Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus

被引:216
作者
Adrianto, Indra [1 ]
Wen, Feng [1 ]
Templeton, Amanda [2 ]
Wiley, Graham [1 ]
King, Jarrod B. [2 ]
Lessard, Christopher J. [1 ,2 ]
Bates, Jared S. [1 ]
Hu, Yanqing [2 ]
Kelly, Jennifer A. [1 ]
Kaufman, Kenneth M. [1 ,2 ,3 ]
Guthridge, Joel M. [1 ]
Alarcon-Riquelme, Marta E. [1 ,4 ]
Anaya, Juan-Manuel [5 ]
Bae, Sang-Cheol [6 ]
Bang, So-Young [6 ]
Boackle, Susan A. [7 ]
Brown, Elizabeth E. [8 ]
Petri, Michelle A. [9 ]
Gallant, Caroline [10 ]
Ramsey-Goldman, Rosalind [11 ]
Reveille, John D. [12 ]
Vila, Luis M. [13 ]
Criswell, Lindsey A. [14 ]
Edberg, Jeffrey C. [15 ]
Freedman, Barry I. [16 ]
Gregersen, Peter K. [17 ]
Gilkeson, Gary S. [18 ]
Jacob, Chaim O. [19 ]
James, Judith A. [1 ,2 ]
Kamen, Diane L. [18 ]
Kimberly, Robert P. [15 ]
Martin, Javier [20 ]
Merrill, Joan T. [21 ]
Niewold, Timothy B. [22 ,23 ]
Park, So-Yeon [6 ]
Pons-Estel, Bernardo A. [24 ]
Scofield, R. Hal [1 ,2 ]
Stevens, Anne M. [25 ,26 ]
Tsao, Betty P. [27 ]
Vyse, Timothy J. [28 ,29 ]
Langefeld, Carl D. [30 ]
Harley, John B. [3 ,31 ]
Moser, Kathy L. [1 ,2 ]
Webb, Carol F. [32 ]
Humphrey, Mary Beth [2 ]
Montgomery, Courtney Gray [1 ]
Gaffney, Patrick M. [1 ]
机构
[1] Oklahoma Med Res Fdn, Arthrit & Clin Immunol Res Program, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Coll Med, Oklahoma City, OK 73190 USA
[3] US Dept Vet Affairs Med Ctr, Oklahoma City, OK USA
[4] Ctr Genom & Oncol Res GENyO, Granada, Spain
[5] Univ Rosario, Ctr Autoimmune Dis Res CREA, Bogota, Colombia
[6] Hanyang Univ Hosp Rheumat Dis, Dept Rheumatol, Seoul, South Korea
[7] Univ Colorado Denver, Div Rheumatol, Aurora, CO USA
[8] Univ Alabama, Dept Epidemiol, Birmingham, AL USA
[9] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[10] Uppsala Univ, Rudbeck Lab, Dept Genet & Pathol, Uppsala, Sweden
[11] Northwestern Univ, Feinberg Sch Med, Div Rheumatol, Chicago, IL 60611 USA
[12] Univ Texas Hlth Sci Ctr Houston, Houston, TX USA
[13] Univ Puerto Rico, Dept Med, Div Rheumatol, San Juan, PR 00936 USA
[14] Univ Calif San Francisco, Rosalind Russell Med Res Ctr Arthrit, San Francisco, CA 94143 USA
[15] Univ Alabama, Dept Med, Birmingham, AL 35294 USA
[16] Wake Forest Univ Hlth Sci, Dept Internal Med, Winston Salem, NC USA
[17] N Shore Long Isl Jewish LIJ Hlth Syst, Feinstein Inst Med Res, Robert S Boas Ctr Genom & Human Genet, Manhasset, NY USA
[18] Univ S Carolina, Div Rheumatol, Charleston, SC USA
[19] Univ So Calif, Dept Med, Los Angeles, CA USA
[20] CSIC, Inst Parasitol & Biomed Lopez Neyra, Granada, Spain
[21] Oklahoma Med Res Fdn, Clin Pharmacol Res Program, Oklahoma City, OK 73104 USA
[22] Univ Chicago, Rheumatol Sect, Chicago, IL 60637 USA
[23] Univ Chicago, Gwen Knapp Ctr Lupus & Immunol Res, Chicago, IL 60637 USA
[24] Sanat Parque, Rosario, Santa Fe, Argentina
[25] Univ Washington, Dept Pediat, Div Rheumatol, Seattle, WA 98195 USA
[26] Seattle Childrens Res Inst, Ctr Immun & Immunotherapies, Seattle, WA USA
[27] Univ Calif Los Angeles, Dept Med, Div Rheumatol, Los Angeles, CA 90024 USA
[28] Kings Coll London, Div Genet & Mol Med, London WC2R 2LS, England
[29] Kings Coll London, Div Immunol Infect & Inflammatory Dis, London WC2R 2LS, England
[30] Wake Forest Univ Hlth Sci, Dept Biostat Sci, Winston Salem, NC USA
[31] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH USA
[32] Oklahoma Med Res Fdn, Immunobiol & Canc Res Program, Oklahoma City, OK 73104 USA
基金
美国国家卫生研究院; 新加坡国家研究基金会; 英国惠康基金; 瑞典研究理事会;
关键词
GENOME-WIDE ASSOCIATION; AFRICAN-AMERICANS; RHEUMATOID-ARTHRITIS; ENZYME A20; ADMIXTURE; HAPLOTYPE; RISK; 6Q23; MAP; POLYMORPHISMS;
D O I
10.1038/ng.766
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Systemic lupus erythematosus (SLE, MIM152700) is an autoimmune disease characterized by self-reactive antibodies resulting in systemic inflammation and organ failure. TNFAIP3, encoding the ubiquitin-modifying enzyme A20, is an established susceptibility locus for SLE. By fine mapping and genomic re-sequencing in ethnically diverse populations, we fully characterized the TNFAIP3 risk haplotype and identified a TT>A polymorphic dinucleotide (deletion T followed by a T to A transversion) associated with SLE in subjects of European (P = 1.58 x 10(-8), odds ratio = 1.70) and Korean (P = 8.33 x 10(-10), odds ratio = 2.54) ancestry. This variant, located in a region of high conservation and regulatory potential, bound a nuclear protein complex composed of NF-kappa B subunits with reduced avidity. Further, compared with the non-risk haplotype, the haplotype carrying this variant resulted in reduced TNFAIP3 mRNA and A20 protein expression. These results establish this TT>A variant as the most likely functional polymorphism responsible for the association between TNFAIP3 and SLE.
引用
收藏
页码:253 / U102
页数:8
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