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Registro Completo |
Biblioteca(s): |
Embrapa Uva e Vinho. |
Data corrente: |
08/06/2018 |
Data da última atualização: |
29/04/2019 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
BOSCO, D. D.; SINSKI, I.; RITSCHEL, P. S.; CAMARGO, U. A.; FAJARDO, T. V. M.; HARAKAVA, R.; QUECINI, V. |
Afiliação: |
DANIELA DAL BOSCO, CNPUV; IRACI SINSKI, CNPUV; PATRICIA SILVA RITSCHEL, CNPUV; Umberto A. Camargo; THOR VINICIUS MARTINS FAJARDO, CNPUV; Ricardo Harakava; VERA MARIA QUECINI, CNPUV. |
Título: |
Expression of disease resistance in genetically modified grapevines correlates with the contents of viral sequences in the T-DNA and global genome methylation. |
Ano de publicação: |
2018 |
Fonte/Imprenta: |
Transgenic Research, p. 1-18, 2018. [Online] |
DOI: |
https://doi.org/10.1007/s11248-018-0082-1 |
Idioma: |
Português |
Conteúdo: |
Increased tolerance to pathogens is an important goal in conventional and biotechnology-assisted grapevine breeding programs worldwide. Fungal and viral pathogens cause direct losses in berry production, but also affect the quality of the final products. Precision breeding strategies allow the introduction of resistance characters in elite cultivars, although the factors determining the plant?s overall performance are not fully characterized. Grapevine plants expressing defense proteins, from fungal or plant origins, or of the coat protein gene of grapevine leafroll-associated virus 3 (GLRaV-3) were generated by Agrobacterium -mediated transformation of somatic embryos and shoot apical meristems. The responses of the transformed lines to pathogen challenges were investigated by biochemical, phytopathological and molecular methods. The expression of a Metarhizium anisopliae chitinase gene delayed pathogenesis and disease progression against the necrotrophic pathogen Botrytis cinerea. Modified lines expressing a Solanum nigrum osmotin-like protein also exhibited slower disease progression, but to a smaller extent. Grapevine lines carrying two hairpin- inducing constructs had lower GLRaV-3 titers when challenged by grafting, although disease symptoms and viral multiplication were detected. The levels of global genome methylation were determined for the genetically engineered lines, and correlation analyses demonstrated the association between higher levels of methylated DNA and larger portions of virus-derived sequences. Resistance expression was also negatively correlated with the contents of introduced viral sequences and genome methylation, indicating that the effectiveness of resistance strategies employing sequences of viral origin is subject to epigenetic regulation in grapevine. Keywords Chitinase, Epigenetics, Fungus, Grapevine leafroll-associated virus 3, Pathogenesis related protein 5, Vitis MenosIncreased tolerance to pathogens is an important goal in conventional and biotechnology-assisted grapevine breeding programs worldwide. Fungal and viral pathogens cause direct losses in berry production, but also affect the quality of the final products. Precision breeding strategies allow the introduction of resistance characters in elite cultivars, although the factors determining the plant?s overall performance are not fully characterized. Grapevine plants expressing defense proteins, from fungal or plant origins, or of the coat protein gene of grapevine leafroll-associated virus 3 (GLRaV-3) were generated by Agrobacterium -mediated transformation of somatic embryos and shoot apical meristems. The responses of the transformed lines to pathogen challenges were investigated by biochemical, phytopathological and molecular methods. The expression of a Metarhizium anisopliae chitinase gene delayed pathogenesis and disease progression against the necrotrophic pathogen Botrytis cinerea. Modified lines expressing a Solanum nigrum osmotin-like protein also exhibited slower disease progression, but to a smaller extent. Grapevine lines carrying two hairpin- inducing constructs had lower GLRaV-3 titers when challenged by grafting, although disease symptoms and viral multiplication were detected. The levels of global genome methylation were determined for the genetically engineered lines, and correlation analyses demonstrated the association between higher levels of methylated DNA and... Mostrar Tudo |
Palavras-Chave: |
Fungus; Pathogenesis related protein 5. |
Thesaurus Nal: |
Chitinase; Epigenetics; Grapevine leafroll-associated virus 3; Vitis. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/178409/1/s11248-018-0082-1-Artigo-v-publicada-Metilacao-DNA-Transgenic-Research-06-06-18.pdf
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Marc: |
LEADER 02824naa a2200277 a 4500 001 2092380 005 2019-04-29 008 2018 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.1007/s11248-018-0082-1$2DOI 100 1 $aBOSCO, D. D. 245 $aExpression of disease resistance in genetically modified grapevines correlates with the contents of viral sequences in the T-DNA and global genome methylation.$h[electronic resource] 260 $c2018 520 $aIncreased tolerance to pathogens is an important goal in conventional and biotechnology-assisted grapevine breeding programs worldwide. Fungal and viral pathogens cause direct losses in berry production, but also affect the quality of the final products. Precision breeding strategies allow the introduction of resistance characters in elite cultivars, although the factors determining the plant?s overall performance are not fully characterized. Grapevine plants expressing defense proteins, from fungal or plant origins, or of the coat protein gene of grapevine leafroll-associated virus 3 (GLRaV-3) were generated by Agrobacterium -mediated transformation of somatic embryos and shoot apical meristems. The responses of the transformed lines to pathogen challenges were investigated by biochemical, phytopathological and molecular methods. The expression of a Metarhizium anisopliae chitinase gene delayed pathogenesis and disease progression against the necrotrophic pathogen Botrytis cinerea. Modified lines expressing a Solanum nigrum osmotin-like protein also exhibited slower disease progression, but to a smaller extent. Grapevine lines carrying two hairpin- inducing constructs had lower GLRaV-3 titers when challenged by grafting, although disease symptoms and viral multiplication were detected. The levels of global genome methylation were determined for the genetically engineered lines, and correlation analyses demonstrated the association between higher levels of methylated DNA and larger portions of virus-derived sequences. Resistance expression was also negatively correlated with the contents of introduced viral sequences and genome methylation, indicating that the effectiveness of resistance strategies employing sequences of viral origin is subject to epigenetic regulation in grapevine. Keywords Chitinase, Epigenetics, Fungus, Grapevine leafroll-associated virus 3, Pathogenesis related protein 5, Vitis 650 $aChitinase 650 $aEpigenetics 650 $aGrapevine leafroll-associated virus 3 650 $aVitis 653 $aFungus 653 $aPathogenesis related protein 5 700 1 $aSINSKI, I. 700 1 $aRITSCHEL, P. S. 700 1 $aCAMARGO, U. A. 700 1 $aFAJARDO, T. V. M. 700 1 $aHARAKAVA, R. 700 1 $aQUECINI, V. 773 $tTransgenic Research, p. 1-18, 2018. [Online]
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Registro original: |
Embrapa Uva e Vinho (CNPUV) |
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Registros recuperados : 181 | |
1. | | CAMARGO, U. A. Banco ativo de germoplasma de uva. In: SIMPÓSIO DE RECURSOS GENÉTICOS VEGETAIS. SESSÃO I - BANCOS ATIVOS DE GERMOPLASMA, 1979, Brasília, DF. Anais... Brasília, DF: EMBRAPA-CENARGEN: EMBRAPA-DID, 1980. p. 112-113.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Uva e Vinho. |
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2. | | CAMARGO, U. A. Banco ativo de germoplasma de uva. In: WORKSHOP PARA CURADORES DE BANCOS DE GERMOPLASMA DE ESPÉCIES FRUTÍFERAS, 1997, Brasília, DF. Recursos genéticos de espécies frutíferas no Brasil: anais. Brasília, DF: Embrapa Recursos Genéticos e Biotecnologia, 1999. p. 184-187.Tipo: Artigo em Anais de Congresso / Nota Técnica |
Biblioteca(s): Embrapa Uva e Vinho. |
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9. | | CAMARGO, U. A. Cultivares. In: MELLO, L. M. R. de; MACHADO, C. A. E. (Ed.). Cadastro vitícola do Rio Grande do Sul: 2005 a 2007. Bento Gonçalves: Embrapa Uva e Vinho, 2008. 1 CD-ROM.Tipo: Capítulo em Livro Técnico-Científico |
Biblioteca(s): Embrapa Uva e Vinho. |
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12. | | CAMARGO, U. A. Melhoramento genético da videira. In: SOUZA LEÃO, P. C. de; SOARES, J. M. (Ed.). A viticultura no semi-árido brasileiro. Petrolina, PE: Embrapa Semi-Árido, 2000. p. 65-91.Tipo: Capítulo em Livro Técnico-Científico | Circulação/Nível: -- - -- |
Biblioteca(s): Embrapa Uva e Vinho. |
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13. | | CAMARGO, U. A. Novas cultivarres de videira para vinho, suco e mesa. In: SIMPÓSIO MINEIRO DE VITICULTURA E ENOLOGIA, 1., 2002, Andradas, MG. Viticultura e Enologia: atualizando conceitos. Caldas: EPAMIG, 2002. p. 33-48 Coordenado por Murilo Albuquerque Regina com colaboração de Luiz Eduardo Correa Antunes.Tipo: Artigo em Anais de Congresso / Nota Técnica | Circulação/Nível: -- - -- |
Biblioteca(s): Embrapa Uva e Vinho. |
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14. | | CAMARGO, U. A. Sinonímia das videiras cultivadas no Rio Grande do Sul. In: SIMPÓSIO LATINO-AMERICANO DE ENOLOGIA, 2.; JORNADA DE VITICULTURA E ENOLOGIA, 2.; SIMPÓSIO ANUAL DE VITIVINICULTURA, 2., 1987, Garibaldi. Trabalhos apresentados... Bento Gonçalves: EMBRAPA-CNPUV, 1987. p. 33-52Tipo: Artigo em Anais de Congresso / Nota Técnica | Circulação/Nível: -- - -- |
Biblioteca(s): Embrapa Uva e Vinho. |
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15. | | CAMARGO, U. A. Suco de uva: matéria-prima para produtos de qualidade e competitividade. In: CONGRESSO LATINO-AMERICANO DE VITICULTURA E ENOLOGIA, 10.; CONGRESSO BRASILEIRO DE VITICULTURA E ENOLOGIA, 11.; SEMINÁRIO FRANCO-BRASILEIRO DE VITICULTURA E ENOLOGIA, 2., 2005, Bento Gonçalves. Anais... Bento Gonçalves: Embrapa Uva e Vinho, 2005. p. 195-199. Série Documentos, 55Tipo: Artigo em Anais de Congresso / Nota Técnica |
Biblioteca(s): Embrapa Uva e Vinho. |
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17. | | CAMARGO, U. A. Uvas do Brasil. Brasília, DF: EMBRAPA-SPI, 1994. 90 p. il., color. (Embrapa Uva e Vinho. Documentos, 9).Tipo: Autoria/Organização/Edição de Livros |
Biblioteca(s): Embrapa Uva e Vinho. |
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Registros recuperados : 181 | |
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Nenhum registro encontrado para a expressão de busca informada. |
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