ELF1 is associated with systemic lupus erythematosus in Asian populations
Systemic lupus erythematosus (SLE) is an autoimmune disease with a strong genetic involvement. The susceptibility genes identified so far can only explain a small proportion of disease heritability. Through a genome-wide association in a Hong Kong Chinese cohort and subsequent replication in two oth...
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Veröffentlicht in: | Human molecular genetics 2011-02, Vol.20 (3), p.601-607 |
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creator | JING YANG WANLING YANG KA WING LEE SIK NIN WONG LEUNG, Alexander Moon Ho LI, Xiang-Pei AVIHINGSANON, Yingyos RIANTHAVORN, Pornpimol DEEKAJORNDEJ, Thavatchai SUPHAPEETIPORN, Kanya SHOTELERSUK, Vorasuk BAUM, Larry HIRANKARN, Nattiya KWAN, Patrick TSZ LEUNG LEE HOK KUNG HO, Marco PUI WAH LEE, Pamela HING SANG WONG, Wilfred SHUAI ZENG JING ZHANG WONG, Chun-Ming OI LIN NG, Irene GARCIA-BARCELO, Maria-Mercè DONG QING YE CHERNY, Stacey S KWONG-HANG TAM, Paul PAK CHUNG SHAM CHAK SING LAU YU LUNG LAU YAN ZHANG PAN, Hai-Feng CHI CHIU MOK TAK MAO CHAN WONG, Raymond Woon Sing MO YIN MOK |
description | Systemic lupus erythematosus (SLE) is an autoimmune disease with a strong genetic involvement. The susceptibility genes identified so far can only explain a small proportion of disease heritability. Through a genome-wide association in a Hong Kong Chinese cohort and subsequent replication in two other Asian populations, with a total of 3164 patients and 4482 matched controls, we identified association of ELF1 (E74-like factor 1) with SLE (rs7329174, OR = 1.26, joint P= 1.47 × 10(-8)). ELF1 belongs to the ETS family of transcription factors and is known to be involved in T cell development and function. Database analysis revealed transcripts making use of three alternative exon1s for this gene. Near equivalent expression levels of distinct transcripts initiated from alternative exon1s were detected in peripheral blood mononuclear cells from both SLE patients and healthy controls. Although a direct association of rs7329174 with the three forms of transcripts for this gene was not detected, these findings support an important role of ELF1 in SLE susceptibility and suggest a potentially tight regulation for the expression of this gene. |
doi_str_mv | 10.1093/hmg/ddq474 |
format | Article |
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The susceptibility genes identified so far can only explain a small proportion of disease heritability. Through a genome-wide association in a Hong Kong Chinese cohort and subsequent replication in two other Asian populations, with a total of 3164 patients and 4482 matched controls, we identified association of ELF1 (E74-like factor 1) with SLE (rs7329174, OR = 1.26, joint P= 1.47 × 10(-8)). ELF1 belongs to the ETS family of transcription factors and is known to be involved in T cell development and function. Database analysis revealed transcripts making use of three alternative exon1s for this gene. Near equivalent expression levels of distinct transcripts initiated from alternative exon1s were detected in peripheral blood mononuclear cells from both SLE patients and healthy controls. Although a direct association of rs7329174 with the three forms of transcripts for this gene was not detected, these findings support an important role of ELF1 in SLE susceptibility and suggest a potentially tight regulation for the expression of this gene.</description><identifier>ISSN: 0964-6906</identifier><identifier>EISSN: 1460-2083</identifier><identifier>DOI: 10.1093/hmg/ddq474</identifier><identifier>PMID: 21044949</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Asian Continental Ancestry Group - genetics ; Biological and medical sciences ; China ; Databases, Genetic ; Ephrin-A2 - genetics ; Fundamental and applied biological sciences. Psychology ; Genetic Predisposition to Disease ; Genetics of eukaryotes. Biological and molecular evolution ; Genome-Wide Association Study ; Genotype ; Haplotypes ; Hong Kong ; Humans ; Lupus Erythematosus, Systemic - genetics ; Medical sciences ; Molecular and cellular biology ; Polymerase Chain Reaction ; Polymorphism, Single Nucleotide ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Sequence Analysis, DNA ; T-Lymphocytes - metabolism ; Thailand ; Transcription Factors</subject><ispartof>Human molecular genetics, 2011-02, Vol.20 (3), p.601-607</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-acb4847998563de2b3327fe1c5aff4b250a6f482938b1b10cd186186bcc91b0d3</citedby><cites>FETCH-LOGICAL-c416t-acb4847998563de2b3327fe1c5aff4b250a6f482938b1b10cd186186bcc91b0d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23879105$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21044949$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>JING YANG</creatorcontrib><creatorcontrib>WANLING YANG</creatorcontrib><creatorcontrib>KA WING LEE</creatorcontrib><creatorcontrib>SIK NIN WONG</creatorcontrib><creatorcontrib>LEUNG, Alexander Moon Ho</creatorcontrib><creatorcontrib>LI, Xiang-Pei</creatorcontrib><creatorcontrib>AVIHINGSANON, Yingyos</creatorcontrib><creatorcontrib>RIANTHAVORN, Pornpimol</creatorcontrib><creatorcontrib>DEEKAJORNDEJ, Thavatchai</creatorcontrib><creatorcontrib>SUPHAPEETIPORN, Kanya</creatorcontrib><creatorcontrib>SHOTELERSUK, Vorasuk</creatorcontrib><creatorcontrib>BAUM, Larry</creatorcontrib><creatorcontrib>HIRANKARN, Nattiya</creatorcontrib><creatorcontrib>KWAN, Patrick</creatorcontrib><creatorcontrib>TSZ LEUNG LEE</creatorcontrib><creatorcontrib>HOK KUNG HO, Marco</creatorcontrib><creatorcontrib>PUI WAH LEE, Pamela</creatorcontrib><creatorcontrib>HING SANG WONG, Wilfred</creatorcontrib><creatorcontrib>SHUAI ZENG</creatorcontrib><creatorcontrib>JING ZHANG</creatorcontrib><creatorcontrib>WONG, Chun-Ming</creatorcontrib><creatorcontrib>OI LIN NG, Irene</creatorcontrib><creatorcontrib>GARCIA-BARCELO, Maria-Mercè</creatorcontrib><creatorcontrib>DONG QING YE</creatorcontrib><creatorcontrib>CHERNY, Stacey S</creatorcontrib><creatorcontrib>KWONG-HANG TAM, Paul</creatorcontrib><creatorcontrib>PAK CHUNG SHAM</creatorcontrib><creatorcontrib>CHAK SING LAU</creatorcontrib><creatorcontrib>YU LUNG LAU</creatorcontrib><creatorcontrib>YAN ZHANG</creatorcontrib><creatorcontrib>PAN, Hai-Feng</creatorcontrib><creatorcontrib>CHI CHIU MOK</creatorcontrib><creatorcontrib>TAK MAO CHAN</creatorcontrib><creatorcontrib>WONG, Raymond Woon Sing</creatorcontrib><creatorcontrib>MO YIN MOK</creatorcontrib><title>ELF1 is associated with systemic lupus erythematosus in Asian populations</title><title>Human molecular genetics</title><addtitle>Hum Mol Genet</addtitle><description>Systemic lupus erythematosus (SLE) is an autoimmune disease with a strong genetic involvement. The susceptibility genes identified so far can only explain a small proportion of disease heritability. Through a genome-wide association in a Hong Kong Chinese cohort and subsequent replication in two other Asian populations, with a total of 3164 patients and 4482 matched controls, we identified association of ELF1 (E74-like factor 1) with SLE (rs7329174, OR = 1.26, joint P= 1.47 × 10(-8)). ELF1 belongs to the ETS family of transcription factors and is known to be involved in T cell development and function. Database analysis revealed transcripts making use of three alternative exon1s for this gene. Near equivalent expression levels of distinct transcripts initiated from alternative exon1s were detected in peripheral blood mononuclear cells from both SLE patients and healthy controls. Although a direct association of rs7329174 with the three forms of transcripts for this gene was not detected, these findings support an important role of ELF1 in SLE susceptibility and suggest a potentially tight regulation for the expression of this gene.</description><subject>Asian Continental Ancestry Group - genetics</subject><subject>Biological and medical sciences</subject><subject>China</subject><subject>Databases, Genetic</subject><subject>Ephrin-A2 - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Genome-Wide Association Study</subject><subject>Genotype</subject><subject>Haplotypes</subject><subject>Hong Kong</subject><subject>Humans</subject><subject>Lupus Erythematosus, Systemic - genetics</subject><subject>Medical sciences</subject><subject>Molecular and cellular biology</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Sequence Analysis, DNA</subject><subject>T-Lymphocytes - metabolism</subject><subject>Thailand</subject><subject>Transcription Factors</subject><issn>0964-6906</issn><issn>1460-2083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0ctKw0AUBuBBFFurGx9AZiOCEDu3zGUppdVCwY2uw8xkYkdyMydB-vamtOpSOHA48PEvzo_QNSUPlBg-31bv8zz_FEqcoCkVkiSMaH6KpsRIkUhD5ARdAHwQQqXg6hxNGCVCGGGmaL3crCiOgC1A46PtQ46_Yr_FsIM-VNHjcmgHwKHb9dtQ2b6B8Yo1foRoa9w27VDaPjY1XKKzwpYQro57ht5Wy9fFc7J5eVovHjeJF1T2ifVOaKGM0ankeWCOc6aKQH1qi0I4lhIrC6GZ4dpRR4nPqZbjOO8NdSTnM3R3yG275nMI0GdVBB_K0tahGSAzqUiN1Er9L4mi6Rhu_pWaMUMY5_vM-4P0XQPQhSJru1jZbpdRku3byMY2skMbI745xg6uCvkv_Xn_CG6PwIK3ZdHZ2kf4c1wrQ0nKvwHXtJJz</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>JING YANG</creator><creator>WANLING YANG</creator><creator>KA WING LEE</creator><creator>SIK NIN WONG</creator><creator>LEUNG, Alexander Moon Ho</creator><creator>LI, Xiang-Pei</creator><creator>AVIHINGSANON, Yingyos</creator><creator>RIANTHAVORN, Pornpimol</creator><creator>DEEKAJORNDEJ, Thavatchai</creator><creator>SUPHAPEETIPORN, Kanya</creator><creator>SHOTELERSUK, Vorasuk</creator><creator>BAUM, Larry</creator><creator>HIRANKARN, Nattiya</creator><creator>KWAN, Patrick</creator><creator>TSZ LEUNG LEE</creator><creator>HOK KUNG HO, Marco</creator><creator>PUI WAH LEE, Pamela</creator><creator>HING SANG WONG, Wilfred</creator><creator>SHUAI ZENG</creator><creator>JING ZHANG</creator><creator>WONG, Chun-Ming</creator><creator>OI LIN NG, Irene</creator><creator>GARCIA-BARCELO, Maria-Mercè</creator><creator>DONG QING YE</creator><creator>CHERNY, Stacey S</creator><creator>KWONG-HANG TAM, Paul</creator><creator>PAK CHUNG SHAM</creator><creator>CHAK SING LAU</creator><creator>YU LUNG LAU</creator><creator>YAN ZHANG</creator><creator>PAN, Hai-Feng</creator><creator>CHI CHIU MOK</creator><creator>TAK MAO CHAN</creator><creator>WONG, Raymond Woon Sing</creator><creator>MO YIN MOK</creator><general>Oxford University Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20110201</creationdate><title>ELF1 is associated with systemic lupus erythematosus in Asian populations</title><author>JING YANG ; WANLING YANG ; KA WING LEE ; SIK NIN WONG ; LEUNG, Alexander Moon Ho ; LI, Xiang-Pei ; AVIHINGSANON, Yingyos ; RIANTHAVORN, Pornpimol ; DEEKAJORNDEJ, Thavatchai ; SUPHAPEETIPORN, Kanya ; SHOTELERSUK, Vorasuk ; BAUM, Larry ; HIRANKARN, Nattiya ; KWAN, Patrick ; TSZ LEUNG LEE ; HOK KUNG HO, Marco ; PUI WAH LEE, Pamela ; HING SANG WONG, Wilfred ; SHUAI ZENG ; JING ZHANG ; WONG, Chun-Ming ; OI LIN NG, Irene ; GARCIA-BARCELO, Maria-Mercè ; DONG QING YE ; CHERNY, Stacey S ; KWONG-HANG TAM, Paul ; PAK CHUNG SHAM ; CHAK SING LAU ; YU LUNG LAU ; YAN ZHANG ; PAN, Hai-Feng ; CHI CHIU MOK ; TAK MAO CHAN ; WONG, Raymond Woon Sing ; MO YIN MOK</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-acb4847998563de2b3327fe1c5aff4b250a6f482938b1b10cd186186bcc91b0d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Asian Continental Ancestry Group - genetics</topic><topic>Biological and medical sciences</topic><topic>China</topic><topic>Databases, Genetic</topic><topic>Ephrin-A2 - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Genome-Wide Association Study</topic><topic>Genotype</topic><topic>Haplotypes</topic><topic>Hong Kong</topic><topic>Humans</topic><topic>Lupus Erythematosus, Systemic - genetics</topic><topic>Medical sciences</topic><topic>Molecular and cellular biology</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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The susceptibility genes identified so far can only explain a small proportion of disease heritability. Through a genome-wide association in a Hong Kong Chinese cohort and subsequent replication in two other Asian populations, with a total of 3164 patients and 4482 matched controls, we identified association of ELF1 (E74-like factor 1) with SLE (rs7329174, OR = 1.26, joint P= 1.47 × 10(-8)). ELF1 belongs to the ETS family of transcription factors and is known to be involved in T cell development and function. Database analysis revealed transcripts making use of three alternative exon1s for this gene. Near equivalent expression levels of distinct transcripts initiated from alternative exon1s were detected in peripheral blood mononuclear cells from both SLE patients and healthy controls. Although a direct association of rs7329174 with the three forms of transcripts for this gene was not detected, these findings support an important role of ELF1 in SLE susceptibility and suggest a potentially tight regulation for the expression of this gene.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>21044949</pmid><doi>10.1093/hmg/ddq474</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Asian Continental Ancestry Group - genetics Biological and medical sciences China Databases, Genetic Ephrin-A2 - genetics Fundamental and applied biological sciences. Psychology Genetic Predisposition to Disease Genetics of eukaryotes. Biological and molecular evolution Genome-Wide Association Study Genotype Haplotypes Hong Kong Humans Lupus Erythematosus, Systemic - genetics Medical sciences Molecular and cellular biology Polymerase Chain Reaction Polymorphism, Single Nucleotide Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Sequence Analysis, DNA T-Lymphocytes - metabolism Thailand Transcription Factors |
title | ELF1 is associated with systemic lupus erythematosus in Asian populations |
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