The CST complex mediates a post-resection non-homologous end joining repair pathway and promotes local deletions in Saccharomyces cerevisiae.

IF 11.1 Q1 CELL BIOLOGY
Oana Ilioaia, Liébaut Dudragne, Clémentine Brocas, Léa Meneu, Romain Koszul, Karine Dubrana, Zhou Xu
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Abstract

The repair of a DNA double-strand break (DSB) by non-homologous end joining (NHEJ) generally leaves an intact or minimally modified sequence. Resection exposes single-stranded DNA and directs repair toward homology-dependent pathways and away from NHEJ. Here, we report that in Saccharomyces cerevisiae, the Cdc13/Stn1/Ten1 (CST) complex, characterized for its telomeric functions, acts after resection initiation to mediate a back-up NHEJ repair. We found a CST-specific mutation signature after repair characterized by deletions of 5-85 bp that were mostly dependent on NHEJ, with a subset dependent on microhomology-mediated end joining (MMEJ). The interaction between CST and Polα-primase is critical for these intermediate-size deletions, suggesting a role for fill-in synthesis, thus limiting extensive resection, which would otherwise lead to MMEJ-dependent deletions of several kilobases. Collectively, these results depict a complex picture of repair pathway choice where CST facilitates post-resection NHEJ repair, promoting local deletions but guarding against larger and potentially more deleterious deletions and rearrangements.

CST复合物介导切除后非同源末端连接修复途径,并促进酿酒酵母的局部缺失。
通过非同源末端连接(NHEJ)修复DNA双链断裂(DSB)通常会留下一个完整或最小修饰的序列。切除暴露单链DNA,并将修复导向同源依赖途径,远离NHEJ。在这里,我们报道了在酿酒酵母中,Cdc13/Stn1/Ten1 (CST)复合物,以其端粒功能为特征,在切除起始后介导备用NHEJ修复。我们发现修复后的cst特异性突变特征为5-85 bp的缺失,主要依赖于NHEJ,其中一小部分依赖于微同源介导的末端连接(MMEJ)。CST和pol α-引物酶之间的相互作用对于这些中等大小的缺失是至关重要的,这表明CST和pol α-引物酶之间存在填补合成的作用,从而限制了广泛的切除,否则会导致数千个碱基的mmej依赖性缺失。总的来说,这些结果描绘了修复途径选择的复杂图景,其中CST促进了切除后NHEJ的修复,促进了局部缺失,但防止了更大的和潜在更有害的缺失和重排。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.10
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