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Research Project:
Molecular mechanisms controlling exit from mitosis

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Contributors

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ID

EC.00111

Authors

Item type:Person,
Çaydaşı, Ayşe Koca
Faculty Member

Publications

Item type:Publication, Access status: Open Access ,
SWR1 chromatin remodeling complex prevents mitotic slippage during spindle position checkpoint arrest
(American Society for Cell Biology, 2023)
Khmelinskii, Anton
;
Darieva, Zoulfia
;
Kurtulmus, Bahtiyar
;
Knop, Michael
;
Pereira, Gislene
Faithful chromosome segregation in budding yeast requires correct positioning of the mitotic spindle along the mother to daughter cell polarity axis. When the anaphase spindle is not correctly positioned, a surveillance mechanism, named as the spindle position checkpoint (SPOC), prevents the progression out of mitosis until correct spindle positioning is achieved. How SPOC works on a molecular level is not well understood. Here we performed a genome-wide genetic screen to search for components required for SPOC. We identified the SWR1 chromatin-remodeling complex (SWR1-C) among several novel factors that are essential for SPOC integrity. Cells lacking SWR1-C were able to activate SPOC upon spindle misorientation but underwent mitotic slippage upon prolonged SPOC arrest. This mitotic slippage required the Cdc14-early anaphase release pathway and other factors including the SAGA (Spt-Ada-Gcn5 acetyltransferase) histone acetyltransferase complex, proteasome components and the mitotic cyclin-dependent kinase inhibitor Sic1. Together, our data establish a novel link between SWR1-C chromatin remodeling and robust checkpoint arrest in late anaphase.

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