Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation [chi][sup 2] (MASC) method: Rejection of the unifying-shared-epitope hypothesis
In order to investigate the HLA component involved in rheumatoid arthritis (RA), the authors tested genetic models by the marker association-segregation [chi][sup 2] (MASC) method, using the HLA genotypic distribution observed in a sample of 97 RA patients. First they tested models assuming the invo...
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Veröffentlicht in: | American journal of human genetics 1993-09, Vol.53:3 |
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container_title | American journal of human genetics |
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creator | Dizier, M.H. Eliaou, J.F. Babron, M.C. Combe, B. Sany, J. Clot, J. Clerget-Darpoux, F. |
description | In order to investigate the HLA component involved in rheumatoid arthritis (RA), the authors tested genetic models by the marker association-segregation [chi][sup 2] (MASC) method, using the HLA genotypic distribution observed in a sample of 97 RA patients. First they tested models assuming the involvement of a susceptibility gene linked to the DR locus. They showed that the present data are compatible with a simple model assuming the effect of a recessive allele of a biallelic locus linked to the DR locus and without any assumption of synergistic effect. Then they considered models assuming the direct involvement of the DR allele products, and tested the unifying-shared-epitope hypothesis, which has been proposed. Under this hypothesis the DR alleles are assumed to be directly involved in the susceptibility to the disease because of the presence of similar or identical amino acid sequences in position 70-74 of the third hypervariable region of the DRBI molecules, shared by the RA-associated DR alleles DR4Dw4, DR4Dw14, and DR1. This hypothesis was strongly rejected with the present data. In the case of the direct involvement of the DR alleles, hypotheses more complex that the unifying-shared-epitope hypothesis would have to be considered. 28 refs., 2 tabs. |
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First they tested models assuming the involvement of a susceptibility gene linked to the DR locus. They showed that the present data are compatible with a simple model assuming the effect of a recessive allele of a biallelic locus linked to the DR locus and without any assumption of synergistic effect. Then they considered models assuming the direct involvement of the DR allele products, and tested the unifying-shared-epitope hypothesis, which has been proposed. Under this hypothesis the DR alleles are assumed to be directly involved in the susceptibility to the disease because of the presence of similar or identical amino acid sequences in position 70-74 of the third hypervariable region of the DRBI molecules, shared by the RA-associated DR alleles DR4Dw4, DR4Dw14, and DR1. This hypothesis was strongly rejected with the present data. 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First they tested models assuming the involvement of a susceptibility gene linked to the DR locus. They showed that the present data are compatible with a simple model assuming the effect of a recessive allele of a biallelic locus linked to the DR locus and without any assumption of synergistic effect. Then they considered models assuming the direct involvement of the DR allele products, and tested the unifying-shared-epitope hypothesis, which has been proposed. Under this hypothesis the DR alleles are assumed to be directly involved in the susceptibility to the disease because of the presence of similar or identical amino acid sequences in position 70-74 of the third hypervariable region of the DRBI molecules, shared by the RA-associated DR alleles DR4Dw4, DR4Dw14, and DR1. This hypothesis was strongly rejected with the present data. In the case of the direct involvement of the DR alleles, hypotheses more complex that the unifying-shared-epitope hypothesis would have to be considered. 28 refs., 2 tabs.</description><subject>990200 -- Mathematics & Computers</subject><subject>ANTIGENS</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>DETECTION</subject><subject>DISEASES</subject><subject>GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE</subject><subject>GENES</subject><subject>GENETIC MAPPING</subject><subject>HISTOCOMPATIBILITY COMPLEX</subject><subject>MAPPING</subject><subject>MATHEMATICAL MODELS</subject><subject>RHEUMATIC DISEASES</subject><subject>SKELETAL DISEASES 550400 -- Genetics</subject><subject>STATISTICAL MODELS</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNqNj81qwzAQhEVpoe7POyw9JQeDbGMn6c2ElhTSS9pbCEGV19amsWS0siHv1werCTn02NMM7PDNzpWIkjybxUUh82sRSSnTeJEuZrfijvkgZZLMZRaJnzc7IAdqVCBnwdUQDMJqXYJ2becs2gBkB3ccsBoNeIN9q4KjCpQPxlMghsmmnMLXCXom25wBrfLf6EExO01ndMzYeLzUbLWh3Zb7DtIdTN7Lj-UUWgzGVc-wwQPqv8_0lurTCI7ZKI9VjB0F1yGYU-fGOxM_iJtaHRkfL3ovnl5fPper2I3L9qwpoDbaWTuC97nM5LxIsn-FfgEzfGqz</recordid><startdate>19930901</startdate><enddate>19930901</enddate><creator>Dizier, M.H.</creator><creator>Eliaou, J.F.</creator><creator>Babron, M.C.</creator><creator>Combe, B.</creator><creator>Sany, J.</creator><creator>Clot, J.</creator><creator>Clerget-Darpoux, F.</creator><scope>OTOTI</scope></search><sort><creationdate>19930901</creationdate><title>Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation [chi][sup 2] (MASC) method: Rejection of the unifying-shared-epitope hypothesis</title><author>Dizier, M.H. ; Eliaou, J.F. ; Babron, M.C. ; Combe, B. ; Sany, J. ; Clot, J. ; Clerget-Darpoux, F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-osti_scitechconnect_50308613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>990200 -- Mathematics & Computers</topic><topic>ANTIGENS</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>DETECTION</topic><topic>DISEASES</topic><topic>GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE</topic><topic>GENES</topic><topic>GENETIC MAPPING</topic><topic>HISTOCOMPATIBILITY COMPLEX</topic><topic>MAPPING</topic><topic>MATHEMATICAL MODELS</topic><topic>RHEUMATIC DISEASES</topic><topic>SKELETAL DISEASES 550400 -- Genetics</topic><topic>STATISTICAL MODELS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dizier, M.H.</creatorcontrib><creatorcontrib>Eliaou, J.F.</creatorcontrib><creatorcontrib>Babron, M.C.</creatorcontrib><creatorcontrib>Combe, B.</creatorcontrib><creatorcontrib>Sany, J.</creatorcontrib><creatorcontrib>Clot, J.</creatorcontrib><creatorcontrib>Clerget-Darpoux, F.</creatorcontrib><collection>OSTI.GOV</collection><jtitle>American journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dizier, M.H.</au><au>Eliaou, J.F.</au><au>Babron, M.C.</au><au>Combe, B.</au><au>Sany, J.</au><au>Clot, J.</au><au>Clerget-Darpoux, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation [chi][sup 2] (MASC) method: Rejection of the unifying-shared-epitope hypothesis</atitle><jtitle>American journal of human genetics</jtitle><date>1993-09-01</date><risdate>1993</risdate><volume>53:3</volume><issn>0002-9297</issn><eissn>1537-6605</eissn><abstract>In order to investigate the HLA component involved in rheumatoid arthritis (RA), the authors tested genetic models by the marker association-segregation [chi][sup 2] (MASC) method, using the HLA genotypic distribution observed in a sample of 97 RA patients. First they tested models assuming the involvement of a susceptibility gene linked to the DR locus. They showed that the present data are compatible with a simple model assuming the effect of a recessive allele of a biallelic locus linked to the DR locus and without any assumption of synergistic effect. Then they considered models assuming the direct involvement of the DR allele products, and tested the unifying-shared-epitope hypothesis, which has been proposed. Under this hypothesis the DR alleles are assumed to be directly involved in the susceptibility to the disease because of the presence of similar or identical amino acid sequences in position 70-74 of the third hypervariable region of the DRBI molecules, shared by the RA-associated DR alleles DR4Dw4, DR4Dw14, and DR1. This hypothesis was strongly rejected with the present data. In the case of the direct involvement of the DR alleles, hypotheses more complex that the unifying-shared-epitope hypothesis would have to be considered. 28 refs., 2 tabs.</abstract><cop>United States</cop></addata></record> |
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source | ScienceDirect Journals (5 years ago - present); EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | 990200 -- Mathematics & Computers ANTIGENS BASIC BIOLOGICAL SCIENCES DETECTION DISEASES GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE GENES GENETIC MAPPING HISTOCOMPATIBILITY COMPLEX MAPPING MATHEMATICAL MODELS RHEUMATIC DISEASES SKELETAL DISEASES 550400 -- Genetics STATISTICAL MODELS |
title | Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation [chi][sup 2] (MASC) method: Rejection of the unifying-shared-epitope hypothesis |
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