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MSH2 响应遗传多态性刺激干扰和非干扰交叉。

MSH2 stimulates interfering and inhibits non-interfering crossovers in response to genetic polymorphism.

机构信息

Laboratory of Genome Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, Poznań, Poland.

Department of Molecular Virology, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznań, Poland.

出版信息

Nat Commun. 2023 Oct 23;14(1):6716. doi: 10.1038/s41467-023-42511-z.

Abstract

Meiotic crossovers can be formed through the interfering pathway, in which one crossover prevents another from forming nearby, or by an independent non-interfering pathway. In Arabidopsis, local sequence polymorphism between homologs can stimulate interfering crossovers in a MSH2-dependent manner. To understand how MSH2 regulates crossovers formed by the two pathways, we combined Arabidopsis mutants that elevate non-interfering crossovers with msh2 mutants. We demonstrate that MSH2 blocks non-interfering crossovers at polymorphic loci, which is the opposite effect to interfering crossovers. We also observe MSH2-independent crossover inhibition at highly polymorphic sites. We measure recombination along the chromosome arms in lines differing in patterns of heterozygosity and observe a MSH2-dependent crossover increase at the boundaries between heterozygous and homozygous regions. Here, we show that MSH2 is a master regulator of meiotic DSB repair in Arabidopsis, with antagonistic effects on interfering and non-interfering crossovers, which shapes the crossover landscape in relation to interhomolog polymorphism.

摘要

减数分裂交叉可以通过干扰途径形成,其中一个交叉阻止另一个在附近形成,或者通过独立的非干扰途径形成。在拟南芥中,同源物之间的局部序列多态性可以以 MSH2 依赖的方式刺激干扰交叉。为了了解 MSH2 如何调节两条途径形成的交叉,我们将提高非干扰交叉的拟南芥突变体与 msh2 突变体结合。我们证明 MSH2 在多态性位点阻断非干扰交叉,这与干扰交叉的效果相反。我们还在高度多态性位点观察到 MSH2 不依赖的交叉抑制。我们在异质型和同质型区域之间的边界处观察到 MSH2 依赖性交叉增加,从而测量了沿染色体臂的重组。在这里,我们表明 MSH2 是拟南芥减数分裂 DSB 修复的主要调节剂,对干扰和非干扰交叉具有拮抗作用,从而根据同源多态性塑造交叉景观。

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