MDA5变体以抗病毒活性换取对自身免疫性疾病的保护。

IF 2.1 4区 医学 Q3 GENETICS & HEREDITY
Chris Wallace, Rahul Singh, Yorgo Modis
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引用次数: 0

摘要

在全基因组关联研究(GWAS)中,病毒和逆转录因子双链RNA的关键传感器MDA5的功能丧失变体与1型糖尿病(T1D)的保护有关。据报道,MDA5功能丧失变异也会增加炎症性肠病(IBD)的风险。这些关联是否与其他疾病有关或延伸到其他疾病尚不清楚。在这里,对四个大型GWAS数据集的精细映射分析表明,保护t1d的功能丧失MDA5变异也可以预防牛皮癣和甲状腺功能减退,同时增加IBD的风险。自身免疫保护程度与IBD风险呈线性正比关系。罕见MDA5变异的自身免疫保护和IBD风险的比值比大于常见变异,这在不同的地理人群中存在差异表达。我们的分析表明,MDA5基因变异在病毒清除和自身免疫组织损伤之间提供了直接的适应性权衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MDA5 variants trade antiviral activity for protection from autoimmune disease.

Loss-of-function variants in MDA5, a key sensor of double-stranded RNA from viruses and retroelements, have been associated with protection from type 1 diabetes (T1D) in genome-wide association studies (GWAS). MDA5 loss-of-function variants have also been reported to increase the risk of inflammatory bowel disease (IBD). Whether these associations are linked or extend to other diseases remains unclear. Here, fine-mapping analysis of four large GWAS datasets shows that T1D-protective loss-of-function MDA5 variants also protect against psoriasis and hypothyroidism, while increasing the risk of IBD. The degree of autoimmune protection and IBD risk were linearly proportional. The magnitudes of the odds ratios for autoimmune protection and IBD risk were larger for rare MDA5 variants than for common variants, which were differentially expressed in different geographic populations. Our analysis suggests MDA5 genetic variants offer a direct fitness trade-off between viral clearance and autoimmune tissue damage.

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来源期刊
BMC Medical Genomics
BMC Medical Genomics 医学-遗传学
CiteScore
3.90
自引率
0.00%
发文量
243
审稿时长
3.5 months
期刊介绍: BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genomics, genome structure, genome-scale population genetics, epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.
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