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1.
Oncogene ; 36(32): 4670, 2017 08 10.
Article in English | MEDLINE | ID: mdl-28368396

ABSTRACT

This corrects the article DOI: 10.1038/onc.2016.209.

2.
Oncogene ; 36(3): 429-438, 2017 01 19.
Article in English | MEDLINE | ID: mdl-27321178

ABSTRACT

Canonical Wnt signaling induces the stabilization of ß-catenin, its translocation to the nucleus and the activation of target promoters. This pathway is initiated by the binding of Wnt ligands to the Frizzled receptor, the association of the LRP5/6 co-receptor and the formation of a complex comprising Dvl-2, Axin and protein kinases CK1α, ɛ, γ and GSK3. Among these, activation of CK1ɛ, constitutively bound to LRP5/6 through p120-catenin, is required for the association of the rest of the components. We describe here that CK1ɛ is activated by the PP2A/PR61ɛ phosphatase. Binding of Wnt ligands promotes the interaction of LRP5/6-associated CK1ɛ with Frizzled-bound PR61ɛ regulatory subunit, facilitating the access of PP2A catalytic subunit to CK1ɛ and its activation, what enables the recruitment of Dvl-2 to the receptor complex and the initiation of the Wnt pathway. Our results uncover the mechanism of activation of the canonical Wnt pathway by its ligands.


Subject(s)
Casein Kinase Idelta/metabolism , Protein Phosphatase 2/metabolism , Frizzled Receptors/metabolism , HEK293 Cells , HT29 Cells , Humans , Wnt Signaling Pathway
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