The 8.5-kb PstI allele of the stress protein gene, Hsp70-2 : An independent risk factor for systemic lupus erythematosus in African Americans?
SLE is dramatically more prevalent in persons of African descent than in other populations. Several genes in the class III region of the MHC have been considered as potential susceptibility loci for this disorder, but the primary association(s) remains unknown. The stress protein gene, hsp70-2, is o...
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Veröffentlicht in: | Human immunology 1996, Vol.45 (1), p.59-63 |
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description | SLE is dramatically more prevalent in persons of African descent than in other populations. Several genes in the class III region of the MHC have been considered as potential susceptibility loci for this disorder, but the primary association(s) remains unknown. The stress protein gene, hsp70-2, is of special interest in this regard because it encodes a protein functionally relevant to antigen processing and presentation and has itself been identified as a putative susceptibility locus in organ-specific autoimmune diseases in Caucasians. To clarify the relationship of the hsp70-2 gene to SLE in African Americans, genomic DNA from 46 patients and 42 appropriately matched control subjects was analyzed for an RFLP of the hsp70-2 gene using the probe pH2.3 and the restriction endonuclease
PstI, which identifies alleles of 8.5 and 9.0 kb. The 8.5-kb hsp70-2 allele was associated with SLE in this population (
x
2 = 8.2473,
p = 0.0044). This association was not due to linkage disequilibrium with the C4A deletion or with HLA-DR3, as has been reported in Caucasians with IDDM. These data suggest that the 8.5-kb hsp70-2 allele may be an independent susceptibility marker for SLE in African Americans. |
doi_str_mv | 10.1016/0198-8859(95)00153-0 |
format | Article |
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PstI, which identifies alleles of 8.5 and 9.0 kb. The 8.5-kb hsp70-2 allele was associated with SLE in this population (
x
2 = 8.2473,
p = 0.0044). This association was not due to linkage disequilibrium with the C4A deletion or with HLA-DR3, as has been reported in Caucasians with IDDM. These data suggest that the 8.5-kb hsp70-2 allele may be an independent susceptibility marker for SLE in African Americans.</description><identifier>ISSN: 0198-8859</identifier><identifier>EISSN: 1879-1166</identifier><identifier>DOI: 10.1016/0198-8859(95)00153-0</identifier><identifier>PMID: 8655362</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alleles ; Base Sequence ; Black or African American ; Black People - genetics ; Deoxyribonucleases, Type II Site-Specific ; Disease Susceptibility ; Genetic Markers ; HSP70 Heat-Shock Proteins - genetics ; Humans ; Lupus Erythematosus, Systemic - etiology ; Lupus Erythematosus, Systemic - genetics ; Molecular Sequence Data ; Polymorphism, Restriction Fragment Length ; Risk Factors</subject><ispartof>Human immunology, 1996, Vol.45 (1), p.59-63</ispartof><rights>1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0198-8859(95)00153-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,4022,27922,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8655362$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jarjour, Wael</creatorcontrib><creatorcontrib>M. Reed, Ann</creatorcontrib><creatorcontrib>Gauthier, Josée</creatorcontrib><creatorcontrib>Hunt, Stephen</creatorcontrib><creatorcontrib>B. Winfield, John</creatorcontrib><title>The 8.5-kb PstI allele of the stress protein gene, Hsp70-2 : An independent risk factor for systemic lupus erythematosus in African Americans?</title><title>Human immunology</title><addtitle>Hum Immunol</addtitle><description>SLE is dramatically more prevalent in persons of African descent than in other populations. Several genes in the class III region of the MHC have been considered as potential susceptibility loci for this disorder, but the primary association(s) remains unknown. The stress protein gene, hsp70-2, is of special interest in this regard because it encodes a protein functionally relevant to antigen processing and presentation and has itself been identified as a putative susceptibility locus in organ-specific autoimmune diseases in Caucasians. To clarify the relationship of the hsp70-2 gene to SLE in African Americans, genomic DNA from 46 patients and 42 appropriately matched control subjects was analyzed for an RFLP of the hsp70-2 gene using the probe pH2.3 and the restriction endonuclease
PstI, which identifies alleles of 8.5 and 9.0 kb. The 8.5-kb hsp70-2 allele was associated with SLE in this population (
x
2 = 8.2473,
p = 0.0044). This association was not due to linkage disequilibrium with the C4A deletion or with HLA-DR3, as has been reported in Caucasians with IDDM. These data suggest that the 8.5-kb hsp70-2 allele may be an independent susceptibility marker for SLE in African Americans.</description><subject>Alleles</subject><subject>Base Sequence</subject><subject>Black or African American</subject><subject>Black People - genetics</subject><subject>Deoxyribonucleases, Type II Site-Specific</subject><subject>Disease Susceptibility</subject><subject>Genetic Markers</subject><subject>HSP70 Heat-Shock Proteins - genetics</subject><subject>Humans</subject><subject>Lupus Erythematosus, Systemic - etiology</subject><subject>Lupus Erythematosus, Systemic - genetics</subject><subject>Molecular Sequence Data</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Risk Factors</subject><issn>0198-8859</issn><issn>1879-1166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUdtqFTEUDWKpp61_oJAnseC0uUxuPiiHorZQqA_1OWQyOxo7N5OMcH7CbzanPfjqw76xFgvWXgi9ouSCEiovCTW60VqYt0acE0IFb8gztKFamYZSKZ-jzT_KC3SS809CiCKqPUbHWgrBJdugP_c_AOsL0Tx0-GsuN9gNAwyA54BLRXJJkDNe0lwgTvg7TPAOX-dFkYbh93g74Tj1sEBtU8Ep5gccnC9zwqFW3uUCY_R4WJc1Y0i7qjm6Mud6VbltSNG7Okd4XPLHM3QU3JDh5WGeom-fP91fXTe3d19urra3DTDDStMz2SoPoe0N6zrBheQhSOoEI95I1bdGcO65Dr0ixCnNvGx51wUjfVedM36K3jzpVme_VsjFjjF7GAY3wbxmqzQRrVLkv0QqpKIt5ZX4-kBcuxF6u6Q4urSzh09X_MMTDtXW7wjJZh9h8tDHBL7Yfo6WErtP1u5js_vYrBH2MVlL-F_xkJQB</recordid><startdate>1996</startdate><enddate>1996</enddate><creator>Jarjour, Wael</creator><creator>M. Reed, Ann</creator><creator>Gauthier, Josée</creator><creator>Hunt, Stephen</creator><creator>B. Winfield, John</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>1996</creationdate><title>The 8.5-kb PstI allele of the stress protein gene, Hsp70-2 : An independent risk factor for systemic lupus erythematosus in African Americans?</title><author>Jarjour, Wael ; M. Reed, Ann ; Gauthier, Josée ; Hunt, Stephen ; B. Winfield, John</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e292t-d2647cef4d92bb53563ff61a520c967d49533c38fd700a782c643bbf96cb65523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Alleles</topic><topic>Base Sequence</topic><topic>Black or African American</topic><topic>Black People - genetics</topic><topic>Deoxyribonucleases, Type II Site-Specific</topic><topic>Disease Susceptibility</topic><topic>Genetic Markers</topic><topic>HSP70 Heat-Shock Proteins - genetics</topic><topic>Humans</topic><topic>Lupus Erythematosus, Systemic - etiology</topic><topic>Lupus Erythematosus, Systemic - genetics</topic><topic>Molecular Sequence Data</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jarjour, Wael</creatorcontrib><creatorcontrib>M. Reed, Ann</creatorcontrib><creatorcontrib>Gauthier, Josée</creatorcontrib><creatorcontrib>Hunt, Stephen</creatorcontrib><creatorcontrib>B. Winfield, John</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jarjour, Wael</au><au>M. Reed, Ann</au><au>Gauthier, Josée</au><au>Hunt, Stephen</au><au>B. Winfield, John</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The 8.5-kb PstI allele of the stress protein gene, Hsp70-2 : An independent risk factor for systemic lupus erythematosus in African Americans?</atitle><jtitle>Human immunology</jtitle><addtitle>Hum Immunol</addtitle><date>1996</date><risdate>1996</risdate><volume>45</volume><issue>1</issue><spage>59</spage><epage>63</epage><pages>59-63</pages><issn>0198-8859</issn><eissn>1879-1166</eissn><abstract>SLE is dramatically more prevalent in persons of African descent than in other populations. Several genes in the class III region of the MHC have been considered as potential susceptibility loci for this disorder, but the primary association(s) remains unknown. The stress protein gene, hsp70-2, is of special interest in this regard because it encodes a protein functionally relevant to antigen processing and presentation and has itself been identified as a putative susceptibility locus in organ-specific autoimmune diseases in Caucasians. To clarify the relationship of the hsp70-2 gene to SLE in African Americans, genomic DNA from 46 patients and 42 appropriately matched control subjects was analyzed for an RFLP of the hsp70-2 gene using the probe pH2.3 and the restriction endonuclease
PstI, which identifies alleles of 8.5 and 9.0 kb. The 8.5-kb hsp70-2 allele was associated with SLE in this population (
x
2 = 8.2473,
p = 0.0044). This association was not due to linkage disequilibrium with the C4A deletion or with HLA-DR3, as has been reported in Caucasians with IDDM. These data suggest that the 8.5-kb hsp70-2 allele may be an independent susceptibility marker for SLE in African Americans.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>8655362</pmid><doi>10.1016/0198-8859(95)00153-0</doi><tpages>5</tpages></addata></record> |
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subjects | Alleles Base Sequence Black or African American Black People - genetics Deoxyribonucleases, Type II Site-Specific Disease Susceptibility Genetic Markers HSP70 Heat-Shock Proteins - genetics Humans Lupus Erythematosus, Systemic - etiology Lupus Erythematosus, Systemic - genetics Molecular Sequence Data Polymorphism, Restriction Fragment Length Risk Factors |
title | The 8.5-kb PstI allele of the stress protein gene, Hsp70-2 : An independent risk factor for systemic lupus erythematosus in African Americans? |
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