p120-catenin in canonical Wnt signaling

被引:31
作者
Dunach, Mireia [1 ]
Del Valle-Perez, Beatriz [1 ]
Garcia de Herreros, Antonio [2 ,3 ]
机构
[1] Univ Autonoma Barcelona, Fac Med, Dept Bioquim & Biol Mol, CEB, E-08193 Bellaterra, Spain
[2] Inst Hosp Mar Invest Med IMIM, Programa Recerca Canc, Barcelona, Spain
[3] Univ Pompeu Fabra, Dept Ciencies Expt & Salut, Barcelona, Spain
关键词
Wnt signaling; beta-catenin; p120-catenin; CK1; Rac1; Kaiso; KINASE-I-EPSILON; BETA-CATENIN DEGRADATION; RHO-FAMILY GTPASES; P120; CATENIN; WNT-3A-INDUCED ACCUMULATION; TRANSCRIPTIONAL REPRESSION; NUCLEAR-LOCALIZATION; NEGATIVE REGULATOR; STRUCTURAL BASIS; PARTNER KAISO;
D O I
10.1080/10409238.2017.1295920
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Canonical Wnt signaling controls -catenin protein stabilization, its translocation to the nucleus and the activation of -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 CK1, 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 -catenin; (iii) the activation of Rac1 small GTPase, required for -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 -catenin stabilization but for -catenin transcriptional activity. Moreover, we discuss the possible future implications, suggesting that the two cellular compartments where -catenin is localized, thus, the adherens junction complex and the Wnt signalosome, are more physically connected that previously thought.
引用
收藏
页码:327 / 339
页数:13
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