Hong Sun Woo, Hong Seong Min, Yoo Jae Wook, Lee Young Chul, Kim Soyoun, Lis John T, Lee Dong-Ki
Department of Chemistry, Global Research Laboratory for RNAi Medicine, BK21 School of Chemical Materials Science, Sungkyunkwan University, Suwon 440-746, Korea.
Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14276-80. doi: 10.1073/pnas.0903642106. Epub 2009 Aug 7.
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.
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。