Beta-catenin N- and C-terminal tails modulate the coordinated binding of adherens junction proteins to beta-catenin

J Biol Chem. 2002 Aug 30;277(35):31541-50. doi: 10.1074/jbc.M204376200. Epub 2002 Jun 20.

Abstract

beta-Catenin plays a central role in the establishment and regulation of adherens junctions because it interacts with E-cadherin and, through alpha-catenin, with the actin cytoskeleton. beta-Catenin is composed of three domains: a central armadillo repeat domain and two N- and C-terminal tails. The C-tail interacts with the armadillo domain and limits its ability to bind E-cadherin and other cofactors. The two beta-catenin tails are mutually inter-regulated because the C-tail is also necessary for binding of the N-tail to the armadillo domain. Moreover, the N-tail restricts the interaction of the C-tail with the central domain. Depletion of either of the two tails has consequences for the binding of factors at the other end: deletion of the C-tail increases alpha-catenin binding, whereas deletion of the N-tail blocks E-cadherin interaction to the armadillo repeats. As an effect of the interconnection of the tails, the association of alpha-catenin and E-cadherin to beta-catenin is interdependent. Thus, binding of alpha-catenin to the N-tail, through conformational changes that affect the C-tail, facilitates the association of E-cadherin. These results indicate that different cofactors of beta-catenin bind coordinately to this protein and indicate how the two terminal ends of beta-catenin exquisitely modulate intermolecular binding within junctional complexes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Amino Acid Sequence
  • Antibodies, Monoclonal
  • Antigens, CD
  • Binding Sites
  • Cadherins
  • Cell Adhesion Molecules / metabolism*
  • Cytoskeletal Proteins / chemistry
  • Cytoskeletal Proteins / metabolism*
  • Molecular Sequence Data
  • Mutagenesis
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Sequence Deletion
  • Trans-Activators / chemistry
  • Trans-Activators / metabolism*
  • beta Catenin

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • CDH2 protein, human
  • Cadherins
  • Cell Adhesion Molecules
  • Cytoskeletal Proteins
  • Peptide Fragments
  • Recombinant Proteins
  • Trans-Activators
  • beta Catenin