Abstract
The p53-related protein p73 has many functions similar to that of p53 including the ability to induce cell-cycle arrest and apoptosis. Both p53 and p73 function as transcription factors, and p73 activates expression of many genes that also are regulated by p53. Despite their similarities, it is evident that p53 and p73 are not interchangeable functionally, with p73 playing a role in normal growth and development that is not shared by p53. In this paper we describe the ability of p73beta but not p53 to activate expression of the cyclin-dependent kinase inhibitor p57(KIP) and KvLQT1, two genes that are coregulated in an imprinted region of the genome. Our results suggest that p73 may regulate expression of genes through mechanisms that are not shared by p53, potentially explaining the different contributions of p53 and p73 to normal development.
MeSH terms
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Animals
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Blotting, Western
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Cell Cycle Proteins*
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Cell Line
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Cyclin-Dependent Kinase Inhibitor p57
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DNA-Binding Proteins / metabolism*
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E2F Transcription Factors
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Genes, Tumor Suppressor
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Genomic Imprinting / genetics
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Humans
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KCNQ Potassium Channels
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KCNQ1 Potassium Channel
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Mice
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Nuclear Proteins / biosynthesis*
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Nuclear Proteins / genetics
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Nuclear Proteins / metabolism*
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Potassium Channels / genetics
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Potassium Channels, Voltage-Gated*
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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Transcription Factors / metabolism
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Tumor Cells, Cultured
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Tumor Protein p73
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Tumor Suppressor Protein p53 / metabolism
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Tumor Suppressor Proteins
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Up-Regulation*
Substances
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CDKN1C protein, human
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Cdkn1c protein, mouse
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Cell Cycle Proteins
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Cyclin-Dependent Kinase Inhibitor p57
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DNA-Binding Proteins
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E2F Transcription Factors
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KCNQ Potassium Channels
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KCNQ1 Potassium Channel
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KCNQ1 protein, human
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Kcnq1 protein, mouse
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Nuclear Proteins
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Potassium Channels
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Potassium Channels, Voltage-Gated
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RNA, Messenger
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TP73 protein, human
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Transcription Factors
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Trp73 protein, mouse
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Tumor Protein p73
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Tumor Suppressor Protein p53
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Tumor Suppressor Proteins