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| 101. |  | DEGENHARDT-GOLDBACH, J.; STACHEVSKI, T. W.; FRANCISCON, L.; BUSS, S.; WENDLING, I.; DUTRA, L. F. Calogênese in vitro a partir de folhas de erva-mate (Ilex paraguariensis St.Hil.) mantidas em casa de vegetação. In: CONGRESO SUDAMERICANO DE LA YERBA MATE, 5., 2011, Posadas. Actas. Posadas: Instituto Nacional de la Yerba Mate, 2011. p. 61-66. 1 CD-ROM.| Biblioteca(s): Embrapa Clima Temperado; Embrapa Florestas. |
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| 102. | | HEIMANN, J. de P.; DEGENHARDT, J.; DUTRA, L. F.; HANSEL, F. A.; FRANCISCON, L. Avaliação de meios de cultura na propagação in vitro de ápices caulinares de Eucalyptus benthamii. In: EVENTO DE INICIAÇÃO CIENTÍFICA DA EMBRAPA FLORESTAS, 8., 2009, Colombo. Anais. Colombo: Embrapa Florestas, 2009. 1 CD-ROM. (Embrapa Florestas. Documentos, 186). EVINCI. Resumo.| Biblioteca(s): Embrapa Florestas. |
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| 103. | | HEIMANN, J. de P.; GOLDBACH, J. D.; DUTRA, L. F.; HANSEL, F. A.; FRANCISCON, L. Avaliação de meios de cultura na propagação in vitro de ápices caulinares de Eucalyptus benthamii. In: EVENTO DE INICIAÇÃO CIENTÍFICA DA EMBRAPA FLORESTAS, 8., 2009, Colombo. Anais. Colombo: Embrapa Florestas, 2009. 1 CD-ROM. (Embrapa Florestas. Documentos, 186).| Biblioteca(s): Embrapa Clima Temperado. |
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| 104. | | SANTOS, D. C. dos; WENDLING, I.; DUTRA, L. F.; FRACARO, L. C. Assepsia para estabelecimento in vitro de erva-mate (Ilex paraguariensis). Horticultura Brasileira, Brasília DF, v. 23, n. 2, p. 638, ago. 2005. Suplemento. Edição dos Resumos do Congresso Brasileiro de Olericultura, 45; Congresso Brasileiro de Floricultura e Plantas Ornamentais, 15; Congresso Brasileiro de Cultura de Tecidos de Plantas, 2., 2005, Fortaleza.| Biblioteca(s): Embrapa Florestas. |
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| 114. | | BRONDANI, G. E.; DUTRA, L. F.; GROSSI, F.; WENDLING, I.; AZEVEDO, J. H.; HANSEL, F. A. Multiplicação e alongamento do híbrido Eucalyptus benthamii Maiden & Cambage x Eucalyptus dunnii Maiden. Revista Brasileira de Horticultura Ornamental, v. 13, p. 982-985, 2007. Suplemento. Edição dos Anais do 16º Congresso Brasileiro de Floricultura e Plantas Ornamentais; 3º Congresso Brasileiro de Cultura de Tecidos de Plantas; 1º Simpósio de Plantas Ornamentais Nativas, Goiânia, 2007.| Biblioteca(s): Embrapa Florestas. |
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| 115. | | LIMA, B. H. de; DUTRA, L. F.; HANSEL, F. A.; MORITZ, A.; BATISTA, C. do R. Multiplicação e alongamento in vitro de Eucalyptus benthamii. Revista Brasileira de Horticultura Ornamental, v. 13, p. 1104-1107, 2007. Suplemento. Edição dos Anais do 16º Congresso Brasileiro de Floricultura e Plantas Ornamentais; 3º Congresso Brasileiro de Cultura de Tecidos de Plantas; 1º Simpósio de Plantas Ornamentais Nativas, Goiânia, 2007.| Biblioteca(s): Embrapa Florestas. |
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| 116. | | TANIGUCHI, M.; COPATTI, A. S.; NICOLAO, R.; FERNANDO, J. A.; HEIDEN, G.; DUTRA, L. F. Organogênese in vitro em butia lallemantii (arecaceae). In: SEMANA INTEGRADA UFPEL, 5.; ENCONTRO DE PÓS-GRADUAÇÃO, 21., 2019, Pelotas. [Anais]. Online. 4 p. ENPOS. Eventos simultâneos: SEMANA INTEGRADA UFPEL, 5.; CONGRESSO DE INICIAÇÃO CIENTÍFICA, 28., 2019, Pelotas. [Anais]. 4 p. ENPOS.| Biblioteca(s): Embrapa Clima Temperado. |
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| 117. | | VILLA, F.; FRÁGUAS, C. B.; DUTRA, L. F.; PIO, L. A. S.; PASQUAL, M. Multiplicação in vitro de amoreira-preta cultivar Brazos. Ciência e Agrotecnologia, Lavras, v. 30, n.2, p. 266-270, mar./abr. 2006| Biblioteca(s): Embrapa Florestas. |
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Registro Completo
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
29/12/2014 |
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Data da última atualização: |
19/08/2024 |
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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: |
BENCKE-MALATO, M.; CABREIRA, C.; WIEBKE-STROHM, B.; BÜCKER-NETO, L.; MANCINI, E.; OSORIO, M. B.; HOMRICH, M. S.; TURCHETTO-ZOLET, A. C.; CARVALHO, M. C. C. G. de; STOLF, R.; WEBER, R. L. M.; WESTERGAARD, G.; CASTAGNARO, A. P.; ABDELNOOR, R. V.; MARCELINO-GUIMARÃES, F. C.; MARGIS-PINHEIRO, M.; BODANESE-ZANETTINI, M. H. |
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Afiliação: |
MARTA BENCKE-MALATO, UFRGS; CAROLINE CABREIRA, UFRGS; BEATRIZ WIEBKE-STROHM, UFRGS; LAURO BÜCKER-NETO, UFRGS; ESTEFANIA MANCINI, INSTITUTO DE AGROBIOTECNOLOGIA ROSARIO SA; MARINA B. OSORIO, UFRGS; MILENA S. HOMRICH, UFRGS; ANDREIA CARINA TURCHETTO-ZOLET, UFRGS; MAYRA C. C. G. DE CARVALHO; RENATA STOLF; RICARDO L. M. WEBER, UFRGS; GASTÓN WESTERGAARD, INSTITUTO DE AGROBIOTECNOLOGIA ROSARIO SA; ATÍLIO P. CASTAGNARO, ESTACIÓN EXPERIMENTAL AGROINDUSTRIAL OBISPO COLOMBRES (EEAOC); RICARDO VILELA ABDELNOOR, CNPSO; FRANCISMAR CORREA MARCELINO-GUIMARÃES, CNPSO; MÁRCIA MARGIS-PINHEIRO, UFRGS; MARIA HELENA BODANESE-ZANETTINI, UFRGS. |
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Título: |
Genome-wide annotation of the soybean WRKY family and functional characterization of genes involved in response to Phakopsora pachyrhizi infection. |
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Ano de publicação: |
2014 |
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Fonte/Imprenta: |
BMC Plant Biology, v. 14, n. 1, article 236, Sept. 2014. |
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Páginas: |
18 p. |
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ISSN: |
1471-2229 |
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DOI: |
10.1186/s12870-014-0236-0 |
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Idioma: |
Inglês |
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Conteúdo: |
Background: Many previous studies have shown that soybean WRKY transcription factors are involved in the plant response to biotic and abiotic stresses. Phakopsora pachyrhizi is the causal agent of Asian Soybean Rust, one of the most important soybean diseases. There are evidences that WRKYs are involved in the resistance of some soybean genotypes against that fungus. The number of WRKY genes already annotated in soybean genome was underrepresented. In the present study, a genome-wide annotation of the soybean WRKY family was carried out and members involved in the response to P. pachyrhizi were identified. Results: As a result of a soybean genomic databases search, 182 WRKY-encoding genes were annotated and 33 putative pseudogenes identified. Genes involved in the response to P. pachyrhizi infection were identified using superSAGE, RNA-Seq of microdissected lesions and microarray experiments. Seventy-five genes were differentially expressed during fungal infection. The expression of eight WRKY genes was validated by RT-qPCR. The expression of these genes in a resistant genotype was earlier and/or stronger compared with a susceptible genotype in response to P. pachyrhizi infection. Soybean somatic embryos were transformed in order to overexpress or silence WRKY genes. Embryos overexpressing a WRKY gene were obtained, but they were unable to convert into plants. When infected with P. pachyrhizi, the leaves of the silenced transgenic line showed a higher number of lesions than the wild-type plants. Conclusions: The present study reports a genome-wide annotation of soybean WRKY family. The participation of some members in response to P. pachyrhizi infection was demonstrated. The results contribute to the elucidation of gene function and suggest the manipulation of WRKYs as a strategy to increase fungal resistance in soybean plants. MenosBackground: Many previous studies have shown that soybean WRKY transcription factors are involved in the plant response to biotic and abiotic stresses. Phakopsora pachyrhizi is the causal agent of Asian Soybean Rust, one of the most important soybean diseases. There are evidences that WRKYs are involved in the resistance of some soybean genotypes against that fungus. The number of WRKY genes already annotated in soybean genome was underrepresented. In the present study, a genome-wide annotation of the soybean WRKY family was carried out and members involved in the response to P. pachyrhizi were identified. Results: As a result of a soybean genomic databases search, 182 WRKY-encoding genes were annotated and 33 putative pseudogenes identified. Genes involved in the response to P. pachyrhizi infection were identified using superSAGE, RNA-Seq of microdissected lesions and microarray experiments. Seventy-five genes were differentially expressed during fungal infection. The expression of eight WRKY genes was validated by RT-qPCR. The expression of these genes in a resistant genotype was earlier and/or stronger compared with a susceptible genotype in response to P. pachyrhizi infection. Soybean somatic embryos were transformed in order to overexpress or silence WRKY genes. Embryos overexpressing a WRKY gene were obtained, but they were unable to convert into plants. When infected with P. pachyrhizi, the leaves of the silenced transgenic line showed a higher number of lesions than ... Mostrar Tudo |
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Thesagro: |
Soja. |
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Thesaurus NAL: |
Soybeans. |
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Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
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URL: |
https://www.alice.cnptia.embrapa.br/alice/bitstream/doc/1003866/1/GenomewideannotationofthesoybeanWRKYfamilyandfunctionalcharacterizationofgenesinvolvedinresponsetoPhakopsorapachyrhiziinfection.pdf
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Marc: |
LEADER 02998naa a2200373 a 4500
001 2003866
005 2024-08-19
008 2014 bl uuuu u00u1 u #d
022 $a1471-2229
024 7 $a10.1186/s12870-014-0236-0$2DOI
100 1 $aBENCKE-MALATO, M.
245 $aGenome-wide annotation of the soybean WRKY family and functional characterization of genes involved in response to Phakopsora pachyrhizi infection.$h[electronic resource]
260 $c2014
300 $a18 p.
520 $aBackground: Many previous studies have shown that soybean WRKY transcription factors are involved in the plant response to biotic and abiotic stresses. Phakopsora pachyrhizi is the causal agent of Asian Soybean Rust, one of the most important soybean diseases. There are evidences that WRKYs are involved in the resistance of some soybean genotypes against that fungus. The number of WRKY genes already annotated in soybean genome was underrepresented. In the present study, a genome-wide annotation of the soybean WRKY family was carried out and members involved in the response to P. pachyrhizi were identified. Results: As a result of a soybean genomic databases search, 182 WRKY-encoding genes were annotated and 33 putative pseudogenes identified. Genes involved in the response to P. pachyrhizi infection were identified using superSAGE, RNA-Seq of microdissected lesions and microarray experiments. Seventy-five genes were differentially expressed during fungal infection. The expression of eight WRKY genes was validated by RT-qPCR. The expression of these genes in a resistant genotype was earlier and/or stronger compared with a susceptible genotype in response to P. pachyrhizi infection. Soybean somatic embryos were transformed in order to overexpress or silence WRKY genes. Embryos overexpressing a WRKY gene were obtained, but they were unable to convert into plants. When infected with P. pachyrhizi, the leaves of the silenced transgenic line showed a higher number of lesions than the wild-type plants. Conclusions: The present study reports a genome-wide annotation of soybean WRKY family. The participation of some members in response to P. pachyrhizi infection was demonstrated. The results contribute to the elucidation of gene function and suggest the manipulation of WRKYs as a strategy to increase fungal resistance in soybean plants.
650 $aSoybeans
650 $aSoja
700 1 $aCABREIRA, C.
700 1 $aWIEBKE-STROHM, B.
700 1 $aBÜCKER-NETO, L.
700 1 $aMANCINI, E.
700 1 $aOSORIO, M. B.
700 1 $aHOMRICH, M. S.
700 1 $aTURCHETTO-ZOLET, A. C.
700 1 $aCARVALHO, M. C. C. G. de
700 1 $aSTOLF, R.
700 1 $aWEBER, R. L. M.
700 1 $aWESTERGAARD, G.
700 1 $aCASTAGNARO, A. P.
700 1 $aABDELNOOR, R. V.
700 1 $aMARCELINO-GUIMARÃES, F. C.
700 1 $aMARGIS-PINHEIRO, M.
700 1 $aBODANESE-ZANETTINI, M. H.
773 $tBMC Plant Biology$gv. 14, n. 1, article 236, Sept. 2014.
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