Abstract
To examine signal transduction events activated by oncogenic p21ras, we have studied kinases that are activated following the scrape loading of p21ras into quiescent cells. We observe rapid activation of 42 kDa and 46 kDa protein kinases. The 42 kDa kinase is the mitogen and extracellular-signal regulated kinase ERK2, (MAP2 kinase), which is activated by phosphorylation on tyrosine and threonine in response to oncogenic p21ras, while the 46 kDa kinase is likely to be another member of the ERK family. Stimulation of these kinases by oncogenic p21ras does not require the presence of growth factors, showing that oncogenic p21ras uncouples kinase activation from external signals. In ras transformed cell lines, these kinases are constitutively activated. We propose that the kinases are important components of the signal transduction pathway activated by p21ras oncoprotein.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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3T3 Cells
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Amino Acid Sequence
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Animals
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Blotting, Western
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Calcium-Calmodulin-Dependent Protein Kinases
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Cell Line, Transformed
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Enzyme Activation
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Flow Cytometry
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Kinetics
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Mice
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Mitogen-Activated Protein Kinase 1
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Molecular Sequence Data
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Phosphates / metabolism
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Phosphorylation
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Phosphotyrosine
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Protein-Tyrosine Kinases / metabolism*
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Proteins / isolation & purification
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Proteins / metabolism*
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Proto-Oncogene Proteins p21(ras) / genetics
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Proto-Oncogene Proteins p21(ras) / isolation & purification
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Proto-Oncogene Proteins p21(ras) / metabolism*
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Recombinant Proteins / metabolism
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Signal Transduction*
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Tyrosine / analogs & derivatives
Substances
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Phosphates
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Proteins
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Recombinant Proteins
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Phosphotyrosine
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Tyrosine
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Protein-Tyrosine Kinases
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Calcium-Calmodulin-Dependent Protein Kinases
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Mitogen-Activated Protein Kinase 1
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Proto-Oncogene Proteins p21(ras)