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原核生物中的 RNA 多聚腺苷酸化及其后果。

RNA polyadenylation and its consequences in prokaryotes.

机构信息

CNRS UMR8261 associated with University Paris Diderot, Institut de Biologie Physico-Chimique, 13 rue P. et M. Curie, 75005 Paris, France

Department of Immunology, Microbiology and Parasitology, University of the Basque Country UPV/EHU, 48940 Leioa, Spain

出版信息

Philos Trans R Soc Lond B Biol Sci. 2018 Nov 5;373(1762):20180166. doi: 10.1098/rstb.2018.0166.

Abstract

Post-transcriptional addition of poly(A) tails to the 3' end of RNA is one of the fundamental events controlling the functionality and fate of RNA in all kingdoms of life. Although an enzyme with poly(A)-adding activity was discovered in more than 50 years ago, its existence and role in prokaryotic RNA metabolism were neglected for many years. As a result, it was not until 1992 that poly(A) polymerase I was purified to homogeneity and its gene was finally identified. Further work revealed that, similar to its role in surveillance of aberrant nuclear RNAs of eukaryotes, the addition of poly(A) tails often destabilizes prokaryotic RNAs and their decay intermediates, thus facilitating RNA turnover. Moreover, numerous studies carried out over the last three decades have shown that polyadenylation greatly contributes to the control of prokaryotic gene expression by affecting the steady-state level of diverse protein-coding and non-coding transcripts including antisense RNAs involved in plasmid copy number control, expression of toxin-antitoxin systems and bacteriophage development. Here, we review the main findings related to the discovery of polyadenylation in prokaryotes, isolation, and characterization and regulation of bacterial poly(A)-adding activities, and discuss the impact of polyadenylation on prokaryotic mRNA metabolism and gene expression.This article is part of the theme issue '5' and 3' modifications controlling RNA degradation'.

摘要

在所有生命领域中,RNA 3' 端添加多聚(A)尾是控制 RNA 功能和命运的基本事件之一。尽管 50 多年前就发现了具有多聚(A)添加活性的酶,但多年来其在原核 RNA 代谢中的存在和作用一直被忽视。结果,直到 1992 年才纯化出多聚(A)聚合酶 I 并最终鉴定其基因。进一步的研究表明,与在真核生物异常核 RNA 的监测中的作用相似,添加多聚(A)尾通常会使原核 RNA 及其降解中间物不稳定,从而促进 RNA 周转。此外,过去三十年来的大量研究表明,多聚腺苷酸化通过影响包括参与质粒拷贝数控制、毒素抗毒素系统表达和噬菌体发育的反义 RNA 在内的多种蛋白编码和非编码转录物的稳态水平,极大地有助于控制原核基因表达。在这里,我们回顾了与原核生物中多聚腺苷酸化的发现、细菌多聚(A)添加活性的分离、鉴定和调控相关的主要发现,并讨论了多聚腺苷酸化对原核 mRNA 代谢和基因表达的影响。本文是主题问题'5'和'3'修饰控制 RNA 降解'的一部分。

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