Translesion DNA synthesis in the context of cancer research

被引:49
作者
Knobel, Philip A. [1 ]
Marti, Thomas M. [1 ]
机构
[1] Univ Zurich Hosp, Mol Oncol Lab, Clin & Polyclin Oncol, CH-8044 Zurich, Switzerland
关键词
XERODERMA-PIGMENTOSUM VARIANT; CELL NUCLEAR ANTIGEN; ESCHERICHIA-COLI DINB; BASE EXCISION-REPAIR; THYMINE DIMER BYPASS; SACCHAROMYCES-CEREVISIAE GENE; UBIQUITIN-BINDING DOMAINS; INTERSTRAND CROSS-LINKS; FREE REPLICATIVE BYPASS; POLYMERASE-BETA;
D O I
10.1186/1475-2867-11-39
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
During cell division, replication of the genomic DNA is performed by high-fidelity DNA polymerases but these error-free enzymes can not synthesize across damaged DNA. Specialized DNA polymerases, so called DNA translesion synthesis polymerases (TLS polymerases), can replicate damaged DNA thereby avoiding replication fork breakdown and subsequent chromosomal instability. We focus on the involvement of mammalian TLS polymerases in DNA damage tolerance mechanisms. In detail, we review the discovery of TLS polymerases and describe the molecular features of all the mammalian TLS polymerases identified so far. We give a short overview of the mechanisms that regulate the selectivity and activity of TLS polymerases. In addition, we summarize the current knowledge how different types of DNA damage, relevant either for the induction or treatment of cancer, are bypassed by TLS polymerases. Finally, we elucidate the relevance of TLS polymerases in the context of cancer therapy.
引用
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页数:19
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共 246 条
[1]   Roles of PCNA-binding and ubiquitin-binding domains in human DNA polymerase η in translesion DNA synthesis [J].
Acharya, Narottam ;
Yoon, Jung-Hoon ;
Gali, Himabindu ;
Unk, Ildiko ;
Haracska, Lajos ;
Johnson, Robert E. ;
Hurvvitz, Jerard ;
Prakash, Louise ;
Prakash, Satya .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (46) :17724-17729
[2]   Genome instability:: a mechanistic view of its causes and consequences [J].
Aguilera, Andres ;
Gomez-Gonzalez, Belen .
NATURE REVIEWS GENETICS, 2008, 9 (03) :204-217
[3]   A role for polymerase η in the cellular tolerance to cisplatin-induced damage [J].
Albertella, MR ;
Green, CM ;
Lehmann, AR ;
O'Connor, MJ .
CANCER RESEARCH, 2005, 65 (21) :9799-9806
[4]   The overexpression of specialized DNA polymerases in cancer [J].
Albertella, MR ;
Lau, A ;
O'Connor, MJ .
DNA REPAIR, 2005, 4 (05) :583-593
[5]   Eukaryotic DNA damage tolerance and translesion syntheses through covalent modifications of PCNA [J].
Andersen, Parker L. ;
Xu, Fang ;
Xiao, Wei .
CELL RESEARCH, 2008, 18 (01) :162-173
[6]   Two novel human and mouse DNA polymerases of the polX family [J].
Aoufouchi, S ;
Flatter, E ;
Dahan, A ;
Faili, A ;
Bertocci, B ;
Storck, S ;
Delbos, F ;
Cocea, L ;
Gupta, N ;
Weill, JC ;
Reynaud, CA .
NUCLEIC ACIDS RESEARCH, 2000, 28 (18) :3684-3693
[7]   Low-fidelity DNA synthesis by human DNA polymerase theta [J].
Arana, Mercedes E. ;
Seki, Mineaki ;
Wood, Richard D. ;
Rogozin, Igor B. ;
Kunkel, Thomas A. .
NUCLEIC ACIDS RESEARCH, 2008, 36 (11) :3847-3856
[8]   The HORMA domain: a common structural denominator in mitotic checkpoints, chromosome synapsis and DNA repair [J].
Aravind, L ;
Koonin, EV .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (08) :284-286
[9]   Quantitative analysis of translesion DNA synthesis across a benzo[a] pyrene-guanine adduct in mammalian cells -: The role of DNA polymerase κ [J].
Avkin, S ;
Goldsmith, M ;
Velasco-Miguel, S ;
Geacintov, N ;
Friedberg, EC ;
Livneh, Z .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (51) :53298-53305
[10]   Efficiency, specificity and DNA polymerase-dependence of translesion replication across the oxidative DNA lesion 8-oxoguanine in human cells [J].
Avkin, S ;
Livneh, Z .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2002, 510 (1-2) :81-90