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Exo1 recruits Cdc5 polo kinase to MutLĪ³ to ensure efficient meiotic crossover formation

1 Dec 2020Proceedings of the National Academy of Sciences

DOI : 10.1073/pnas.2013012117

Authors

Aurore Sanchez, CĆ©line Adam, Felix Rauh, Yann Duroc, Lepakshi Ranjha, BĆ©rangĆØre Lombard, Xiaojing Mu, MĆ©lody Wintrebert, Damarys Loew, Alba GuarnĆ©, Stefano Gnan, Chun-Long Chen, Scott Keeney, Petr Cejka, RaphaĆ«l GuĆ©rois, Franz Klein, Jean-Baptiste Charbonnier, ValĆ©rie Borde

Abstract

Significance

Meiotic crossovers are essential for the production of gametes with balanced chromosome content. MutLĪ³ (Mlh1ā€“Mlh3) endonuclease, a mismatch repair heterodimer, also functions during meiosis to generate crossovers. Its activity requires Exo1 as well as the MutSĪ³ heterodimer (Msh4ā€“Msh5). Crossovers also require the polo kinase Cdc5 in a way that is poorly understood. We show that Exo1 directly interacts with Cdc5, and that this promotes the activation of MutLĪ³ for crossovers. Since Cdc5 also controls other key meiotic processes, including kinetochores mono-orientation and disassembly of the synaptonemal complex, this direct interaction with the crossover proteins may be a way to coordinate meiotic chromosome segregation events to avoid untimely activation of the MutLĪ³ endonuclease once recruited to future crossover sites.

Members

VALERIE BORDE

Directeur de recherche CNRS

CHUNLONG CHEN

Directeur de recherche CNRS