共 246 条
Translesion DNA synthesis in the context of cancer research
被引:49
作者:

Knobel, Philip A.
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机构:
Univ Zurich Hosp, Mol Oncol Lab, Clin & Polyclin Oncol, CH-8044 Zurich, Switzerland Univ Zurich Hosp, Mol Oncol Lab, Clin & Polyclin Oncol, CH-8044 Zurich, Switzerland

Marti, Thomas M.
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机构:
Univ Zurich Hosp, Mol Oncol Lab, Clin & Polyclin Oncol, CH-8044 Zurich, Switzerland Univ Zurich Hosp, Mol Oncol Lab, Clin & Polyclin Oncol, CH-8044 Zurich, Switzerland
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.
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