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 | Acesso ao texto completo restrito à biblioteca da Embrapa Gado de Leite. Para informações adicionais entre em contato com cnpgl.biblioteca@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Gado de Leite. |
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Data corrente: |
05/02/2014 |
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Data da última atualização: |
05/02/2024 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
OLIVEIRA, C. S.; SARAIVA, N. Z.; CRUZ, M. H. C.; MAZETI, B.; OLIVEIRA, L. Z.; LOPES, F. L.; GARCIA, J. M. |
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Afiliação: |
CLARA SLADE OLIVEIRA, CNPGL; NAIARA ZOCCAL SARAIVA, UNESP; MARIA HELENA COELHO CRUZ, UNESP; BRUNA MAZETI, UNESP; LETICIA ZOCCOLARO OLIVEIRA, UNESP; FLAVIA LOMBARDI LOPES, UNESP; JOAQUIM MANSANO GARCIA, UNESP. |
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Título: |
HDAC inhibition decreases XIST expression on female IVP bovine blastocysts. |
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Ano de publicação: |
2013 |
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Fonte/Imprenta: |
Reproduction, v. 145, n. 1, p. 9-17, 2013. |
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DOI: |
https://doi.org/10.1530/rep-11-0343 |
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Idioma: |
Inglês |
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Conteúdo: |
During initial development, both X chromosomes are active in females, and one of them must be silenced at the appropriate time in order to dosage compensate their gene expression levels to male counterparts. Silencing involves epigenetic mechanisms, including histone deacetylation. Major X chromosome inactivation (XCI) in bovine occurs between hatching and implantation, although in vitro culture conditions might disrupt the silencing process, increasing or decreasing X-linked gene expression. In this study, we aimed to address the roles of histone deacetylase inhibition by trichostatin A (TSA) on female preimplantation development. We tested the hypothesis that by enhancing histone acetylation, TSA would increase the percentage of embryos achieving 16-cell stage, reducing percentage of embryos blocked at 8-cell stage, and interfere with XCI in IVF embryos. We noticed that after TSA treatment, acetylation levels in individual blastomeres of 8-16 cell embryos were increased twofold on treated embryos, and the same was detected for blastocysts. Changes among blastomere levels within the same embryo were diminished on TSA group, as low-acetylated blastomeres were no longer detected. The percentage of embryos that reached the 5th cleavage cycle 118 h after IVF, analyzed by Hoechst staining, remained unaltered after TSA treatment. Then, we assessed XIST and G6PD expression in individual female bovine blastocysts by quantitative real-time PCR. Even though G6PD expression remained unaltered after TSA exposure, XIST expression was eightfold decreased, and we also detected a major decrease in the percentage of blastocysts expressing detectable XIST levels after TSA treatment. Based on these results, we conclude that HDAC is involved on XCI process in bovine embryos, and its inhibition might delay X chromosome silencing and attenuate aberrant XIST expression described for IVF embryos. MenosDuring initial development, both X chromosomes are active in females, and one of them must be silenced at the appropriate time in order to dosage compensate their gene expression levels to male counterparts. Silencing involves epigenetic mechanisms, including histone deacetylation. Major X chromosome inactivation (XCI) in bovine occurs between hatching and implantation, although in vitro culture conditions might disrupt the silencing process, increasing or decreasing X-linked gene expression. In this study, we aimed to address the roles of histone deacetylase inhibition by trichostatin A (TSA) on female preimplantation development. We tested the hypothesis that by enhancing histone acetylation, TSA would increase the percentage of embryos achieving 16-cell stage, reducing percentage of embryos blocked at 8-cell stage, and interfere with XCI in IVF embryos. We noticed that after TSA treatment, acetylation levels in individual blastomeres of 8-16 cell embryos were increased twofold on treated embryos, and the same was detected for blastocysts. Changes among blastomere levels within the same embryo were diminished on TSA group, as low-acetylated blastomeres were no longer detected. The percentage of embryos that reached the 5th cleavage cycle 118 h after IVF, analyzed by Hoechst staining, remained unaltered after TSA treatment. Then, we assessed XIST and G6PD expression in individual female bovine blastocysts by quantitative real-time PCR. Even though G6PD expression remained u... Mostrar Tudo |
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Palavras-Chave: |
Cultured Female Fertilization; Drug effects. |
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Thesaurus Nal: |
Blastocyst; Embryology; Metabolism. |
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Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
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Marc: |
LEADER 02665naa a2200265 a 4500
001 1978655
005 2024-02-05
008 2013 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1530/rep-11-0343$2DOI
100 1 $aOLIVEIRA, C. S.
245 $aHDAC inhibition decreases XIST expression on female IVP bovine blastocysts.$h[electronic resource]
260 $c2013
520 $aDuring initial development, both X chromosomes are active in females, and one of them must be silenced at the appropriate time in order to dosage compensate their gene expression levels to male counterparts. Silencing involves epigenetic mechanisms, including histone deacetylation. Major X chromosome inactivation (XCI) in bovine occurs between hatching and implantation, although in vitro culture conditions might disrupt the silencing process, increasing or decreasing X-linked gene expression. In this study, we aimed to address the roles of histone deacetylase inhibition by trichostatin A (TSA) on female preimplantation development. We tested the hypothesis that by enhancing histone acetylation, TSA would increase the percentage of embryos achieving 16-cell stage, reducing percentage of embryos blocked at 8-cell stage, and interfere with XCI in IVF embryos. We noticed that after TSA treatment, acetylation levels in individual blastomeres of 8-16 cell embryos were increased twofold on treated embryos, and the same was detected for blastocysts. Changes among blastomere levels within the same embryo were diminished on TSA group, as low-acetylated blastomeres were no longer detected. The percentage of embryos that reached the 5th cleavage cycle 118 h after IVF, analyzed by Hoechst staining, remained unaltered after TSA treatment. Then, we assessed XIST and G6PD expression in individual female bovine blastocysts by quantitative real-time PCR. Even though G6PD expression remained unaltered after TSA exposure, XIST expression was eightfold decreased, and we also detected a major decrease in the percentage of blastocysts expressing detectable XIST levels after TSA treatment. Based on these results, we conclude that HDAC is involved on XCI process in bovine embryos, and its inhibition might delay X chromosome silencing and attenuate aberrant XIST expression described for IVF embryos.
650 $aBlastocyst
650 $aEmbryology
650 $aMetabolism
653 $aCultured Female Fertilization
653 $aDrug effects
700 1 $aSARAIVA, N. Z.
700 1 $aCRUZ, M. H. C.
700 1 $aMAZETI, B.
700 1 $aOLIVEIRA, L. Z.
700 1 $aLOPES, F. L.
700 1 $aGARCIA, J. M.
773 $tReproduction$gv. 145, n. 1, p. 9-17, 2013.
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| 6. |  | AVILA, A. C. de; HAAN, P. de; KITAJIMA, E. W.; RESENDE, R. de O.; GOLDBACH, R. W.; PETERS, D. Characterization of a distinct isolate of tomato spotted wilt virus (TSWV) from impatiens in the Netherlands. Fitopatologia Brasileira, Brasilia, v.16, n.2, p.25, jun. 1991. Resumo.| Biblioteca(s): Embrapa Hortaliças. |
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| 7. | | AVILA, A. C. de; HAAN, P. de; SMEETS, M. L. L.; RESENDE, R. de O.; KORMELINK, R.; KITAJIMA, E. W.; GOLDBACH, R. W.; PETERS, D. Distinct levels of relationship between tospovirus isolates. Archives of Virology, v. 128, p. 211-227, 1993.| Biblioteca(s): Embrapa Hortaliças. |
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| 8. | | AVILA, A. C. de; HAAN, de P.; KITAJIMA, E. W.; KORMELINK, R.; RESENDE R. de O.; GOLDBACH, R. W.; PETERS, D. Characterization of a distinct isolate of tomato spotted wilt virus (TSWV) from impatiens sp. in the Netherlands. Phytopathology, v. 134, n. 2, p. 133-151, 1992.| Biblioteca(s): Embrapa Hortaliças. |
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| 9. | | AVILA, A. C. de; HAAN, P. de; KORMELINK, R.; RESENDE, R. de O.; POELWIJK, F. van; WIJKAMP, I.; GOLDBACH, R. W.; PETERS, D. Tomato spotted wilt virus: genne structure, classification, detection and genetically engineered resistance. In: RISHI, N.; AHUJA, K.L.; SINGH, B.P., (Ed.). Virology in the tropics. New Delhi: Malhotra Publishing House, 1994. p. 95-105.| Biblioteca(s): Embrapa Hortaliças. |
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