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J Cell Biol. 2010 Jul 26;190(2):209-22. doi: 10.1083/jcb.201002026.

Oscillations in Cdc14 release and sequestration reveal a circuit underlying mitotic exit.

Author information

  • 1The Italian Foundation for Cancer Research Institute of Molecular Oncology, 20139 Milan, Italy.

Abstract

In budding yeast, the phosphatase Cdc14 orchestrates progress through anaphase and mitotic exit, thereby resetting the cell cycle for a new round of cell division. Two consecutive pathways, Cdc fourteen early anaphase release (FEAR) and mitotic exit network (MEN), contribute to the progressive activation of Cdc14 by regulating its release from the nucleolus, where it is kept inactive by Cfi1. In this study, we show that Cdc14 activation requires the polo-like kinase Cdc5 together with either Clb-cyclin-dependent kinase (Cdk) or the MEN kinase Dbf2. Once active, Cdc14 triggers a negative feedback loop that, in the presence of stable levels of mitotic cyclins, generates periodic cycles of Cdc14 release and sequestration. Similar phenotypes have been described for yeast bud formation and centrosome duplication. A common theme emerges where events that must happen only once per cycle, although intrinsically capable of oscillations, are limited to one occurrence by the cyclin-Cdk cell cycle engine.

PMID:
20660629
[PubMed - indexed for MEDLINE]
PMCID:
PMC2930283
Free PMC Article

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