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染色体融合而非染色体倒位激活了一种依赖PCH-2的检查点,该检查点促进了……中的交叉形成。

Chromosomal fusions, but not chromosomal inversions, activate a PCH-2 dependent checkpoint that promotes crossover formation in .

作者信息

Patel Bhumil, Grobler Maryke, Bhalla Needhi

机构信息

Molecular, Cellular, and Developmental Biology, University of California, Santa Cruz, Santa Cruz, California, United States.

出版信息

MicroPubl Biol. 2023 Jun 19;2023. doi: 10.17912/micropub.biology.000839. eCollection 2023.

Abstract

Meiotic crossovers promote accurate chromosome segregation during gametogenesis. In , a highly conserved AAA ATPase, PCH-2, ensures that homologous chromosomes have at least one crossover, preventing meiotic defects. PCH-2 localizes to meiotic chromosomes and this localization is extended when there are defects in meiotic recombination, suggesting a role in responding to defects. Here, we show that, unlike in other systems, PCH-2 does not persist on meiotic chromosomes when there are chromosomal inversions but does persist when there are whole chromosome fusions. Moreover, this persistence correlates with an increase in crossovers, demonstrating that PCH-2's localization to chromosomes promotes crossover formation.

摘要

减数分裂交叉互换在配子发生过程中促进染色体的准确分离。在一个高度保守的AAA型ATP酶PCH-2中,它确保同源染色体至少有一次交叉互换,从而防止减数分裂缺陷。PCH-2定位于减数分裂染色体上,当减数分裂重组出现缺陷时,这种定位会扩展,这表明它在应对缺陷方面发挥作用。在这里,我们表明,与其他系统不同,当存在染色体倒位时,PCH-2不会持续存在于减数分裂染色体上,但当存在全染色体融合时则会持续存在。此外,这种持续性与交叉互换的增加相关,表明PCH-2在染色体上的定位促进了交叉互换的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67fb/10318441/2b86d2742575/25789430-2023-micropub.biology.000839.jpg

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