The regulation of cadherin-mediated adhesion by tyrosine phosphorylation/dephosphorylation of β-catenin

J Lilien, J Balsamo - Current opinion in cell biology, 2005 - Elsevier
J Lilien, J Balsamo
Current opinion in cell biology, 2005Elsevier
The formation of stable cell–cell adhesions by type I cadherins depends on the association
of their cytoplasmic domain with β-catenin, and of β-catenin with α-catenin. The binding of β-
catenin to these partners is regulated by phosphorylation of at least three critical tyrosine
residues. Each of these residues is targeted by one or more specific kinases: Y142 by Fyn,
Fer and cMet; Y489 by Abl; and Y654 by Src and the epidermal growth factor receptor.
Developmental and physiological signals have been identified that initiate the specific …
The formation of stable cell–cell adhesions by type I cadherins depends on the association of their cytoplasmic domain with β-catenin, and of β-catenin with α-catenin. The binding of β-catenin to these partners is regulated by phosphorylation of at least three critical tyrosine residues. Each of these residues is targeted by one or more specific kinases: Y142 by Fyn, Fer and cMet; Y489 by Abl; and Y654 by Src and the epidermal growth factor receptor. Developmental and physiological signals have been identified that initiate the specific phosphorylation and dephosphorylation of these residues, regulating cadherin function during neurite outgrowth, permeability of airway epithelium and synapse remodeling, and possibly initiating epithelial cell migration during development and metastasis.
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