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是什么让小RNA发挥作用?

What makes a small RNA work?

作者信息

Alquethamy Saleh, Lalaouna David, Tree Jai J

机构信息

School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney 2052, NSW, Australia.

Université de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, Strasbourg 67000, France.

出版信息

Nucleic Acids Res. 2025 Jun 20;53(12). doi: 10.1093/nar/gkaf563.

Abstract

Bacterial small RNAs (sRNAs) are key regulators of gene expression, interacting with target messenger RNAs (mRNAs) through imperfect base pairing. Unlike other non-coding RNAs such as microRNAs and PIWI-interacting RNAs, bacterial sRNAs exhibit significant sequence and structural diversity, complicating functional predictions. Recent high-throughput profiling of the sRNA interactome has accentuated this problem by revealing a highly complex network of sRNA interactions. It is clear that there is an incredible diversity of sRNA interactions with different RNA classes in vivo, including different interaction modes with mRNAs. In this review, we attempt to summarize the known sequence and structural features that contribute to sRNA function in bacteria. As many of these features drive recruitment of protein partners, we necessarily focus on interactions with chaperones and ribonucleases, the best studied being Hfq and RNase E. Where possible, we have included examples outside this well-studied system as diversity and rule breaking appear to be central themes of sRNA biology. Understanding the sequences and structures that drive sRNA function will enhance our ability to predict regulatory outcomes, and this may inform the development of effective RNA therapeutics that are inspired by bacterial sRNA mechanisms.

摘要

细菌小RNA(sRNA)是基因表达的关键调节因子,通过不完全碱基配对与靶信使RNA(mRNA)相互作用。与其他非编码RNA(如微小RNA和PIWI相互作用RNA)不同,细菌sRNA表现出显著的序列和结构多样性,这使得功能预测变得复杂。最近对sRNA相互作用组的高通量分析揭示了一个高度复杂的sRNA相互作用网络,进一步凸显了这一问题。很明显,在体内,sRNA与不同RNA类别之间存在着令人难以置信的相互作用多样性,包括与mRNA的不同相互作用模式。在这篇综述中,我们试图总结已知的有助于细菌sRNA功能的序列和结构特征。由于许多这些特征驱动了蛋白质伴侣的招募,我们必然会关注与分子伴侣和核糖核酸酶的相互作用,其中研究得最好的是Hfq和核糖核酸酶E。在可能的情况下,我们纳入了这个研究充分的系统之外的例子,因为多样性和打破规则似乎是sRNA生物学的核心主题。了解驱动sRNA功能的序列和结构将增强我们预测调控结果的能力,这可能为受细菌sRNA机制启发的有效RNA疗法的开发提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c4d/12205990/e6c46f6273fa/gkaf563figgra1.jpg

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