Mitochondrial DNA repair pathways

被引:169
作者
Croteau, DL
Stierum, RH
Bohr, VA
机构
[1] NIA, Mol Genet Lab, NIH, Baltimore, MD 21224 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
来源
MUTATION RESEARCH-DNA REPAIR | 1999年 / 434卷 / 03期
关键词
mitochondrial DNA repair pathways; base excision repair; nucleotide excision repair;
D O I
10.1016/S0921-8777(99)00025-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
DNA repair mechanisms are fairly well characterized for nuclear DNA while knowledge regarding the repair mechanisms operable in mitochondria is limited. Several lines of evidence suggest that mitochondria contain DNA repair mechanisms. DNA lesions are removed from mtDNA in cells exposed to various chemicals. Protein activities that process damaged DNA have been detected in mitochondria. As will be discussed, there is evidence for base excision repair (BER), direct damage reversal, mismatch repair, and recombinational repair mechanisms in mitochondria, while nucleotide excision repair (NER), as we know it from nuclear repair, is not present. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:137 / 148
页数:12
相关论文
共 73 条
[1]  
ANDERSON CTM, 1980, NUCLEIC ACIDS RES, V8, P875
[2]   Homogenous repair of singlet oxygen-induced DNA damage in differentially transcribed regions and strands of human mitochondrial DNA [J].
Anson, RM ;
Croteau, DL ;
Stierum, RH ;
Filburn, C ;
Parsell, R ;
Bohr, VA .
NUCLEIC ACIDS RESEARCH, 1998, 26 (02) :662-668
[3]   Cloning and characterization of a functional human homolog of Escherichia coli endonuclease III [J].
Aspinwall, R ;
Rothwell, DG ;
RoldanArjona, T ;
Anselmino, C ;
Ward, CJ ;
Cheadle, JP ;
Sampson, JR ;
Lindahl, T ;
Harris, PC ;
Hickson, ID .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (01) :109-114
[4]   Purification, characterization, gene cloning, and expression of Saccharomyces cerevisiae redoxyendonuclease, a homolog of Escherichia coli endonuclease III [J].
Augeri, L ;
Lee, YM ;
Barton, AB ;
Doetsch, PW .
BIOCHEMISTRY, 1997, 36 (04) :721-729
[5]  
Beckman K B, 1996, Methods Enzymol, V264, P442, DOI 10.1016/S0076-6879(96)64040-3
[6]   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
[7]   SUBSTRATE-SPECIFICITY OF THE ESCHERICHIA-COLI FPG PROTEIN (FORMAMIDOPYRIMIDINE DNA GLYCOSYLASE) - EXCISION OF PURINE LESIONS IN DNA PRODUCED BY IONIZING-RADIATION OR PHOTOSENSITIZATION [J].
BOITEUX, S ;
GAJEWSKI, E ;
LAVAL, J ;
DIZDAROGLU, M .
BIOCHEMISTRY, 1992, 31 (01) :106-110
[8]   SELECTION BY GENETIC-TRANSFORMATION OF A SACCHAROMYCES-CEREVISIAE MUTANT DEFECTIVE FOR THE NUCLEAR URACIL-DNA-GLYCOSYLASE [J].
BURGERS, PMJ ;
KLEIN, MB .
JOURNAL OF BACTERIOLOGY, 1986, 166 (03) :905-913
[9]  
CHENG KC, 1992, J BIOL CHEM, V267, P166
[10]   ABSENCE OF A PYRIMIDINE DIMER REPAIR MECHANISM IN MAMMALIAN MITOCHONDRIA [J].
CLAYTON, DA ;
DODA, JN ;
FRIEDBER.EC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (07) :2777-2781