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TFIIH激酶对RNA聚合酶II C端结构域的磷酸化对于酿酒酵母基因组的转录并非必不可少。

Phosphorylation of the RNA polymerase II C-terminal domain by TFIIH kinase is not essential for transcription of Saccharomyces cerevisiae genome.

作者信息

Hong Sun Woo, Hong Seong Min, Yoo Jae Wook, Lee Young Chul, Kim Soyoun, Lis John T, Lee Dong-Ki

机构信息

Department of Chemistry, Global Research Laboratory for RNAi Medicine, BK21 School of Chemical Materials Science, Sungkyunkwan University, Suwon 440-746, Korea.

出版信息

Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14276-80. doi: 10.1073/pnas.0903642106. Epub 2009 Aug 7.

Abstract

Ser-5 phosphorylation of the RNA polymerase II (Pol II) C-terminal domain by TFIIH kinase has been implicated in critical steps in mRNA synthesis, such as Pol II promoter escape and mRNA 5'-capping. However, the general requirement and precise role of TFIIH kinase in Pol II transcription still remain elusive. Here we use a chemical genetics approach to show that, for a majority of budding-yeast genes, specific inhibition of the yeast TFIIH kinase results in a dramatic reduction in both mRNA level and Ser-5 C-terminal domain phosphorylation. Surprisingly, inhibition of TFIIH kinase activity only partially affected both Pol II density and Ser-2 phosphorylation level. The discrepancy between mRNA level and Pol II density is attributed to the defective 5'-capping, which results in the destabilization of mRNAs. Therefore, contrary to the current belief, our study points strongly toward a minor role of TFIIH kinase in Pol II transcription, and a more significant role in mRNA capping in budding yeast.

摘要

TFIIH激酶对RNA聚合酶II(Pol II)羧基末端结构域的丝氨酸5位点进行磷酸化,这一过程与mRNA合成的关键步骤有关,比如Pol II启动子逃逸和mRNA 5'端加帽。然而,TFIIH激酶在Pol II转录中的总体需求和精确作用仍不清楚。在此,我们采用化学遗传学方法来表明,对于大多数芽殖酵母基因而言,特异性抑制酵母TFIIH激酶会导致mRNA水平和丝氨酸5羧基末端结构域磷酸化显著降低。令人惊讶的是,抑制TFIIH激酶活性仅部分影响Pol II密度和丝氨酸2磷酸化水平。mRNA水平与Pol II密度之间的差异归因于有缺陷的5'端加帽,这导致mRNA不稳定。因此,与当前的认知相反,我们的研究有力地表明TFIIH激酶在芽殖酵母的Pol II转录中作用较小,而在mRNA加帽中作用更为显著。

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