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复制依赖性双链断裂修复中的链不对称性。

Strand asymmetry in the repair of replication dependent double-strand breaks.

作者信息

Kimble Michael T, Sane Aakanksha, Reid Robert Jd, Johnson Matthew J, Rothstein Rodney, Symington Lorraine S

出版信息

bioRxiv. 2024 Jun 19:2024.06.17.598707. doi: 10.1101/2024.06.17.598707.

DOI:10.1101/2024.06.17.598707
PMID:38948862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11212877/
Abstract

Single-strand breaks (SSBs) are one of the most common endogenous lesions and have the potential to give rise to cytotoxic double-strand breaks (DSBs) during DNA replication. To investigate the mechanism of replication fork collapse at SSBs and subsequent repair, we employed Cas9 nickase (nCas9) to generate site and strand-specific nicks in the budding yeast genome. We show that nCas9-induced nicks are converted to mostly double-ended DSBs during S-phase. We find that repair of replication-dependent DSBs requires homologous recombination (HR) and is independent of canonical non-homologous end joining. Consistent with a strong bias to repair these lesions using a sister chromatid template, we observe minimal induction of inter-chromosomal HR by nCas9. Using nCas9 and a gRNA to nick either the leading or lagging strand template, we carried out a genome-wide screen to identify factors necessary for the repair of replication-dependent DSBs. All the core HR genes were recovered in the screen with both gRNAs, but we recovered components of the replication-coupled nucleosome assembly (RCNA) pathway with only the gRNA targeting the leading strand template. By use of additional gRNAs, we find that the RCNA pathway is especially important to repair a leading strand fork collapse.

摘要

单链断裂(SSB)是最常见的内源性损伤之一,在DNA复制过程中有可能引发细胞毒性双链断裂(DSB)。为了研究单链断裂处复制叉崩溃及后续修复的机制,我们利用Cas9切口酶(nCas9)在芽殖酵母基因组中产生位点和链特异性切口。我们发现,nCas9诱导的切口在S期大多会转化为双端DSB。我们发现,复制依赖性DSB的修复需要同源重组(HR),且不依赖于经典的非同源末端连接。与使用姐妹染色单体模板修复这些损伤的强烈偏好一致,我们观察到nCas9对染色体间HR的诱导作用极小。利用nCas9和一个gRNA对前导链或后随链模板进行切口,我们进行了全基因组筛选,以确定复制依赖性DSB修复所需的因子。使用两种gRNA进行筛选时,所有核心HR基因均被回收,但只有在使用靶向前导链模板的gRNA时,我们才回收了复制偶联核小体组装(RCNA)途径的组分。通过使用其他gRNA,我们发现RCNA途径对于修复前导链叉崩溃尤为重要。