A cell cycle-regulated inhibitor of cyclin-dependent kinases.
AUTOR(ES)
Hengst, L
RESUMO
Cyclin-dependent kinases (Cdks) previously have been shown to drive the major cell cycle transitions in eukaryotic organisms ranging from yeast to humans. We report here the identification of a 28-kDa protein, p28Ick (inhibitor of cyclin-dependent kinase), that binds to and inhibits the kinase activity of preformed Cdk/cyclin complexes from human cells. p28 inhibitory activity fluctuates during the cell cycle with maximal levels in G1 and accumulates in G1- and G0-arrested cells. These results suggest that control of the G1/S transition may be influenced by a family of Cdk inhibitors that include p28Ick and the recently described inhibitors p21Cip1/Waf1/Cap20 and p16Ink4.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=43980Documentos Relacionados
- Cell cycle control by Xenopus p28Kix1, a developmentally regulated inhibitor of cyclin-dependent kinases.
- KAP: a dual specificity phosphatase that interacts with cyclin-dependent kinases.
- Phosphorylation and inactivation of protein phosphatase 1 by cyclin-dependent kinases.
- Specific regulation of E2F family members by cyclin-dependent kinases.
- Inhibition of p53-mediated growth arrest by overexpression of cyclin-dependent kinases.