Casein kinase 1 γ couples Wnt receptor activation to cytoplasmic signal transduction
Gary Davidson (),
Wei Wu,
Jinlong Shen,
Josipa Bilic,
Ursula Fenger,
Peter Stannek,
Andrei Glinka and
Christof Niehrs ()
Additional contact information
Gary Davidson: Deutsches Krebsforschungszentrum
Wei Wu: Deutsches Krebsforschungszentrum
Jinlong Shen: Deutsches Krebsforschungszentrum
Josipa Bilic: Deutsches Krebsforschungszentrum
Ursula Fenger: Deutsches Krebsforschungszentrum
Peter Stannek: Deutsches Krebsforschungszentrum
Andrei Glinka: Deutsches Krebsforschungszentrum
Christof Niehrs: Deutsches Krebsforschungszentrum
Nature, 2005, vol. 438, issue 7069, 867-872
Abstract:
Abstract Signalling by Wnt proteins (Wingless in Drosophila) has diverse roles during embryonic development and in adults, and is implicated in human diseases, including cancer1,2. LDL-receptor-related proteins 5 and 6 (LRP5 and LRP6; Arrow in Drosophila) are key receptors required for transmission of Wnt/β-catenin signalling in metazoa3. Although the role of these receptors in Wnt signalling is well established, their coupling with the cytoplasmic signalling apparatus remains poorly defined. Using a protein modification screen for regulators of LRP6, we describe the identification of Xenopus Casein kinase 1 γ (CK1γ), a membrane-bound member of the CK1 family. Gain-of-function and loss-of-function experiments show that CK1γ is both necessary and sufficient to transduce LRP6 signalling in vertebrates and Drosophila cells. In Xenopus embryos, CK1γ is required during anterio-posterior patterning to promote posteriorizing Wnt/β-catenin signalling. CK1γ is associated with LRP6, which has multiple, modular CK1 phosphorylation sites. Wnt treatment induces the rapid CK1γ-mediated phosphorylation of these sites within LRP6, which, in turn, promotes the recruitment of the scaffold protein Axin. Our results reveal an evolutionarily conserved mechanism that couples Wnt receptor activation to the cytoplasmic signal transduction apparatus.
Date: 2005
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Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:438:y:2005:i:7069:d:10.1038_nature04170
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DOI: 10.1038/nature04170
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