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  Essential role of BCL9-2 in the switch between β-catenin's adhesive and transcriptional functions

Brembeck, F. H., Schwarz-Romond, T., Bakkers, J., Wilhelm, S., Hammerschmidt, M., & Birchmeier, W. (2004). Essential role of BCL9-2 in the switch between β-catenin's adhesive and transcriptional functions. Genes & Development, 18, 2225-2230.

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 Creators:
Brembeck, Felix H., Author
Schwarz-Romond, Thomas, Author
Bakkers, Jeroen1, Author           
Wilhelm, Sabine, Author
Hammerschmidt, Matthias1, Author           
Birchmeier, Walter, Author
Affiliations:
1Georges Köhler Laboratory, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243653              

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Free keywords: BCL9/legless; α-catenin; Wnt8; tyrosine phosphorylation; epithelial-mesenchymal transition; mesoderm patterning
 Abstract: β-Catenin controls both cadherin-mediated cell adhesion and activation of Wnt target genes. We demonstrate here that the β-catenin-binding protein BCL9-2, a homolog of the human proto-oncogene product BCL9, induces epithelial-mesenchymal transitions of nontransformed cells and increases β-catenin-dependent transcription. RNA interference of BCL9-2 in carcinoma cells induces an epithelial phenotype and translocates β-catenin from the nucleus to the cell membrane. The switch between β-catenin's adhesive and transcriptional functions is modulated by phosphorylation of Tyr 142 of β-catenin, which favors BCL9-2 binding and precludes interaction with α-catenin. During zebrafish embryogenesis, BCL9-2 acts in the Wnt8-signaling pathway and regulates mesoderm patterning.

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Language(s): eng - English
 Dates: 2004
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 207237
 Degree: -

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Title: Genes & Development
Source Genre: Journal
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Pages: - Volume / Issue: 18 Sequence Number: - Start / End Page: 2225 - 2230 Identifier: -