Centre for mRNP Biogenesis and Metabolism, Department of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.
Wiley Interdiscip Rev RNA. 2013 May-Jun;4(3):233-46. doi: 10.1002/wrna.1156. Epub 2013 Feb 28.
RNA polymerase II (RNAPII)-mediated gene transcription initiates at promoters and ends at terminators. Transcription termination is intimately connected to 3'-end processing of the produced RNA and already when loaded at the promoter, RNAPII starts to become configured for this downstream event. Conversely, RNAPII is 'reset' as part of the 3'-end processing/termination event, thus preparing the enzyme for its next round of transcription--possibly on the same gene. There is both direct and circumstantial evidence for preferential recycling of RNAPII from the gene terminator back to its own promoter, which supposedly increases the efficiency of the transcription process under conditions where RNAPII levels are rate limiting. Here, we review differences and commonalities between initiation and 3'-end processing/termination processes on various types of RNAPII transcribed genes. In doing so, we discuss the requirements for efficient 3'-end processing/termination and how these may relate to proper recycling of RNAPII.
RNA 聚合酶 II(RNAPII)介导的基因转录起始于启动子,终止于终止子。转录终止与产生的 RNA 的 3'端加工密切相关,并且当 RNA 聚合酶加载到启动子时,它就开始为下游事件进行配置。相反,RNAPII 作为 3'端加工/终止事件的一部分被“重置”,从而为下一轮转录做好准备——可能是在同一个基因上。有直接和间接的证据表明,RNAPII 从基因终止子优先回收回其自身的启动子,这据称在 RNAPII 水平限制转录速度的条件下提高了转录过程的效率。在这里,我们回顾了各种类型的 RNAPII 转录基因的起始和 3'端加工/终止过程之间的差异和共同点。在这样做的过程中,我们讨论了有效 3'端加工/终止的要求,以及这些要求如何与 RNAPII 的适当回收相关。