Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/3042
Appears in Collections:Aquaculture Journal Articles
Peer Review Status: Refereed
Title: Expression of fatty acyl desaturase and elongase genes, and evolution of DHA:EPA ratio during development of unfed larvae of Atlantic bluefin tuna (Thunnus thynnus L.)
Author(s): Morais, Sofia
Mourente, Gabriel
Ortega, Aurelio
Tocher, Jamie A
Tocher, Douglas R
Contact Email: drt1@stir.ac.uk
Keywords: Atlantic bluefin tuna
yolk sac larvae
lipid content and composition
fatty acid composition
fatty acyl desaturase
fatty acyl elongase
gene expression
development
Fishes Feeding and feeds
Fishes Nutrition
Issue Date: 15-Mar-2011
Date Deposited: 3-Jun-2011
Citation: Morais S, Mourente G, Ortega A, Tocher JA & Tocher DR (2011) Expression of fatty acyl desaturase and elongase genes, and evolution of DHA:EPA ratio during development of unfed larvae of Atlantic bluefin tuna (Thunnus thynnus L.). Aquaculture, 313 (1-4), pp. 129-139. http://www.sciencedirect.com/science/journal/00448486; https://doi.org/10.1016/j.aquaculture.2011.01.031
Abstract: The concentration of n-3 long-chain polyunsaturated fatty acids (LC-PUFA) in neural tissues is known to be crucial for effective prey capture from the time of first feeding in marine fish larvae. Furthermore, tissues of tunids, including Atlantic bluefin tuna, have relatively high levels of DHA (docosahexaenic acid, 22:6n-3) and a high ratio of DHA:EPA (eicosapentaenoic acid; 20:5n-3) compared to most other species. Although the lipid biochemistry underpinning the high DHA:EPA ratio in tuna is unclear, it has been generally assumed that they must selectively accumulate and retain DHA in their tissues. In the present study, we investigated lipid and fatty acid metabolism during early development of Atlantic bluefin tuna and determined the changes in lipid content, lipid class composition and total, phospholipid and neutral lipid fatty acid profiles in unfed larvae during yolk sac utilisation. In addition, we studied the LC-PUFA biosynthesis pathway by quantifying expression of fatty acyl desaturase and elongase genes. To this end, we cloned and functionally characterized two cDNAs by heterologous expression in yeast, showing them to code for a Δ6 desaturase and Elovl5 elongase, respectively, that could both be involved in the conversion of EPA to DHA. The level of DHA was maintained, but the proportion of EPA declined, and so the DHA:EPA ratio increased in bluefin tuna larvae during yolk sac utilization. Although this could be the result of relative retention of DHA during a period of generally high fatty acid oxidation and utilization, there was also a great increase in desaturase and elongase expression with larval development. This suggests that increased activity of these enzymes is important for the normal development of tuna larvae related to the provision of adequate DHA for the formation of biomembranes, particularly in neural (brain and eye) tissues.
URL: http://www.sciencedirect.com/science/journal/00448486
DOI Link: 10.1016/j.aquaculture.2011.01.031
Rights: Published in Aquaculture by Elsevier. Aquaculture, Volume 313, Issues 1-4, March 2011, pp. 129 - 139.; This is the peer reviewed version of this article.; NOTICE: this is the author’s version of a work that was accepted for publication in Aquaculture. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Aquaculture, VOL 313, ISSUE 1-4, (March 2011). DOI: 10.1016/j.aquaculture.2011.01.031

Files in This Item:
File Description SizeFormat 
Morais et al (FINAL).pdfFulltext - Accepted Version1.2 MBAdobe PDFView/Open



This item is protected by original copyright



Items in the Repository are protected by copyright, with all rights reserved, unless otherwise indicated.

The metadata of the records in the Repository are available under the CC0 public domain dedication: No Rights Reserved https://creativecommons.org/publicdomain/zero/1.0/

If you believe that any material held in STORRE infringes copyright, please contact library@stir.ac.uk providing details and we will remove the Work from public display in STORRE and investigate your claim.