Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia

Nat Genet. 2001 Mar;27(3):313-7. doi: 10.1038/85886.

Abstract

The Wiskott-Aldrich syndrome protein (WASP; encoded by the gene WAS) and its homologs are important regulators of the actin cytoskeleton, mediating communication between Rho-family GTPases and the actin nucleation/crosslinking factor, the Arp2/3 complex. Many WAS mutations impair cytoskeletal control in hematopoietic tissues, resulting in functional and developmental defects that define the X-linked Wiskott-Aldrich syndrome (WAS) and the related X-linked thrombocytopenia (XLT). These diseases seem to result from reduced WASP signaling, often through decreased transcription or translation of the gene. Here we describe a new disease, X-linked severe congenital neutropenia (XLN), caused by a novel L270P mutation in the region of WAS encoding the conserved GTPase binding domain (GBD). In vitro, the mutant protein is constitutively activated through disruption of an autoinhibitory domain in the wild-type protein, indicating that loss of WASP autoinhibition is a key event in XLN. Our findings highlight the importance of precise regulation of WASP in hematopoietic development and function, as impairment versus enhancement of its activity give rise to distinct spectra of cellular defects and clinical phenotypes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • DNA / genetics
  • DNA Primers / genetics
  • Female
  • Genetic Linkage*
  • Humans
  • Lymphocyte Subsets
  • Male
  • Models, Molecular
  • Neutropenia / blood
  • Neutropenia / congenital*
  • Neutropenia / genetics*
  • Pedigree
  • Point Mutation*
  • Protein Conformation
  • Proteins / chemistry
  • Proteins / genetics*
  • Wiskott-Aldrich Syndrome / genetics
  • Wiskott-Aldrich Syndrome Protein
  • X Chromosome / genetics*

Substances

  • DNA Primers
  • Proteins
  • WAS protein, human
  • Wiskott-Aldrich Syndrome Protein
  • DNA