Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA 02142, USA.
Science. 2014 Mar 7;343(6175):1246980. doi: 10.1126/science.1246980.
Little is known about how human genetic variation affects the responses to environmental stimuli in the context of complex diseases. Experimental and computational approaches were applied to determine the effects of genetic variation on the induction of pathogen-responsive genes in human dendritic cells. We identified 121 common genetic variants associated in cis with variation in expression responses to Escherichia coli lipopolysaccharide, influenza, or interferon-β (IFN-β). We localized and validated causal variants to binding sites of pathogen-activated STAT (signal transducer and activator of transcription) and IRF (IFN-regulatory factor) transcription factors. We also identified a common variant in IRF7 that is associated in trans with type I IFN induction in response to influenza infection. Our results reveal common alleles that explain interindividual variation in pathogen sensing and provide functional annotation for genetic variants that alter susceptibility to inflammatory diseases.
关于人类遗传变异如何影响复杂疾病背景下对环境刺激的反应,人们知之甚少。本研究应用实验和计算方法来确定遗传变异对人类树突状细胞中病原体反应基因诱导的影响。我们鉴定了 121 个常见的遗传变异,这些变异与大肠杆菌脂多糖、流感或干扰素-β(IFN-β)的表达反应变异呈顺式相关。我们定位并验证了致病变体到病原体激活 STAT(信号转导和转录激活因子)和 IRF(IFN 调节因子)转录因子结合位点。我们还在 IRF7 中发现了一个常见的变异,该变异与流感感染时 I 型 IFN 的诱导呈反式相关。我们的研究结果揭示了常见的等位基因,这些等位基因解释了病原体感知的个体间差异,并为改变炎症性疾病易感性的遗传变异提供了功能注释。