Administration of nucleic acid sequence to female animal

专利摘要:
Growth is improved by administering a nucleic acid sequence of GHRH or an analog thereof to a female animal, preferably via a parenteral route of administration, using a growth promoting potential method. Pups born in sows injected with GHRH encoding DNA have greater effect without further vector administration, as evidenced in later pregnancy.
公开号:KR20040039187A
申请号:KR10-2003-7007872
申请日:2001-12-12
公开日:2004-05-10
发明作者:슈바르츠로버트제이；카펜터로버트에이취；드라기아-아클리록상드라；케른더글라스알；스미쓰로이지
申请人:베일러 칼리지 오브 메디신；아드비시스 인코포레이티드；
IPC主号:

专利说明:

Administration of nucleic acid sequence to female animal
[1] This application claims priority to US Patent Provisional Application No. 60 / 255,021, filed December 12, 2000.
[3] Growth hormone (GH) production pathways consist of a series of interdependent genes of products required for normal growth. The GH pathway genes are (1) ligands such as GH and insulin-like growth factor-I (IGF-I), (2) precursors of pit 1 or transcription factors such as prop 1 and pit 1, and (3) growth hormone secretion, respectively. Agonists and antagonists such as hormones (GHRH) and somatostatin and (4) receptors such as GHRH receptors (GHRH-R) and GH receptors (GH-R). These genes are expressed in different organs and tissues including the hypothalamus, pituitary gland, liver and bone. Not only is efficient and regulated expression of the GH pathway essential for optimal primary growth, but also the homeostasis of carbohydrate, protein and fat metabolism GH synthesis and secretion from the anterior pituitary gland is stimulated by GHRH, inhibited by somatostatin, GHRH and somatostatin All are hypothalamic hormones. The central role of GH in regulating somatic cell growth in humans and other vertebrates and the physiologically related pathways regulating GH secretion from the pituitary gland are well known. GH primarily increases the production of IGF-I in the liver and other target organs. IGF-I and GH in turn feed back from the hypothalamus and pituitary gland to inhibit GHRH and GH secretion. GH acts directly and indirectly on peripheral tissues, and the indirect effects are mainly mediated by IGF-I.
[4] There are many clinical conditions in children and adults that respond to GH or GHRH therapy with balanced primary growth (prepubertal patients) or body composition. In all cases the GHRH-GH-IGF-I axis functions but does not necessarily function with optimal sensitivity or reactivity for several possible reasons.
[5] The main feature of GH deficiency in children is the dwarf. Similar phenotypes are seen in non-GH-deleted dwarfs as well as genetic defects at other points in the GH axis (Parks et al., 1995). Non-GH-defectives indicate other pathologies, such as (1) Turner syndrome as a hereditary disease (Jacobs et al., 1990; Skuse et al., 1999), cartilage dysfunction (Tanaka et al., 1998; Key and Gross, 1996) and Crohn's disease (Savage et al., 1999); (2) intrauterine growth disorders (Albanese and Stanhope, 1997; Azcona et al., 1998); And (3) chronic kidney deficiency (Sohmiya et al., 1998; Benfield and Kohaut, 1997). If the GH axis is not affected (ie, the patient has normal hormones, genes and receptors), it accounts for more than 50% of all patients with growth disorders. In these cases, GHRH or GH therapy has been shown to be effective (Gesundheit and Alexander, 1995).
[6] Reduced GH secretion from the anterior pituitary gland causes loss of bone mass in the age group of 25 to old. The GHRH-GH-IGF-I axis undergoes drastic changes in aging and in adults (D'Costa et al., 1993), with reduced GH production rate and GH half-life, and reduced IGF-I response to GH and GHRH stimulation Loss of mass (sarcopenia), osteoporosis and fat gain and weight loss (Bartke, 1998). Previous studies have shown a significant decrease in serum GH and IGF levels by 70-80% from 13-19 years of age in a significant number of normal adults (Corpas et al., 1993; Iranmanesh et al., 1991). The development of muscle loss has been demonstrated to be recoverable with GH therapy. However, this therapy is opposed due to cost and frequent side effects in adults.
[7] The production of recombinant proteins serves as a useful tool for the treatment of these conditions. Although GH replacement therapy is widely used in patients with growth deficiency, it provides satisfactory growth and has a positive mental effect on the child being treated (Rosenbaum and Saigal, 1996; Erling, 1999). For example, impractical (Monti et al., 1997; Heptulla et al., 1997) and undesirable secondary effects of frequent administration of GH (Blethen et al., 1996; Watkins, 1996; Shalet et al., 1997; Allen et al., 1997).
[8] Extracranial secreted GHRH is a mature peptide or truncated molecule (as observed with pancreatic islet cell tumors and variously located carcinoids) and is often known to be biologically active and even cause acromegaly (Esch et al. , 1982; Thorner et al., 1984). Administration of recombinant GHRH to GH-deficient children or adults raises IGF-I levels, increases GH secretion in proportion to the GHRH dose, and induces a response to the clotting dose of GHRH (Bercu and Walker, 1997). Thus, GHRH administration is a more physiological alternative to increasing sub-normal GH and IGF-I levels (Corpas et al., 1993).
[9] Although GHRH protein therapy induces and stimulates the normal GH secretion cycle without substantially causing side effects, the short in vivo half-life of GHRH is frequent (one to three times daily) intravenously, subcutaneously or intranasally (300-fold higher doses). Need. Therefore, GHRH administration is not practical as a long term treatment. However, extracranial secreted GHRH is biologically active as a processed protein species (Tyr1-40 or Tyr1-Leu44) or even as a shorter truncated molecule (Thorner et al., 1984). Importantly, low levels of GHRH in the blood supply (100 pg / ml) stimulate GH secretion (Corpas et al., 1993), whereby GHRH is an excellent candidate for gene therapy expression. Direct plasmid DNA gene transfer is the basis of many gene therapy strategies currently being discussed, and thus do not require viral genes or lipid particles (Muramatsu et al., 1998; Aihara and Miyazaki, 1998). Bone muscle is a preferred target tissue because of its long lifespan and can be transduced by circular DNA plasmids expressed over months or years in immunocompetent hosts (Davis et al., 1993; Tripathy et al., 1996). Previous reports have demonstrated that human GHRH cDNA can be delivered by muscle expression vectors injectable into the muscles of mice, in which case GHRH moderately stimulated GH secretion over two weeks (Draghia-Akli et al. , 1997).
[10] Wild type GHRH has a relatively short half-life in the circulation of humans (Frohman et al., 1984) and livestock. 95% of GHRH (1-44) NH2 is degraded after 60 minutes of incubation in plasma, while under similar conditions, the shorter (1-40) OH form of the hormone shows only 77% of degradation after 60 minutes of culture ( Frohman et al., 1989). Insertion of a coding cDNA of a specific protease-resistant GHRH analog into a gene therapy vector leads to molecules with longer half-lives, increased potency in serum and provides more GH secretion in plasmid injected animals (Draghia-Akli et al. , 1999, incorporated herein by reference). Mutagenesis through amino acid substitutions of protease sensitive amino acids extends the serum half-life of the hGHRH molecule. In addition, increased biological activity of GHRH is achieved using super-active analogues that can increase binding affinity for specific receptors (Draghia-Akli et al., 1999).
[11] Novel GHRH analogue proteins for the purpose of increasing the secretion of growth hormone (US Pat. Nos. 5,847,066; 5,846,936; 5,792,747; 5,776,901; 5,696,089; 5,486,505; 5,137,872; 5,084,442; 5,036,045; 5,023,322; 4,839,344; 4,410,512; RE33,699 or synthetic or natural peptide fragments of GHRH (US Pat. Nos. 4,833,166; 4,228,158; 4,228,156; 4,226,857; 4,224,316) 4,223,021; 4,223,020; 4,223,019). GHRH analogs have been reported containing the following mutations (US Pat. No. 5,846,936): Tyr at position 1 is His; Ala at position 2 is Val, Leu or others; Asn at position 8 is Gln, Ser, or Thr; Gly at position 15 is Ala or Leu; Met at position 27 is Nle or Leu; And Ser at position 28 is Asn. GHRH analogs that are the subject of U.S. Patent No. 60 / 145,624 (incorporated herein by reference) do not contain all amino acid substitutions as required for activity and reported in U.S. Patent No. 5,846,936. The invention of U.S. Patent No. 60 / 145,624 differs from U.S. Patent No. 5,756,264 in two respects. First, the invention of U.S. Patent Application No. 60 / 145,624 improves the function as a GH secretagogue (i.e., prolongs the therapeutic effect ability, thereby reducing the sensitivity and increasing the stability to proteases; and Increase in biological activity) and with analogues of wild type and other growth hormone secreting hormones. Analogs of U.S. Patent No. 60 / 145,624 have no substitution with Gln, Ser or Thr at position 8 present in the GHRG analogs of U.S. Patent 5,756,264. In addition, the invention of U.S. Patent Application 60 / 145,624 contains, in one aspect, a proximal serum response element (SRE) from a skeletal α-actin, multiple MEF-2 sites, a MEF-1 site and a TEF-1 binding site and a natural muscle composition. DNA encoding a GHRH analogue linked to a specific synthetic promoter called SPc5-12 (Li et al., 1999) that significantly surpasses the transcriptional efficacy of the promoter. The specificity of such synthetic promoters is a significant improvement over, for example, patents on muscle promoters and their use (eg US Pat. No. 5,374,544) or systems for muscle expression of nucleic acid sequences (eg US Pat. No. 5,298,422). .
[12] US Pat. No. 5,061,690 relates to increasing birth weight and milk production by feeding an effective amount of hGRF or one of its analogs to a pregnant female mammal for 10 to 20 days. Application of the analog continues throughout the lactation period. However, several administrations are presented and there is no description of administration of growth hormone secreting hormone (or factor) as a DNA molecule as in gene therapy techniques.
[13] U.S. Patent Nos. 5,134,120 and 5,292,721 similarly do not provide techniques for the administration of growth hormone secreting hormones in the form of DNA. These patents also relate to multiple administrations of recombinant protein GH within the last two weeks of conception and within three weeks of birth. There is also no discussion of any non-wild type forms as provided in the present invention.
[14] Administration of growth hormone (GH) to livestock enhances lean tissue tissue erosion and / or milk production while increasing feeding efficiency (Etherton et al., 1986; Klindt et al., 1998). Many studies have shown that GH significantly reduces the amount of carcass fat, and consequently, meat quality increases. However, long-term GH administration has practical and physiological limitations and potentially diminishes its usefulness and utility (Chung et al., 1985; Gopinath and Etherton, 1989). Experimental GH-secreting hormone (GHRH) was used as a more physiological alternative. For large species such as pigs or cows, the use of GHRH, an upstream stimulator of GH, is an alternative that can increase production efficiency from substantial and metabolic aspects, as well as growth and milk production, more importantly (Dubreuil et al., 1990). Farmer et al., 1992). However, the high cost and required frequency of administration of recombinant peptides currently limits the use of this treatment. Their main disadvantage can be avoided by using gene therapy which induces translocation production of GHRH, provided that its production can last long term. Pituitary tissue-specific expression of the GHRH gene is not required for activity as extracranial secreted GHRH may be biologically active (Faglia et al., 1992; Melmed, 1991). Gene therapy that delivers GHRH is advantageous because genes, cDNAs, and natural and several mutated molecules are well characterized in pigs, cows, and many other species, and treatment decisions are easy and accurate. Osteotomy is a perfect candidate for target tissue because intramuscular injection can be easily performed in an industrial setting, the longevity of myofibrils and transduced by circular DNA plasmids (Bettan et al., 2000; Everett et al., 2000). Thus, there is no need for re-administration and transgenes can be efficiently expressed over months or years in immunocompetent hosts (Wolff et al., 1992).
[15] Summary of the Invention
[16] In one aspect of the invention, the promoter, nucleotide sequence and 3 ′ non-toxic region are provided with an effective amount of a vector comprising the nucleotide sequence expressed and under the conditions that the introduction and expression of the vector provides improved or enhanced growth results for progeny. Methods of improving or enhancing the growth of offspring from a female animal are provided, including introducing into or before the conception of a female offspring into the cells of the female animal. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In yet another particular embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another particular embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another particular embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny conceived. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another specific embodiment, administration of the ligand is oral administration.
[17] In a further aspect of the present invention, an effective amount of a vector comprising a promoter, a nucleotide sequence and a 3 ′ non-toxic region, under conditions in which the nucleotide sequence is expressed and the introduction and expression of the vector results in an increase in the growth hormone levels of the offspring A method of increasing growth hormone levels of a descendant from a female animal is provided, the method comprising introducing into the cells of the female animal before or during the conception of the female descendant. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In yet another particular embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another particular embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another particular embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny conceived. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another particular embodiment, the administration of the ligand is oral administration.
[18] In another aspect of the invention, a female, comprising an effective amount of a vector comprising a promoter, a nucleotide sequence and a 3 ′ non-toxic region, under conditions where the nucleotide sequence is expressed and the introduction and expression of the vector provides increased lean body mass results. Methods of increasing lean body mass of a descendant from a female animal are provided, including introducing into or before the conception of a female descendant into the cells of the animal. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In yet another particular embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another particular embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another particular embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny concept. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another particular embodiment, the administration of the ligand is oral administration.
[19] In another aspect of the invention, a promoter, nucleotide sequence and 3 ′ non-toxic region of a vector comprising a nucleotide sequence is expressed under conditions in which the nucleotide sequence is expressed and the introduction and expression of the vector provides increased IGF-I levels of descendants. A method of increasing the level of IGF-I in a descendant from a female animal is provided, including introducing an effective amount into or before the conception of the female offspring into the cells of the female animal. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In yet another particular embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another particular embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another specific embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny conceived. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another particular embodiment, the administration of the ligand is oral administration.
[20] In still another aspect of the invention, a promoter, nucleotide sequence and 3 ′ non-toxic region of a vector comprising a nucleotide sequence is expressed under conditions in which the nucleotide sequence is expressed and the introduction and expression of the vector provides increased feed efficiency results in progeny. A method of increasing feed efficiency of a descendant from a female animal is provided, including introducing an effective amount into or before the conception of the female offspring into the cells of the female animal. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In yet another particular embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another particular embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another particular embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny conceived. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another particular embodiment, the administration of the ligand is oral administration.
[21] In another embodiment of the invention, the promoter, nucleotide sequence and 3 ′ non-toxic region are provided with an effective amount of a vector comprising the nucleotide sequence expressed and under the conditions that the introduction and expression of the vector provides increased growth rate results for progeny. A method of increasing the rate of growth of a descendant from a female animal is provided, including introducing into or before the conception of the female offspring into the cells of the female animal. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In yet another particular embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another specific embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another particular embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny conceived. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another particular embodiment, the administration of the ligand is oral administration.
[22] In another aspect of the invention, the promoter, nucleotide sequence, and 3 ′ non-toxic region are characterized in that the nucleotide sequence is expressed and the introduction and expression of the vector provides increased growth hormone secretion cells to other hormone-producing cell ratios of descendants. Under conditions, introducing an effective amount of the comprising vector into the cells of the female animal before or during the conception of the female offspring, thereby increasing the ratio of growth hormone secreting cells to other hormone-producing cells in the pituitary gland of the female offspring. A method is provided. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In another further specific embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another particular embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another particular embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny conceived. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another particular embodiment, the administration of the ligand is oral administration.
[23] In another embodiment of the present invention, a female animal comprising a promoter, a nucleotide sequence and a 3 ′ non-toxic region, under conditions in which the nucleotide sequence is expressed and the introduction and expression of the vector provides a delayed birth result of the offspring, the female animal A method of delaying the birth of a descendant from a female animal is provided, including the step of introducing prior to or during the conception of a female descendant into the cells of the female. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In yet another particular embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another particular embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another particular embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny conceived. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another particular embodiment, the administration of the ligand is oral administration. In certain embodiments, the hormone producing cells are selected from the group consisting of adrenal cortical hormone secreting cells, prolactin secreting cells and gonadotropin secreting cells.
[24] In another embodiment of the present invention, an effective amount of a vector comprising a promoter, a nucleotide sequence and a 3 ′ non-toxic region, under conditions where the nucleotide sequence is expressed and the introduction and expression of the vector provides increased milk production results in the animal. A method of increasing milk production in an animal is provided, including introducing into an animal's cells. In certain embodiments, the cells of said female animal comprise diploid cells. In another particular embodiment, the cells of the female animal comprise muscle cells. In a further particular embodiment, the nucleic acid sequence encodes a growth hormone secreting hormone or analogue thereof. In yet another particular embodiment, the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8 or an individual analog thereof. In another further particular embodiment, the promoter comprises a synthesized muscle promoter. In yet another particular embodiment, the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region. In another further particular embodiment, the vector is introduced into the cells of a female animal via electroporation, viral vectors, binding to a carrier or parenteral route. In yet another particular embodiment, the female animal is a human, pet, farm animal, edible animal or working animal. In a further particular embodiment, the female animal is human, pig, cow, sheep, goat or chicken. In yet another particular embodiment, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In another particular embodiment, the vector is introduced into the female in a single dose. In another further embodiment, the introduction occurs in a 6-9 month period of progeny conceived. In another further particular embodiment, the method comprises administering to the female a ligand for a growth hormone secretagogue receptor. In another particular embodiment, the administration of the ligand is oral administration.
[25] Other and further objects, features, and advantages will be apparent and more readily understood with reference to examples of preferred embodiments of the invention provided for the purpose of the accompanying drawings or the description, which read the following specification and constitute a part thereof.
[2] The present invention relates generally to endocrinology, medicine and cell biology. More specifically, the present invention provides for the development of growth and function, i.e., the growth of growth hormone production in an animal using administration of DNA encoding stimulation and growth hormone secretion hormone to female animals at levels above those associated with normal growth. It's about promotion. The invention also relates to the application of nucleotide sequences that promote growth, particularly growth hormone secreting hormones or analogs thereof, regulated by muscle-specific promoters into muscle tissue using electroporation techniques.
[26] 1A-1C demonstrate that GHRH super-active analogues increase GH secretagogue activity and stability. 1A compares the pig wild type (1-40) OH amino acid sequence with analog HV-GHRH. 1B shows the effect of different GHRH species on porcine GH secretion in porcine primary pituitary cultures. 1C demonstrates the change in stability that occurred in HV-GHRH and wild-type porcine GHRH over 6 hours of incubation.
[27] 2A-2E demonstrate an increase in GHRH, GH and IGF-I serum levels over two months after a single injection of the super-active analog GHRH muscle expression vector. 2A depicts a construct containing a SPc5-12 synthetic promoter and a 3 ′ UTR of GH. As a model of the mutated protein, an HV-GHRH construct was used and compared with the pig wild type as a positive control and the β-galactosidase construct as a negative control. 2B depicts the relative serum GHRH levels in pSP-GHRH injected pigs versus placebo injected control pigs. 2C demonstrates serum GHRH absolute levels in control pigs corrected for pSP-GHRH injected pigs versus weight / blood dose increase. 2D shows the change in GH levels in pigs injected with pSP-HV-GHRH. 2E shows plasma IGF-I levels after direct intramuscular injection of pSP-GHRH construct.
[28] 3A-3C demonstrate the effect of muscle GHRH expression vectors on pig growth. 3A shows the mean weight change of pigs for 2 months after injection of pSP-GHRH or pSP-HV-GHRH into pigs. 3C compares pSP-HV-GHRH injected pigs and placebo injected control pigs over 45 days post injection.
[29] 4 shows the effect of different amounts of pSP-HV-GHRH injected on 10-day-old young pigs on IGF-I levels.
[30] 5 shows the effect of different amounts of pSP-HV-GHRH injected on 10-day-old young pigs on IGF-I levels.
[31] 6 illustrates the time course for injection of the pSP-HV-GHRH plasmid into young pigs.
[32] FIG. 7 illustrates another preferred embodiment of the invention versus an external caliper electrode for the injectable electrode. At the top is an illustration of an external caliper electrode with a 2 square plate / 1.5 cm side. Shown below is a 6-needle arrangement with a 2 cm long, 18-26 g needle present in a 1 cm diameter array. The left side is from the side and the right side is from the bottom.
[33] 8 demonstrates the newborn weight of control and experimental young pigs.
[34] Figure 9 illustrates the body weight at weaning time of the experimental and control young pigs.
[35] FIG. 10 compares the weights of control groups reared with hybrids to the injected animals and their litters.
[36] FIG. 11 compares the body weights of young pigs from GHRH-treated sows reared in control sows with their litters.
[37] FIG. 12 illustrates the overall increase in body weight for the control fed to control sows.
[38] Figure 13 compares experimental and control meat weights.
[39] FIG. 14 illustrates the weight of offspring at 3, 10 and 24 weeks.
[40] 15 shows muscle weight per body weight at 3 weeks of age.
[41] Figure 16 demonstrates pituitary body weight per body weight of offspring.
[42] Figure 17 shows RNA analysis of GH, GHRH and PRL of descendants and demonstrates that GHRH acts as a growth factor in the pituitary gland.
[43] 18 illustrates DAB staining of GH-secreting cells.
[44] FIG. 19 demonstrates IGF-I concentrations of offspring at 3, 12, and 6 months.
[45] It will be apparent to those skilled in the art that the invention described herein may be variously substituted and modified without departing from the scope and spirit of the invention.
[46] The term indefinite article (a or an) as used herein may mean one or more. When used in combination with the word "comprising" as used in the claims, the indefinite article (a or an) may mean two or more.
[47] As used herein, the term "animal" includes all species of animals. In a preferred embodiment, the animals are more specifically humans, wild animals, pets (birds, dogs, cats, horses), animals used for work (horses, cows, dogs) and animals that feed food (chicken, Cattle, fish), livestock (pigs, horses, cattle, sheep, chickens), or animals of their own food (frog, chicken, fish, crab, crayfish), shrimp, shellfish, scallops, goats, boar, cattle, sheep, sows , Ostrich, emu, eel) and other animals well known in the art.
[48] As used herein, the term "effective amount" is defined as the amount of composition necessary to effect on a host that can be monitored using several endpoints known to those skilled in the art. In certain embodiments, these endpoints are alternative labels.
[49] As used herein, the term “feed conversion efficiency” is defined as the amount of body weight an animal gains relative to the amount of food the animal consumes each day. The term "efficiency" or "feed efficiency" as used herein may be interchanged with "feed conversion efficiency".
[50] As used herein, the term “growth deficiency” is defined as a medical condition, medical condition or disease in which growth is less than normal. Deficiency may be a departure result that directly affects the growth hormone pathway (eg, the GHRH-GH-IGF-I axis), indirectly affects the growth hormone pathway, or does not affect the growth hormone pathway at all. .
[51] The term "growth hormone" as used herein relates to growth and is defined as a hormone that acts as a chemical transporter and acts on target cells.
[52] The term "growth hormone secreting hormone" as used herein is defined as a hormone that promotes or stimulates the secretion of growth hormone.
[53] As used herein, the term “growth hormone secreting hormone analog” refers to a function that contains amino acid variations and / or deletions that are not naturally present in the GHRH molecule in its native form (no synthetic dextrose or cyclic amino acids). It is defined as a protein that maintains and enhances the synthesis and secretion of growth hormone.
[54] The term "growth hormone secretagogue receptor" (GHS-R) as used herein is defined as a receptor for small synthetic compounds that is directly or indirectly associated with the secretion of growth hormone from the pituitary gland.
[55] As used herein, the term "lean fat mass" is defined as the body mass of an animal belonging to adipose tissue, such as muscle.
[56] As used herein, the term “ligand for growth hormone secretagogue receptor” is defined as a compound that acts as an agonist against growth hormone secretagogue receptor. Ligands may be synthetic or natural. Ligands can be peptides, proteins, sugars, carbohydrates, lipids, nucleic acids or combinations thereof.
[57] The term "muscle" as used herein specifically refers to muscle tissue.
[58] As used herein, the term "neonatal" refers to an animal at all maturity or growth stages immediately after and after birth.
[59] As used herein, the term "offspring" refers to offspring, including fetuses or newborns.
[60] The term "parenteral" as used herein refers to a mechanism other than the intestine for introducing a substance into an animal. In certain embodiments, parenterals include subcutaneous, intramuscular, intravenous, intradural, intraperitoneal and other methods.
[61] As used herein, the term “pharmaceutically acceptable” refers to a compound that is acceptable to the recipient animal when administered.
[62] As used herein, the term “secretagogue” refers to a natural or synthetic molecule that increases the synthesis and secretion of a reduced-regulated molecule (eg, GHRH is a secretagogue of GH).
[63] As used herein, the term “growth hormone secreting cell” refers to a cell that produces growth hormone.
[64] As used herein, the term "therapeutically effective amount" refers to a dose of a physiologically significant compound. If the presence of a substance causes a technical change in the physiology of the recipient animal, the substance is physiologically significant. For example, in the treatment of growth deficiency, a composition that enhances growth may be therapeutically effective; For consumable diseases, compositions that can reduce loss or increase growth are therapeutically effective.
[65] As used herein, the term "vector" refers to a vehicle that delivers nucleic acid into a cell or organism. Examples thereof include plasmids, viral vectors, liposomes or cationic lipids. In certain embodiments, liposomes and cationic lipids are adjuvants (carriers) that can form complexes with other vectors to increase uptake of plasmids or viral vectors by target cells. In a preferred embodiment, the vector comprises a nucleotide sequence encoding a promoter, preferably a growth hormone secreting hormone, or an analog thereof and a 3 ′ untranslated region. In another preferred embodiment, the promoter, nucleotide sequence, and 3 ′ nontoxic region are operably linked for expression in eukaryotic cells.
[66] As used herein, the term "consumable condition" is defined as the condition and condition associated with wasting disease or chronic wasting disease.
[67] This application is related to the subject matter of US Provisional Patent Application No. 60 / 145,624, filed July 26, 1999, and US Patent Application No. 09 / 624,268, filed July 24, 2000. These patent applications are incorporated herein by reference.
[68] To evaluate the growth effect of growth hormone secretion hormone (GHRH) gene usage, muscles containing wild type (pSP-wt-GHRH) or mutated (pSP-HV-GHRH) GHRH cDNA in sows 6-9 months of pregnancy. Vector 10 mg was injected. Following the injection, electroporation was given. Non-injected / electropored sows were used as controls. Young pigs from GHRH injected sows were larger at birth (mean 1.65 ± 0.06 kg HV-GHRH, p <0.00002 and 1.46 ± 0.05 kg wt-GHRH, p <0.0014, control 1.27 ± 0.02 kg). Cross parenting studies were conducted. The offspring of sows injected at weaning were larger than controls. The cross-bred control sucked from sows injected was significantly larger than litters. This continued and the offspring of the injected sows were 135.7 kg for HV-GHRH and 129.3 kg for wt-GHRH at 170 days postnatal. Several biochemical measures were performed on young pigs. In the sows of injected sows, total protein increased, blood urea levels decreased at all time points throughout the test period, and both constants demonstrated improved protein metabolism. Creatinine concentrations were normal, indicating normal kidney function. Glucose and insulin levels were normal. Thus, sows pups treated with gene therapy using plasmid DNA constructs encoding GHRH show growth patterns above normal levels up to at least 170 days after birth and are lean body mass while maintaining normal homeostasis. This increase likewise contributes to increased milk production and deformation of the hypothalamic pituitary axis of the posterior bovine. This evidence of key experiments demonstrates that plasmid mediated delivery can be used to enhance the characteristics of certain animals throughout generations while avoiding the side effects associated with classical protein treatment.
[69] As an aspect of the present invention, it is possible to increase growth, promote growth, increase feed conversion rate, increase lean body mass, increase IGF-I levels, increase growth rate, growth hormone secretory cells versus other hormones- Nucleic acid sequences are used in the methods of the invention that increase the proportion of producing cells, delay procreation or increase milk production in female offspring. In certain embodiments, the nucleic acid sequence is a growth hormone secretion hormone, IGF-I, prolactin or an analog thereof. The female may be a surrogate mother, such as a mother, a female who has never had a pregnancy or childbirth or a pregnancy by placental transplantation.
[70] Preferred embodiments of the invention utilize growth hormone-secreting hormone analogs having the amino acid sequence of SEQ ID NO: 1 or SEQ ID NO: 8 (wt GHRH). The term "wild type" as used herein may be an endogenous form of GHRH of all animals or may be a slightly modified form of a hormone such as porcine GHRH. One skilled in the art knows that endogenous GHRH has 44 amino acids and amide groups at the ends, and the exact notation of this form is (1-44) NH ₂ -GHRH. In certain embodiments, forms having only 40 amino acids (lacking the last 4 amino acids) and also not containing an amide group are used and may be designated (1-40) OH-GHRH. As used herein, this form is wild type because it does not contain internal mutations as compared to wild type sequences, as opposed to other forms discussed herein (eg HV) having internal mutations introduced by site directed mutagenesis. May also be mentioned. Those skilled in the art will appreciate that forms 1-40 and shorter forms (e.g. 1-32 or 1-29) are naturally present in humans and other mammals (even other types of GHRH-secreting tumors) and are native (1-44) NH ₂ It is known that it has similar activity to. As a preferred embodiment of the present invention, GHRH with increased stability compared to wild type GHRH is used.
[71] In another embodiment, other species of GHRH or analogs of GHRH are within the scope of the present invention. For the purposes of the present invention, residues encoded by DNA are not modified after translation under the nature of nucleic acid administration.
[72] The following species are within the scope of the present invention. US Pat. No. 4,223,019 discloses the amino acid sequence NH ₂ --Y--Z--E--G--J-COOH, wherein Y is selected from the group consisting of D-lysine and D-arginine; Z and J are Is independently selected from the group consisting of tyrosine, tryptophan and phenylalanine; E and G are independently selected from the group consisting of D-tyrosine, D-tryptophan and D-phenylalanine). . US Pat. No. 4,223,020 discloses the amino acid sequence NH ₂ --Y--Z--E--G-COOH, wherein Y and G are independently selected from the group consisting of tyrosine, tryptophan and phenylalanine; Z and E Are independently selected from the group consisting of D-tyrosine, D-tryptophan and D-phenylalanine). US Pat. No. 4,223,021 discloses the amino acid sequence NH ₂ --Y--Z--E--G--J-COOH, wherein Y and G are independently selected from the group consisting of tyrosine, tryptophan and phenylalanine; Z is selected from the group consisting of glycine, alanine, valine, leucine, isoleucine, proline, hydroxyproline, serine, threonine, cysteine and methionine; E and Z are independently D-tyrosine, D-tryptophan and D Peptapeptides are selected from the group consisting of -phenylalanine. U.S. Pat. No. 4,224,316 discloses the amino acid sequence NH ₂ -YZEGJ-COOH, wherein Y and E are independently selected from the group consisting of D-tyrosine, D-tryptophan and D-phenylalanine; Z and G are tyrosine, tryptophan And phenylalanine; J is glycine, alanine, valine, leucine, isoleucine, proline, hydroxyproline, serine, threonine, cysteine, methionine, aspartic acid, glutamic acid, asparagine, glutamine, arginine and Pentapeptides are selected from the group consisting of lysine. U.S. Patent No. 4,226,857 discloses the amino acid sequence NH ₂ -YZEGJ-COOH, wherein Y and G are independently selected from the group consisting of tyrosine, tryptophan and phenylalanine; Z and J are independently D-tyrosine, D -Is selected from the group consisting of tryptophan and D-phenylalanine; E is glycine, alanine, valine, leucine, isoleucine, proline, hydroxyproline, serine, threonine, cysteine, methionine, aspartic acid, glutamic acid, asparagine, Pentapeptides are selected from the group consisting of glutamine and histidine). US 4,228,155 discloses the amino acid sequence NH ₂ -YZEGJ-COOH, wherein Y is selected from the group consisting of tyrosine, D-tyrosine, tryptophan, D-tryptophan, phenylalanine and D-phenylalanine; Independently, it is selected from the group consisting of D-tyrosine, D-tryptophan and D-phenylalanine; G is selected from the group consisting of lysine and arginine; J is glycine, alanine, valine, leucine, isoleucine, proline, Pentapeptides are selected from the group consisting of hydroxyproline, serine, threonine, cysteine and histidine. U.S. Patent No. 4,228,156 discloses the amino acid sequence NH ₂ -YZE-COOH, wherein Y and Z are independently selected from the group consisting of D-tyrosine, D-tryptophan and D-phenylalanine; E is tyrosine, tryptophan and phenylalanine Is selected from the group consisting of. U.S. Patent No. 4,833,166 discloses a synthetic peptide having the formula H-Asp-Pro-Val-Asn-Ile-Arg-Ala-Phe-Asp-Asp-Val-Leu-Y, wherein Y is OH or NH ₂ ; Non-toxic salts and formulas H-Val-Glu-Pro-Gly-Ser-Leu-Phe-Leu-Val-Pro-Leu-Leu-Pro-Val-His-Asp-Phe-Val-Gln-Gln-Phe-Ala Synthetic peptides with -Gly-Ile-Y, wherein Y is OH or NH _2, or nontoxic salts thereof, are described. Draghia-Akli et al. (1997) initially described the 228-bp fragment of hGHRH encoding the 31-amino acid signal peptide described by Mayo et al. (1995) and the fully mature peptide human GHRH (1-44) OH (Tyr1-Leu44). Use Guillemin et al. (1992) also determine the sequence of human pancreatic growth hormone secretion factor (hpGRE).
[73] A further aspect of the present invention is a method for improving the growth capacity of (1) offspring; (2) stimulating offspring's growth hormone production to levels higher than those associated with normal growth; And (3) a method of increasing growth of offspring. All these methods include introducing a plasmid vector into the mother of the offspring during or during the pregnancies of the offspring, wherein the vector is a sequentially operably linked promoter, nucleotide sequence (eg , SEQ ID NO: 1 or SEQ ID NO: 8) and 3 'non-toxic region.
[74] In a further particular embodiment, a vector comprising a 3 'untranslated region and a nucleotide sequence encoding a sequentially operably linked promoter, sequence 1 or sequence 8, at appropriate distances for functional expression, is subjected to Methods are provided for stimulating progeny growth hormone production at levels above that associated with normal growth, including introducing into the mother. More levels than those associated with normal growth include basal, intrinsic growth of animals at growth levels similar to other similar animals in the colony, including growth-associated deficiency animals or animals without growth-related deficiencies.
[75] In a preferred embodiment, an effective amount of a vector comprising a promoter, a nucleotide sequence encoding SEQ ID NO: 1 or SEQ ID NO: 8, and a 3 'untranslated region is inserted into the animal by a suitable distance for appropriate expression for functional expression. Provided are methods for enhancing growth. Animals whose growth is enhanced may or may not have growth deficiency.
[76] It is an object of the present invention to increase the growth and / or growth rate of offspring from animals, preferably mothers. In a preferred embodiment, the growth and / or growth rate of the animal proceeds for a long time, such as more than a few weeks or more than several months. In a particular embodiment, this is achieved by administering growth hormone secreting hormone to the mother of the offspring, preferably in the form of a nucleic acid. In a preferred embodiment, GHRH nucleic acids are maintained as episomes in muscle cells. In certain embodiments, an increase in GHRH affects the pituitary gland by increasing the number of growth hormone producing cells, thus causing changes in their cell lineage. In certain embodiments, the proportion of growth hormone secreting cells (growth hormone producing cells) is increased compared to other hormone producing cells in the pituitary gland, such as adrenal cortical stimulating hormone secreting cells, prolactin secreting cells, gonadotropin secreting cells and the like. In certain embodiments, the increase in growth hormone associated with an increase in the number of growth hormone-producing cells is reflected in the increase in IGF-I levels. In another particular embodiment, an increase in growth hormone levels is associated with an increase in lean body mass and an increase in the rate of growth of offspring. In another particular embodiment, the increase in lean body mass is associated with an increase in bone line growth. In a further particular embodiment, the feed conversion rate of descendants is increased. In another particular embodiment, the birth of offspring is delayed, and in a preferred embodiment it is associated with an improved or increased growth rate of the fetus.
[77] In a preferred embodiment, the promoter is a synthetic muscle promoter and the hGH 3 ′ nontoxic region is in the 3 ′ nontoxic region. However, the 3 ′ non-toxic region may be from any natural or synthetic region. In a particular embodiment of the invention, it contains a proximal serum response element (SRE) from bone α-actin, multiple MEF-2 sites, MEF-1 sites and TEF-1 binding sites and significantly exceeds the transcriptional efficacy of native muscle promoters. A synthetic promoter called SPc5-12 (Li et al., 1999) (SEQ ID NO: 6) is used. In a preferred embodiment, the promoters used in the present invention do not cease or significantly decrease activity by endogenous cell mechanisms or factors. Other elements including trans-acting factor binding sites and enhancers can be used in accordance with this aspect of the invention. In another embodiment, natural root promoters are used and those skilled in the art are familiar with how to obtain such promoter sequences from a GenBank database of the National Center for Biotechnology Information (NCBI) or from a database including the NCBI PubMed site. Those skilled in the art can use these world wide web sites to obtain sequences or documents related to the present invention.
[78] In certain embodiments, the hGH 3 ′ non-toxic region (SEQ ID NO: 7) is used in nucleic acid vectors such as plasmids.
[79] In certain embodiments, the vector is selected from the group consisting of plasmids, viral vectors, liposomes and cationic lipids. In a more particular embodiment, the vector is introduced into muscle cells or muscle tissue. In a further particular embodiment, the animal is a human, pet, working animal or an edible animal.
[80] In addition to certain embodiments of introducing such a construct into an animal via a plasmid vector, a delivery system for transfecting nucleic acids into an animal known in the art or a cell thereof may be used. For example, other non-viral or viral methods can be used. Those skilled in the art recognize that a target system in a nonviral form of DNA or RNA requires four components: 1) the DNA or RNA of interest; 2) residues that recognize and bind to cell surface receptors or antigens; 3) DNA binding residues; And 4) soluble residues that allow the transport of the complex from the cell surface to the cytoplasm. In addition, liposomes and cationic lipids can be used to deliver therapeutic gene combinations to achieve the same effect. Potential viral vectors include expression vectors derived from viruses such as adenoviruses, vaccinia viruses, herpes viruses, and bovine papilloma viruses. Also, episomal vectors can be used. Other DNA vectors and transfer systems are known in the art.
[81] One skilled in the art knows that expression vectors derived from various bacterial plasmids, retroviruses, adenoviruses, herpes or vaccinia viruses can be used to deliver nucleotide sequences to target organs, tissues or cell populations. Methods well known to those skilled in the art can be used to construct recombinant vectors that express genes encoding growth hormone secreting hormone analogs. Transient expression can persist for more than a month with a non-replicating vector and can last longer if the appropriate replication element is part of the vector system.
[82] It is an object of the present invention to provide a regimen in which a single administration of growth hormone secreting hormone is sufficient for several gestation periods and also enhances young pig performance on meat weight with increased growth and altered body composition.
[83] Nucleic acid
[84] 1. Vector
[85] As used herein, the term “vector” refers to a carrier nucleic acid molecule that can be inserted to introduce a nucleic acid sequence into a cell that the vector can replicate and express the nucleic acid sequence. Nucleic acid sequences can be exogenous, meaning that they are exogenous to the cell into which the vector is introduced or are homologous to a sequence located in the nucleic acid of a host cell in the cell but no sequence is normally found. Vectors include plasmids, cosmids, viruses (vector bacteriophages, animal viruses and plant viruses) and artificial chromosomes (eg YAC). One skilled in the art can construct vectors through standard recombinant techniques, which are described in Maniatis et al., 1988 and Ausubel et al., 1994. All of which are incorporated herein by reference.
[86] The term "expression vector" refers to a vector containing a nucleic acid sequence encoding at least a portion of a gene product that can be transcribed. In certain embodiments, the nucleic acid sequence encodes some or all of the GHRH. In some cases, RNA molecules are translated into proteins, polypeptides or peptides. In other cases they are not translated, eg, in the production of antisense molecules or ribozymes. Expression vectors can contain a variety of “regulatory sequences,” which refer to nucleic acid sequences necessary for the transcription and possible translation of coding sequences operably linked in a particular host organism. In addition to regulatory sequences that control transcription and translation, vectors and expression vectors may provide other functions and contain nucleic acid sequences as described herein.
[87] In a preferred embodiment, the vector of the present invention is a plasmid comprising a nucleotide sequence encoding a synthesized muscle (muscle-specific) promoter, a growth hormone secreting hormone or an analog thereof and a 3 ′ non-toxic region. In another embodiment, the vector is a viral vector, such as an adeno-associated virus, adenovirus or retrovirus. As another aspect, the skeletal alpha-actin promoter, myosin light chain promoter, cytomegalobarus promoter or SV40 promoter can be used. In another embodiment, human growth hormone, bovine growth hormone, SV40 or skeletal alpha actin 3 ′ non-toxic regions are used in the vector.
[88] a. Promoter and Enhancer
[89] A "promoter" is a regulatory sequence that is a region of a nucleic acid sequence whose transcription initiation and rate are regulated. It may contain genetic elements to which regulatory proteins and molecules can bind, such as RNA polymerase and other transcription factors. The terms “operably positioned”, “operably linked”, “under control” and “under transcription control” refer to the exact operating position and / or relative to the nucleic acid sequence in which the promoter controls transcription initiation and / or expression of the sequence. Means in direction. A promoter may or may not be used in conjunction with an enhancer, which refers to a cis-functional regulatory sequence involved in transcriptional activation of the nucleic acid sequence.
[90] The promoter may be one of the native coding sequences located upstream of the coding fragment and / or exon. Such promoters are endogenous. Similarly, an enhancer may be one that is naturally associated with a nucleic acid sequence located upstream or downstream of that sequence. Alternatively, certain advantages can be obtained by placing the coding nucleic acid fragments under the control of a recombinant or heterologous promoter. Such a promoter refers to a promoter that is not normally associated with a nucleic acid sequence in its natural environment. Such promoters or enhancers may include those promoters or enhancers of other genes, promoters or enhancers isolated from other prokaryotic, viral or prokaryotic cells, and mutations that do not exist naturally, ie, alter other elements and / or expression of different transcriptional regulatory regions. Containing promoters or enhancers. In addition to the synthetic production of nucleic acid sequences of promoters and enhancers, sequences can be prepared using nucleic acid amplification techniques and / or recombinant cloning, including PCR ^™ , in connection with the compositions described herein (see US Patent No. 4,683,202 and 5,928,906, the contents of which are incorporated herein by reference). In addition, regulatory sequences may also be used that direct transcription and / or expression of sequences in nonnuclear organelles such as mitochondria, chloroplasts and the like.
[91] Naturally, it is important to use promoters and / or enhancers that effectively direct the expression of DNA fragments in cell types, organelles and organisms selected for expression. The skilled artisan of molecular biology generally knows the use of a combination of promoters, enhancers and cell types for protein expression (Sambrook et al. (1989)-the contents of which are incorporated herein by reference). The promoters used may be constitutive, tissue-specific, inducible and / or useful under appropriate conditions that induce high levels of expression of the introduced DNA fragments as advantageous in mass production of recombinant proteins and / or peptides. Promoters can be heterogeneous or endogenous. In a particular embodiment, the promoter is a muscular promoter synthesized as described in Li et al (1999).
[92] Assays to characterize the identity of tissue-specific promoters or elements as well as their activity are well known to those skilled in the art. Examples of such regions include human LIMK2 gene (Nomoto et al. 1999), somatostatin receptor 2 gene (Kraus et al. 1998), rat epididymal retinic acid-binding gene (Lareyre et al., 1999), human CD4 (Zhao-Emonet et al. 1998), mouse alpha 2 (XI) collagen (Tsumaki, et al., 1998), D1A dopamine receptor gene (Lee, et al., 1997), insulin-like growth factor II (Wu et al., 1997) ), Human platelet endothelial cell adsorption molecule-1 (Almendro et al., 1996).
[93] b. Initiation signal and internal liposome binding site
[94] Certain initiation signals may also be required for efficient translation of coding sequences. These signals include ATG start codons or contiguous sequences. Exogenous detoxification control signals, including ATG start codons, may need to be provided. One skilled in the art can readily determine this and provide the necessary signal. It is well known that the initiation codon must be within the frame of reading of the desired coding sequence to ensure translation of the complete insert. Exogenous detoxification control signals and initiation codons can be natural or synthetic. Expression efficiency can be enhanced by including appropriate transcriptional enhancer elements.
[95] In certain embodiments of the invention, internal ribosomal entry site (IRES) elements are used to generate multigene or polycistronic messages. IRES elements can bypass the ribosomal scanning model of 5 ′ methylated Cap dependent translation and initiate translation at internal sites (Pelletier and Sonenberg, 1988). IRES elements (Macejak and Sarnow, 1991) from two components of the piconavirus family (Polio and myocarditis) as well as IRES from mammalian messages (Macejak and Sarnow, 1991) are known. IRES elements may be linked to heterogeneous open reading frames. Multiple open read frames can be transcribed together, each separated by an IRES to create a polycistronic message. Due to the IRES element, each open reading frame is close to ribosomes for efficient readout. Multiple genes can be efficiently expressed using a single promoter / enhancer to transcribe a single message (see US Pat. Nos. 5,925,565 and 5,935,819, the contents of which are incorporated herein by reference).
[96] c. Multiple cloning site
[97] The vector may comprise multiple cloning sites (MCS), which are nucleic acid regions containing multiple restriction enzyme sites. Any restriction enzyme site can be used to degrade the vector in combination with standard recombinant techniques. (See Carbonelli et al., 1999, Levenson et al., 1998 and Cocea, 1997, the contents of which are incorporated herein by reference). "Restriction enzyme digestion" refers to catalytic cleavage of a nucleic acid molecule by an enzyme that acts only at a specific position of the nucleic acid molecule. Many restriction enzymes are commercially available. The use of such enzymes is well understood by those skilled in the art. Often, vectors are linearized or fragmented using restriction enzymes that cleave in foreign MCS to link foreign sequences to the vector. "Linking" refers to the process of forming a phosphodiester bond between two nucleic acid fragments that may or may not be adjacent to each other. Techniques involving restriction enzymes and linkage reactions are well known to those skilled in the recombinant art.
[98] d. Splicing area
[99] Most transcribed eukaryotic RNA molecules will undergo RNA splicing to remove introns from the primary transcript. Vectors containing genomic eukaryotic sequences may require donor and / or acceptor splicing sites to ensure proper processing of transcripts for protein expression. (Chandler et al., 1997, the contents of which are incorporated herein by reference).
[100] e. Polyadenylation signal
[101] In expression, it is typical to include a polyadenylation signal for proper polyadenylation of the transcript. The nature of the polyadenylation signal is not critical to the successful practice of the invention and / or any such sequence can be used. Preferred embodiments include SV40 polyadenylation signals and / or bovine or human growth hormone polyadenylation signals, which are known to be convenient and / or function well in various target cells. Also considered are transcription termination sites as elements of an expression cassette. These elements may serve to increase message levels and / or minimize reading from cassettes to other sequences.
[102] f. Replica Origin
[103] To propagate a vector in a host cell, it may contain one or more replication origin sites (often denoted by "ori"), which are the specific nucleic acid sequences from which replication is initiated. Alternatively, autologous replication sequences (ARS) can be used when the host cell is yeast.
[104] g. Selection and Screening Markers
[105] In certain embodiments of the invention, the cells contain the nucleic acid constructs of the invention, and the cells can be identified in vitro or in vivo by including markers in the expression vector. Such markers provide identifiable changes to the cell to allow for easy identification of the cell containing the expression vector. In general, a selection marker is one that provides a property that allows selection. Positive selection markers are those whose presence allows selection while negative selection markers are those whose presence prevents selection. An example of a positive selection marker is a drug resistance marker.
[106] Usually, the insertion of drug resistance markers play a secondary role in the cloning and identification of transformants. For example, genes that provide resistance to neomycin, puromycin, hygromycin, DHFR, GPT, zeocin and histidinol are useful selection markers. In addition to markers that provide a phenotype that allows identification of transformants based on the fulfillment of conditions, other types of markers are also contemplated, including selectable markers such as GFP based on colorimetric analysis. As another alternative, selection enzymes such as herpes simplex virus thymidine kinase (tk) or chloramphenicol acetyltransferase (CAT) can be used. Those skilled in the art also know how to use immunological markers in combination with possible FACS analysis. The marker used is not believed to be important as long as it can be expressed simultaneously with the nucleic acid encoding the gene product. Examples of selection and selection markers are well known to those skilled in the art.
[107] 2. Host Cells
[108] As used herein, the terms "cell", "cell line" and "cell culture" can be used interchangeably. All these terms also include their descendants and all subsequent generations. It will be understood that all descendants may not be identical due to intentional or accidental mutations. In terms of expressing a heterologous nucleic acid sequence, a “host cell” refers to any prokaryotic or eukaryotic cell and includes any transgenic organism capable of replicating a vector and / or expressing a heterologous gene encoded by the vector. Host cells can be used and have been used as receptors for vectors. Host cells can be transformed or transfected, and these terms refer to the process by which foreign nucleic acid is delivered or introduced into the host cell. Transformed cells include primary subject cells and their descendants.
[109] Host cells may be derived from prokaryotic or eukaryotic cells depending on whether the desired result is replication of the vector or expression of some or all of the vector-encoded nucleic acid sequence. Many cell lines and cultures are used as host cells and they are available through the American Type Culture Collection (ATCC). It is an organ that serves as a repository of living cultures and genetic material (www.atcc.org). Suitable hosts can be determined by one skilled in the art based on the vector backbone and the desired result. Plasmids or cosmids can be introduced into prokaryotic host cells, for example for replication of many vectors. Bacterial cells used as host cells for vector replication and / or expression include many commercial bacterial hosts such as DH5a, JM109 and KC8 as well as SURE® competent cells and SOLOPACKa Gold cells (STRATAGENE®, La Jolla). As another way, Lee. Bacterial cells such as E. coli LE392 can be used as host cells for phage virus.
[110] Examples of eukaryotic host cells for replication and / or expression of the vector include HeLa, NIH3T3, Jurkat, 293, Cos, CHO, Saos and PC12. Many host cells from various cell types and organisms are used and known to those skilled in the art. Similarly, viral vectors can be used in combination with eukaryotic or prokaryotic host cells, especially cells that allow for replication or expression of the vector.
[111] Some vectors may use regulatory sequences that allow for replication and / or expression in both prokaryotic and eukaryotic cells. Those skilled in the art understand the conditions under which they are maintained for all of the host cells described above and cultured to enable replication of the vector. In addition, techniques and conditions are understood and known that allow for the mass production of vectors as well as the production of nucleic acids encoded by the vectors and their cognate polypeptides, proteins or peptides.
[112] 3. Expression system
[113] Many expression systems exist that include at least some or all of the compositions described above. Prokaryotic- and / or eukaryotic-based systems can be used in the present invention to generate nucleic acid sequences or their cognate polypeptides, proteins and peptides. Many such systems are commercially available and widely used.
[114] Insect cell / baculovirus systems can produce high levels of protein expression of heterologous nucleic acid fragments, such as those described in US Pat. Nos. 5,871,986 and 4,879,236, the contents of which are incorporated herein by reference. They can be purchased, for example, under the tradename BACPACK ^™ BACULOVIRUSEXPRESSION SYSTEM® from INVITROGEN® under the tradename MAXBAC® 2.0 and CLONTECH®.
[115] Another example of an expression system is the COMPLETE CONTROLa inducible mammalian expression system of STRATAGENE® or E. coli containing a synthetic ecdyson-induced receptor. PET expression system, which is an E. coli expression system. Another example of an inducible expression system is available from INVITROGEN®, which has the T-REX ™ (tetracycline-regulated expression) system, which is an inducible mammalian expression system using a full length CMV promoter. INVITROGEN provides a yeast expression system called Pichia metanolica expression system. This system is designed for high-level production of recombinant proteins in methylsoluble yeast Pichia methanolica. One skilled in the art knows how to express a vector, such as an expression construct, to produce a nucleic acid sequence or syngeneic polypeptide, protein or peptide thereof.
[116] Mutagenesis
[117] Mutagenesis, when used, is accomplished by several standard mutation procedures. Mutation is the process by which changes occur in the amount or structure of an organism. Mutations can include a single gene, a block of genes or a change in the nucleotide sequence of the entire chromosome. Changes in a single gene may be the result of point mutations involving the removal, addition or substitution of a single nucleotide base in a DNA sequence or may be the result of a change involving insertion or deletion of many nucleotides.
[118] Mutations can occur simultaneously as a result of progression such as the accuracy of DNA replication or a mistake in the migration of translocation genetic elements (transpozones) in the genome. They are also induced after exposure to chemicals or physical mutagens. Such mutation-inducing agents include polycyclic aromatic hydrocarbons and alkylating agents that can interact directly or indirectly (usually after some metabolic biotransformation) with ionizing radiation, ultraviolet light and various chemicals, such as nucleic acids. DNA lesions induced by such environmental agents can induce modifications of the nucleotide sequence when the affected DNA is replicated or restored and as a result can induce mutations. Mutations can also be site directed through the use of specific target methods.
[119] Site-directed mutation
[120] Structure-guided site specific mutations represent a powerful tool for the cleavage and engineering of protein-ligand interactions (Wells, 1996, Braisted et al., 1996). This technique provides for the preparation and testing of sequence variants by introducing one or more nucleotide sequence changes into the selected DNA.
[121] Site specific mutagenesis utilizes a sufficient number of contiguous modified nucleotides as well as specific oligonucleotide sequences that encode the DNA sequence of the desired mutation. In this case, sufficient size and complexity are provided to form a stable double strand on both sides of the deletion junction that traverses the primer sequence. Primers of about 17 to 25 nucleotides are preferred, with about 5 to 10 residues mutated on both sides of the sequence junction.
[122] This technique typically uses bacteriophage vectors that exist in both single and double strand forms. Vectors useful for site directed mutagenesis include vectors such as M13 phage. These phage vectors are commercially available and their use is generally well known to those skilled in the art. Double-stranded plasmids are also commonly used in site directed mutagenesis, which eliminates the transfer of the gene from phage to the plasmid.
[123] In general, initially a single chain vector encoding the desired protein or genetic element in the sequence is obtained or two strands of the double stranded vector are melted. The oligonucleotide primers containing the desired mutant sequences synthetically prepared are then annealed with single chain DNA preparations and the degree of mismatch is taken into account when selecting hybridization conditions. The hybridized product was subjected to E. coli to complete the synthesis of the mutation-containing strands. It is applied to DNA polymerase such as E. coli polymerase I (Clenow fragment). Thus a heterologous double strand is formed wherein one strand encodes the original non-mutated sequence and the other strand contains the desired mutation. Then use this heterologous heteroprint vector. Suitable clones of cells, such as E. coli cells, are transformed and clones comprising the recombinant vector with the mutated sequence sequence are selected.
[124] Comprehensive information and amount of information of functional significance for a given residue of protein can be obtained by saturation mutagenesis, which examines all 19 amino acid substitutions. The drawback of this method is the poor logic of multi-residual saturation mutagenesis (warren et al., 1996, Brown et al., 1996; Zeng et al., 1996; Burton and Barbas, 1994; Yelton et al., 1995; Jackson et al., 1995; Short et al., 1995; Wong et al., 1996; Hilton et al., 1996). Hundreds and even thousands of site specific mutations should be studied. However, improved techniques make the generation and rapid selection of mutations much easier (see for description of “walk-through” mutagenesis: US Pat. Nos. 5,798,208 and 5,830,650).
[125] Other methods of site directed mutagenesis are described in US Pat. Nos. 5,220,007, 5,284,760, 5,354,670, 5,366,878, 5,389,514, 5,635,377 and 5,789,166.
[126] Dosage and Formulation
[127] The composition of the present invention (active ingredient: a vector comprising a promoter and a nucleotide sequence encoding SEQ ID NO: 1 or SEQ ID NO: 8 and a 3'untranslated region) that is operably linked at appropriate distances for functional expression is active in the body of an animal Formulations and administrations may be made to affect a variety of growth deficient conditions by means of creating contact between the component and the active site of action of the formulation. Compositions of the invention are defined as vectors containing nucleotide sequences encoding compounds of the invention that are amino acid sequence analogs described herein. The composition is administered in an amount sufficient to generate a therapeutically effective amount of the compound. Those skilled in the art recognize that the terms "administered" and "introduced" can be used interchangeably. These may be administered by conventional means used in combination with pharmaceuticals as individual therapeutically active ingredients or as a combination of therapeutically active ingredients. In a preferred embodiment, the active ingredient may be administered alone or in a buffer such as PBS, but with a pharmaceutical carrier selected based on the chosen route of administration and standard pharmaceutical examples. Such pharmaceutical compositions can be used for therapeutic or diagnostic purposes in both human and veterinary clinical medicine. For example, they are useful for the treatment of growth-related diseases such as hypopituitary subauthentication caused by abnormalities in growth hormone production. They can also be used to stimulate the growth of animals raised for meat production or to improve feed conversion efficiency, enhance milk production and stimulate egg production.
[128] Dosages are therapeutically effective amounts of the active ingredient, as well as the pharmacokinetic characteristics of the particular active ingredient and its mode and route of administration, the type of animal, the age of the beneficiary, the sex of the beneficiary, the reproductive status of the beneficiary, the weight of the beneficiary, the symptoms Will depend on known factors such as the nature and extent of the treatment, the type of concurrent treatment, the frequency of treatment and the desired effect. Appropriate dosages of the vectors according to the invention will vary slightly depending on the individual subject and other variables. One skilled in the art will be able to determine the appropriate dose based on known circulating levels of growth hormone associated with normal growth and growth hormone secretion activity of the vector. As is well known in the art, treating females or mothers to produce larger animals is essential to varying doses individually depending on the degree of increased growth hormone production required.
[129] Accordingly, the present invention provides a method of increasing growth of offspring, including administering to a female or mother of offspring an amount of an analog of the invention sufficient to increase production of growth hormone to a level higher than that associated with normal growth. to provide. Normal levels of growth hormone vary widely and individually, and for a given individual subject, levels of circulating growth hormone vary significantly during the day.
[130] The present invention also provides a method of increasing the growth rate of an animal by administering an amount of GHRH analogs sufficient to stimulate growth hormone growth at levels higher than those associated with normal growth.
[131] Gene therapy
[132] If desired, gene therapy vectors may be formulated in solid, semisolid, liquid or gaseous formulations by methods known in the art for the individual route of administration. Means known in the art can be used to prevent release and absorption of the composition or to ensure timely release of the composition until the composition reaches the target organ. Pharmaceutically acceptable forms should be used to effect the compositions of the present invention. In pharmaceutical dosage forms, the compositions can be used alone or in combination with other pharmaceutically active compounds as well as appropriate combinations.
[133] Thus, the pharmaceutical compositions of the present invention can be delivered to various sites in the animal body through several routes to achieve specific effects (see Rosenfeld et al. (1991); Rosenfeld et al., (1991a); Jaffe et al). , 1992). One skilled in the art knows that although more than one route can be used for administration, certain routes can provide a more immediate and more effective response than other routes. Local or visual delivery can be achieved by application or drip of the formulation into the body cavity, administration including inhalation or aspiration of aerosol or parenteral introduction or intramuscular, intravenous, intraperitoneal, subcutaneous, intradermal and topical administration.
[134] One skilled in the art knows that other methods of delivery can be used to administer the vector to the cell. Examples include (1) methods using physical means, such as applying electroporation (electricity), gene guns (physical forces) or large amounts of liquid (pressure); And (2) complexing the vector with other entities such as liposomes or transporter molecules.
[135] Accordingly, the present invention provides a method of delivering a therapeutic gene to a host, including administering a vector of the invention preferably as part of a composition using such routes of administration or alternative routes known to those skilled in the art and appropriate for a particular application. . Effective gene delivery of a vector to a host cell according to the present invention can be monitored in terms of therapeutic effect (mitigation of some symptoms associated with the particular disease to be treated) or also evidence of expression of the gene or expression of that gene delivered in the host (e.g., Encoding with sequencing using polymerase chain reaction, Northone or Southern hybridization or transcription assays to detect nucleic acids in host cells, immunoblot analysis, antibody-mediated detection, mRNA or protein half-life studies or delivered nucleic acids Or specialized assays for detecting proteins or polypeptides that are affected by the level or function due to such delivery).
[136] These methods described herein are not the only ones and there are other methods that are specific to a particular use and will be apparent to those skilled in the art. In addition, an effective amount of the composition can be adjusted through similarity with known compounds to exert the desired effect.
[137] In addition, the actual dosage and schedule may vary depending on whether the composition is administered in combination with other pharmaceutical compositions or upon individual differences in pharmacokinetics, drug properties and metabolism. Likewise, the amount may vary in in vitro application depending on the particular cell line used (eg, the number of vector receptors present on the cell surface or the ability of a particular vector used for gene transfer to replicate in that cell line). In addition, the amount of vector added per cell will vary depending on the nature of the sequence as well as the length and stability of the therapeutic gene inserted into the vector and in particular variables that may need to be determined empirically and due to factors that do not belong to the methods of the invention. to be. Those skilled in the art can simply make appropriate adjustments according to the requirements of the particular situation.
[138] The following examples illustrate the invention in more detail but do not limit the scope of the invention in any way.
[139] Example 1
[140] GHRH hyperactive analogues that increase GH secretagogue activity and stability
[141] GHRH has a relatively short half-life of about 12 minutes in the circulatory system of humans (Frohman et al., 1984) and pigs. Enhancement of GH secretion is achieved using GHRH analogs that extend the biological half-life of GHRH and / or increase the GH secretagogue activity of GHRH. GHRH mutants were prepared by site directed mutagenesis. Gly15 was used instead of Ala15 to increase α-helix morphology and affinity structure with reduced cleavage by trypsin-like enzymes (Su et al., 1991). The affinity of the GHRH analogue with the Ala15 substituent to the GHRH receptor was increased by 4-5 folds (Campbell et al., 1991). Molecules with free COOH termini were used to replace Met27 and Ser28 instead of Leu27 and Asn28 to reduce the loss of biological activity due to Met oxidation in a slightly more stable form. This resulted in the formation of a triple amino acid substitution mutant represented by GHRH-15 / 27/28. Dipeptidyl peptidase IV is a major serum GHRH degrading enzyme (Walter et al., 1980; Martin et al., 1993). To make a poorer dipeptidase substrate, Ile2 was replaced by Ala2 (GHRH-TI) or Val2 (GHRH-TV) using GHRH15 / 27/28, or Tyr1 and Ala2 were replaced by His1 and Val2 (GHRH). -HV (FIG. 1A); H1V2A15L27N28).
[142] Example 2
[143] DNA constructs
[144] In a specific embodiment, the plasmid of SEQ ID NO: 9 (pSPc5-12-HV-GHRH) was used in the present invention. In another embodiment, pVC0289 backbone (SEQ ID NO: 10); A promoter such as SEQ ID NO: 6; GHRH cDNA (mutated HV-GHRH cDNA) such as porcine HV-GHRH (SEQ ID NO: 11); And 3 'UTRs, such as 3' UTRs derived from human GH (SEQ ID NO: 7).
[145] To test the biological potential of mutated porcine GHRH cDNA sequences, the proximity serum response factor, multiple MEF-2 sites, multiple MEF-1 sites, and TEF-1 binding sites (skeletal α-actin) (Li et al., 1999) A novel synthetic muscle promoter, SPc5-12, was used to construct plasmid vectors capable of inducing large amounts of skeletal muscle specific gene expression. The 31 amino acid signal peptide and the mature peptide porcine GHRH (Tyr1-Gly40) whole and / or porcine GHRH 228 bp fragment encoding the GHRH mutant and then the 3 ′ non-toxic region of human GH cDNA were subjected to methods known in the art. According to the muscle GHRH expression vector. This plasmid pSPc5-12 contains the 360 bp SacI / BamHI fragment of the SPc5-12 synthetic promoter (Li et al., 1999) within the SacI / BamHI site of the pSK-GHRH backbone (Draghia-Akli et al., 1997).
[146] Wild-type and mutated porcine GHRH cDNAs were obtained by site directed mutagenesis of human GHRH cDNA using the kit (Altered Sites II in vitro Mutagenesis System, Promega, Madison, Wisconsin). Human GHRH cDNA was subcloned into the corresponding site of the pALTER Promega vector as a BamHI-Hind III fragment and mutagenesis was performed according to the manufacturer's instructions. Porcine wild type cDNA was obtained from human cDNA by changing human amino acids 34 and 38 using the primers of SEQ ID NO: 2 5'-AGGCAGCAGGGAGAGAGGAACCAAGAGCAAGGAGCATAATGACTGC-AG-3 '. Porcine HV mutations were prepared using the primers of SEQ ID NO: 3: 5'-ACCCTCAGGATGCGGCGGCACGTAGATGCCATCTTCACCAAC-3 '. Porcine 15Ala mutants were prepared using the primers of SEQ ID NO: 4: 5'-CGGAAGGTGCTGGCCCAGCTGTCCGCC-3 '. Porcine 27Leu28Asn mutations were prepared using primers of SEQ ID NO: 5'-CTGCTCCAGGACATCCTGAACAGGCAGCAGGGAGAG-3 '. To verify the correctness of the clones obtained after mutagenesis, they were sequenced and then subcloned into the BamHI / HindIII site of pSK-GHRH described in this example by methods known to those skilled in the art.
[147] Example 3
[148] Cell Culture and Transfection
[149] Experiments were performed using pig anterior pituitary cultures and primitive chick myoblast cultures at the same success rate. However, the figure only exemplifies data presented by pig pituitary cultures. Primitive chick myoblast cultures were obtained as follows. Chick embryogenic tissue was harvested, skin and cartilage tissue was incised and separated by machine. After the cell suspension is passed through a lens paper and cotton mesh plate and cultured at a density of 1x10 ⁸ to 2x10 ⁸ to 100mm plastic petri dishes. A population of cells in a suspension state was collagen culture plate at a density of 2x10 ⁶ to 3x10 ⁶ cells in the 100mm coated plastic dishes and incubated under a constant temperature 37 ℃ in 5% CO ₂ environment. Then, minimum essential medium supplemented with 10% heat inactivated horse serum (HIHS), 5% chick pear extract (CEE) (Gibco BRL; Grand Island, NY) and gentamicin 24 hours before cells were transfected (MEM) ) Were incubated at a density of 1.5 × ¹⁰ 6/100 mm plates. See Draghia-Akli et al., 1997 and Bergsma et al., 1986 for a more detailed description. Anterior pituitary cultures of pigs were obtained as nearly described in Tanner et al., 1990. Briefly, pituitary tissue was plated for a time sufficient to dissociate under enzymatic conditions and attach on plastic dishes. Cells were then washed and exposed to incubation medium prior to the experiment. See Tanner et al (1990).
[150] Cells were transfected with lipofectamine with 4 μg of plasmid per 100 mm plate according to the manufacturer's instructions. After transfection, cells were differentiated by replacing the medium with MEM containing 2% HIHS and 2% CEE. Media and cells were harvested 72 hours after differentiation. The infection rate was estimated to be 10% as assessed by β-galactosidase histochemistry of the control plate. One day prior to harvesting cells were washed twice with antimony balanced salt solution (HBSS) and the medium was exchanged with MEM supplemented with 0.1% bovine serum albumin. The crude medium was treated with 1% trifluoroacetic acid and 0.25 volume of 1 mM phenylmethylsulfonylfluoride, frozen at −80 ° C. and lyophilized, and C-18 Sep-column (Penninsula Levorito, Belmont, CA). And then resuspended and radioimmunized or resuspended in media adjusted for primitive porcine pituitary progenitor cell culture.
[151] Example 4
[152] GHRH hyperactive analogues that increase GH secretagogue activity and stability
[153] Skeletal myoblasts were transfected with each construct as in Example 3 and analyzed for growth hormone secreted into porcine pituitary anterior lobe cell cultures purified from culture medium cells. As shown in FIG. 1B, modified GHRH species (GH15 / 27/28; GHRH-TI; GHRH-TV) were found to be higher than wild type pig GHRH in media collected after 24 hours and quantified by swine specific GH-radioimmunoassay. There was a slight increase in GH secretion amounting to about 20-50%. Only one of the four mutants, GHRH-HV, showed a significant increase in GH secretagogue activity, with pig GH levels rising to 1600 ng / ml at baseline of 200 ng / ml (FIG. 1B).
[154] Example 5
[155] Plasma Culture of HV-GHRH Molecules
[156] Pig plasma pools were collected from control pigs and stored at -80 ° C. Chemically synthesized HV-GHRH was prepared by peptide synthesis. Porcine plasma was thawed, centrifuged and left at 37 ° C. to equilibrate. GHRH mutants were dissolved in plasma samples at a final concentration of 100 μg / ml. Immediately after addition of the GHRH mutant, after 15 minutes, after 30 minutes, after 60 minutes, after 120 minutes and after 240 minutes, 1 ml of plasma was recovered and acidified with 1 ml of 1M TFA. Acidified plasma was purified and lyophilized on a C18 affinity SEP-Pak column, followed by Walters 600 multisystem delivery system, Walters intelligent sample processor type 717 and Walters spectromonitor 490 (Walters Associates, Milipore Corp., Milford MA). ) Was analyzed by HPLC. Detection was carried out at 214 nm. The proportion of peptides digested at this point was determined by peak integration.
[157] The stability of wild type GHRH and analog GHRH-HV was then tested in pig plasma through incubation of GHRH peptides and subsequent solid phase extraction and HPLC analysis. As shown in FIG. 1C, 95% of wild-type GHRH (1-44) NH 2 was degraded within 60 minutes of incubation in plasma. In contrast, incubation of GHRH-HV in pig plasma showed that at least 75% of the polypeptide was protected against enzymatic degradation during 4-6 hours of incubation. Thus, under the same conditions, wild type GHRH was completely degraded while a significant portion of GHRH-HV remained intact, indicating a significant increase in the stability of GHRH-HV against serum proteases.
[158] Example 6
[159] Animal research
[160] Three groups of five hybrid hybrid castrated boars (Yorkshire, Landrace, Hampshire and Duroc) of 3 to 4 weeks old were used for the GHRH study. 6% of the water and body weight diets (24% protein pig diet, Producers Cooperative Association, Bryan, TX) received each animal freely. Animal weights were measured every other day at 8:30 am and feeding continued. Animals were maintained in accordance with the NIH Guide, USDA and Animal Welfare Guidelines.
[161] Example 7
[162] Intramuscular injection of plasmid DNA into pigs
[163] pSPc5-12-HV-GHRH, pSPc5-12-wt-GHRH and pSPc5-12bgal endotoxin depleted plasmid (Qiagen Inc., Chatsworth, CA) at 1 mg / ml in PBS (pH 7.4) Diluted. Animals were allocated equally to one treatment group. Pigs were anesthetized with isoflurane (2-6% concentration for induction of anesthesia and 1-3% for anesthesia maintenance). Three days, seven days, 14 days, 21 days, 28 days, 45 days, and 65 days after plasmid injection, surgery was performed to collect blood from the animals and the catheter was injected into the cervix. During anesthesia, 10 mg of plasmid was injected directly into the pig's half tendon muscle. Two minutes after injection, the injection site muscle was placed between sets of calipers and electroporated by performing four 60 millisecond pulses under an optimum condition of 200 V / cm (Aihara et al., 1998). 65 days after the injection, the animals were killed, the internal organs and the injection site muscles were collected, weighed, frozen under liquid nitrogen and stored at -80 ° C. Conductors were weighed and analyzed for neutron activity. Back fat was measured.
[164] Example 8
[165] PSP-HV-GHRH intramuscular injection to increase pig GHRH; For two months
[166] GH and IGF-I Serum Levels
[167] The activity of optimized protease resistant pSP-HV-GHRH vectors that facilitate long-term expression of GHRH and stimulate GH and IGF-I secretion levels was measured. pSP-HV-GHRH and wild type construct pSP-wt-GHRH (wild type control) and synthetic muscle promoter E. A schematic map of the coli β-galactosidase expression vector pSP-β-gal (placebo control) is shown in FIG. 2A. Blood samples were collected without anesthesia by anesthetizing a 3 week old castrated boar and inserting a jugular catheter. Plasmid expression vector DNA (pSP-HV-GHRH; pSP-wt-GHRH; or 10 mg of DNA of pSP-β gal) was injected directly into the half tendon muscle and then electroporated (see Example 7).
[168] Example 9
[169] Porcine GHRH, GH and IGF-I Measurements
[170] Swine GHRH was measured by a heterogeneous human analysis system (Penisula Revoriatores, Belmont, CA). The sensitivity of this assay system is 1 pg / tube. Porcine GH in plasma was measured by the specific dual antibody procedure RIA (The Pennsylvania State University). The sensitivity of this assay is 4 ng / tube. Porcine IGF-I was measured by heterogeneous human assay (Diagnostic System Lab., Webster, TX). Data was analyzed with the Microsoft Excel Statistical Analysis Package. The values given in the figures are mean values ± s.e.m. to be. Specific p values were obtained comparatively using the Student's t assay. The p <0.05 value is the statistical validity level. In pigs injected with pSP-HV-GHRH in hemiform muscles, GHRH levels increased on day 7 post-injection (Figure 2b), and on day 14 they were 150% above the level of control group (652/4 ± 77 pg / ml vs. 419.6). ± 13 pg / ml). pSV-HV-GHRH expression activity reached a peak of about 2-3 times higher than that of the control group injected with placebo by 60 days. The absolute amount of serum GHRH secreted from pigs injected with pSP-HV-GHRH and corrected for weight gain between 0 and 60 days (blood volume corresponds to 8% of total body weight) was greater than that of the control group injected with placebo. More than threefold higher (1426.49 ± 10.47ng vs. 266.84 ± 25.45ng) (FIG. 2C). Animals injected with wild-type pSP-GHRH in hemimuscular muscle showed only a slight increase in GHRH levels from 45 days after injection but doubled until 60 days after injection (779.36 ng), which was sufficient to induce biological effects. It was a level.
[171] Young animals have very high levels of GH, which decreases gradually with age. Blood samples taken every 15 minutes for 24 hours 7 days and 14 days after the first injection were analyzed for pGH concentrations, and the analysis estimated the total rate of change of pGH content. In pigs injected with pSP-HV-GHRH (FIG. 2D), 7 days after injection (HV Δ change = + 1.52, wt = −0.73 vs. control = −3.2ng / ml) and 14 days after injection (HV Δ change = + 1.09, wt = -4.42 vs. control = -6.88 ng / ml), showing a clear increase in GH content.
[172] An increase in GH systemic concentration can also be confirmed by an increase in IGF-I levels. Serum porcine IGF-I levels began to rise in pigs injected with pSP-HV-GHRH about 3 days post injection (FIG. 2E). On day 21, the increase in mean serum IGF-I levels in these animals was about threefold, which was maintained for at least 60 days (p <0.03). For comparison, pigs injected with wild-type pSP-GHRH expression vector had only a 40% increase in hematogenous IGF-I levels (p = 0.39) (FIG. 2E).
[173] Example 10
[174] Muscle GHRH Expression Vectors That Increase Pig Growth
[175] Porcine GH secreted into the systemic circulation following intramuscular injection of muscle pSP-GHRH expression vector promotes growth for more than 65 days in castrated young boars. Body composition measurements were performed 30 days and 65 days after injection in vivo (densitometer, K40) or post-mortem (organ, conductor, body fat treated in neutron activation chamber after direct separation). Animals injected with wild-type pSP-GHRH averaged 21.5% heavier (37.125 kg vs. 29.375 kg) than placebo controls, whereas pigs injected with pSP-HV-GHRH were 37.8% heavier (41.775 kg; p = 0.014) (FIG. 3a). Feed conversion efficiency was also increased by 20% in pigs injected with the GHRH construct compared to the control (0.267 kg / day feed per kg body weight gain for pSP-HV-GHRH and 0.274 kg for pSP-wt-GHRH). , 0.334 kg for pigs injected with pSP-β-gal, see FIG. 3B). In body composition studies with densitometry, K40 potassium chambers and neutron activation chambers, animals injected with GHRH showed a proportional increase in all body composition without any signs of tracheal hypertrophy, relative proportions of body fat and associated pathology. 45 days later, photographs of control pigs injected with placebo and pigs injected with pSP-HV-GHRH are shown in FIG. 3C.
[176] The metabolic profile of pigs injected with pSP-HV-GHRH shown in Table 1 suggests a significant decrease in serum urea levels compared to pSP-GHRH and pSP-HV-GHRH, respectively (control 9 ± 0.9 mg / dl, injected). 8.3 ± 1 mg / dl and 6.875 ± 0.5 mg / dl (p = 0.006) in swine, indicating a decrease in amino acid metabolism. Serum glucose levels were similar between control and pigs injected with plasmid GHRH [99.2 ± 4.8 mg / dl in control pigs, 104.8 ± 6.9 mg / dl in pigs injected with pSP-HV-GHRH, wild type pSP-GHRH injected pigs. 97.5 ± 8 mg / dl (p <0.27)]. No other metabolic changes were found.
[177] Metabolic profile (mg / ml) of pigs and controls injected with GHRHGlucose Urea Creatinine Total protein Control 99.2 ± 4.8 9 ± 0.9 0.82 ± 0.06 4.6 ± 0.22 pSP-wt-GHRH 97.5 ± 8 8.3 ± 1 0.83 ± 0.056 4.76 ± 0.35 pSP-HV-GHRH 104.8 ± 6.9 6.875 ± 0.5 0.78 ± 0.04 4.88 ± 0.23
[178] Example 11
[179] Experiment with different levels of pSP-HV-GHRH
[180] To further investigate the effect of pSP-HV-GHRH on the growth of piglets, pSP-HV-GHRH (3 mg, 1 mg, 100 μg) was injected. This electrode was 10 times more effective than caliper electrodes known in the art as a result of pretesting. Therefore, the needle electrode is preferred for use in the method of the present invention. As shown in FIG. 4, the group injected with 100 μg of plasmid showed the maximum growth curve, and showed statistically significant difference with the control group after 50 days. One animal in the group injected with 3 mg formed antibodies, showing a significant decrease in growth pattern.
[181] In addition, two piglets groups were injected with the indicated doses of pSP-HV-GHRH 10 days after birth. IGF-I values began to rise 10 days after injection, and pigs injected with 100 μg of plasmid 35 days after injection had an average 10.62 times higher IGF-I value than controls. Pigs injected with 1 mg were 7.94 times higher on average than controls, and pigs injected with 3 mg were 1.16 times higher than the controls.
[182] Thus, in certain embodiments a low dose of pSP-HV-GHRH is injected. In one specific embodiment about 100 μg (1 mg) of the plasmid is used. In another embodiment, about 200-300 μg is injected. In yet further embodiments, 50-100 μg is administered.
[183] Example 12
[184] Age comparison with pSP-HV-GHRH
[185] Two piglets were injected with 2 mg of pSP-HV-GHRH from birth to investigate the ages most suitable for pSP-HV-GHRH injection. As shown in FIG. 6, the group receiving the injection at 14 days after birth showed the largest growth curve, and showed a significant statistical difference at each time point compared to the control group. One of the groups injected at day 21 formed antibodies and showed a significant decrease in growth pattern. Treatment too early (ie, less than about 10 to 14 days of age) can be insulin resistant. In certain embodiments, the therapy may be most effective at the lowest natural GH and IGF-I levels (approximately 10 to 14 days old) and counterproductive when the GHRH levels are usually high. In certain embodiments, if the immune surveillance system is reduced during pregnancy, pregnant animals have fewer antibodies generated against modified GHRH than non-pregnant animals.
[186] Example 13
[187] Specific embodiments
[188] In summary, the optimal injection time point is 14 days after birth (average 8 pounds heavier than the control group at 40 days post-injection (p <0.04)). Preferred injection doses are 100 μg in 2-5 ml doses (average 6 pounds heavier than controls on day 40 post injection (p <0.02)). Hormones and biochemical constants correlated with weight gain in normal (IGF-I, IGF-BP3, insulin, urea, glucose, total protein, creatinine in sows 1 sows (time course) and sows 3 sows (dose curves)). )to be. Body composition results from previous experiments indicate that HV-GHRH determines a uniform increase in all body composition (similar to control but body composition, but larger), whereas wt-GHRH determines an increase in lean body mass and fat loss. Showed.
[189] If an increase in growth hormone can result in an increase in body temperature, in a preferred embodiment the sows are injected under conditions such that the body temperature is from about 62 ° F. to about 80 ° F.
[190] Example 14
[191] Injection of GHRH Muscle Vectors into Pregnant Sows Before First Birth
[192] In order to analyze the growth effect of GHRH muscle vector, 10mg of vector containing GHRH was injected into pregnant sows during the last 3 months of pregnancy. In this example 10 mg of the pSP-HV-GHRH vector was injected into sows (approximately 800 pounds) at 90 days of gestation during the first trimester. The method of administration may use any method known in the art. In this embodiment, the plasmid was administered as in Example 7 except for using an electroporation caliper electrode (FIG. 7). This electrode has six needles 22g on a circular plastic support 2cm long and 1cm in diameter.
[193] Table 2 shows the weight (kg) over time of piglets born from sows injected with pSP-HV-GHRH (p2) by electroporation at day 90 of gestation. Table 3 shows the body weight (kg) of control animals born from sows (p3) not injected with the same data as in Table 2. Table 4 shows body composition data (average% fat / BW / d) of piglets born from sows injected with pSP-HV-GHRH and non-transfected sows. This table shows the relative ratio of fat to body weight and shows that the injected sow piglets had 18.5% less fat per unit of weight. Swine p2 / 1 and p2 / 6 were killed to obtain sieve composition data. The biochemical composition of the piglets was similar to that identified during the second trimester of this sow (Example 15). p values were very similar at all time points. This table clearly shows that piglets born to sows injected with pSP-HV-GHRH during pregnancy are much heavier than piglets born to control sows. Without limiting the scope and scope of the present invention without limiting its scope, Applicants estimate that GHRH injected into muscle cells is secreted and passes through the placenta. As a result of the hypertrophic and hyperplastic effects of GHRH on the pituitary gland, the number of pituitary cells releasing GH is increased.
[194] Example 15
[195] Second sow of an injected sow
[196] Table 5 shows the weight data of the second offspring of sows injected with pSP-HV-GHRH during the first trimester.
[197] Sieve composition of piglets over timeApril 27 May 1 5/4/2000 5/8/2000 5/11/2000 5/16/2000 5/18/2000 5/23/2000 7/13/2000 sow 1 day 5 days 7 days 11th 14 days 19th 21st 26 days 77 days Pig 1 2.097 3.26 4.22 5.627 6.505 8.4 9.1 10.75 36.32 Pig 2 2.264 3.512 4.46 5.882 6.799 8.7 9.4 11.25 37.228 Pig 3 1.758 2.78 3.68 4.817 5.7 7.5 8.25 10.25 35.866 Pig 4 1.895 2.843 3.62 4.733 5.714 7.1 7.6 8.9 32.234 Pig 5 2.397 3.458 4.24 5.704 6.692 8.85 9.6 11.35 39.498 Pig 7 2.457 3.599 4.68 6.132 7.05 8.9 9.65 11.55 37.682 Pig 8 1.907 2.882 3.58 4.767 5.593 6.95 7.55 9.65 36.32 Pig 9 2.381 3.52 4.23 5.635 6.45 8.25 8.9 10.65 34.504 Pig 10 2.473 3.655 4.57 5.935 6.87 8.6 9.25 10.7 39.952 Average 2.181 3.2787 4.14222 5.47022 6.37478 8.13889 8.81111 10.56111 36.62267 STDEV 0.2733 0.3509 0.41817 0.54711 0.55986 0.75778 0.81616 0.85322 2.3808 SE 0.1933 0.2481 0.29569 0.38686 0.39588 0.53583 0.57711 0.60332 1.68348 increase 0 1.0977 1.96122 3.28922 4.19378 5.95789 6.63011 8.38011 34.44167 Sum (kg) 19.629 29.509 37.28 49.232 57.373 73.25 79.3 95.05 329.604 pound 43.183 64.919 82.016 108.3104 126.2206 161.15 174.46 209.11 725.1288 Average daily increase 0.32231 0.44729
[198] GHRH has not been administered to sows since or during pregnancy. The second pup was larger after birth (average weight of piglets at birth in other sows bred in similar settings was 1.71 kg, which averaged 2.181 kg at birth). On the 21st day, the total weight of all single piglets characteristic of the breeds averaged about 130 pounds (approximately 59 kg) and sow piglets previously injected with pSP-HV-GHRH totaled 174 pounds (approximately 79 kg). This advantage was maintained, even at 77 days after birth, on average 11 to 15 pounds (5.5 to 6 kg) heavier weight per pig compared to the best breed known in the art. Animals injected even at 168 days after birth averaged 22 pounds (10 kg) heavier than controls (p <0.0007).
[199] The sows were anesthetized only during the injection / electroporation procedure, using a 2.2 mg / kg dose of TELAZOL ^R (a mixture of tiletamine hydrochloride and zolazepam hydrochloride). Piglets were anesthetized using a combination of ketamine / xylazine HCl when they had to lie back on a double X-ray density meter (DEXA) for about 15 minutes while assessing sieve composition. Specifically, ketamine 20 mg / kg + xylazine 1 mg / kg (typically the xylazine dose is 2 mg / kg) is used. In another embodiment, other anesthetics known in the art, such as ketamine 15 mg / kg + acepromazine 0.4 mg / kg, are administered. In another embodiment, the piglets may not require anesthesia for blood collection or injection.
[200] Pigs and some other animals are generally sensitive to several types of anesthetics and sometimes given atropine if they can die from large changes in the temperature control process (hypothermic or solid temperature, the latter occurring much more often) after anesthesia. Atropine is an anticholinergic drug often used before anesthesia, which facilitates the drying of secretions, reduces the need for anesthesia, prevents deep arrhythmias during anesthesia, and reduces the number of undesirably high fever occurrences, resulting in animal comfort during anesthesia recovery. It is thought to increase. In certain embodiments, atropine 0.05 mg / kg subq (subcutaneous) pretreatment is included. As an alternative to atropine, other similar drugs known in the art may be used.
[201] Multiple biochemical measurements were obtained from piglets. Tables 6-12 provide data for this measurement. Insulin experiments (Table 6) were measured on May 25, 2000. The mean value of all previous controls tested was 6.8 μU / ml and the mean value of experimental piglets was 4.785 μU / ml with no statistical significance (p = 0.07).
[202] Piglet's insulin concentration25 days Pig 1 4.3827 Pig 2 4.131 Pig 3 4.8176 Pig 4 5.7899 Pig 5 4.4267 Pig 7 4.3076 Pig 8 4.1648 Pig 9 6.0912 Pig 10 4.9527 Average 4.78501 STDEV 0.71397 SE 0.23799
[203] IGF-I analysis was performed on May 25, 2000 (Table 7). The mean value of the experimental group was 145.509 ng / ml and the mean value of all the conventional control groups tested was 53.08 ng / ml. Therefore, the p value is very significant (p <0.0001). If GH stimulates the production and release of IGF-I, the IGF-I assay is an indicator of increased GHRH levels and is widely used in the art as is.
[204] IGF-I Concentration in Piglets1 day 10 days 18 days 25 days Pig 1 290.46 118.63 185.01 356.02 Pig 2 265.7 115.62 117.99 172.28 Pig 3 109.27 77.389 200.75 109.99 Pig 4 94.689 36.746 93.795 65.113 Pig 5 155.98 95.946 138.24 179.3 Pig 7 171.41 19.463 213.29 226.43 Pig 8 178.3 101.55 98.478 165.88 Pig 9 104.86 78.872 84.7 77.214 Pig 10 262.4 131.36 206.23 138.99 Average 181.4521 86.17511 148.7203 165.6908 STDEV 74.91415 37.61337 52.67175 57.96496 SE 24.97138 12.53779 17.55725 29.32165
[205] In Table 8 IGF-BP3 (IGF binding protein 3) immunoradioactivity assay (IRMA) was tested on May 25, 2000. IRMA uses a two-site immunoradiometric assay. Miles LEM, Lipschitz DA, Bieber CP and Cook JD: Measurements of serum ferritin by a 2-site immunoradiometric assay. Analyt Biochem 61: 209-224, 1974. IRMA is a noncompetitive assay in which the analyte to be measured is "sandwiched" between two antibodies. The first antibody is fixed to the inner wall of the tube. Other antibodies are radiolabeled for detection. Analytes present in unknown samples, standards and controls bind to both antibodies to form a "sandwich" complex. Unbound material is removed by tilting or washing the tube. The measurements in Table 8 include the correction factor x 50. Table 8 shows that the mean value of the experimental group is 238.88 ng / ml, while the mean value of all the conventional controls tested is 205.44 ng / ml. p <0.048, which is statistically significant.
[206] IGF-BP3 Concentration in Piglets1 day 10 days 18 days 25 days 1 day 10 days 18 days 25 days Pig 1 7.9841 3.917 7.1657 3.5957 399.205 195.85 358.285 179.785 Pig 2 7.5463 3.4327 3.3382 4.4706 377.315 171.635 166.91 223.53 Pig 3 3.4187 4.9039 6.7961 6.3021 170.935 245.195 339.805 315.105 Pig 4 5.6354 4.2184 3.8551 1.9101 281.77 210.92 192.755 95.505 Pig 5 4.282 4.5592 5.2783 3.8224 214.1 227.96 263.915 191.12 Pig 7 3.7328 4.4454 2.9426 4.8232 186.64 222.27 147.13 241.16 Pig 8 5.4265 3.3285 4.1714 7.1258 271.325 166.425 208.57 356.29 Pig 9 3.7912 5.6354 3.9117 6.7643 189.56 281.77 195.585 338.215 Pig 10 4.7668 5.6099 5.24 3.8474 238.34 280.495 262 192.37 Average 5.17598 4.45004 4.74434 4.74018 258.7989 222.5022 237.2172 237.0089 STDEV 1.652 0.83658 1.48489 1.70536 82.6 41.8289 74.24472 85.2679 SE 0.55067 0.27886 0.49496 0.56845 27.53333 13.94297 24.74824 28.42263
[207] Table 9 shows the total protein concentration (g / dl). The mean value of the experimental group was 5.3 g / dl, while the mean value of all the conventional controls tested was 4.02 g / dl. The statistical significance is very high as p <0.0001.
[208] Total protein concentration in piglets1 day 10 days 18 days 25 days Pig 1 5.7 5.9 G.H. 5.5 Pig 2 5.3 5.6 5.5 5 Pig 3 5.2 5.3 5.3 5.4 Pig 4 5.3 5.5 4.9 5.4 Pig 5 5.8 5.3 5. 5.4 Pig 7 5.6 5.4 5.3 5.2 Pig 8 4.5 5 G.H. 4 Pig 9 5.3 5.1 5.3 5.2 Pig 10 6.3 5 5.2 5.5 Average 5.44444 5.34444 5.21429 5.17778 STDEV 0.49526 0.29627 0.20354 0.47111 SE 0.16509 0.09876 0.06795 0.15704
[209] Table 10 shows the creatine concentration (mg / dl). The mean value of the experimental group is 0.936 mg / dl, while the mean value of all the conventional controls tested is 0.982 mg / dl. There was no statistical significance (p <0.34), indicating normal kidney function.
[210] Creatine Concentration of Piglet1 day 10 days 18 days 25 days Pig 1 0.75 0.96 G.H. 1.14 Pig 2 0.73 1.03 0.98 1.46 Pig 3 0.69 0.92 0.95 1.1 Pig 4 0.65 0.94 1.18 1.18 Pig 5 0.64 0.8 0.91 0.92 Pig 7 0.72 0.93 1.02 1.12 Pig 8 0.68 0.9 0.83 1.2 Pig 9 0.68 0.87 One 1.07 Pig 10 0.74 1.02 1.02 1.03 Average 0.69778 0.93 0.98625 1.13556 STDEV 0.0393 0.07124 0.10113 0.14783 SE 0.0131 0.02375 0.03371 0.04928
[211] Table 11 shows BUM (blood urea levels) (mg / dl). The mean value of the experimental group is 3.88 mg / dl, while the mean value of all the conventional controls tested is 8.119 mg / dl. Statistical significance was significant as p <0.0012.
[212] BUN concentration in piglets1 day 10 days 18 days 25 days Pig 1 4 3 5 4 Pig 2 4 3 3 6 Pig 3 6 6 5 7 Pig 4 5 3 4 5 Pig 5 3 2 3 3 Pig 7 3 3 3 3 Pig 8 2 3 5 7 Pig 9 3 3 4 4 Pig 10 3 3 3 4 Average 3.66667 3.22222 3.88889 4.77778 STDEV 1.22474 1.09291 0.92796 1.56347 SE 0.40825 0.3643 0.30932 0.52116
[213] Table 12 shows glucose concentrations (mg / d). The mean value of the experimental group is 123.23 mg / dl, while the mean value of all the conventional controls tested is 122.8 mg / dl. There was no statistical significance (p <0.67). The term G.H. refers to total hemolytic action. Biochemical constants in this sample could not be measured.
[214] Glucose concentration in piglets1 day 10 days 18 days 25 days Pig 1 117 115 G.H. 115 Pig 2 112 137 130 119 Pig 3 133 138 143 115 Pig 4 125 127 132 90 Pig 5 115 123 133 120 Pig 7 114 120 123 115 Pig 8 126 123 G.H. 116 Pig 9 118 129 124 119 Pig 10 142 134 136 112 Average 122.4444 127.3333 131.5714 113.4444 STDEV 9.98888 7.88987 6.90066 9.15302 SE 3.32963 2.62996 2.30022 3.05101
[215] As shown in the tables above, IGH and IGH-BP3 increased (as a result of stimulation of the GH axis), urea decreased and total protein increased (indication of improved protein metabolism), while insulin and glucose remained normal. . Normal levels of insulin and glucose are an advantage of the present invention because classical GH therapy yields a condition such as "diabetes" with hyperglycemia. Normal creatinine in this experiment is a variable used to measure kidney function, which may sometimes be compromised in animals under inappropriate metabolic conditions.
[216] Thus, in certain embodiments, piglets born from subsequent multiple pregnancies of sows receiving pSP-HV-GHRH at the first trimester are superior to animals born from sows not injected with DNA that encodes normal or any form of GHRH. Showed an increase in growth.
[217] In certain embodiments, administration of a nucleic acid encoding GHRH to a female or mother is involved in an increase in about 25-50% of GH producing cells.
[218] In another embodiment, non-pregnant sows are injected before pregnancy.
[219] In another embodiment, other growth hormone releasing hormone analogs known in the art may be used instead of administering the pSP-HV-GHRH vector of the present invention. For example, wild type GHRH may be used. Experiments are conducted similarly to the teachings presented herein.
[220] In another embodiment, the pituitary gland is harvested immediately after killing piglets to analyze changes in pituitary content. That is, piglets are killed when they reach a commercial weight (about 100 kg) to collect the pituitary gland. The analysis includes the relative pituitary content of several hormone-secreting cells (relative proportion of cells that secrete growth hormone, prolactin, progesterone, etc.).
[221] Example 16
[222] additional experiment
[223] In certain embodiments, more sows, such as about 20, have been injected with the same or similar treatments as set forth in Examples 14 and 15. Various plasmid contents ranging from 100 μg to 10 mg were treated for groups using 5 sows per treatment group. The offspring were compared to the offspring of the uninjected sows. In certain embodiments, this experiment is carried out on a farm in order to be able to normalize the data to literature data.
[224] Example 17
[225] Optimization experiment
[226] Pregnant rats were used to determine the optimal injection time during the first trimester. The gestation period of rats is about 21 days. Pregnant females were injected from 5 to 18 days of gestation and their offspring were tested at various time points after birth. Specific experiments include body weight, body composition and relative content of the pituitary gland (relative ratio of cells secreting growth hormone, prolactin, FSH, etc.) of various hormone secreting cells.
[227] Example 18
[228] How to increase milk production
[229] One embodiment of the present invention provides a method of increasing milk production (also called lactation), comprising introducing an effective amount of a vector into an animal's cells under conditions where a nucleotide sequence encoding a growth hormone releasing hormone is expressed. Where the vector is a promoter; Nucleotide sequences encoding the growth hormone releasing hormone; A 3 ′ non-toxic region operably linked to functionally express this nucleotide sequence; The introduction and expression of this vector results in increased animal milk production. In this embodiment the animal is human, cow, pig, goat or sheep.
[230] The introduction of a vector comprising GHRH into an animal by the methods described herein increases milk production in the animal. In certain embodiments the animal is female, mother or pregnant female. In another specific embodiment the offspring of a female or mother grows faster due to increased milk production of the female or mother within approximately the first two weeks. As described herein, an increase in milk production occurs when animals are injected once with nucleic acid encoding GHRH.
[231] Those skilled in the art will be familiar with how to measure the increase in milk production [eg, US Pat. No. 5,061,690; 5,134,120; 5,134,120; And 5,292,721 or Peel et al., J. Nutr., 1981, 111: 1662.
[232] Milk samples are hand-woven at the time of childbirth (colostrum) and at 13 and 20 days of milk production. 40 IU of oxytocin is administered by intramuscular injection (except for colostrum collection) and milked as quickly as possible until no more milk comes from the two mammary glands per sow. Samples of the two mammary glands were mixed well and a certain amount was placed in two vials with a preservative such as potassium dichromate. Bayer was frozen until analysis. Milk fat, anhydrides and proteins are measured according to standard procedures known in the art, such as the A.O.A.C. (1980) procedure. In certain embodiments lactose of milk is semi-automated (Model 27 Industrial Analyzer, Yellow Springs Instrument Co., Inc., Yellow Springs, Ohio) Enzyme Procedure (Operation Procedure No. OP-025, Monsanto Co., St. Louis, Mo.) Analyzed. The milk yield of each sow is measured on the 13th and 20th days of weighing pigs hourly before and after mammaling in certain embodiments as described by Lewis et al. (1978) and Mahan et al. (1971). Care should be taken during this period to prevent or consider the loss of urine and bowel movements. In certain embodiments, sows and offspring are adapted through the first two mammalian periods and not included in calculating daily milk yield. The milk yield is calculated by multiplying the yield obtained for six consecutive hours by four.
[233] Example 19
[234] Another embodiment
[235] In another embodiment of the invention, the ligand of the growth hormone secretagogue receptor (GHS-R) provides results similar to GHRH nucleic acid delivery. Those skilled in the art will be familiar with the many different GHS-R ligand structural forms known in the art, all of which work through GHS-R. Examples include MK-0677 (Merck, Whitehouse Station, NJ), GHRP-6 (see Bows, 1998) and the endogenous ligand ghrelin (Kojima et al., 1999; Dieguez and Casanueva, 2000). Other examples include all compounds that act as agonists on hexarelin (Europeptide), L-692,943 (Merck & Co .; Whitehouse Station, NJ), NN703 (Novo Nordisk; Bagsvaerd, Denmark) or GHS-R receptors. And all of which are known to those skilled in the art (eg, Pong et al. (1996); Howard et al. (1996); or Smith et al. (1997)).
[236] It is well known to those skilled in the art that GHS-R is upstream of GHRH and increases GHRH release from the pituitary gland. In certain embodiments, the GHS-R ligand is administered orally (eg, in addition to feed or drinking water), which amplifies the effect of GHRH when inducing GH release from the pituitary gland. In this embodiment, the GHRH nucleic acid delivery of the present invention provides an additional enhancing effect. Without limiting the scope of the present invention, the inventors found that a similar mechanism of action increased the expression of additional GHRH by pit-1, a transcription factor involved in the development of GH producing cells, which are growth stimulatory cells in the anterior pituitary gland during embryonic development. Estimate. Activation of GHS-R also increases pit-1 expression. Pit-1 expression is also increased by cAMP and the GHS-R ligand increases the amount of cAMP produced in response to GHRH. Thus, it is possible that, at birth, pigs have increased concentrations of stimulatory cells. Therefore, pigs produce more GH. Thus in certain embodiments the GHRH nucleic acid delivery of the invention is administered with one or more GHS-R ligands. GHS-R ligands are administered in pharmaceutically acceptable compositions.
[237] All patents and publications described in this specification are indicative of the level of skill of those skilled in the art to which this invention belongs. All patents and publications are cited to the same extent as if each document were specifically incorporated by reference.
[238] Example 20
[239] Multiple effects of GHRH administration on sows and offspring
[240] For the purposes of the present invention, aberrantly occurring GHRH in pregnant animals is delivered to the offspring, for example through the placenta, to improve prolonged GH production of the offspring, after which they show increased growth and changes in body composition. At the same time, the injected sows produce significantly more milk.
[241] In order to measure the effect of growth on the offspring and the effect of GHRH on sow milk production after injection of the GHRH muscle vector into large mammals, the plasmid DNA pSP-HV-GHRH (n = 4) or 10 mg pSP-wt-GHRH (n = 2). Significant advances have recently been made in the art of using muscle for aberrant gene expression by using electroporation techniques to increase plasmid uptake in vivo in rodents and large mammals (Bettan et al., 2000; Draghia- Akli et al., 1999; Mir et al., 1999). In this case plasmid injections were first performed and then electroporated using the 6 needle array electrode and conditions as described herein and described in Draghia-Akli et al., 1999. Six equivalent sows were used as controls. The animals gave birth to each other within 24 hours. In subsequent studies a total of 132 piglets were analyzed.
[242] Administration of recombinant GHRH by injection two weeks before delivery is known to increase pig body weight and increase pig survival at day 13 and weaning (Etienne et al., 1992). In this case, sows piglets injected with GHRH were much larger at birth (average HV-GHRH 1.65 ± 0.06 kg, p <0.00002 and wt-GHRH 1.46 ± 0.05 kg, p <0.0014 vs. control 1.27 ± 0.02 kg) 8).
[243] Piglets were weaned on day 21 and analyzed for slaughter weight on day 170 postnatal. The sows piglets injected were 18% larger on weaning time (FIG. 9). Half of each litter was crossed reared to control sows (pigs of injected sows) or injected sows (pigs of control sows). Interestingly, the control group reared in the injected animals was significantly larger (up to 12.2%) than their litter (p <0.02, FIG. 10). Changes in body weight of control animals cross-bred to such GHRH-treated animals indicate a significantly increased milk production of injected sows. Nevertheless, piglets from GHRH-treated sows cross-bred to control sows are Tended to be smaller (up to 5.8%) than the litter, but the figure was not statistically significant, indicating that there is an endogenous change in the hypothalamic-pituitary axis where the offspring of GHRH treated animals increase growth. Indicates. The overall increase over control (feeding control sows) is shown in FIG. 12.
[244] This advantage was maintained up to the commercial weight, meaning that on day 170 the body weight averaged 135.7 ± 1.89kg for HV-GHRH and 129.3 ± 2.17kg for wt-GHRH, whereas the mean weight of the control group was 125.3 ± 1.74kg (FIG. 13). . Body weight difference was statistically significant at every hour (p value was between 0.05 and 10 ⁻⁵ ).
[245] Multiple biochemical measurements were made (Tables 13a and 13b). An increase in total protein and albumin concentration (g / dl) was seen in the experimental group as an indication of an increase in assimilation. Slight differences in the time points tested (50 and 170 days after birth) resulted in an 8% increase in total protein and an 7.5% increase in albumin (Tables 13a and 13b).
[246]
[247]
[248] Creatine concentration is normal (0.936 mg / dl vs. control 0.982 mg / dl, p <0.34), indicating normal kidney function.
[249] Glucose concentrations were normal at all time points tested (Tables 14a and 14b).
[250]
[251]
[252] Insulin levels were normal. Normal levels of insulin and glucose are an advantage of the present invention because classical GH therapy yields a "diabetes" -like condition with hyperglycemia (Pursel et al., 1990).
[253] Survival during the previous study was significantly higher for descendants of treated sows (Table 15). Incidence was also much less in the treated group.
[254] Pig Category Gun # Pig # Dead pig Dead % pathology Clinical record Control 63 7 11.11 Sudden death One Hernia One Amputee One Hind legs enteritis One 7/26 hernia-10/10 enteritis Swollen joints 2 Tenderfooted Hermiths 8/30 tumor Bleeding ulcers One Wasting-anemia WT-GHRH 18 One 5.56 Sudden death One HV-GHRH 42 2 4.76 Sudden death One Amputee One 8/21 damaged leg struggle
[255] Unlike injection of porcine recombinant growth-stimulating cells (rpST), which can cause hemolytic ulcers, fear of liver and kidney or even death of sows (Smith et al.), GHRH gene therapy is well tolerated and in animals There were no side effects observed. It should be noted that increased growth is obtained even in the offspring of treated animals without the GHRH plasmid. Tissue / fiber type specific hGH containing plasmids that have been regulated have been conventionally used to deliver and stably produce GH in livestock and GH-deficient hosts by mutagenesis, muscle metastasis or liposome mediated intravenous injection (Dahler et al., 1994; Pursel et al., 1990; Barr and Leiden, 1991). However, these techniques have the following significant drawbacks that cannot be used in large-scale operations and / or feed animals: 1) possible toxic or immune responses associated with liposome delivery; 2) the need for comprehensive ex vivo manipulation techniques in transfected myoblast methods; And / or 3) risk of significant side effects or inefficiencies in mutagenesis (Mililer et al., 1989; Dhawan et al., 1991). Compared to these techniques, plasmid DNA injection is simple and effective and has no problems with delivery systems or overexpression.
[256] The data presented herein show improved biological potential in the offspring of large mammals injected with the GHRH plasmid, as well as an increase in physiological levels of GH production and secretion and a reduction in mortality and incidence. Treated sows show significantly higher milk yield. Descending piglets did not experience any side effects from treatment and showed a normal biochemical profile without associated pathology or organ hypertrophy. Significant improvement in growth suggests that aberrant expression of muscle GHRH vectors could replace the classical GH treatment regimen and stimulate the GH axis in a more physiologically appropriate manner. HV-GHRH molecules, which show high stability and GH secretory activity in pigs, may be useful in other mammals because the serum protease that degrades GHRH is similar in most animals.
[257] Hereinafter, materials and methods used in the present embodiment will be described.
[258] DNA constructs
[259] Plasmid pSPc5-12 contains a 360 bp SacI / BamHI fragment of the SPc5-12 synthetic promoter at the SacI / BamHI site of the pSK-GHRH backbone (Draghia-Akli et al., 1997). Wild type porcine GHRH was obtained by site directed mutagenesis of human GHRH cDNA (1-40) OH by mutating Ser at position 34 to Arg and position 38 Arg to Glu; Mutant porcine HV-GHRH DNA was site-directed mutagenesis of human GHRH cDNA (1-40) OH, Tyr at position 1 to His, Ala at position 2 to Val, Gly to position 15 to Ala, Met at position 27 To Leu, Ser to position 28 to Asn, Ser to position 34 to Arg, Arg to position 38 to Glu (Altered Sites II in vitro Mutagenesis System, Promega, Madison, Wis.), BamHI of pSP-GHRH Cloned to / HinIII site. The 3 'non-toxic region of human growth hormone was placed after GHRH cDNA to obtain pSPc5-12-wt-GHRH and pSPc5-12-HV-GHRH. Plasmids in the control group contained E. coli under the control of the same synthetic promoter. PSP-bgal was obtained by containing the coli beta-galactosidase gene.
[260] Animal research
[261] In this GHRH study, 22 first-born sows from the PIC line weighing about 365 kg were used. The animals were transferred to a farm facility on day 87 and individually housed in a livestock barn, where they had an endless supply of water and feed for the end of the 25-day lactation period. Experiments began in March and the first pups were born in April and analyzed until mid-October. The farm building was equipped with a cooling system capable of maintaining a maximum temperature of 2-5 ° C. lower than the outside temperature even in a hot climate. Average maximum temperatures in July, August and September were 40.6 ° C, 41.6 ° C and 36.6 ° C, respectively. Animals were cared according to the NIH Guide, USDA and Animal Welfare Guidelines.
[262] Intramuscular injection of plasmid DNA into pigs
[263] Endotoxin-free pSPc5-12-HV-GHRH and pSPc5-12-wt-GHRH (Qiagen Inc., Chatsworth, CA, USA) plasmid preparations were diluted to 1 mg / ml with PBS at pH 7.4. One sow was given to each sow. Four sows were injected with pSPc5-12-HV-GHRH, two sows were injected with pSPc5-12-wt-GHRH and six sows were used as controls. On day 95 gestation, animals were lightly anesthetized with 2.2 mg / kg terrazole. A total of 10 mg of plasmid was injected directly into the pig's left half tendon muscle. After 2 minutes, the injected muscle was electroporated using a 6 needle array injection electrode (1 cm in diameter, 22 gauge, 2 cm in length) under the following conditions: 6 pulses, alternation between needles, 200 V / cm, 60 mm Sec / pulse (see Draghia-Akli et al., 1999; Aihara and Miyazai, 1998).
[264] Cross parenting research
[265] Immediately after birth, each pup was divided into two groups. Half of the pups were left to their mother and the other half were cross-bred to the other group (e.g., control piglets were crossed to HV or wt-injected animals or wt-born piglets were crossed to control animals). Parenting). Body weights were recorded weekly.
[266] food
[267] After weaning on day 21, piglets were fed 60 days with Nutrena 18% Medicated Pig Starter (Cargill, Minneapolis, MN) containing 1.012% lysine. The Custom Mix Pig Starter protein containing 1.4% lysine was then fed for 45 days, then the Custom Mix 22.7% protein containing 1.4% lysine for 45 days, followed by 20% with 1.2% lysine for the remainder of the study. Incubated with a custom mix containing protein.
[268] biochemistry
[269] Serum was collected 50 and 170 days after birth and analyzed in an independent laboratory (Antech Diagnostics, Irvine, CA).
[270] Pig IGF-I RIA
[271] Porcine IGF-I was measured by a heterologous human IGF-I assay (Diagnostic System Lab., Webster, TX).
[272] Porcine Insulin RIA
[273] Porcine insulin was measured by heterogeneous human assay (Linco Research Inc .; St. Charles, Missouri). The sensitivity of this assay was 2 μU / ml.
[274] Sieve composition data
[275] The study weighed twice a week using the same adjusted balance (certified accuracy of ± 0.2 kg, coefficient of variation 0.3%).
[276] statistics
[277] Data was analyzed using the Microsoft Excel Statistical Analysis Package. The values given in the figures are mean values ± s.e.m. Value. Specific p-values can be obtained by comparison with the Student's assay. p <0.05 was set at a statistically significant level.
[278] Example 21
[279] Multiple Effects of Rats Treated with GHRH
[280] Growth hormone secretion was stimulated with growth hormone releasing hormone (GHRH), a natural GH secretagogue and inhibited with somatostatin (SS), both of which are hypothalamic hormones (Thorner et al., 1995). GH pulses are the result of GHRH secretion associated with decreased or withdrawn somatostatin secretion. This pulse generator mechanism also appears to be adjusted by GH negative feedback. In addition, guerrelin, a novel peptide isolated for the first time in rats, is recognized as an important regulator of GH secretion and energy homeostasis. Guirelin is an endogenous ligand of growth hormone secretagogue receptor, and its in vivo GH releasing activity is dependent on GHRH (Hataya et al., 2001). In healthy mature mammals, GH is released in highly regulated, unique vibration patterns that appear four to eight times within 24 hours and is of profound importance for its biological activity (Argente et al., 1996). Abnormal patterns of secretion are associated with optimally induced physiological effects at the peripheral level (Veldurs, 1998). The expression, processing and / or release of GH isoforms and the relative ratios between them are differentially regulated during the growth and development stages (Araburo et al., 2000).
[281] The regulation and differentiation of growth stimulatory cells also depends on the paracrine process within the pituitary gland itself and growth factors and several neuropeptides such as angiogenic enteric peptides (Rawlings et al., 1995), angiotensin 2, endothelin (Tomic) et al., 1999) and activin (Billesbup et al., 1990). Effective and regulated expression of the GH and insulin-like growth factor I (IGF-I) pathways is essential to provide optimal linear growth, homeostasis of carbohydrates, protein and fat metabolism and positive nitrogen equilibrium (Murray and Shalet, 2000). . GHRH, GH, guerrelin, prolactin (PRL) and IGF-I play important roles in the regulation of humoral and cellular immune responses in physiological as well as pathological conditions (Geffner et al., 1997; Hattori et al., 2001).
[282] Hypothalamic tissue specific expression of the GHRH gene is not essential for its activity because the extracranial secreted GHRH is biologically active (Faglia et al., 1992; Melmed, 1991). Pathological GHRH stimulation of GH activity (regardless of its source, from mutant models to pancreatic tumors) can lead to proliferation, aberrant proliferation and adenocarcinoma of the pituitary cells (Asa et al., 1992; Sano et al. , 1988). Nevertheless, the long-term effects of sustained GHRH treatment in the offspring of the treated animals are not yet known.
[283] It has already been shown that aberrant expression of novel serum protease resistant pig GHRH from expression plasmids controlled by synthetic muscle specific promoters leads to high GH and IGF-I levels in pigs after intramuscular injection and delivery by in vivo electroporation. (Lopez-Calderon et al., 1999). The purpose of the experiments described in this example is to evaluate whether GHRH delivered by plasmid DNA gene therapy improves the growth and changes the body composition of animal offspring treated during the last 3 weeks of pregnancy.
[284] In certain embodiments, GHRH produced abnormally in pregnant animals is passed through the placenta to the offspring, which influences pituitary aberration and improves long-term offspring's GH production to increase growth and change body composition. Mammalian rats were injected with 30 μg of plasmid DNA pSP-HV-GHRH or pSP-βgal on day 16 of gestation to determine the growth effect on offspring by injecting GHRH muscle vector into mammals. Electroporation was performed after injection to increase plasmid uptake.
[285] All animals gave birth on 20-22 days of gestation. The average number of offspring from litters was similar between groups (treatment group (T), n = 10.8 litters / half; control (C) n = 11.75 litters / half). The number of pups was evenly between 10 mothers per mother. At 2 weeks postpartum the mean weight of pups increased 9% in the treatment group: T = 31.47 ± 0.52g vs. C = 28.86 ± 0.75g, p <0.014.
[286] Weaning weight was significantly increased in T's offspring: T females average 51.97 ± 0.83g, control females (CF) 47.07 ± 4.4g (p <0.043), and treated males average 60.89 ± 1.02g The control male (CM) was 49.85 ± 4.9 g (p <0.001) (FIG. 14). This advantage lasted for 10 weeks, and by 24 weeks the weight difference became meaningless.
[287] Both females and males showed muscle hypertrophy with significant differences between the calf muscles (G) and anterior tibialis muscle (TA) per 3 weeks of age (FIG. 15). TF maintained muscle hypertrophy during the study while males showed no signs of muscle hypertrophy after 10 weeks of age. These changes are thought to be due to changes in sex steroids at maturity in males, which slows down the effects of physiologically increased GH in skeletal muscle.
[288] The pituitary gland was isolated and weighed within one minute after death. The ratio of pituitary weight to total body weight increased significantly in IF until 12 weeks after birth (FIG. 16). An increase in pituitary weight is known because GHRH can stimulate GH synthesis and secretion from the anterior pituitary gland and has a specific hypertrophy effect on growth stimulating cells (Morel et al., 1999; Murray et al., 2000). It is thought that the most likely cause is growth stimulation cell abnormal growth. This is evidenced by hormonal (FIG. 17) and histological (FIG. 18) evidence. Northern blot analysis of the pituitary gland of injected animals showed a significant increase in GH and PRL mRNA levels and a decrease in endogenous rat GHRH mRNA levels. By histological techniques, specific anti-rat GH antibodies show an increase in the number of growth stimulating cells.
[289] Systemic increases in GHRH and GH levels may also result in increased serum IGF-I levels. Rat serum IGH-I was significantly higher in descendants of rats injected with pSP-HV-GHRH up to 24 weeks postpartum (p <0.05 at all time points tested, FIG. 19).
[290] Organs (lungs, heart, liver, kidneys, stomach, intestines, adrenal glands, gonads, brain) were collected and weighed. There was no associated pathology observed in the animals. Among the non-viral techniques of gene transfer in vivo, direct injection of plasmid DNA into muscle is simple, inexpensive and safe, but the application of this method has the disadvantage that the expression rate of the transferred DNA expression vector is relatively low. In certain embodiments there is a need for the use of innovative initiatives in which target animals are not directly processed to regulate growth and body composition by gene therapy but have improved biological properties due to the treatment of pregnant mothers. Another significant improvement of plasmid vectors as described herein is the use of genes encoding HV-GHRH, which is a more stable GHRH analogue (Draghia-Akli et al., 1999). Electrogenic therapeutic transfer methods allow genes to be efficiently transferred and expressed in the desired organ or tissue and can provide long term expression after a single dose. This method is a new method of highly effective nucleic acid transfer that does not require viral genes or particles.
[291] For large mammals such as pigs or sheep, the use of GHRH, an upstream stimulator of GH, is an alternative strategy that can increase production efficiency in terms of growth capacity or milk production and, more importantly, practical and metabolic (Dubreuil et. al., 1990). However, various uses of this therapy are currently limited due to the high cost of the recombinant peptide and the frequency of administration required. This major drawback can be addressed by using nucleic acid transfer methods that induce aberrant production of GHRH, especially when their production lasts for a long time.
[292] Thus, after one electroporation injection of the plasmid expressing the mutated growth hormone releasing hormone (GHRH) cDNA into the anterior tibialis muscle of mature pregnant rats, the growth of the animals in the offspring appeared. Newborn rats (F1) were significantly larger at birth. Long body weight and body composition studies have shown differences between sex with age. Hormonal and biochemical measurements were consistent with growth patterns. F1 showed higher pituitary gland, growth stimulatory cell abnormal growth and GH content. Plasma IGF-I levels of F1 were significantly elevated. In summary, this new finding demonstrates that GHRH can be used to enhance certain animal characteristics over generations after plasmid-based gene therapy.
[293] Hereinafter, the experiment performed in the present embodiment will be described.
[294] DNA constructs
[295] Plasmid pSPc5-12 contains a 360 bp SacI / BamHI fragment of the SPc5-12 synthetic promoter (Li et al., 1999) at the SacI / BamHI site of the pSK-GHRH backbone (Draghia-Akli et al., 1997). Mutated porcine GHRH cDNA was obtained by site directed mutagenesis of human GHRH cDNA (Altered Sites II in vitro Mutagenesis System, Promega, Madison, Wis.). The mutated 228 bp fragment (part of exon 2, all of exon 3 and part of exon 4) encoding 31 amino acid signal peptides and the mutated porcine GHRH (1-40) OH is characterized by the following amino acid substitutions: : Conversion of GLy15 → Ala, Met27 → Leu and Ser28 → Asn, Tyr1 to His, Ala2 → Val. This fragment was cloned into the BamHI / HinIII site of pSP-GHRH. hGH pA is a 3 'non-toxic region and a poly (A) signal derived from the human GH gene. The plasmid is 2 Proliferation was performed in Coli DH5α (Gibco BRL, Carlbad, Calif.). Endotoxin-depleted plasmid (Quiagen Inc., Chatsworth, Calif., USA) preparation was diluted to 1 mg / ml with PBS at pH 7.4.
[296] Intramuscular Injection and Electroporation of Plasmids
[297] Time-adjusted mature Vista female rats were housed in an animal rearing facility at Baylor Medical College, Houston, Texas. Animals were cared for in accordance with the NIH Guide, USDA and Animal Welfare Guidelines under environmental conditions of 10 h light / 14 h dark and the protocol was approved by the Animal Care Use Committee. The experiment was repeated twice. On day 16 of gestation, animals (n = 20 groups) were weighed and dosed from 0.5 to 0.7 ml / kg using a combination of ketamine 42.8 mg / ml, xylazine 8.2 mg / ml and aceproazine 0.7 mg / ml Anesthetized by intramuscular administration. Rat left anterior tibialis muscle was injected with 30 mg of pSP-HV-GHRH dissolved in 100 ml PBS using a 0.3 cc insulin syringe (Becton-Dickinson, Franklin Lakes, NJ). Control animals were injected with only PBS. For both groups caliper electroporation was performed as described in Draghia-Akli et al., 1999 after injection. Briefly, two minutes after injection, the rat's legs were placed between two needle electrodes (1 cm long, 26 gauge, 1 cm distance between needles) (Genetronics, San Diego, Calif.) And an electrical pulse was applied to the site. A 60 ms pulse was applied three times in one orientation and an electric field was reversed by applying a voltage of 100 V / cm three more times in the opposite direction. Pulses were generated with a T-820 Electro Square Porator (Genetronics, San Diego, Calif.).
[298] Posterity
[299] All injected rats gave birth on days 20-22 gestation. 240 descendants in the first study and 60 descendants in the second study from birth to 5 months of age (birth, 2 weeks, 3 weeks, 6 weeks, 8 weeks, 12 weeks, 16 weeks and 22 weeks of age) It was. Body weights were recorded at each time point using the same adjusted scale. At the end of the experiment, the body composition was analyzed after death. Blood was collected and immediately centrifuged at 0 ° C. and stored at −80 ° C. until analysis. Injected animals and organs of the control group (heart, liver, spleen, kidney, pituitary gland, brain, adrenal gland, skeletal muscle- anterior shin muscle (TA), calf muscle (G), rhizo muscle (S) and long toe pump muscle (EDL)), Carcasses and fats were separated, weighed on an analytical balance and flash frozen under liquid nitrogen. The shin length was measured and recorded.
[300] Northern blot analysis of the pituitary gland
[301] The pituitary gland was immediately frozen, placed in solution D, homogenized and extracted. 20 mg of total RNA was treated with DNaseI, size separated on 1.5% agarose-formaldehyde gel and then transferred to nylon membrane. This membrane was hybridized with 32P labeled specific GHRHcDNA probe by random priming.
[302] IGF-I Radioimmunoassay in Rats
[303] Rat IGF-I was determined by specific radioimmunoassay (Diagnostic System Laboratories, Webster, Texas). The sensitivity of this assay was 0.8 ng / ml with intra- and inter-analysis deviations of 2.4% and 4.1%, respectively.
[304] statistics
[305] The values given in the figures are mean values ± s.e.m. to be. Specific p values were obtained by comparison with Student's t-test or ANOVA analysis. p <0.05 was set at a statistically significant level.
[306] U.S. Patent Literature cited herein
[307] US Patent No. 5,847,066, issued December 8, 1998 to Coy, et al.
[308] U.S. Patent No. 5,846,936, issued December 8, 1998 to Felix et al., Registered as inventor;
[309] U. S. Patent No. 5,792, 747, issued August 11, 1998 to Schally et al.
[310] US Patent No. 5,776,901, issued July 7, 1998, to Bowers et al., Registered as inventor;
[311] US Patent No. 5,756,264, issued May 26, 1998 to Schwartz et al., Registered as inventor;
[312] U.S. Patent No. 5,696,089, issued December 9, 1997, to Felix et al., Registered as inventor;
[313] US Patent No. 5,486,505, issued January 23, 1996 to Bauers et al., Registered as inventor;
[314] U.S. Patent No. 5,292,721, issued March 8, 1994 to Boyd et al., Registered as inventor;
[315] U. S. Patent No. 5,137, 872, issued August 11, 1992 to Seely et al., Registered as inventor;
[316] U.S. Patent No. 5,134.210, issued July 28, 1992 to Boyd et al., Registered as inventor;
[317] U.S. Patent No. 5,084,442, issued January 28, 1992 to Felix et al., Registered as inventor;
[318] U. S. Patent No. 5,061, 690, issued October 29, 1991 to Kann et al.
[319] U.S. Patent No. 5,036,045, issued July 30, 1991 to Thorner et al.
[320] US Patent No. 5,023,322, issued June 11, 1991 to Kovacs et al., Registered as inventor;
[321] U.S. Patent No. 4,839,344, issued June 13, 1989 to Bauers et al.
[322] US Patent No. 4,410,512, issued October 18, 1983 to Bauers et al., Registered as inventor;
[323] US Patent No. RE33,699, issued September 24, 1991, to Drengler et al., Registered as inventor.
[324] US Patent No. 4,833,166, issued May 23, 1989 to Grosvenor et al., Registered as inventor;
[325] U.S. Patent No. 4,228,158, issued October 14, 1980 to Momany et al., Registered as inventor;
[326] U.S. Patent No. 4,228,156, issued October 14, 1980, to Momani et al.
[327] U.S. Patent No. 4,226,857, issued October 7, 1980 to Mommani et al.
[328] U.S. Patent No. 4,224,316, issued Sep. 23, 1980, to Momani et al.
[329] U.S. Patent No. 4,223,021, issued September 16, 1980, to Momani et al.
[330] U.S. Patent No. 4,223,020, issued September 16, 1980 to Mommani et al.
[331] U.S. Patent No. 4,223,019, issued September 16, 1980 to Mommani et al., Registered as inventor.
[332] Reference
[333]
[334]
[335]
[336]
[337]
[338]
[339]
[340] The person skilled in the art recognizes that the present invention is widely applied not only to inherent advantages but also to accomplishing the purpose and obtaining the results and advantages. The growth hormones, growth hormone secreting hormones, analogs, plasmids, vectors, pharmaceutical compositions, treatments, methods, processes and techniques described herein are representative of the presently preferred embodiments and are intended to be illustrative and not intended to limit the scope of the invention. . Those skilled in the art will recognize that changes and other uses are limited by the scope of the appended claims contained within the spirit of the invention.

权利要求:
Claims (136)
[1" claim-type="Currently amended] Under the condition that the nucleotide sequence is expressed and the introduction and expression of the vector improves or enhances the growth of the offspring, an effective amount of the vector comprising the promoter, the nucleotide sequence and the 3 'toxin region is transferred into the cells of the female animal before the conception of the female offspring. Or introducing during the process of improving or enhancing the growth of offspring from a female animal.
[2" claim-type="Currently amended] The method of claim 1, wherein the cells of the female animal comprise diploid cells.
[3" claim-type="Currently amended] The method of claim 1, wherein the cells of the female animal comprise muscle cells.
[4" claim-type="Currently amended] The method of claim 1, wherein the nucleic acid sequence encodes a growth hormone secreting hormone or an analog thereof.
[5" claim-type="Currently amended] The method of claim 4, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[6" claim-type="Currently amended] The method of claim 1, wherein the promoter comprises a synthetic muscle promoter.
[7" claim-type="Currently amended] The method of claim 1, wherein the 3 ′ nontoxic region comprises a hGH 3 ′ nontoxic region.
[8" claim-type="Currently amended] The method of claim 1, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of a female animal by electroporation, by parenteral routes, or by a combination thereof.
[9" claim-type="Currently amended] The method of claim 1 wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[10" claim-type="Currently amended] The method of claim 1 wherein the female animal is human, pig, cow, sheep, goat or chicken.
[11" claim-type="Currently amended] The vector according to claim 1, which is a plasmid, viral vector, liposome, cationic lipid or a combination thereof.
[12" claim-type="Currently amended] The method of claim 1, wherein the vector is introduced into the female in a single dose.
[13" claim-type="Currently amended] The method of claim 1, wherein the introduction is during the pre-birth 1/3 period of the offspring.
[14" claim-type="Currently amended] The method of claim 1, further comprising administering a ligand to the growth hormone secretagogue receptor to the female.
[15" claim-type="Currently amended] The method of claim 14, wherein the ligand administration is oral administration.
[16" claim-type="Currently amended] Prior to the conception of a female offspring into a cell of a female animal, an effective amount of a vector comprising a promoter, a nucleotide sequence and a 3 'toxin region is expressed under conditions where the nucleotide sequence is expressed and the introduction and expression of the vector increases the growth hormone level of the offspring. A method for increasing growth hormone levels in offspring from a female animal, comprising the step of introducing during the process.
[17" claim-type="Currently amended] The method of claim 16, wherein the cells of the female animal comprise diploid cells.
[18" claim-type="Currently amended] The method of claim 16, wherein the cells of the female animal comprise muscle cells.
[19" claim-type="Currently amended] The method of claim 16, wherein the nucleic acid sequence encodes a growth hormone secreting hormone or analog thereof.
[20" claim-type="Currently amended] The method of claim 19, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[21" claim-type="Currently amended] The method of claim 16, wherein the promoter comprises a synthetic muscle promoter.
[22" claim-type="Currently amended] The method of claim 16, wherein the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region.
[23" claim-type="Currently amended] The method of claim 16, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of a female animal by electroporation, by parenteral routes, or by a combination thereof.
[24" claim-type="Currently amended] The method of claim 16, wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[25" claim-type="Currently amended] The method of claim 16, wherein the female animal is human, pig, cow, sheep, goat or chicken.
[26" claim-type="Currently amended] The vector according to claim 16, which is a plasmid, viral vector, liposome, cationic lipid or a combination thereof.
[27" claim-type="Currently amended] The method of claim 16, wherein the vector is introduced into the female in a single administration.
[28" claim-type="Currently amended] 17. The method of claim 16, wherein the introduction is during the pre-birth 1/3 of the offspring.
[29" claim-type="Currently amended] The method of claim 16, further comprising administering a ligand to the growth hormone secretagogue receptor in the female.
[30" claim-type="Currently amended] The method of claim 29, wherein the ligand administration is oral administration.
[31" claim-type="Currently amended] Under conditions where the nucleotide sequence is expressed and the introduction and expression of the vector increases the lean mass of the progeny, an effective amount of the vector comprising the promoter, the nucleotide sequence and the 3 ′ nonpoisonous region into or before the conception of the female progeny into the cells of the female animal. A method of increasing lean body mass of offspring from a female animal, comprising the step of introducing.
[32" claim-type="Currently amended] 32. The method of claim 31, wherein the cells of the female animal comprise diploid cells.
[33" claim-type="Currently amended] The method of claim 31, wherein the cells of the female animal comprise muscle cells.
[34" claim-type="Currently amended] 32. The method of claim 31, wherein the nucleic acid sequence encodes a growth hormone secreting hormone or analog thereof.
[35" claim-type="Currently amended] The method of claim 34, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[36" claim-type="Currently amended] 32. The method of claim 31, wherein the promoter comprises a synthetic muscle promoter.
[37" claim-type="Currently amended] The method of claim 31, wherein the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region.
[38" claim-type="Currently amended] The method of claim 31, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of a female animal by electroporation, by parenteral routes, or by a combination thereof.
[39" claim-type="Currently amended] The method of claim 31, wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[40" claim-type="Currently amended] 32. The method of claim 31 wherein the female animal is human, pig, cow, sheep, goat or chicken.
[41" claim-type="Currently amended] The vector according to claim 31, which is a plasmid, viral vector, liposome, cationic lipid or a combination thereof.
[42" claim-type="Currently amended] The method of claim 31, wherein the vector is introduced into the female in a single administration.
[43" claim-type="Currently amended] 32. The method of claim 31, wherein the introduction is during the pre-birth 1/3 of the offspring.
[44" claim-type="Currently amended] 32. The method of claim 31, further comprising administering a ligand to the growth hormone secretagogue receptor in the female.
[45" claim-type="Currently amended] 45. The method of claim 44, wherein the ligand administration is oral administration.
[46" claim-type="Currently amended] Under the condition that the nucleotide sequence is expressed and the introduction and expression of the vector increases the IGF-I level of the progeny, an effective amount of the vector comprising the promoter, the nucleotide sequence and the 3 'toxin region is transferred into the cells of the female animal before the conception of the female offspring. Or during the step of increasing the IGF-I level of the offspring from the female animal.
[47" claim-type="Currently amended] The method of claim 46, wherein the cells of the female animal comprise diploid cells.
[48" claim-type="Currently amended] The method of claim 46, wherein the cells of the female animal comprise muscle cells.
[49" claim-type="Currently amended] 47. The method of claim 46, wherein the nucleic acid sequence encodes a growth hormone secreting hormone or analog thereof.
[50" claim-type="Currently amended] The method of claim 49, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[51" claim-type="Currently amended] 47. The method of claim 46, wherein the promoter comprises a synthetic muscle promoter.
[52" claim-type="Currently amended] 47. The method of claim 46, wherein the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region.
[53" claim-type="Currently amended] 47. The method of claim 46, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of a female animal by electroporation, by parenteral routes, or by a combination thereof.
[54" claim-type="Currently amended] 47. The method of claim 46, wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[55" claim-type="Currently amended] 47. The method of claim 46, wherein the female animal is human, pig, cow, sheep, goat or chicken.
[56" claim-type="Currently amended] The vector according to claim 46, which is a plasmid, viral vector, liposome, cationic lipid or a combination thereof.
[57" claim-type="Currently amended] The method of claim 46, wherein the vector is introduced into the female in a single administration.
[58" claim-type="Currently amended] 47. The method of claim 46, wherein the introduction is during the pre-birth 1/3 of the offspring.
[59" claim-type="Currently amended] 47. The method of claim 46, further comprising administering a ligand to the growth hormone secretagogue receptor to the female.
[60" claim-type="Currently amended] 60. The method of claim 59, wherein the ligand administration is oral administration.
[61" claim-type="Currently amended] Under conditions where the nucleotide sequence is expressed and the introduction and expression of the vector increases feed efficiency of the offspring, an effective amount of the vector comprising a promoter, a nucleotide sequence and a 3'untranslated region is transferred to or before the conception of the female offspring into the cells of the female animal. A method of increasing feed efficiency of offspring from female animals, the method comprising introducing.
[62" claim-type="Currently amended] 62. The method of claim 61, wherein the cells of the female animal comprise diploid cells.
[63" claim-type="Currently amended] The method of claim 61, wherein the cells of the female animal comprise muscle cells.
[64" claim-type="Currently amended] 62. The method of claim 61, wherein the nucleic acid sequence encodes a growth hormone secreting hormone or analog thereof.
[65" claim-type="Currently amended] 65. The method of claim 64, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[66" claim-type="Currently amended] 62. The method of claim 61, wherein the promoter comprises a synthetic muscle promoter.
[67" claim-type="Currently amended] 62. The method of claim 61, wherein the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region.
[68" claim-type="Currently amended] 62. The method of claim 61, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of a female animal by electroporation, by parenteral routes, or by a combination thereof.
[69" claim-type="Currently amended] 62. The method of claim 61, wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[70" claim-type="Currently amended] 62. The method of claim 61, wherein the female animal is human, pig, cow, sheep, goat or chicken.
[71" claim-type="Currently amended] The vector according to claim 61, which is a plasmid, viral vector, liposome, cationic lipid or a combination thereof.
[72" claim-type="Currently amended] The method of claim 61, wherein the vector is introduced into the female in a single administration.
[73" claim-type="Currently amended] 62. The method of claim 61, wherein the introduction is during the pre-birth 1/3 of the offspring.
[74" claim-type="Currently amended] 62. The method of claim 61, further comprising administering a ligand to the growth hormone secretagogue receptor to the female.
[75" claim-type="Currently amended] The method of claim 74, wherein the ligand administration is oral administration.
[76" claim-type="Currently amended] Under conditions where the nucleotide sequence is expressed and the introduction and expression of the vector increases the growth rate of the progeny, an effective amount of the vector comprising the promoter, the nucleotide sequence and the 3 ′ nonpoisonous region into or before the conception of the female progeny into the cells of the female animal. A method of increasing the growth rate of offspring from a female animal, the method comprising introducing.
[77" claim-type="Currently amended] The method of claim 76, wherein the cells of the female animal comprise diploid cells.
[78" claim-type="Currently amended] The method of claim 76, wherein the cells of the female animal comprise muscle cells.
[79" claim-type="Currently amended] The method of claim 76, wherein the nucleic acid sequence encodes a growth hormone secretory hormone or analog thereof.
[80" claim-type="Currently amended] 80. The method of claim 79, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[81" claim-type="Currently amended] 77. The method of claim 76, wherein the promoter comprises a synthetic muscle promoter.
[82" claim-type="Currently amended] 77. The method of claim 76, wherein the 3 'nontoxic region comprises an hGH 3' nontoxic region.
[83" claim-type="Currently amended] The method of claim 76, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of the female animal by electroporation, by parenteral routes, or by a combination thereof.
[84" claim-type="Currently amended] 77. The method of claim 76, wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[85" claim-type="Currently amended] The method of claim 76, wherein the female animal is human, pig, cow, sheep, goat or chicken.
[86" claim-type="Currently amended] The vector according to claim 76, which is a plasmid, viral vector, liposome, cationic lipid or a combination thereof.
[87" claim-type="Currently amended] The method of claim 76, wherein the vector is introduced into the female in a single administration.
[88" claim-type="Currently amended] 77. The method of claim 76, wherein the introduction is during the pre-birth 1/3 of the offspring.
[89" claim-type="Currently amended] 77. The method of claim 76, further comprising administering a ligand to the growth hormone secretagogue receptor to the female.
[90" claim-type="Currently amended] 90. The method of claim 89, wherein the ligand administration is oral administration.
[91" claim-type="Currently amended] An effective amount of a vector comprising a promoter, a nucleotide sequence, and a 3 ′ non-toxic region, under conditions in which the nucleotide sequence is expressed and the introduction and expression of the vector increases the ratio of growth hormone secreting cells to other hormone-producing cells in the posterior pituitary gland. A method of increasing the ratio of growth hormone secreting cells to other hormone-producing cells in the pituitary gland of the offspring from the female animal, comprising introducing into or into the cells of the female animal prior to or during the conception of the female offspring.
[92" claim-type="Currently amended] 92. The method of claim 91, wherein the cells of the female animal comprise diploid cells.
[93" claim-type="Currently amended] 92. The method of claim 91, wherein the cells of the female animal comprise muscle cells.
[94" claim-type="Currently amended] 92. The method of claim 91, wherein the nucleic acid sequence encodes a growth hormone secreting hormone or analog thereof.
[95" claim-type="Currently amended] 95. The method of claim 94, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[96" claim-type="Currently amended] 92. The method of claim 91, wherein the promoter comprises a synthetic muscle promoter.
[97" claim-type="Currently amended] 92. The method of claim 91, wherein the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region.
[98" claim-type="Currently amended] 92. The method of claim 91, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of a female animal by electroporation, by parenteral routes, or by a combination thereof.
[99" claim-type="Currently amended] 92. The method of claim 91, wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[100" claim-type="Currently amended] 92. The method of claim 91, wherein the female animal is human, pig, cow, sheep, goat or chicken.
[101" claim-type="Currently amended] 92. The vector according to claim 91, which is a plasmid, viral vector, liposome, cationic lipid or a combination thereof.
[102" claim-type="Currently amended] 92. The method of claim 91, wherein the vector is introduced into the female in a single administration.
[103" claim-type="Currently amended] 92. The method of claim 91, wherein the introduction is during the pre-birth 1/3 of the offspring.
[104" claim-type="Currently amended] 92. The method of claim 91, further comprising administering a ligand to the growth hormone secretagogue receptor to the female.
[105" claim-type="Currently amended] 105. The method of claim 104, wherein the ligand administration is oral administration.
[106" claim-type="Currently amended] 92. The method of claim 91, wherein the hormone-producing cells are selected from the group consisting of adrenal cortical stimulating hormone secreting cells, prolactin secreting cells and gonadotropin secreting cells.
[107" claim-type="Currently amended] An effective amount of a vector comprising a promoter, a nucleotide sequence, and a 3 ′ non-toxin region is introduced into the cells of a female animal before or during the conception of a female offspring, under conditions in which the nucleotide sequence is expressed and the introduction and expression of the vector delay the birth of the offspring. Delaying the birth of offspring from the female animal.
[108" claim-type="Currently amended] 107. The method of claim 107, wherein the cells of the female animal comprise diploid cells.
[109" claim-type="Currently amended] 107. The method of claim 107, wherein the cells of the female animal comprise muscle cells.
[110" claim-type="Currently amended] 107. The method of claim 107, wherein the nucleic acid sequence encodes a growth hormone secreting hormone or analog thereof.
[111" claim-type="Currently amended] 119. The method of claim 110, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[112" claim-type="Currently amended] 107. The method of claim 107, wherein the promoter comprises a synthetic muscle promoter.
[113" claim-type="Currently amended] 107. The method of claim 107, wherein the 3 ′ nontoxic region comprises an hGH 3 ′ nontoxic region.
[114" claim-type="Currently amended] 107. The method of claim 107, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of a female animal by electroporation, by parenteral routes, or by a combination thereof.
[115" claim-type="Currently amended] 107. The method of claim 107, wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[116" claim-type="Currently amended] 107. The method of claim 107, wherein the female animal is human, pig, cow, sheep, goat or chicken.
[117" claim-type="Currently amended] 108. The vector according to claim 107 which is a plasmid, viral vector, liposome, cationic lipid or a combination thereof.
[118" claim-type="Currently amended] 107. The method of claim 107, wherein the vector is introduced into the female in a single administration.
[119" claim-type="Currently amended] 108. The method of claim 107, wherein the introduction is during the pre-birth 1/3 period of the offspring.
[120" claim-type="Currently amended] 107. The method of claim 107, further comprising administering a ligand to the growth hormone secretagogue receptor to the female.
[121" claim-type="Currently amended] 121. The method of claim 120, wherein the ligand administration is oral administration.
[122" claim-type="Currently amended] Introducing into the animal's cells an effective amount of a vector comprising a promoter, a nucleotide sequence, and a 3 ′ non-toxin region under conditions in which the nucleotide sequence is expressed and the introduction and expression of the vector increases the milk production of the animal, How to increase milk production from
[123" claim-type="Currently amended] 123. The method of claim 122, wherein the cells of the female animal comprise diploid cells.
[124" claim-type="Currently amended] 123. The method of claim 122, wherein the cells of the female animal comprise muscle cells.
[125" claim-type="Currently amended] 123. The method of claim 122, wherein the nucleic acid sequence encodes a growth hormone secretory hormone or analog thereof.
[126" claim-type="Currently amended] 126. The method of claim 125, wherein the growth hormone secreting hormone is SEQ ID NO: 1, SEQ ID NO: 8, or each analog thereof.
[127" claim-type="Currently amended] 123. The method of claim 122, wherein the promoter comprises a synthetic muscle promoter.
[128" claim-type="Currently amended] 123. The method of claim 122, wherein the 3 ′ nontoxic region comprises a hGH 3 ′ nontoxic region.
[129" claim-type="Currently amended] 123. The method of claim 122, wherein the vector is combined with the carrier via a viral vector and introduced into the cells of a female animal by electroporation, by parenteral routes, or by a combination thereof.
[130" claim-type="Currently amended] 123. The method of claim 122, wherein the female animal is a human, pet, farm animal, edible animal or working animal.
[131" claim-type="Currently amended] 123. The method of claim 122, wherein the female animal is human, pig, cow, sheep, goat or chicken.
[132" claim-type="Currently amended] The vector according to claim 122, which is a plasmid, viral vector, liposome, cationic lipid or combination thereof.
[133" claim-type="Currently amended] 123. The method of claim 122, wherein the vector is introduced into the female in a single administration.
[134" claim-type="Currently amended] 123. The method of claim 122, wherein the introduction is during the pre-birth third of the offspring.
[135" claim-type="Currently amended] 123. The method of claim 122, further comprising administering a ligand to the growth hormone secretagogue receptor to the female.
[136" claim-type="Currently amended] 137. The method of claim 135, wherein the ligand administration is oral administration.

类似技术:

---

公开号 | 公开日 | 专利标题

---

JP2019187419A|2019-10-31|Glucagon analogs

---

US8603976B2|2013-12-10|Methods of enhancing functioning of the large intestine

---

Butler et al.2001|Control of growth by the somatropic axis: growth hormone and the insulin-like growth factors have related and independent roles

---

Behringer et al.1990|Expression of insulin-like growth factor I stimulates normal somatic growth in growth hormone-deficient transgenic mice

---

Johnson et al.2000|Evidence for leptin expression in fishes

---

Machlin1972|Effect of porcine growth hormone on growth and carcass composition of the pig

---

Peel et al.1987|Somatotropin and lactation

---

JP5189723B2|2013-04-24|Methods of using GLP for the treatment, prevention, diagnosis and prognosis of bone and nutrition related diseases

---

JP3366644B2|2003-01-14|Treatment of partial growth hormone insensitivity syndrome

---

Bühler et al.1998|Small intestinal morphology in eight-day-old calves fed colostrum for different durations or only milk replacer and treated with long-R3-insulin-like growth factor I and growth hormone

---

Lobie et al.1990|Growth hormone receptor expression in the rat gastrointestinal tract

---

Chung et al.1985|Stimulation of swine growth by porcine growth hormone

---

US20140066368A1|2014-03-06|Methods For Affecting Body Composition

---

McCormick et al.1992|Stimulation of coho salmon growth by insulin-like growth factor I

---

Anthony et al.1995|Placental-fetal hormonal interactions: impact on fetal growth

---

Mathews et al.1988|Growth enhancement of transgenic mice expressing human insulin-like growth factor I

---

US5166191A|1992-11-24|Use of relaxin in cardiovascular therapy

---

US8722621B2|2014-05-13|Stabilized insulin-like growth factor polypeptides

---

CA2274596C|2004-11-09|Compositions and methods for enhancing intestinal function

---

Pursel et al.1989|Genetic engineering of livestock

---

Burrin et al.1996|Orally administered IGF-I increases intestinal mucosal growth in formula-fed neonatal pigs

---

SEMSARIAN et al.1999|Insulin-like growth factor | induces myotube hypertrophy associated with an increase in anaerobic glycolysis in a clonal skeletal-muscle cell model

---

Juskevich et al.1990|Bovine growth hormone: human food safety evaluation

---

EP2060266B1|2011-08-10|Y4 selective receptor agonist PP2-36 for therapeutic interventions

---

Clark1997|The somatogenic hormones and insulin-like growth factor-1: stimulators of lymphopoiesis and immune function

同族专利:

---

公开号 | 公开日

---

EP1364004A2|2003-11-26|

---

CA2430921C|2016-06-07|

---

PL366116A1|2005-01-24|

---

WO2002061037A3|2003-10-02|

---

WO2002061037B1|2004-01-15|

---

AR035671A1|2004-06-23|

---

CN1575301A|2005-02-02|

---

MXPA03005236A|2005-04-08|

---

WO2002061037A2|2002-08-08|

---

BR0116472A|2005-04-05|

---

AU2002248194B2|2007-04-05|

---

CA2430921A1|2002-08-08|

---

EP1364004A4|2005-11-09|

引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

法律状态:
2000-12-12|Priority to US25502100P

---

2000-12-12|Priority to US60/255,021

---

2001-12-12|Application filed by 베일러 칼리지 오브 메디신, 아드비시스 인코포레이티드

---

2001-12-12|Priority to PCT/US2001/048726

---

2004-05-10|Publication of KR20040039187A

优先权:

---

申请号 | 申请日 | 专利标题

---

US25502100P| true| 2000-12-12|2000-12-12|

---

US60/255,021|2000-12-12|

---

PCT/US2001/048726|WO2002061037A2|2000-12-12|2001-12-12|Administration of nucleic acid sequence to female animal|