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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/132327
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dc.contributor.authorPerecin, F.-
dc.contributor.authorMéo, S. C.-
dc.contributor.authorYamazaki, W.-
dc.contributor.authorFerreira, C. R.-
dc.contributor.authorMerighe, G. K F-
dc.contributor.authorMeirelles, F. V.-
dc.contributor.authorGarcia, J. M.-
dc.date.accessioned2014-05-27T11:23:55Z-
dc.date.accessioned2016-10-25T21:25:34Z-
dc.date.available2014-05-27T11:23:55Z-
dc.date.available2016-10-25T21:25:34Z-
dc.date.issued2009-06-15-
dc.identifierhttp://dx.doi.org/10.4238/vol8-1gmr541-
dc.identifier.citationGenetics and Molecular Research, v. 8, n. 1, p. 76-85, 2009.-
dc.identifier.issn1676-5680-
dc.identifier.urihttp://hdl.handle.net/11449/132327-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/132327-
dc.description.abstractCloning by nuclear transfer is often associated with poor results due to abnormal nuclear reprogramming of somatic donor cells and altered gene expression patterns. We investigated the expression patterns of imprinted genes IGF2 and IGF2R in 33- to 36-day bovine embryos and chorio-allantoic membranes derived from in vivo- and in vitro-produced embryos by somatic cell nuclear transfer (SCNT), parthenogenetic activation, and in vitro fertilization (IVF). There was a lower IGF2 expression rate in the SCNT (0.19) and parthenogenetic (0.02) groups when compared to in vivo and IVF embryos (2.01; P<0.05). In the chorio-allantoic membranes, IGF2 showed a baseline expression pattern (P<0.05) in parthenotes (0.001) when compared to in vivo, IVF (3.13), and SCNT (0.98) groups. IGF2R was less expressed (P<0.05) in SCNT chorio-allantoic membranes (0.25) when compared to the in vivo group. The low expression of IGF2 in parthenogenetic embryos and chorio-allantoic membranes confirms its imprinted status in cattle. Alterations in the relative frequency of IGF2 and IGF2R transcripts were observed in SCNT-derived bovine embryos and chorio- allantoic membranes, respectively, supporting the hypothesis that abnormalities in the expression of imprinted genes are causes of the low efficiency of SCNT procedures in this species.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent76-85-
dc.language.isoeng-
dc.publisherFunpec-editora-
dc.sourceScopus-
dc.subjectCattle-
dc.subjectEpigenetics-
dc.subjectF2-
dc.subjectG-
dc.subjectGenomic imprinting-
dc.subjectI-
dc.subjectIGF2-
dc.subjectNuclear transfer-
dc.subjectR-
dc.subjectGlyceraldehyde 3 phosphate dehydrogenase-
dc.subjectGrowth factor receptor-
dc.subjectMessenger RNA-
dc.subjectSomatomedin A-
dc.subjectSomatomedin a receptor-
dc.subjectUnclassified drug-
dc.subjectSomatomedin B-
dc.subjectSomatomedin B receptor-
dc.subjectAnimal cell-
dc.subjectAnimal experiment-
dc.subjectAnimal tissue-
dc.subjectCell nucleus transplantation-
dc.subjectChorioallantois-
dc.subjectControlled study-
dc.subjectCow-
dc.subjectEmbryo-
dc.subjectFemale-
dc.subjectFertilization in vitro-
dc.subjectGene activation-
dc.subjectGene expression-
dc.subjectGene frequency-
dc.subjectGenetic transcription-
dc.subjectGenome imprinting-
dc.subjectIn vitro study-
dc.subjectIn vivo study-
dc.subjectNonhuman-
dc.subjectNucleotide sequence-
dc.subjectSomatic cell-
dc.subjectAnimal-
dc.subjectAnimal embryo-
dc.subjectCattle-
dc.subjectGenetics-
dc.subjectMale-
dc.subjectMetabolism-
dc.subjectParthenogenesis-
dc.subjectBos-
dc.subjectBovinae-
dc.subjectAnimals-
dc.subjectChorioallantoic Membrane-
dc.subjectEmbryo, Mammalian-
dc.subjectFemale-
dc.subjectFertilization in Vitro-
dc.subjectGene Expression-
dc.subjectGenomic Imprinting-
dc.subjectInsulin-Like Growth Factor II-
dc.subjectMale-
dc.subjectNuclear Transfer Techniques-
dc.subjectParthenogenesis-
dc.subjectReceptor, IGF Type 2-
dc.titleImprinted gene expression in in vivo- And in vi/ro-produced bovine embryos and chorio-allantoic membranesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)-
dc.description.affiliationDepartamento de Medicina Veterinária Preventiva e Reprodução Animal Faculdade de Ciências Agrárias e Veterinárias Universidade Estadual Paulista, Jaboticabal, SP-
dc.description.affiliationDepartamento de Ciências Básicas Faculdade de Zootecnia e Engenharia de Alimentos Universidade de São Paulo, Pirassununga, SP-
dc.description.affiliationEmbrapa Pecuária Sudeste, Sao Carlos, SP-
dc.description.affiliationDepartamento de Medicina Veterinaria Preventiva e Reproducao Animal Faculdade de Ciencias Agrarias e Veterinarias Universidade Estadual Paulista, Jaboticabal, SP-
dc.description.affiliationUnespDepartamento de Medicina Veterinária Preventiva e Reprodução Animal Faculdade de Ciências Agrárias e Veterinárias Universidade Estadual Paulista, Jaboticabal, SP-
dc.description.affiliationUnespDepartamento de Medicina Veterinaria Preventiva e Reproducao Animal Faculdade de Ciencias Agrarias e Veterinarias Universidade Estadual Paulista, Jaboticabal, SP-
dc.identifier.doi10.4238/vol8-1gmr541-
dc.identifier.wosWOS:000265578600009-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-66349090503.pdf-
dc.relation.ispartofGenetics and Molecular Research-
dc.identifier.scopus2-s2.0-66349090503-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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