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Registros recuperados : 31 | |
2. | | ANGELO, P. C. da S.; PEREIRA, L. F. P.; SERA, G. H.; SETA, T. Coffee microspore cultivation to attain doubled-haploid plantlets. Acta Horticulturae, v. 31, n. 1359, p. 123-130, 2023. Apresentado no INTERNATIONAL HORTICULTURAL CONGRESS, 31., 2022, Angers, França. Biblioteca(s): Embrapa Café. |
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10. | | ANGELO, P. C. da S.; PEREIRA, L. F. P.; SERA, G. H.; CAIXETA, E. T. Some Coffea liberica SH3-LRR-coding sequences are highly distinguishable. Acta Horticulturae, v. 31, n. 1362, p. 283-287, 2023. Apresentado no INTERNATIONAL HORTICULTURAL CONGRESS, 31., 2022, Angers, França. Biblioteca(s): Embrapa Café. |
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11. | | ANGELO, P. C. da S.; FERREIRA, I. B.; CARVALHO, C. H. S. de; MATIELLO, J. B.; SERA, G. H. Arabica coffee fruits phenology assessed through degree days, precipitation, and solar radiation exposure on a daily basis. International Journal of Biometeorology, v. 63, n. 7, p. 831-843, 2019 Biblioteca(s): Embrapa Café. |
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12. | | ANGELO, P. C. da S.; CAIXETA, E. T.; PEREIRA, L. F. P.; RIBAS, A. F.; SERA, G. H. Os loci SH3 envolvidos na resistência à ferrugem são complexos, multialélicos e divergentes em genomas de coffea. Brasília, DF: Embrapa Café, 2022. 21 p. PDF. (Embrapa Café. Boletim de Pesquisa e Desenvolvimento, 3). Título em inglês: SH3 loci involved in the resistance to leaf rust are complex, multi allelic and divergent in coffea. Biblioteca(s): Embrapa Café. |
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13. | | ANGELO, P. C. da S.; ARIYOSHI, C.; CAIXETA, E. T.; PEREIRA, L. F. P.; RIBAS, A. F.; SERA, G. H. Variabilidade no domínio LRR de peptídeos codificados em "clusters" homólogos ao SH3 em diferentes genomas de Coffea. In: SIMPÓSIO DE PESQUISA DOS CAFÉS DO BRASIL, 10., 2019, Vitória, ES. Pesquisa, inovação e sustentabilidade dos cafés do Brasil. Brasília, DF: Embrapa Café, 2019. Título em inglês: LRR domain variability for peptides encoded in gene clusters homologous to the SH3 in different Coffea genomes. Biblioteca(s): Embrapa Café. |
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14. | | CHARMETANT, P.; PEREIRA, L. F.; SERA, G. H.; MARRACCINI, P.; ANDRADE, A. C.; MOUEN, J.; AUKOUMOU, M. M.; ANNEBIQUE, F.; LEROY, T. Adaptation of Coffea arabica F1 Hybrids to various environmental conditions. In: EUCARPIA GENETIC RESOURCES, 2017, Montpellier. Abstracts book... Montpellier: INRA, 2017. Biblioteca(s): Embrapa Café. |
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15. | | CARVALHO, C. H. S. de; BARTELEGA, L.; SERA, G. H.; MATIELLO, J. B.; ALMEIDA, S. R. de; SANTINATO, F.; HOTZ, A. L. Catálogo de cultivares de café arábica. Brasília, DF: Embrapa Café, 2022. 115 p. PDF. (Embrapa Café. Documentos, 16). Biblioteca(s): Embrapa Café; Embrapa Unidades Centrais. |
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16. | | GASPARINI, A. K. dos S.; CINTRA, L. A.; CARDUCCI, F. C.; SHIGUEOKA, L. H.; SERA, G. H.; SERA, T.; ANGELO, P. C. da S. Indução in vivo de poliploidia em Coffea canephora resistente a nematoides. In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA PARA O PROGRESSO DA CIÊNCIA, 73., 2021, Juiz de Fora, MG. Anais... Juiz de Fora, MG: SBPC, 2021. 4 p. Biblioteca(s): Embrapa Café. |
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17. | | RIEDE, C. R.; CAMPOS, L. A. C.; GARBUGLIO, D. D.; OKUYAMA, L. A.; SCHOLZ, M. B. dos; SERA, G. H.; SHIOGA, P. S.; POLA, J. N. IPR Catuara TM - cultivar de trigo melhorador. In: REUNIÃO DA COMISSÃO BRASILEIRA DE PESQUISA DE TRIGO E TRITICALE, 5., 2011, Dourados. Ata e resumos... Dourados: Embrapa Agropecuária Oeste, 2011. 4 p. Melhoramento, Aptidão Industrial e Sementes. 1 CD-ROM. Biblioteca(s): Embrapa Trigo. |
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18. | | SERA, G. H.; SERA, T.; MATA, J. S. da; ALEGRE, C. R.; FONSECA, I. C. de B.; ITO, D. S.; KANAYAMA, F. S.; BARRETO, P. C. Reaction of coffee cultivars Tupi IAC 1669-33 and IPR 100 to nematode Meloidogyne paranaensis. Crop Breeding and Applied Biotechnology, Londrina, v. 9, n. 4, p. 293-298, Dec. 2009. Biblioteca(s): Embrapa Agricultura Digital. |
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19. | | SERA, G. H.; CARVALHO, C. H. S. de; ABRAHÃO, J. C. de R.; POZZA, E. A.; MATIELLO, J. B.; ALMEIDA, S. R. de; BARTELEGA, L.; BOTELHO, D. M. dos S. Coffee leaf rust in Brazil: historical events, current situation, and control measures. Agronomy, v. 12, n. 2, 2022. 19 p. Biblioteca(s): Embrapa Café. |
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20. | | ANGELO, P. C. da S.; YAMAGISHI, M. E. B.; SILVA, A. G.; PONCE, T. P.; ARIYOSHI, C.; SHIGUEOKA, L. H.; ARANTES, T.; GASPARINI, A. K.; SERA, G. H.; PEREIRA, L. F. P.; CAIXETA, E. T. Could genes allocated to SH3 loci contribute to other resistance factors? In: ASIC CONFERENCE ON COFFEE SCIENCE, 29., 2023, Hanoi, Vietnam. Books of abstracts... Montpellier: ASIC, 2023. p. 167. ASIC 2023. Biblioteca(s): Embrapa Agricultura Digital; Embrapa Café. |
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Registros recuperados : 31 | |
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Registro Completo
Biblioteca(s): |
Embrapa Café. |
Data corrente: |
12/04/2023 |
Data da última atualização: |
13/04/2023 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
ANGELO, P. C. da S.; PEREIRA, L. F. P.; SERA, G. H.; CAIXETA, E. T. |
Afiliação: |
PAULA CRISTINA DA SILVA ANGELO, CNPCa; L. F. P. PEREIRA; G. H. SERA, IDR-Parana; E. T. CAIXETA, Embrapa Coffee - University of Viçosa. |
Título: |
Some Coffea liberica SH3-LRR-coding sequences are highly distinguishable. |
Ano de publicação: |
2022 |
Fonte/Imprenta: |
INTERNATIONAL HORTICULTURAL CONGRESS, 31., 2022, Angers, França. |
DOI: |
10.17660/ActaHortic.2023.1362.38 |
Idioma: |
Inglês |
Notas: |
E-poster. |
Conteúdo: |
Genes in coffee SH3 loci are involved in the interaction with the fungus Hemileia vastatrix. Previously we found, by comparison to data published for C. arabica ?IAPAR 59?, that SH3 loci are multi-alellic and complex in the publicly available genomes of Coffea arabica ?Caturra?, C. eugenioides and C. canephora. The above cited SH3 loci display different numbers of copies of a CC-NBS-LRR gene, in distinctive organizations. In its turn, C. liberica is considered to display an SH3 configuration ideal to provide durable resistance to leaf rust, which is highly desirable and pursued. The CC-NBS-LRR genes in the coffee SH3 loci display highly conserved as well as hypervariable regions. Sets of primers designated to amplify the hypervariable LRR-carboxy terminals were used to clone and sequence S H3 variants in C. liberica and ?IAPAR 59?. Neighbor-joining was used to graphically represent pairwise divergence indexes between the deduced peptide sequences. ?IAPAR 59? was re-accessed as a testimony for the approach?s effectiveness because it was possible to verify that all the variants previously reported elsewhere for SH3 genes in ?IAPAR 59? BAC clones were also cloned using our primer sets. Indeed, it was considered that all the variants present in the accessed C. liberica plant had also been cloned. This was further checked by contrasting the restriction fragment maps coming from genomic DNA × cloned amplicons in the two genotypes: patterns for both DNA sources of a same genotype were equal, and diverged from those in the other genotype. Regarding sequences, at least three out of six carboxy-terminal variants found in C. liberica seem to be exclusive when contrasted to the other four genotypes accessed. Differences found in the restriction maps and sequences are very likely related to susceptibility or resistance reactions verified during coffee plants-H. vastatrix physiological race interactions. MenosGenes in coffee SH3 loci are involved in the interaction with the fungus Hemileia vastatrix. Previously we found, by comparison to data published for C. arabica ?IAPAR 59?, that SH3 loci are multi-alellic and complex in the publicly available genomes of Coffea arabica ?Caturra?, C. eugenioides and C. canephora. The above cited SH3 loci display different numbers of copies of a CC-NBS-LRR gene, in distinctive organizations. In its turn, C. liberica is considered to display an SH3 configuration ideal to provide durable resistance to leaf rust, which is highly desirable and pursued. The CC-NBS-LRR genes in the coffee SH3 loci display highly conserved as well as hypervariable regions. Sets of primers designated to amplify the hypervariable LRR-carboxy terminals were used to clone and sequence S H3 variants in C. liberica and ?IAPAR 59?. Neighbor-joining was used to graphically represent pairwise divergence indexes between the deduced peptide sequences. ?IAPAR 59? was re-accessed as a testimony for the approach?s effectiveness because it was possible to verify that all the variants previously reported elsewhere for SH3 genes in ?IAPAR 59? BAC clones were also cloned using our primer sets. Indeed, it was considered that all the variants present in the accessed C. liberica plant had also been cloned. This was further checked by contrasting the restriction fragment maps coming from genomic DNA × cloned amplicons in the two genotypes: patterns for both DNA sources of a same genotype w... Mostrar Tudo |
Thesaurus NAL: |
Gene interaction; Leucine; Plant pathogens. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1153107/1/Some-Coffea-liberica-eposter.pdf
|
Marc: |
LEADER 02562nam a2200205 a 4500 001 2153107 005 2023-04-13 008 2022 bl uuuu u00u1 u #d 024 7 $a10.17660/ActaHortic.2023.1362.38$2DOI 100 1 $aANGELO, P. C. da S. 245 $aSome Coffea liberica SH3-LRR-coding sequences are highly distinguishable.$h[electronic resource] 260 $aINTERNATIONAL HORTICULTURAL CONGRESS, 31., 2022, Angers, França.$c2022 500 $aE-poster. 520 $aGenes in coffee SH3 loci are involved in the interaction with the fungus Hemileia vastatrix. Previously we found, by comparison to data published for C. arabica ?IAPAR 59?, that SH3 loci are multi-alellic and complex in the publicly available genomes of Coffea arabica ?Caturra?, C. eugenioides and C. canephora. The above cited SH3 loci display different numbers of copies of a CC-NBS-LRR gene, in distinctive organizations. In its turn, C. liberica is considered to display an SH3 configuration ideal to provide durable resistance to leaf rust, which is highly desirable and pursued. The CC-NBS-LRR genes in the coffee SH3 loci display highly conserved as well as hypervariable regions. Sets of primers designated to amplify the hypervariable LRR-carboxy terminals were used to clone and sequence S H3 variants in C. liberica and ?IAPAR 59?. Neighbor-joining was used to graphically represent pairwise divergence indexes between the deduced peptide sequences. ?IAPAR 59? was re-accessed as a testimony for the approach?s effectiveness because it was possible to verify that all the variants previously reported elsewhere for SH3 genes in ?IAPAR 59? BAC clones were also cloned using our primer sets. Indeed, it was considered that all the variants present in the accessed C. liberica plant had also been cloned. This was further checked by contrasting the restriction fragment maps coming from genomic DNA × cloned amplicons in the two genotypes: patterns for both DNA sources of a same genotype were equal, and diverged from those in the other genotype. Regarding sequences, at least three out of six carboxy-terminal variants found in C. liberica seem to be exclusive when contrasted to the other four genotypes accessed. Differences found in the restriction maps and sequences are very likely related to susceptibility or resistance reactions verified during coffee plants-H. vastatrix physiological race interactions. 650 $aGene interaction 650 $aLeucine 650 $aPlant pathogens 700 1 $aPEREIRA, L. F. P. 700 1 $aSERA, G. H. 700 1 $aCAIXETA, E. T.
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