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从RNA合成到转录起始并过渡到延伸阶段的结构洞察

Structural Insights into Transcription Initiation from RNA Synthesis to Transitioning into Elongation.

作者信息

Zuo Yuhong, De Swastik, Feng Yingang, Steitz Thomas A

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA.

Howard Hughes Medical Institute, New Haven, CT 06510, USA.

出版信息

iScience. 2020 Aug 11;23(9):101445. doi: 10.1016/j.isci.2020.101445. eCollection 2020 Sep 25.

Abstract

In bacteria, the dissociable σ subunit of the RNA polymerase (RNAP) is responsible for initiating RNA synthesis from specific DNA sites. As nascent RNA grows, downstream DNA unwinds and is pulled into the RNAP, causing stress accumulation and initiation complex destabilization. Processive transcription elongation requires at least partial separation of the σ factor from the RNAP core enzyme. Here, we present a series of transcription complexes captured between the early initiation and elongation phases via in-crystal RNA synthesis and cleavage. Crystal structures of these complexes indicate that stress accumulation during transcription initiation is not due to clashing of the growing nascent RNA with the σ loop, but results from scrunching of the template strand DNA that is contained inside the RNAP by the σ domain. Our results shed light on how scrunching of template-strand DNA drives both abortive initiation and σ-RNAP core separation to transition transcription from initiation to elongation.

摘要

在细菌中,RNA聚合酶(RNAP)的可解离σ亚基负责从特定DNA位点起始RNA合成。随着新生RNA的生长,下游DNA解旋并被拉入RNAP,导致应力积累和起始复合物不稳定。连续的转录延伸需要σ因子与RNAP核心酶至少部分分离。在这里,我们展示了一系列通过晶体中的RNA合成和切割捕获的处于早期起始和延伸阶段之间的转录复合物。这些复合物的晶体结构表明,转录起始期间的应力积累不是由于生长的新生RNA与σ环发生冲突,而是由σ结构域将包含在RNAP内部的模板链DNA压缩所致。我们的结果揭示了模板链DNA的压缩如何驱动流产起始和σ-RNAP核心分离,从而使转录从起始过渡到延伸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5975/7452309/bc6d90f29753/fx1.jpg

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