RNA聚合酶Ⅱ
抄写(语言学)
BRD4
延伸系数
生物
细胞生物学
延伸率
发起人
溴尿嘧啶
基因
调节器
转录因子
聚四氟乙烯
基因表达
遗传学
核糖核酸
表观遗传学
核糖体
语言学
哲学
材料科学
极限抗拉强度
冶金
作者
Elisabeth Altendorfer,Yelizaveta Mochalova,Andreas Mayer
出处
期刊:Transcription
[Informa]
日期:2022-05-27
卷期号:13 (1-3): 70-81
被引量:20
标识
DOI:10.1080/21541264.2022.2108302
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI