ISI Web of Knowledge Take the next step  
Web of Science®
 
Previous Record (inactive) Record 1  of  1 Next Record (inactive)
Record from Web of Science®
The Saccharomyces cerevisiae homologue of human Wiskott-Aldrich syndrome protein Las17p interacts with the Arp2/3 complex
Author(s): Madania A, Dumoulin P, Grava S, Kitamoto H, Scharer-Brodbeck C, Soulard A, Moreau V, Winsor B
Source: MOLECULAR BIOLOGY OF THE CELL    Volume: 10    Issue: 10    Pages: 3521-3538    Published: OCT 1999  
Times Cited: 93     References: 79     
Abstract: Yeast Las17 protein is homologous to the Wiskott-Aldrich Syndrome protein, which is implicated in severe immunodeficiency. Las17p/Bee1p has been shown to he important for actin patch assembly and actin polymerization. Here we show that Las17p interacts with the Arp2/3 complex. LAS17 is an allele-specific multicopy suppressor of ARP2 and ARP3 mutations; overexpression restores both actin patch organization and endocytosis defects in ARP2 temperature-sensitive (ts) cells. Six of seven ARP2 ts mutants and at least one ARP3 ts mutant are synthetically lethal with las17 Delta ts confirming functional interaction with the Arp2/3 complex. Further characterization of las17 Delta cells showed that receptor-mediated internalization of alpha factor by the Ste2 receptor is severely defective. The polarity of normal bipolar bud site selection is lost. Las17-gfp remains localized in cortical patches in vivo independently of polymerized actin and is required for the polarized localization of Arp2/3 as well as actin. Coimmunoprecipitation of Arp2p with Las17p indicates that Las17p interacts directly with the complex. Two hybrid results also suggest that Las17p interacts with actin, verprolin, Rvs167p and several other proteins including Src homology 3 (SH3) domain proteins, suggesting that Las17p cascades destined for the Arp2/3p complex and may integrate signals from different regulatory the actin cytoskeleton.
Document Type: Article
Language: English
Reprint Address: Winsor, B (reprint author), CNRS, Inst Biol Mol & Cellulaire, Div Mecanismes Mol & Cellulaire Dev, Unit Propre Recherche, 9005, F-67084 Strasbourg, France
Addresses:
1. CNRS, Inst Biol Mol & Cellulaire, Div Mecanismes Mol & Cellulaire Dev, Unit Propre Recherche, F-67084 Strasbourg, France
2. Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
Publisher: AMER SOC CELL BIOLOGY, PUBL OFFICE, 9650 ROCKVILLE PIKE, BETHESDA, MD 20814 USA
Subject Category: Cell Biology
IDS Number: 245PE
ISSN: 1059-1524
Previous Record (inactive) Record 1  of  1 Next Record (inactive)
Record from Web of Science®
  
Thomson Reuters Logo