A yeast model system for functional analysis of beta-catenin signaling

J Cell Biol. 2002 Sep 16;158(6):1067-78. doi: 10.1083/jcb.200204063. Epub 2002 Sep 16.

Abstract

We have developed a novel Saccharomyces cerevisiae model system to dissect the molecular events of beta-catenin (beta-cat) signaling. Coexpression of mammalian beta-cat with TCF4 or LEF1 results in nuclear accumulation of these proteins and a functional complex that activates reporter gene transcription from constructs containing leukocyte enhancer factor (LEF)/T cell factor (TCF) response elements. Reporter transcription is constitutive, requires expression of both beta-cat and TCF4 or LEF1, and is not supported by mutated LEF/TCF binding elements or by TCF4 or LEF1 mutants. A cytoplasmic domain of E-cadherin or a functional fragment of adenomatous polyposis coli (APC) protein (APC-25) complexes with beta-cat, reduces beta-cat binding to TCF4, and leads to increased cytoplasmic localization of beta-cat and a reduction in reporter activation. Systematic mutation of putative nuclear export signal sequences in APC-25 decreases APC-25 binding to beta-cat and restores reporter gene transcription. Additional beta-cat signaling components, Axin and glycogen synthase kinase 3beta, form a multisubunit complex similar to that found in mammalian cells. Coexpression of the F-box protein beta-transducin repeat-containing protein reduces the stability of beta-cat and decreases reporter activation. Thus, we have reconstituted a functional beta-cat signal transduction pathway in yeast and show that beta-cat signaling can be regulated at multiple levels, including protein subcellular localization, protein complex formation, and protein stability.

MeSH terms

  • Active Transport, Cell Nucleus
  • Adenomatous Polyposis Coli Protein / metabolism
  • Alanine / metabolism
  • Amino Acid Substitution
  • Axin Protein
  • Biological Transport, Active
  • Cadherins / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinases / chemistry
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Cytoplasm / metabolism
  • Cytoskeletal Proteins / metabolism
  • Cytoskeletal Proteins / physiology*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Gene Deletion
  • Gene Expression Regulation
  • Genes, Reporter
  • Glycogen Synthase Kinases
  • Humans
  • Lymphoid Enhancer-Binding Factor 1
  • Models, Biological
  • Oligopeptides
  • Peptides / metabolism
  • Proteins / chemistry
  • Proteins / metabolism
  • Repressor Proteins*
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism*
  • Signal Transduction*
  • TCF Transcription Factors
  • Trans-Activators / metabolism
  • Trans-Activators / physiology*
  • Transcription Factor 7-Like 2 Protein
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transducin / metabolism
  • beta Catenin

Substances

  • Adenomatous Polyposis Coli Protein
  • Axin Protein
  • CTNNB1 protein, human
  • Cadherins
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • LEF1 protein, human
  • Lymphoid Enhancer-Binding Factor 1
  • Oligopeptides
  • Peptides
  • Proteins
  • Repressor Proteins
  • TCF Transcription Factors
  • TCF7L2 protein, human
  • Trans-Activators
  • Transcription Factor 7-Like 2 Protein
  • Transcription Factors
  • beta Catenin
  • FLAG peptide
  • Glycogen Synthase Kinases
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Transducin
  • Alanine