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使启动子开放与起始位点扫描解偶联。

Uncoupling Promoter Opening from Start-Site Scanning.

作者信息

Murakami Kenji, Mattei Pierre-Jean, Davis Ralph E, Jin Huiyan, Kaplan Craig D, Kornberg Roger D

机构信息

Department of Structural Biology, Stanford University, Stanford, CA 94305, USA.

Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843-2128, USA.

出版信息

Mol Cell. 2015 Jul 2;59(1):133-8. doi: 10.1016/j.molcel.2015.05.021. Epub 2015 Jun 11.

Abstract

Whereas RNA polymerase II (Pol II) transcription start sites (TSSs) occur about 30-35 bp downstream of the TATA box in metazoans, TSSs are located 40-120 bp downstream in S. cerevisiae. Promoter melting begins about 12 bp downstream in all eukaryotes, so Pol II is presumed to "scan" further downstream before starting transcription in yeast. Here we report that removal of the kinase complex TFIIK from TFIIH shifts the TSS in a yeast system upstream to the location observed in metazoans. Conversely, moving the normal TSS to an upstream location enables a high level of TFIIK-independent transcription in the yeast system. We distinguish two stages of the transcription initiation process: bubble formation by TFIIH, which fills the Pol II active center with single-stranded DNA, and subsequent scanning downstream, also driven by TFIIH, which requires displacement of the initial bubble. Omission of TFIIK uncouples the two stages of the process.

摘要

在后生动物中,RNA聚合酶II(Pol II)转录起始位点(TSS)位于TATA框下游约30 - 35 bp处,而在酿酒酵母中,TSS位于下游40 - 120 bp处。在所有真核生物中,启动子解链始于下游约12 bp处,因此推测在酵母中,Pol II在开始转录前会进一步“扫描”下游区域。在此我们报告,在酵母系统中,从TFIIH中去除激酶复合物TFIIK会使TSS向上游移动至后生动物中观察到的位置。相反,将正常的TSS移至上游位置能在酵母系统中实现高水平的不依赖TFIIK的转录。我们区分了转录起始过程的两个阶段:由TFIIH形成气泡,用单链DNA填充Pol II活性中心,以及随后同样由TFIIH驱动的下游扫描,这需要初始气泡的移位。省略TFIIK会使该过程的两个阶段解偶联。

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