Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/27954
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dc.contributor.authorLi, Yuanyouen_UK
dc.contributor.authorYin, Ziyanen_UK
dc.contributor.authorDong, Yeweien_UK
dc.contributor.authorWang, Shuqien_UK
dc.contributor.authorMonroig, Óscaren_UK
dc.contributor.authorTocher, Douglas Ren_UK
dc.contributor.authorYou, Cuihongen_UK
dc.date.accessioned2018-10-12T00:01:30Z-
dc.date.available2018-10-12T00:01:30Z-
dc.date.issued2019-02en_UK
dc.identifier.urihttp://hdl.handle.net/1893/27954-
dc.description.abstractAs the first marine teleost demonstrated to have the ability of long-chain polyunsaturated fatty acids (LC-PUFA) biosynthesis from C18 PUFA precursors, the rabbitfish Siganus canaliculatus provides us a unique model for clarifying the regulatory mechanisms of LC-PUFA biosynthesis in teleosts aiming at the replacement of dietary fish oil (rich in LC-PUFA) with vegetable oils (rich in C18 PUFA precursors but devoid of LC-PUFA). In the study of transcription regulation of gene encoding the Δ6Δ5 fatty acyl desaturase (Δ6Δ5 Fads), a rate-limiting enzyme catalyzing the first step of LC-PUFA biosynthesis in rabbitfish, a binding site for the transcription factor (TF), peroxisome proliferator-activated receptor γ (Pparγ), was predicted in Δ6Δ5 fads2 promoter by bioinformatics analysis, and thus the present study focused on the regulatory roles of Pparγ on Δ6Δ5 fads2. First, the activity of the Δ6Δ5 fads2 promoter was proved to be downregulated by pparγ overexpression and upregulated by treatment of Pparγ antagonist (GW9662), respectively, in HEK 293T cells with the dual luciferase reporter assay. Pparγ was further confirmed to interact with the promoter by electrophoretic mobility shift assay. Moreover, in S. canaliculatus hepatocyte line (SCHL) cells, GW9662 decreased the expression of pparγ together with increase of Δ6Δ5 fads2 mRNA. Besides, Δ6Δ5 fads2 expression was increased by pparγ RNAi knockdown and reduced by its mRNA overexpression. Furthermore, knockdown of pparγ induced a high conversion of 18:3n−3 to 18:4n−3 and 18:2n−6 to 18:3n−6, while pparγ mRNA overexpression led to a lower conversion of that, and finally a significant decrease of 20:4n-6(ARA), 20:5n-3(EPA), and 22:6n-3(DHA) production. The results indicate that Pparγ is involved in the transcriptional regulation of liver LC-PUFA biosynthesis by targeting Δ6Δ5 fads2 in rabbitfish, which is the first report of Pparγ involvement in the regulation of LC-PUFA biosynthesis in teleosts.en_UK
dc.language.isoenen_UK
dc.publisherBMCen_UK
dc.relationLi Y, Yin Z, Dong Y, Wang S, Monroig Ó, Tocher DR & You C (2019) Pparγ Is Involved in the Transcriptional Regulation of Liver LC-PUFA Biosynthesis by Targeting the Δ6Δ5 Fatty Acyl Desaturase Gene in the Marine Teleost Siganus canaliculatus. Marine Biotechnology, 21 (1), pp. 19-29. https://doi.org/10.1007/s10126-018-9854-0en_UK
dc.rightsThis 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. This is a post-peer-review, pre-copyedit version of an article published in Marine Biotechnology. The final authenticated version is available online at: https://doi.org/10.1007/s10126-018-9854-0en_UK
dc.subjectLC-PUFAen_UK
dc.subjectFatty acyl desaturaseen_UK
dc.subjectTranscriptional regulationen_UK
dc.subjectSiganus canaliculatusen_UK
dc.titlePparγ Is Involved in the Transcriptional Regulation of Liver LC-PUFA Biosynthesis by Targeting the Δ6Δ5 Fatty Acyl Desaturase Gene in the Marine Teleost Siganus canaliculatusen_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate2019-09-12en_UK
dc.rights.embargoreason[Li et al Manuscript -final accepted.pdf] Publisher requires embargo of 12 months after formal publication.en_UK
dc.identifier.doi10.1007/s10126-018-9854-0en_UK
dc.identifier.pmid30206714en_UK
dc.citation.jtitleMarine Biotechnologyen_UK
dc.citation.issn1436-2236en_UK
dc.citation.issn1436-2228en_UK
dc.citation.volume21en_UK
dc.citation.issue1en_UK
dc.citation.spage19en_UK
dc.citation.epage29en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusAM - Accepted Manuscripten_UK
dc.author.emaild.r.tocher@stir.ac.uken_UK
dc.citation.date11/09/2018en_UK
dc.contributor.affiliationSouth China Agricultural Universityen_UK
dc.contributor.affiliationShantou Universityen_UK
dc.contributor.affiliationSouth China Agricultural Universityen_UK
dc.contributor.affiliationShantou Universityen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationShantou Universityen_UK
dc.identifier.isiWOS:000459406500003en_UK
dc.identifier.scopusid2-s2.0-85053491378en_UK
dc.identifier.wtid1030881en_UK
dc.contributor.orcid0000-0001-8712-0440en_UK
dc.contributor.orcid0000-0002-8603-9410en_UK
dc.date.accepted2018-08-28en_UK
dcterms.dateAccepted2018-08-28en_UK
dc.date.filedepositdate2018-10-11en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionAMen_UK
local.rioxx.authorLi, Yuanyou|en_UK
local.rioxx.authorYin, Ziyan|en_UK
local.rioxx.authorDong, Yewei|en_UK
local.rioxx.authorWang, Shuqi|en_UK
local.rioxx.authorMonroig, Óscar|0000-0001-8712-0440en_UK
local.rioxx.authorTocher, Douglas R|0000-0002-8603-9410en_UK
local.rioxx.authorYou, Cuihong|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2019-09-12en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved||2019-09-11en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/all-rights-reserved|2019-09-12|en_UK
local.rioxx.filenameLi et al Manuscript -final accepted.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1436-2236en_UK
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