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      A comparative analysis of the response of the hepatic transcriptome to dietary docosahexaenoic acid in Atlantic salmon ( Salmo salar) post-smolts

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          Abstract

          Background

          The present study aimed to explore the impact of dietary docosahexaenoic acid (DHA) on aspects of the metabolism of Atlantic salmon ( Salmo salar). The effects of diets containing increasing levels of DHA (1 g kg −1, 3 g kg −1, 6 g kg −1, 10 g kg −1 and 13 g kg −1) on the liver transcriptome of post-smolt salmon was examined to elucidate patterns of gene expression and responses of specific metabolic pathways. Total RNA was isolated from the liver of individual fish and analyzed using a custom gene expression 44K feature Atlantic salmon oligo-microarray.

          Results

          The expression of up to 911 unique annotated genes was significantly affected by dietary DHA inclusion relative to a low DHA reference diet. Analysis of a total of 797 unique genes were found with a significant linear correlation between expression level and dietary DHA. Gene-Set Enrichment Analysis (GSEA) identified a range of pathways that were significantly affected by dietary DHA content.

          Conclusions

          Pathways that showed a significant response to dietary DHA level included those for long-chain polyunsaturated fatty acid biosynthesis, fatty acid elongation, steroid biosynthesis, glycan biosynthesis, protein export and protein processing in the endoplasmic reticulum. These findings suggest that in addition to clear roles in influencing lipid metabolic pathways, DHA might also have key functional roles in other pathways distinct from lipid metabolism.

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          Most cited references42

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          Complex N-glycan number and degree of branching cooperate to regulate cell proliferation and differentiation.

          The number of N-glycans (n) is a distinct feature of each glycoprotein sequence and cooperates with the physical properties of the Golgi N-glycan-branching pathway to regulate surface glycoprotein levels. The Golgi pathway is ultrasensitive to hexosamine flux for the production of tri- and tetra-antennary N-glycans, which bind to galectins and form a molecular lattice that opposes glycoprotein endocytosis. Glycoproteins with few N-glycans (e.g., TbetaR, CTLA-4, and GLUT4) exhibit enhanced cell-surface expression with switch-like responses to increasing hexosamine concentration, whereas glycoproteins with high numbers of N-glycans (e.g., EGFR, IGFR, FGFR, and PDGFR) exhibit hyperbolic responses. Computational and experimental data reveal that these features allow nutrient flux stimulated by growth-promoting high-n receptors to drive arrest/differentiation programs by increasing surface levels of low-n glycoproteins. We have identified a mechanism for metabolic regulation of cellular transition between growth and arrest in mammals arising from apparent coevolution of N-glycan number and branching.
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            Protein-glycan interactions in the control of innate and adaptive immune responses.

            The importance of protein glycosylation in the migration of immune cells throughout the body has been extensively appreciated. However, our awareness of the impact of glycosylation on the regulation of innate and adaptive immune responses is relatively new. An increasing number of studies reveal the relevance of glycosylation to pathogen recognition, to the modulation of the innate immune system and to the control of immune cell homeostasis and inflammation. Similarly important is the effect of glycan-containing 'information' in the development of autoimmune diseases and cancer. In this review, we provide an overview of these new directions and their impact in the field of glycoimmunology.
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              Short technical reports. Modification of the TRI reagent procedure for isolation of RNA from polysaccharide- and proteoglycan-rich sources.

              A modification of the TRI Reagent procedure has been elaborated for isolation of RNA from polysaccharide- and proteoglycan-rich material. In the modified procedure, RNA is precipitated from the aqueous phase by the combined action of isopropanol and a high-salt concentration. Under these conditions, RNA is effectively precipitated while contaminating polysaccharides and proteoglycans remain in the soluble form. The modified precipitation does not prolong or increase the complexity of the TRI Reagent procedure. The new procedure was tested by isolation of RNA from polysaccharide- and proteoglycan-rich tissues such as rat liver and aorta.
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                Author and article information

                Contributors
                brett.glencross@gmail.com
                christian.desantis@stir.ac.uk
                beatrix.berdal@stir.ac.uk
                j.b.taggart@stir.ac.uk
                j.e.bron@stir.ac.uk
                m.b.betancor@stir.ac.uk
                d.r.tocher@stir.ac.uk
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                7 September 2015
                7 September 2015
                2015
                : 16
                : 1
                : 684
                Affiliations
                [ ]CSIRO Aquaculture, GPO Box 2583, Brisbane, QLD 4001 Australia
                [ ]Institute of Aquaculture, School of Natural Sciences, Stirling University, Stirling, FK9 4LA Scotland, UK
                Article
                1810
                10.1186/s12864-015-1810-z
                4562122
                26345987
                c71b67f6-0e41-44c3-99ae-4cc6b946ad47
                © Glencross et al. 2015

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 20 January 2015
                : 3 August 2015
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2015

                Genetics
                essential fatty acid,dha,gene expression,transcriptome,atlantic salmon,microarray
                Genetics
                essential fatty acid, dha, gene expression, transcriptome, atlantic salmon, microarray

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