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dc.contributor.authorPemmasani, Jhansi K.
dc.contributor.authorPottinger, Tom G.
dc.contributor.authorCairns, Michael T.
dc.date.accessioned2016-05-24T10:51:35Z
dc.date.available2016-05-24T10:51:35Z
dc.date.issued2011-12
dc.identifier.citationPemmasani, JK,Pottinger, TG,Cairns, MT (2011) 'Analysis of stress-induced hepatic gene expression in rainbow trout (Oncorhynchus mykiss) selected for high- and low-responsiveness to stress'. Comparative Biochemistry And Physiology D-Genomics & Proteomics, 6 :406-419.en_IE
dc.identifier.issn1744-117X
dc.identifier.urihttp://hdl.handle.net/10379/5833
dc.description.abstractThe production and welfare of intensively reared fish would be improved by reducing stress responsiveness. One approach to achieving this goal is selective breeding utilising stress-responsive genes as direct genetic markers of the desirable trait. As a first step in this process, microarray analysis has been carried out on liver tissues of rainbow trout selectively bred for high (HR) or low (LR) responsiveness to a stressor. Microarray hybridizations provided gene expression profiles for pooled samples of fish confined for 6 h, 24 h and 168 h and for individual fish (168 h only). 161 genes were shown to be differentially regulated in HR and LR fish during confinement exposure and eight of these gene expression profiles were validated by quantitative PCR. Genes of particular interest included intelectin-2 precursor which showed greater than 100-fold higher expression in HR fish compared to LR fish irrespective of whether the fish were confined or not; interferon inducible transmembrane protein 3 which was differentially stress-induced between the two lines; and hepatic pro-opiomelanocortin B (POMC B) which was upregulated during stress in HR fish but downregulated in LR fish. All these offer potential as direct markers of low stress responsiveness in a marker-assisted selection scheme. (C) 2011 Elsevier Inc. All rights reserved.en_IE
dc.description.sponsorshipEuropean Commission, the Natural Environment Research Council of the UK, and Enterprise Ireland. European Commission support was through contract no. Q5RS-2001-002211-STRESSGENES, contract no. 513692-AQUAFIRST, and a Marie Curie Host Fellowship to Jhansi K. Pemmasani (contract no. MTKD-CT-2004-013701-DIAGNOMICS).en_IE
dc.formatapplication/pdfen_IE
dc.language.isoenen_IE
dc.publisherElsevieren_IE
dc.relation.ispartofComparative Biochemistry And Physiology D-Genomics & Proteomicsen
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectCortisolen_IE
dc.subjectGenetic markersen_IE
dc.subjectLiveren_IE
dc.subjectMicroarrayen_IE
dc.subjectSelective breedingen_IE
dc.subjectSalmon salmo-salaren_IE
dc.subjectSparus-aurata L.en_IE
dc.subjectConfinement exposureen_IE
dc.subjectLiveren_IE
dc.subjectPropiomelanocortinen_IE
dc.subjectLectinsen_IE
dc.subjectProteinen_IE
dc.subjectFamilyen_IE
dc.subjectTissueen_IE
dc.subjectModelen_IE
dc.titleAnalysis of stress-induced hepatic gene expression in rainbow trout (Oncorhynchus mykiss) selected for high- and low-responsiveness to stressen_IE
dc.typeArticleen_IE
dc.date.updated2016-05-17T09:43:25Z
dc.identifier.doiDOI 10.1016/j.cbd.2011.09.001
dc.local.publishedsourcehttp://www.sciencedirect.com/science/article/pii/S1744117X11000608en_IE
dc.description.peer-reviewedpeer-reviewed
dc.contributor.funder|~|
dc.internal.rssid2720982
dc.local.contactMichael Cairns, Glycoscience Group, Ncbes, Biomedical Sciences, Dangan, Newcastle Rd. 2094 Email: michael.cairns@nuigalway.ie
dc.local.copyrightcheckedYes
dc.local.versionPUBLISHED
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