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RNA 聚合酶 II 和许多转录因子与 Pol III 基因密切相关。

Close association of RNA polymerase II and many transcription factors with Pol III genes.

机构信息

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

出版信息

Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3639-44. doi: 10.1073/pnas.0911315106. Epub 2010 Feb 5.

DOI:10.1073/pnas.0911315106
PMID:20139302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2840497/
Abstract

Transcription of the eukaryotic genomes is carried out by three distinct RNA polymerases I, II, and III, whereby each polymerase is thought to independently transcribe a distinct set of genes. To investigate a possible relationship of RNA polymerases II and III, we mapped their in vivo binding sites throughout the human genome by using ChIP-Seq in two different cell lines, GM12878 and K562 cells. Pol III was found to bind near many known genes as well as several previously unidentified target genes. RNA-Seq studies indicate that a majority of the bound genes are expressed, although a subset are not suggestive of stalling by RNA polymerase III. Pol II was found to bind near many known Pol III genes, including tRNA, U6, HVG, hY, 7SK and previously unidentified Pol III target genes. Similarly, in vivo binding studies also reveal that a number of transcription factors normally associated with Pol II transcription, including c-Fos, c-Jun and c-Myc, also tightly associate with most Pol III-transcribed genes. Inhibition of Pol II activity using alpha-amanitin reduced expression of a number of Pol III genes (e.g., U6, hY, HVG), suggesting that Pol II plays an important role in regulating their transcription. These results indicate that, contrary to previous expectations, polymerases can often work with one another to globally coordinate gene expression.

摘要

真核生物基因组的转录由三种不同的 RNA 聚合酶 I、II 和 III 进行,每种聚合酶被认为独立转录一组不同的基因。为了研究 RNA 聚合酶 II 和 III 之间可能存在的关系,我们使用 ChIP-Seq 在两种不同的细胞系 GM12878 和 K562 中,在整个人类基因组中绘制了它们的体内结合位点。结果发现,Pol III 结合在许多已知基因附近,也结合在几个以前未鉴定的靶基因附近。RNA-Seq 研究表明,大多数结合基因都有表达,尽管有一部分不太可能是由 RNA 聚合酶 III 引起的停滞。Pol II 被发现结合在许多已知的 Pol III 基因附近,包括 tRNA、U6、HVG、hY、7SK 和以前未鉴定的 Pol III 靶基因。同样,体内结合研究也表明,许多通常与 Pol II 转录相关的转录因子,包括 c-Fos、c-Jun 和 c-Myc,也与大多数 Pol III 转录的基因紧密结合。使用α-鹅膏蕈碱抑制 Pol II 活性会降低许多 Pol III 基因(如 U6、hY、HVG)的表达,表明 Pol II 在调节它们的转录中起着重要作用。这些结果表明,与先前的预期相反,聚合酶通常可以相互协作,全局协调基因表达。

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