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      A cytoplasmic inhibitor of the JNK signal transduction pathway.

      Science (New York, N.Y.)
      Activating Transcription Factor 2, Animals, COS Cells, Calcium-Calmodulin-Dependent Protein Kinases, metabolism, Carrier Proteins, chemistry, Cell Nucleus, Cell Transformation, Neoplastic, Cells, Cultured, Cloning, Molecular, Cyclic AMP Response Element-Binding Protein, Cytoplasm, Fusion Proteins, bcr-abl, Gene Expression Regulation, JNK Mitogen-Activated Protein Kinases, Mitogen-Activated Protein Kinase 9, Mitogen-Activated Protein Kinases, Molecular Sequence Data, Phosphorylation, Protein Kinases, Proto-Oncogene Proteins c-jun, Recombinant Fusion Proteins, Signal Transduction, Transcription Factors, Transcriptional Activation, Transfection

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          Abstract

          The c-Jun amino-terminal kinase (JNK) is a member of the stress-activated group of mitogen-activated protein (MAP) kinases that are implicated in the control of cell growth. A murine cytoplasmic protein that binds specifically to JNK [the JNK interacting protein-1 (JIP-1)] was characterized and cloned. JIP-1 caused cytoplasmic retention of JNK and inhibition of JNK-regulated gene expression. In addition, JIP-1 suppressed the effects of the JNK signaling pathway on cellular proliferation, including transformation by the Bcr-Abl oncogene. This analysis identifies JIP-1 as a specific inhibitor of the JNK signal transduction pathway and establishes protein targeting as a mechanism that regulates signaling by stress-activated MAP kinases.

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