Gene-gene interaction and RNA splicing profiles of MAP2K4 gene in rheumatoid arthritis

被引:11
|
作者
Shchetynsky, Klementy [1 ]
Protsyuk, Darya [1 ]
Ronninger, Marcus [1 ]
Diaz-Gallo, Lina-Marceta [1 ]
Klareskog, Lars [1 ]
Padyukov, Leonid [1 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Dept Med, Rheumatol Unit, S-17176 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Rheumatoid arthritis; Gene-gene interaction; MAP2K4; Alternative splicing; RNA expression; RISK; INFLAMMATION; ASSOCIATION; EXPRESSION; SMOKING; DISEASE; PTPN22; MAPKS;
D O I
10.1016/j.clim.2015.02.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We performed gene gene interaction analysis, with HLA-DRB1 shared epitope (SE) alleles for 195 SNPs within immunologically important MAP2K, MAP3K and MAP4K gene families, in 2010 rheumatoid arthritis (RA) patients and 2280 healthy controls. We found a significant statistical interaction for rs10468473 with SE alleles in autoantibody-positive RA. Individuals heterozygous for rs10468473 demonstrated higher expression of total MAP2K4 mRNA in blood, compared to A-allele homozygous. We discovered a novel, putatively translated, "cassette exon" RNA splice form of MAP2K4, differentially expressed in peripheral blood mononuclear cells from 88 RA cases and controls. Within the group of RA patients, we observed a correlation of MAP2K4 isoform expression with carried SE alleles, autoantibody, and rheumatoid factor profiles. TNF-dependent modulation of isoform expression pattern was detected in the Jurkat cell line. Our data suggest a genetic interaction between MAP2K4 and HLA-DRB1, and the importance of rs10468473 and MAP2K4 splice variants in the development of autoantibody-positive RA. (C) 2015 The Authors. Published by Elsevier Inc.
引用
收藏
页码:19 / 28
页数:10
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