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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.
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页码:327 / 339
页数:13
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