Abstract
The transcriptional co-activator p300 has been reported to regulate the tumor suppressor p53 and its ortholog p73. Here we describe a study showing that this coactivator also regulates the transcriptional function of p63. p300 bound to the N-terminal domain of p63gamma, and p63gamma bound to the N terminus of p300 in vitro and in cells. p300, but not its acetylase-defective mutant AT2, stimulated p63gamma-dependent transcription and induction of p21 in cells, consequently leading to G1 arrest. Inversely, the deltaN-p63gamma isoform as well as p300AT2 inhibited the induction of p21 by p63gamma. These results suggest that p300 regulates p63-dependent transcription of p21.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adenoviridae / genetics
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Cell Cycle
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Cell Cycle Proteins / metabolism
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Cell Line
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Cell Line, Tumor
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Cyclin-Dependent Kinase Inhibitor p21
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DNA-Binding Proteins
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Genes, Tumor Suppressor / physiology*
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Glutathione Transferase / metabolism
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Histidine / chemistry
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Humans
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Immunoprecipitation
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Mutation
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Nuclear Proteins / metabolism
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Nuclear Proteins / physiology*
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Phosphoproteins / genetics
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Phosphoproteins / physiology*
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Plasmids / metabolism
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Protein Binding
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Protein Structure, Tertiary
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Recombinant Fusion Proteins / metabolism
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Trans-Activators / genetics
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Trans-Activators / metabolism
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Trans-Activators / physiology*
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Transcription Factors
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Transcription, Genetic*
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Transcriptional Activation
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Transfection
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Tumor Suppressor Proteins
Substances
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CDKN1A protein, human
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Cell Cycle Proteins
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Cyclin-Dependent Kinase Inhibitor p21
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DNA-Binding Proteins
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Nuclear Proteins
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Phosphoproteins
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Recombinant Fusion Proteins
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TP63 protein, human
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Trans-Activators
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Transcription Factors
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Tumor Suppressor Proteins
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Histidine
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Glutathione Transferase