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Registro Completo |
Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
Data corrente: |
19/01/2017 |
Data da última atualização: |
08/02/2017 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
CASTRO, J. A.; OLIVEIRA, E. J. de; JESUS, O. N. de; SOARES, T. L.; MARGARIDO, G. R. A. |
Afiliação: |
J. A. CASTRO, UFRB; EDER JORGE DE OLIVEIRA, CNPMF; ONILDO NUNES DE JESUS, CNPMF; T. L. SOARES; G. R. A. MARGARIDO, ESALQ. |
Título: |
Molecular markers for conservation genetic resources of fourPassiflora species. |
Ano de publicação: |
2016 |
Fonte/Imprenta: |
Scientia Horticulturae, v., 212, p. 251-261, 2016. |
ISSN: |
0304-4238 |
Idioma: |
Inglês |
Conteúdo: |
tThe aim of this study was to use microsatellite markers (SSR) for the characterization of the Passifloraspecies and to verify the effect of random selection of individuals in parameters that characterize thegenetic variability of germplasm for conservation purposes. Four species, Passiflora edulis f. flavicarpaDegener, P. cincinnata Mast., P. alata Curtis and P. setacea D.C., were evaluated. For each species tworandom samples were evaluated, one consisting of 60 plants (S60) and the other of 10 plants (S10)randomly selected from the S60. Initially, the S10 and S60 were used to calculate the genetic parametersof number of alleles, expected and observed heterozygosity, effective population size, inbreeding andpolymorphic information content based on 40 microsatellite markers developed for P. edulis and 20 for P.alata. Further bootstrap analysis was performed to identify the minimum number of individuals neededto represent the variability of each Passiflora species from a range of 2 to 59. The number of polymorphicmicrosatellites was 15, 9, 6 and 2 on P. edulis f. flavicarpa, P. cincinnata, P. alata and P. setacea, respectively.The allelic loss due to the under-representation of the samples was 19 (30%), 16 (43%) and nine (39%)alleles, respectively, for P. edulis f. flavicarpa, P. cincinnata and P. alata. No allelic loss was observed forP. setacea, probably because only two polymorphic microsatellites were identified. In general, there aredifferences between S10 and S60 because of lost genetic variability on S10, indicating that the use of these10 individuals to represent the Passiflora species is insufficient for long-term preservation. In contrast,the bootstrap analysis revealed that the stability of the genetic parameters due to the increase in samplesize was close to 30, 23, 25 and 24 individuals for P. cincinnata, P. edulis f. flavicarpa, P. setacea and P. alata,respectively. The difference of genetic estimates between samples S10 and S60 demonstrated that 23?30individuals are the minimum range of population to represent the Passiflora species studied. This studymay optimize the strategies for conservation the Passiflora germplasm avoiding the under-representationof samples and consequent loss of genetic variability during sexual propagation. MenostThe aim of this study was to use microsatellite markers (SSR) for the characterization of the Passifloraspecies and to verify the effect of random selection of individuals in parameters that characterize thegenetic variability of germplasm for conservation purposes. Four species, Passiflora edulis f. flavicarpaDegener, P. cincinnata Mast., P. alata Curtis and P. setacea D.C., were evaluated. For each species tworandom samples were evaluated, one consisting of 60 plants (S60) and the other of 10 plants (S10)randomly selected from the S60. Initially, the S10 and S60 were used to calculate the genetic parametersof number of alleles, expected and observed heterozygosity, effective population size, inbreeding andpolymorphic information content based on 40 microsatellite markers developed for P. edulis and 20 for P.alata. Further bootstrap analysis was performed to identify the minimum number of individuals neededto represent the variability of each Passiflora species from a range of 2 to 59. The number of polymorphicmicrosatellites was 15, 9, 6 and 2 on P. edulis f. flavicarpa, P. cincinnata, P. alata and P. setacea, respectively.The allelic loss due to the under-representation of the samples was 19 (30%), 16 (43%) and nine (39%)alleles, respectively, for P. edulis f. flavicarpa, P. cincinnata and P. alata. No allelic loss was observed forP. setacea, probably because only two polymorphic microsatellites were identified. In general, there aredifferences between S10 and S60 becaus... Mostrar Tudo |
Palavras-Chave: |
Passionfruit. |
Thesagro: |
Maracujá. |
Categoria do assunto: |
-- |
Marc: |
LEADER 02875naa a2200205 a 4500 001 2061183 005 2017-02-08 008 2016 bl uuuu u00u1 u #d 022 $a0304-4238 100 1 $aCASTRO, J. A. 245 $aMolecular markers for conservation genetic resources of fourPassiflora species.$h[electronic resource] 260 $c2016 520 $atThe aim of this study was to use microsatellite markers (SSR) for the characterization of the Passifloraspecies and to verify the effect of random selection of individuals in parameters that characterize thegenetic variability of germplasm for conservation purposes. Four species, Passiflora edulis f. flavicarpaDegener, P. cincinnata Mast., P. alata Curtis and P. setacea D.C., were evaluated. For each species tworandom samples were evaluated, one consisting of 60 plants (S60) and the other of 10 plants (S10)randomly selected from the S60. Initially, the S10 and S60 were used to calculate the genetic parametersof number of alleles, expected and observed heterozygosity, effective population size, inbreeding andpolymorphic information content based on 40 microsatellite markers developed for P. edulis and 20 for P.alata. Further bootstrap analysis was performed to identify the minimum number of individuals neededto represent the variability of each Passiflora species from a range of 2 to 59. The number of polymorphicmicrosatellites was 15, 9, 6 and 2 on P. edulis f. flavicarpa, P. cincinnata, P. alata and P. setacea, respectively.The allelic loss due to the under-representation of the samples was 19 (30%), 16 (43%) and nine (39%)alleles, respectively, for P. edulis f. flavicarpa, P. cincinnata and P. alata. No allelic loss was observed forP. setacea, probably because only two polymorphic microsatellites were identified. In general, there aredifferences between S10 and S60 because of lost genetic variability on S10, indicating that the use of these10 individuals to represent the Passiflora species is insufficient for long-term preservation. In contrast,the bootstrap analysis revealed that the stability of the genetic parameters due to the increase in samplesize was close to 30, 23, 25 and 24 individuals for P. cincinnata, P. edulis f. flavicarpa, P. setacea and P. alata,respectively. The difference of genetic estimates between samples S10 and S60 demonstrated that 23?30individuals are the minimum range of population to represent the Passiflora species studied. This studymay optimize the strategies for conservation the Passiflora germplasm avoiding the under-representationof samples and consequent loss of genetic variability during sexual propagation. 650 $aMaracujá 653 $aPassionfruit 700 1 $aOLIVEIRA, E. J. de 700 1 $aJESUS, O. N. de 700 1 $aSOARES, T. L. 700 1 $aMARGARIDO, G. R. A. 773 $tScientia Horticulturae$gv., 212, p. 251-261, 2016.
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Registros recuperados : 154 | |
1. | | SOARES, T. L. Eficiência do sistema reprodutivo de bananeira. 2011. 70 p. Tese (Doutorado em Ciências Agrárias) - Universidade Federal do Recôncavo da Bahia, Cruz das Almas, 2011. Maria Angélica Pereira de Carvalho Costa, Orientador; Janay Almeida dos Santos-Serejo, CNPMF; Co-Orientador; Sebastião de Oliveira e...Tipo: Orientação de Tese de Pós-Graduação |
Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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5. | | SAMPAIO, S. R.; SOARES, T. L.; OLIVEIRA, E. J. de; JESUS, O. N. de. Aspectos da biologia reprodutiva de Passiflora spp. In: JORNADA CIENTÍFICA EMBRAPA MANDIOCA E FRUTICULTURA, 8., 2014, Cruz das Almas, Ba. Pesquisa: despertando mentes para a inovação e transformando o futuro: [anais]. Cruz das Almas, BA, Embrapa Mandioca e Fruticultura, 2014.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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10. | | MARTlNS, C. A. D.; SOARES, T. L.; OLIVEIRA, E. J. de; JESUS, O. N. de. Caracterização morfológica e reação à virose de híbridos interespecíficos de maracujazeiro. In: REUNIÃO ANUAL DE CIÊNCIA, TECNOLOGIA, INOVAÇÃO E CULTURA NO RECÔNCAVO DA BAHIA - RECONCITEC, 2., 2012, Cruz das Almas. Energias Renováveis, Educação, Tecnologia e Sociedade. Cruz das Almas, BA: UFRB, 2012.Tipo: Artigo em Anais de Congresso |
Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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17. | | GIRARDI, E. A.; JESUS, O. N. de; SOARES, T. L.; LIMA, L. K. S. Tecnologia de mudas enxertadas de maracujazeiro via enxertia hipocotiledonar. In: MORERA, M. P.; COSTA, A. M.; FALEIRO, F. G.; CARLOSAMA, A. R.; CARRANZA, C. Maracujá: dos recursos genéticos ao desenvolvimento tecnológico. Brasília, DF: Proimpress, 2018. p. 123-129.Tipo: Capítulo em Livro Técnico-Científico |
Biblioteca(s): Embrapa Cerrados. |
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19. | | SOARES, T. L.; SOUZA, F. V. D.; SOUZA, E. H. de; VIEIRA, L. de J. Viabilidade de pólen de abacaxizeiro Ananas comosus var. comosus. In: SIMPÓSIO BRASILEIRO DE RECURSOS GENÉTICOS, 2., 2008, Brasília, DF. Anais... Brasília, DF: Embrapa Recursos Genéticos e Biotecnologia, 2008. p. 400.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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Registros recuperados : 154 | |
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