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Mediation Analysis Demonstrates That Trans-eQTLs Are Often Explained by Cis-Mediation: A Genome-Wide Analysis among 1800 South Asians

机译:调解分析表明反式eQTL通常由顺式调解解释:在1800名南亚人中进行的全基因组分析

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摘要

A large fraction of human genes are regulated by genetic variation near the transcribed sequence (cis-eQTL, expression quantitative trait locus), and many cis-eQTLs have implications for human disease. Less is known regarding the effects of genetic variation on expression of distant genes (trans-eQTLs) and their biological mechanisms. In this work, we use genome-wide data on SNPs and array-based expression measures from mononuclear cells obtained from a population-based cohort of 1,799 Bangladeshi individuals to characterize cis- and trans-eQTLs and determine if observed trans-eQTL associations are mediated by expression of transcripts in cis with the SNPs showing trans-association, using Sobel tests of mediation. We observed 434 independent trans-eQTL associations at a false-discovery rate of 0.05, and 189 of these trans-eQTLs were also cis-eQTLs (enrichment P<0.0001). Among these 189 trans-eQTL associations, 39 were significantly attenuated after adjusting for a cis-mediator based on Sobel P<10-5. We attempted to replicate 21 of these mediation signals in two European cohorts, and while only 7 trans-eQTL associations were present in one or both cohorts, 6 showed evidence of cis-mediation. Analyses of simulated data show that complete mediation will be observed as partial mediation in the presence of mediator measurement error or imperfect LD between measured and causal variants. Our data demonstrates that trans-associations can become significantly stronger or switch directions after adjusting for a potential mediator. Using simulated data, we demonstrate that this phenomenon is expected in the presence of strong cis-trans confounding and when the measured cis-transcript is correlated with the true (unmeasured) mediator. In conclusion, by applying mediation analysis to eQTL data, we show that a substantial fraction of observed trans-eQTL associations can be explained by cis-mediation. Future studies should focus on understanding the mechanisms underlying widespread cis-mediation and their relevance to disease biology, as well as using mediation analysis to improve eQTL discovery.
机译:人类基因的很大一部分受转录序列(顺式-eQTL,表达数量性状基因座)附近的遗传变异的调控,许多顺式-eQTL对人类疾病有影响。关于遗传变异对远距离基因(trans-eQTL)表达及其生物学机制的影响知之甚少。在这项工作中,我们使用SNPs的全基因组数据和从1799名孟加拉国人群的人群中获得的单核细胞的基于阵列的表达量度来表征顺式和反式eQTL,并确定是否观察到反式eQTL关联通过使用Sobel中介试验,通过在顺式中表达转录物,使SNP显示反式缔合。我们观察到434个独立的反式eQTL关联,错误发现率为0.05,其中189个反式eQTL也是顺式eQTL(富集P <0.0001)。在这189个trans-eQTL关联中,有39个在基于Sobel P <10 -5 调整顺式介体后显着减弱。我们试图在两个欧洲队列中复制21个这些调解信号,而在一个或两个队列中仅存在7个trans-eQTL关联,但有6个显示了顺式调解的证据。对模拟数据的分析表明,在存在介体测量错误或被测变量与因果变量之间存在不完善的LD的情况下,完全中介将被视为部分中介。我们的数据表明,在调节潜在的介体后,反式关联可以变得更加强大或改变方向。使用模拟数据,我们证明在强烈的顺式- trans 混杂的情况下以及当测得的 cis -转录本与真实(未测量)介体相关时,这种现象是可以预期的。总之,通过将中介分析应用于eQTL数据,我们表明,观察到的 trans -eQTL关联的很大一部分可以通过 cis 中介进行解释。未来的研究应侧重于理解广泛的顺式介导的机制及其与疾病生物学的相关性,以及使用介导分析来改善eQTL发现。

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