Lemay Jean-François, Bachand François
a Department of Biochemistry ; Faculté de Médecine et des Sciences de la Santé; Université de Sherbrooke; Pavillon de Recherche Appliquée sur le Cancer (PRAC) ; Sherbrooke, Quebec.
RNA Biol. 2015;12(9):927-32. doi: 10.1080/15476286.2015.1073433.
Termination of RNA polymerase II (RNAPII) transcription is a fundamental step of gene expression that involves the release of the nascent transcript and dissociation of RNAPII from the DNA template. As transcription termination is intimately linked to RNA 3' end processing, termination pathways have a key decisive influence on the fate of the transcribed RNA. Quite remarkably, when reaching the 3' end of genes, a substantial fraction of RNAPII fail to terminate transcription, requiring the contribution of alternative or "fail-safe" mechanisms of termination to release the polymerase. This point of view covers redundant mechanisms of transcription termination and how they relate to conventional termination models. In particular, we expand on recent findings that propose a reverse torpedo model of termination, in which the 3'5' exonucleolytic activity of the RNA exosome targets transcription events associated with paused and backtracked RNAPII.
RNA聚合酶II(RNAPII)转录的终止是基因表达的一个基本步骤,它涉及新生转录本的释放以及RNAPII与DNA模板的解离。由于转录终止与RNA 3'末端加工密切相关,终止途径对转录RNA的命运具有关键的决定性影响。非常值得注意的是,当到达基因的3'末端时,相当一部分RNAPII无法终止转录,这就需要替代或“故障安全”终止机制的作用来释放聚合酶。本文观点涵盖了转录终止的冗余机制以及它们与传统终止模型的关系。特别是,我们详述了最近提出的一种反向鱼雷终止模型的研究结果,在该模型中,RNA外切体的3'→5'核酸外切酶活性靶向与暂停和回溯的RNAPII相关的转录事件。