Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/23504
Appears in Collections:Aquaculture Journal Articles
Peer Review Status: Refereed
Title: Regulatory divergence of homeologous Atlantic salmon elovl5 genes following the salmonid-specific whole genome duplication
Authors: Carmona-Antonanzas, Greta
Zheng, Xiaozhong
Tocher, Douglas R
Leaver, Michael
Contact Email: mjl1@stir.ac.uk
Keywords: Atlantic salmon
DNA transposon
homeologous genes
neofunctionalisation
transposable elements
whole-genome duplication
fatty acid biosynthesis
Issue Date: 10-Oct-2016
Publisher: Elsevier
Citation: Carmona-Antonanzas G, Zheng X, Tocher DR & Leaver M (2016) Regulatory divergence of homeologous Atlantic salmon elovl5 genes following the salmonid-specific whole genome duplication, Gene, 591 (1), pp. 34-42.
Abstract: Fatty acyl elongase 5 (elovl5) is a critical enzyme in the vertebrate biosynthetic pathway which produces the physiologically essential long chain polyunsaturated fatty acids (LC-PUFA), docosahexenoic acid (DHA) and eicosapentenoic acid (EPA) from 18 carbon fatty acids precursors. In contrast to most other vertebrates, Atlantic salmon possess two copies of elovl5 (elovl5a and elovl5b) as a result of a whole genome duplication (WGD) which occurred at the base of the salmonid lineage. WGDs have had a major influence on vertebrate evolution, providing extra genetic material, enabling neofunctionalization to accelerate adaptation and speciation. However, little is known about the mechanisms by which such duplicated homeologous genes diverge. Here we show that homeologous Atlantic salmon elovl5a and elovl5b genes have been asymmetrically colonised by transposon-like elements. Identical locations and identities of insertions are also present in the rainbow trout duplicate elovl5 genes, but not in the nearest extant representative preduplicated teleost, the northern pike. Both elovl5 salmon duplicates possessed conserved regulatory elements that promoted Srebp1- and Srebp2-dependent transcription, and differences in the magnitude of Srebp response between promoters could be attributed to a tandem duplication of SRE and NF-Y cofactor binding sites in elovl5b. Furthermore, an insertion in the promoter region of elovl5a confers responsiveness to Lxr/Rxr transcriptional activation. Our results indicate that most, but not all transposon mobilisation into elovl5 genes occurred after the split from the common ancestor of pike and salmon, but before more recent salmonid speciations, and that divergence of elovl5 regulatory regions have enabled neofuntionalization by promoting differential expression of these homeologous genes.
Type: Journal Article
URI: http://hdl.handle.net/1893/23504
DOI Link: http://dx.doi.org/10.1016/j.gene.2016.06.056
Rights: This item has been embargoed for a period. During the embargo please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study. Accepted refereed manuscript of: Carmona-Antonanzas G, Zheng X, Tocher DR & Leaver M (2016) Regulatory divergence of homeologous Atlantic salmon elovl5 genes following the salmonid-specific whole genome duplication, Gene, 591 (1), pp. 34-42. DOI: 10.1016/j.gene.2016.06.056 © 2016, Elsevier. Licensed under the Creative Commons Attribution- NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/
Affiliation: Aquaculture
Aquaculture
Aquaculture
Aquaculture

Files in This Item:
File Description SizeFormat 
M Leaver Gene 300516 (2).pdf885.78 kBAdobe PDFUnder Embargo until 30/6/2017     Request a copy

Note: If any of the files in this item are currently embargoed, you can request a copy directly from the author by clicking the padlock icon above. However, this facility is dependant on the depositor still being contactable at their original email address.

This item is protected by original copyright



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

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.