| Literature DB >> 27129770 |
Eva-Maria Brinkmann1, Benjamin Mattes2, Rahul Kumar1, Anja I H Hagemann2, Dietmar Gradl3, Steffen Scholpp2, Herbert Steinbeisser1, Lilian T Kaufmann4, Suat Özbek5.
Abstract
Convergent extension movements during vertebrate gastrulation require a balanced activity of non-canonical Wnt signaling pathways, but the factors regulating this interplay on the molecular level are poorly characterized. Here we show that sFRP2, a member of the secreted frizzled-related protein (sFRP) family, is required for morphogenesis and papc expression during Xenopus gastrulation. We further provide evidence that sFRP2 redirects non-canonical Wnt signaling from Frizzled 7 (Fz7) to the receptor tyrosine kinase-like orphan receptor 2 (Ror2). During this process, sFRP2 promotes Ror2 signal transduction by stabilizing Wnt5a-Ror2 complexes at the membrane, whereas it inhibits Fz7 signaling, probably by blocking Fz7 receptor endocytosis. The cysteine-rich domain of sFRP2 is sufficient for Ror2 activation, and related sFRPs can substitute for this function. Notably, direct interaction of the two receptors via their cysteine-rich domains also promotes Ror2-mediated papc expression but inhibits Fz7 signaling. We propose that sFRPs can act as a molecular switch, channeling the signal input for different non-canonical Wnt pathways during vertebrate gastrulation.Entities:
Keywords: Fz7; Ror2; Wnt signaling; Xenopus; development; embryo; papc; sFRP2; zebrafish
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Year: 2016 PMID: 27129770 PMCID: PMC4919455 DOI: 10.1074/jbc.M116.733766
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157