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The cell cycle inhibitor p21CIP is phosphorylated by cyclin A-CDK2 complexes
M Jaumot1, J M Estañol, O Casanovas
1Department of Cell Biology, Faculty of Medicine, University of Barcelona, Spain.
Biochemical and Biophysical Research Communications
|January 13, 1998
Abstract:
We report here experimental evidence indicating that the p21CIP, the universal inhibitor of cyclin-dependent protein kinases, general inhibitor CDKs is a substrate oof cyclin A-cdk2. The evidence comes from phosphorylation experiments in which the endogenous p21CIP present in using the original cyclin A-cdk2 complexes immunoprecipitated from HeLa cells extracts can be phosphorylated by the cdk2 of the same complexes. In vitro experiments showing that reconstituted GSTcyclin A-GSTcdk2 complexes from phosphorylate recombinant GSTp21CIP confirms that p21CIP is a cyclin A-cdk2 substrate.