单分子洞察扭转和障碍在细菌转录延伸。

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Transcription-Austin Pub Date : 2021-08-01 Epub Date: 2021-11-01 DOI:10.1080/21541264.2021.1997315
Jin Qian, Wenxuan Xu, David Dunlap, Laura Finzi
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引用次数: 1

摘要

在转录过程中,RNA聚合酶(RNAP)沿着螺旋模板DNA易位,同时保持高转录保真度。然而,所有的基因组都是动态扭曲、扭曲的,并被结合的蛋白质和运动酶修饰。在原核生物中,与DNA结合的蛋白质,无论是否特异性,经常将DNA压缩成构象,通过阻断RNAP使基因沉默。RNAP与这些结构蛋白的碰撞可能导致RNAP停滞和/或蛋白质路障的位移。重要的是要了解转录RNAPs在不同水平的超螺旋或存在障碍的情况下如何快速运作。鉴于转录复合物表现出广泛的异步动力学,单分子分析,如原子力显微镜、荧光检测、光学和磁镊子等,非常适合以足够的空间和时间分辨率检测和量化活性。在这里,我们总结了目前对扭曲和路障对原核转录影响的理解,重点是提供实时检测和读出的单分子分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Single-molecule insights into torsion and roadblocks in bacterial transcript elongation.

Single-molecule insights into torsion and roadblocks in bacterial transcript elongation.

During transcription, RNA polymerase (RNAP) translocates along the helical template DNA while maintaining high transcriptional fidelity. However, all genomes are dynamically twisted, writhed, and decorated by bound proteins and motor enzymes. In prokaryotes, proteins bound to DNA, specifically or not, frequently compact DNA into conformations that may silence genes by obstructing RNAP. Collision of RNAPs with these architectural proteins, may result in RNAP stalling and/or displacement of the protein roadblock. It is important to understand how rapidly transcribing RNAPs operate under different levels of supercoiling or in the presence of roadblocks. Given the broad range of asynchronous dynamics exhibited by transcriptional complexes, single-molecule assays, such as atomic force microscopy, fluorescence detection, optical and magnetic tweezers, etc. are well suited for detecting and quantifying activity with adequate spatial and temporal resolution. Here, we summarize current understanding of the effects of torsion and roadblocks on prokaryotic transcription, with a focus on single-molecule assays that provide real-time detection and readout.

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来源期刊
Transcription-Austin
Transcription-Austin BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
6.50
自引率
5.60%
发文量
9
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