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Registro Completo |
Biblioteca(s): |
Embrapa Algodão. |
Data corrente: |
15/02/2011 |
Data da última atualização: |
15/02/2011 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
QUEIROZ, C. M.; LIMA, L. M. de; SANTOS, R. C. dos; BATISTA, V. G. L.; PINHEIRO, M. P. N. |
Afiliação: |
LIZIANE MARIA DE LIMA, CNPA; ROSEANE CAVALCANTI DOS SANTOS, CNPA. |
Título: |
Identificação e validação da expressão de genes relacionados com botão floral de algodoeiro. |
Ano de publicação: |
2010 |
Fonte/Imprenta: |
In: ENCONTRO DE PRODUÇÃO CIENTÍFICA DA EMBRAPA ALGODÃO - EPC 2010, 5., 2010, Campina Grande. [Resumos...]. Campina Grande: Embrapa Algodão, 2010. |
Páginas: |
p. 19 |
ISSN: |
0103-0205 |
Idioma: |
Português |
Palavras-Chave: |
Biblioteca subtrativa; Melhoramento genético; RT-PCR. |
Categoria do assunto: |
-- |
Marc: |
LEADER 00738naa a2200217 a 4500 001 1877330 005 2011-02-15 008 2010 bl uuuu u00u1 u #d 022 $a0103-0205 100 1 $aQUEIROZ, C. M. 245 $aIdentificação e validação da expressão de genes relacionados com botão floral de algodoeiro. 260 $c2010 300 $ap. 19 653 $aBiblioteca subtrativa 653 $aMelhoramento genético 653 $aRT-PCR 700 1 $aLIMA, L. M. de 700 1 $aSANTOS, R. C. dos 700 1 $aBATISTA, V. G. L. 700 1 $aPINHEIRO, M. P. N. 773 $tIn: ENCONTRO DE PRODUÇÃO CIENTÍFICA DA EMBRAPA ALGODÃO - EPC 2010, 5., 2010, Campina Grande. [Resumos...]. Campina Grande: Embrapa Algodão, 2010.
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Embrapa Algodão (CNPA) |
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Registro Completo
Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
Data corrente: |
24/12/2008 |
Data da última atualização: |
15/01/2009 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
GUERRA, M.; MORAES, A. P.; MIRKOV, E.; BRASILEIRO-VIDAL, A. C.; SILVA, A. E. B. e; SOARES FILHO, W. dos S. |
Afiliação: |
M. Guerra, UFPE; A. P. Moraes, UFPE; E. Mirkov, AgriLife Research; A. C. Brasileiro-Vidal, UFPE; A. E. Barros e Silva, UFPE; Walter dos Santos Soares Filho, CNPMF. |
Título: |
Molecular characterization of chromosomes of Poncirus trifoliata using different DNA sequences. |
Ano de publicação: |
2008 |
Fonte/Imprenta: |
In: INTERNATIONAL CITRUS CONGRESS, 11., 2008, Wuhan,China. Program and abstracts... Wuhan: The International Society of Citriculture, 2008. p. 25. 19. |
Idioma: |
Inglês |
Conteúdo: |
In order to get a first molecular cytogenetic map of each chromosome of Poncirus trifoliata, we localized by fluorescent in situ hybridization (FISH) several different probes. Chromosomes were firstly stained with the fluorochromes CMA and DAPI which allow the identification of heterochromatin as CMA+/DAPI- bands, dividing the nine chromosome pairs into three groups: two chromosome pairs bearing a proximal and a terminal band (B type), four having only a single terminal band (D type) and three others without any band (F type). Sequential CMA/DAPI staining and FISH using the 5S and 45S rDNA probes showed that these two probes were always adjacent to each other. The 45S rDNA probe co-located with the proximal band of all B type chromosome and with the single band of one D chromosome. A satelite DNA sequence isolated from Citrus sinensis, using primers based on the 181 bp satelite sequence of C. ichangensis described by Beridze et al. (1992), hybridzed at all CMA+ bands except the rDNA sites and a single terminal band in a B chromosome, suggesting that this is the main satelite sequence of Citrus and Poncirus. Further, 24 BACs from a P. trifoliata genomic library were selected and hybridized in situ, including four BACs from the Ctv resistance gene region. Seven out of the 24 probes gave disperse signals, four did not give any signal and 13 produced single copy homozygous signals in seven of the nine chromosome pairs (two D pairs were not labeled). The four BACs from the Ctv region were located very close to each other at the smallest F chromosome type, precisely in the interstitial region of the more distended arm. MenosIn order to get a first molecular cytogenetic map of each chromosome of Poncirus trifoliata, we localized by fluorescent in situ hybridization (FISH) several different probes. Chromosomes were firstly stained with the fluorochromes CMA and DAPI which allow the identification of heterochromatin as CMA+/DAPI- bands, dividing the nine chromosome pairs into three groups: two chromosome pairs bearing a proximal and a terminal band (B type), four having only a single terminal band (D type) and three others without any band (F type). Sequential CMA/DAPI staining and FISH using the 5S and 45S rDNA probes showed that these two probes were always adjacent to each other. The 45S rDNA probe co-located with the proximal band of all B type chromosome and with the single band of one D chromosome. A satelite DNA sequence isolated from Citrus sinensis, using primers based on the 181 bp satelite sequence of C. ichangensis described by Beridze et al. (1992), hybridzed at all CMA+ bands except the rDNA sites and a single terminal band in a B chromosome, suggesting that this is the main satelite sequence of Citrus and Poncirus. Further, 24 BACs from a P. trifoliata genomic library were selected and hybridized in situ, including four BACs from the Ctv resistance gene region. Seven out of the 24 probes gave disperse signals, four did not give any signal and 13 produced single copy homozygous signals in seven of the nine chromosome pairs (two D pairs were not labeled). The four BACs from the Ctv... Mostrar Tudo |
Palavras-Chave: |
Citros. |
Thesagro: |
Biotecnologia. |
Categoria do assunto: |
-- |
Marc: |
LEADER 02333naa a2200205 a 4500 001 1655685 005 2009-01-15 008 2008 bl uuuu u00u1 u #d 100 1 $aGUERRA, M. 245 $aMolecular characterization of chromosomes of Poncirus trifoliata using different DNA sequences. 260 $c2008 520 $aIn order to get a first molecular cytogenetic map of each chromosome of Poncirus trifoliata, we localized by fluorescent in situ hybridization (FISH) several different probes. Chromosomes were firstly stained with the fluorochromes CMA and DAPI which allow the identification of heterochromatin as CMA+/DAPI- bands, dividing the nine chromosome pairs into three groups: two chromosome pairs bearing a proximal and a terminal band (B type), four having only a single terminal band (D type) and three others without any band (F type). Sequential CMA/DAPI staining and FISH using the 5S and 45S rDNA probes showed that these two probes were always adjacent to each other. The 45S rDNA probe co-located with the proximal band of all B type chromosome and with the single band of one D chromosome. A satelite DNA sequence isolated from Citrus sinensis, using primers based on the 181 bp satelite sequence of C. ichangensis described by Beridze et al. (1992), hybridzed at all CMA+ bands except the rDNA sites and a single terminal band in a B chromosome, suggesting that this is the main satelite sequence of Citrus and Poncirus. Further, 24 BACs from a P. trifoliata genomic library were selected and hybridized in situ, including four BACs from the Ctv resistance gene region. Seven out of the 24 probes gave disperse signals, four did not give any signal and 13 produced single copy homozygous signals in seven of the nine chromosome pairs (two D pairs were not labeled). The four BACs from the Ctv region were located very close to each other at the smallest F chromosome type, precisely in the interstitial region of the more distended arm. 650 $aBiotecnologia 653 $aCitros 700 1 $aMORAES, A. P. 700 1 $aMIRKOV, E. 700 1 $aBRASILEIRO-VIDAL, A. C. 700 1 $aSILVA, A. E. B. e 700 1 $aSOARES FILHO, W. dos S. 773 $tIn: INTERNATIONAL CITRUS CONGRESS, 11., 2008, Wuhan,China. Program and abstracts... Wuhan: The International Society of Citriculture, 2008. p. 25. 19.
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Embrapa Mandioca e Fruticultura (CNPMF) |
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