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
相关论文
共 37 条
[1]   Damage-induced ubiquitylation of human RNA polymerase II by the ubiquitin ligase Nedd4, but not Cockayne syndrome proteins or BRCA1 [J].
Anindya, Roy ;
Ayguen, Ozan ;
Svejstrup, Jesper Q. .
MOLECULAR CELL, 2007, 28 (03) :386-397
[2]   Molecular cloning of DNAs encoding the regulatory subunits of elongin from Saccharomyces cerevisiae and Drosophila melanogaster [J].
Aso, T ;
Conrad, MN .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 241 (02) :334-340
[3]  
Beaudenon SL, 1999, MOL CELL BIOL, V19, P6972
[4]   DNA-REPAIR IN AN ACTIVE GENE - REMOVAL OF PYRIMIDINE DIMERS FROM THE DHFR GENE OF CHO CELLS IS MUCH MORE EFFICIENT THAN IN THE GENOME OVERALL [J].
BOHR, VA ;
SMITH, CA ;
OKUMOTO, DS ;
HANAWALT, PC .
CELL, 1985, 40 (02) :359-369
[5]   UV-induced ubiquitination of RNA polymerase II: A novel modification deficient in cockayne syndrome cells [J].
Bregman, DB ;
Halaban, R ;
vanGool, AJ ;
Henning, KA ;
Friedberg, EC ;
Warren, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (21) :11586-11590
[6]   Yeast Rpb9 plays an important role in ubiquitylation and degradation of Rpb1 in response to UV-induced DNA damage [J].
Chen, Xuefeng ;
Ruggiero, Christine ;
Li, Shisheng .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (13) :4617-4625
[7]   Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects [J].
Fousteri, Maria ;
Mullenders, Leon H. F. .
CELL RESEARCH, 2008, 18 (01) :73-84
[8]   RETRACTED: Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo (Retracted article. See vol. 81, pg. 5112, 2021) [J].
Fousteri, Maria ;
Vermeulen, Wim ;
van Zeeland, Albert A. ;
Mullenders, Leon H. F. .
MOLECULAR CELL, 2006, 23 (04) :471-482
[9]   Structural basis of transcription:: An RNA polymerase II elongation complex at 3.3 Å resolution [J].
Gnatt, AL ;
Cramer, P ;
Fu, JH ;
Bushnell, DA ;
Kornberg, RD .
SCIENCE, 2001, 292 (5523) :1876-1882
[10]   The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage [J].
Groisman, R ;
Polanowska, J ;
Kuraoka, I ;
Sawada, J ;
Saijo, M ;
Drapkin, R ;
Kisselev, AF ;
Tanaka, K ;
Nakatani, Y .
CELL, 2003, 113 (03) :357-367