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Proc Natl Acad Sci U S A ; 96(5): 2147-52, 1999 Mar 02.
Article in English | MEDLINE | ID: mdl-10051609

ABSTRACT

The p53 tumor suppressor controls multiple cell cycle checkpoints regulating the mammalian response to DNA damage. To identify the mechanism by which p53 regulates G2, we have derived a human ovarian cell that undergoes p53-dependent G2 arrest at 32 degrees C. We have found that p53 prevents G2/M transition by decreasing intracellular levels of cyclin B1 protein and attenuating the activity of the cyclin B1 promoter. Cyclin B1 is the regulatory subunit of the cdc2 kinase and is a protein required for mitotic initiation. The ability of p53 to control mitotic initiation by regulating intracellular cyclin B1 levels suggests that the cyclin B-dependent G2 checkpoint has a role in preventing neoplastic transformation.


Subject(s)
Cell Cycle/physiology , Cyclin B/physiology , Tumor Suppressor Protein p53/genetics , Tumor Suppressor Protein p53/metabolism , Animals , CDC2 Protein Kinase/metabolism , Cell Line , Cyclin B/genetics , Cyclin B1 , Female , G2 Phase , Gene Expression Regulation , Genes, Reporter , Humans , Mice , Mitosis , Ovarian Neoplasms , Protein Kinases/metabolism , Recombinant Proteins/metabolism , Transfection , Tumor Cells, Cultured
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