
The SH3 binding protein, 3BP-1, was originally cloned as a partial cDNA from an expression library using the Abl SH3 domain as a probe. In addition to an SH3 binding domain, 3BP-1 displayed homology to a class of GTPase activating proteins (GAPs) active against Rac and Rho proteins. We report here a full length cDNA of 3BP-1 which extends the homology to GAP proteins previously noted. 3BP-1 functions in vitro as a GAP with a specificity for Rac-related G proteins. Microinjection of the 3BP-1 protein into serum-starved fibroblasts produces an inhibition of platelet-derived growth factor (PDGF)-induced membrane ruffling mediated by Rac. Co-injection of 3BP-1 with an activated Rac mutant that is unresponsive to GAPs, counter-acts this inhibition. 3BP-1 does not show in vitro activity towards Rho and, in agreement with this finding, microinjection of 3BP-1 into fibroblasts has no effect on lysophosphatidic acid (LPA)-induced stress fiber assembly mediated by Rho. Thus 3BP-1 is a new and specific Rac GAP that can act in cells to counter Rac-mediated membrane ruffling. How its SH3 binding site interacts with its GAP activity remains to be understood.
570, Molecular Sequence Data, 3BP-I, 610, Phosphatidic Acids, Mice, GTP-Binding Proteins, Animals, Amino Acid Sequence, Growth Substances, Oncogene Proteins, Base Sequence, Cell Membrane, GTPase-Activating Proteins, cytoskeleton, GAP, 3T3 Cells, Fibroblasts, Actins, Rac, SH3, Genes, src, Gene Expression Regulation, Mutation, Guanosine Triphosphate, Lysophospholipids, Carrier Proteins
570, Molecular Sequence Data, 3BP-I, 610, Phosphatidic Acids, Mice, GTP-Binding Proteins, Animals, Amino Acid Sequence, Growth Substances, Oncogene Proteins, Base Sequence, Cell Membrane, GTPase-Activating Proteins, cytoskeleton, GAP, 3T3 Cells, Fibroblasts, Actins, Rac, SH3, Genes, src, Gene Expression Regulation, Mutation, Guanosine Triphosphate, Lysophospholipids, Carrier Proteins
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