Binding to cadherins antagonizes the signaling activity of β-catenin during axis formation in Xenopus Journal Article


Authors: Fagotto, F.; Funayama, N.; Glück, U.; Gumbiner, B. M.
Article Title: Binding to cadherins antagonizes the signaling activity of β-catenin during axis formation in Xenopus
Abstract: β-Catenin, a cytoplasmic protein known for its association with cadherin cell adhesion molecules, is also part of a signaling cascade involved in embryonic patterning processes such as the determination of the dorsoventral axis in Xenopus and determination of segment polarity in Drosophila. Previous studies suggest that increased cytoplasmic levels of β-catenin correlate with signaling, raising questions about the need for interaction with cadherins in this process. We have tested the role of the β-catenin-cadherin interaction in axis formation. Using β-catenin deletion mutants, we demonstrate that significant binding to cadherins can be eliminated without affecting the signaling activity. Also, depletion of the soluble, cytosolic pool of β-catenin by binding to overexpressed C-cadherin completely inhibited β-catenin-inducing activity. We conclude that binding to cadherins is not required for β-catenin signaling, and therefore the signaling function of β-catenin is independent of its role in cell adhesion. Moreover, because β-catenin signaling is antagonized by binding to cadherins, we suggest that cadherins can act as regulators of the intracellular β-catenin signaling pathway.
Keywords: signal transduction; controlled study; sequence deletion; nonhuman; animal cell; animals; embryo; protein protein interaction; protein binding; morphogenesis; immunofluorescence; embryo, nonmammalian; amino acid sequence; molecular sequence data; messenger rna; immunoprecipitation; trans-activators; beta catenin; cadherin; cell adhesion; cadherins; larva; polyacrylamide gel electrophoresis; cytoskeletal proteins; xenopus; xenopus laevis; embryo axis; embryonic induction; xenopus proteins; priority journal; article
Journal Title: Journal of Cell Biology
Volume: 132
Issue: 6
ISSN: 0021-9525
Publisher: Rockefeller University Press  
Date Published: 1996-03-14
Start Page: 1105
End Page: 1114
Language: English
DOI: 10.1083/jcb.132.6.1105
PUBMED: 8601588
PROVIDER: scopus
PMCID: PMC2120760
DOI/URL:
Notes: Article -- Export Date: 22 November 2017 -- Source: Scopus
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  1. Francois Fagotto
    12 Fagotto