BRD4:转录延伸的一般调节因子。

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Transcription-Austin Pub Date : 2022-02-01 Epub Date: 2022-09-01 DOI:10.1080/21541264.2022.2108302
Elisabeth Altendorfer, Yelizaveta Mochalova, Andreas Mayer
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引用次数: 9

摘要

RNA聚合酶II (Pol II)的转录延伸已成为基因表达的调控枢纽。一个关键的控制点发生在早期转录延伸,当Pol II暂停在启动子-近端区域在哺乳动物细胞的大多数基因和在果蝇的一大组基因。越来越多的交互作用因子与启动子-近端暂停有关。有些因素有助于建立暂停,而其他因素则是Pol II释放到生产伸长所必需的。这个延伸控制点的功能障碍导致基因表达异常,并可能导致疾病的发展。BET溴结构域蛋白BRD4与伸长控制有关。然而,直到最近才发现brd4在Pol II转录延伸中的直接特异性功能。这主要是由于技术的进步,允许选择性和快速消融细胞中的BRD4,以及捕获新生转录的直接后果的方法的可用性。这篇综述揭示了导致BRD4作为转录伸长的一般调节因子的新兴观点的实验突破。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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BRD4: a general regulator of transcription elongation.

Transcription elongation by RNA polymerase II (Pol II) has emerged as a regulatory hub in gene expression. A key control point occurs during early transcription elongation when Pol II pauses in the promoter-proximal region at the majority of genes in mammalian cells and at a large set of genes in Drosophila. An increasing number of trans-acting factors have been linked to promoter-proximal pausing. Some factors help to establish the pause, whereas others are required for the release of Pol II into productive elongation. A dysfunction of this elongation control point leads to aberrant gene expression and can contribute to disease development. The BET bromodomain protein BRD4 has been implicated in elongation control. However, only recently direct BRD4-specific functions in Pol II transcription elongation have been uncovered. This mainly became possible with technological advances that allow selective and rapid ablation of BRD4 in cells along with the availability of approaches that capture the immediate consequences on nascent transcription. This review sheds light on the experimental breakthroughs that led to the emerging view of BRD4 as a general regulator of transcription elongation.

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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
期刊最新文献
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