The dishevelled protein is modified by wingless signaling in Drosophila

Genes Dev. 1995 May 1;9(9):1087-97. doi: 10.1101/gad.9.9.1087.

Abstract

Wingless (Wg) is an important signaling molecule in the development of Drosophila, but little is known about its signal transduction pathway. Genetic evidence indicates that another segment polarity gene, dishevelled (dsh) is required for Wg signaling. We have recently developed a cell culture system for Wg protein activity, and using this in vitro system as well as intact Drosophila embryos, we have analyzed biochemical changes in the Dsh protein as a consequence of Wg signaling. We find that Dsh is a phosphoprotein, normally present in the cytoplasm. Wg signaling generates a hyperphosphorylated form of Dsh, which is associated with a membrane fraction. Overexpressed Dsh becomes hyperphosphorylated in the absence of extracellular Wg and increases levels of the Armadillo protein, thereby mimicking the Wg signal. A deletional analysis of Dsh identifies several conserved domains essential for activity, among which is a so-called GLGF/DHR motif. We conclude that dsh, a highly conserved gene, is not merely a permissive factor in Wg signaling but encodes a novel signal transduction molecule, which may function between the Wg receptor and more downstream signaling molecules.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Armadillo Domain Proteins
  • Base Sequence
  • Cell Extracts
  • Cell Membrane / chemistry
  • Cells, Cultured
  • Conserved Sequence / genetics
  • Cytoplasm / chemistry
  • Dishevelled Proteins
  • Drosophila / embryology
  • Drosophila / genetics*
  • Drosophila Proteins*
  • Gene Expression Regulation
  • Gene Expression Regulation, Developmental
  • Genes, Insect / genetics
  • Molecular Sequence Data
  • Molecular Weight
  • Phosphoproteins* / analysis
  • Phosphoproteins* / chemistry
  • Phosphoproteins* / physiology
  • Protein Biosynthesis
  • Proteins* / analysis
  • Proteins* / chemistry
  • Proteins* / physiology
  • Proto-Oncogene Proteins / physiology*
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / immunology
  • Sequence Deletion / physiology
  • Signal Transduction / genetics*
  • Trans-Activators*
  • Transcription Factors
  • Wnt1 Protein

Substances

  • ARM protein, Drosophila
  • Adaptor Proteins, Signal Transducing
  • Armadillo Domain Proteins
  • Cell Extracts
  • Dishevelled Proteins
  • Drosophila Proteins
  • Phosphoproteins
  • Proteins
  • Proto-Oncogene Proteins
  • Recombinant Fusion Proteins
  • Trans-Activators
  • Transcription Factors
  • Wnt1 Protein
  • dsh protein, Drosophila
  • wg protein, Drosophila