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Mol. Cells 2010; 29(3): 233-237

Published online January 21, 2010

https://doi.org/10.1007/s10059-010-0030-2

© The Korean Society for Molecular and Cellular Biology

δ-Catenin Affects the Localization and Stability of p120-Catenin by Competitively Interacting with E-Cadherin

Ilhwan Yang, Ockyoung Chang, Qun Lu1, and Kwonseop Kim*

The College of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 500-757, Korea, 1Department of Anatomy and Cell Biology, The Brody School of Medicine, East Carolina University, Greenville, NC 27834, USA

Correspondence to : *Correspondence: koskim@chonnam.ac.kr

Received: June 22, 2009; Revised: November 26, 2009; Accepted: November 27, 2009

Abstract

E-cadherin is a member of the cadherin family of Ca2+-dependent cell-cell adhesion molecules. p120-Catenin and δ-catenin are known to bind to similar juxtamembrane regions of E-cadherin, and p120-catenin is known to stabilize E-cadherin. However, the function of competition between p120-catenin and δ-catenin for E-cadherin has not been fully explained. In this report, we show that cells overexpressing δ-catenin contain less p120-catenin than control cells at the cell-cell interface and that this causes the re-localization of p120-catenin from the plasma membrane to the cytosol. We show that successful binding by one to E-cadherin adversely affects the stability of the other.

Keywords δ-catenin, adherens junction, E-cadherin, p120-catenin, protein stability

Article

Research Article

Mol. Cells 2010; 29(3): 233-237

Published online March 31, 2010 https://doi.org/10.1007/s10059-010-0030-2

Copyright © The Korean Society for Molecular and Cellular Biology.

δ-Catenin Affects the Localization and Stability of p120-Catenin by Competitively Interacting with E-Cadherin

Ilhwan Yang, Ockyoung Chang, Qun Lu1, and Kwonseop Kim*

The College of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 500-757, Korea, 1Department of Anatomy and Cell Biology, The Brody School of Medicine, East Carolina University, Greenville, NC 27834, USA

Correspondence to:*Correspondence: koskim@chonnam.ac.kr

Received: June 22, 2009; Revised: November 26, 2009; Accepted: November 27, 2009

Abstract

E-cadherin is a member of the cadherin family of Ca2+-dependent cell-cell adhesion molecules. p120-Catenin and δ-catenin are known to bind to similar juxtamembrane regions of E-cadherin, and p120-catenin is known to stabilize E-cadherin. However, the function of competition between p120-catenin and δ-catenin for E-cadherin has not been fully explained. In this report, we show that cells overexpressing δ-catenin contain less p120-catenin than control cells at the cell-cell interface and that this causes the re-localization of p120-catenin from the plasma membrane to the cytosol. We show that successful binding by one to E-cadherin adversely affects the stability of the other.

Keywords: δ-catenin, adherens junction, E-cadherin, p120-catenin, protein stability

Mol. Cells
Nov 30, 2023 Vol.46 No.11, pp. 655~725
COVER PICTURE
Kim et al. (pp. 710-724) demonstrated that a pathogen-derived Ralstonia pseudosolanacearum type III effector RipL delays flowering time and enhances susceptibility to bacterial infection in Arabidopsis thaliana. Shown is the RipL-expressing Arabidopsis plant, which displays general dampening of the transcriptional program during pathogen infection, grown in long-day conditions.

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