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细菌中 RNA 介导的转录调控的结构见解。

Structural insights into RNA-mediated transcription regulation in bacteria.

机构信息

Department of Integrated Structural Biology, IGBMC, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), 67400 Illkirch, France; Université de Strasbourg, IGBMC UMR 7104-UMR-S 1258, 67400 Illkirch, France; CNRS, UMR 7104, 67400 Illkirch, France; Inserm, UMR-S 1258, 67400 Illkirch, France.

Department of Integrated Structural Biology, IGBMC, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), 67400 Illkirch, France; Université de Strasbourg, IGBMC UMR 7104-UMR-S 1258, 67400 Illkirch, France; CNRS, UMR 7104, 67400 Illkirch, France; Inserm, UMR-S 1258, 67400 Illkirch, France.

出版信息

Mol Cell. 2022 Oct 20;82(20):3885-3900.e10. doi: 10.1016/j.molcel.2022.09.020. Epub 2022 Oct 10.

Abstract

RNA can regulate its own synthesis without auxiliary proteins. For example, U-rich RNA sequences signal RNA polymerase (RNAP) to pause transcription and are required for transcript release at intrinsic terminators in all kingdoms of life. In contrast, the regulatory RNA putL suppresses pausing and termination in cis. However, how nascent RNA modulates its own synthesis remains largely unknown. We present cryo-EM reconstructions of RNAP captured during transcription of putL variants or an unrelated sequence at a U-rich pause site. Our results suggest how putL suppresses pausing and promotes its synthesis. We demonstrate that transcribing a U-rich sequence, a ubiquitous trigger of intrinsic termination, promotes widening of the RNAP nucleic-acid-binding channel. Widening destabilizes RNAP interactions with DNA and RNA to facilitate transcript dissociation reminiscent of intrinsic transcription termination. Surprisingly, RNAP remains bound to DNA after transcript release. Our results provide the structural framework to understand RNA-mediated intrinsic transcription termination.

摘要

RNA 可以在没有辅助蛋白的情况下调节自身的合成。例如,富含 U 的 RNA 序列信号 RNA 聚合酶 (RNAP) 暂停转录,并在所有生命领域的内在终止子处释放转录本。相比之下,调节 RNA putL 在顺式中抑制暂停和终止。然而,新生 RNA 如何调节自身的合成在很大程度上仍是未知的。我们展示了在富含 U 的暂停位点转录 putL 变体或不相关序列时捕获的 RNAP 的冷冻电镜重建结果。我们的结果表明了 putL 如何抑制暂停并促进其合成。我们证明,转录富含 U 的序列,这是内在终止的普遍触发因素,会促进 RNAP 核酸结合通道的变宽。变宽会破坏 RNAP 与 DNA 和 RNA 的相互作用,从而促进类似于内在转录终止的转录本解离。令人惊讶的是,转录本释放后,RNAP 仍与 DNA 结合。我们的结果提供了理解 RNA 介导的内在转录终止的结构框架。

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