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NusG通过稳定最小转录泡来抑制RNA聚合酶回溯。

NusG inhibits RNA polymerase backtracking by stabilizing the minimal transcription bubble.

作者信息

Turtola Matti, Belogurov Georgiy A

机构信息

Department of Biochemistry, University of Turku, Turku, Finland.

出版信息

Elife. 2016 Oct 4;5:e18096. doi: 10.7554/eLife.18096.

Abstract

Universally conserved factors from NusG family bind at the upstream fork junction of transcription elongation complexes and modulate RNA synthesis in response to translation, processing, and folding of the nascent RNA. NusG enhances transcription elongation in vitro by a poorly understood mechanism. Here we report that NusG slows Gre factor-stimulated cleavage of the nascent RNA, but does not measurably change the rates of single nucleotide addition and translocation by a non-paused RNA polymerase. We demonstrate that NusG slows RNA cleavage by inhibiting backtracking. This activity is abolished by mismatches in the upstream DNA and is independent of the gate and rudder loops, but is partially dependent on the lid loop. Our comprehensive mapping of the upstream fork junction by base analogue fluorescence and nucleic acids crosslinking suggests that NusG inhibits backtracking by stabilizing the minimal transcription bubble.

摘要

来自NusG家族的普遍保守因子结合在转录延伸复合物的上游叉状连接处,并根据新生RNA的翻译、加工和折叠来调节RNA合成。NusG通过一种尚不清楚的机制增强体外转录延伸。在此,我们报告NusG减缓了Gre因子刺激的新生RNA切割,但并未显著改变非暂停RNA聚合酶的单核苷酸添加和转位速率。我们证明NusG通过抑制回溯来减缓RNA切割。上游DNA中的错配会消除这种活性,并且该活性独立于门环和舵环,但部分依赖于盖环。我们通过碱基类似物荧光和核酸交联对上游叉状连接处进行的全面图谱分析表明,NusG通过稳定最小转录泡来抑制回溯。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1b/5100998/ddcfe00a1161/elife-18096-fig1.jpg

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