4.8 Article

LDL-receptor-related proteins in Wnt signal transduction

Journal

NATURE
Volume 407, Issue 6803, Pages 530-535

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NATURE PUBLISHING GROUP
DOI: 10.1038/35035117

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The Wnt family of secreted signalling molecules are essential in embryo development and tumour formation(1). The Frizzled (Fz) family of serpentine receptors function as Wnt receptors(2-10), but how Fz proteins transduce signalling is not understood. In Drosophila, arrow phenocopies the wingless (DWnt-1) phenotype(11), and encodes a transmembrane protein(11) that is homologous to two members of the mammalian low-density lipoprotein receptor (LDLR)-related protein (LRP) family, LRP5 and LRP6 (refs 12-15). Here we report that LRP6 functions as a co-receptor for Wnt signal transduction. In Xenopus embryos, LRP6 activated Wnt-Fz signalling, and induced Wnt responsive genes, dorsal axis duplication and neural crest formation. An LRP6 mutant lacking the carboxyl intracellular domain blocked signalling by Wnt or Wnt-Fz, but not by Dishevelled or beta-catenin, and inhibited neural crest development. The extracellular domain of LRP6 bound Wnt-1 and associated with Fz in a Wnt-dependent manner. Our results indicate that LRP6 may be a component of the Wnt receptor complex.

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