Abstract
The nuclear factor of activated T cells (NFAT) group of transcription factors is retained in the cytoplasm of quiescent cells. NFAT activation is mediated in part by induced nuclear import. This process requires calcium-dependent dephosphorylation of NFAT caused by the phosphatase calcineurin. The c-Jun amino-terminal kinase (JNK) phosphorylates NFAT4 on two sites. Mutational removal of the JNK phosphorylation sites caused constitutive nuclear localization of NFAT4. In contrast, JNK activation in calcineurin-stimulated cells caused nuclear exclusion of NFAT4. These findings show that the nuclear accumulation of NFAT4 promoted by calcineurin is opposed by the JNK signal transduction pathway.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Binding Sites
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COS Cells
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Calcineurin / metabolism
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Calcineurin Inhibitors
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Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
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Cell Line
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Cell Nucleus / metabolism*
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Cyclosporine / pharmacology
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Cytoplasm / metabolism
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / metabolism*
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Humans
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JNK Mitogen-Activated Protein Kinases
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Jurkat Cells
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Mitogen-Activated Protein Kinase Kinases
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Mitogen-Activated Protein Kinases*
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Mutation
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NFATC Transcription Factors
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Nuclear Proteins*
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Phosphorylation
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Protein Kinases / metabolism
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Recombinant Fusion Proteins / metabolism
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Signal Transduction*
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T-Lymphocytes / metabolism
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Transcription Factors / genetics
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Transcription Factors / metabolism*
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Transcription, Genetic
Substances
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Calcineurin Inhibitors
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DNA-Binding Proteins
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NFATC Transcription Factors
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NFATC3 protein, human
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Nuclear Proteins
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Recombinant Fusion Proteins
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Transcription Factors
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Cyclosporine
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Protein Kinases
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Calcium-Calmodulin-Dependent Protein Kinases
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JNK Mitogen-Activated Protein Kinases
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Mitogen-Activated Protein Kinases
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Mitogen-Activated Protein Kinase Kinases
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Calcineurin