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    • 专利摘要:
    The present application relates to a disease gene of chronic joint rheumatism located within ± 1 cm of the DNA sequence hybridized by the microceterite markers D1S214, D1S253, D8S556, DXS1001, DXS1047, DXS1205, DXS1227 and / or DXS1232. PCR amplification of genomic DNA of a subject using at least one as a primer, and comparing the PCR products with the same PCR products of healthy subjects, the diagnostic method of chronic joint rheumatism and the causative factors of chronic joint rheumatism Provide a decision method.
    公开号:KR20010012591A
    申请号:KR1019997010549
    申请日:1998-04-10
    公开日:2001-02-15
    发明作者:시오자와순이찌
    申请人:시오자와 순이찌；
    IPC主号:
    专利说明:

    A Gene Causative of Rheumatoid Arthritis, Method for Diagnosing Rheumatoid Arthritis, and Method for Identifying Causative Factors of Rheumatoid Arthritis}
    The pattern of arthritis and joint destruction, especially the pathology of chronic joint rheumatism, especially their pathology, has been gradually revealed through various studies. However, many autoimmune diseases including chronic rheumatoid arthritis have many causes. Because of the polymerization and development and amplification of diseases, the body itself of various factor interactions must be identified for accurate explanation and proper treatment of these diseases.
    Chronic joint rheumatism is a disease with a morbidity rate of less than 1% worldwide (N. Engl. J. Med. 322: 1277-1289, 1990), but more than about 8% of symptoms develop in the compatriots of the disease (Cell 85: 311-318, 1996) are expected to act as genetic factors as one of the causative factors. However, the molecular genetic techniques and genetic engineering techniques commonly used to specify the genetic factors of disease do not function effectively against autoimmune diseases. For some reason, autoimmune diseases are not caused by a biologically simple mechanism called aberrant proliferation of a gene that causes mutations such as cancer. In addition, the conventional classical genetics method for obtaining the genetic basis of the disease clarifies that autoimmune disease is caused by multifactor inheritance, but cannot enter the body or the body. Thus, for genes related to chronic joint rheumatism, the reality was that the locus on the chromosome was not completely detected.
    Meanwhile, chain analysis and positional cloning with polymorphic markers have revolutionized the study of hereditary diseases in recent years. By using these methods, not only the chromosomal localization of disease genes, which have not been available in the past, has been clarified, but the causal genes have been isolated and analyzed for many diseases (experimental medicine vol.12 no. 6: 80-85, 1994). In recent years, as a polymorphic marker, a microanalytic marker (Nature, 359: 794 to 801, 1992; Nature Genet., 7: 246 to 339) has been used for the analysis of a patient's household, which is a technique of classical genetics. The cause gene of type I diabetes was isolated by the Korean-American analysis method combined with the analysis (Nature, 171: 130-136, 1994), and it was pointed out that the cause gene can be identified in incurable diseases including autoimmune diseases. have.
    In light of the above circumstances, the present application has been undertaken with the latest research trends, and the presence of chronic joint rheumatism as an indicator of the disease genes and mutations in these genes of the newly identified chronic joint rheumatism on the human chromosome. It aims to provide a diagnostic method and a method of determining the cause factors.
    The present invention relates to a method for diagnosing and determining the causative factors of chronic joint rheumatoid disease genes and chronic joint rheumatism as an indicator of the mutation of these genes.
    BRIEF DESCRIPTION OF THE DRAWINGS It is the 1st-5th chromosome map of the microsetterite marker used for specification of the locus of this invention.
    Fig. 2 shows the sixth to fifteenth chromosome maps of the microceterite markers used for specifying the locus of the present invention.
    Fig. 3 is a chromosome map and sex chromosome map of the 16th to 22nd micromarkers used for the specification of the locus of the present invention.
    4 is an example of gel electrophoresis of PCR products.
    5 is an example of interpretation by a Genotyper of a PCR product.
    FIG. 6 shows the results of plotting MLS values for the analyzed microceterite markers on chromosomes 1 to 6. FIG.
    7 is a result of plotting the MLS values for the analyzed microceterite markers on chromosomes 7-12.
    FIG. 8 is a result of plotting MLS values for the analyzed microsetterite markers on chromosomes 13 to 18. FIG.
    9 shows the results of plotting the MLS values for the analyzed microceterite markers on chromosomes 19 to X.
    Figure 10 shows the MLS values of each microceterite marker on the first chromosome (top), the eighth chromosome (middle) and the X chromosome (bottom) for a plurality of marker sites containing marker sites indicating the disease genes of the present invention. Is a graph showing the relationship between the genetic distance of the target gene and the unit of cm.
    This application provides the following genes as an invention which solves the said subject.
    (1) The disease gene of chronic joint rheumatism, which is located within ± 1 cm of the DNA sequence hybridized by the microsetterite markers D1S214 and / or D1S253 of the human first chromosome.
    (2) The disease gene of chronic joint rheumatism, which is located within ± 1 cm of the DNA sequence hybridized by microsetterite marker D8S556 of the human eighth chromosome.
    (3) The disease gene of chronic joint rheumatism located within ± 1 cm of the DNA sequence hybridized by the microsetterite markers DXS1001, DXS1047, DXS1205, DXS1227 and / or DXS1232 of the human X chromosome.
    In addition, the present application PCR amplifies the genomic DNA of the subject using at least one of the microsetter markers D1S214, D1S253, D8S556, DXS1001, DXS1047, DXS1205, DXS1227 and / or DXS1232 as a primer, and the PCR products are subjected to the same It provides a diagnostic method of chronic joint rheumatism, characterized in that compared with the PCR product.
    Furthermore, the present application PCR amplifies a subject's genomic DNA using at least one of microsetter markers D1S214, D1S253, D8S556, DXS1001, DXS1047, DXS1205, DXS1227 and / or DXS1232 as a primer, and the PCR products are subjected to the same It provides a method for determining the causative factors of chronic joint rheumatism, characterized in that compared with the PCR product.
    Hereinafter, the specific method of the gene of the present invention will be described in detail.
    The genes of the present invention are a plurality of genes whose chromosomal loci are specified by performing a chain analysis using a microceterite marker to a chronic rheumatism patient and its kinase. In other words, the present inventors use a polymorphism on the DNA of the microceterite marker gene (a polymorph of length by repeating a CA) over the entire length of the human chromosome to identify a transgene locus related to disease susceptibility of chronic joint rheumatism. decided. The specific method is as follows.
    (1) Extraction of genomic DNA
    Consistent with the diagnostic criteria of the American Rheumatology Society, patients with chronic joint rheumatoid patients (A), other rheumatoid patients (B), and their healthy compatriots (C) who have a stage 2 or higher degree of joint destruction, A total of 35 articles were analyzed. Each person was bled (10 mL) using EDTA, and 20 mL of buffer-I [0.32 M sucrose, 5% v / v Triton X-100, 5 mM MgCl 2 , 12 mM Tris HCl (pH 7.6) ] And gently mixed to dissolve the cell membrane. During centrifugation, the precipitated nuclei were reacted with buffer-II [4M guanidine thiocyanate, 12 mM EDTA, 375 mM NaCl, 0.5% sodium N-lauroyl sarcosinate, 0.1 M β-mercaptoethanol, 12 mM Tris HCl (pH 7.6)]. After dissolving, DNA was extracted by ethanol precipitation.
    (2) PCR amplification and sizing of microceterite DNA
    Using the extracted genomic DNA as a template, the microceterite marker gene corresponding to the chromosomal locus shown in Figs. 1 to 3 was PCR amplified using a fluorescent label primer (Perkin Elmer Co., Ltd.). Moreover, marker D1S502 was not used because DNA amplification is technically difficult. In addition, the genes of D6S299, D6S265, and D6S273 were amplified instead of D6D276 to analyze the HLA-D region in detail. In addition to the amplification of the microceterite DNA described above, genes near the HLA-DRB1 region were also PCR amplified using restriction fragment fragment polymorphism (RFLP) markers, and a total of 359 marker sites were searched.
    In addition, the composition of the PCR reaction solution (15 µl) in the amplification of microceterite DNA was DNA (30ng); Primer mixed mole (0.2 μM); dNTPs (0.2 mM each); DNA polymerase (1 unit); MgCl 2 (2.5 mM); 1 × PCR buffer-II, and the conditions for the amplification reaction were 10 minutes at 94 ° C., denaturation (94 ° C., 30 seconds); Annealing (55 ° C., 1 min); Elongation (72 degreeC, 2 minutes) was made into 27 cycles and finally, 72 degreeC for 5 minutes.
    Each PCR product labeled with 6-FAM, TET or HEX was labeled with a DNA sequencer (ABI 377: Applied Biosystems Inc.) on one panel of gel (4% acrylamide / 6M ruea) with a TAMURA labeled size standard. Electrophoresis inside. 4 is an example of this electrophoresis, but in this method, the peak, size, and region of the DNA fragment are analyzed with reference to the size standard recognized as a pattern, so that the error due to electrophoresis can be extremely low. Then, they were put into a computer to size each marker gene at the position of the fluorescence image, and it was determined how genes of parent-induced genes were propagated for each household. Moreover, the results of electrophoresis were sized with Genotype analysis software through Gene scanning analysis. 5 is an example of an analysis result by the genotyper.
    (3) Chain Analysis
    Korean compatriot analysis using chain analysis by microceterite markers is well known in the identification of the causative agent of type I diabetes (Proc. Natl. Acad. Sci., 92: 8560-885, 1995), but chronic rheumatoid arthritis In the case of a target, this method cannot be used as it is. Because the common compatriot analysis determines the genetic pattern of identical genes (IBD) between the patient and his parents, in the case of chronic joint rheumatism, an old age disease, This is because most of them are dead, and it is impossible to determine the IBD value uniquely.
    Therefore, in the present invention, when calculating the IBD value, a combination of three patients (A), three patients (B), and healthy compatriots (C) was set as one set, and analyzed for set of 35 sets. In other words, the IBD value becomes 1 when the gene a possessed by the original parent is distributed to both diseased compatriots, and the diseased compatriots share respective alleles, or If each of them is from one side of the parent then IBD = 2. IBD cannot be uniquely determined when the parents are already dead and the parents' genes cannot be typed. However, once the distribution of gene markers of the phosphorus in the ethnic group to be interpreted is determined, the allotype frequency of the gene can be used to determine the IBD value. In other words, the appearance of IBD between three patients (A), patients (B) and healthy Koreans (C)
    (IBD value between A-B, IBD value between A-C, IBD value between B-C)
    Let's focus on arbitrary genes and make it a, The probability to be obtained is 27 as shown in Table 1.
    Table 1
    Case 1: (ａａａａ, ａａ), (ａ , ａ , ａ ), ( , , )
    Case 2: (a, a, ), ( , , ａａ)
    Case 3: (ａａ, , ａａ), ( , ａａ, ａａ), (ａａ, , ), ( , ａａ, )
    Case 4: (ａａａａ, ａ ), (ａ , ａ , ａａ), (ａ , ａ , ), ( , , ａ )
    Case 5: (ａａａ , ａａ), (ａ , ａａ, ａａ), (ａａ, ａ , ａ ), (ａ , ａａ, ａ ), (ａ , , ａ ), ( , ａ , ａ ), (ａ , , ), ( , , )
    Case 6: (ａａ, , a ), ( , ａａ, ａ )
    Case 7: (a, a , ), (ａ , ａａ, ), (ａ , , ａ), ( , a , ａａ)
    The load value (Lod value; L value) is determined by Equation 1 of Holmans & Clayton (Am. J. Hum. Genet. 57: 1221 to 1232, 1995), with the frequency of the allotype of gene a being Pa. Saved.
    Equation 1:
    For example, when L values are calculated as L 11 , L 12 , and L 13 , respectively, as in Case 1 3 of Table 1, these values are obtained by the equations 2, 3, and 4, respectively.
    Equation 2: L 11 = Pa 4 z 0 + 1/2 Pa 3 (1 + Pa) z 1 + 1 / 4Pa 3 (1 + Pa) 2 z 2
    Equation 3: L 13 = Pa 4 z 0 + 1/2 Pa 8 (1 + Pa) z 1 + 1 / 4Pa 2 (1 + Pa) 3 z 2
    Equation 4: L 13 = 3 Pa 3 Pa 2 z 0 + 1/2 PaPa (1 + 2PaPa) Z 1 + PaPa (1 + 1 / 2PaPa) z 3
    Similarly, L values from L 11 to L 72 are calculated. In addition, by calculating the same for all subjects, the L value of gene a in the population is obtained by Equation 5.
    Equation 5:
    Then, the L value by varying the full range of variables Z 0, Z 1, Z 2 under Z 0 ≤1 / 2, Z 0 ≤1 / 2Z 1, Z 0 + Z 1 + Z 2 = 1 condition of maximum Find the L value (L max ). On the other hand, the L value (L null ) in the case where there is no correlation between the marker and the actual gene is fixed at Z 0 = 0.25, Z 1 = 0.50, and Z 2 = 0.25, and is obtained by the following equation.
    Equation 6:
    Finally, the maximum load score (MLS) is obtained by Equation 7.
    Equation 7:
    6 to 9 show the results of plotting the MLS values of all 359 microsetterite markers analyzed for each chromosome. Here, one can be seen that the corresponding relationship between the causal gene and the marker region in which the MLS value is around 3.0. In other words, the MLS value is the probability compared with the case where the correspondence between the marker and the causal may occur by chance, and the logarithmic value log 10 shows the probability that the MLS value is 1000 times higher than that by chance. A correspondence exists. That is, it was understood that the microsetter markers D1S214, D1S253, D8S556, and DXS1232 have extremely high MLS values of around 3.0 and indicate very close positions of the causal genes.
    10 shows MLS values and diseases of the microceterite markers of the first chromosome (upper), the eighth chromosome (intermediate) and the X chromosome (lower) for a plurality of marker regions including the four marker regions. It is a graph showing the relationship between the genetic distance (unit: cm hair) of the gene. As shown in FIG. 10, it is understood that a target gene for chronic joint rheumatism exists at a position very close to the mark region of the microceterite markers D1S214 and / or D1S253 for the human first chromosome. Similarly, the disease gene is present at a position very close to the mark region of the microceterite marker D8S556 on the human eighth chromosome, and to the mark region of the microceterite marker DXS1001, DXS1047, DXS1205, DXS1227 and / or DXS1232 on the X chromosome. It is understood.
    The chronic joint rheumatoid disease gene of the present invention is a gene present at a specific chromosome locus as described above (a gene present in at least one or more places within ± 1 cm of the 8 mark region of the microceterite marker described above), For example, the code region can be identified by a known method such as positional cloning, and further, the base sequence can be determined, thereby greatly contributing to the establishment of an effective treatment. In addition, PCR amplification and interpretation of the microceterite gene used in the present invention can be applied to the diagnosis of chronic joint rheumatism and determination of the causative factor. In other words, the genomic DNA of a subject with a possibility of morbidity is PCR amplified using a marker corresponding to the chromosome locus as a primer, and compared with that of a healthy person by interpretation by a genotyper as shown in FIG. Subsequent outbreaks can be determined with high precision.
    The present invention provides a method for diagnosing and determining the cause factors of chronic joint rheumatism, the disease gene of human chronic rheumatoid arthritis and the mutation of these disease genes. These inventions can be used for drug development and medical technology development.
    权利要求:
    Claims (5)
    [1" claim-type="Currently amended] A disease gene of chronic joint rheumatism located within ± 1 cm of the DNA sequence hybridized by the microsetterite markers D1S214 and / or D1S253 of the human first chromosome.
    [2" claim-type="Currently amended] The disease gene of chronic joint rheumatism located within ± 1 cm of the DNA sequence hybridized by microsetterite marker D8S556 of the human eighth chromosome.
    [3" claim-type="Currently amended] A disease gene of chronic joint rheumatism located within ± 1 cm of the DNA sequence hybridized by the microsetterite markers DXS1001, DXS1047, DXS1205, DXS1227 and / or DXS1232 of the human X chromosome.
    [4" claim-type="Currently amended] PCR amplification of the genomic DNA of a subject using at least one of the microsetter markers D1S214, D1S253, D8S556, DXS1001, DXS1047, DXS1205, DXS1227, and DXS1232 as a primer, and comparing these PCR products with the same PCR products of healthy subjects. Chronic joint rheumatism diagnostic method.
    [5" claim-type="Currently amended] PCR amplification of the genomic DNA of a subject using at least one of the microsetter markers D1S214, D1S253, D8S556, DXS1001, DXS1047, DXS1205, DXS1227, and DXS1232 as a primer, and comparing these PCR products with the same PCR products of healthy subjects. Method of determining the causative factors of chronic joint rheumatism.
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    同族专利:
    公开号 | 公开日
    US6623924B1|2003-09-23|
    AU730817B2|2001-03-15|
    AU6748698A|1998-12-08|
    WO1998051791A9|1999-12-23|
    CA2289961A1|1998-11-19|
    EP1008648A1|2000-06-14|
    EP1008648A4|2001-07-04|
    CA2289961C|2009-03-31|
    WO1998051791A1|1998-11-19|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1997-05-15|Priority to JP12589997
    1997-05-15|Priority to JP97-125899
    1998-02-13|Priority to JP98-031840
    1998-02-13|Priority to JP3184098
    1998-04-10|Application filed by 시오자와 순이찌
    2001-02-15|Publication of KR20010012591A
    优先权:
    申请号 | 申请日 | 专利标题
    JP12589997|1997-05-15|
    JP97-125899|1997-05-15|
    JP98-031840|1998-02-13|
    JP3184098|1998-02-13|
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