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人类转录因子结合的变异性。

Variation in transcription factor binding among humans.

机构信息

Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520, USA.

出版信息

Science. 2010 Apr 9;328(5975):232-5. doi: 10.1126/science.1183621. Epub 2010 Mar 18.

Abstract

Differences in gene expression may play a major role in speciation and phenotypic diversity. We examined genome-wide differences in transcription factor (TF) binding in several humans and a single chimpanzee by using chromatin immunoprecipitation followed by sequencing. The binding sites of RNA polymerase II (PolII) and a key regulator of immune responses, nuclear factor kappaB (p65), were mapped in 10 lymphoblastoid cell lines, and 25 and 7.5% of the respective binding regions were found to differ between individuals. Binding differences were frequently associated with single-nucleotide polymorphisms and genomic structural variants, and these differences were often correlated with differences in gene expression, suggesting functional consequences of binding variation. Furthermore, comparing PolII binding between humans and chimpanzee suggests extensive divergence in TF binding. Our results indicate that many differences in individuals and species occur at the level of TF binding, and they provide insight into the genetic events responsible for these differences.

摘要

基因表达的差异可能在物种形成和表型多样性中起主要作用。我们通过使用染色质免疫沉淀 followed by sequencing 的方法,检测了几个人类和一只黑猩猩的转录因子 (TF) 结合的全基因组差异。在 10 个淋巴母细胞系中绘制了 RNA 聚合酶 II (PolII) 和免疫反应关键调节剂核因子 kappaB (p65) 的结合位点,发现个体之间分别有 25%和 7.5%的相应结合区域存在差异。结合差异通常与单核苷酸多态性和基因组结构变异有关,并且这些差异通常与基因表达的差异相关,表明结合变异的功能后果。此外,比较人类和黑猩猩之间的 PolII 结合表明 TF 结合的广泛分歧。我们的结果表明,个体和物种之间的许多差异都发生在 TF 结合水平上,并且为这些差异的遗传事件提供了深入了解。

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