Interactions between Sox9 and beta-catenin control chondrocyte differentiation

Genes Dev. 2004 May 1;18(9):1072-87. doi: 10.1101/gad.1171104.

Abstract

Chondrogenesis is a multistep process that is essential for endochondral bone formation. Previous results have indicated a role for beta-catenin and Wnt signaling in this pathway. Here we show the existence of physical and functional interactions between beta-catenin and Sox9, a transcription factor that is required in successive steps of chondrogenesis. In vivo, either overexpression of Sox9 or inactivation of beta-catenin in chondrocytes of mouse embryos produces a similar phenotype of dwarfism with decreased chondrocyte proliferation, delayed hypertrophic chondrocyte differentiation, and endochondral bone formation. Furthermore, either inactivation of Sox9 or stabilization of beta-catenin in chondrocytes also produces a similar phenotype of severe chondrodysplasia. Sox9 markedly inhibits activation of beta-catenin-dependent promoters and stimulates degradation of beta-catenin by the ubiquitination/proteasome pathway. Likewise, Sox9 inhibits beta-catenin-mediated secondary axis induction in Xenopus embryos. Beta-catenin physically interacts through its Armadillo repeats with the C-terminal transactivation domain of Sox9. We hypothesize that the inhibitory activity of Sox9 is caused by its ability to compete with Tcf/Lef for binding to beta-catenin, followed by degradation of beta-catenin. Our results strongly suggest that chondrogenesis is controlled by interactions between Sox9 and the Wnt/beta-catenin signaling pathway.

Publication types

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

MeSH terms

  • Animals
  • Binding Sites
  • Cell Differentiation
  • Cell Division
  • Chondrocytes / cytology*
  • Chondrocytes / physiology
  • Cyclin D1 / metabolism
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / physiology*
  • Enhancer Elements, Genetic
  • Gene Expression
  • Heterozygote
  • High Mobility Group Proteins / chemistry
  • High Mobility Group Proteins / genetics
  • High Mobility Group Proteins / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Mice, Transgenic
  • Models, Biological
  • Phenotype
  • SOX9 Transcription Factor
  • Signal Transduction
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Transcription Factors / chemistry
  • Transcription Factors / genetics
  • Transcription Factors / physiology*
  • Transcription, Genetic
  • Xenopus Proteins
  • Xenopus laevis
  • beta Catenin

Substances

  • CTNNB1 protein, Xenopus
  • CTNNB1 protein, mouse
  • Cytoskeletal Proteins
  • High Mobility Group Proteins
  • SOX9 Transcription Factor
  • Sox9 protein, mouse
  • Trans-Activators
  • Transcription Factors
  • Xenopus Proteins
  • beta Catenin
  • Cyclin D1