Sister chromatid separation and chromosome re-duplication are regulated by different mechanisms in response to spindle damage
- PMID: 10329618
- PMCID: PMC1171353
- DOI: 10.1093/emboj/18.10.2707
Sister chromatid separation and chromosome re-duplication are regulated by different mechanisms in response to spindle damage
Abstract
In yeast, anaphase entry depends on Pds1 proteolysis, while chromosome re-duplication in the subsequent S-phase involves degradation of mitotic cyclins such as Clb2. Sequential proteolysis of Pds1 and mitotic cyclins is mediated by the anaphase-promoting complex (APC). Lagging chromosomes or spindle damage are detected by surveillance mechanisms (checkpoints) which block anaphase onset, cytokinesis and DNA re-replication. Until now, the MAD and BUB genes implicated in this regulation were thought to function in a single pathway that blocks APC activity. We show that spindle damage blocks sister chromatid separation solely by inhibiting APCCdc20-dependent Pds1 proteolysis and that this process requires Mad2. Blocking APCCdh1-mediated Clb2 proteolysis and chromosome re-duplication does not require Mad2 but a different protein, Bub2. Our data imply that Mad1, Mad2, Mad3 and Bub1 regulate APCCdc20, whereas Bub2 regulates APCCdh1.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
