Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/28735
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dc.contributor.authorJin, Ye Hwaen_UK
dc.contributor.authorDavie, Andrewen_UK
dc.contributor.authorMigaud, Herveen_UK
dc.date.accessioned2019-02-12T01:01:26Z-
dc.date.available2019-02-12T01:01:26Z-
dc.date.issued2019-03-10en_UK
dc.identifier.urihttp://hdl.handle.net/1893/28735-
dc.description.abstractPrimordial germ cells (PGCs) are specified by maternally provided determinants in fish. PGCs migrate then into prospective gonadal sites during early development and give rise to germ cell lineage. PGC disrupted animals do not sexually mature which has a range of commercial as well as environmental benefits. To find potential target genes for sterilisation of Nile tilapia, relative mRNA abundance patterns and tissue distribution of four nanos, two piwil, dnd1, vasa and three pum genes were investigated during ontogenic development from unfertilised eggs to newly hatched larvae and in adult tissues, respectively. The ontogenic pattern of RNA abundance revealed that all the investigated gene transcripts are maternally deposited to varying degrees, except for nanos2 which is not expressed in eggs. The ontogenic patterns of relative RNA abundance could be grouped into three categories. The first one, including nanos3, piwil1, piwil2, dnd1 and vasa, showed abundant transcript levels during early developmental stages which are then degraded during the period of maternal to zygotic transition between blastula and gastrula stages with a reduction in expression of four to five orders of magnitude by hatching stage. Another, including pum2 and pum3, showed similar patterns to the first group, but the transcript levels are reduced by only two orders of magnitude. The third group, including nanos1a, nanos1b and pum1, was characterised by a zygotic increase. nanos2 had no detectable transcripts until hatching stage. The tissue screening of nanos1a, nanos1b, pum1, pum2 and pum3 showed that they are expressed in various tissues, implying their potential pleiotropic effects in these tissues apart from gonads. In contrast, nanos3, piwil1, piwil2, dnd1 and vasa appeared to be exclusively expressed in gonads (both ovary and testis), and nanos2 showed testis-specific expression. Based on these results nanos3, piwil1, piwil2, dnd1 and vasa were prioritised among the 11 selected genes as potential target genes for sterilisation in Nile tilapia as they have no significant zygotic expression during embryogenesis, they are expressed exclusively in gonads and maternally deposited. These features suggest a potential role of these genes in the specification and maintenance of PGCs during the ontogenic development of Nile tilapia.en_UK
dc.language.isoenen_UK
dc.publisherElsevieren_UK
dc.relationJin YH, Davie A & Migaud H (2019) Expression pattern of nanos, piwil, dnd, vasa and pum genes during ontogenic development in Nile tilapia Oreochromis niloticus. Gene, 688, pp. 62-70. https://doi.org/10.1016/j.gene.2018.11.078en_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. Accepted refereed manuscript of: Jin YH, Davie A & Migaud H (2019) Expression pattern of nanos, piwil, dnd, vasa and pum genes during ontogenic development in Nile tilapia Oreochromis niloticus. Gene, 688, pp. 62-70. DOI: https://doi.org/10.1016/j.gene.2018.11.078 © 2018, Elsevier. Licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/en_UK
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_UK
dc.subjectPrimordial germ cellsen_UK
dc.subjectMaternal transcriptsen_UK
dc.subjectMaternal to zygotic transitionen_UK
dc.subjectEarly developmenten_UK
dc.titleExpression pattern of nanos, piwil, dnd, vasa and pum genes during ontogenic development in Nile tilapia Oreochromis niloticusen_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate2019-12-01en_UK
dc.rights.embargoreason[GENE-D-18-00838_revision_29_08_18_Not_highlighted11.pdf] Publisher requires embargo of 12 months after formal publication.en_UK
dc.identifier.doi10.1016/j.gene.2018.11.078en_UK
dc.identifier.pmid30503393en_UK
dc.citation.jtitleGeneen_UK
dc.citation.issn0378-1119en_UK
dc.citation.volume688en_UK
dc.citation.spage62en_UK
dc.citation.epage70en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusAM - Accepted Manuscripten_UK
dc.author.emailherve.migaud@stir.ac.uken_UK
dc.citation.date30/11/2018en_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.identifier.isiWOS:000457662200009en_UK
dc.identifier.scopusid2-s2.0-85057757359en_UK
dc.identifier.wtid1079234en_UK
dc.contributor.orcid0000-0002-9524-618Xen_UK
dc.contributor.orcid0000-0002-5404-7512en_UK
dc.date.accepted2018-11-22en_UK
dcterms.dateAccepted2018-11-22en_UK
dc.date.filedepositdate2019-02-11en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionAMen_UK
local.rioxx.authorJin, Ye Hwa|en_UK
local.rioxx.authorDavie, Andrew|0000-0002-9524-618Xen_UK
local.rioxx.authorMigaud, Herve|0000-0002-5404-7512en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2019-12-01en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved||2019-11-30en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by-nc-nd/4.0/|2019-12-01|en_UK
local.rioxx.filenameGENE-D-18-00838_revision_29_08_18_Not_highlighted11.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source0378-1119en_UK
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