Sutton Mark D
Department of Biochemistry, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, 3435 Main Street, 140 Farber Hall, Buffalo, NY 14214, USA.
Biochim Biophys Acta. 2010 May;1804(5):1167-79. doi: 10.1016/j.bbapap.2009.06.010. Epub 2009 Jun 21.
With the discovery that organisms possess multiple DNA polymerases (Pols) displaying different fidelities, processivities, and activities came the realization that mechanisms must exist to manage the actions of these diverse enzymes to prevent gratuitous mutations. Although many of the Pols encoded by most organisms are largely accurate, and participate in DNA replication and DNA repair, a sizeable fraction display a reduced fidelity, and act to catalyze potentially error-prone translesion DNA synthesis (TLS) past lesions that persist in the DNA. Striking the proper balance between use of these different enzymes during DNA replication, DNA repair, and TLS is essential for ensuring accurate duplication of the cell's genome. This review highlights mechanisms that organisms utilize to manage the actions of their different Pols. A particular emphasis is placed on discussion of current models for how different Pols switch places with each other at the replication fork during high fidelity replication and potentially error-pone TLS.
随着发现生物体拥有多种具有不同保真度、持续合成能力和活性的DNA聚合酶(Pols),人们意识到必须存在一些机制来管理这些不同酶的作用,以防止无端突变。尽管大多数生物体编码的许多Pols在很大程度上是准确的,并参与DNA复制和DNA修复,但相当一部分显示出较低的保真度,并在DNA中持续存在的损伤处催化潜在易错的跨损伤DNA合成(TLS)。在DNA复制、DNA修复和TLS过程中,在使用这些不同酶之间取得适当平衡对于确保细胞基因组的准确复制至关重要。本综述重点介绍了生物体用于管理其不同Pols作用的机制。特别强调了关于在高保真复制和潜在易错TLS过程中不同Pols如何在复制叉处相互交换位置的当前模型的讨论。