Development and validation of a mixed-tissue oligonucleotide DNA microarray for Atlantic bluefin tuna, Thunnus thynnus (Linnaeus, 1758). (December 2015)

• Record Type: Journal Article
• Authors: Trumbić, Željka; Bekaert, Michaël; Taggart, John; Bron, James; Gharbi, Karim; Mladineo, Ivona
• Is Part Of: BMC genomics. Volume 16:Number 1(2015)
• Page Start: 1
• Page End: 17
• Publication Date: 2015-12
• Subjects: Thunnus thynnus -- transcriptome -- Microarray -- Tissue gene expression, genome mapping; Genomes -- Periodicals; Gene mapping -- Periodicals; Genomics -- Periodicals; Base Sequence -- Periodicals; Chromosome Mapping -- Periodicals; Genetic Techniques -- Periodicals; Sequence Analysis, DNA -- Periodicals; 572.8605
• DOI: 10.1186/s12864-015-2208-7
• Languages: English
• ISSNs: 1471-2164

Abstract

Abstract Background The largest of the tuna species, Atlantic bluefin tuna (Thunnus thynnus ), inhabits the North Atlantic Ocean and the Mediterranean Sea and is considered to be an endangered species, largely a consequence of overfishing.T. thynnus aquaculture, referred to as fattening or farming, is a capture based activity dependent on yearly renewal from the wild. Thus, the development of aquaculture practices independent of wild resources can provide an important contribution towards ensuring security and sustainability of this species in the longer-term. The development of such practices is today greatly assisted by large scale transcriptomic studies. Results We have used pyrosequencing technology to sequence a mixed-tissue normalised cDNA library, derived from adultT. thynnus . A total of 976, 904 raw sequence reads were assembled into 33, 105 unique transcripts having a mean length of 893 bases and an N50 of 870. Of these, 33.4 % showed similarity to known proteins or gene transcripts and 86.6 % of them were matched to the congeneric Pacific bluefin tuna (Thunnus orientalis ) genome, compared to 70.3 % for the more distantly related Nile tilapia (Oreochromis niloticus ) genome. Transcript sequences were used to develop a novel 15 K Agilent oligonucleotide DNA microarray forT. thynnus and comparative tissue gene expression profiles were inferred for gill, heart, liver, ovaries and testes. Functional contrasts were strongest between gills and ovaries. Gills were particularly associated with immune system, signal transduction and cell communication, while ovaries displayed signatures of glycan biosynthesis, nucleotide metabolism, transcription, translation, replication and repair. Conclusions Sequence data generated from a novel mixed-tissueT. thynnus cDNA library provide an important transcriptomic resource that can be further employed for study of various aspects ofT. thynnus ecology and genomics, with strong applications in aquaculture. Tissue-specific gene expression profiles inferred through the use of novel oligo-microarray can serve in the design of new and more focused transcriptomic studies for future research of tuna physiology and assessment of the welfare in a production environment.