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RESEARCH PAPER
-catenin signaling is sufficient and necessary for synovial joint formation
Genetic Disease Research Branch, National Human Genome Research Institute, Bethesda, Maryland 20892, USA
A critical step in skeletal morphogenesis is the formation of synovial
joints, which define the relative size of discrete skeletal elements and are
required for the mobility of vertebrates. We have found that several
Wnt genes, including Wnt4, Wnt14, and Wnt16, were
expressed in overlapping and complementary patterns in the developing synovial
joints, where
-catenin protein levels and transcription activity were
up-regulated. Removal of
-catenin early in mesenchymal
progenitor cells promoted chondrocyte differentiation and blocked the activity
of Wnt14 in joint formation. Ectopic expression of an activated form
of
-catenin or Wnt14 in early differentiating
chondrocytes induced ectopic joint formation both morphologically and
molecularly. In contrast, genetic removal of
-catenin in
chondrocytes led to joint fusion. These results demonstrate that the
Wnt/
-catenin signaling pathway is necessary and sufficient to induce
early steps of synovial joint formation. Wnt4, Wnt14, and
Wnt16 may play redundant roles in synovial joint induction by
signaling through the
-catenin-mediated canonical Wnt pathway.
Received June 10, 2004; revised version accepted August 9, 2004.
Article published online ahead of print. Article and publication date are at http://www.genesdev.org/cgi/doi/10.1101/gad.1230704.
1 These authors contributed equally to this work.
2 Present address: Department of Biochemistry and State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing 210093, P. R. China
3 Corresponding author.
E-MAIL
yyang{at}nhgri.nih.gov;
FAX (301) 402-2170.
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