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 | Acesso ao texto completo restrito à biblioteca da Embrapa Soja. Para informações adicionais entre em contato com valeria.cardoso@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
26/11/2014 |
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Data da última atualização: |
07/04/2022 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
HOSSAIN, M. M.; AKAMATSU, H.; MORISHITA, M.; MORI, T.; YAMAOKA, Y.; SUENAGA, K.; SOARES, R. M.; BOGADO, A. N.; IVANCOVICH, A. J. G.; YAMANAKA, N. |
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Afiliação: |
JIRCAS; JIRCAS; JIRCAS; JIRCAS; Faculty of Life and Environmental Sciences, University of Tsukuba; Faculty of Life and Environmental Sciences, University of Tsukuba; RAFAEL MOREIRA SOARES, CNPSO; CICM/IPTA; INTA - EEA Pergamino; JIRCAS. |
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Título: |
Molecular mapping of Asian soybean rust resistance in soybean landraces PI 594767A, PI 587905 and PI 416764. |
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Ano de publicação: |
2015 |
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Fonte/Imprenta: |
Plant Pathology, London, v. 64, n. 1, p. 147-156, 2015. |
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DOI: |
10.1111/ppa.12226 |
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Idioma: |
Inglês |
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Conteúdo: |
Asian soybean rust (ASR), caused by Phakopsora pachyrhizi, is one of the most serious diseases of soybean. The soybean landraces PI 594767A, PI 587905 and PI 416764 previously showed high levels of resistance to a wide range of ASR fungus, while the genetic basis of the resistance has yet to be understood. In this study, the ASR resistance loci were mapped using three independent mapping populations, POP-1, POP-2 and POP-3 derived from crosses BRS184 × PI 594767A, BRS184 × PI 587905 and BRS184 × PI 416764, respectively. In each population, the resistance to ASR segregated as a single gene, but the resistance was dominant in PI 594767A and PI 587905 and incompletely dominant in PI 416764. The resistance genes from both PI 594767A and PI 587905 were mapped on chromosome 18 corresponding to the same location as known resistance locus Rpp1. Quantitative trait locus (QTL) analysis performed on POP-3 identified the putative ASR resistance locus in PI 416764 on the defined region of chromosome 6 where Rpp3 was located. The QTLs detected by the mapping explained about 67?72% of the phenotypic variation in POP-3. Cluster analysis based on disease reactions to 64 ASR populations demonstrated the presence of at least two types of functional resistant Rpp1 alleles: strong and weak allele(s), e.g. soybean accession PI 594767A and PI 587905 carry the strong resistant Rpp1 allele(s). Introducing or pyramiding strong Rpp1 allele(s) in elite soybean cultivars is expected to be useful against the South American rust population. MenosAsian soybean rust (ASR), caused by Phakopsora pachyrhizi, is one of the most serious diseases of soybean. The soybean landraces PI 594767A, PI 587905 and PI 416764 previously showed high levels of resistance to a wide range of ASR fungus, while the genetic basis of the resistance has yet to be understood. In this study, the ASR resistance loci were mapped using three independent mapping populations, POP-1, POP-2 and POP-3 derived from crosses BRS184 × PI 594767A, BRS184 × PI 587905 and BRS184 × PI 416764, respectively. In each population, the resistance to ASR segregated as a single gene, but the resistance was dominant in PI 594767A and PI 587905 and incompletely dominant in PI 416764. The resistance genes from both PI 594767A and PI 587905 were mapped on chromosome 18 corresponding to the same location as known resistance locus Rpp1. Quantitative trait locus (QTL) analysis performed on POP-3 identified the putative ASR resistance locus in PI 416764 on the defined region of chromosome 6 where Rpp3 was located. The QTLs detected by the mapping explained about 67?72% of the phenotypic variation in POP-3. Cluster analysis based on disease reactions to 64 ASR populations demonstrated the presence of at least two types of functional resistant Rpp1 alleles: strong and weak allele(s), e.g. soybean accession PI 594767A and PI 587905 carry the strong resistant Rpp1 allele(s). Introducing or pyramiding strong Rpp1 allele(s) in elite soybean cultivars is expected to be useful against... Mostrar Tudo |
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Palavras-Chave: |
Genetic mapping; Pathogenic diversity; QTL analysis. |
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Thesagro: |
Phakopsora Pachyrhizi. |
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Thesaurus Nal: |
cluster analysis. |
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Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
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Marc: |
LEADER 02423naa a2200301 a 4500
001 2000961
005 2022-04-07
008 2015 bl uuuu u00u1 u #d
024 7 $a10.1111/ppa.12226$2DOI
100 1 $aHOSSAIN, M. M.
245 $aMolecular mapping of Asian soybean rust resistance in soybean landraces PI 594767A, PI 587905 and PI 416764.$h[electronic resource]
260 $c2015
520 $aAsian soybean rust (ASR), caused by Phakopsora pachyrhizi, is one of the most serious diseases of soybean. The soybean landraces PI 594767A, PI 587905 and PI 416764 previously showed high levels of resistance to a wide range of ASR fungus, while the genetic basis of the resistance has yet to be understood. In this study, the ASR resistance loci were mapped using three independent mapping populations, POP-1, POP-2 and POP-3 derived from crosses BRS184 × PI 594767A, BRS184 × PI 587905 and BRS184 × PI 416764, respectively. In each population, the resistance to ASR segregated as a single gene, but the resistance was dominant in PI 594767A and PI 587905 and incompletely dominant in PI 416764. The resistance genes from both PI 594767A and PI 587905 were mapped on chromosome 18 corresponding to the same location as known resistance locus Rpp1. Quantitative trait locus (QTL) analysis performed on POP-3 identified the putative ASR resistance locus in PI 416764 on the defined region of chromosome 6 where Rpp3 was located. The QTLs detected by the mapping explained about 67?72% of the phenotypic variation in POP-3. Cluster analysis based on disease reactions to 64 ASR populations demonstrated the presence of at least two types of functional resistant Rpp1 alleles: strong and weak allele(s), e.g. soybean accession PI 594767A and PI 587905 carry the strong resistant Rpp1 allele(s). Introducing or pyramiding strong Rpp1 allele(s) in elite soybean cultivars is expected to be useful against the South American rust population.
650 $acluster analysis
650 $aPhakopsora Pachyrhizi
653 $aGenetic mapping
653 $aPathogenic diversity
653 $aQTL analysis
700 1 $aAKAMATSU, H.
700 1 $aMORISHITA, M.
700 1 $aMORI, T.
700 1 $aYAMAOKA, Y.
700 1 $aSUENAGA, K.
700 1 $aSOARES, R. M.
700 1 $aBOGADO, A. N.
700 1 $aIVANCOVICH, A. J. G.
700 1 $aYAMANAKA, N.
773 $tPlant Pathology, London$gv. 64, n. 1, p. 147-156, 2015.
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Registro original: |
Embrapa Soja (CNPSO) |
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Biblioteca |
ID |
Origem |
Tipo/Formato |
Classificação |
Cutter |
Registro |
Volume |
Status |
URL |
Voltar
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Registro Completo
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Biblioteca(s): |
Embrapa Mandioca e Fruticultura; Embrapa Recursos Genéticos e Biotecnologia. |
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Data corrente: |
16/08/2010 |
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Data da última atualização: |
03/02/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
B - 2 |
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Autoria: |
MILLER, R. N. G.; PASSOS, M. A. N.; MENEZES, N. N. P.; SOUZA JUNIOR, M. T.; COSTA, M. M. do C.; AZEVEDO, V. C. R.; AMORIM, E. P.; PAPPAS JUNIOR, G. J.; CIAMPI, A. Y. |
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Afiliação: |
ROBERT NEIL GERARD MILLER., UnB; Marco A. N. Passos, UCB; Natália N. Pereira Menezes, UCB; MANOEL TEIXEIRA SOUZA JUNIOR, Labex Europa; MARCOS MOTA DO CARMO COSTA, CENARGEN; VANIA CRISTINA RENNO AZEVEDO, CENARGEN; EDSON PERITO AMORIM, CNPMF; GEORGIOS JOANNIS PAPPAS JUNIOR, CENARGEN; ANA YAMAGUISHI CIAMPI, CENARGEN. |
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Título: |
Characterization of novel microsatellite markers in Musa acuminata subsp. burmannicoides, var. Calcutta 4. |
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Ano de publicação: |
2010 |
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Fonte/Imprenta: |
BMC Research Notes, v.3, n.148, 2010. |
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Idioma: |
Inglês |
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Notas: |
Disponível em:.Acesso em: 16 ago. 2010. |
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Conteúdo: |
Banana is a nutritionally important crop across tropical and sub-tropical countries in sub-Saharan Africa, Central and South America and Asia. Although cultivars have evolved from diploid, triploid and tetraploid wild Asian species of Musa acuminata (A genome) and Musa balbisiana (B genome), many of today's commercial cultivars are sterile triploids or diploids, with fruit developing via parthenocarpy. As a result of restricted genetic variation, improvement has been limited, resulting in a crop frequently lacking resistance to pests and disease. Considering the importance of molecular tools to facilitate development of disease resistant genotypes, the objectives of this study were to develop polymorphic microsatellite markers from BAC clone sequences for M. acuminata subsp. burmannicoides, var. Calcutta 4. This wild diploid species is used as a donor cultivar in breeding programs as a source of resistance to diverse biotic stresses. |
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Thesagro: |
Banana; Marcador Molecular; Melhoramento Genético Vegetal; Musa sp. |
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Thesaurus NAL: |
varieties. |
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Categoria do assunto: |
G Melhoramento Genético |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/25772/1/BMC3.pdf
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Marc: |
LEADER 01876naa a2200289 a 4500
001 1871790
005 2023-02-03
008 2010 bl uuuu u00u1 u #d
100 1 $aMILLER, R. N. G.
245 $aCharacterization of novel microsatellite markers in Musa acuminata subsp. burmannicoides, var. Calcutta 4.$h[electronic resource]
260 $c2010
500 $aDisponível em:<http://www.biomedcentral.com/1756-0500/3/148#refs>.Acesso em: 16 ago. 2010.
520 $aBanana is a nutritionally important crop across tropical and sub-tropical countries in sub-Saharan Africa, Central and South America and Asia. Although cultivars have evolved from diploid, triploid and tetraploid wild Asian species of Musa acuminata (A genome) and Musa balbisiana (B genome), many of today's commercial cultivars are sterile triploids or diploids, with fruit developing via parthenocarpy. As a result of restricted genetic variation, improvement has been limited, resulting in a crop frequently lacking resistance to pests and disease. Considering the importance of molecular tools to facilitate development of disease resistant genotypes, the objectives of this study were to develop polymorphic microsatellite markers from BAC clone sequences for M. acuminata subsp. burmannicoides, var. Calcutta 4. This wild diploid species is used as a donor cultivar in breeding programs as a source of resistance to diverse biotic stresses.
650 $avarieties
650 $aBanana
650 $aMarcador Molecular
650 $aMelhoramento Genético Vegetal
650 $aMusa sp
700 1 $aPASSOS, M. A. N.
700 1 $aMENEZES, N. N. P.
700 1 $aSOUZA JUNIOR, M. T.
700 1 $aCOSTA, M. M. do C.
700 1 $aAZEVEDO, V. C. R.
700 1 $aAMORIM, E. P.
700 1 $aPAPPAS JUNIOR, G. J.
700 1 $aCIAMPI, A. Y.
773 $tBMC Research Notes$gv.3, n.148, 2010.
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Embrapa Recursos Genéticos e Biotecnologia (CENARGEN) |
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