Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/151827
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dc.contributor.authorDuran, Bruno Oliveira da Silva-
dc.contributor.authorDal-Pai-Silva, Maeli-
dc.contributor.authorGarcía de la Serrana Castillo, Daniel-
dc.date.accessioned2020-03-03T15:20:22Z-
dc.date.available2020-12-23T06:10:17Z-
dc.date.issued2019-12-23-
dc.identifier.issn0022-0949-
dc.identifier.urihttp://hdl.handle.net/2445/151827-
dc.description.abstractMuscle fibres are classified as fast, intermediate and slow. In vitro myoblast cell culture model from fast muscle is a very useful tool to study muscle growth and development; however, similar models for slow muscle do not exist. Owing to the compartmentalization of fish muscle fibres, we have developed a slow myoblast cell culture for rainbow trout (Oncorhynchus mykiss). Slow and fast muscle-derived myoblasts have similar morphology, but with differential expression of slow muscle markers such as slow myhc, sox6 and pgc-1α. We also characterized the mir-133 and mir-499 microRNA families in trout slow and fast myoblasts as a case study during myogenesis and in response to electrostimulation. Three mir-133 (a-1a, a-1b and a-2) and four mir-499 (aa, ab, ba and bb) paralogues were identified for rainbow trout and named base on their phylogenetic relationship to zebrafish and Atlantic salmon orthologues. Omy-mir-499ab and omy-mir-499bb had 0.6 and 0.5-fold higher expression in slow myoblasts compared with fast myoblasts, whereas mir-133 duplicates had similar levels in both phenotypes and little variation during development. Slow myoblasts also showed increased expression for omy-mir-499b paralogues in response to chronic electrostimulation (7-fold increase for omy-mir-499ba and 2.5-fold increase for omy-mir-499bb). The higher expression of mir-499 paralogues in slow myoblasts suggests a role in phenotype determination, while the lack of significant differences of mir-133 copies during culture development might indicate a different role in fish compared with mammals. We have also found signs of sub-functionalization of mir-499 paralogues after electrostimulation, with omy-mir-499b copies more responsive to electrical signals.-
dc.format.extent12 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherThe Company of Biologists-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1242/jeb.216390-
dc.relation.ispartofJournal of Experimental Biology, 2019, vol. 223, p. 216390-
dc.relation.urihttps://doi.org/10.1242/jeb.216390-
dc.rights(c) The Company of Biologists, 2019-
dc.sourceArticles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)-
dc.subject.classificationEsquelet humà-
dc.subject.classificationFibres-
dc.subject.classificationMúsculs-
dc.subject.otherHuman skeleton-
dc.subject.otherFibers-
dc.subject.otherMuscles-
dc.titleRainbow trout slow myoblast cell culture as a model to study slow skeletal muscle and the characterization of mir-133 and mir-499 families as a case study-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec694842-
dc.date.updated2020-03-03T15:20:23Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)

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