DNA损伤反应激酶Mec1ATR及其激活子Rad24RAD17在减数分裂重组中的分离作用。

IF 4 2区 生物学 Q1 GENETICS & HEREDITY PLoS Genetics Pub Date : 2024-12-09 eCollection Date: 2024-12-01 DOI:10.1371/journal.pgen.1011485
Margaret R Crawford, Jon A Harper, Tim J Cooper, Marie-Claude Marsolier-Kergoat, Bertrand Llorente, Matthew J Neale
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引用次数: 0

摘要

在减数分裂过程中,拓扑异构酶样酶Spo11通过检查点钳加载器Rad24RAD17激活DNA损伤反应(DDR)激酶Mec1ATR,形成程序性DNA双链断裂(DSBs)。在单个位点上,Mec1和Rad24活性的丧失会改变DSB的形成和重组结果,但它们在全基因组中的作用尚未得到详细研究。在这里,我们利用两种策略——缺失错配修复蛋白Msh2和通过调节Ndt80转录因子控制减数分裂前期长度——来帮助表征Mec1和Rad24在减数分裂重组中的作用,从而实现减数分裂后代的全基因组定位。与之前的研究一致,我们观察到由于前期缩短导致的rad24缺失严重影响了孢子活力,并且重组频率降低。相比之下,Mec1功能的缺失增加了重组频率,与其在DSB交叉干扰中的作用一致,对孢子活力的影响较小。尽管存在这些差异,但由紧密间隔的DSB引发的复杂多染色单体事件(在野生型细胞中很少见)在缺乏Rad24或Mec1的情况下发生得更频繁,这表明两者在DSB形成水平上都失去了空间调节。Mec1和Rad24在交叉(COs)的空间调控中也有重要作用。当Mec1或Rad24丢失时,CO分布变得更加随机,这表明干扰的全球表现减少。这种影响与‘ZMM’突变体(如zip3Δ)的表型相似,但不那么极端,并且可能是由干扰COs比例的减少所驱动的。总的来说,除了在CO调节中的共同作用外,我们的研究结果还强调了Rad24作为CO前因子和Mec1作为重组频率调节剂的可分离作用,它们的缺失有助于抑制由于DDR的废除而导致的CO调节中的任何更广泛的缺陷。
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Separable roles of the DNA damage response kinase Mec1ATR and its activator Rad24RAD17 during meiotic recombination.

During meiosis, programmed DNA double-strand breaks (DSBs) are formed by the topoisomerase-like enzyme, Spo11, activating the DNA damage response (DDR) kinase Mec1ATR via the checkpoint clamp loader, Rad24RAD17. At single loci, loss of Mec1 and Rad24 activity alters DSB formation and recombination outcome, but their genome-wide roles have not been examined in detail. Here, we utilise two strategies-deletion of the mismatch repair protein, Msh2, and control of meiotic prophase length via regulation of the Ndt80 transcription factor-to help characterise the roles Mec1 and Rad24 play in meiotic recombination by enabling genome-wide mapping of meiotic progeny. In line with previous studies, we observe severely impacted spore viability and a reduction in the frequency of recombination upon deletion of RAD24-driven by a shortened prophase. By contrast, loss of Mec1 function increases recombination frequency, consistent with its role in DSB trans-interference, and has less effect on spore viability. Despite these differences, complex multi-chromatid events initiated by closely spaced DSBs-rare in wild-type cells-occur more frequently in the absence of either Rad24 or Mec1, suggesting a loss of spatial regulation at the level of DSB formation in both. Mec1 and Rad24 also have important roles in the spatial regulation of crossovers (COs). Upon loss of either Mec1 or Rad24, CO distributions become more random-suggesting reductions in the global manifestation of interference. Such effects are similar to, but less extreme than, the phenotype of 'ZMM' mutants such as zip3Δ, and may be driven by reductions in the proportion of interfering COs. Collectively, in addition to shared roles in CO regulation, our results highlight separable roles for Rad24 as a pro-CO factor, and for Mec1 as a regulator of recombination frequency, the loss of which helps to suppress any broader defects in CO regulation caused by abrogation of the DDR.

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PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
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2.20%
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438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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