Genetic interaction between Wnt/beta-catenin and BMP receptor signaling during formation of the AER and the dorsal-ventral axis in the limb

Genes Dev. 2003 Aug 15;17(16):1963-8. doi: 10.1101/gad.263003.

Abstract

By conditional gene ablation in mice, we found that beta-catenin, an essential downstream effector of canonical Wnt signaling, is a key regulator of formation of the apical ectodermal ridge (AER) and of the dorsal-ventral axis of the limbs. By generation of compound mutants, we also show that beta-catenin acts downstream of the BMP receptor IA in AER induction, but upstream or parallel in dorsal-ventral patterning. Thus, AER formation and dorsal-ventral patterning of limbs are tightly controlled by an intricate interplay between Wnt/beta-catenin and BMP receptor signaling.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Patterning / genetics
  • Bone Morphogenetic Protein Receptors
  • Bone Morphogenetic Protein Receptors, Type I
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism*
  • Ectoderm / metabolism
  • Extremities / embryology*
  • Fibroblast Growth Factor 8
  • Fibroblast Growth Factors / metabolism
  • Hindlimb / abnormalities
  • Limb Deformities, Congenital / genetics
  • Mice
  • Mice, Mutant Strains
  • Mice, Transgenic
  • Mutation
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins / metabolism*
  • Receptors, Growth Factor / metabolism*
  • Signal Transduction*
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Wnt Proteins
  • Zebrafish Proteins*
  • beta Catenin

Substances

  • CTNNB1 protein, mouse
  • Cytoskeletal Proteins
  • Fgf8 protein, mouse
  • Proto-Oncogene Proteins
  • Receptors, Growth Factor
  • Trans-Activators
  • Wnt Proteins
  • Zebrafish Proteins
  • beta Catenin
  • Fibroblast Growth Factor 8
  • Fibroblast Growth Factors
  • Protein Serine-Threonine Kinases
  • Bmpr1a protein, mouse
  • Bone Morphogenetic Protein Receptors
  • Bone Morphogenetic Protein Receptors, Type I