dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorOliveira, Clara S.
dc.creatorSaraiva, Naiara Z.
dc.creatorde Souza, Marcela M.
dc.creatorTetzner, Tatiane A. D.
dc.creatorde Lima, Marina R.
dc.creatorGarcia, Joaquim Mansano
dc.date2014-05-20T15:30:27Z
dc.date2016-10-25T18:05:58Z
dc.date2014-05-20T15:30:27Z
dc.date2016-10-25T18:05:58Z
dc.date2010-01-01
dc.date.accessioned2017-04-06T00:17:05Z
dc.date.available2017-04-06T00:17:05Z
dc.identifierReproduction Fertility and Development. Collingwood: Csiro Publishing, v. 22, n. 6, p. 1041-1048, 2010.
dc.identifier1031-3613
dc.identifierhttp://hdl.handle.net/11449/39827
dc.identifierhttp://acervodigital.unesp.br/handle/11449/39827
dc.identifier10.1071/RD09238
dc.identifierWOS:000279384100016
dc.identifierhttp://dx.doi.org/10.1071/RD09238
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/882671
dc.descriptionTrichostatin A (TSA) induces histone hyperacetylation by inhibiting histone deacetylases and consequently increasing gene expression. The hypothesis was that TSA supplementation during the in vitro culture (IVC) of bovine embryos would increase the blastocyst rate, particularly in low-quality and female embryos. Oocytes were fertilised separately with X and Y spermatozoa and, 70 h after IVF, the IVC medium was supplemented with 5 nM and 15 nM TSA for 48 or 144 h. Incubation of female embryos with 5 nM and 15 nM TSA resulted in similar increases in acetylated histone H3K9 levels. However, to see comparable effects on acetylated histone H3K9 levels in male embryos, the culture medium needed to be supplemented with 15 nM TSA (as opposed to 5 nM TSA for female embryos). Treatment of male and female embryos with 5 nM TSA for 48 h or female embryos with 5 nM for 144 h had no effect on blastocyst rates, although 15 nM TSA compromised embryonic development. The terminal deoxyribonucleotidyl transferase-mediated dUTP-digoxigenin nick end-labelling (TUNEL) assay revealed increased apoptosis in female embryos treated with 5 nM TSA for 144 h, as well as in male and female embryos treated with 15 nM TSA for 48 h, but this increase in apoptosis was not observed in low-quality embryos. The results of the present study suggest that TSA treatment promotes histone hyperacetylation, but has no beneficial effects on the in vitro production of male and female bovine embryos during preimplantation development.
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.languageeng
dc.publisherCSIRO Publishing
dc.relationReproduction, Fertility and Development
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectEpigenetics
dc.subjecthistone deacetylase inhibition
dc.subjecthistone H3 lys9 acetylation
dc.subjectimmunocytochemistry
dc.subjecttrichostatin A
dc.subjectTUNEL assay
dc.titleEffects of histone hyperacetylation on the preimplantation development of male and female bovine embryos
dc.typeOtro


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