Interaction of axin and Dvl-2 proteins regulates Dvl-2-stimulated TCF-dependent transcription

EMBO J. 1999 May 17;18(10):2823-35. doi: 10.1093/emboj/18.10.2823.

Abstract

Axin promotes the phosphorylation of beta-catenin by GSK-3beta, leading to beta-catenin degradation. Wnt signals interfere with beta-catenin turnover, resulting in enhanced transcription of target genes through the increased formation of beta-catenin complexes containing TCF transcription factors. Little is known about how GSK-3beta-mediated beta-catenin turnover is regulated in response to Wnt signals. We have explored the relationship between Axin and Dvl-2, a member of the Dishevelled family of proteins that function upstream of GSK-3beta. Expression of Dvl-2 activated TCF-dependent transcription. This was blocked by co-expression of GSK-3beta or Axin. Expression of a 59 amino acid GSK-3beta-binding region from Axin strongly activated transcription in the absence of an upstream signal. Introduction of a point mutation into full-length Axin that prevented GSK-3beta binding also generated a transcriptional activator. When co-expressed, Axin and Dvl-2 co-localized within expressing cells. When Dvl-2 localization was altered using a C-terminal CAAX motif, Axin was also redistributed, suggesting a close association between the two proteins, a conclusion supported by co-immunoprecipitation data. Deletion analysis suggested that Dvl-association determinants within Axin were contained between residues 603 and 810. The association of Axin with Dvl-2 may be important in the transmission of Wnt signals from Dvl-2 to GSK-3beta.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Amino Acid Sequence
  • Animals
  • Axin Protein
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
  • Cell Line
  • DNA-Binding Proteins / genetics
  • Dishevelled Proteins
  • Dogs
  • Fluorescent Antibody Technique
  • Gene Expression Regulation
  • Glycogen Synthase Kinase 3
  • Lymphoid Enhancer-Binding Factor 1
  • Mice
  • Molecular Sequence Data
  • Mutation
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Proteins / genetics
  • Proteins / metabolism*
  • Recombinant Fusion Proteins / genetics
  • Repressor Proteins*
  • Signal Transduction
  • Transcription Factors / genetics
  • Transcriptional Activation
  • Transfection

Substances

  • Adaptor Proteins, Signal Transducing
  • Axin Protein
  • DNA-Binding Proteins
  • Dishevelled Proteins
  • Dvl2 protein, mouse
  • Lymphoid Enhancer-Binding Factor 1
  • Phosphoproteins
  • Proteins
  • Recombinant Fusion Proteins
  • Repressor Proteins
  • Transcription Factors
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Glycogen Synthase Kinase 3