Lopez Martinez David, Svejstrup Jesper Q
Centre for Gene Expression, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
J Mol Biol. 2025 Jan 1;437(1):168735. doi: 10.1016/j.jmb.2024.168735. Epub 2024 Aug 2.
RNA polymerase II (RNAPII) is responsible for the synthesis of a diverse set of RNA molecules, including protein-coding messenger RNAs (mRNAs) and many short non-coding RNAs (ncRNAs). For this purpose, RNAPII relies on a multitude of factors that regulate the transcription cycle, from initiation and promoter-proximal pausing, through elongation and finally termination. RNAPII transcription termination at the end of genes ensures the release of RNAPII from the DNA template and its efficient recycling for further rounds of transcription. Termination of RNAPII is tightly coupled to 3'-end mRNA processing, which constitutes an important trigger for the subsequent transcription termination event. In this review, we discuss the current understanding of RNAPII termination mechanisms, focusing on 'canonical' termination at the 3'-end of genes. We also integrate the allosteric and 'torpedo' models into a unified model of termination, and describe the different termination factors that have been identified to date, paying special attention to the human factors and their mechanism of action at the molecular level. Indeed, in recent years the development of novel approaches in structural biology, biochemistry and cell biology have together led to a more detailed comprehension of the different mechanisms of RNAPII termination, and a better understanding of their importance in regulating gene expression, especially under cellular stress and pathological situations.
RNA聚合酶II(RNAPII)负责合成多种RNA分子,包括蛋白质编码信使RNA(mRNA)和许多短链非编码RNA(ncRNA)。为此,RNAPII依赖于众多调节转录周期的因子,从起始和启动子近端暂停,到延伸,最后终止。基因末端的RNAPII转录终止确保了RNAPII从DNA模板上释放,并使其有效地循环用于进一步的转录轮次。RNAPII的终止与3'端mRNA加工紧密偶联,这构成了随后转录终止事件的重要触发因素。在本综述中,我们讨论了目前对RNAPII终止机制的理解,重点是基因3'端的“经典”终止。我们还将变构模型和“鱼雷”模型整合到一个统一的终止模型中,并描述了迄今为止已鉴定的不同终止因子,特别关注人类因子及其在分子水平上的作用机制。事实上,近年来结构生物学、生物化学和细胞生物学中新方法的发展共同导致了对RNAPII终止不同机制的更详细理解,以及对其在调节基因表达中的重要性的更好理解,特别是在细胞应激和病理情况下。