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Large-Scale trans-eQTLs Affect Hundreds of Transcripts and Mediate Patterns of Transcriptional Co-regulation

机译:大规模的trans-eQTL影响数百个笔录和中介转录调控的模式。

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摘要

Efforts to decipher the causal relationships between differences in gene regulation and corresponding differences in phenotype have been stymied by several basic technical challenges. Although detecting local, cis-eQTLs is now routine, trans-eQTLs, which are distant from the genes of origin, are far more difficult to find because millions of SNPs must currently be compared to thousands of transcripts. Here, we demonstrate an alternative approach: we looked for SNPs associated with the expression of many genes simultaneously and found that hundreds of trans-eQTLs each affect hundreds of transcripts in lymphoblastoid cell lines across three African populations. These trans-eQTLs target the same genes across the three populations and show the same direction of effect. We discovered that target transcripts of a high-confidence set of trans-eQTLs encode proteins that interact more frequently than expected by chance, are bound by the same transcription factors, and are enriched for pathway annotations indicative of roles in basic cell homeostasis. We thus demonstrate that our approach can uncover trans-acting transcriptional control circuits that affect co-regulated groups of genes: a key to understanding how cellular pathways and processes are orchestrated.
机译:几个基本的技术挑战已阻碍了努力解释基因调控差异和相应的表型差异之间的因果关系。尽管现在检测局部的顺式eQTL很常规,但是与起源基因相距较远的反式eQTL却很难找到,因为目前必须将数百万个SNP与数千个转录本进行比较。在这里,我们展示了一种替代方法:我们同时寻找与许多基因表达相关的SNP,并发现数百个反式eQTL分别影响三个非洲人群中成淋巴细胞样细胞系中的数百个转录本。这些反式eQTL在三个种群中靶向相同的基因,并显示相同的作用方向。我们发现,一组高可信度的trans-eQTL的目标转录本编码的蛋白质相互作用比偶然预期的要频繁得多,并受相同的转录因子结合,并丰富了指示在基本细胞体内稳态中作用的途径注释。因此,我们证明了我们的方法可以揭示影响共同调节的基因组的反式转录控制电路:这是了解如何协调细胞途径和过程的关键。

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