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dc.contributor.authorCalduch-Giner, Josep A
dc.contributor.authorDavey, Grace
dc.contributor.authorSaera-Vila, Alfonso
dc.contributor.authorHoueix, Benoit
dc.contributor.authorTalbot, Anita
dc.contributor.authorPrunet, Patrick
dc.contributor.authorCairns, Michael T
dc.contributor.authorPerez-Sanchez, Jaume
dc.date.accessioned2018-09-20T16:02:24Z
dc.date.available2018-09-20T16:02:24Z
dc.date.issued2010-01-01
dc.identifier.citationCalduch-Giner, Josep A; Davey, Grace; Saera-Vila, Alfonso; Houeix, Benoit; Talbot, Anita; Prunet, Patrick; Cairns, Michael T; Perez-Sanchez, Jaume (2010). Use of microarray technology to assess the time course of liver stress response after confinement exposure in gilthead sea bream (sparus aurata l.). BMC Genomics 11 ,
dc.identifier.issn1471-2164
dc.identifier.urihttp://hdl.handle.net/10379/10650
dc.description.abstractBackground: Selection programs for growth and stress traits in cultured fish are fundamental to the improvement of aquaculture production. The gilthead sea bream ( Sparus aurata) is the main aquacultured species in the Mediterranean area and there is considerable interest in the genetic improvement of this species. With the aim of increasing the genomic resources in gilthead sea bream and identifying genes and mechanisms underlying the physiology of the stress response, we developed a cDNA microarray for gilthead sea bream that is enriched by suppression substractive hybridization with stress and immunorelevant genes. This microarray is used to analyze the dynamics of gilthead sea bream liver expression profile after confinement exposure. Results: Groups of confined and control juvenile fish were sampled at 6, 24, 72 and 120 h post exposure. GeneSpring analyses identified 202 annotated genes that appeared differentially expressed at least at one sampling time (P < 0.05). Gene expression results were validated by quantitative PCR of 10 target genes, and K-means clustering of differently expressed genes identified four major temporal gene expression profiles. Set 1 encompassed a rapid metabolic readjustment with enhanced uptake and intracellular transport of fatty acids as metabolic fuels. Set 2 was associated with a wide variety of tissue repair and remodeling processes that were mostly mediated by the stress response of the endoplasmic reticulum ( ER). Sets 3 and 4 encompassed the re-establishment of cellular homeostasis with increased intracellular trafficking and scavenging of reactive oxygen species (ROS), accompanied by a bidirectional regulation of the immune system and a general decline of ROS production. Conclusions: Collectively, these findings show the complex nature of the adaptive stress response with a clear indication that the ER is an important control point for homeostatic adjustments. The study also identifies metabolic pathways which could be analyzed in greater detail to provide new insights regarding the transcriptional regulation of the stress response in fish.
dc.publisherSpringer Nature
dc.relation.ispartofBMC Genomics
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjecttrout oncorhynchus-mykiss
dc.subjectsuppression subtractive hybridization
dc.subjectunfolded protein response
dc.subjectgene-expression profiles
dc.subjectretinol-binding-protein
dc.subjectrainbow-trout
dc.subjectcortisol response
dc.subjectoxidative stress
dc.subjectatlantic salmon
dc.subjectplasma-cortisol
dc.titleUse of microarray technology to assess the time course of liver stress response after confinement exposure in gilthead sea bream (sparus aurata l.)
dc.typeArticle
dc.identifier.doi10.1186/1471-2164-11-193
dc.local.publishedsourcehttps://bmcgenomics.biomedcentral.com/track/pdf/10.1186/1471-2164-11-193?site=bmcgenomics.biomedcentral.com
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