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Rad51 依赖性断裂诱导复制过程中不匹配模板的修复。

Repair of mismatched templates during Rad51-dependent Break-Induced Replication.

机构信息

Department of Biology and Rosenstiel Basic Medical Sciences Research Center, Brandeis University, Waltham, Massachusetts, United States of America.

Department of Biochemistry & Molecular Biophysics, Columbia University, New York, New York, United States of America.

出版信息

PLoS Genet. 2022 Sep 2;18(9):e1010056. doi: 10.1371/journal.pgen.1010056. eCollection 2022 Sep.

Abstract

Using budding yeast, we have studied Rad51-dependent break-induced replication (BIR), where the invading 3' end of a site-specific double-strand break (DSB) and a donor template share 108 bp of homology that can be easily altered. BIR still occurs about 10% as often when every 6th base is mismatched as with a perfectly matched donor. Here we explore the tolerance of mismatches in more detail, by examining donor templates that each carry 10 mismatches, each with different spatial arrangements. Although 2 of the 6 arrangements we tested were nearly as efficient as the evenly-spaced reference, 4 were significantly less efficient. A donor with all 10 mismatches clustered at the 3' invading end of the DSB was not impaired compared to arrangements where mismatches were clustered at the 5' end. Our data suggest that the efficiency of strand invasion is principally dictated by thermodynamic considerations, i.e., by the total number of base pairs that can be formed; but mismatch position-specific effects are also important. We also addressed an apparent difference between in vitro and in vivo strand exchange assays, where in vitro studies had suggested that at a single contiguous stretch of 8 consecutive bases was needed to be paired for stable strand pairing, while in vivo assays using 108-bp substrates found significant recombination even when every 6th base was mismatched. Now, using substrates of either 90 or 108 nt-the latter being the size of the in vivo templates-we find that in vitro D-loop results are very similar to the in vivo results. However, there are still notable differences between in vivo and in vitro assays that are especially evident with unevenly-distributed mismatches. Mismatches in the donor template are incorporated into the BIR product in a strongly polar fashion up to ~40 nucleotides from the 3' end. Mismatch incorporation depends on the 3'→ 5' proofreading exonuclease activity of DNA polymerase δ, with little contribution from Msh2/Mlh1 mismatch repair proteins, or from Rad1-Rad10 flap nuclease or the Mph1 helicase. Surprisingly, the probability of a mismatch 27 nt from the 3' end being replaced by donor sequence was the same whether the preceding 26 nucleotides were mismatched every 6th base or fully homologous. These data suggest that DNA polymerase δ "chews back" the 3' end of the invading strand without any mismatch-dependent cues from the strand invasion structure. However, there appears to be an alternative way to incorporate a mismatch at the first base at the 3' end of the donor.

摘要

我们使用芽殖酵母研究了依赖 Rad51 的断裂诱导复制(BIR),其中特定双链断裂(DSB)的 3' 末端和供体模板具有可轻易改变的 108bp 同源性。即使每第六个碱基错配,BIR 的发生频率也与完全匹配的供体相同,约为 10%。在这里,我们通过检查每个携带 10 个错配的供体模板,更详细地研究了错配的容忍度,每个错配都有不同的空间排列。尽管我们测试的 6 种排列中的 2 种与均匀间隔的参考排列一样有效,但 4 种排列的效率明显较低。与错配聚集在 DSB 5' 末端的排列相比,聚集在 3' 入侵末端的供体没有受到影响。我们的数据表明,链入侵的效率主要由热力学因素决定,即可以形成的碱基对总数;但错配位置特异性效应也很重要。我们还解决了体外和体内链交换测定之间的一个明显差异,其中体外研究表明,需要连续 8 个碱基对配对才能稳定链配对,而使用 108-bp 底物的体内测定发现,即使每第六个碱基错配,也存在显著的重组。现在,我们使用 90 或 108 个核苷酸的底物 - 后者是体内模板的大小 - 发现体外 D-loop 结果与体内结果非常相似。然而,体内和体外测定之间仍然存在明显差异,尤其是在不均匀分布的错配情况下。供体模板中的错配以强烈的极性方式掺入 BIR 产物中,直到 3' 端约 40 个核苷酸处。错配掺入取决于 DNA 聚合酶 δ 的 3'→5' 校对外切酶活性,Msh2/Mlh1 错配修复蛋白或 Rad1-Rad10 瓣状核酸内切酶或 Mph1 解旋酶的贡献很小。令人惊讶的是,距离 3' 端 27 个核苷酸的错配被供体序列取代的概率与前面 26 个核苷酸每第六个碱基错配或完全同源时相同。这些数据表明,DNA 聚合酶 δ“向后咀嚼”入侵链的 3' 末端,而无需来自链入侵结构的任何错配依赖性线索。然而,似乎有一种替代方法可以在供体 3' 端的第一个碱基处掺入一个错配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd7d/9477423/d96ec6dc795d/pgen.1010056.g001.jpg

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