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The fidelity of DNA synthesis by yeast DNA polymerase zeta alone and with accessory proteins

机译:酵母DNA聚合酶zeta单独和与辅助蛋白一起进行DNA合成的保真度

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摘要

DNA polymerase zeta (pol ζ) participates in several DNA transactions in eukaryotic cells that increase spontaneous and damage-induced mutagenesis. To better understand this central role in mutagenesis in vivo, here we report the fidelity of DNA synthesis in vitro by yeast pol ζ alone and with RFC, PCNA and RPA. Overall, the accessory proteins have little effect on the fidelity of pol ζ. Pol ζ is relatively accurate for single base insertion/deletion errors. However, the average base substitution fidelity of pol ζ is substantially lower than that of homologous B family pols α, δ and ɛ. Pol ζ is particularly error prone for substitutions in specific sequence contexts and generates multiple single base errors clustered in short patches at a rate that is unprecedented in comparison with other polymerases. The unique error specificity of pol ζ in vitro is consistent with Pol ζ-dependent mutagenic specificity reported in vivo. This fact, combined with the high rate of single base substitution errors and complex mutations observed here, indicates that pol ζ contributes to mutagenesis in vivo not only by extending mismatches made by other polymerases, but also by directly generating its own mismatches and then extending them.
机译:DNA聚合酶zeta(polζ)参与真核细胞中的几种DNA交易,这些交易增加了自发的和损伤诱导的诱变作用。为了更好地了解在体内诱变中的这种中心作用,在这里我们报告了单独使用酵母polζ和RFC,PCNA和RPA在体外进行DNA合成的保真度。总体而言,辅助蛋白对polζ的保真度影响很小。 Polζ对于单个碱基的插入/缺失错误相对准确。但是,polζ的平均碱基取代保真度明显低于同源B族polsα,δ和that。 Polζ特别容易在特定序列上下文中发生替换,并且会以短于其他补丁的簇集方式生成多个单碱基错误,其速率是其他聚合酶所无法比拟的。 polζ在体外的独特错误特异性与体内报道的Polζ依赖性诱变特异性一致。这一事实,加上此处观察到的高单碱基取代错误率和复杂突变的发生率,表明polζ不仅通过扩大其他聚合酶产生的错配,而且还通过直接产生其自身的错配然后扩大它们来促进体内诱变。

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