<?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>2026-04-13T02:59:08Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10230/25478" metadataPrefix="marc">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><record xmlns="http://www.loc.gov/MARC21/slim" 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://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Valle Pérez, Beatriz del</subfield>
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      <subfield code="a">Casagolda, David</subfield>
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      <subfield code="a">Lugilde, Ero</subfield>
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      <subfield code="a">Valls, Gabriela</subfield>
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      <subfield code="a">Codina, Montserrat</subfield>
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      <subfield code="a">Dave, Natàlia</subfield>
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      <subfield code="a">García de Herreros, Antonio</subfield>
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      <subfield code="a">Duñach, Mireia</subfield>
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      <subfield code="c">2015-12-18T18:55:36Z</subfield>
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      <subfield code="c">2015-12-18T18:55:36Z</subfield>
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      <subfield code="c">2011</subfield>
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      <subfield code="a">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.</subfield>
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      <subfield code="a">Cadherines</subfield>
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      <subfield code="a">Proteïnes Fixació</subfield>
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      <subfield code="a">Fosforilació</subfield>
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      <subfield code="a">Factors de transcripció</subfield>
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      <subfield code="a">Wnt signaling</subfield>
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      <subfield code="a">p120-catenin</subfield>
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      <subfield code="a">Kaiso</subfield>
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      <subfield code="a">CK1 phosphorylation</subfield>
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      <subfield code="a">Wnt controls the transcriptional activity of Kaiso through CK1ε-dependent phosphorylation of p120-catenin</subfield>
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