Abstract
Jab1 interacts with a variety of cell cycle and signal transduction regulators to control cell proliferation, differentiation, and tumorigenesis. In this study, we employed a non-denaturing gel electrophoresis method to separate different Jab1-containing complexes, the COP9 signalosome complex and the small Jab1-containing subcomplex. The formation of the small Jab1 complex was dependent on a low cell density and anchorage to a solid support, and enhanced during the early G1 phase of the cell cycle, which was abrogated in ras-transformed cells. The small Jab1-containing subcomplex may be a novel mediator of anchorage and cell-cell contact-dependent signal transduction.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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COP9 Signalosome Complex
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Cell Adhesion
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Cell Count
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Cell Cycle*
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Cell Line
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Cell Transformation, Neoplastic*
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Contact Inhibition
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DNA-Binding Proteins / metabolism*
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Intracellular Signaling Peptides and Proteins
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Mice
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Multiprotein Complexes / chemistry
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Multiprotein Complexes / isolation & purification
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Multiprotein Complexes / metabolism
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Peptide Hydrolases
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Protein Binding
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Transcription Factors / metabolism*
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ras Proteins / genetics
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ras Proteins / metabolism*
Substances
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DNA-Binding Proteins
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Intracellular Signaling Peptides and Proteins
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Multiprotein Complexes
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Transcription Factors
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Peptide Hydrolases
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Cops5 protein, mouse
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COP9 Signalosome Complex
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ras Proteins