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16. | | SILVA, G. A. da; SILVA, S. de S.; SOUSA, M. V. R. de; GUIMARÃES, L. M.; MESQUITA, E. F. de. Estudo da fitomassa das folhas e caule da mamoneira EBDA MPA 11 submetidos às diferentes dosagens de nitrogênio no campus IV da UEPB Catolé do Rocha-PB. . In: CONGRESSO BRASILEIRO DE MAMONA, 5.; SIMPÓSIO INTERNACIONAL DE OLEAGINOSAS ENERGÉTICAS, 2.; FÓRUM CAPIXABA DE PINHÃO-MANSO, 1., 2012, Guarapari. Desafios e Oportunidades: anais. Campina Grande: Embrapa Algodão, 2012. p. 90 Biblioteca(s): Embrapa Algodão. |
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17. | | LIMA, C. M. R. de; SA, M. F. G. de; SANTANA, E.; SOUSA, M. V.; MORTHY, L. The cytolyn enterobolin is present in the cytosol and nucleus of Entorolobium contortisiliquum seed cells. In: REUNIAO ANUAL DA SOCIEDADE BRASILEIRA DE BIOQUIMICA E BIOLOGIA MOLECULAR, 24., 1995, Caxambu, MG. Programa e resumos. Caxambu: SociedadeBrasileira de Bioquimica e Biologia Molecular, 1995. p.65. Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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18. | | SILVA, G. A. da; GUIMARÃES, L. M.; SOUSA, M. V. R. de; SILVA, S. de S.; MESQUITA, E. F. de. Crescimento da mamoneira EBDA MPA 11 sob o efeito da adubação nitrogenada. In: CONGRESSO BRASILEIRO DE MAMONA, 5.; SIMPÓSIO INTERNACIONAL DE OLEAGINOSAS ENERGÉTICAS, 2.; FÓRUM CAPIXABA DE PINHÃO-MANSO, 1., 2012, Guarapari. Desafios e Oportunidades: anais. Campina Grande: Embrapa Algodão, 2012. p. 71 Biblioteca(s): Embrapa Algodão. |
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19. | | FERREIRA, P.; PAES, N. S.; SOUZA, C. R. B.; GERHARDT, I. R.; COUTINHO, M. V.; MELLO, L. V.; SOUSA, M. V.; GROSSI DE SA, M. F. Arcelin 5 protein: purification, analysis, developing seeds study and imunocytolocalization. In: REUNIAO ANUAL DA SOCIEDADE BRASILEIRA DE BIOQUIMICA E BIOLOGIA MOLECULAR, 23., 1994, Caxambu, MG. Programa e resumos. Caxambu: Sociedade Brasileira de Bioquimica e Biologia Molecular, 1994. p.49. E-39. p.49 Resumo. Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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20. | | RIBEIRO, D. G.; ALMEIDA, R. F.; FONTES, W.; CASTRO, M. de S.; SOUSA, M. V. de; RICART, C. A. O.; PEREIRA, J. E. S.; MEHTA, A. Identificação de proteínas envolvidas na aquisição de competência embriogênica em dendezeiros (Elaeis guineensis Jacq. var. tenera) utilizando proteômica Shotgun. In: CONGRESSO NACIONAL DE BOTÂNICA, 67., 2016, Vitória, ES. Conectando diversidades, revelando o desconhecido: resumos. Brasília, DF: Sociedade Botânica do Brasil, 2016. Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| Acesso ao texto completo restrito à biblioteca da Embrapa Arroz e Feijão. Para informações adicionais entre em contato com cnpaf.biblioteca@embrapa.br. |
Registro Completo
Biblioteca(s): |
Embrapa Arroz e Feijão; Embrapa Recursos Genéticos e Biotecnologia. |
Data corrente: |
24/04/2021 |
Data da última atualização: |
12/07/2021 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
TÁVORA, F. T. P. K.; BEVITORI, R.; MELLO, R. N. de; CINTRA, M. M. D. F.; OLIVEIRA NETO, O. B.; FONTES, W.; CASTRO, M. S.; SOUSA, M. V.; FRANCO, O. L.; REIS, A. M. dos. |
Afiliação: |
FABIANO T. P. K. TÁVORA, UNIVERSIDADE FEDERAL DE JUIZ DE FORA, MG; ROSANGELA BEVITORI, CNPAF; RAQUEL NEVES DE MELLO, CNPAF; MARIA MONICA DOMINGUES F CINTRA, CNPAF; OSMUNDO B. OLIVEIRA NETO, CENTRO UNIVERSITARIO UNIEURO, Brasília-DF; WAGNER FONTES, UNIVERSIDADE DE BRASÍLIA; MARIANA S. CASTRO, UNIVERSIDADE DE BRASÍLIA; MARCELO V. SOUSA, UNIVERSIDADE DE BRASÍLIA; OCTAVIO L. FRANCO, UNIVERSIDADE CATÓLICA DE BRASÍLIA; ANGELA MEHTA DOS REIS, Cenargen. |
Título: |
Shotgun proteomics coupled to transient-inducible gene silencing reveal rice susceptibility genes as new sources for blast disease resistance. |
Ano de publicação: |
2021 |
Fonte/Imprenta: |
Journal of Proteomics, v. 241, 104223, June 2021. |
ISSN: |
1874-3919 |
DOI: |
https://doi.org/10.1016/j.jprot.2021.104223 |
Idioma: |
Inglês Português |
Notas: |
Na publicação: Angela Mehta. |
Conteúdo: |
A comparative proteomic analysis between two near-isogenic rice lines, displaying a resistant and susceptible phenotype upon infection with Magnaporthe oryzae was performed. We identified and validated factors associ-ated with rice disease susceptibility, representing a flourishing source toward a more resolute rice-blast resis-tance. Proteome profiles were remarkably different during early infection (12 h post-inoculation), revealing several proteins with increased abundance in the compatible interaction. Potential players of rice susceptibility were selected and gene expression was evaluated by RT-qPCR. Gene Ontology analysis disclosed susceptibility gene-encoded proteins claimed to be involved in fungus sustenance and suppression of plant immunity, such as sucrose synthase 4-like, serpin-ZXA-like, nudix hydrolase15, and DjA2 chaperone protein. Two other candidate genes, picked from a previous transcriptome study, were added into our downstream analysis including pyr-abactin resistant-like 5 (OsPYL5), and rice ethylene-responsive factor 104 (OsERF104). Further, we validated their role in susceptibility by Transient-Induced Gene Silencing (TIGS) using short antisense oligodeoxyr-ibonucleotides that resulted in a remarkable reduction of foliar disease symptoms in the compatible interaction. Therefore, we successfully employed shotgun proteomics and antisense-based gene silencing to prospect and functionally validate rice potential susceptibility factors, which could be further explored to build rice-blast resistance. Significance: R gene-mediated disease resistance is race-specific and often not durable in the field. More recently, advancements in new breeding techniques (NBTs) have made plant disease susceptibility genes (S-genes) a new target to build a broad spectrum and more durable resistance, hence an alternative source to R-genes in breeding programs. We successfully coupled shotgun proteomics and gene silencing tools to prospect and validate new rice-bast susceptibility genes that can be further exploited toward a more resolute blast disease resistance. MenosA comparative proteomic analysis between two near-isogenic rice lines, displaying a resistant and susceptible phenotype upon infection with Magnaporthe oryzae was performed. We identified and validated factors associ-ated with rice disease susceptibility, representing a flourishing source toward a more resolute rice-blast resis-tance. Proteome profiles were remarkably different during early infection (12 h post-inoculation), revealing several proteins with increased abundance in the compatible interaction. Potential players of rice susceptibility were selected and gene expression was evaluated by RT-qPCR. Gene Ontology analysis disclosed susceptibility gene-encoded proteins claimed to be involved in fungus sustenance and suppression of plant immunity, such as sucrose synthase 4-like, serpin-ZXA-like, nudix hydrolase15, and DjA2 chaperone protein. Two other candidate genes, picked from a previous transcriptome study, were added into our downstream analysis including pyr-abactin resistant-like 5 (OsPYL5), and rice ethylene-responsive factor 104 (OsERF104). Further, we validated their role in susceptibility by Transient-Induced Gene Silencing (TIGS) using short antisense oligodeoxyr-ibonucleotides that resulted in a remarkable reduction of foliar disease symptoms in the compatible interaction. Therefore, we successfully employed shotgun proteomics and antisense-based gene silencing to prospect and functionally validate rice potential susceptibility factors, which could be furth... Mostrar Tudo |
Palavras-Chave: |
Gene ontology; Plant immunity; PTO-based TIGS; RT-qPCR; S-gene; Transient-Induced gene silencing. |
Thesagro: |
Arroz; Brusone; Doença de Planta; Oryza Sativa. |
Thesaurus NAL: |
blast disease; disease resistance; foliar diseases; Magnaporthe oryzae; plant diseases and disorders; proteomics; rice. |
Categoria do assunto: |
-- S Ciências Biológicas |
Marc: |
LEADER 03484naa a2200469 a 4500 001 2131497 005 2021-07-12 008 2021 bl uuuu u00u1 u #d 022 $a1874-3919 024 7 $ahttps://doi.org/10.1016/j.jprot.2021.104223$2DOI 100 1 $aTÁVORA, F. T. P. K. 245 $aShotgun proteomics coupled to transient-inducible gene silencing reveal rice susceptibility genes as new sources for blast disease resistance.$h[electronic resource] 260 $c2021 500 $aNa publicação: Angela Mehta. 520 $aA comparative proteomic analysis between two near-isogenic rice lines, displaying a resistant and susceptible phenotype upon infection with Magnaporthe oryzae was performed. We identified and validated factors associ-ated with rice disease susceptibility, representing a flourishing source toward a more resolute rice-blast resis-tance. Proteome profiles were remarkably different during early infection (12 h post-inoculation), revealing several proteins with increased abundance in the compatible interaction. Potential players of rice susceptibility were selected and gene expression was evaluated by RT-qPCR. Gene Ontology analysis disclosed susceptibility gene-encoded proteins claimed to be involved in fungus sustenance and suppression of plant immunity, such as sucrose synthase 4-like, serpin-ZXA-like, nudix hydrolase15, and DjA2 chaperone protein. Two other candidate genes, picked from a previous transcriptome study, were added into our downstream analysis including pyr-abactin resistant-like 5 (OsPYL5), and rice ethylene-responsive factor 104 (OsERF104). Further, we validated their role in susceptibility by Transient-Induced Gene Silencing (TIGS) using short antisense oligodeoxyr-ibonucleotides that resulted in a remarkable reduction of foliar disease symptoms in the compatible interaction. Therefore, we successfully employed shotgun proteomics and antisense-based gene silencing to prospect and functionally validate rice potential susceptibility factors, which could be further explored to build rice-blast resistance. Significance: R gene-mediated disease resistance is race-specific and often not durable in the field. More recently, advancements in new breeding techniques (NBTs) have made plant disease susceptibility genes (S-genes) a new target to build a broad spectrum and more durable resistance, hence an alternative source to R-genes in breeding programs. We successfully coupled shotgun proteomics and gene silencing tools to prospect and validate new rice-bast susceptibility genes that can be further exploited toward a more resolute blast disease resistance. 650 $ablast disease 650 $adisease resistance 650 $afoliar diseases 650 $aMagnaporthe oryzae 650 $aplant diseases and disorders 650 $aproteomics 650 $arice 650 $aArroz 650 $aBrusone 650 $aDoença de Planta 650 $aOryza Sativa 653 $aGene ontology 653 $aPlant immunity 653 $aPTO-based TIGS 653 $aRT-qPCR 653 $aS-gene 653 $aTransient-Induced gene silencing 700 1 $aBEVITORI, R. 700 1 $aMELLO, R. N. de 700 1 $aCINTRA, M. M. D. F. 700 1 $aOLIVEIRA NETO, O. B. 700 1 $aFONTES, W. 700 1 $aCASTRO, M. S. 700 1 $aSOUSA, M. V. 700 1 $aFRANCO, O. L. 700 1 $aREIS, A. M. dos 773 $tJournal of Proteomics$gv. 241, 104223, June 2021.
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