延伸因子在RNA聚合酶II泛素化和降解中的新作用。

IF 2.6 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Joseph C. Reese
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引用次数: 0

摘要

RNA聚合酶II(RNAPII)在完成基因信使核糖核酸合成的过程中遇到了许多障碍。暂停和停滞的RNAPII被延伸因子重新激活或拯救,延伸因子在聚合酶转录DNA时与聚合酶一起传播。然而,当RNAPII未能恢复转录时,例如当它遇到不可修复的庞大DNA损伤时,它通过靶向其最大的亚基Rpb1而被去除,以供泛素-蛋白酶体系统(UPS)降解。我们开始更好地了解这个过程,以及UPS如何标记Rbp1的退化。这篇综述将集中在最新进展上,并描述伸长因子的新功能,这些伸长因子曾被认为只在去除和降解RNAPII的非应力条件下促进伸长。我提出,除了RNAPII结构的变化外,延伸复合物中延伸因子的组成和修饰决定了是拯救还是降解RNAPII。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New roles for elongation factors in RNA polymerase II ubiquitylation and degradation

RNA polymerase II (RNAPII) encounters numerous impediments on its way to completing mRNA synthesis across a gene. Paused and arrested RNAPII are reactivated or rescued by elongation factors that travel with polymerase as it transcribes DNA. However, when RNAPII fails to resume transcription, such as when it encounters an unrepairable bulky DNA lesion, it is removed by the targeting of its largest subunit, Rpb1, for degradation by the ubiquitin-proteasome system (UPS). We are starting to understand this process better and how the UPS marks Rbp1 for degradation. This review will focus on the latest developments and describe new functions for elongation factors that were once thought to only promote elongation in unstressed conditions in the removal and degradation of RNAPII. I propose that in addition to changes in RNAPII structure, the composition and modification of elongation factors in the elongation complex determine whether to rescue or degrade RNAPII.

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来源期刊
CiteScore
9.20
自引率
2.10%
发文量
63
审稿时长
44 days
期刊介绍: BBA Gene Regulatory Mechanisms includes reports that describe novel insights into mechanisms of transcriptional, post-transcriptional and translational gene regulation. Special emphasis is placed on papers that identify epigenetic mechanisms of gene regulation, including chromatin, modification, and remodeling. This section also encompasses mechanistic studies of regulatory proteins and protein complexes; regulatory or mechanistic aspects of RNA processing; regulation of expression by small RNAs; genomic analysis of gene expression patterns; and modeling of gene regulatory pathways. Papers describing gene promoters, enhancers, silencers or other regulatory DNA regions must incorporate significant functions studies.
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