Answers are grounded in this paper and cite their sources.
SUMMARY Faithful cell division requires precise control of spindle assembly and disassembly. In budding yeast, spindle breakdown at mitotic exit depends on Cdk1 inactivation and ubiquitin-mediated degradation of spindle stabilizing factors, including the kinesin-5 Cin8 and the crosslinker Ase1/PRC1. Timely degradation of Cin8 by APC Cdh1 prevents spindle over-elongation and deformation. We have identified SUMOylation and the SUMO-targeted ubiquitin ligase Slx5 as regulators of spindle disassembly. Cin8 is SUMOylated and interacts with Slx5, suggesting that it is a substrate of Slx5. Deletion of the SLX5 gene or expression of a SUMOylation-defective Cin8 mutant cause spindle disassembly defects that resemble those of degradation-resistant Cin8 mutants. Reduction of Cin8 SUMOylation partly stabilizes spindles in ase1Δ cells. In addition, SUMOylation of Cin8 and Slx5 are required for timely actomyosin-ring contraction and Cin8 clearance from the mitotic spindle. We propose that SUMOylation regulates Cin8 activity and that SUMO-targeted ubiquitylation facilitates removal Cin8 from the spindle, promoting spindle disassembly at the end of mitosis.
No takes yet. Share an insight, caveat, or question.
Gaven et al. (2025) studied this question.
Synapse has enriched 8 closely related papers on similar clinical questions. Consider them for comparative context: