Identification of a motif in the carboxyl terminus of beta -arrestin2 responsible for activation of JNK3.
Accumulating evidence indicates that the beta-arrestins act as scaffold molecules that couple G-protein-coupled receptors to mitogen-activated protein (MAP) kinase signaling pathways. Recently, we identified the c-Jun N-terminal kinase 3 (JNK3) as a beta-arrestin2-interacting protein in yeast-two hybrid and co-immunoprecipitation studies. Beta-arrestin2 acts as a scaffold to enhance signaling to JNK3 ... stimulated by overexpression of the MAP3 kinase ASK1 or by agonist activation of the angiotensin 1A receptor. Whereas beta-arrestin2 is a very strong activator of JNK3 signaling, beta-arrestin1 is very weak in this regard. The data also indicate that the specific step enhanced by beta-arrestin2 involves phosphorylation of JNK3 by the MAP2 kinase MKK4. We reasoned that defining the region (or domain) in beta-arrestin2 responsible for high level JNK3 activation would provide insight into the mechanism by which beta-arrestin2 enhances the activity of this signaling pathway. Using chimeric beta-arrestins, we have determined that sequences in the carboxyl-terminal region of beta-arrestin2 are important for the enhancement of JNK3 phosphorylation. More detailed analysis of the carboxyl-terminal domains of the beta-arrestins indicated that beta-arrestin2, but not beta-arrestin1, contains a sequence (RRSLHL) highly homologous to the conserved docking motif present in many MAP kinase-binding proteins. Replacement of the beta-arrestin2 RRS residues with the corresponding KP residues present in beta-arrestin1 dramatically reduced both JNK3 interaction and enhancement of JNK3 phosphorylation. Conversely, replacement of the KP residues in beta-arrestin1 with RRS significantly increased both JNK3 binding and enhancement of JNK3 phosphorylation. These results delineate a mechanism by which beta-arrestin2 functions as a scaffold protein in the JNK3 signaling pathway and implicate the conserved docking site in beta-arrestin2 as an important factor in binding JNK3 and stimulating the phosphorylation of JNK3 by MKK4.
Mesh Terms:
Amino Acid Motifs, Amino Acid Sequence, Animals, Arabidopsis Proteins, Arrestins, COS Cells, Dose-Response Relationship, Drug, Enzyme Activation, Immunoblotting, Mitogen-Activated Protein Kinase 10, Mitogen-Activated Protein Kinase Kinases, Mitogen-Activated Protein Kinases, Models, Biological, Molecular Sequence Data, Phosphorylation, Plant Proteins, Plasmids, Precipitin Tests, Protein Binding, Protein Structure, Tertiary, Protein-Tyrosine Kinases, Receptors, Adrenergic, beta-2, Sequence Homology, Amino Acid, Signal Transduction
Amino Acid Motifs, Amino Acid Sequence, Animals, Arabidopsis Proteins, Arrestins, COS Cells, Dose-Response Relationship, Drug, Enzyme Activation, Immunoblotting, Mitogen-Activated Protein Kinase 10, Mitogen-Activated Protein Kinase Kinases, Mitogen-Activated Protein Kinases, Models, Biological, Molecular Sequence Data, Phosphorylation, Plant Proteins, Plasmids, Precipitin Tests, Protein Binding, Protein Structure, Tertiary, Protein-Tyrosine Kinases, Receptors, Adrenergic, beta-2, Sequence Homology, Amino Acid, Signal Transduction
J. Biol. Chem.
Date: Jul. 27, 2001
PubMed ID: 11356842
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