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Registro Completo |
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Biblioteca(s): |
Embrapa Agrobiologia; Embrapa Agropecuária Oeste; Embrapa Unidades Centrais. |
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Data corrente: |
04/06/2003 |
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Data da última atualização: |
12/01/2010 |
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Autoria: |
GUERRA, J. G. M.; ALMEIDA, D. L. de; FERNANDES, M. S.; SOUTO, S. M. |
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Título: |
Variação estacional de Brachiaria decumbens sob adubação com fontes de fósforo |
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Ano de publicação: |
1998 |
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Fonte/Imprenta: |
Seropédica: EMBRAPA-CNPAB, 1998. |
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Páginas: |
7 p. |
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Série: |
(EMBRAPA-CNPAB. Comunicado Técnico, 26). |
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ISSN: |
0104-8945 |
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Idioma: |
Português |
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Palavras-Chave: |
P; Variação estacional. |
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Thesagro: |
Adubação; Brachiaria Decumbens; Capim Brachiaria; Fertilizante; Fósforo; Pastagem; Rocha Fosfatada; Variação Sazonal. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/CNPAB-2010/27152/1/cot026.pdf
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Marc: |
LEADER 00804nam a2200289 a 4500
001 1623695
005 2010-01-12
008 1998 bl uuuu u0uu1 u #d
022 $a0104-8945
100 1 $aGUERRA, J. G. M.
245 $aVariação estacional de Brachiaria decumbens sob adubação com fontes de fósforo
260 $aSeropédica: EMBRAPA-CNPAB$c1998
300 $a7 p.
490 $a(EMBRAPA-CNPAB. Comunicado Técnico, 26).
650 $aAdubação
650 $aBrachiaria Decumbens
650 $aCapim Brachiaria
650 $aFertilizante
650 $aFósforo
650 $aPastagem
650 $aRocha Fosfatada
650 $aVariação Sazonal
653 $aP
653 $aVariação estacional
700 1 $aALMEIDA, D. L. de
700 1 $aFERNANDES, M. S.
700 1 $aSOUTO, S. M.
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Registro original: |
Embrapa Agrobiologia (CNPAB) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Pecuária Sudeste. Para informações adicionais entre em contato com cppse.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Pecuária Sudeste. |
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Data corrente: |
23/08/2012 |
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Data da última atualização: |
22/02/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
B - 2 |
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Autoria: |
SARAIVA, N. Z.; OLIVEIRA, C. S.; TETZNER, T. A. D.; LIMA, M. R. de; MELO, D. S. de; NICIURA, S. C. M.; GARCIA, J. M. |
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Afiliação: |
NAIARA ZOCCAL SARAIVA, Universidade Estadual Paulista; CLARA SLADE OLIVEIRA, UNESP; TATIANE ALMEIDA DRUMMOND TETZNER, UNESP; MARINA RAGAGNIN DE LIMA, UNESP/JABOTICABAL; DANILAS SALINET DE MELO, UNESP/JABOTICABAL; SIMONE CRISTINA MEO NICIURA, CPPSE; JOAQUIM MANSANO GARCIA, UNESP/JABOTICABAL. |
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Título: |
Chemically assisted enucleation results in higher G6PD expression in early bovine female embryos obtained by somatic cell nuclear transfer. |
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Ano de publicação: |
2012 |
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Fonte/Imprenta: |
Cellular Reprogramming, v. 14, n. 5, p. 1-11, 2012. |
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DOI: |
10.1089/cell.2011.0077 |
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Idioma: |
Inglês |
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Conteúdo: |
Despite extensive efforts, low efficiency is still an issue in bovine somatic cell nuclear transfer (SCNT). The hypothesis of our study was that the use of cytoplasts produced by chemically assisted enucleation (EN) would improve nuclear reprogramming in nuclear transfer (NT)?derived embryos because it results in lower damage and higher cytoplasm content than conventional EN. For that purpose, we investigated the expression of two X-linked genes: X inactive-specific transcript (XIST) and glucose 6-phosphate dehydrogenase (G6PD). In the first experiment, gene expression was assessed in day-7 female blastocysts from embryonic cell NT (ECNT) groups [conventional, ECNT conv; chemically assisted, ECNT deme (demecolcine)]. Where as in the ECNT conv group, only one embryo (25%; n = 4) expressed XIST transcripts, most embryos showed XIST expression (75%; n = 4) in the ECNT deme group. However, no significant differences in transcript abundance of XIST and G6PD were found when comparing the embryos from all groups. In a second experiment using somatic cells as nuclear donors, we evaluated gene expression profiles in female SCNT-derived embryos. No significant differences in relative abundance (RA) of XIST transcripts were observed among the groups. Nonetheless, higher ( p < 0.05) levels of G6PD were observed in SCNT deme and in vitro?derived groups in comparison to SCNT conv. To know whether higher G6PD expression in embryos derived from SCNT chemically assisted EN indicates higher metabolism in embryos considered of superior quality or if the presence of higher reactive oxygen species (ROS) levels generated by the increased oxygen consumption triggers G6PD activation, the expression of genes related to stress response should be investigated in embryos produced by that technique. MenosDespite extensive efforts, low efficiency is still an issue in bovine somatic cell nuclear transfer (SCNT). The hypothesis of our study was that the use of cytoplasts produced by chemically assisted enucleation (EN) would improve nuclear reprogramming in nuclear transfer (NT)?derived embryos because it results in lower damage and higher cytoplasm content than conventional EN. For that purpose, we investigated the expression of two X-linked genes: X inactive-specific transcript (XIST) and glucose 6-phosphate dehydrogenase (G6PD). In the first experiment, gene expression was assessed in day-7 female blastocysts from embryonic cell NT (ECNT) groups [conventional, ECNT conv; chemically assisted, ECNT deme (demecolcine)]. Where as in the ECNT conv group, only one embryo (25%; n = 4) expressed XIST transcripts, most embryos showed XIST expression (75%; n = 4) in the ECNT deme group. However, no significant differences in transcript abundance of XIST and G6PD were found when comparing the embryos from all groups. In a second experiment using somatic cells as nuclear donors, we evaluated gene expression profiles in female SCNT-derived embryos. No significant differences in relative abundance (RA) of XIST transcripts were observed among the groups. Nonetheless, higher ( p < 0.05) levels of G6PD were observed in SCNT deme and in vitro?derived groups in comparison to SCNT conv. To know whether higher G6PD expression in embryos derived from SCNT chemically assisted EN indicates higher m... Mostrar Tudo |
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Palavras-Chave: |
Higher G6PD; Nuclear transfer; Somatic cell. |
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Categoria do assunto: |
G Melhoramento Genético |
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Marc: |
LEADER 02567naa a2200241 a 4500
001 1932049
005 2023-02-22
008 2012 bl uuuu u00u1 u #d
024 7 $a10.1089/cell.2011.0077$2DOI
100 1 $aSARAIVA, N. Z.
245 $aChemically assisted enucleation results in higher G6PD expression in early bovine female embryos obtained by somatic cell nuclear transfer.$h[electronic resource]
260 $c2012
520 $aDespite extensive efforts, low efficiency is still an issue in bovine somatic cell nuclear transfer (SCNT). The hypothesis of our study was that the use of cytoplasts produced by chemically assisted enucleation (EN) would improve nuclear reprogramming in nuclear transfer (NT)?derived embryos because it results in lower damage and higher cytoplasm content than conventional EN. For that purpose, we investigated the expression of two X-linked genes: X inactive-specific transcript (XIST) and glucose 6-phosphate dehydrogenase (G6PD). In the first experiment, gene expression was assessed in day-7 female blastocysts from embryonic cell NT (ECNT) groups [conventional, ECNT conv; chemically assisted, ECNT deme (demecolcine)]. Where as in the ECNT conv group, only one embryo (25%; n = 4) expressed XIST transcripts, most embryos showed XIST expression (75%; n = 4) in the ECNT deme group. However, no significant differences in transcript abundance of XIST and G6PD were found when comparing the embryos from all groups. In a second experiment using somatic cells as nuclear donors, we evaluated gene expression profiles in female SCNT-derived embryos. No significant differences in relative abundance (RA) of XIST transcripts were observed among the groups. Nonetheless, higher ( p < 0.05) levels of G6PD were observed in SCNT deme and in vitro?derived groups in comparison to SCNT conv. To know whether higher G6PD expression in embryos derived from SCNT chemically assisted EN indicates higher metabolism in embryos considered of superior quality or if the presence of higher reactive oxygen species (ROS) levels generated by the increased oxygen consumption triggers G6PD activation, the expression of genes related to stress response should be investigated in embryos produced by that technique.
653 $aHigher G6PD
653 $aNuclear transfer
653 $aSomatic cell
700 1 $aOLIVEIRA, C. S.
700 1 $aTETZNER, T. A. D.
700 1 $aLIMA, M. R. de
700 1 $aMELO, D. S. de
700 1 $aNICIURA, S. C. M.
700 1 $aGARCIA, J. M.
773 $tCellular Reprogramming$gv. 14, n. 5, p. 1-11, 2012.
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