|Appears in Collections:||Aquaculture Journal Articles|
|Peer Review Status:||Refereed|
|Title:||Functional desaturase fads1 (delta5) and fads2 (delta6) orthologues evolved before the origin of jawed vertebrates|
|Author(s):||Costa Castro, Luıs Filipe|
Tocher, Douglas R
|Citation:||Costa Castro LF, Monroig O, Leaver M, Wilson J, Cunha I & Tocher DR (2012) Functional desaturase fads1 (delta5) and fads2 (delta6) orthologues evolved before the origin of jawed vertebrates. PLoS ONE, 7 (2), p. e31950. https://doi.org/10.1371/journal.pone.0031950|
|Abstract:||Long-chain polyunsaturated fatty acids (LC-PUFAs) such as arachidonic (ARA), eicosapentaenoic (EPA) and docosahexaenoic (DHA) acids are essential components of biomembranes, particularly in neural tissues. Endogenous synthesis of ARA, EPA and DHA occurs from precursor dietary essential fatty acids such as linoleic and α- linolenic acid through elongation and Δ5 and Δ6 desaturations. With respect to desaturation activities some noteworthy differences have been noted in vertebrate classes. In mammals, the Δ5 activity is allocated to the Fads1 gene, while Fads2 is a Δ6 desaturase. In contrast, teleosts show distinct combinations of desaturase activities (e.g. bifunctional or separate Δ5 and Δ6 desaturases) apparently allocated to Fads2- type genes. To determine the timing of Fads1-Δ5 and Fads2-Δ6 evolution we used a combination of comparative and functional genomics with the analysis of key phylogenetic species. Our data show that Fads1 and Fads2 genes with Δ5 and Δ6 activities respectively, evolved before gnathostome radiation, since the catshark Scyliorhinus canicula has functional orthologues of both gene families. Consequently, the loss of Fads1 in teleosts is a secondary episode, while the existence of Δ5 activities in the same group most likely occurred through independent mutations into Fads2 type genes. Unexpectedly, we also establish that events of Fads1 gene expansion have taken place in birds and reptiles. Finally, a fourth Fads gene (Fads4) was found with an exclusive occurrence in mammalian genomes. Our findings enlighten the history of a crucially important gene family in vertebrate fatty acid metabolism and physiology and provide an explanation of how observed lineagespecific gene duplications, losses and diversifications might be linked to habitatspecific food web structures in different environments and over geological timescales.|
|Rights:||Publisher is open-access. Open access publishing allows free access to and distribution of published articles where the author retains copyright of their work by employing a Creative Commons attribution licence. Proper attribution of authorship and correct citation details should be given. Publisher’s policy available from http://creativecommons.org/licenses/by/2.5/|
|journal.pone.0031950.pdf||Fulltext - Published Version||647.04 kB||Adobe PDF||View/Open|
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