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We show here that the cell cycle-dependent DNA-binding and transcriptional activity of p53 correlates with E2F expression in human primary fibroblasts. E2F1 binds and stimulates DNA-binding, transactivation and apoptotic functions of p53 but not p63 and p73. E2F1 binds residues 347-370 of p53 and enhances nuclear retention of Ser315 phosphorylated p53. This regulation of p53 by E2F1 is cell cycle dependent, as the cellular distribution of Ser315 phosphorylated p53 is associated with the periodic expression of E2F and cyclin A throughout the cell cycle. This is the first demonstration that the activities of p53 are regulated during the cell cycle by E2F/p53 interactions and that phosphorylation of p53 at Ser315 is required for this regulation.

Original publication

DOI

10.1038/sj.emboj.7600735

Type

Journal article

Journal

EMBO J

Publication Date

03/08/2005

Volume

24

Pages

2768 - 2782

Keywords

Amino Acid Sequence, Cell Cycle, Cell Cycle Proteins, Cell Nucleus, DNA, DNA-Binding Proteins, E2F Transcription Factors, E2F1 Transcription Factor, Genes, Tumor Suppressor, Humans, Molecular Sequence Data, Nuclear Proteins, Phosphoproteins, Phosphorylation, Serine, Trans-Activators, Transcription Factors, Transcription, Genetic, Tumor Protein p73, Tumor Suppressor Protein p53, Tumor Suppressor Proteins