Abstract
The protein scaffold and signaling regulator p62 is important in critical cellular functions, including bone homeostasis, obesity, and cancer, because of its interactions with various signaling intermediaries. p62 is overexpressed in human cancers and is induced during cell transformation. Its genetic ablation inhibits lung tumorigenesis in vivo and cell proliferation in culture by regulating the TRAF6/NF-κB signaling cascade to control reactive oxygen species (ROS) production and apoptosis. Here we show that cdk1 phosphorylates p62 in vitro and in vivo at T269 and S272, which is necessary for the maintenance of appropriate cyclin B1 levels and the levels of cdk1 activity necessary to allow cells to properly enter and exit mitosis. The lack of cdk1-mediated phosphorylation of p62 leads to a faster exit from mitosis, which translates into enhanced cell proliferation and tumorigenesis in response to Ras-induced transformation. Therefore, p62 emerges as a node for the control of not only cell survival but also cell transit through mitosis.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Binding Sites
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CDC2 Protein Kinase / genetics
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CDC2 Protein Kinase / metabolism*
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Cell Line
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Cell Line, Tumor
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Cell Proliferation
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Cell Transformation, Neoplastic / genetics
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Cell Transformation, Neoplastic / metabolism*
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Cells, Cultured
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Cyclin B1 / metabolism
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Genes, ras
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Humans
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Male
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Mice
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Mice, Knockout
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Mice, Nude
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Mitosis / genetics
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Mitosis / physiology*
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Molecular Sequence Data
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Mutant Proteins / genetics
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Mutant Proteins / metabolism
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Phosphoproteins / chemistry
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Phosphoproteins / genetics
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Phosphoproteins / metabolism*
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Phosphorylation
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Recombinant Proteins / genetics
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Recombinant Proteins / metabolism
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Sequence Homology, Amino Acid
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Signal Transduction
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Tandem Mass Spectrometry
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Transcription Factor TFIIH
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Transcription Factors / chemistry
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Transcription Factors / deficiency
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Transcription Factors / genetics
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Transcription Factors / metabolism*
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Transcription Factors, TFII / chemistry
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Transcription Factors, TFII / genetics
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Transcription Factors, TFII / metabolism*
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Transfection
Substances
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CCNB1 protein, human
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Cyclin B1
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GTF2H1 protein, human
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Gtf2h1 protein, mouse
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Mutant Proteins
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Phosphoproteins
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Recombinant Proteins
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Transcription Factors
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Transcription Factors, TFII
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Transcription Factor TFIIH
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CDC2 Protein Kinase