含rna毒素-抗毒素系统的结构和功能多样性。

IF 4.8 2区 生物学 Q1 CELL BIOLOGY
Harshita Dutta, Salik Noor, Kavyashree Nadig, Mahavir Singh
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引用次数: 0

摘要

毒素-抗毒素(TA)系统是普遍存在的原核生物遗传模块,位于质粒和染色体上,有助于质粒稳定,维持基因组完整性,噬菌体防御和细菌发病。通常,这些系统编码代谢稳定的毒素和不稳定的抗毒素,在稳态条件下中和毒素活性。应激诱导的抗毒素降解释放毒素,通过抑制各种细胞过程,包括翻译、DNA复制和细胞壁合成,导致生长停滞。根据抗毒素特性和作用方式,TA系统分为八种类型(I-VIII型)。其中,I型、III型和VIII型代表含有RNA的TA系统,其中要么只有抗毒素(I型和III型),要么毒素和抗毒素(VIII型)都是RNA分子。I型系统利用小的顺式或反式编码的反义RNA抗毒素,与毒素mrna碱基配对,阻止翻译或促进降解;它们的毒素通常是靶向膜或诱导类核凝结的小疏水性肽。III型系统编码核糖核酸内酶毒素和结构RNA抗毒素,这些抗毒素组装成化学计量核糖核蛋白复合物。毒素、CptIN和AbiF III型TA复合物的结构研究强调了假结和含有抗毒素的茎环,这些抗毒素具有高特异性地参与毒素活性位点。VIII型系统,如CreTA,是完全基于rna的系统,其中毒素隔离罕见的trna,抗毒素模仿CRISPR rna介导cas依赖性的毒素转录抑制。在这篇综述中,我们总结了目前对这些系统的理解,强调了它们的组装和作用的分子机制以及它们在生物技术和治疗学中的新应用。本文分类为:RNA与蛋白质和其他分子的相互作用> RNA-蛋白质复合物调控RNA /RNAi/核糖开关>调控RNA RNA结构和动力学>生物系统中RNA结构的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural and Functional Diversity of RNA-Containing Toxin-Antitoxin Systems.

Toxin-antitoxin (TA) systems are ubiquitous prokaryotic genetic modules located on plasmids and chromosomes, contributing to plasmid stabilization, maintenance of genome integrity, phage defense, and bacterial pathogenesis. Canonically, these systems encode a metabolically stable toxin and a labile antitoxin that neutralizes the toxin activity under homeostatic conditions. Stress-induced antitoxin degradation unleashes the toxin, leading to growth arrest through inhibition of various cellular processes, including translation, DNA replication, and cell wall synthesis. TA systems are classified into eight types (type I-VIII) based on antitoxin identity and mode of action. Among these, types I, III, and VIII represent RNA-containing TA systems in which either only antitoxin (types I and III) or both toxin and antitoxin (type VIII) are RNA molecules. Type I systems utilize small cis- or trans-encoded antisense RNA antitoxins that base-pair with toxin mRNAs to block translation or promote degradation; their toxins are typically small hydrophobic peptides targeting membranes or inducing nucleoid condensation. Type III systems encode endoribonuclease toxins and structured RNA antitoxins that assemble into stoichiometric ribonucleoprotein complexes. Structural studies of ToxIN, CptIN, and AbiF type III TA complexes have highlighted the pseudoknot and stem-loop containing antitoxins that engage toxin active sites with high specificity. Type VIII systems, such as CreTA, are fully RNA-based systems, where the toxin sequesters rare tRNAs and the antitoxin mimics CRISPR RNAs to mediate Cas-dependent transcriptional repression of the toxin. In this review, we summarize current understanding of these systems, emphasizing their molecular mechanisms of assembly and action and their emerging applications in biotechnology and therapeutics. This article is categorized under: RNA Interactions with Proteins and Other Molecules > RNA-Protein Complexes Regulatory RNAs/RNAi/Riboswitches > Regulatory RNAs RNA Structure and Dynamics > Influence of RNA Structure in Biological Systems.

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来源期刊
CiteScore
14.80
自引率
4.10%
发文量
67
审稿时长
6-12 weeks
期刊介绍: WIREs RNA aims to provide comprehensive, up-to-date, and coherent coverage of this interesting and growing field, providing a framework for both RNA experts and interdisciplinary researchers to not only gain perspective in areas of RNA biology, but to generate new insights and applications as well. Major topics to be covered are: RNA Structure and Dynamics; RNA Evolution and Genomics; RNA-Based Catalysis; RNA Interactions with Proteins and Other Molecules; Translation; RNA Processing; RNA Export/Localization; RNA Turnover and Surveillance; Regulatory RNAs/RNAi/Riboswitches; RNA in Disease and Development; and RNA Methods.
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