活细胞中的 RNA 二级结构集合图谱确定了保守的 RNA 调控开关和温度计

Ivana Borovska, Chundan Zhang, Edoardo Morandi, Daphne van den Homberg, Michael T. Wolfinger, Willem Velema, Danny Incarnato
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引用次数: 0

摘要

RNA 分子可以填充多种可选结构构象组合,但全面绘制活细胞内的 RNA 构象图谱是一项重大挑战,因此迄今为止仍难以实现。在这里,我们以大肠杆菌为模型,首次生成了活细胞中 RNA 二级结构组合的转录组尺度图谱。我们的分析发现了结构动态区域的特征,以及数百种高度保守的细菌 RNA 结构元素的存在。条件结构图揭示了冷休克期间 RNA 组合的广泛重组,从而在 cspG、cspI、cpxP 和 lpxP mRNA 的 5′ UTR 中发现了几种新型 RNA 温度计。我们从机理上描述了这些温度计如何在应对冷休克时切换结构,并揭示了 cspE 合子介导的 lpxP 调控。总之,这项工作揭示了活细胞中 RNA 结构动态的复杂性,而这种复杂性以前从未被认识到,它为大大加快发现调控 RNA 开关提供了关键资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA secondary structure ensemble mapping in a living cell identifies conserved RNA regulatory switches and thermometers
RNA molecules can populate ensembles of alternative structural conformations, but comprehensively mapping RNA conformational landscapes within living cells presents significant challenges and has, as such, so far remained elusive. Here, we generated the first transcriptome-scale maps of RNA secondary structure ensembles in a living cell, using Escherichia coli as a model. Our analysis uncovered features of structurally-dynamic regions, as well as the existence of hundreds of highly-conserved bacterial RNA structural elements. Conditional structure mapping revealed extensive restructuring of RNA ensembles during cold shock, leading to the discovery of several novel RNA thermometers in the 5′ UTRs of the cspG, cspI, cpxP and lpxP mRNAs. We mechanistically characterized how these thermometers switch structure in response to cold shock and revealed the cspE chaperone-mediated regulation of lpxP. Collectively, this work reveals a previously unappreciated complexity of RNA structural dynamics in living cells, and it provides a key resource to significantly accelerate the discovery of regulatory RNA switches.
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