[PDF][PDF] Mutual antagonism between dickkopf1 and dickkopf2 regulates Wnt/β-catenin signalling

W Wu, A Glinka, H Delius, C Niehrs - Current Biology, 2000 - cell.com
W Wu, A Glinka, H Delius, C Niehrs
Current Biology, 2000cell.com
Wnts are secreted glycoproteins implicated in diverse processes during embryonic
patterning in metazoans. They signal through seven-transmembrane receptors of the
Frizzled (Fz) family [1] to stabilise β-catenin [2]. Wnts are antagonised by several
extracellular inhibitors including the product of the dickkopf1 (dkk1) gene, which was
identified in Xenopus embryos and is a member of a multigene family. The dkk1 gene acts
upstream of the Wnt pathway component dishevelled but its mechanism of action is …
Abstract
Wnts are secreted glycoproteins implicated in diverse processes during embryonic patterning in metazoans. They signal through seven-transmembrane receptors of the Frizzled (Fz) family [1] to stabilise β-catenin [2]. Wnts are antagonised by several extracellular inhibitors including the product of the dickkopf1 (dkk1) gene, which was identified in Xenopus embryos and is a member of a multigene family. The dkk1 gene acts upstream of the Wnt pathway component dishevelled but its mechanism of action is unknown [3]. Although the function of Dkk1 as a Wnt inhibitor in vertebrates is well established [3–6], the effect of other Dkks on the Wnt/β-catenin pathway is unclear. Here, we report that a related family member, Dkk2, activates rather than inhibits the Wnt/β-catenin signalling pathway in Xenopus embryos. Dkk2 strongly synergised with Wnt receptors of the Fz family to induce Wnt signalling responses. The study identifies Dkk2 as a secreted molecule that is able to activate Wnt/β-catenin signalling. The results suggest that a coordinated interplay between inhibiting dkk1 and activating dkk2 can modulate Fz signalling.
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