IDENTIFICATION OF G(1) KINASE-ACTIVITY FOR CDK6, A NOVEL CYCLIN-D PARTNER

Citation
M. Meyerson et E. Harlow, IDENTIFICATION OF G(1) KINASE-ACTIVITY FOR CDK6, A NOVEL CYCLIN-D PARTNER, Molecular and cellular biology, 14(3), 1994, pp. 2077-2086
Citations number
74
Categorie Soggetti
Biology
ISSN journal
02707306
Volume
14
Issue
3
Year of publication
1994
Pages
2077 - 2086
Database
ISI
SICI code
0270-7306(1994)14:3<2077:IOGKFC>2.0.ZU;2-N
Abstract
A family of vertebrate cdc2-related kinases has been identified, and t hese kinases are candidates for roles in cell cycle regulation. Here, we show that the human PLSTIRE gene product is a novel cyclin-dependen t kinase, cdk6. The cdk6 kinase is associated with cyclins D1, D2, and D3 in lysates of human cells and is activated by coexpression with D- type cyclins in Sf9 insect cells. Furthermore, we demonstrate that end ogenous cdk6 from human cell extracts is an active kinase which can ph osphorylate pRB, the product of the retinoblastoma tumor suppressor ge ne. The activation of cdk6 kinase occurs during mid-G, in phytohemaggl utinin-stimulated T cells, well prior to the activation of cdk2 kinase . This timing suggests that cdk6, and by analogy its homolog cdk4, lin ks growth factor stimulation with the onset of cell cycle progression.