生物
单核苷酸多态性
炎症
促炎细胞因子
内质网
遗传学
遗传变异
免疫学
单倍型
基因
等位基因
基因型
作者
Joanne E. Curran,Jeremy B. M. Jowett,Kate Elliott,Yuan Gao,Kristi Gluschenko,Jianmin Wang,Dalia M Abel Azim,Guowen Cai,Michael C. Mahaney,Anthony G. Comuzzie,Thomas D. Dyer,Ken Walder,Paul Zimmet,Jean W. MacCluer,Greg R. Collier,Ahmed H. Kissebah,John Blangero
出处
期刊:Nature Genetics
[Springer Nature]
日期:2005-10-09
卷期号:37 (11): 1234-1241
被引量:363
摘要
Chronic inflammation has a pathological role in many common diseases and is influenced by both genetic and environmental factors. Here we assess the role of genetic variation in selenoprotein S (SEPS1, also called SELS or SELENOS), a gene involved in stress response in the endoplasmic reticulum and inflammation control. After resequencing SEPS1, we genotyped 13 SNPs in 522 individuals from 92 families. As inflammation biomarkers, we measured plasma levels of IL-6, IL-1β and TNF-α. Bayesian quantitative trait nucleotide analysis identified associations between SEPS1 polymorphisms and all three proinflammatory cytokines. One promoter variant, −105G → A, showed strong evidence for an association with each cytokine (multivariate P = 0.0000002). Functional analysis of this polymorphism showed that the A variant significantly impaired SEPS1 expression after exposure to endoplasmic reticulum stress agents (P = 0.00006). Furthermore, suppression of SEPS1 by short interfering RNA in macrophage cells increased the release of IL-6 and TNF-α. To investigate further the significance of the observed associations, we genotyped −105G → A in 419 Mexican American individuals from 23 families for replication. This analysis confirmed a significant association with both TNF-α (P = 0.0049) and IL-1β (P = 0.0101). These results provide a direct mechanistic link between SEPS1 and the production of inflammatory cytokines and suggest that SEPS1 has a role in mediating inflammation.
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