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dc.contributor.authorLaing, LV
dc.contributor.authorViana, J
dc.contributor.authorDempster, EL
dc.contributor.authorTrznadel, M
dc.contributor.authorTrunkfield, LA
dc.contributor.authorWebster, TM
dc.contributor.authorvan Aerle, R
dc.contributor.authorPaull, GC
dc.contributor.authorWilson, RJ
dc.contributor.authorMill, J
dc.contributor.authorSantos, EM
dc.date.accessioned2016-04-28T13:22:39Z
dc.date.issued2016-04-27
dc.description.abstractBisphenol A (BPA) is a commercially important high production chemical widely used in epoxy resins and polycarbonate plastics, and is ubiquitous in the environment. Previous studies demonstrated that BPA activates estrogenic signaling pathways associated with adverse effects on reproduction in vertebrates and that exposure can induce epigenetic changes. We aimed to investigate the reproductive effects of BPA in a fish model and to document its mechanisms of toxicity. We exposed breeding groups of zebrafish (Danio rerio) to 0.01, 0.1, and 1 mg/L BPA for 15 days. We observed a significant increase in egg production, together with a reduced rate of fertilization in fish exposed to 1 mg/L BPA, associated with significant alterations in the transcription of genes involved in reproductive function and epigenetic processes in both liver and gonad tissue at concentrations representing hotspots of environmental contamination (0.1 mg/L) and above. Of note, we observed reduced expression of DNA methyltransferase 1 (dnmt1) at environmentally relevant concentrations of BPA, along with a significant reduction in global DNA methylation, in testes and ovaries following exposure to 1 mg/L BPA. Our findings demonstrate that BPA disrupts reproductive processes in zebrafish, likely via estrogenic mechanisms, and that environmentally relevant concentrations of BPA are associated with altered transcription of key enzymes involved in DNA methylation maintenance. These findings provide evidence of the mechanisms of action of BPA in a model vertebrate and advocate for its reduction in the environment.en_GB
dc.description.sponsorshipWe thank the Aquatic Resources Centre technical team for support with zebrafish husbandry. This work was funded by a PhD studentship from the Fisheries Society of the British Isles (http://www.fsbi.org.uk/) and the University of Exeter (http://www.exeter.ac.uk/) to LVL and EMS. TMUW was funded by a Natural Environment Research Council CASE PhD studentship (grant no. NE/I528326/1) and the Salmon & Trout Association (http://www.salmon-trout.org/).en_GB
dc.identifier.doi10.1080/15592294.2016.1182272
dc.identifier.urihttp://hdl.handle.net/10871/21294
dc.language.isoenen_GB
dc.publisherTaylor & Francisen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/27120497en_GB
dc.rightsThis is the author accepted manuscript. The final version is available from Taylor & Francis via the DOI in this record.en_GB
dc.subjectaquaticen_GB
dc.subjectendocrineen_GB
dc.subjectmethylationen_GB
dc.subjectplasticizersen_GB
dc.subjectteleosten_GB
dc.subjectvertebrateen_GB
dc.subjectwasteen_GB
dc.titleBisphenol A causes reproductive toxicity, decreases dnmt1 transcription, and reduces global DNA methylation in breeding zebrafish (Danio rerio).en_GB
dc.typeArticleen_GB
dc.identifier.issn1559-2294
dc.identifier.journalEpigeneticsen_GB


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