E-Cadherin negatively modulates delta-catenin-induced morphological changes and RhoA activity reduction by competing with p190RhoGEF for delta-catenin
- ECU Author/Contributor (non-ECU co-authors, if there are any, appear on document)
- Hangun Kim (Creator)
- Kwonseop Kim (Creator)
- Qun Lu (Creator)
- Minsoo Oh (Creator)
- Institution
- East Carolina University (ECU )
- Web Site: http://www.ecu.edu/lib/
Abstract: δ-Catenin is a member of the p120-catenin subfamily of armadillo proteins. Here we describe istinctive features of δ-catenin localization and its association with E-cadherin in HEK293 epithelial ells. In HEK293 cells maintained in low cell densities approximately 15% of cells overexpressing ´-catenin showed dendrite-like process formation but there was no detectable change in RhoA ctivity. In addition δ-catenin was localized mainly in the cytoplasm and was associated with 190RhoGEF. However at high cell densities δ-catenin localization was shifted to the plasma embrane. The association of δ-catenin with E-cadherin was strengthened whereas its interaction ith p190RhoGEF was weakened. In mouse embryonic fibroblast cell ectopic expression of Ecadherin ecreased the effect of δ-catenin on the reduction of RhoA activity as well as on dendritelike rocess formation. These results suggest that δ-catenin is more dominantly bound to E-cadherin han to p190RhoGEF and that δ-catenin’s function is dependent on its cellular binding partner. Originally published Biochem Biophys Res Commun Vol. 377 No. 2 Dec 2008
Additional Information
- Publication
- Other
- Biochemical and Biophysical Research Communications. 377:2(December 2008) p. 636-641.
- Language: English
- Date: 2011
- Keywords
- delta-catenin, cadherin, dendrogenesis, adherens junction, RhoA
Title | Location & Link | Type of Relationship |
E-Cadherin negatively modulates delta-catenin-induced morphological changes and RhoA activity reduction by competing with p190RhoGEF for delta-catenin | http://hdl.handle.net/10342/3322 | The described resource references, cites, or otherwise points to the related resource. |