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dc.contributor.authorMorena-Barrio, María Eugenia de la-
dc.contributor.authorBuil, Alfonso-
dc.contributor.authorAntón, Ana Isabel-
dc.contributor.authorMartínez-Martínez, Irene-
dc.contributor.authorMiñano, Antonia-
dc.contributor.authorGuriérrez-Gallego, Ricardo-
dc.contributor.authorNavarro-Fernandez, José-
dc.contributor.authorÁguila, Sonia-
dc.contributor.authorSouto, Juan Carlos-
dc.contributor.authorVicente, Vicente-
dc.contributor.authorSoria, José Manuel-
dc.contributor.authorCorral, Javier-
dc.date.accessioned2024-02-07T13:01:15Z-
dc.date.available2024-02-07T13:01:15Z-
dc.date.issued2013-
dc.identifier.citationPlos One, 2013; 8(5): e64998.es
dc.identifier.issnElectronic: 1932-6203-
dc.identifier.urihttp://hdl.handle.net/10201/138893-
dc.description©<2013>. This manuscript version is made available under the CC-BY-NC 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ This document is the, Published, version of a Published Work that appeared in final form in Plos One. To access the final edited and published work see: https://doi.org/10.1371/journal.pone.0064998-
dc.description.abstractThe haemostatic relevance of antithrombin together with the low genetic variability of SERPINC1, and the high heritability of plasma levels encourage the search for modulating genes. We used a hypothesis-free approach to identify these genes, evaluating associations between plasma antithrombin and 307,984 polymorphisms in the GAIT study (352 individuals from 21 Spanish families). Despite no SNP reaching the genome wide significance threshold, we verified milder positive associations in 307 blood donors from a different cohort. This validation study suggested LARGE, a gene encoding a protein with xylosyltransferase and glucuronyltransferase activities that forms heparin-like linear polysaccharides, as a potential modulator of antithrombin based on the significant association of one SNPs, rs762057, with anti-FXa activity, particularly after adjustment for age, sex and SERPINC1 rs2227589 genotype, all factors influencing antithrombin levels (p = 0.02). Additional results sustained this association. LARGE silencing inHepG2 and HEK-EBNA cells did not affect SERPINC1 mRNA levels but significantly reduced the secretion of antithrombin with moderate intracellular retention. Milder effects were observed on a1-antitrypsin, prothrombin and transferrin. Our study suggests LARGE as the first known modifier of plasma antithrombin, and proposes a new role for LARGE in modulating extracellular secretion of certain glycoproteins.es
dc.formatapplication/pdfes
dc.format.extent8es
dc.languageenges
dc.publisherPublic Library of Science-
dc.relationÁmbito internacional This study was supported partially by 04515/GERM/06 (Fundacio´n Se´neca de la Regio´n de Murcia), SAF2009-08993 and SAF2008/01859 (Spanish Ministerio de Ciencia y Tecnologı´a & Fondo Europeo de Desarrollo Regional de la Unio´n Europea FEDER), PI-08/0756, PI-11/0184 and RECAVA RD06/0014/0039 & RD06/0014/0016 (Spanish Instituto de Salud Carlos III & Fondo Europeo de Desarrollo Regional de la Unio´n Europea FEDER), and Centre National du Genotypage (Evry, France). MEMB is a holder of a predoctoral research grant from Spanish Instituto de Salud Carlos III (FI09/00190). IMM is a researcher from Fundacio´n para la Formacio´n e Investigacio´n Sanitarias. JNF is a postdoctoral researcher of the University of Murcia. JM Soria was supported by ‘‘Programa d’ Estabilitzacio´ d’Investigadors de la Direccio´ d’Estrategia i Coordinacio´ del Departament de Salut’’ (Generalitat de Catalunya). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAntithrombinen
dc.subjectLargeen
dc.subjectGlycosylationen
dc.subjectModulating genesen
dc.titleIdentification of Antithrombin-Modulating Genes. Role of LARGE, a Gene Encoding a Bifunctional Glycosyltransferase, in the Secretion of Proteins?es
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0064998-
dc.contributor.departmentDepartamento de Medicina-
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