Toda K, et al. (2012) APC/C-Cdh1-dependent anaphase and telophase progression during mitotic slippage. Cell Div 7(1):4
Abstract: ABSTRACT: BACKGROUND: The spindle assembly checkpoint (SAC) inhibits anaphase progression in the presence of insufficient kinetochore-microtubule attachments, but cells can eventually escape from this mitotic arrest by a process known as called mitotic slippage or adaptation. This is a problem for cancer chemotherapy using microtubule poisons. RESULTS: Here we describe mitotic slippage in budding yeast. Precocious activation of anaphase promoting complex/cyclosome (APC/C)-Cdh1 caused mitotic slippage in the presence of nocodazole, while SAC was still active. APC/C-Cdh1, but not APC/C-Cdc20, triggered anaphase progression (securin degradation, separase-mediated cohesin cleavage and sister-chromatid separation), in addition to telophase onset (mitotic exit), during mitotic slippage. This demonstrates that an inhibitory system not only of APC/C-Cdc20 but also of APC/C-Cdh1 is critical for accurate chromosome segregation in the presence of unsatisfied kinetochore-microtubule attachments. CONCLUSIONS: The sequential activation of APC/C-Cdc20-to-APC/C-Cdh1 during mitosis is the heart of accurate mitosis. Precocious activation of APC/C-Cdh1 in metaphase (pre-anaphase) causes mitotic slippage in nocodazole-treated cells. For prevention of mitotic slippage, concomitant inhibition of APC/C-Cdh1 may be effective for tumor therapy with mitotic spindle poisons in human.
|Status: Epub ahead of print||Type: Journal Article||PubMed ID: 22321970|
Topics addressed in this paper
Number of different genes curated to this paper: 7
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