Regulation of the cell cycle by the cdk2 protein kinase in cultured human fibroblasts.

Michele Pagano(European Molecular Biology Laboratory), Rainer Pepperkok(European Molecular Biology Laboratory), Jiří Lukáš(European Molecular Biology Laboratory), Véronique Baldin(European Molecular Biology Laboratory), W. Ansorge(European Molecular Biology Laboratory), Jiří Bártek(490 BioTech (United States)), Giulio Draetta(European Molecular Biology Laboratory)
The Journal of Cell Biology
April 1, 1993
Cited by 325Open Access
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Abstract

In mammalian cells inhibition of the cdc2 function results in arrest in the G2-phase of the cell cycle. Several cdc2-related gene products have been identified recently and it has been hypothesized that they control earlier cell cycle events. Here we have studied the relationship between activation of one of these cdc2 homologs, the cdk2 protein kinase, and the progression through the cell cycle in cultured human fibroblasts. We found that cdk2 was activated and specifically localized to the nucleus during S phase and G2. Microinjection of affinity-purified anti-cdk2 antibodies but not of affinity-purified anti-cdc2 antibodies, during G1, inhibited entry into S phase. The specificity of these effects was demonstrated by the fact that a plasmid-driven cdk2 overexpression counteracted the inhibition. These results demonstrate that the cdk2 protein kinase is involved in the activation of DNA synthesis.


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