Department of Pathology, The Joseph Gottstien Memorial Cancer Research Laboratory, University of Washington, Seattle, WA 98195-7705, USA.
Environ Mol Mutagen. 2012 Dec;53(9):666-82. doi: 10.1002/em.21745. Epub 2012 Oct 13.
The eukaryotic genome is in a constant state of modification and repair. Faithful transmission of the genomic information from parent to daughter cells depends upon an extensive system of surveillance, signaling, and DNA repair, as well as accurate synthesis of DNA during replication. Often, replicative synthesis occurs over regions of DNA that have not yet been repaired, presenting further challenges to genomic stability. DNA polymerase δ (pol δ) occupies a central role in all of these processes: catalyzing the accurate replication of a majority of the genome, participating in several DNA repair synthetic pathways, and contributing structurally to the accurate bypass of problematic lesions during translesion synthesis. The concerted actions of pol δ on the lagging strand, pol ϵ on the leading strand, associated replicative factors, and the mismatch repair (MMR) proteins results in a mutation rate of less than one misincorporation per genome per replication cycle. This low mutation rate provides a high level of protection against genetic defects during development and may prevent the initiation of malignancies in somatic cells. This review explores the role of pol δ in replication fidelity and genome maintenance.
真核生物基因组处于不断修饰和修复的状态。基因组信息从亲代细胞到子细胞的忠实传递依赖于广泛的监控、信号转导和 DNA 修复系统,以及复制过程中 DNA 的准确合成。通常,复制合成发生在尚未修复的 DNA 区域,这对基因组稳定性提出了进一步的挑战。DNA 聚合酶 δ(pol δ)在所有这些过程中都起着核心作用:催化大多数基因组的准确复制,参与几种 DNA 修复合成途径,并在跨损伤合成过程中结构上有助于准确绕过有问题的损伤。pol δ 在滞后链上、pol ϵ 在前导链上、相关复制因子和错配修复(MMR)蛋白的协同作用导致每个复制周期每个基因组的突变率低于一次错误掺入。这种低突变率为发育过程中的遗传缺陷提供了高度保护,并可能防止体细胞恶性肿瘤的发生。本综述探讨了 pol δ 在复制保真度和基因组维护中的作用。