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 | Acesso ao texto completo restrito à biblioteca da Embrapa Gado de Corte. Para informações adicionais entre em contato com cnpgc.biblioteca@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Gado de Corte. |
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Data corrente: |
10/07/2009 |
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Data da última atualização: |
25/07/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
BOLDRINI, K. R.; PAGLIARINI, M. S.; VALLE, C. B. do. |
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Afiliação: |
KELLEN REGINA BOLDRINI, UNIVERSIDADE ESTADUAL DE MARINGÁ; MARIA SUELY PAGLIARINI, UNIVERSIDADE ESTADUAL DE MARINGÁ; CACILDA BORGES DO VALLE, CNPGC. |
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Título: |
Abnormal timing of cytokinesis in microsporogenesis in Brachiaria humidicola (Poaceae: Paniceae). |
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Ano de publicação: |
2006 |
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Fonte/Imprenta: |
Journal of Genetics, Bangalore, v. 85, n. 3, p. 225-228, Dec. 2006 |
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Idioma: |
Inglês |
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Notas: |
Research note. |
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Conteúdo: |
Meiosis is controlled by a large number of genes, generally dominant, whose expression is stage-specific, site-specific and time-specific (Gottschalk and Kaul 1974, 1980a,b; Baker et al. 1976; Golubovskaya 1979, 1989). Among genes acting in the meiotic process, those responsible for the partitioning of the cytoplasm after nuclear division play a very important role in the formation of viable gametes. After two rounds of chromosome segregation (karyokinesis) and one simultaneous or two successive cytoplasmic divisions (cytokinesis), the final product of male meiosis in flowering plants emerges as a tetrad of haploid microspores enclosed in a callose wall. The timing of cytokinesis varies among angiosperms. In most monocot plants, cytokinesis is successive, i.e. one partitioning of the cytoplasm occurs after telophase I and another after telophase II, so that there is a distinct dyad stage. However, in most dicots, it is simultaneous and occurs after telophase II (Peirson et al. 1996). Many meiosis mutations affecting the pattern of cytokinesis have been reported in higher plants (Peirson et al. 1996). In Brachiaria, a promising African genus of forage grass for the Brazilian savannas, absence of cytokinesis leading to 2n microspores and binucleated or tetranucleated microspores have been reported in B. brizantha (Risso-Pascotto et al. 2003) and B. nigropedata (Utsunomiya et al. 2005). The present study details meiotic and postmeiotic abnormalities related to cytokinesis observed in one accession of B. humidicola. MenosMeiosis is controlled by a large number of genes, generally dominant, whose expression is stage-specific, site-specific and time-specific (Gottschalk and Kaul 1974, 1980a,b; Baker et al. 1976; Golubovskaya 1979, 1989). Among genes acting in the meiotic process, those responsible for the partitioning of the cytoplasm after nuclear division play a very important role in the formation of viable gametes. After two rounds of chromosome segregation (karyokinesis) and one simultaneous or two successive cytoplasmic divisions (cytokinesis), the final product of male meiosis in flowering plants emerges as a tetrad of haploid microspores enclosed in a callose wall. The timing of cytokinesis varies among angiosperms. In most monocot plants, cytokinesis is successive, i.e. one partitioning of the cytoplasm occurs after telophase I and another after telophase II, so that there is a distinct dyad stage. However, in most dicots, it is simultaneous and occurs after telophase II (Peirson et al. 1996). Many meiosis mutations affecting the pattern of cytokinesis have been reported in higher plants (Peirson et al. 1996). In Brachiaria, a promising African genus of forage grass for the Brazilian savannas, absence of cytokinesis leading to 2n microspores and binucleated or tetranucleated microspores have been reported in B. brizantha (Risso-Pascotto et al. 2003) and B. nigropedata (Utsunomiya et al. 2005). The present study details meiotic and postmeiotic abnormalities related to cytokinesis obser... Mostrar Tudo |
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Palavras-Chave: |
Braquiária; Microsporogênese. |
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Thesagro: |
Brachiaria Humidicola; Gramínea Forrageira; Melhoramento Genético Vegetal; Pastagem; Poliploidia. |
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Thesaurus Nal: |
Cytokinesis; Forage grasses; Meiosis; Microsporogenesis; Polyploidy. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02404naa a2200301 a 4500
001 1327021
005 2023-07-25
008 2006 bl uuuu u00u1 u #d
100 1 $aBOLDRINI, K. R.
245 $aAbnormal timing of cytokinesis in microsporogenesis in Brachiaria humidicola (Poaceae$bPaniceae).
260 $c2006
500 $aResearch note.
520 $aMeiosis is controlled by a large number of genes, generally dominant, whose expression is stage-specific, site-specific and time-specific (Gottschalk and Kaul 1974, 1980a,b; Baker et al. 1976; Golubovskaya 1979, 1989). Among genes acting in the meiotic process, those responsible for the partitioning of the cytoplasm after nuclear division play a very important role in the formation of viable gametes. After two rounds of chromosome segregation (karyokinesis) and one simultaneous or two successive cytoplasmic divisions (cytokinesis), the final product of male meiosis in flowering plants emerges as a tetrad of haploid microspores enclosed in a callose wall. The timing of cytokinesis varies among angiosperms. In most monocot plants, cytokinesis is successive, i.e. one partitioning of the cytoplasm occurs after telophase I and another after telophase II, so that there is a distinct dyad stage. However, in most dicots, it is simultaneous and occurs after telophase II (Peirson et al. 1996). Many meiosis mutations affecting the pattern of cytokinesis have been reported in higher plants (Peirson et al. 1996). In Brachiaria, a promising African genus of forage grass for the Brazilian savannas, absence of cytokinesis leading to 2n microspores and binucleated or tetranucleated microspores have been reported in B. brizantha (Risso-Pascotto et al. 2003) and B. nigropedata (Utsunomiya et al. 2005). The present study details meiotic and postmeiotic abnormalities related to cytokinesis observed in one accession of B. humidicola.
650 $aCytokinesis
650 $aForage grasses
650 $aMeiosis
650 $aMicrosporogenesis
650 $aPolyploidy
650 $aBrachiaria Humidicola
650 $aGramínea Forrageira
650 $aMelhoramento Genético Vegetal
650 $aPastagem
650 $aPoliploidia
653 $aBraquiária
653 $aMicrosporogênese
700 1 $aPAGLIARINI, M. S.
700 1 $aVALLE, C. B. do
773 $tJournal of Genetics, Bangalore$gv. 85, n. 3, p. 225-228, Dec. 2006
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| 5. |  | OLIVEIRA, M. G. de C.; REZENDE, R. C. Análise do processo de recebimento e expedição de grãos em unidade armazenadora, no sudoeste goiano, por meio da simulação computacional. Revista Brasileira de Armazenamento, Viçosa, MG, v. 36, n. 1, p. 3-12, 2011.| Tipo: Artigo em Periódico Indexado | Circulação/Nível: B - 3 |
| Biblioteca(s): Embrapa Arroz e Feijão. |
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| 11. | | OLIVEIRA, M. G. de C.; BASSINELLO, P. Z.; DEVILLA, I. A.; PENHA, W. F. da. Composição de micro e macro nutrientes de diferentes proporções da mistura de arroz tipo 1: polido e parboilizado. In: CONGRESSO BRASILEIRO DE ENGENHARIA AGRÍCOLA, 36., 2007, Bonito, MS. Anais... Bonito, MS: SBEA, 2007.| Tipo: Artigo em Anais de Congresso / Nota Técnica |
| Biblioteca(s): Embrapa Arroz e Feijão. |
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| 12. | | OLIVEIRA, M. G. de C.; BASSINELLO, P. Z.; DEVILLA, I. A.; ASCHERI, D. P. R. Caracterização da qualidade de diferentes proporções da mistura de arroz tipo 1: branco e parboilizado. Revista Brasileira de Armazenamento, Viçosa, MG, v. 34, n. 2, p. 111-121, 2009.| Tipo: Artigo em Periódico Indexado | Circulação/Nível: B - 3 |
| Biblioteca(s): Embrapa Arroz e Feijão. |
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| 19. | | PENHA, W. F. da; DEVILLA, I. A.; BASSINELLO, P. Z.; OLIVEIRA, M. G. de C. Propriedades físicas dos grãos de quinoa (Chenopodium quinoa Willd). In: CONGRESSO BRASILEIRO DE ENGENHARIA AGRÍCOLA, 36., 2007, Bonito, MS. Anais... Bonito, MS: SBEA, 2007.| Tipo: Artigo em Anais de Congresso |
| Biblioteca(s): Embrapa Arroz e Feijão. |
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| Registros recuperados : 36 | |
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