Abstract
The biological functions of the tumor suppressor ING1 have been studied extensively in the past 5 years since it was cloned. Of the three alternatively spliced forms of ING1, p24(ING1) has been the focus of much of past research. Information on the other currently known isoforms, p47(ING1), p32(ING1), and p27(ING1), has been lacking. ING1 shares many biological functions with p53. It has been reported to mediate growth arrest, senescence, apoptosis, anchorage-dependent growth, and chemosensitivity. Some of these functions, such as cell-cycle arrest and apoptosis, have been shown to be dependent on the activity of both ING1 and p53 proteins. In this review, we will examine what is known about ING1 up to this point and clarify the cloning errors originating from the isolation of this gene.
Copyright 2001 Academic Press.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Alternative Splicing
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Animals
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Cell Cycle Proteins
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DNA-Binding Proteins
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Genes, Tumor Suppressor / physiology*
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Growth Inhibitors / genetics*
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Growth Inhibitors / metabolism
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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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Mice
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Multigene Family
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Neoplasms / metabolism
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Nuclear Proteins
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Organ Specificity
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Protein Isoforms / genetics
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Protein Isoforms / metabolism
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Proteins / genetics*
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Proteins / metabolism
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RNA, Messenger / biosynthesis
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Sequence Homology, Amino Acid
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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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Growth Inhibitors
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ING1 protein, human
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Ing1 protein, mouse
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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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RNA, Messenger
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Tumor Suppressor Proteins