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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/17128
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dc.contributor.authorAlves de Almeida, Fernanda Losi-
dc.contributor.authorCarvalho, Robson Francisco-
dc.contributor.authorPinhal, Danillo-
dc.contributor.authorPadovani, Carlos Roberto-
dc.contributor.authorMartins, Cesar-
dc.contributor.authorDal Pai-Silva, Maeli-
dc.date.accessioned2014-05-20T13:48:03Z-
dc.date.accessioned2016-10-25T17:01:07Z-
dc.date.available2014-05-20T13:48:03Z-
dc.date.available2016-10-25T17:01:07Z-
dc.date.issued2008-12-01-
dc.identifierhttp://dx.doi.org/10.1016/j.micron.2008.02.011-
dc.identifier.citationMicron. Oxford: Pergamon-Elsevier B.V. Ltd, v. 39, n. 8, p. 1306-1311, 2008.-
dc.identifier.issn0968-4328-
dc.identifier.urihttp://hdl.handle.net/11449/17128-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/17128-
dc.description.abstractSkeletal muscle is the edible part of the fish. It grows by hypertrophy and hyperplasia, events regulated by differential expression of myogenic regulatory factors (MRFs). The study of muscle growth mechanisms in fish is very important in fish farming development. Pacu (Piaractus mesopotamicus) is one of the most important food species farmed in Brazil and has been extensively used in Brazilian aquaculture programs. The aim of this study was to analyze hyperplasia and hypertrophy and the MRF MyoD expression pattern in skeletal muscle of pacu (P. mesopotamicus) during juvenile and adult growth stages. Juvenile (n = 5) and adult (n = 5) fish were anaesthetized, sacrificed, and weight (g) and total length (cm) determined. White dorsal region muscle samples were collected and immersed in liquid nitrogen. Transverse sections (10 mu m thick) were stained with Haematoxilin-Eosin (HE) for morphological and morphometric analysis. Smallest fiber diameter from 100 muscle fibers per animal was calculated in each growth phase. These fibers were grouped into three classes (<20, 20-50, and >50 mu m) to evaluate hypertrophy and hyperplasia in white skeletal muscle. MyoD gene expression was determined by semi-quantitative RTPCR. PCR products were cloned and sequenced. juvenile and adult pacu skeletal muscle had similar morphology. The large number of <20 mu m diameter muscle fibers observed in juvenile fish confirms active hyperplasia. In adult fish, most fibers were over 50 mu m diameter and denote more intense muscle fiber hypertrophy. The MyoD mRNA level in juveniles was higher than in adults. A consensus partial sequence for MyoD gene (338 base pairs) was obtained. The Pacu MyoD nucleotide sequence displayed high similarity among several vertebrates, including teleosts. The differential MyoD gene expression observed in pacu white muscle is possibly related to differences in growth patterns during the phases analyzed, with hyperplasia predominant in juveniles and hypertrophy in adult fish. These results should provide a foundation for understanding the molecular control of skeletal muscle growth in economically important Brazilian species, with a view to improving production quality. (C) 2008 Elsevier Ltd. All rights reserved.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent1306-1311-
dc.language.isoeng-
dc.publisherPergamon-Elsevier B.V. Ltd-
dc.sourceWeb of Science-
dc.subjectFishen
dc.subjectSkeletal muscle growthen
dc.subjectHyperplasiaen
dc.subjectHypertrophyen
dc.subjectSemi-quantitative RT-PCRen
dc.titleDifferential expression of myogenic regulatory factor MyoD in pacu skeletal muscle (Piaractus mesopotamicus Holmberg 1887: Serrasalminae, Characidae, Teleostei) during juvenile and adult growth phasesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.description.affiliationUniv Estadual Paulista, Inst Biosci, Dept Morphol, BR-18618000 São Paulo, Brazil-
dc.description.affiliationUniv Estadual Campinas, Dept Cellular Biol, Inst Biol, BR-13084971 São Paulo, Brazil-
dc.description.affiliationUNESP, Dept Biostat, BR-18618000 Botucatu, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biosci, Dept Morphol, BR-18618000 São Paulo, Brazil-
dc.description.affiliationUnespUNESP, Dept Biostat, BR-18618000 Botucatu, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 04/12756-3-
dc.description.sponsorshipIdFAPESP: 05/56587-3-
dc.identifier.doi10.1016/j.micron.2008.02.011-
dc.identifier.wosWOS:000260873600035-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofMicron-
dc.identifier.orcid0000-0002-4901-7714pt
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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