Gilman Benjamin, Drullinger Linda F, Kugel Jennifer F, Goodrich James A
Department of Chemistry, University of Colorado, Boulder, Colorado 80309-0215, USA.
J Biol Chem. 2009 Apr 3;284(14):9093-8. doi: 10.1074/jbc.M900019200. Epub 2009 Feb 4.
To better understand the mechanism of steps in early transcription by RNA polymerase II (pol II), we investigated the molecular determinants of transcript slipping within complexes assembled on promoters containing a pre-melted transcription bubble from -9 to +3. Transcript slippage occurs when an RNA transcript contains a repetitive sequence that allows the transcript to slip back and pair with the template strand of the DNA at a new register before transcription continues. We established the contributions of individual transcription factors, DNA elements, and RNA length to slipping on a heteroduplex template using a highly purified human pol II transcription system. We found that transcripts slip at a very defined point in the transcription reaction, after pol II completes phosphodiester bond synthesis at register +5. This point is set by the position of the polymerase active site on the DNA template, as opposed to the length of the transcript, as well as by a repetitive CUCU sequence that must occur from +2 to +5. Interestingly, slipping at this juncture is induced by TATA-binding protein and transcription factor IIB and requires a TATA box but not a transcription factor IIB recognition sequence. We propose a model in which transcribing complexes, upon completing phosphodiester bond synthesis at register +5, enter one of two branches in which they either complete productive synthesis of the transcript or undergo multiple rounds of transcript slipping.
为了更好地理解RNA聚合酶II(pol II)早期转录步骤的机制,我们研究了在含有从-9到+3预熔解转录泡的启动子上组装的复合物中转录本滑动的分子决定因素。当RNA转录本包含一个重复序列,使得转录本在转录继续之前能够回滑并与DNA模板链在新的读框处配对时,就会发生转录本滑动。我们使用高度纯化的人类pol II转录系统,确定了单个转录因子、DNA元件和RNA长度对异源双链模板上滑动的贡献。我们发现,转录本在转录反应中一个非常明确的点发生滑动,即在pol II在+5读框完成磷酸二酯键合成之后。这一点是由DNA模板上聚合酶活性位点的位置决定的,而不是由转录本的长度决定的,同时也由必须从+2到+5出现的重复CUCU序列决定。有趣的是,此时的滑动是由TATA结合蛋白和转录因子IIB诱导的,并且需要一个TATA盒,但不需要转录因子IIB识别序列。我们提出了一个模型,在该模型中,转录复合物在+5读框完成磷酸二酯键合成后,进入两个分支之一,在这两个分支中,它们要么完成转录本的有效合成,要么经历多轮转录本滑动。