Mechanisms of human DNA repair: an update

被引:410
作者
Christmann, M [1 ]
Tomicic, MT [1 ]
Roos, WP [1 ]
Kaina, B [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Inst Toxicol, Div Appl Toxicol, D-55131 Mainz, Germany
关键词
DNA-repair gene; DNA-repair protein; DNA-damage signaling;
D O I
10.1016/S0300-483X(03)00287-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The human genome, comprising three billion base pairs coding for 30 000-40 000 genes, is constantly attacked by endogenous reactive metabolites, therapeutic drugs and a plethora of environmental mutagens that impact its integrity. Thus it is obvious that the stability of the genome must be under continuous surveillance. This is accomplished by DNA repair mechanisms, which have evolved to remove or to tolerate pre-cytotoxic, pre-mutagenic and pre-clastogenic DNA lesions in an error-free, or in some cases, error-prone way. Defects in DNA repair give rise to hypersensitivity to DNA-damaging agents, accumulation of mutations in the genome and finally to the development of cancer and various metabolic disorders. The importance of DNA repair is illustrated by DNA repair deficiency and genomic instability syndromes, which are characterised by increased cancer incidence and multiple metabolic alterations. Up to 130 genes have been identified in humans that are associated with DNA repair. This review is aimed at updating our current knowledge of the various repair pathways by providing an overview of DNA-repair genes and the corresponding proteins, participating either directly in DNA repair, or in checkpoint control and signaling of DNA damage. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:3 / 34
页数:32
相关论文
共 391 条
[31]   Nucleotide-promoted release of hMutSα from heteroduplex DNA is consistent with an ATP-dependent translocation Mechanism [J].
Blackwell, LJ ;
Martik, D ;
Bjornson, KP ;
Bjornson, ES ;
Modrich, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :32055-32062
[32]   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
[33]  
Boldogh I, 1998, CANCER RES, V58, P3950
[34]   DNA-REPAIR - ENGAGEMENT WITH TRANSCRIPTION [J].
BOOTSMA, D ;
HOEIJMAKERS, JHJ .
NATURE, 1993, 363 (6425) :114-115
[35]   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
[36]   MODE OF ACTION OF POLY(ADP-RIBOSE) GLYCOHYDROLASE [J].
BROCHU, G ;
DUCHAINE, C ;
THIBEAULT, L ;
LAGUEUX, J ;
SHAH, GM ;
POIRIER, GG .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1994, 1219 (02) :342-350
[37]   The mismatch repair system is required for S-phase checkpoint activation [J].
Brown, KD ;
Rathi, A ;
Kamath, R ;
Beardsley, DI ;
Zhan, QM ;
Mannino, JL ;
Baskaran, R .
NATURE GENETICS, 2003, 33 (01) :80-84
[38]   Eukaryotic DNA polymerases: Proposal for a revised nomenclature [J].
Burgers, PMJ ;
Koonin, EV ;
Bruford, E ;
Blanco, L ;
Burtis, KC ;
Christman, MF ;
Copeland, WC ;
Friedberg, EC ;
Hanaoka, F ;
Hinkle, DC ;
Lawrence, CW ;
Nakanishi, M ;
Ohmori, H ;
Prakash, L ;
Prakash, S ;
Reynaud, CA ;
Sugino, A ;
Todo, T ;
Wang, ZG ;
Weill, JC ;
Woodgate, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (47) :43487-43490
[39]  
Bürkle A, 2001, CHEMBIOCHEM, V2, P725, DOI 10.1002/1439-7633(20011001)2:10<725::AID-CBIC725>3.0.CO
[40]  
2-3