Ectodermal Wnt3/β-catenin signaling is required for the establishment and maintenance of the apical ectodermal ridge

  1. Jeffery R. Barrow1,
  2. Kirk R. Thomas2,
  3. Oreda Boussadia-Zahui3,4,
  4. Robert Moore3,5,
  5. Rolf Kemler3,
  6. Mario R. Capecchi2, and
  7. Andrew P. McMahon1,6
  1. 1Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA; 2Howard Hughes Medical Institute, Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA; 3Department of Molecular Embryology, Max-Planck Institute of Immunobiology, D-79108 Freiberg, Germany.

Abstract

The formation of the apical ectodermal ridge (AER) is critical for the distal outgrowth and patterning of the vertebrate limb. Recent work in the chick has demonstrated that interplay between the Wntand Fgf signaling pathways is essential in the limb mesenchyme and ectoderm in the establishment and perhaps the maintenance of the AER. In the mouse, whereas a role for Fgfs for AER establishment and function has been clearly demonstrated, the role ofWnt/β-catenin signaling, although known to be important, is obscure. In this study, we demonstrate that Wnt3, which is expressed ubiquitously throughout the limb ectoderm, is essential for normal limb development and plays a critical role in the establishment of the AER. We also show that the conditional removal ofβ-catenin in the ventral ectodermal cells is sufficient to elicit the mutant limb phenotype. In addition, removingβ-catenin after the induction of the ridge results in the disappearance of the AER, demonstrating the requirement for continuedβ-catenin signaling for the maintenance of this structure. Finally, we demonstrate that Wnt/β-catenin signaling lies upstream of the Bmp signaling pathway in establishment of the AER and regulation of the dorsoventral polarity of the limb.

Keywords

Footnotes

  • Present addresses: 4Nucleis, Parc technologique des capucins, Bâtiment Montéclair, F-49033 Angers, cedex 01, France; 5Génétique du Développement des Mélanocytes, Institut Curie, F-91405 Orsay, France.

  • 6 Corresponding author.

  • E-MAIL amcmahon{at}mcb.harvard.edu; FAX (617) 496-3763.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1044903.

    • Received September 25, 2002.
    • Accepted December 6, 2002.
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