Abstract
The serine/threonine kinase Cot triggers NF-kappaB-dependent transactivation and activation of various MAPKinases. Here we identify Cot as a novel p65 interacting protein kinase. Cot expression induces p65 phosphorylation at serines 536 and 468 in dependence from its kinase function. Accordingly, shRNA-mediated knockdown of Cot expression interferes with TNF-induced NF-kappaB-dependent gene expression. Also the C-terminally truncated, oncogenic form of Cot is able to trigger p65 phosphorylation. In vitro kinase assays and dominant negative mutants revealed that NIK functions downstream of Cot to mediate p65 phosphorylation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cell Line
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Gene Expression / drug effects
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Gene Expression Regulation
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Humans
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MAP Kinase Kinase Kinases / genetics
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MAP Kinase Kinase Kinases / metabolism*
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Mutation
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NF-kappaB-Inducing Kinase
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Phosphorylation
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Protein Serine-Threonine Kinases / genetics
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Protein Serine-Threonine Kinases / metabolism*
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Proto-Oncogene Proteins / genetics
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Proto-Oncogene Proteins / metabolism*
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RNA, Small Interfering / genetics
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Transcription Factor RelA / metabolism*
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Tumor Necrosis Factor-alpha / pharmacology
Substances
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Proto-Oncogene Proteins
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RNA, Small Interfering
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Transcription Factor RelA
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Tumor Necrosis Factor-alpha
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Protein Serine-Threonine Kinases
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MAP Kinase Kinase Kinases
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MAP3K8 protein, human