Abstract
In this issue of Molecular Cell, two manuscripts (Sykes et al., 2006) propose that the decision to undergo apoptosis upon DNA damage is mediated through acetylation of p53 within its DNA-binding domain by MYST histone acetyltransferases.
MeSH terms
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Acetylation
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Animals
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Apoptosis
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Apoptosis Regulatory Proteins / metabolism
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Cell Cycle
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Cyclin-Dependent Kinase Inhibitor p21 / metabolism
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Histone Acetyltransferases / metabolism*
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Histone Acetyltransferases / physiology*
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Humans
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Lysine Acetyltransferase 5
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Proto-Oncogene Proteins / metabolism
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Proto-Oncogene Proteins c-mdm2 / metabolism
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Transcriptional Activation*
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Tumor Suppressor Protein p53 / metabolism*
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p300-CBP Transcription Factors / physiology
Substances
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Apoptosis Regulatory Proteins
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BBC3 protein, human
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CDKN1A protein, human
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Cyclin-Dependent Kinase Inhibitor p21
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Proto-Oncogene Proteins
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Tumor Suppressor Protein p53
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Histone Acetyltransferases
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KAT5 protein, human
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KAT8 protein, human
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Lysine Acetyltransferase 5
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p300-CBP Transcription Factors
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MDM2 protein, human
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Proto-Oncogene Proteins c-mdm2