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Registro Completo |
Biblioteca(s): |
Biblioteca Rui Tendinha. |
Data corrente: |
29/04/2015 |
Data da última atualização: |
01/09/2015 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
ABREU, P. M. V.; ANTUNES, T. F. S.; MAGAÑA-ÁLVAREZ, A.; PÉREZ-BRITO, D.; TAPIA-TUSSEL, R.; VENTURA, J. A.; FERNANDES, A. A. R.; FERNANDES, P. M. B. |
Afiliação: |
Paolla M. V. Abreu; Tathiana F. S. Antunes; Anuar Magaña-Álvarez; Daisy Pérez-Brito; Raúl Tapia-Tussell; Jose Aires Ventura, Incaper; Antonio A. R. Fernandes; Patricia M. B. Fernandes. |
Título: |
A Current Overview of the Papaya meleira virus, an Unusual Plant Virus. |
Ano de publicação: |
2015 |
Fonte/Imprenta: |
Viruses, v. 7, p. 1853-1870, 2015. |
DOI: |
10.3390/v7041853 |
Idioma: |
Inglês |
Conteúdo: |
Papaya meleira virus (PMeV) is the causal agent of papaya sticky disease, which is characterized by a spontaneous exudation of fluid and aqueous latex from the papaya fruit and leaves. The latex oxidizes after atmospheric exposure, resulting in a sticky feature on the fruit from which the name of the disease originates. PMeV is an isometric virus particle with a double-stranded RNA (dsRNA) genome of approximately 12 Kb. Unusual for a plant virus, PMeV particles are localized on and linked to the polymers present in the latex. The ability of the PMeV to inhabit such a hostile environment demonstrates an intriguing interaction of the virus with the papaya. A hypersensitivity response is triggered against PMeV infection, and there is a reduction in the proteolytic activity of papaya latex during sticky disease. In papaya leaf tissues, stress responsive proteins, mostly calreticulin and proteasome-related proteins, are up regulated and proteins related to metabolism are down-regulated. Additionally, PMeV modifies the transcription of several miRNAs involved in the modulation of genes related to the ubiquitin-proteasome system. Until now, no PMeV resistant papaya genotype has been identified and roguing is the only viral control strategy available. However, a single inoculation of papaya plants with PMeV dsRNA delayed the progress of viral infection. |
Thesaurus NAL: |
DsRNA genome virus; Laticifers colonization; Papaya sticky disease; Phytopathogenic virus. |
Categoria do assunto: |
G Melhoramento Genético |
URL: |
http://biblioteca.incaper.es.gov.br/digital/bitstream/item/748/1/CurrentOverviewofthePapayameleiravirusVentura.pdf
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Marc: |
LEADER 02150naa a2200265 a 4500 001 1006363 005 2015-09-01 008 2015 bl uuuu u00u1 u #d 024 7 $a10.3390/v7041853$2DOI 100 1 $aABREU, P. M. V. 245 $aA Current Overview of the Papaya meleira virus, an Unusual Plant Virus.$h[electronic resource] 260 $c2015 520 $aPapaya meleira virus (PMeV) is the causal agent of papaya sticky disease, which is characterized by a spontaneous exudation of fluid and aqueous latex from the papaya fruit and leaves. The latex oxidizes after atmospheric exposure, resulting in a sticky feature on the fruit from which the name of the disease originates. PMeV is an isometric virus particle with a double-stranded RNA (dsRNA) genome of approximately 12 Kb. Unusual for a plant virus, PMeV particles are localized on and linked to the polymers present in the latex. The ability of the PMeV to inhabit such a hostile environment demonstrates an intriguing interaction of the virus with the papaya. A hypersensitivity response is triggered against PMeV infection, and there is a reduction in the proteolytic activity of papaya latex during sticky disease. In papaya leaf tissues, stress responsive proteins, mostly calreticulin and proteasome-related proteins, are up regulated and proteins related to metabolism are down-regulated. Additionally, PMeV modifies the transcription of several miRNAs involved in the modulation of genes related to the ubiquitin-proteasome system. Until now, no PMeV resistant papaya genotype has been identified and roguing is the only viral control strategy available. However, a single inoculation of papaya plants with PMeV dsRNA delayed the progress of viral infection. 650 $aDsRNA genome virus 650 $aLaticifers colonization 650 $aPapaya sticky disease 650 $aPhytopathogenic virus 700 1 $aANTUNES, T. F. S. 700 1 $aMAGAÑA-ÁLVAREZ, A. 700 1 $aPÉREZ-BRITO, D. 700 1 $aTAPIA-TUSSEL, R. 700 1 $aVENTURA, J. A. 700 1 $aFERNANDES, A. A. R. 700 1 $aFERNANDES, P. M. B. 773 $tViruses$gv. 7, p. 1853-1870, 2015.
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Registro original: |
Biblioteca Rui Tendinha (BRT) |
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Registro Completo |
Biblioteca(s): |
Biblioteca Rui Tendinha. |
Data corrente: |
07/01/2015 |
Data da última atualização: |
09/09/2019 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
- - - |
Autoria: |
FONSECA, A. F. A. da.; SEDIYAMA, T.; CRUZ, C. D.; SAKIYAMA, N. S.; FERRÃO, R. G.; FERRÃO, M. A. G.; BRAGANÇA, S. M. |
Afiliação: |
Aymbiré Francisco Almeida da Fonseca, Incaper/Embrapa Café; Cosme Damião Cruz; Ney Sussumu Sakiyama; Romário Gava Ferrão, Incaper; Maria Amélia Gava Ferrão, Incaper/Embrapa Café; Scheilla Marina Bragança, Incaper. |
Título: |
Discriminant analysis for the classification and clustering of robusta coffee genotypes. |
Ano de publicação: |
2004 |
Fonte/Imprenta: |
Crop Breeding and Applied Biotechnology, v. 4, n. 3, p. 285-289, 2004. |
ISSN: |
1518-7853 |
Idioma: |
Inglês |
Conteúdo: |
This study evaluated the adequacy of the composition of three clonal Coffea canephora varieties recommended for the State of Espírito Santo by a multivariate method designated discriminant analysis. This method consists in the establishment of functions that enable the classification of a given individual into one, among various distinct populations, reducing the probability of a misclassification. It simultaneously considers measures of several traits, in order to give the new variety homogeneity. The original classification of genotypes in the three studied varieties, based on agronomical criteria, maintained expressive concordance with the results of the discriminant analysis, with an apparent deviation rate of only 6.25%. Corrected discriminant functions were also proposed, capable of classifying a new genotype into one of the three clonal varieties to be used in improvement programs, eliminating the subjectivity of the clustering process. |
Palavras-Chave: |
Biotecnología; Café conilon; Coffea canephora; Genética; Genotipos; Plantas para uso industrial. |
Thesaurus NAL: |
Coffee; Genetic improvement; Genotypes. |
Categoria do assunto: |
-- |
URL: |
http://biblioteca.incaper.es.gov.br/digital/bitstream/item/444/1/2004-trabalho1-MaAmelia-AYMBIRE.pdf
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Marc: |
LEADER 01859naa a2200313 a 4500 001 1004803 005 2019-09-09 008 2004 bl uuuu u00u1 u #d 022 $a1518-7853 100 1 $aFONSECA, A. F. A. da. 245 $aDiscriminant analysis for the classification and clustering of robusta coffee genotypes.$h[electronic resource] 260 $c2004 520 $aThis study evaluated the adequacy of the composition of three clonal Coffea canephora varieties recommended for the State of Espírito Santo by a multivariate method designated discriminant analysis. This method consists in the establishment of functions that enable the classification of a given individual into one, among various distinct populations, reducing the probability of a misclassification. It simultaneously considers measures of several traits, in order to give the new variety homogeneity. The original classification of genotypes in the three studied varieties, based on agronomical criteria, maintained expressive concordance with the results of the discriminant analysis, with an apparent deviation rate of only 6.25%. Corrected discriminant functions were also proposed, capable of classifying a new genotype into one of the three clonal varieties to be used in improvement programs, eliminating the subjectivity of the clustering process. 650 $aCoffee 650 $aGenetic improvement 650 $aGenotypes 653 $aBiotecnología 653 $aCafé conilon 653 $aCoffea canephora 653 $aGenética 653 $aGenotipos 653 $aPlantas para uso industrial 700 1 $aSEDIYAMA, T. 700 1 $aCRUZ, C. D. 700 1 $aSAKIYAMA, N. S. 700 1 $aFERRÃO, R. G. 700 1 $aFERRÃO, M. A. G. 700 1 $aBRAGANÇA, S. M. 773 $tCrop Breeding and Applied Biotechnology$gv. 4, n. 3, p. 285-289, 2004.
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