| Literature DB >> 9652094 |
B Novak1, A Csikasz-Nagy, B Gyorffy, K Chen, J J Tyson.
Abstract
All events of the fission yeast cell cycle can be orchestrated by fluctuations of a single cyclin-dependent protein kinase, the Cdc13/Cdc2 heterodimer. The G1/S transition is controlled by interactions of Cdc13/Cdc2 and its stoichiometric inhibitor, Rum1. The G2/M transition is regulated by a kinase-phosphatase pair, Wee1 and Cdc25, which determine the phosphorylation state of the Tyr-15 residue of Cdc2. The meta/anaphase transition is controlled by interactions between Cdc13/Cdc2 and the anaphase promoting complex, which labels Cdc13 subunits for proteolysis. We construct a mathematical model of fission yeast growth and division that encompasses all three crucial checkpoint controls. By numerical simulations we show that the model is consistent with a broad selection of cell cycle mutants, and we predict the phenotypes of several multiple-mutant strains that have not yet been constructed.Entities:
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Year: 1998 PMID: 9652094 DOI: 10.1016/s0301-4622(98)00133-1
Source DB: PubMed Journal: Biophys Chem ISSN: 0301-4622 Impact factor: 2.352