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| Registros recuperados : 7 | |
| 1. |  | MORGANTE, C. V.; ARRAES, F. B. M.; PINTO, C. E. M.; MELO, B. P. de; GROSSI-DE-SA, M. F. Modulação da expressão gênica em plantas via tecnologia CRISPR/dCas9. In: MOLINARI, H. B. C.; VIEIRA, L. R.; SILVA, N. V. e; PRADO, G. S.; LOPES FILHO, J. H. (Ed.). Tecnologia CRISPR na edição genômica de plantas: biotecnologia aplicada à agricultura. Brasília, DF: Embrapa, 2020. cap. 4, p. 125-177.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia; Embrapa Semiárido. |
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| 2. | | BASSO, M. F.; LOURENCO-TESSUTTI, I. T.; MENDES, R. A. G.; PINTO, C. E. M.; BOURNAUD, C.; GILLET, F.-X.; TOGAWA, R. C.; MACEDO, L. L. P. de; ENGLER, J. d A.; GROSSI-DE-SA, M. F. MiDaf16-like and MiSkn1-like gene families are reliable targets to develop biotechnological tools for the control and management of Meloidogyne incognita. Scientific Reports, v. 10, n. 1, p. 1-13, 2020.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 3. | | IBARRA, L. N.; ALVES, A. E. O. de A.; ANTONINO, J. D.; PRADO, G. S.; PINTO, C. E. M.; SOCCOL, C. R.; VASCONCELOS, E. A. R. de; GROSSI-DE-SA, M. F. Enzymatic activity of a recombinant beta-1,4-endoglucanase from the Cotton Boll Weevil (Anthonomus grandis) aiming second generation ethanol production. Scientific Reports, v. 9, 19580, 2019.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 4. | | FARIAS, D. F.; VIANA, M. P.; OLIVEIRA, G. R.; SANTOS, V. O.; PINTO, C. E. M.; VIANA, D. A.; VASCONCELOS, I. M.; SA, M. F. G. de; CARVALHO, A. F. U. Food safety assessment of Cry8Ka5 mutant protein using Cry1Ac as a control Bt protein. Food and Chemical Toxicology, v. 81, p. 81-91, 2015.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 5. | | BASSO, M. F.; LOURENCO-TESSUTTI, I. T.; BUSANELLO, C.; PINTO, C. E. M.; FREITAS, E. de O.; RIBEIRO, T. P.; ENGLER, J. de A.; OLIVEIRA, A. C. de; MORGANTE, C. V.; ALVES-FERREIRA, M.; GROSSI-DE-SA, M. F. Insights obtained using different modules of the cotton uceA1.7 promoter. Planta, v. 251, n. 2, 2020.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia; Embrapa Semiárido. |
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| 6. | | COSTA, L. S. de L.; ALVES, N. S. de F.; PINTO, C. E. M.; FLORENTINO, L. H.; MELO, B. P. de; MOREIRA, V. J. V.; SÁ, M. E. L. de; ARRAES, F. B. M.; RECH FILHO, E. L.; MORGANTE, C. V.; SA, M. F. G. de. Depleção do quadro de leitura upstream como nova estratégia para manipular a tradução de gmpr10 usando crispr/cas9 para aumentar a tolerância da soja a fitonematoides. In: SIMPÓSIO BRASILEIRO DE GENÉTICA MOLECULAR DE PLANTAS, 8, 2023, Florianópolis, SC. Anais... Florianópolis: SBG, 2023. p. 131.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 7. | | COSTA, L. S. de L.; ALVES, N. S. de F.; PINTO, C. E. M.; FLORENTINO, L. H.; MELO, B. P. de; MOREIRA, V. J. V.; SÁ, M. E. L. de; ARRAES, F. B. M.; RECH FILHO, E. L.; MORGANTE, C. V.; SA, M. F. G. de. Depleção do quadro de leitura upstream como nova estratégia para manipular a tradução de gmpr10 usando crispr/cas9 para aumentar a tolerância da soja a fitonematoides. In: SIMPÓSIO BRASILEIRO DE GENÉTICA MOLECULAR DE PLANTAS, 8, 2023, Florianópolis, SC. Anais... Florianópolis: SBG, 2023. p. 131.| Biblioteca(s): Embrapa Semiárido. |
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| Registros recuperados : 7 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Recursos Genéticos e Biotecnologia. Para informações adicionais entre em contato com cenargen.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia; Embrapa Semiárido. |
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Data corrente: |
28/04/2020 |
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Data da última atualização: |
19/11/2020 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 1 |
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Autoria: |
BASSO, M. F.; LOURENCO-TESSUTTI, I. T.; BUSANELLO, C.; PINTO, C. E. M.; FREITAS, E. de O.; RIBEIRO, T. P.; ENGLER, J. de A.; OLIVEIRA, A. C. de; MORGANTE, C. V.; ALVES-FERREIRA, M.; GROSSI-DE-SA, M. F. |
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Afiliação: |
MARCOS FERNANDO BASSO; ISABELA TRISTAN LOURENCO TESSUTTI, Cenargen; CARLOS BUSANELLO, UFPEL; CLIDIA EDUARDA MOREIRA PINTO, UNB; ELINEA DE OLIVEIRA FREITAS, UNB; JANICE DE ALMEIDA ENGLER, INRA/CNRS/UNS, FRANCE; ANTONIO COSTA DE OLIVEIRA, UFPEL; CAROLINA VIANNA MORGANTE, CPATSA; MARCIO ALVES-FERREIRA, UFRJ; MARIA FATIMA GROSSI DE SA, Cenargen. |
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Título: |
Insights obtained using different modules of the cotton uceA1.7 promoter. |
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Ano de publicação: |
2020 |
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Fonte/Imprenta: |
Planta, v. 251, n. 2, 2020. |
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DOI: |
https://doi.org/10.1007/s00425-020-03348-8 |
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Idioma: |
Inglês |
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Conteúdo: |
Transcriptional promoters are among the primary genetic engineering elements used to control genes of interest (GOIs) associated with agronomic traits. Cotton uceA1.7 was previously characterized as a constitutive promoter with activity higher than that of the constitutive promoter from the Cauliflower mosaic virus (CaMV) 35S gene in various plant tissues. In this study, we generated Arabidopsis thaliana homozygous events stably overexpressing the gfp reporter gene driven by different modules of the uceA1.7 promoter. The expression level of the reporter gene in different plant tissues and the transcriptional stability of these modules was determined compared to its full-length promoter and the 35S promoter. The full-length uceA1.7 promoter exhibited higher activity in different plant tissues compared to the 35S promoter. Two modules of the promoter produced a low and unstable transcription level compared to the other promoters. The other two modules rich in cis-regulatory elements showed similar activity levels to full-length uceA1.7 and 35S promoters but were less stable. This result suggests the location of a minimal portion of the promoter that is required to initiate transcription properly (the core promoter). Additionally, the full-length uceA1.7 promoter containing the 5?-untranslated region (UTR) is essential for higher transcriptional stability in various plant tissues. These findings confirm the potential use of the full-length uceA1.7 promoter for the development of new biotechnological tools (NBTs) to achieve higher expression levels of GOIs in, for example, the root or flower bud for the efficient control of phytonematodes and pest-insects, respectively, in important crops. MenosTranscriptional promoters are among the primary genetic engineering elements used to control genes of interest (GOIs) associated with agronomic traits. Cotton uceA1.7 was previously characterized as a constitutive promoter with activity higher than that of the constitutive promoter from the Cauliflower mosaic virus (CaMV) 35S gene in various plant tissues. In this study, we generated Arabidopsis thaliana homozygous events stably overexpressing the gfp reporter gene driven by different modules of the uceA1.7 promoter. The expression level of the reporter gene in different plant tissues and the transcriptional stability of these modules was determined compared to its full-length promoter and the 35S promoter. The full-length uceA1.7 promoter exhibited higher activity in different plant tissues compared to the 35S promoter. Two modules of the promoter produced a low and unstable transcription level compared to the other promoters. The other two modules rich in cis-regulatory elements showed similar activity levels to full-length uceA1.7 and 35S promoters but were less stable. This result suggests the location of a minimal portion of the promoter that is required to initiate transcription properly (the core promoter). Additionally, the full-length uceA1.7 promoter containing the 5?-untranslated region (UTR) is essential for higher transcriptional stability in various plant tissues. These findings confirm the potential use of the full-length uceA1.7 promoter for the development o... Mostrar Tudo |
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Palavras-Chave: |
Cotton constitutive promoter; New biotechnological tools; Transcriptional core promoter; Transgenic crops. |
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Thesagro: |
Algodão; Gene Marcador; Genética. |
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Thesaurus NAL: |
Gene expression. |
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Categoria do assunto: |
--
G Melhoramento Genético |
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Marc: |
LEADER 02743naa a2200349 a 4500
001 2123510
005 2020-11-19
008 2020 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1007/s00425-020-03348-8$2DOI
100 1 $aBASSO, M. F.
245 $aInsights obtained using different modules of the cotton uceA1.7 promoter.$h[electronic resource]
260 $c2020
520 $aTranscriptional promoters are among the primary genetic engineering elements used to control genes of interest (GOIs) associated with agronomic traits. Cotton uceA1.7 was previously characterized as a constitutive promoter with activity higher than that of the constitutive promoter from the Cauliflower mosaic virus (CaMV) 35S gene in various plant tissues. In this study, we generated Arabidopsis thaliana homozygous events stably overexpressing the gfp reporter gene driven by different modules of the uceA1.7 promoter. The expression level of the reporter gene in different plant tissues and the transcriptional stability of these modules was determined compared to its full-length promoter and the 35S promoter. The full-length uceA1.7 promoter exhibited higher activity in different plant tissues compared to the 35S promoter. Two modules of the promoter produced a low and unstable transcription level compared to the other promoters. The other two modules rich in cis-regulatory elements showed similar activity levels to full-length uceA1.7 and 35S promoters but were less stable. This result suggests the location of a minimal portion of the promoter that is required to initiate transcription properly (the core promoter). Additionally, the full-length uceA1.7 promoter containing the 5?-untranslated region (UTR) is essential for higher transcriptional stability in various plant tissues. These findings confirm the potential use of the full-length uceA1.7 promoter for the development of new biotechnological tools (NBTs) to achieve higher expression levels of GOIs in, for example, the root or flower bud for the efficient control of phytonematodes and pest-insects, respectively, in important crops.
650 $aGene expression
650 $aAlgodão
650 $aGene Marcador
650 $aGenética
653 $aCotton constitutive promoter
653 $aNew biotechnological tools
653 $aTranscriptional core promoter
653 $aTransgenic crops
700 1 $aLOURENCO-TESSUTTI, I. T.
700 1 $aBUSANELLO, C.
700 1 $aPINTO, C. E. M.
700 1 $aFREITAS, E. de O.
700 1 $aRIBEIRO, T. P.
700 1 $aENGLER, J. de A.
700 1 $aOLIVEIRA, A. C. de
700 1 $aMORGANTE, C. V.
700 1 $aALVES-FERREIRA, M.
700 1 $aGROSSI-DE-SA, M. F.
773 $tPlanta$gv. 251, n. 2, 2020.
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