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dc.contributor.authorOrtiz-Villanueva, Elenaes_ES
dc.contributor.authorNavarro-Martín, Laiaes_ES
dc.contributor.authorJaumot, Joaquimes_ES
dc.contributor.authorBenavente, Fernandoes_ES
dc.contributor.authorSanz-Nebot, Victoria M.es_ES
dc.contributor.authorPiña, Benjamínes_ES
dc.contributor.authorTauler, Romàes_ES
dc.date.accessioned2017-12-11T10:39:55Z-
dc.date.available2017-12-11T10:39:55Z-
dc.date.issued2017-
dc.identifier.citationEnvironmental Pollution: 231: 22-36 (2017)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/158053-
dc.description.abstractAlthough bisphenol A (BPA) is commonly recognized as an endocrine disruptor, the metabolic consequences of its exposure are still poorly understood. In this study, we present a non-targeted LC-MS based metabolomic analysis in combination with a full-genome, high-throughput RNA sequencing (RNA-Seq) to reveal the metabolic effects and the subjacent regulatory pathways of exposing zebrafish embryos to BPA during the first 120 hours post-fertilization. We applied multivariate data analysis methods to extract biochemical information from the LC-MS and RNA-Seq complex datasets and to perform testable predictions of the phenotypic adverse effects. Metabolomic and transcriptomic data revealed a similar subset of altered pathways, despite the large difference in the number of identified biomarkers (around 50 metabolites and more than 1000 genes). These results suggest that even a moderate coverage of zebrafish metabolome may be representative of the global metabolic changes. These multi-omic responses indicate a specific metabolic disruption by BPA affecting different signaling pathways, such as retinoid and prostaglandin metabolism. The combination of transcriptomic and metabolomic data allowed a dynamic interpretation of the results that could not be drawn from either single dataset. These results illustrate the utility of -omic integrative analyses for characterizing the physiological effects of toxicants beyond the mere indication of the affected pathways. © 2017 Elsevier Ltdes_ES
dc.description.sponsorshipThis work was supported by the European Research Council under the European Union's Seventh Framework Programme (FP/ 2007-2013)/ERC Grant Agreement n. 320737. Some part of this study was also supported by a grant from the Spanish Ministry of Economy and Competitiveness (CTQ2014-56777-R). LNM was supported by a Beatriu de Pinos Postdoctoral Fellow (2013BP-B- 00088) awarded by the Secretary for Universities and Research of the Ministry of Economy and Knowledge of the Government of Catalonia and the Cofund programme of the Marie Curie Actions of the 7th R&D Framework Programme of the European Union.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/320737es_ES
dc.relationMINECO/ICTI2013-2016/CTQ2014-56777-R-
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccessen_EN
dc.subjectBisphenol Aes_ES
dc.subjectMetabolic disruptiones_ES
dc.subjectNon-targeted metabolomicses_ES
dc.subjectTranscriptomicses_ES
dc.subjectZebrafishes_ES
dc.titleMetabolic disruption of zebrafish (Danio rerio) embryos by bisphenol A. An integrated metabolomic and transcriptomic approaches_ES
dc.typeartículoes_ES
dc.identifier.doi10.1016/j.envpol.2017.07.095-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.envpol.2017.07.095es_ES
dc.embargo.terms2019-12-01es_ES
dc.rights.licensehttp://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.contributor.funderEuropean Commissiones_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
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