| Literature DB >> 28276699 |
Mireia Duñach1, Beatriz Del Valle-Pérez1, Antonio García de Herreros2,3.
Abstract
Canonical Wnt signaling controls β-catenin protein stabilization, its translocation to the nucleus and the activation of β-catenin/Tcf-4-dependent transcription. In this review, we revise and discuss the recent results describing actions of p120-catenin in different phases of this pathway. More specifically, we comment its involvement in four different steps: (i) the very early activation of CK1ɛ, essential for Dvl-2 binding to the Wnt receptor complex; (ii) the internalization of GSK3 and Axin into multivesicular bodies, necessary for a complete stabilization of β-catenin; (iii) the activation of Rac1 small GTPase, required for β-catenin translocation to the nucleus; and (iv) the release of the inhibitory action caused by Kaiso transcriptional repressor. We integrate these new results with the previously known action of other elements in this pathway, giving a particular relevance to the responses of the Wnt pathway not required for β-catenin stabilization but for β-catenin transcriptional activity. Moreover, we discuss the possible future implications, suggesting that the two cellular compartments where β-catenin is localized, thus, the adherens junction complex and the Wnt signalosome, are more physically connected that previously thought.Entities:
Keywords: CK1ɛ; Kaiso; Rac1; Wnt signaling; p120-catenin; β-catenin
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Year: 2017 PMID: 28276699 DOI: 10.1080/10409238.2017.1295920
Source DB: PubMed Journal: Crit Rev Biochem Mol Biol ISSN: 1040-9238 Impact factor: 8.250