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Registro Completo |
Biblioteca(s): |
Embrapa Agroenergia; Embrapa Recursos Genéticos e Biotecnologia; Embrapa Semiárido. |
Data corrente: |
23/11/2022 |
Data da última atualização: |
08/12/2023 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
ARRAES, F. B. M.; VASQUEZ, D. D. N.; TAHIR, M.; PINHEIRO, D. H.; FAHEEM, M.; FREITAS-ALVES, N. S.; MOREIRA-PINTO, C. E.; MOREIRA, V. J. V.; PAES-DE-MELO, B.; LISEI-DE-SA, M. E.; MORGANTE, C. V.; MOTA, A. P. Z.; LOURENCO, I. T.; TOGAWA, R. C.; GRYNBERG, P.; FRAGOSO, R. da R.; ALMEIDA-ENGLER, J. de; LARSEN, M. R.; GROSSI-DE-SA, M. F. |
Afiliação: |
FABRICIO B. M. ARRAES, FEDERAL UNIVERSITY OF RIO GRANDE DO SUL; DANIEL D. N. VASQUEZ, FEDERAL UNIVERSITY OF RIO GRANDE DO SUL; MUHAMMED TAHIR, UNIVERSITY OF SOUTHERN DENMARK; DANIELE H. PINHEIRO, NATIONAL INSTITUTE OF SCIENCE AND TECHNOLOGY; MUHAMMED FAHEEM, NATIONAL UNIVERSITY OF MEDICAL SCIENCES, PAKISTAN; NAYARA S. FREITAS-ALVES, FEDERAL UNIVERSITY OF PARANÁ; CLÍDIA E. MOREIRA-PINTO, CNPAE; VALDEIR J. V. MOREIRA, UNIVERSITY OF BRASÍLIA; BRUNO PAES-DE-MELO, CNPAE; MARIA E. LISEI-DE-SA, MINAS GERAIS AGRICULTURAL RESEARCH COMPANY; CAROLINA VIANNA MORGANTE, CPATSA; ANA P. Z. MOTA, INRAE; ISABELA TRISTAN LOURENCO TESSUTTI, Cenargen; ROBERTO COITI TOGAWA, Cenargen; PRISCILA GRYNBERG, Cenargen; RODRIGO DA ROCHA FRAGOSO, CNPAE; JANICE DE ALMEIDA-ENGLER, INRAE; MARTIN R. LARSEN, UNIVERSITY OF SOUTHERN DENMARK; MARIA FATIMA GROSSI-DE-SA, Cenargen. |
Título: |
Integrated omic approaches reveal molecular mechanisms of tolerance during soybean and meloidogyne incognita interactions. |
Ano de publicação: |
2022 |
Fonte/Imprenta: |
Plants, v. 11, 2744, 2022. |
ISSN: |
2223-7747 |
DOI: |
https:// doi.org/10.3390/plants11202744 |
Idioma: |
Inglês |
Conteúdo: |
The root-knot nematode (RKN), Meloidogyne incognita, is a devastating soybean pathogen worldwide. The use of resistant cultivars is the most effective method to prevent economic losses caused by RKNs. To elucidate the mechanisms involved in resistance to RKN, we determined the proteome and transcriptome profiles from roots of susceptible (BRS133) and highly tolerant (PI595099) Glycine max genotypes 4, 12, and 30 days after RKN infestation. After in silico analysis, we described major defense molecules and mechanisms considered constitutive responses to nematodeinfestation, such as mTOR, PI3K-Akt, relaxin, and thermogenesis. The integrated data allowed us to identify protein families and metabolic pathways exclusively regulated in tolerant soybean genotypes. Among them, we highlighted the phenylpropanoid pathway as an early, robust, and systemic defense process capable of controlling M. incognita reproduction. Associated with this metabolic pathway, 29 differentially expressed genes encoding 11 different enzymes were identified, mainly from the flavonoid and derivative pathways. Based on differential expression in transcriptomic and proteomic data, as well as in the expression profile by RT?qPCR, and previous studies, we selected and overexpressed the GmPR10 gene in transgenic tobacco to assess its protective effect against M. incognita. Transgenic plants of the T2 generation showed up to 58% reduction in the M. incognita reproduction factor. Finally, data suggest that GmPR10 overexpression can be effective against the plant parasitic nematodeM. incognita, but its mechanism of action remains unclear. These findings will help develop new engineered soybean genotypes with higher performance in response to RKN infections. MenosThe root-knot nematode (RKN), Meloidogyne incognita, is a devastating soybean pathogen worldwide. The use of resistant cultivars is the most effective method to prevent economic losses caused by RKNs. To elucidate the mechanisms involved in resistance to RKN, we determined the proteome and transcriptome profiles from roots of susceptible (BRS133) and highly tolerant (PI595099) Glycine max genotypes 4, 12, and 30 days after RKN infestation. After in silico analysis, we described major defense molecules and mechanisms considered constitutive responses to nematodeinfestation, such as mTOR, PI3K-Akt, relaxin, and thermogenesis. The integrated data allowed us to identify protein families and metabolic pathways exclusively regulated in tolerant soybean genotypes. Among them, we highlighted the phenylpropanoid pathway as an early, robust, and systemic defense process capable of controlling M. incognita reproduction. Associated with this metabolic pathway, 29 differentially expressed genes encoding 11 different enzymes were identified, mainly from the flavonoid and derivative pathways. Based on differential expression in transcriptomic and proteomic data, as well as in the expression profile by RT?qPCR, and previous studies, we selected and overexpressed the GmPR10 gene in transgenic tobacco to assess its protective effect against M. incognita. Transgenic plants of the T2 generation showed up to 58% reduction in the M. incognita reproduction factor. Finally, data suggest that GmPR10... Mostrar Tudo |
Palavras-Chave: |
Differential expression; Root-knot nematode. |
Thesagro: |
Glycine Max; Meloidogyne Incognita; Soja. |
Thesaurus Nal: |
Phenylpropanoids; Proteome; Transcriptome. |
Categoria do assunto: |
-- G Melhoramento Genético |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1148619/1/Integrated-omic-approaches.pdf
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Marc: |
LEADER 03069naa a2200457 a 4500 001 2148619 005 2023-12-08 008 2022 bl uuuu u00u1 u #d 022 $a2223-7747 024 7 $ahttps:// doi.org/10.3390/plants11202744$2DOI 100 1 $aARRAES, F. B. M. 245 $aIntegrated omic approaches reveal molecular mechanisms of tolerance during soybean and meloidogyne incognita interactions.$h[electronic resource] 260 $c2022 520 $aThe root-knot nematode (RKN), Meloidogyne incognita, is a devastating soybean pathogen worldwide. The use of resistant cultivars is the most effective method to prevent economic losses caused by RKNs. To elucidate the mechanisms involved in resistance to RKN, we determined the proteome and transcriptome profiles from roots of susceptible (BRS133) and highly tolerant (PI595099) Glycine max genotypes 4, 12, and 30 days after RKN infestation. After in silico analysis, we described major defense molecules and mechanisms considered constitutive responses to nematodeinfestation, such as mTOR, PI3K-Akt, relaxin, and thermogenesis. The integrated data allowed us to identify protein families and metabolic pathways exclusively regulated in tolerant soybean genotypes. Among them, we highlighted the phenylpropanoid pathway as an early, robust, and systemic defense process capable of controlling M. incognita reproduction. Associated with this metabolic pathway, 29 differentially expressed genes encoding 11 different enzymes were identified, mainly from the flavonoid and derivative pathways. Based on differential expression in transcriptomic and proteomic data, as well as in the expression profile by RT?qPCR, and previous studies, we selected and overexpressed the GmPR10 gene in transgenic tobacco to assess its protective effect against M. incognita. Transgenic plants of the T2 generation showed up to 58% reduction in the M. incognita reproduction factor. Finally, data suggest that GmPR10 overexpression can be effective against the plant parasitic nematodeM. incognita, but its mechanism of action remains unclear. These findings will help develop new engineered soybean genotypes with higher performance in response to RKN infections. 650 $aPhenylpropanoids 650 $aProteome 650 $aTranscriptome 650 $aGlycine Max 650 $aMeloidogyne Incognita 650 $aSoja 653 $aDifferential expression 653 $aRoot-knot nematode 700 1 $aVASQUEZ, D. D. N. 700 1 $aTAHIR, M. 700 1 $aPINHEIRO, D. H. 700 1 $aFAHEEM, M. 700 1 $aFREITAS-ALVES, N. S. 700 1 $aMOREIRA-PINTO, C. E. 700 1 $aMOREIRA, V. J. V. 700 1 $aPAES-DE-MELO, B. 700 1 $aLISEI-DE-SA, M. E. 700 1 $aMORGANTE, C. V. 700 1 $aMOTA, A. P. Z. 700 1 $aLOURENCO, I. T. 700 1 $aTOGAWA, R. C. 700 1 $aGRYNBERG, P. 700 1 $aFRAGOSO, R. da R. 700 1 $aALMEIDA-ENGLER, J. de 700 1 $aLARSEN, M. R. 700 1 $aGROSSI-DE-SA, M. F. 773 $tPlants$gv. 11, 2744, 2022.
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Registro original: |
Embrapa Agroenergia (CNPAE) |
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Registro Completo
Biblioteca(s): |
Embrapa Amazônia Ocidental; Embrapa Pantanal; Embrapa Unidades Centrais. |
Data corrente: |
28/10/2013 |
Data da última atualização: |
16/12/2013 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
DAIRIKI, J. K.; BORGHESI, R.; DIAS, C. T. dos S.; CYRINO, J. E. P. |
Afiliação: |
JONY KOJI DAIRIKI, CPAA; RICARDO BORGHESI, CPAP; Carlos Tadeu dos Santos Dias, Universidade de São Paulo; José Eurico Possebon Cyrino, ESALQ. |
Título: |
Lysine and arginine requirements of Salminus brasiliensis. |
Ano de publicação: |
2013 |
Fonte/Imprenta: |
Pesquisa Agropecuária Brasileira, Brasília, DF, v. 48, n. 8, p. 1012-1020, ago. 2013. |
DOI: |
10.1590/S0100-204X2013000800029 |
Idioma: |
Inglês Português |
Conteúdo: |
The objective of this work was to determine the dietary lysine (DL) and dietary arginine (DA) requirements of dourado (Salminus brasiliensis), through dose?response trials using the amino acid profiles of whole carcasses as a reference. Two experiments were carried out in a completely randomized design (n=4). In the first experiment, groups of 12 feed?conditioned dourado juveniles (11.4±0.2 g) were stocked in 60 L cages placed in 300 L plastic indoor tanks in a closed circulation system. Fish were fed for 60 days on diets containing 1.0, 1.5, 2.0, 2.5, 3.0, or 3.5 % dietary lysine. In the second experiment, dourado juveniles (27.0±0.8 g) were fed for 60 days on semipurified diets containing arginine at 1.0, 1.5, 2.0, 2.5 or 3.0%, in similar conditions to those of the first experiment. Optimal DL requirements, as determined by broken?line analysis method for final weight, weight gain and specific growth rate, were 2.15% DL or 5% lysine in dietary protein, and 1.48% DA or 3.43% arginine in dietary protein. The best feed conversion ratio is attained with 2.5% DL or 5.8% lysine in dietary protein and 1.4% DA or 3.25% arginine in dietary protein. |
Palavras-Chave: |
Amino acid; Dose-reposta; Dose-resposta; Regressão. |
Thesagro: |
Aminoácido; Dourado. |
Thesaurus NAL: |
Amino acids; Salminus brasiliensis. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/91743/1/Dairiki-et-al-lysine-and-arginine-requirements-of-dourado-PAB-2013-definitivo.pdf
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/92619/1/10837-79331-1-PB.pdf
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/162134/1/Lysine-and-arginine-requirements.pdf
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Marc: |
LEADER 01912naa a2200265 a 4500 001 1969536 005 2013-12-16 008 2013 bl uuuu u00u1 u #d 024 7 $a10.1590/S0100-204X2013000800029$2DOI 100 1 $aDAIRIKI, J. K. 245 $aLysine and arginine requirements of Salminus brasiliensis. 260 $c2013 520 $aThe objective of this work was to determine the dietary lysine (DL) and dietary arginine (DA) requirements of dourado (Salminus brasiliensis), through dose?response trials using the amino acid profiles of whole carcasses as a reference. Two experiments were carried out in a completely randomized design (n=4). In the first experiment, groups of 12 feed?conditioned dourado juveniles (11.4±0.2 g) were stocked in 60 L cages placed in 300 L plastic indoor tanks in a closed circulation system. Fish were fed for 60 days on diets containing 1.0, 1.5, 2.0, 2.5, 3.0, or 3.5 % dietary lysine. In the second experiment, dourado juveniles (27.0±0.8 g) were fed for 60 days on semipurified diets containing arginine at 1.0, 1.5, 2.0, 2.5 or 3.0%, in similar conditions to those of the first experiment. Optimal DL requirements, as determined by broken?line analysis method for final weight, weight gain and specific growth rate, were 2.15% DL or 5% lysine in dietary protein, and 1.48% DA or 3.43% arginine in dietary protein. The best feed conversion ratio is attained with 2.5% DL or 5.8% lysine in dietary protein and 1.4% DA or 3.25% arginine in dietary protein. 650 $aAmino acids 650 $aSalminus brasiliensis 650 $aAminoácido 650 $aDourado 653 $aAmino acid 653 $aDose-reposta 653 $aDose-resposta 653 $aRegressão 700 1 $aBORGHESI, R. 700 1 $aDIAS, C. T. dos S. 700 1 $aCYRINO, J. E. P. 773 $tPesquisa Agropecuária Brasileira, Brasília, DF$gv. 48, n. 8, p. 1012-1020, ago. 2013.
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Embrapa Amazônia Ocidental (CPAA) |
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