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RESEARCH ARTICLE |
T-Catenin: a novel tissue-specific ß-catenin-binding protein mediating strong cell-cell adhesion
1 Molecular Cell Biology Unit, Department of Molecular Biology, Flanders Interuniversity Institute for Biotechnology (VIB)-Ghent University, B-9000 Ghent, Belgium
2 Department of Pathology, University Hospital Antwerp (UZA), B-2650 Edegem, Belgium
3 Department of Radiotherapy, Nuclear Medicine and Experimental Cancerology, University Hospital Ghent, B-9000 Ghent, Belgium
*Author for correspondence (e-mail: f.vanroy{at}dmb.rug.ac.be)
Accepted May 28, 2001
Cadherins are major cell-cell adhesion proteins whose cytoplasmic domains bind to catenin proteins. Strong intercellular adhesion depends on linkage of the cadherin/catenin complex to the actin cytoskeleton via
-catenin. To date, it is not clear how different cell types achieve the variable strength of cell-cell adhesion clearly needed in a multicellular organism. Here, we report the cloning and molecular characterization of
T(testis)-catenin, a novel human cDNA encoding a protein with homology to both human
E(epithelial)-catenin and
N(neural)-catenin. Although originally discovered in testis,
T-catenin is expressed in other tissues, the highest levels being observed in heart. Immunohistochemical analysis showed human
T-catenin localization at intercalated discs of cardiomyocytes and in peritubular myoid cells of testis. In cells transfected with
T-catenin cDNA, interaction with ß-catenin was demonstrated by co-immunoprecipitation. Transfection of
-catenin-deficient colon carcinoma cells recruited E-cadherin and ß-catenin to cell-cell contacts and functional cadherin-mediated cell-cell adhesion was restored in this way. Moreover, compaction of these cells was at least as prominent as in the case of cells expressing endogenous
E-catenin. We propose that
T-catenin is necessary for the formation of stretch-resistant cell-cell adhesion complexes, in particular, muscle cells.
Key words: Catenin, Cadherin, Muscle, Heart, Testis
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