期刊
JOURNAL OF MEDICAL GENETICS
卷 50, 期 1, 页码 25-33出版社
BMJ PUBLISHING GROUP
DOI: 10.1136/jmedgenet-2012-101085
关键词
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资金
- Ministerio de Economia y Competitividad (MINECO)-Fondos Europeos de Desarrollo Regional (FEDER) [SAF2009-11491]
- Fondo de Investigacion Sanitaria (FIS) [RETICS-REEM RD07/0060, CP 10/00526, PI10/1985, PS09/02105]
- Junta de Andaluc~a-Fondos Europeos de Desarrollo Regional (FEDER) [P07-CVI-02551, P09-CTS-5218]
- Basque Foundation for Science (Bilbao)
- Fundacion Ilundain
- ICREA Funding Source: Custom
Background and aim Several studies have highlighted the association of the 12q13.3-12q14.1 region with coeliac disease, type 1 diabetes, rheumatoid arthritis and multiple sclerosis (MS); however, the causal variants underlying diseases are still unclear. The authors sought to identify the functional variant of this region associated with MS. Methods Tag-single nucleotide polymorphism (SNP) analysis of the associated region encoding 15 genes was performed in 2876 MS patients and 2910 healthy Caucasian controls together with expression regulation analyses. Results rs6581155, which tagged 18 variants within a region where 9 genes map, was sufficient to model the association. This SNP was in total linkage disequilibrium (LD) with other polymorphisms that associated with the expression levels of FAM119B, AVIL, TSFM, TSPAN31 and CYP27B1 genes in different expression quantitative trait loci studies. Functional annotations from Encyclopedia of DNA Elements (ENCODE) showed that six out of these rs6581155-tagged-SNPs were located in regions with regulatory potential and only one of them, rs10877013, exhibited allele-dependent (ratio A/G=9.5-fold) and orientation-dependent (forward/reverse=2.7-fold) enhancer activity as determined by luciferase reporter assays. This enhancer is located in a region where a long-range chromatin interaction among the promoters and promoter-enhancer of several genes has been described, possibly affecting their expression simultaneously. Conclusions This study determines a functional variant which alters the enhancer activity of a regulatory element in the locus affecting the expression of several genes and explains the association of the 12q13.3-12q14.1 region with MS.
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