A Genome-Wide Association Study Identified as a Susceptibility Locus for Systemic Lupus Eyrthematosus in Japanese
Systemic lupus erythematosus (SLE) is an autoimmune disease that causes multiple organ damage. Although recent genome-wide association studies (GWAS) have contributed to discovery of SLE susceptibility genes, few studies has been performed in Asian populations. Here, we report a GWAS for SLE examining 891 SLE cases and 3,384 controls and multi-stage replication studies examining 1,387 SLE cases and 28,564 controls in Japanese subjects. Considering that expression quantitative trait loci (eQTLs) have been implicated in genetic risks for autoimmune diseases, we integrated an eQTL study into the results of the GWAS. We observed enrichments of cis-eQTL positive loci among the known SLE susceptibility loci (30.8%) compared to the genome-wide SNPs (6.9%). In addition, we identified a novel association of a variant in the AF4/FMR2 family, member 1 (AFF1) gene at 4q21 with SLE susceptibility (rs340630; P = 8.3×10−9, odds ratio = 1.21). The risk A allele of rs340630 demonstrated a cis-eQTL effect on the AFF1 transcript with enhanced expression levels (P<0.05). As AFF1 transcripts were prominently expressed in CD4+ and CD19+ peripheral blood lymphocytes, up-regulation of AFF1 may cause the abnormality in these lymphocytes, leading to disease onset.
Vyšlo v časopise:
A Genome-Wide Association Study Identified as a Susceptibility Locus for Systemic Lupus Eyrthematosus in Japanese. PLoS Genet 8(1): e32767. doi:10.1371/journal.pgen.1002455
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1002455
Souhrn
Systemic lupus erythematosus (SLE) is an autoimmune disease that causes multiple organ damage. Although recent genome-wide association studies (GWAS) have contributed to discovery of SLE susceptibility genes, few studies has been performed in Asian populations. Here, we report a GWAS for SLE examining 891 SLE cases and 3,384 controls and multi-stage replication studies examining 1,387 SLE cases and 28,564 controls in Japanese subjects. Considering that expression quantitative trait loci (eQTLs) have been implicated in genetic risks for autoimmune diseases, we integrated an eQTL study into the results of the GWAS. We observed enrichments of cis-eQTL positive loci among the known SLE susceptibility loci (30.8%) compared to the genome-wide SNPs (6.9%). In addition, we identified a novel association of a variant in the AF4/FMR2 family, member 1 (AFF1) gene at 4q21 with SLE susceptibility (rs340630; P = 8.3×10−9, odds ratio = 1.21). The risk A allele of rs340630 demonstrated a cis-eQTL effect on the AFF1 transcript with enhanced expression levels (P<0.05). As AFF1 transcripts were prominently expressed in CD4+ and CD19+ peripheral blood lymphocytes, up-regulation of AFF1 may cause the abnormality in these lymphocytes, leading to disease onset.
Zdroje
1. LipskyPE 2001 Systemic lupus erythematosus: an autoimmune disease of B cell hyperactivity. Nat Immunol 2 764 766
2. SestakALShaverTSMoserKLNeasBRHarleyJB 1999 Familial aggregation of lupus and autoimmunity in an unusual multiplex pedigree. J Rheumatol 26 1495 1499
3. SigurdssonSNordmarkGGoringHHLindroosKWimanAC 2005 Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus. Am J Hum Genet 76 528 537
4. GrahamRRKozyrevSVBaechlerECReddyMVPlengeRM 2006 A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus. Nat Genet 38 550 555
5. GrahamRRKyogokuCSigurdssonSVlasovaIADaviesLR 2007 Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus. Proc Natl Acad Sci U S A 104 6758 6763
6. RemmersEFPlengeRMLeeATGrahamRRHomG 2007 STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus. N Engl J Med 357 977 986
7. Cunninghame GrahamDSGrahamRRMankuHWongAKWhittakerJC 2008 Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus. Nat Genet 40 83 89
8. NathSKHanSKim-HowardXKellyJAViswanathanP 2008 A nonsynonymous functional variant in integrin-alpha(M) (encoded by ITGAM) is associated with systemic lupus erythematosus. Nat Genet 40 152 154
9. HarleyJBAlarcon-RiquelmeMECriswellLAJacobCOKimberlyRP 2008 Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. Nat Genet 40 204 210
10. KozyrevSVAbelsonAKWojcikJZaghloolALinga ReddyMV 2008 Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus. Nat Genet 40 211 216
11. HomGGrahamRRModrekBTaylorKEOrtmannW 2008 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. N Engl J Med 358 900 909
12. GrahamRRCotsapasCDaviesLHackettRLessardCJ 2008 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. Nat Genet 40 1059 1061
13. MusoneSLTaylorKELuTTNitithamJFerreiraRC 2008 Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus. Nat Genet 40 1062 1064
14. HanJWZhengHFCuiYSunLDYeDQ 2009 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. Nat Genet 41 1234 1237
15. GatevaVSandlingJKHomGTaylorKEChungSA 2009 A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus. Nat Genet 41 1228 1233
16. YangWShenNYeDQLiuQZhangY 2010 Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus. PLoS Genet 6 e1000841 doi:10.1371/journal.pgen.1000841
17. LessardCJAdriantoIKellyJAKaufmanKMGrundahlKM 2011 Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study. Am J Hum Genet 88 83 91
18. YangJYangWHirankarnNYeDQZhangY 2011 ELF1 is associated with systemic lupus erythematosus in Asian populations. Hum Mol Genet 20 601 607
19. HopkinsonNDDohertyMPowellRJ 1994 Clinical features and race-specific incidence/prevalence rates of systemic lupus erythematosus in a geographically complete cohort of patients. Ann Rheum Dis 53 675 680
20. DanchenkoNSatiaJAAnthonyMS 2006 Epidemiology of systemic lupus erythematosus: a comparison of worldwide disease burden. Lupus 15 308 318
21. YangJBenyaminBMcEvoyBPGordonSHendersAK 2010 Common SNPs explain a large proportion of the heritability for human height. Nat Genet 42 565 569
22. RaychaudhuriSPlengeRMRossinEJNgACPurcellSM 2009 Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions. PLoS Genet 5 e1000534 doi:10.1371/journal.pgen.1000534
23. CantorRMLangeKSinsheimerJS 2010 Prioritizing GWAS results: A review of statistical methods and recommendations for their application. Am J Hum Genet 86 6 22
24. DuboisPCTrynkaGFrankeLHuntKARomanosJ 2010 Multiple common variants for celiac disease influencing immune gene expression. Nat Genet 42 295 302
25. CooksonWLiangLAbecasisGMoffattMLathropM 2009 Mapping complex disease traits with global gene expression. Nat Rev Genet 10 184 194
26. KochiYOkadaYSuzukiAIkariKTeraoC 2010 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. Nat Genet 42 515 519
27. Yamaguchi-KabataYNakazonoKTakahashiASaitoSHosonoN 2008 Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies. Am J Hum Genet 83 445 456
28. StrangerBENicaACForrestMSDimasABirdCP 2007 Population genomics of human gene expression. Nat Genet 39 1217 1224
29. The International HapMap Consortium 2003 The International HapMap Project. Nature 426 789 796
30. PearsonJVHuentelmanMJHalperinRFTembeWDMelquistS 2007 Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. Am J Hum Genet 80 126 139
31. XiaZBPopovicRChenJTheislerCStuartT 2005 The MLL fusion gene, MLL-AF4, regulates cyclin-dependent kinase inhibitor CDKN1B (p27kip1) expression. Proc Natl Acad Sci U S A 102 14028 14033
32. IsnardPCoreNNaquetPDjabaliM 2000 Altered lymphoid development in mice deficient for the mAF4 proto-oncogene. Blood 96 705 710
33. SchadtEEMolonyCChudinEHaoKYangX 2008 Mapping the genetic architecture of gene expression in human liver. PLoS Biol 6 e107 doi:10.1371/journal.pbio.0060107
34. ErnstJKheradpourPMikkelsenTSShoreshNWardLD 2011 Mapping and analysis of chromatin state dynamics in nine human cell types. Nature 473 43 49
35. StahlEARaychaudhuriSRemmersEFXieGEyreS 2010 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat Genet 42 508 514
36. NakamuraY 2007 The BioBank Japan Project. Clin Adv Hematol Oncol 5 696 697
37. HochbergMC 1997 Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 40 1725
38. SuzukiAYamadaRKochiYSawadaTOkadaY 2008 Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population. Nat Genet 40 1224 1229
39. ShimaneKKochiYHoritaTIkariKAmanoH 2010 The association of a nonsynonymous single-nucleotide polymorphism in TNFAIP3 with systemic lupus erythematosus and rheumatoid arthritis in the Japanese population. Arthritis Rheum 62 574 579
40. MyouzenKKochiYShimaneKFujioKOkamuraT 2010 Regulatory polymorphisms in EGR2 are associated with susceptibility to systemic lupus erythematosus. Hum Mol Genet 19 2313 2320
41. PurcellSNealeBTodd-BrownKThomasLFerreiraMA 2007 PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81 559 575
42. PriceALPattersonNJPlengeRMWeinblattMEShadickNA 2006 Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38 904 909
43. LiYWillerCSannaSAbecasisG 2009 Genotype imputation. Annu Rev Genomics Hum Genet 10 387 406
44. OkadaYTakahashiAOhmiyaHKumasakaNKamataniY 2011 Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. Hum Mol Genet 20 1224 1231
45. AikawaYYamamotoMYamamotoTMorimotoKTanakaK 2002 An anti-rheumatic agent T-614 inhibits NF-kappaB activation in LPS- and TNF-alpha-stimulated THP-1 cells without interfering with IkappaBalpha degradation. Inflamm Res 51 188 194
46. AkamatsuSTakataRAshikawaKHosonoNKamataniN 2010 A functional variant in NKX3.1 associated with prostate cancer susceptibility down-regulates NKX3.1 expression. Hum Mol Genet 19 4265 4272
47. JohnsonADHandsakerREPulitSLNizzariMMO'DonnellCJ 2008 SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 24 2938 2939
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
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