RNA 聚合酶 II 在基因 3'- 端终止的机制。

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2024-08-02 DOI:10.1016/j.jmb.2024.168735
David Lopez Martinez, Jesper Q Svejstrup
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引用次数: 0

摘要

RNA 聚合酶 II(RNAPII)负责合成各种 RNA 分子,包括编码蛋白质的信使 RNA(mRNA)和许多短的非编码 RNA(ncRNA)。为此,RNAPII 依靠多种因子调节转录周期,从启动和启动子近端暂停,到延伸,最后终止。基因末端的 RNAPII 转录终止可确保 RNAPII 从 DNA 模板中释放出来,并有效地循环用于下一轮转录。RNAPII 的终止与 mRNA 3'-end 处理紧密相关,后者是后续转录终止事件的重要触发因素。在这篇综述中,我们讨论了目前对 RNAPII 终止机制的理解,重点是基因 3'- 端的 "规范 "终止。我们还将异构模型和 "鱼雷 "模型整合到一个统一的终止模型中,并描述了迄今已发现的不同终止因子,特别关注了人为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新方法的发展,使人们对 RNAPII 终止的不同机制有了更详细的了解,并更好地理解了它们在调节基因表达(尤其是在细胞应激和病理情况下)中的重要性。
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Mechanisms of RNA Polymerase II Termination at the 3'-End of Genes.

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.

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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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