Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes

dc.contributor.authorRodríguez Ubreva, Javier
dc.contributor.authorCiudad, Laura
dc.contributor.authorGómez Cabrero, David
dc.contributor.authorParra Bola, Mª Isabel
dc.contributor.authorBussmann, Lars H.
dc.contributor.authorTullio, Alessandro di
dc.contributor.authorKallin, Eric M.
dc.contributor.authorTegnér, Jesper
dc.contributor.authorGraf, Thomas
dc.contributor.authorBallestar Tarín, Esteban
dc.date.accessioned2018-11-28T10:13:41Z
dc.date.available2018-11-28T10:13:41Z
dc.date.issued2012-03-01
dc.date.updated2018-07-24T12:56:06Z
dc.description.abstractTranscription factor-induced lineage reprogramming or transdifferentiation experiments are essential for understanding the plasticity of differentiated cells. These experiments helped to define the specific role of transcription factors in conferring cell identity and played a key role in the development of the regenerative medicine field. We here investigated the acquisition of DNA methylation changes during C/EBP alpha-induced pre-B cell to macrophage transdifferentiation. Unexpectedly, cell lineage conversion occurred without significant changes in DNA methylation not only in key B cell- and macrophage-specific genes but also throughout the entire set of genes differentially methylated between the two parental cell types. In contrast, active and repressive histone modification marks changed according to the expression levels of these genes. We also demonstrated that C/EBP alpha and RNA Pol II are associated with the methylated promoters of macrophage-specific genes in reprogrammed macrophages without inducing methylation changes. Our findings not only provide insights about the extent and hierarchy of epigenetic events in pre-B cell to macrophage transdifferentiation but also show an important difference to reprogramming towards pluripotency where promoter DNA demethylation plays a pivotal role.
dc.format.extent15 p.
dc.format.mimetypeapplication/pdf
dc.identifier.pmid22086955
dc.identifier.urihttps://hdl.handle.net/2445/126530
dc.language.isoeng
dc.publisherOxford University Press
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1093/nar/gkr1015
dc.relation.ispartofNucleic Acids Research, 2012, vol. 40, num. 5, p. 1954-1968
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/208119/EU//HDAC HEMATOPOIESIS
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/223920/EU//VPH NOE
dc.relation.urihttps://doi.org/10.1093/nar/gkr1015
dc.rightscc by-nc (c) Rodríguez Ubreva et al., 2012
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationADN
dc.subject.classificationCèl·lules B
dc.subject.otherDNA
dc.subject.otherB cells
dc.titlePre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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