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Translesion Synthesis: Insights into the Selection and Switching of DNA Polymerases

机译:跨病变合成:洞察DNA聚合酶的选择和转换

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摘要

DNA replication is constantly challenged by DNA lesions, noncanonical DNA structures and difficult-to-replicate DNA sequences. Two major strategies to rescue a stalled replication fork and to ensure continuous DNA synthesis are: (1) template switching and recombination-dependent DNA synthesis; and (2) translesion synthesis (TLS) using specialized DNA polymerases to perform nucleotide incorporation opposite DNA lesions. The former pathway is mainly error-free, and the latter is error-prone and a major source of mutagenesis. An accepted model of translesion synthesis involves DNA polymerase switching steps between a replicative DNA polymerase and one or more TLS DNA polymerases. The mechanisms that govern the selection and exchange of specialized DNA polymerases for a given DNA lesion are not well understood. In this review, recent studies concerning the mechanisms of selection and switching of DNA polymerases in eukaryotic systems are summarized.
机译:DNA复制一直受到DNA损伤,非规范DNA结构和难以复制的DNA序列的挑战。挽救停滞的复制叉并确保连续的DNA合成的两种主要策略是:(1)模板转换和依赖重组的DNA合成; (2)使用专门的DNA聚合酶进行跨病变合成(TLS),以进行与DNA病变相对的核苷酸掺入。前者途径主要是无差错的,而后者是容易出错的且是诱变的主要来源。公认的跨病变合成模型涉及复制性DNA聚合酶和一种或多种TLS DNA聚合酶之间的DNA聚合酶转换步骤。对于给定的DNA损伤,控制选择和交换专门的DNA聚合酶的机制还不是很清楚。在这篇综述中,总结了有关真核系统中DNA聚合酶选择和转换机制的最新研究。

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