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dc.contributor.authorZheng, D
dc.contributor.authorKille, P
dc.contributor.authorFeeney, GP
dc.contributor.authorCunningham, P
dc.contributor.authorHandy, Richard
dc.contributor.authorHogstrand, C
dc.date.accessioned2018-04-12T10:13:21Z
dc.date.issued2010-12
dc.identifier.issn1471-2164
dc.identifier.issn1471-2164
dc.identifier.other553
dc.identifier.urihttp://hdl.handle.net/10026.1/11257
dc.description.abstract

<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>Dietary zinc supplementation may help to promote growth, boost the immune system, protect against diabetes, and aid recovery from diarrhoea. We exploited the zebrafish (<jats:italic>Danio rerio</jats:italic>) gill as a unique vertebrate ion transporting epithelium model to study the time-dependent regulatory networks of gene-expression leading to homeostatic control during zinc supplementation. This organ forms a conduit for zinc uptake whilst exhibiting conservation of zinc trafficking components.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Fish were maintained with either zinc supplemented water (4.0 μM) and diet (2023 mg zinc kg<jats:sup>-1</jats:sup>) or water and diet containing Zn<jats:sup>2+</jats:sup> at 0.25 μM and 233 mg zinc kg<jats:sup>-1</jats:sup>, respectively. Gill tissues were harvested at five time points (8 hours to 14 days) and transcriptome changes analysed in quintuplicate using a 16 K microarray with results anchored to gill Zn<jats:sup>2+</jats:sup> influx and whole body nutrient composition (protein, carbohydrate, lipid, elements). The number of regulated genes increased up to day 7 but declined as the fish acclimated. In total 525 genes were regulated (having a fold-change more than 1.8 fold change and an adjusted P-value less than 0.1 which is controlling a 10% False discovery rate, FDR) by zinc supplementation, but little overlap was observed between genes regulated at successive time-points. Many genes displayed cyclic expression, typical for homeostatic control mechanisms. Annotation enrichment analysis revealed strong overrepresentation of "transcription factors", with specific association evident with "steroid hormone receptors". A suite of genes linked to "development" were also statistically overrepresented. More specifically, early regulation of genes was linked to a few key transcription factors (e.g. Mtf1, Jun, Stat1, Ppara, Gata3) and was followed by hedgehog and bone morphogenic protein signalling.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>The results suggest that zinc supplementation reactivated developmental pathways in the gill and stimulated stem cell differentiation, a response likely reflecting gill remodelling in response to its altered environment. This provides insight to the role of zinc during cell differentiation and illustrates the critical nature of maintaining zinc status. The study also highlights the importance of temporal transcriptomics analysis in order resolve the discrete elements of biological processes, such as zinc acclimation.</jats:p> </jats:sec>

dc.format.extent553-
dc.format.mediumElectronic
dc.languageen
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.subject5' Untranslated Regions
dc.subjectAnimals
dc.subjectBinding Sites
dc.subjectDietary Supplements
dc.subjectGene Expression Profiling
dc.subjectGene Expression Regulation
dc.subjectGene Regulatory Networks
dc.subjectGills
dc.subjectMolecular Sequence Annotation
dc.subjectRNA, Messenger
dc.subjectReproducibility of Results
dc.subjectReverse Transcriptase Polymerase Chain Reaction
dc.subjectSignal Transduction
dc.subjectTime Factors
dc.subjectTranscription Factors
dc.subjectTranscription, Genetic
dc.subjectZebrafish
dc.subjectZebrafish Proteins
dc.subjectZinc
dc.titleDynamic transcriptomic profiles of zebrafish gills in response to zinc supplementation
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000283552900001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue1
plymouth.volume11
plymouth.publication-statusPublished
plymouth.journalBMC Genomics
dc.identifier.doi10.1186/1471-2164-11-553
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering/School of Biological and Marine Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA06 Agriculture, Veterinary and Food Science
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Marine Institute
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeEngland
dcterms.dateAccepted2010-10-11
dc.identifier.eissn1471-2164
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1186/1471-2164-11-553
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2010-10-11
rioxxterms.typeJournal Article/Review


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