Y-family DNA polymerases in mammalian cells

被引:123
作者
Guo, Caixia [1 ,2 ]
Kosarek-Stancel, J. Nicole [1 ]
Tang, Tie-Shan [3 ]
Friedberg, Errol C. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Pathol, Lab Mol Pathol, Dallas, TX 75390 USA
[2] Chinese Acad Sci, Beijing Inst Genom, Beijing 100029, Peoples R China
[3] Chinese Acad Sci, Inst Zool, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100101, Peoples R China
关键词
Y-family polymerase; PCNA; Replication foci; Translesion DNA synthesis; Mutagenesis; Polymerase switching; Somatic hypermutation; XERODERMA-PIGMENTOSUM VARIANT; S-PHASE CHECKPOINT; IMMUNOGLOBULIN GENE HYPERMUTATION; NUCLEAR ANTIGEN UBIQUITINATION; EFFICIENT PCNA UBIQUITINATION; DAMAGE-INDUCED MUTAGENESIS; CLASS-SWITCH RECOMBINATION; REV1 PROTEIN INTERACTS; ESCHERICHIA-COLI DINB; THYMINE DIMER BYPASS;
D O I
10.1007/s00018-009-0024-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eukaryotic genomes are replicated with high fidelity to assure the faithful transmission of genetic information from one generation to the next. The accuracy of replication relies heavily on the ability of replicative DNA polymerases to efficiently select correct nucleotides for the polymerization reaction and, using their intrinsic exonuclease activities, to excise mistakenly incorporated nucleotides. Cells also possess a variety of specialized DNA polymerases that, by a process called translesion DNA synthesis (TLS), help overcome replication blocks when unrepaired DNA lesions stall the replication machinery. This review considers the properties of the Y-family (a subset of specialized DNA polymerases) and their roles in modulating spontaneous and genotoxic-induced mutations in mammals. We also review recent insights into the molecular mechanisms that regulate PCNA monoubiquitination and DNA polymerase switching during TLS and discuss the potential of using Y-family DNA polymerases as novel targets for cancer prevention and therapy.
引用
收藏
页码:2363 / 2381
页数:19
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