Suffering in silence: The tolerance of DNA damage

被引:211
作者
Friedberg, EC [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Pathol, Lab Mol Pathol, Dallas, TX 75390 USA
关键词
D O I
10.1038/nrm1781
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
When cells that are actively replicating DNA encounter sites of base damage or strand breaks, replication might stall or arrest. In this situation, cells rely on DNA-damage-tolerance mechanisms to bypass the damage effectively. One of these mechanisms, known as translesion DNA synthesis, is supported by specialized DNA polymerases that are able to catalyse nucleotide incorporation opposite lesions that cannot be negotiated by high-fidelity replicative polymerases. A second category of tolerance mechanism involves alternative replication strategies that obviate the need to replicate directly across sites of template- strand damage.
引用
收藏
页码:943 / 953
页数:11
相关论文
共 133 条
[51]   Eukaryotic polymerases ι and ζ act sequentially to bypass DNA lesions [J].
Johnson, RE ;
Washington, MT ;
Haracska, L ;
Prakash, S ;
Prakash, L .
NATURE, 2000, 406 (6799) :1015-1019
[52]   hRAD30 mutations in the variant form of xeroderma pigmentosum [J].
Johnson, RE ;
Kondratick, CM ;
Prakash, S ;
Prakash, L .
SCIENCE, 1999, 285 (5425) :263-265
[53]   THE SACCHAROMYCES-CEREVISIAE RAD18 GENE ENCODES A PROTEIN THAT CONTAINS POTENTIAL ZINC FINGER DOMAINS FOR NUCLEIC-ACID BINDING AND A PUTATIVE NUCLEOTIDE BINDING SEQUENCE [J].
JONES, JS ;
WEBER, S ;
PRAKASH, L .
NUCLEIC ACIDS RESEARCH, 1988, 16 (14) :7119-7131
[54]   Xeroderma pigmentosum variant and error-prone DNA polymerases [J].
Kannouche, P ;
Stary, A .
BIOCHIMIE, 2003, 85 (11) :1123-1132
[55]   Localization of DNA polymerases η and ι to the replication machinery is tightly co-ordinated in human cells [J].
Kannouche, P ;
de Henestrosa, ARF ;
Coull, B ;
Vidal, AE ;
Gray, C ;
Zicha, D ;
Woodgate, R ;
Lehmann, AR .
EMBO JOURNAL, 2002, 21 (22) :6246-6256
[56]   Interaction of human DNA polymerase η with monoubiquitinated PCNA:: A possible mechanism for the polymerase switch in response to DNA damage [J].
Kannouche, PL ;
Wing, J ;
Lehmann, AR .
MOLECULAR CELL, 2004, 14 (04) :491-500
[57]   ISOLATION AND CHARACTERIZATION OF MUTANTS OF ESCHERICHIA-COLI DEFICIENT IN INDUCTION OF MUTATIONS BY ULTRAVIOLET-LIGHT [J].
KATO, T ;
SHINOURA, Y .
MOLECULAR & GENERAL GENETICS, 1977, 156 (02) :121-131
[58]   Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase λ-deficient mice:: Possible implication for the pathogenesis of immotile cilia syndrome [J].
Kobayashi, Y ;
Watanabe, M ;
Okada, Y ;
Sawa, H ;
Takai, H ;
Nakanishi, M ;
Kawase, Y ;
Suzuki, H ;
Nagashima, K ;
Ikeda, K ;
Motoyama, N .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (08) :2769-2776
[59]   The DNA replication priming protein, PriA, is required for homologous recombination and double-strand break repair [J].
Kogoma, T ;
Cadwell, GW ;
Barnard, KG ;
Asai, T .
JOURNAL OF BACTERIOLOGY, 1996, 178 (05) :1258-1264
[60]   Initiation of genetic recombination and recombination-dependent replication [J].
Kowalczykowski, SC .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (04) :156-165