Abstract
The tumor suppressor protein, p53, is part of the cell's emergency team that is called upon following cellular insult. How do cells sense DNA damage and other cellular stresses and what signal transduction pathways are used to alert p53? How is the resulting nuclear accumulation of p53 accomplished and what determines the outcome of p53 induction? Many posttranslational modifications of p53, such as phosphorylation, dephosphorylation, acetylation and ribosylation, have been shown to occur following cellular stress. Some of these modifications may activate the p53 protein, interfere with MDM2 binding and/or dictate cellular localization of p53. This review will focus on recent findings about how the p53 response may be activated following cellular stress.
Publication types
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
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Review
MeSH terms
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Animals
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Cysteine Endopeptidases / physiology
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DNA / metabolism
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DNA Damage
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DNA Repair
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Gene Expression Regulation
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Humans
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Mitogen-Activated Protein Kinase 8
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Mitogen-Activated Protein Kinases / physiology
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Multienzyme Complexes / physiology
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Nuclear Proteins*
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Proteasome Endopeptidase Complex
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Proto-Oncogene Proteins / physiology
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Proto-Oncogene Proteins c-mdm2
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RNA Polymerase II / radiation effects
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Tumor Suppressor Protein p53 / physiology*
Substances
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Multienzyme Complexes
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Nuclear Proteins
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Proto-Oncogene Proteins
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Tumor Suppressor Protein p53
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DNA
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MDM2 protein, human
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Proto-Oncogene Proteins c-mdm2
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Mitogen-Activated Protein Kinase 8
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Mitogen-Activated Protein Kinases
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RNA Polymerase II
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Cysteine Endopeptidases
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Proteasome Endopeptidase Complex