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RNA 聚合酶在蛋白质路障处暂停会通过启动子阻断增强转录干扰。

RNA polymerase pausing at a protein roadblock can enhance transcriptional interference by promoter occlusion.

机构信息

Department of Molecular and Biomedical Science, School of Biological Sciences, The University of Adelaide, Adelaide, Australia.

CSIRO Synthetic Biology Future Science Platform, Canberra, Australia.

出版信息

FEBS Lett. 2019 May;593(9):903-917. doi: 10.1002/1873-3468.13365. Epub 2019 Mar 29.

Abstract

Convergent promoters exert transcriptional interference (TI) by several mechanisms including promoter occlusion, where elongating RNA polymerases (RNAPs) block access to a promoter. Here, we tested whether pausing of RNAPs by obstructive DNA-bound proteins can enhance TI by promoter occlusion. Using the Lac repressor as a 'roadblock' to induce pausing over a target promoter, we found only a small increase in TI, with mathematical modelling suggesting that rapid termination of the stalled RNAP was limiting the occlusion effect. As predicted, the roadblock-enhanced occlusion was significantly increased in the absence of the Mfd terminator protein. Thus, protein roadblocking of RNAP may cause pause-enhanced occlusion throughout genomes, and the removal of stalled RNAP may be needed to minimize unwanted TI.

摘要

聚合酶启动子通过几种机制发挥转录干扰 (TI) 作用,包括启动子阻断,其中延伸的 RNA 聚合酶 (RNAP) 阻止进入启动子。在这里,我们测试了由阻塞性 DNA 结合蛋白引起的 RNAP 暂停是否可以通过启动子阻断增强 TI。我们使用 Lac 阻遏物作为“路障”诱导靶启动子上的暂停,发现 TI 仅略有增加,数学建模表明,暂停的 RNAP 的快速终止限制了阻断效应。如预测的那样,在没有 Mfd 终止蛋白的情况下,路障增强的阻断作用显著增加。因此,RNAP 的蛋白路障可能会导致整个基因组中暂停增强的阻断,并且可能需要去除停滞的 RNAP 以最小化不必要的 TI。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfda/6593788/6c27f77c9cf1/FEB2-593-903-g001.jpg

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