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dc.contributor.authorLafita Navarro, María Carmen
dc.contributor.authorBlanco Fernández, Rosa Fernanda
dc.contributor.authorMata Garrido, Jorge 
dc.contributor.authorLiaño Pons, Judit
dc.contributor.authorTapia Martínez, Olga
dc.contributor.authorGarcía Gutiérrez, Lucía
dc.contributor.authorGarcía Alegría, E.
dc.contributor.authorBerciano Blanco, María Teresa 
dc.contributor.authorLafarga Coscojuela, Miguel Ángel 
dc.contributor.authorLeón Serrano, Javier 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2016-10-14T10:54:44Z
dc.date.available2016-10-14T10:54:44Z
dc.date.issued2016
dc.identifier.issn1949-2553
dc.identifier.otherSAF2014-53526, BFU2014-54754P,RETIC-RD012-036-033, CIBERNED CB06/05/0037
dc.identifier.urihttp://hdl.handle.net/10902/9296
dc.description.abstractMXD1 is a protein that interacts with MAX, to form a repressive transcription factor. MXD1-MAX binds E-boxes. MXD1-MAX antagonizes the transcriptional activity of the MYC oncoprotein in most models. It has been reported that MYC overexpression leads to augmented RNA synthesis and ribosome biogenesis, which is a relevant activity in MYC-mediated tumorigenesis. Here we describe that MXD1, but not MYC or MNT, localizes to the nucleolus in a wide array of cell lines derived from different tissues (carcinoma, leukemia) as well as in embryonic stem cells. MXD1 also localizes in the nucleolus of primary tissue cells as neurons and Sertoli cells. The nucleolar localization of MXD1 was confirmed by co-localization with UBF. Co-immunoprecipitation experiments showed that MXD1 interacted with UBF and proximity ligase assays revealed that this interaction takes place in the nucleolus. Furthermore, chromatin immunoprecipitation assays showed that MXD1 was bound in the transcribed rDNA chromatin, where it co-localizes with UBF, but also in the ribosomal intergenic regions. The MXD1 involvement in rRNA synthesis was also suggested by the nucleolar segregation upon rRNA synthesis inhibition by actinomycin D. Silencing of MXD1 with siRNAs resulted in increased synthesis of pre-rRNA while enforced MXD1 expression reduces it. The results suggest a new role for MXD1, which is the control of ribosome biogenesis. This new MXD1 function would be important to curb MYC activity in tumor cells.es_ES
dc.format.extent13 p.es_ES
dc.language.isoenges_ES
dc.publisherImpact Journalses_ES
dc.rightsAtribución 3.0 Españaes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceOncotarget. 2016 Aug 31es_ES
dc.subject.otherMXD1es_ES
dc.subject.otherUBFes_ES
dc.subject.othernucleoluses_ES
dc.subject.otherpre-rRNAes_ES
dc.subject.othertranscription regulationes_ES
dc.titleMXD1 localizes in the nucleolus, binds UBF and impairs rRNA synthesises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.18632/oncotarget.11766
dc.type.versionpublishedVersiones_ES


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Atribución 3.0 EspañaExcept where otherwise noted, this item's license is described as Atribución 3.0 España