The complex choreography of transcription-coupled repair

被引:35
作者
Spivak, Graciela [1 ]
Ganesan, Ann K. [1 ]
机构
[1] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
关键词
Nucleotide excision repair; Transcription-coupled repair; DNA damage; DNA repair; NUCLEOTIDE-EXCISION-REPAIR; UV-SENSITIVE SYNDROME; RNA-POLYMERASE-II; OXIDATIVE DNA LESIONS; COCKAYNE-SYNDROME; STRUCTURAL BASIS; R-LOOPS; DAMAGE; ELONGATION; CHROMATIN;
D O I
10.1016/j.dnarep.2014.03.025
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A quarter of a century has elapsed since the discovery of transcription-coupled repair (TCR), and yet our fascination with this process has not diminished. Nucleotide excision repair (NER) is a versatile pathway that removes helix-distorting DNA lesions from the genomes of organisms across the evolutionary scale, from bacteria to humans. TCR, defined as a subpathway of NER, is dedicated to the repair of lesions that, by virtue of their location on the transcribed strands of active genes, encumber elongation by RNA polymerases. In this review, we will report on newly identified proteins, protein modifications, and protein complexes that participate in TCR in Escherichia coli and in human cells. We will discuss general models for the biochemical pathways and how and when cells might choose to utilize TCR or other pathways for repair or bypass of transcription-blocking DNA alterations. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 70
页数:7
相关论文
共 68 条
[11]  
Deaconescu AM, 2006, CELL, V124, P507, DOI 10.1016/j.cell.2005.11.045
[12]   Enhanced Chromatin Dynamics by FACT Promotes Transcriptional Restart after UV-Induced DNA Damage [J].
Dinant, Christoffel ;
Ampatziadis-Michailidis, Giannis ;
Lans, Hannes ;
Tresini, Maria ;
Lagarou, Anna ;
Grosbart, Malgorzata ;
Thei, Arjan F. ;
van Cappellen, Wiggert A. ;
Kimura, Hiroshi ;
Bartek, Jiri ;
Fousteri, Maria ;
Houtsmuller, Adriaan B. ;
Vermeulen, Wim ;
Marteijn, Jurgen A. .
MOLECULAR CELL, 2013, 51 (04) :469-479
[13]   UvrD facilitates DNA repair by pulling RNA polymerase backwards [J].
Epshtein, Vitaly ;
Kamarthapu, Venu ;
McGary, Katelyn ;
Svetlov, Vladimir ;
Ueberheide, Beatrix ;
Proshkin, Sergey ;
Mironov, Alexander ;
Nudler, Evgeny .
NATURE, 2014, 505 (7483) :372-+
[14]   KIAA1530 Protein Is Recruited by Cockayne Syndrome Complementation Group Protein A (CSA) to Participate in Transcription-coupled Repair (TCR) [J].
Fei, Jia ;
Chen, Junjie .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (42) :35118-35126
[15]   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
[16]   A new connection of mRNP biogenesis and export with transcription-coupled repair [J].
Gaillard, Helene ;
Wellinger, Ralf Erik ;
Aguilera, Andres .
NUCLEIC ACIDS RESEARCH, 2007, 35 (12) :3893-3906
[17]   Transcription coupled repair at the interface between transcription elongation and mRNP biogenesis [J].
Gaillard, Helene ;
Aguilera, Andres .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2013, 1829 (01) :141-150
[18]   Transcription-Coupled DNA Repair in Prokaryotes [J].
Ganesan, Ann ;
Spivak, Graciela ;
Hanawalt, Philip C. .
MECHANISMS OF DNA REPAIR, 2012, 110 :25-40
[19]   Comet-FISH with strand-specific probes reveals transcription-coupled repair of 8-oxoGuanine in human cells [J].
Guo, Jia ;
Hanawalt, Philip C. ;
Spivak, Graciela .
NUCLEIC ACIDS RESEARCH, 2013, 41 (16) :7700-7712
[20]   Stalled transcription complexes promote DNA repair at a distance [J].
Haines, Nia M. ;
Kim, Young-In T. ;
Smith, Abigail J. ;
Savery, Nigel J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (11) :4037-4042