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Correction of non-random mutational biases along a linear bacterial chromosome by the mismatch repair endonuclease NucS

机译:通过错配修复核酸内切酶 NucS 校正沿线性细菌染色体的非随机突变偏倚

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摘要

The linear chromosome of Streptomyces exhibits a highly compartmentalized structure with a conserved central region flanked by variable arms. As double strand break (DSB) repair mechanisms play a crucial role in shaping the genome plasticity of Streptomyces, we investigated the role of EndoMS/NucS, a recently characterized endonuclease involved in a non-canonical mismatch repair (MMR) mechanism in archaea and actinobacteria, that singularly corrects mismatches by creating a DSB. We showed that Streptomyces mutants lacking NucS display a marked colonial phenotype and a drastic increase in spontaneous mutation rate. In vitro biochemical assays revealed that NucS cooperates with the replication clamp to efficiently cleave G/T, G/G and T/T mismatched DNA by producing DSBs. These findings are consistent with the transition-shifted mutational spectrum observed in the mutant strains and reveal that NucS-dependent MMR specific task is to eliminate G/T mismatches generated by the DNA polymerase during replication. Interestingly, our data unveil a crescent-shaped distribution of the transition frequency from the replication origin towards the chromosomal ends, shedding light on a possible link between NucS-mediated DSBs and Streptomyces genome evolution.
机译:链霉菌的线性染色体表现出高度区室化的结构,具有保守的中央区域,两侧是可变臂。由于双链断裂 (DSB) 修复机制在塑造链霉菌的基因组可塑性中起着至关重要的作用,我们研究了 EndoMS/NucS 的作用,EndoMS/NucS 是一种最近表征的核酸内切酶,参与古细菌和放线菌中的非经典错配修复 (MMR) 机制,它通过产生 DSB 来单独纠正错配。我们发现缺乏 NucS 的链霉菌突变体表现出显着的菌落表型和自发突变率的急剧增加。体外生化分析显示,NucS 与复制钳配合,通过产生 DSB 有效切割 G/T、G/G 和 T/T 错配的 DNA。这些发现与在突变菌株中观察到的过渡转移突变谱一致,并揭示了 NucS 依赖性 MMR 特异性任务是消除 DNA 聚合酶在复制过程中产生的 G/T 错配。有趣的是,我们的数据揭示了从复制起点到染色体末端的转换频率的新月形分布,揭示了 NucS 介导的 DSB 和链霉菌基因组进化之间的可能联系。

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