Proteasome-dependent degradation of human CDC25B phosphatase. - Archive ouverte HAL Access content directly
Journal Articles Molecular Biology Reports Year : 1999

Proteasome-dependent degradation of human CDC25B phosphatase.

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The CDC25 dual specificity phosphatase is a universal cell cycle regulator. The evolutionary conservation of this enzyme from yeast to man bears witness to its major role in the control of cyclin-dependent kinases (CDK) activity that are central regulators of the cell cycle machinery. CDC25 phosphatase both dephosphorylates and activates CDKs. Three human CDC25s have been identified. CDC25A is involved in the control of G1/S, and CDC25C at G2/M throught the activation of CDK 1-cyclin B. The exact function of CDC25B however remains elusive. We have found that CDC25B is degraded by the proteasome pathway in vitro and in vivo. This degradation is dependent upon phosphorylation by the CDK1-cyclin A complex, but not by CDK1-cyclin B. Together with the observations of others made in yeast and mammals, our results suggest that CDC25B might act as a 'mitotic starter' triggering the activation of an auto-amplification loop before being degraded.

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hal-02353446 , version 1 (07-11-2019)



Christophe Cans, Bernard Ducommun, Véronique Baldin. Proteasome-dependent degradation of human CDC25B phosphatase.. Molecular Biology Reports, 1999, 26 (1/2), pp.53-57. ⟨10.1023/a:1006912105352⟩. ⟨hal-02353446⟩
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