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Mre11 核酸酶活性促使 Ku 和 MRN 从 DNA 末端释放,并且 Ctp1 对于双链断裂的同源重组修复是必需的。

Release of Ku and MRN from DNA ends by Mre11 nuclease activity and Ctp1 is required for homologous recombination repair of double-strand breaks.

机构信息

Department of Molecular Biology, The Scripps Research Institute, La Jolla, California, United States of America.

出版信息

PLoS Genet. 2011 Sep;7(9):e1002271. doi: 10.1371/journal.pgen.1002271. Epub 2011 Sep 8.

Abstract

The multifunctional Mre11-Rad50-Nbs1 (MRN) protein complex recruits ATM/Tel1 checkpoint kinase and CtIP/Ctp1 homologous recombination (HR) repair factor to double-strand breaks (DSBs). HR repair commences with the 5'-to-3' resection of DNA ends, generating 3' single-strand DNA (ssDNA) overhangs that bind Replication Protein A (RPA) complex, followed by Rad51 recombinase. In Saccharomyces cerevisiae, the Mre11-Rad50-Xrs2 (MRX) complex is critical for DSB resection, although the enigmatic ssDNA endonuclease activity of Mre11 and the DNA-end processing factor Sae2 (CtIP/Ctp1 ortholog) are largely unnecessary unless the resection activities of Exo1 and Sgs1-Dna2 are also eliminated. Mre11 nuclease activity and Ctp1/CtIP are essential for DSB repair in Schizosaccharomyces pombe and mammals. To investigate DNA end resection in Schizo. pombe, we adapted an assay that directly measures ssDNA formation at a defined DSB. We found that Mre11 and Ctp1 are essential for the efficient initiation of resection, consistent with their equally crucial roles in DSB repair. Exo1 is largely responsible for extended resection up to 3.1 kb from a DSB, with an activity dependent on Rqh1 (Sgs1) DNA helicase having a minor role. Despite its critical function in DSB repair, Mre11 nuclease activity is not required for resection in fission yeast. However, Mre11 nuclease and Ctp1 are required to disassociate the MRN complex and the Ku70-Ku80 nonhomologous end-joining (NHEJ) complex from DSBs, which is required for efficient RPA localization. Eliminating Ku makes Mre11 nuclease activity dispensable for MRN disassociation and RPA localization, while improving repair of a one-ended DSB formed by replication fork collapse. From these data we propose that release of the MRN complex and Ku from DNA ends by Mre11 nuclease activity and Ctp1 is a critical step required to expose ssDNA for RPA localization and ensuing HR repair.

摘要

多功能 Mre11-Rad50-Nbs1(MRN)蛋白复合物招募 ATM/Tel1 检查点激酶和 CtIP/Ctp1 同源重组(HR)修复因子到双链断裂(DSB)。HR 修复始于 DNA 末端的 5'到 3'切除,产生 3'单链 DNA(ssDNA)突出端,与复制蛋白 A(RPA)复合物结合,随后是 Rad51 重组酶。在酿酒酵母中,Mre11-Rad50-Xrs2(MRX)复合物对于 DSB 切除至关重要,尽管 Mre11 的神秘 ssDNA 内切酶活性和 DNA 末端加工因子 Sae2(CtIP/Ctp1 同源物)在很大程度上是不必要的,除非 Exo1 和 Sgs1-Dna2 的切除活性也被消除。Mre11 核酸酶活性和 Ctp1/CtIP 对于裂殖酵母和哺乳动物的 DSB 修复是必不可少的。为了研究裂殖酵母中的 DNA 末端切除,我们采用了一种直接测量特定 DSB 处 ssDNA 形成的测定法。我们发现 Mre11 和 Ctp1 对于有效启动切除至关重要,这与它们在 DSB 修复中的同等关键作用一致。Exo1 主要负责从 DSB 延伸切除长达 3.1kb,其活性依赖于 Rqh1(Sgs1)DNA 解旋酶,其作用较小。尽管 Mre11 核酸酶活性在 DSB 修复中具有关键功能,但在裂殖酵母中,切除并不需要 Mre11 核酸酶活性。然而,Mre11 核酸酶和 Ctp1 对于从 DSB 上解离 MRN 复合物和 Ku70-Ku80 非同源末端连接(NHEJ)复合物是必要的,这对于有效 RPA 定位是必需的。消除 Ku 使 Mre11 核酸酶活性对于 MRN 解离和 RPA 定位不再是必需的,同时改善了由复制叉崩溃形成的单端 DSB 的修复。根据这些数据,我们提出 Mre11 核酸酶活性和 Ctp1 通过释放 DNA 末端的 MRN 复合物和 Ku 是暴露 ssDNA 以进行 RPA 定位和随后的 HR 修复的关键步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bc5/3169521/3cd8579daf10/pgen.1002271.g001.jpg

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