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Recruitment of Polo-like kinase couples synapsis to meiotic progression via inactivation of CHK-2.


ABSTRACT: Meiotic chromosome segregation relies on synapsis and crossover (CO) recombination between homologous chromosomes. These processes require multiple steps that are coordinated by the meiotic cell cycle and monitored by surveillance mechanisms. In diverse species, failures in chromosome synapsis can trigger a cell cycle delay and/or lead to apoptosis. How this key step in 'homolog engagement' is sensed and transduced by meiotic cells is unknown. Here we report that in C. elegans, recruitment of the Polo-like kinase PLK-2 to the synaptonemal complex triggers phosphorylation and inactivation of CHK-2, an early meiotic kinase required for pairing, synapsis, and double-strand break (DSB) induction. Inactivation of CHK-2 terminates DSB formation and enables CO designation and cell cycle progression. These findings illuminate how meiotic cells ensure CO formation and accurate chromosome segregation.

SUBMITTER: Zhang L 

PROVIDER: S-EPMC9998088 | biostudies-literature | 2023 Jan

REPOSITORIES: biostudies-literature

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Recruitment of Polo-like kinase couples synapsis to meiotic progression via inactivation of CHK-2.

Zhang Liangyu L   Stauffer Weston T WT   Wang John S JS   Wu Fan F   Yu Zhouliang Z   Liu Chenshu C   Kim Hyung Jun HJ   Dernburg Abby F AF  

eLife 20230126


Meiotic chromosome segregation relies on synapsis and crossover (CO) recombination between homologous chromosomes. These processes require multiple steps that are coordinated by the meiotic cell cycle and monitored by surveillance mechanisms. In diverse species, failures in chromosome synapsis can trigger a cell cycle delay and/or lead to apoptosis. How this key step in 'homolog engagement' is sensed and transduced by meiotic cells is unknown. Here we report that in <i>C. elegans</i>, recruitmen  ...[more]

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