The Role of Cdh1p in Maintaining Genomic Stability in Budding Yeast

Corresponding author: Orna Cohen-Fix, 8 Center Dr., Bldg. 8, Rm. 319, Bethesda, MD 20892-0840., ornacf{at}helix.nih.gov (E-mail)

Communicating editor: B. ANDREWS

Cdh1p, a substrate specificity factor for the cell cycle-regulated ubiquitin ligase, the anaphase-promoting complex/cyclosome (APC/C), promotes exit from mitosis by directing the degradation of a number of proteins, including the mitotic cyclins. Here we present evidence that Cdh1p activity at the M/G₁ transition is important not only for mitotic exit but also for high-fidelity chromosome segregation in the subsequent cell cycle. CDH1 showed genetic interactions with MAD2 and PDS1, genes encoding components of the mitotic spindle assembly checkpoint that acts at metaphase to prevent premature chromosome segregation. Unlike cdh1 and mad2 single mutants, the mad2 cdh1 double mutant grew slowly and exhibited high rates of chromosome and plasmid loss. Simultaneous deletion of PDS1 and CDH1 caused extensive chromosome missegregation and cell death. Our data suggest that at least part of the chromosome loss can be attributed to kinetochore/spindle problems. Our data further suggest that Cdh1p and Sic1p, a Cdc28p/Clb inhibitor, have overlapping as well as nonoverlapping roles in ensuring proper chromosome segregation. The severe growth defects of both mad2 cdh1 and pds1 cdh1 strains were rescued by overexpressing Swe1p, a G₂/M inhibitor of the cyclin-dependent kinase, Cdc28p/Clb. We propose that the failure to degrade cyclins at the end of mitosis leaves cdh1 mutant strains with abnormal Cdc28p/Clb activity that interferes with proper chromosome segregation.

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