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Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota

机译:全基因组关联分析确定了维生素D受体和其他影响肠道菌群的宿主因素的变异

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Human gut microbiota is an important determinant for health and disease, and recent studies emphasize the numerous factors shaping its diversity. Here we performed a genome-wide association study (GWAS) of the gut microbiota using two cohorts from northern Germany totaling 1,812 individuals. Comprehensively controlling for diet and non-genetic parameters, we identify genome-wide significant associations for overall microbial variation and individual taxa at multiple genetic loci, including the VDR gene (encoding vitamin D receptor). We observe significant shifts in the microbiota of Vdr(-/-) mice relative to control mice and correlations between the microbiota and serum measurements of selected bile and fatty acids in humans, including known ligands and downstream metabolites of VDR. Genome-wide significant (P < 5 x 10(-8)) associations at multiple additional loci identify other important points of host-microbe intersection, notably several disease susceptibility genes and sterol metabolism pathway components. Non-genetic and genetic factors each account for approximately 10% of the variation in gut microbiota, whereby individual effects are relatively small.
机译:人体肠道菌群是健康和疾病的重要决定因素,最近的研究强调了影响其多样性的众多因素。在这里,我们使用来自德国北部的两个队列,共1,812个个体,对肠道菌群进行了全基因组关联研究(GWAS)。全面控制饮食和非遗传参数,我们确定了整个基因组范围内整个微生物变异和多个遗传位点(包括VDR基因(编码维生素D受体)的单个分类单元)的显着关联。我们观察到相对于对照小鼠,Vdr(-/-)小鼠的微生物区系发生了显着变化,并且微生物群与人中所选胆汁和脂肪酸的血清测量值之间的相关性,包括VDR的已知配体和下游代谢产物。在多个其他基因座处的全基因组显着(P <5 x 10(-8))关联确定了宿主-微生物交集的其他重要点,特别是几个疾病易感基因和固醇代谢途径成分。非遗传因素和遗传因素各自约占肠道菌群变异的10%,因此个体效应相对较小。

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