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Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in Saccharomyces cerevisiae

机译:Ku DNA末端结合活性促进酿酒酵母的保真度和影响非同源末端连接过程中的最终加工。

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摘要

The Ku heterodimer acts centrally in nonhomologous end-joining (NHEJ) of DNA double-strand breaks (DSB). Saccharomyces cerevisiae Ku, like mammalian Ku, binds and recruits NHEJ factors to DSB ends. Consequently, NHEJ is virtually absent in yeast Ku null (∆ or ∆) strains. Previously, we unexpectedly observed imprecise NHEJ proficiency in a yeast Ku mutant with impaired DNA end-binding (DEB). However, how DEB impairment supported imprecise NHEJ was unknown. Here, we found imprecise NHEJ proficiency to be a feature of a panel of DEB-impaired Ku mutants and that DEB impairment resulted in a deficiency in precise NHEJ. These results suggest that DEB-impaired Ku specifically promotes error-prone NHEJ. Epistasis analysis showed that classical NHEJ factors, as well as novel and previously characterized NHEJ-specific residues of Ku, are required for the distinct error-prone repair in a Ku DEB mutant. However, sequencing of repair junctions revealed that imprecise repair in Ku DEB mutants was almost exclusively characterized by small deletions, in contrast to the majority of insertions that define imprecise repair in wild-type strains. Notably, while sequencing indicated a lack of -dependent insertions at the site of repair, exonuclease activity, which mediates small deletions in NHEJ, contributed to imprecise NHEJ in a Ku DEB mutant. The deletions were smaller than in Ku-independent microhomology-mediated end-joining (MMEJ) and were neither promoted by nuclease activity nor . Thus, the quality of Ku’s engagement at the DNA end influences end-processing during NHEJ and DEB impairment unmasks a Ku-dependent error-prone pathway of end-joining distinct from MMEJ.
机译:Ku异二聚体在DNA双链断裂(DSB)的非同源末端连接(NHEJ)中集中作用。酿酒酵母Ku和哺乳动物Ku一样,将NHEJ因子结合并募集到DSB末端。因此,酵母Ku null(∆或∆)菌株中实际上不存在NHEJ。以前,我们出乎意料地观察到DNA末端结合(DEB)受损的酵母Ku突变体中NHEJ能力不精确。但是,尚不清楚DEB减损如何支持不精确的NHEJ。在这里,我们发现不精确的NHEJ能力是一组DEB受损的Ku突变体的特征,并且DEB损伤导致精确的NHEJ缺乏。这些结果表明,DEB损害的Ku特别促进了容易出错的NHEJ。上位性分析表明,经典的NHEJ因子,以及新的和先前表征的Ku的NHEJ特异性残基,对于Ku DEB突变体中易于出错的独特修复是必需的。然而,修复接头的测序显示,与大多数在野生型菌株中定义不精确修复的插入相反,Ku DEB突变体中不精确修复的特征几乎完全是由小缺失组成。值得注意的是,虽然测序表明在修复位点缺乏依赖性插入,但介导NHEJ中小缺失的核酸外切酶活性却导致了Ku DEB突变体中NHEJ的不精确。缺失小于Ku独立的微同源介导的末端连接(MMEJ),并且既不被核酸酶活性促进也不被。因此,Ku在DNA末端的参与质量会影响NHEJ和DEB损伤期间的末端加工,从而掩盖了不同于MMEJ的Ku依赖性易错末端连接途径。

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