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4. |  | BRAGANÇA, S. M.; MARTINEZ, H. E. P.; LEITE, H. G.; SANTOS, L. P.; LANI, J. A.; SEDIYAMA, C. S.; ALVAREZ, V. H. V.; MOSQUIM, P. R. Acumulação de macronutrientes pelo cafeeiro conilon. In: SIMPÓSIO DE PESQUISA DOS CAFÉS DO BRASIL, 5., 2007, Águas de Lindóia, SP. Anais... Brasília, DF: Embrapa Café, 2007. 5p.Biblioteca(s): Biblioteca Rui Tendinha. |
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5. |  | BRAGANÇA, S. M.; MARTINEZ, H. E. P.; LEITE, H. G.; SANTOS, L. P.; LANI, J. A.; SEDIYAMA, C. S.; ALVAREZ V., V. H. Acumulação de matéria seca pelo cafeeiro Conilon. Revista Ceres, Viçosa v. 57, n.1, p. 048-052, jan./fev. 2010.Biblioteca(s): Biblioteca Rui Tendinha. |
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6. |  | BRAGANÇA, S. M.; MARTINEZ, H. E. P.; LEITE, H. G.; SANTOS, L. P.; LANI, J. A.; SEDIYAMA, C. S.; ALVAREZ, V. H. V.; MOSQUIM, P. R. Acumulação de micronutrientes pelo cafeeiro conilon. In: SIMPÓSIO DE PESQUISA DOS CAFÉS DO BRASIL, 5., 2007, Águas de Lindóia, SP. Anais... Brasília, DF: Embrapa Café, 2007 5p.Biblioteca(s): Biblioteca Rui Tendinha. |
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7. |  | BRAGANÇA, S. M.; MARTINEZ, H. E. P.; LEITE, H. G.; SANTOS, L. P.; SEDIYAMA, C. S.; ALVAREZ, V. H. V.; LANI, J. A. Acúmulo de B, CU, FE, MN e ZN pelo cafeeiro Conilon. Revista Ceres, Viçosa v. 54, n. 314, p. 398-404, jan./fev. 2007.Biblioteca(s): Biblioteca Rui Tendinha. |
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8. |  | TOMAZ, M. A.; FERRARI, R. B.; CRUZ, C. D.; MARTINEZ, H. E. P.; FONSECA, A. F. A. da.; SAKIYAMA, N. S. Crescimento de raiz e parte aérea de cafeeiros enxertados cultivados em vaso. Revista Ceres, Viçosa, v. 53, n. 308, p.507-512, 2006. p.507-512Biblioteca(s): Biblioteca Rui Tendinha. |
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11. |  | AMARAL, J. F. T. do.; FONSECA, A. F. A. da.; MARTINEZ, H. E. P; PEREIRA, P. R.; FONTES,P. C. R. Deficiências de macronutrientes, Fe e B em manjericão (Ocimum sp.) em cultivo hidropônico. Revista Ceres, Viçosa, mg, v.46, n.265, p.297-308,1999.Biblioteca(s): Biblioteca Rui Tendinha. |
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12. |  | QUEIROZ, R. B.; LOPES, M. C.; COSTA, T. L.; SILVA, R. S. da; GALDINO, T. V. S.; GONTIJO, P. da C.; MARTINEZ, H. E. P.; PICANÇO, M. C. Influence of tomato plants nutritional status on the fitness and damage of Tuta absoluta (Lepidoptera: Gelechiidae). Agricultural and Forest Entomology, p. 1-7, 2022.Biblioteca(s): Biblioteca Rui Tendinha. |
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Registro Completo |
Biblioteca(s): |
Biblioteca Rui Tendinha. |
Data corrente: |
17/04/2018 |
Data da última atualização: |
17/04/2018 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
MADRONERO, J.; RODRIGUES, S. P.; ANTUNES, T. F. S.; ABREU, P. M. V.; VENTURA, J. A.; FERNANDES, A. A. R.; FERNANDES, P. M. B. |
Afiliação: |
Johana Madroñero, UFES; Silas P. Rodrigues, UFES; Tathiana F. S. Antunes, UFES; Paolla M. V. Abreu, UFES; Jose Aires Ventura, Incaper; A. Alberto R. Fernandes, UFES; Patricia Machado Bueno Fernandes, UFES. |
Título: |
Transcriptome analysis provides insights into the delayed sticky disease symptoms in Carica papaya |
Ano de publicação: |
2018 |
Fonte/Imprenta: |
Plant Cell Reports, p. 1-14, 2018. |
Idioma: |
Português |
Conteúdo: |
Carica papaya plants develop the papaya sticky disease (PSD) as a result of the combined infection of papaya meleira virus (PMeV) and papaya meleira virus 2 (PMeV2), or PMeV complex. PSD symptoms appear only after C. papaya flowers. To understand the mechanisms involved in this phenomenon, the global gene expression patterns of PMeV complex-infected C. papaya at pre-and post-flowering stages were assessed by RNA-Seq. The result was 633 and 88 differentially expressed genes at pre- and post-flowering stages, respectively. At pre-flowering stage, genes related to stress and transport were up-regulated while metabolism-related genes were down-regulated. It was observed that induction of several salicylic acid (SA)-activated genes, including PR1, PR2, PR5, WRKY transcription factors, ROS and callose genes, suggesting SA signaling involvement in the delayed symptoms. In fact, pre-flowering C. papaya treated with exogenous SA showed a tendency to decrease the PMeV and PMeV2 loads when compared to control plants. However, pre-flowering C. papaya also accumulated transcripts encoding a NPR1-inhibitor (NPR1-I/NIM1-I) candidate, genes coding for UDP-glucosyltransferases (UGTs) and several genes involved with ethylene pathway, known to be negative regulators of SA signaling. At post-flowering, when PSD symptoms appeared, the down-regulation of PR-1 encoding gene and the induction of BSMT1 and JA metabolism-related genes were observed. Hence, SA signaling likely operates at the pre-flowering stage of PMeV complex-infected C. papaya inhibiting the development of PSD symptoms, but the induction of its negative regulators prevents the full-scale and long-lasting tolerance. MenosCarica papaya plants develop the papaya sticky disease (PSD) as a result of the combined infection of papaya meleira virus (PMeV) and papaya meleira virus 2 (PMeV2), or PMeV complex. PSD symptoms appear only after C. papaya flowers. To understand the mechanisms involved in this phenomenon, the global gene expression patterns of PMeV complex-infected C. papaya at pre-and post-flowering stages were assessed by RNA-Seq. The result was 633 and 88 differentially expressed genes at pre- and post-flowering stages, respectively. At pre-flowering stage, genes related to stress and transport were up-regulated while metabolism-related genes were down-regulated. It was observed that induction of several salicylic acid (SA)-activated genes, including PR1, PR2, PR5, WRKY transcription factors, ROS and callose genes, suggesting SA signaling involvement in the delayed symptoms. In fact, pre-flowering C. papaya treated with exogenous SA showed a tendency to decrease the PMeV and PMeV2 loads when compared to control plants. However, pre-flowering C. papaya also accumulated transcripts encoding a NPR1-inhibitor (NPR1-I/NIM1-I) candidate, genes coding for UDP-glucosyltransferases (UGTs) and several genes involved with ethylene pathway, known to be negative regulators of SA signaling. At post-flowering, when PSD symptoms appeared, the down-regulation of PR-1 encoding gene and the induction of BSMT1 and JA metabolism-related genes were observed. Hence, SA signaling likely operates at the pre-flow... Mostrar Tudo |
Thesaurus NAL: |
Carica papaya; Defense responses; Papaya meleira virus; Transcriptome Plant'virus interaction. |
Categoria do assunto: |
-- |
Marc: |
LEADER 02422naa a2200241 a 4500 001 1020018 005 2018-04-17 008 2018 bl uuuu u00u1 u #d 100 1 $aMADRONERO, J. 245 $aTranscriptome analysis provides insights into the delayed sticky disease symptoms in Carica papaya$h[electronic resource] 260 $c2018 520 $aCarica papaya plants develop the papaya sticky disease (PSD) as a result of the combined infection of papaya meleira virus (PMeV) and papaya meleira virus 2 (PMeV2), or PMeV complex. PSD symptoms appear only after C. papaya flowers. To understand the mechanisms involved in this phenomenon, the global gene expression patterns of PMeV complex-infected C. papaya at pre-and post-flowering stages were assessed by RNA-Seq. The result was 633 and 88 differentially expressed genes at pre- and post-flowering stages, respectively. At pre-flowering stage, genes related to stress and transport were up-regulated while metabolism-related genes were down-regulated. It was observed that induction of several salicylic acid (SA)-activated genes, including PR1, PR2, PR5, WRKY transcription factors, ROS and callose genes, suggesting SA signaling involvement in the delayed symptoms. In fact, pre-flowering C. papaya treated with exogenous SA showed a tendency to decrease the PMeV and PMeV2 loads when compared to control plants. However, pre-flowering C. papaya also accumulated transcripts encoding a NPR1-inhibitor (NPR1-I/NIM1-I) candidate, genes coding for UDP-glucosyltransferases (UGTs) and several genes involved with ethylene pathway, known to be negative regulators of SA signaling. At post-flowering, when PSD symptoms appeared, the down-regulation of PR-1 encoding gene and the induction of BSMT1 and JA metabolism-related genes were observed. Hence, SA signaling likely operates at the pre-flowering stage of PMeV complex-infected C. papaya inhibiting the development of PSD symptoms, but the induction of its negative regulators prevents the full-scale and long-lasting tolerance. 650 $aCarica papaya 650 $aDefense responses 650 $aPapaya meleira virus 650 $aTranscriptome Plant'virus interaction 700 1 $aRODRIGUES, S. P. 700 1 $aANTUNES, T. F. S. 700 1 $aABREU, P. M. V. 700 1 $aVENTURA, J. A. 700 1 $aFERNANDES, A. A. R. 700 1 $aFERNANDES, P. M. B. 773 $tPlant Cell Reports, p. 1-14, 2018.
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