Abstract
ING1b is a candidate tumor suppressor that can stimulate the transcriptional activity of p53 and inhibit cell proliferation. The molecular basis of how ING1b activates p53 function remains unclear. Here we show that ING1b could stimulate the activity of p53 by increasing the level and stability of the p53 protein. The stabilization and activation of p53 by ING1b could be reversed by MDM2 in a dose-dependent manner. Conversely, ING1b could reverse the inhibition and degradation of p53 caused by MDM2 in a dose-dependent manner. Furthermore, ING1b and MDM2 bound to p53 in a mutually exclusive manner. In agreement with these observations, we found that similarly to MDM2, ING1b binds to the NH(2)-terminal region of p53. These data suggest a model in which ING1b disrupts the interaction between p53 and MDM2, leading to the stabilization of p53 and growth inhibition.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Binding, Competitive
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Carcinoma, Non-Small-Cell Lung / genetics
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Carcinoma, Non-Small-Cell Lung / metabolism
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Carcinoma, Non-Small-Cell Lung / pathology
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Cell Cycle Proteins
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Cell Division / physiology
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DNA-Binding Proteins
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Genes, Tumor Suppressor
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Humans
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Inhibitor of Growth Protein 1
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Intracellular Signaling Peptides and Proteins
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Lung Neoplasms / genetics
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Lung Neoplasms / metabolism
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Lung Neoplasms / pathology
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Nuclear Proteins
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Protein Isoforms
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Proteins / metabolism
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Proteins / physiology*
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Transcription, Genetic
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Tumor Cells, Cultured
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Tumor Suppressor Protein p53 / genetics
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Tumor Suppressor Protein p53 / metabolism
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Tumor Suppressor Protein p53 / physiology*
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Tumor Suppressor Proteins
Substances
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Cell Cycle Proteins
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DNA-Binding Proteins
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ING1 protein, human
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Inhibitor of Growth Protein 1
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Intracellular Signaling Peptides and Proteins
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Nuclear Proteins
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Protein Isoforms
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Proteins
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Tumor Suppressor Protein p53
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Tumor Suppressor Proteins