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dc.contributor.authorAlonso Pérez, Elisa
dc.contributor.authorFernández Poceiro, Romina
dc.contributor.authorLalonde, Emilie
dc.contributor.authorKwan, Tony
dc.contributor.authorCalaza Cabanas, Manuel
dc.contributor.authorGómez-Reino Carnota, Juan Jesús 
dc.contributor.authorMajewski, Jacek
dc.contributor.authorGonzález Martínez-Pedrayo, Antonio 
dc.date.accessioned2017-06-07T07:02:24Z
dc.date.available2017-06-07T07:02:24Z
dc.date.issued2013
dc.identifier.issn1478-6354
dc.identifier.urihttp://hdl.handle.net/20.500.11940/1941
dc.description.abstractBackground: Polymorphisms in the interferon regulatory factor 5 (IRF5) gene are associated with susceptibility to systemic lupus erythematosus, rheumatoid arthritis and other diseases through independent risk and protective haplotypes. Several functional polymorphisms are already known, but they do not account for the protective haplotypes that are tagged by the minor allele of rs729302. Methods: Polymorphisms in linkage disequilibrium (LD) with rs729302 or particularly associated with IRF5 expression were selected for functional screening, which involved electrophoretic mobility shift assays (EMSAs) and reporter gene assays. Results: A total of 54 single-nucleotide polymorphisms in the 5' region of IRF5 were genotyped. Twenty-four of them were selected for functional screening because of their high LD with rs729302 or protective haplotypes. In addition, two polymorphisms were selected for their prominent association with IRF5 expression. Seven of these twenty-six polymorphisms showed reproducible allele differences in EMSA. The seven were subsequently analyzed in gene reporter assays, and three of them showed significant differences between their two alleles: rs729302, rs13245639 and rs11269962. Haplotypes including the cis-regulatory polymorphisms correlated very well with IRF5 mRNA expression in an analysis based on previous data. Conclusion: We have found that three polymorphisms in LD with the protective haplotypes of IRF5 have differential allele effects in EMSA and in reporter gene assays. Identification of these cis-regulatory polymorphisms will allow more accurate analysis of transcriptional regulation of IRF5 expression, more powerful genetic association studies and deeper insight into the role of IRF5 in disease susceptibility.
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAutoimmune Diseases
dc.subject.meshElectrophoretic Mobility Shift Assay
dc.subject.meshGenetic Predisposition to Disease
dc.subject.meshInterferon Regulatory Factors
dc.subject.meshPolymorphism, Single Nucleotide
dc.subject.meshRheumatic Diseases
dc.titleIdentification of three new cis-regulatory IRF5 polymorphisms: in vitro studies
dc.typeArtigoes
dc.authorsophosAlonso-Perez, E.
dc.authorsophosFernandez-Poceiro, R.
dc.authorsophosLalonde, E.
dc.authorsophosKwan, T.
dc.authorsophosCalaza, M.
dc.authorsophosGomez-Reino, J. J.
dc.authorsophosMajewski, J.
dc.authorsophosGonzalez, A.
dc.identifier.doi10.1186/ar4262
dc.identifier.isi330628300012
dc.identifier.pmid23941291
dc.identifier.sophos12442
dc.issue.number4
dc.journal.titleARTHRITIS RESEARCH & THERAPY
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Reumatoloxía
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago::IDIS.- Instituto de investigaciones sanitarias de Santiago
dc.page.initialR82
dc.rights.accessRightsopenAccess
dc.subject.decsEnfermedades Autoinmunes
dc.subject.decsEnsayo de Cambio de Movilidad Electroforética
dc.subject.decsPredisposición Genética a la Enfermedad
dc.subject.decsFactores Reguladores del Interferón
dc.subject.decsPolimorfismo de Nucleótido Simple
dc.subject.decsEnfermedades Reumáticas
dc.typesophosArtículo Original
dc.volume.number15


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