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Registro Completo |
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Biblioteca(s): |
Embrapa Hortaliças. |
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Data corrente: |
11/10/2010 |
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Data da última atualização: |
05/02/2020 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
QUEZADO DUVAL, A. M.; HENZ, G. P.; PAZ-LIMA, M. L.; MEDEIROS, A. R.; PFENNING, L. H.; REIS, A. |
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Afiliação: |
ALICE MARIA QUEZADO DUVAL, CNPH; GILMAR PAULO HENZ, CNPH; UNB; AGÊNCIA NACIONAL DO PETRÔLEO, GÁS NATURAL E BIOCOMBUSTÍVEIS; UFLA; AILTON REIS, CNPH. |
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Título: |
New Host of Myrothecium spp. in Brazil and a preliminary in vitro assay of fungicides. |
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Ano de publicação: |
2010 |
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Fonte/Imprenta: |
Brazilian Journal of Microbiology, São Paulo, v. 41, n. 1, p. 246-252, 2010. |
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DOI: |
10.1590/S1517-83822010000100034. |
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Idioma: |
Inglês |
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Palavras-Chave: |
Anthurium andrearum; Batata-doce; Brasil; Dieffenbachia amoena; Nicandra physaloides; Ocorrência; Planta daninha; Solanum lycopersicon; Spathiphyllum wallisii. |
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Thesagro: |
Capsicum Annuum; Erva daninha; Etiologia; Hortaliça; Ipomoea Batatas; Pimentão; Planta hospedeira; Tomate. |
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Thesaurus Nal: |
Myrothecium roridum; Solidago canadensis. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/176699/1/v41n1a34.pdf
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Marc: |
LEADER 01200naa a2200409 a 4500
001 1863994
005 2020-02-05
008 2010 bl uuuu u00u1 u #d
024 7 $a10.1590/S1517-83822010000100034.$2DOI
100 1 $aQUEZADO DUVAL, A. M.
245 $aNew Host of Myrothecium spp. in Brazil and a preliminary in vitro assay of fungicides.$h[electronic resource]
260 $c2010
650 $aMyrothecium roridum
650 $aSolidago canadensis
650 $aCapsicum Annuum
650 $aErva daninha
650 $aEtiologia
650 $aHortaliça
650 $aIpomoea Batatas
650 $aPimentão
650 $aPlanta hospedeira
650 $aTomate
653 $aAnthurium andrearum
653 $aBatata-doce
653 $aBrasil
653 $aDieffenbachia amoena
653 $aNicandra physaloides
653 $aOcorrência
653 $aPlanta daninha
653 $aSolanum lycopersicon
653 $aSpathiphyllum wallisii
700 1 $aHENZ, G. P.
700 1 $aPAZ-LIMA, M. L.
700 1 $aMEDEIROS, A. R.
700 1 $aPFENNING, L. H.
700 1 $aREIS, A.
773 $tBrazilian Journal of Microbiology, São Paulo$gv. 41, n. 1, p. 246-252, 2010.
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Registro original: |
Embrapa Hortaliças (CNPH) |
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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. |
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: |
20/07/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
MENDES-BONATO, A. B.; PAGLIARINI, M. S.; VALLE, C. B. do; JANK, L. |
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Afiliação: |
ANDRÉA BEATRIZ MENDES -BONATO, UNIVERSIDADE ESTADUAL DE MARINGÁ; MARIA SUELY PAGLIARINI, UNIVERSIDADE ESTADUAL DE MARINGÁ; CACILDA BORGES DO VALLE, CNPGC; LIANA JANK, CNPGC. |
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Título: |
Abnormal pollen mitoses (PM I and PM II) in an interspecific hybrid of Brachiaria ruziziensis and Brachiaria decumbens (Gramineae). |
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Ano de publicação: |
2004 |
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Fonte/Imprenta: |
Journal of Genetics, Bangalore, v. 83, n. 3, p. 279-283, Dec. 2004. |
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Idioma: |
Inglês |
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Notas: |
Research note. |
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Conteúdo: |
Microgametogenesis was analysed in an interspecific hybrid resulting from a cross between an artificially tetraploidized sexual accession of Brachiaria ruziziensis (2n = 4x = 36) and the apomictic cultivar (cv. Basilisk) of B. decumbens (2n = 4x = 36). Although each microspore initiated its differentiation by pollen mitosis, polarization of the nucleus was not observed in 28.85% of the microspores, and the typical hemispherical cell plate was not detected as well. The usual asymmetry was not seen at first pollen mitosis (PM I), and microspores therefore lacked differentiation between the vegetative and the generative cell. After telophase, each cell entered PM II, but this was not always followed by cytokinesis. Tripolar spindle and restitutional nuclei were observed among microspores that lacked the first cytokinesis. Pollen from such abnormal divisions were sterile and larger than those resulting from the normal ones. Male gametogenesis in flowering plants depends on a determinative asymmetry in the cell division at pollen mitosis I (PM I), which gives rise to a larger vegetative cell and a smaller generative cell. To achieve this asymmetry, the microspore undergoes several unique cellular events, including the establishment of cell polarity through nuclear migration, development of an asymmetric mitotic spindle, and an expected process of cytokinesis to form a hemispherical cell plate. Control of gametophytic cytokinesis is, therefore, a critical process in pollen cell fate determination which results in the asymmetric distribution of cellular components that presumably include cell fate determinants (Twell et al. 1998; Park and Twell 2001). During cell division in somatic cells, a pre-prophase band of microtubules marks the future division plane and the exact site of cytokinesis, and the cell plate arises from the phragmoplast and grows toward the cell wall (Sylvester 2000). On the other hand, in gametophytic cytokinesis at PM I the pre-prophase band is absent and a unique hemispherical cell plate is formed and surrounds the generative nucleus (Terasaka and Niitsu 1990). Asymmetric cytoplasm cleavage is ensured by a curved profile of phragmoplast microtubules that appear to guide the centrifugal growth of the cell plate from its margin (Brown and Lemmon 1991). Mutations altering cell division asymmetry during pollen mitosis have been reported in Arabidopsis thaliana (Park et al. 1998) and B. decumbens (Junqueira Filho et al. 2003). This paper reports a new occurrence of symmetry in pollen mitoses (PM I and PM II) in a hybrid involving B. decumbens as the male genitor. Absence of cytokinesis following PM I and PM II was also observed. MenosMicrogametogenesis was analysed in an interspecific hybrid resulting from a cross between an artificially tetraploidized sexual accession of Brachiaria ruziziensis (2n = 4x = 36) and the apomictic cultivar (cv. Basilisk) of B. decumbens (2n = 4x = 36). Although each microspore initiated its differentiation by pollen mitosis, polarization of the nucleus was not observed in 28.85% of the microspores, and the typical hemispherical cell plate was not detected as well. The usual asymmetry was not seen at first pollen mitosis (PM I), and microspores therefore lacked differentiation between the vegetative and the generative cell. After telophase, each cell entered PM II, but this was not always followed by cytokinesis. Tripolar spindle and restitutional nuclei were observed among microspores that lacked the first cytokinesis. Pollen from such abnormal divisions were sterile and larger than those resulting from the normal ones. Male gametogenesis in flowering plants depends on a determinative asymmetry in the cell division at pollen mitosis I (PM I), which gives rise to a larger vegetative cell and a smaller generative cell. To achieve this asymmetry, the microspore undergoes several unique cellular events, including the establishment of cell polarity through nuclear migration, development of an asymmetric mitotic spindle, and an expected process of cytokinesis to form a hemispherical cell plate. Control of gametophytic cytokinesis is, therefore, a critical process in pollen cell fa... Mostrar Tudo |
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Palavras-Chave: |
Braquiária. |
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Thesagro: |
Brachiaria Decumbens; Brachiaria Ruziziensis; Gramínea Forrageira; Melhoramento Genético Vegetal; Mitose; Pastagem. |
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Thesaurus NAL: |
Pollen. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 03495naa a2200265 a 4500
001 1327022
005 2023-07-20
008 2004 bl uuuu u00u1 u #d
100 1 $aMENDES-BONATO, A. B.
245 $aAbnormal pollen mitoses (PM I and PM II) in an interspecific hybrid of Brachiaria ruziziensis and Brachiaria decumbens (Gramineae).
260 $c2004
500 $aResearch note.
520 $aMicrogametogenesis was analysed in an interspecific hybrid resulting from a cross between an artificially tetraploidized sexual accession of Brachiaria ruziziensis (2n = 4x = 36) and the apomictic cultivar (cv. Basilisk) of B. decumbens (2n = 4x = 36). Although each microspore initiated its differentiation by pollen mitosis, polarization of the nucleus was not observed in 28.85% of the microspores, and the typical hemispherical cell plate was not detected as well. The usual asymmetry was not seen at first pollen mitosis (PM I), and microspores therefore lacked differentiation between the vegetative and the generative cell. After telophase, each cell entered PM II, but this was not always followed by cytokinesis. Tripolar spindle and restitutional nuclei were observed among microspores that lacked the first cytokinesis. Pollen from such abnormal divisions were sterile and larger than those resulting from the normal ones. Male gametogenesis in flowering plants depends on a determinative asymmetry in the cell division at pollen mitosis I (PM I), which gives rise to a larger vegetative cell and a smaller generative cell. To achieve this asymmetry, the microspore undergoes several unique cellular events, including the establishment of cell polarity through nuclear migration, development of an asymmetric mitotic spindle, and an expected process of cytokinesis to form a hemispherical cell plate. Control of gametophytic cytokinesis is, therefore, a critical process in pollen cell fate determination which results in the asymmetric distribution of cellular components that presumably include cell fate determinants (Twell et al. 1998; Park and Twell 2001). During cell division in somatic cells, a pre-prophase band of microtubules marks the future division plane and the exact site of cytokinesis, and the cell plate arises from the phragmoplast and grows toward the cell wall (Sylvester 2000). On the other hand, in gametophytic cytokinesis at PM I the pre-prophase band is absent and a unique hemispherical cell plate is formed and surrounds the generative nucleus (Terasaka and Niitsu 1990). Asymmetric cytoplasm cleavage is ensured by a curved profile of phragmoplast microtubules that appear to guide the centrifugal growth of the cell plate from its margin (Brown and Lemmon 1991). Mutations altering cell division asymmetry during pollen mitosis have been reported in Arabidopsis thaliana (Park et al. 1998) and B. decumbens (Junqueira Filho et al. 2003). This paper reports a new occurrence of symmetry in pollen mitoses (PM I and PM II) in a hybrid involving B. decumbens as the male genitor. Absence of cytokinesis following PM I and PM II was also observed.
650 $aPollen
650 $aBrachiaria Decumbens
650 $aBrachiaria Ruziziensis
650 $aGramínea Forrageira
650 $aMelhoramento Genético Vegetal
650 $aMitose
650 $aPastagem
653 $aBraquiária
700 1 $aPAGLIARINI, M. S.
700 1 $aVALLE, C. B. do
700 1 $aJANK, L.
773 $tJournal of Genetics, Bangalore$gv. 83, n. 3, p. 279-283, Dec. 2004.
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