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Arp2/3 complex-independent actin regulatory function of WAVE.

Abstract
We report that WAVE1/Scar1, a WASP-family protein that functions downstream of Rac in membrane ruffling, can induce part of the reorganization of the actin cytoskeleton without Arp2/3 complex. WAVE1 has been reported to associate and activate Arp2/3 complex at its C-terminal region that is rich in acidic residues. The deletion of the acidic residues abolished the interaction with and the activation ability of Arp2/3 complex. The expression of the mutant WAVE1 lacking the acidic residues (DeltaA), however, induced actin-clustering in cells as the wild-type WAVE1 did. In addition, this actin-clustering could not be suppressed by the coexpression of the Arp2/3 complex-sequestering fragment (CA-region) derived from N-WASP, which clearly inhibits Rac-induced membrane ruffling. This study therefore demonstrates that WAVE1 reorganizes the actin cytoskeleton not only through Arp2/3 complex but also through another unidentified mechanism that may be important but has been neglected thus far.
AuthorsN Sasaki, H Miki, T Takenawa
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 272 Issue 2 Pg. 386-90 (Jun 07 2000) ISSN: 0006-291X [Print] United States
PMID10833423 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2000 Academic Press.
Chemical References
  • Actin-Related Protein 2
  • Actin-Related Protein 3
  • Actins
  • Actr2 protein, mouse
  • Actr3 protein, mouse
  • Biopolymers
  • Cytoskeletal Proteins
  • Microfilament Proteins
  • Nerve Tissue Proteins
  • Peptide Fragments
  • Recombinant Fusion Proteins
  • Wasf1 protein, mouse
  • Wasl protein, mouse
  • Wiskott-Aldrich Syndrome Protein Family
  • Wiskott-Aldrich Syndrome Protein, Neuronal
Topics
  • 3T3 Cells
  • Actin-Related Protein 2
  • Actin-Related Protein 3
  • Actins (metabolism)
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Biopolymers (metabolism)
  • Cytoskeletal Proteins
  • Cytoskeleton (metabolism)
  • Hydrogen-Ion Concentration
  • Mice
  • Microfilament Proteins (chemistry, genetics, metabolism)
  • Molecular Sequence Data
  • Nerve Tissue Proteins (chemistry, genetics, metabolism)
  • Peptide Fragments (chemistry, genetics, metabolism)
  • Protein Binding
  • Recombinant Fusion Proteins (chemistry, genetics, metabolism)
  • Sequence Deletion (genetics)
  • Wiskott-Aldrich Syndrome Protein Family
  • Wiskott-Aldrich Syndrome Protein, Neuronal

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