dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorSchool of Biology
dc.contributorPhysiology and Immunology
dc.date.accessioned2020-12-12T01:13:39Z
dc.date.accessioned2022-12-19T20:41:16Z
dc.date.available2020-12-12T01:13:39Z
dc.date.available2022-12-19T20:41:16Z
dc.date.created2020-12-12T01:13:39Z
dc.date.issued2020-01-01
dc.identifierJournal of Experimental Biology, v. 223, n. 2, 2020.
dc.identifier0022-0949
dc.identifierhttp://hdl.handle.net/11449/198465
dc.identifier10.1242/jeb.216390
dc.identifier2-s2.0-85078692026
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5379099
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 omymir-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.languageeng
dc.relationJournal of Experimental Biology
dc.sourceScopus
dc.subjectCell culture
dc.subjectElectrostimulation
dc.subjectMiRNA
dc.subjectMyoblasts
dc.subjectSlow skeletal muscle
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.typeArtículos de revistas


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