Damage control: DNA repair, transcription, and the ubiquitin-proteasome system

被引:50
作者
Daulny, Anne [1 ]
Tansey, William P. [1 ]
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
基金
美国国家卫生研究院;
关键词
RNA polymerase II; Ubiquitin; DNA damage; Transcription elongation; RNA-POLYMERASE-II; COCKAYNE-SYNDROME; SACCHAROMYCES-CEREVISIAE; LARGE SUBUNIT; EXCISION-REPAIR; DHFR GENE; DEGRADATION; UBIQUITYLATION; PROTEIN; CELLS;
D O I
10.1016/j.dnarep.2009.01.017
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The presence of DNA damage within an actively transcribed gene poses an immediate threat to cellular viability. Bulky DNA adducts, such as those induced by ultraviolet light, can profoundly influence patterns of gene expression by causing the irreversible arrest of RNA polymerase II at sites of DNA damage. It is critical that processes exist to either specifically repair transcribed genes or clear stalled RNA polymerase, so that general repair can occur and transcription resume. A growing body of evidence indicates that clearance of stalled polymerase is achieved, in part, by ubiquitin-mediated destruction of the largest subunit of RNA polymerase II. In this review, we shall discuss how an intimate connection between RNA polymerase II and the ubiquitylation machinery acts to restore normal transcription after DNA damage, and other forms of transcriptional arrest, has occurred. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:444 / 448
页数:5
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