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doi: 10.1242/10.1242/dev.00435
1 Division of Morphogenesis, Department of Developmental Biology, National
Institute for Basic Biology, 38 Nishigonaka, Myodaiji, Okazaki 444-8585,
Japan
2 Department of Anatomy and Developmental Biology, University College London,
Gower Street, London WC1E 6BT, UK
* Author for correspondence (e-mail: nueno{at}nibb.ac.jp)
Accepted 12 February 2003
Coordinated morphogenetic cell movements during gastrulation are crucial for establishing embryonic axes in animals. Most recently, the non-canonical Wnt signaling cascade (PCP pathway) has been shown to regulate convergent extension movements in Xenopus and zebrafish. Heparan sulfate proteoglycans (HSPGs) are known as modulators of intercellular signaling, and are required for gastrulation movements in vertebrates. However, the function of HSPGs is poorly understood. We analyze the function of Xenopus glypican 4 (Xgly4), which is a member of membrane-associated HSPG family. In situ hybridization revealed that Xgly4 is expressed in the dorsal mesoderm and ectoderm during gastrulation. Reducing the levels of Xgly4 inhibits cell-membrane accumulation of Dishevelled (Dsh), which is a transducer of the Wnt signaling cascade, and thereby disturbs cell movements during gastrulation. Rescue analysis with different Dsh mutants and Wnt11 demonstrated that Xgly4 functions in the non-canonical Wnt/PCP pathway, but not in the canonical Wnt/ß-catenin pathway, to regulate gastrulation movements. We also provide evidence that the Xgly4 protein physically binds Wnt ligands. Therefore, our results suggest that Xgly4 functions as positive regulator in non-canonical Wnt/PCP signaling during gastrulation.
Key words: Heparan sulfate proteoglycan, Wnt signaling pathway, Gastrulation movements, Xenopus
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