Guo Caixia, Kosarek-Stancel J Nicole, Tang Tie-Shan, Friedberg Errol C
Laboratory of Molecular Pathology, Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9072, USA.
Cell Mol Life Sci. 2009 Jul;66(14):2363-81. doi: 10.1007/s00018-009-0024-4. Epub 2009 Apr 15.
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.
真核生物基因组以高保真度进行复制,以确保遗传信息从一代到下一代的准确传递。复制的准确性在很大程度上依赖于复制性DNA聚合酶有效地为聚合反应选择正确核苷酸的能力,以及利用其固有的核酸外切酶活性切除错误掺入的核苷酸的能力。细胞还拥有多种特殊的DNA聚合酶,通过一种称为跨损伤DNA合成(TLS)的过程,当未修复的DNA损伤使复制机制停滞时,帮助克服复制障碍。本综述考虑了Y家族(特殊DNA聚合酶的一个子集)的特性及其在调节哺乳动物自发和基因毒性诱导突变中的作用。我们还综述了对TLS过程中调节PCNA单泛素化和DNA聚合酶切换的分子机制的最新见解,并讨论了将Y家族DNA聚合酶用作癌症预防和治疗新靶点的潜力。