<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-17T11:56:32Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10230/25478" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10230/25478</identifier><datestamp>2025-12-20T17:04:23Z</datestamp><setSpec>com_2072_6</setSpec><setSpec>col_2072_452952</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Wnt controls the transcriptional activity of Kaiso through CK1ε-dependent phosphorylation of p120-catenin</dc:title>
   <dc:creator>Valle Pérez, Beatriz del</dc:creator>
   <dc:creator>Casagolda, David</dc:creator>
   <dc:creator>Lugilde, Ero</dc:creator>
   <dc:creator>Valls, Gabriela</dc:creator>
   <dc:creator>Codina, Montserrat</dc:creator>
   <dc:creator>Dave, Natàlia</dc:creator>
   <dc:creator>García de Herreros, Antonio</dc:creator>
   <dc:creator>Duñach, Mireia</dc:creator>
   <dc:subject>Cadherines</dc:subject>
   <dc:subject>Proteïnes Fixació</dc:subject>
   <dc:subject>Fosforilació</dc:subject>
   <dc:subject>Factors de transcripció</dc:subject>
   <dc:subject>Wnt signaling</dc:subject>
   <dc:subject>p120-catenin</dc:subject>
   <dc:subject>Kaiso</dc:subject>
   <dc:subject>CK1 phosphorylation</dc:subject>
   <dcterms:abstract>p120-catenin is an E-cadherin-associated protein that modulates E-cadherin function and stability. In response to Wnt3a, p120-catenin is phosphorylated at Ser268 and Ser269, disrupting its interaction with E-cadherin. Here, we describe that Wnt-induced p120-catenin phosphorylation at Ser268 and Ser269 also enhances its binding to the transcriptional factor Kaiso, preventing Kaiso-mediated inhibition of the β-catenin-Tcf-4 transcriptional complex. Kaiso-mediated repression of this complex is due to its association not only with Tcf-4 but also with β-catenin. Disruption of Tcf-4-Kaiso and β-catenin-Kaiso interactions by p120-catenin not only releases Tcf-4 and β-catenin enabling its mutual association and the formation of the transcriptional complex but also permits Kaiso binding to methylated CpG islands, an interaction that is weakly inhibited by p120-catenin. Consequently, Wnt stimulates Kaiso association to the CDKN2A promoter, which contains CpG sequences, in cells where these sequences are extensively methylated, such as HT-29 M6, an effect accompanied by decreased expression of its gene product. These results indicate that, when released from E-cadherin by Wnt3a-stimulated phosphorylation, p120-catenin controls the activity of the Kaiso transcriptional factor, enhancing its binding to repressed promoters and relieving its inhibition of the β-catenin-Tcf-4 transcriptional complex.</dcterms:abstract>
   <dcterms:issued>2015-12-18T18:55:36Z</dcterms:issued>
   <dcterms:issued>2015-12-18T18:55:36Z</dcterms:issued>
   <dcterms:issued>2011</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:relation>Journal of cell science. 2011;124(Pt 13):2298-309</dc:relation>
   <dc:rights>© Company of Biologists http://jcs.biologists.org/content/124/13/2298.long DOI 10.1242/jcs.082693</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Company of Biologists</dc:publisher>
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