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      The interaction between N-WASP and the Arp2/3 complex links Cdc42-dependent signals to actin assembly.

      Cell
      Actin-Related Protein 2, Actin-Related Protein 3, Actins, metabolism, Animals, Biopolymers, Cattle, Cell Cycle Proteins, Cytoskeletal Proteins, Female, GTP-Binding Proteins, In Vitro Techniques, Macromolecular Substances, Models, Biological, Nerve Tissue Proteins, chemistry, genetics, Oocytes, Peptide Fragments, Phosphatidylinositol 4,5-Diphosphate, Rats, Recombinant Proteins, Signal Transduction, Wiskott-Aldrich Syndrome Protein, Neuronal, Xenopus, cdc42 GTP-Binding Protein

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          Abstract

          Although small GTP-binding proteins of the Rho family have been implicated in signaling to the actin cytoskeleton, the exact nature of the linkage has remained obscure. We describe a novel mechanism that links one Rho family member, Cdc42, to actin polymerization. N-WASP, a ubiquitously expressed Cdc42-interacting protein, is required for Cdc42-stimulated actin polymerization in Xenopus egg extracts. The C terminus of N-WASP binds to the Arp2/3 complex and dramatically stimulates its ability to nucleate actin polymerization. Although full-length N-WASP is less effective, its activity can be greatly enhanced by Cdc42 and phosphatidylinositol (4,5) bisphosphate. Therefore, N-WASP and the Arp2/3 complex comprise a core mechanism that directly connects signal transduction pathways to the stimulation of actin polymerization.

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