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G1 control in mammalian cells.
Reed, S I; Bailly, E; Dulic, V; Hengst, L; Resnitzky, D; Slingerland, J.
Afiliación
  • Reed SI; Department of Molecular Biology, Scripps Research Institute, La Jolla, CA 92037.
J Cell Sci Suppl ; 18: 69-73, 1994.
Article en En | MEDLINE | ID: mdl-7883795
Cyclin-dependent kinases (Cdks) control the major cell cycle transitions in eukaryotic cells. On the basis of a variety of experiments where cyclin function either is impaired or enhanced, D-type cyclins as well as cyclins E and A have been linked to G1 and G1/S phase roles in mammalian cells. We therefore sought to determine if agents that block the G1/S phase transition do so at the level of regulating the Cdk activities associated with these cyclins. A variety of conditions that lead to G1 arrest were found to correlate with accumulation of G1-specific Cdk inhibitors, including treatment of fibroblasts with ionizing radiation, treatment of epithelial cells with TGF-beta, treatment of HeLa cells with the drug lovastatin, and removal of essential growth factors from a variety of different cell types. Mechanistically, inhibition of Cdks was found to involve the stoichiometric binding of Cdk inhibitor proteins. p21Waf1/Cip1 was associated with DNA damage induced arrest while p27Kip1/p28Ick1 accumulated under a variety of antiproliferative conditions.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fase G1 / Ciclinas / Quinasas Ciclina-Dependientes Límite: Animals / Humans Idioma: En Revista: J Cell Sci Suppl Año: 1994 Tipo del documento: Article Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fase G1 / Ciclinas / Quinasas Ciclina-Dependientes Límite: Animals / Humans Idioma: En Revista: J Cell Sci Suppl Año: 1994 Tipo del documento: Article Pais de publicación: Reino Unido