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| Registros recuperados : 121 | |
| 8. |  | ASSIS, G. M. L. de; CAMPOS, T. de; BIANCHINI, P. C.; MATOS, L. R. A. de. Banco de germoplasma de amendoim forrageiro: conservação e utilização. In: CONGRESSO BRASILEIRO DE RECURSOS GENÉTICOS, 2., 2012, Belém, PA. Anais... Brasília, DF: Sociedade Brasileira de Recursos Genéticos, 2012. 4 p. 1 CD-ROM.| Biblioteca(s): Embrapa Acre. |
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| 11. | | CAVALCANTE, L. do N.; SOUZA, C. S. de; CAMPOS, T. de. Estudo da diversidade genética de acessos de seringueira das coleções da Embrapa. In: SEMINÁRIO DA EMBRAPA ACRE DE INICIAÇÃO CIENTÍFICA E PÓS-GRADUAÇÃO, 1., 2018, Rio Branco, AC. Pesquisa e inovação para a Agropecuária no Acre: anais. Rio Branco, AC: Embrapa Acre, 2019. p. 21-26. Apresentação oral. (Embrapa Acre. Eventos técnicos & científicos, 1).| Biblioteca(s): Embrapa Acre. |
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| 12. | | FERREIRA, J. A.; CUNHA, M. O. da; ASSIS, G. M. L. de; CAMPOS, T. de. Certificação molecular de hibridação intraespecífica em amendoim forrageiro por meio de marcadores SSRS. In: CONGRESSO BRASILEIRO DE RECURSOS GENÉTICOS, 2., 2012, Belém, PA. Anais... Brasília, DF: Sociedade Brasileira de Recursos Genéticos, 2012. 4 p. 1 CD-ROM.| Biblioteca(s): Embrapa Acre. |
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| 13. | | FERREIRA, J. A.; SILVA, H. F.; ASSIS, G. M. L. de; CAMPOS, T. de. Caracterização da diversidade genética de genitores de amendoim forrageiro por meio de marcadores microssatélites. In: CONGRESSO BRASILEIRO DE RECURSOS GENÉTICOS, 2., 2012, Belém, PA. Anais... Brasília, DF: Sociedade Brasileira de Recursos Genéticos, 2012. 4 p. 1 CD-ROM.| Biblioteca(s): Embrapa Acre. |
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| 14. | | SIVIERO, A.; BERGO, C. L.; SILVA, L. M. da; KLEIN, M. A.; CAMPOS, T. de. Caracterização de etnovariedades de mandioca utilizadas na produção de farinha de Cruzeiro do Sul. In: CONGRESSO BRASILEIRO DE MANDIOCA, 17.; CONGRESSO LATINO-AMERICANO E CARIBENHO DE MANDIOCA, 2., 2018, Belém, PA. Anais... Belém, PA: SBM, 2018. p. 197-200.| Biblioteca(s): Embrapa Acre. |
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| 15. | | SILVA, V. S.; MARTINS, K.; CAMPOS, T. de; WADT, L. H. de O. Diversidade genética de populações naturais de castanheira (Bertholletia excelsa) com marcadores ISSR. In: CONGRESSO BRASILEIRO DE RECURSOS GENÉTICOS, 2., 2012, Belém, PA. Anais... Brasília, DF: Sociedade Brasileira de Recursos Genéticos, 2012. 4 p. 1 CD-ROM.| Biblioteca(s): Embrapa Acre. |
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| Registros recuperados : 121 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Acre. Para informações adicionais entre em contato com cpafac.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Acre. |
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Data corrente: |
25/10/2023 |
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Data da última atualização: |
13/05/2024 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 3 |
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Autoria: |
OLIVEIRA, J. C. de; SILVA, A. L. D. da; SILVA, L. M. da; FORMIGHIERI, E. F.; PETERS, L. P.; ASSIS, G. M. L. de; SILVA, C. C. da; SOUZA, A. P. de; CAMPOS, T. de. |
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Afiliação: |
JÔNATAS CHAGAS DE OLIVEIRA, UNIVERSIDADE FEDERAL DO ACRE; ANDRÉ LUCAS DOMINGOS DA SILVA, UNIVERSIDADE FEDERAL DO ACRE; LUCIELIO MANOEL DA SILVA, CPATC; EDUARDO FERNANDES FORMIGHIERI, CNPAE; LEILA PRISCILA PETERS, UNIVERSIDADE FEDERAL DO ACRE; GISELLE MARIANO LESSA DE ASSIS, CPAF-AC; CARLA CRISTINA DA SILVA, UNIVERSIDADE DE CAMPINAS; ANETE PEREIRA DE SOUZA, UNIVERSIDADE DE CAMPINAS; TATIANA DE CAMPOS, CPAF-AC. |
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Título: |
Novel microsatellite markers derived from Arachis pintoi transcriptome sequencing for cross-species transferability and varietal identification. |
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Ano de publicação: |
2024 |
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Fonte/Imprenta: |
Plant Molecular Biology Reporter, v. 42, p. 183-192, Mar. 2024. |
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DOI: |
https://doi.org/10.1007/s11105-023-01402-9 |
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Idioma: |
Inglês |
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Conteúdo: |
Forage peanut (Arachis pintoi) is an important leguminous forage that has gained popularity due to increased livestock productivity. Furthermore, the species helps with soil fertility and the restoration of degraded areas. However, A. pintoi has a limited number of molecular markers. The objective of this study was to create and characterize gene-derived microsatellite markers as well as to test their transferability to the peanut (Arachis hypogaea) and other six wild Arachis species. A total of 4461 putative simple sequence repeats (SSR) were identified, and PCR primer pairs were designed for 999 SSR regions after filtering out primers with the same annealing site and searching for sequences related to open reading frames (ORFs). The dinucleotide motif was the most common (628; 62.86%). For validation, 186 primer pairs were chosen at random, of which 63 (33.87%) were polymorphic, with an average of 7.37 alleles per locus. Polymorphic information content (PIC=0.70) and discriminatory power (D=0.80) were both high on average. The functional annotation discovered 120 sequences that were assigned to 87 gene ontology functional groups divided into three main categories: molecular function (27 sub-categories), cellular components (21 sub-categories), and biological process (39 sub-categories). Thirty-three SSRs were tested for transferability to peanut and six other wild Arachis species, resulting in variable cross-species amplification (63.64 to 100%). Here, we present the first gene-derived SSR for A. pintoi. These new informative microsatellites may be linked to agronomically important genes to be used in genetic studies. MenosForage peanut (Arachis pintoi) is an important leguminous forage that has gained popularity due to increased livestock productivity. Furthermore, the species helps with soil fertility and the restoration of degraded areas. However, A. pintoi has a limited number of molecular markers. The objective of this study was to create and characterize gene-derived microsatellite markers as well as to test their transferability to the peanut (Arachis hypogaea) and other six wild Arachis species. A total of 4461 putative simple sequence repeats (SSR) were identified, and PCR primer pairs were designed for 999 SSR regions after filtering out primers with the same annealing site and searching for sequences related to open reading frames (ORFs). The dinucleotide motif was the most common (628; 62.86%). For validation, 186 primer pairs were chosen at random, of which 63 (33.87%) were polymorphic, with an average of 7.37 alleles per locus. Polymorphic information content (PIC=0.70) and discriminatory power (D=0.80) were both high on average. The functional annotation discovered 120 sequences that were assigned to 87 gene ontology functional groups divided into three main categories: molecular function (27 sub-categories), cellular components (21 sub-categories), and biological process (39 sub-categories). Thirty-three SSRs were tested for transferability to peanut and six other wild Arachis species, resulting in variable cross-species amplification (63.64 to 100%). Here, we present the first... Mostrar Tudo |
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Palavras-Chave: |
Amendoim forrageiro; Anotação funcional; Cacahuetes forrajeros; Fitomejoramiento; Forage peanut; Identificación de especies; Marcadores genéticos; Repeticiones de microsatélite; RNA-Seq; Transcriptoma; Transferencia de genes. |
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Thesagro: |
Arachis Hypogaea; Genoma; Identificação de Estirpe; Marcador Molecular; Melhoramento Genético Vegetal. |
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Thesaurus NAL: |
Arachis pintoi; Gene transfer; Genetic markers; Genome; Microsatellite repeats; Plant breeding; Species identification; Transcriptome. |
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Categoria do assunto: |
G Melhoramento Genético |
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Marc: |
LEADER 03263naa a2200517 a 4500
001 2157490
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008 2024 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1007/s11105-023-01402-9$2DOI
100 1 $aOLIVEIRA, J. C. de
245 $aNovel microsatellite markers derived from Arachis pintoi transcriptome sequencing for cross-species transferability and varietal identification.$h[electronic resource]
260 $c2024
520 $aForage peanut (Arachis pintoi) is an important leguminous forage that has gained popularity due to increased livestock productivity. Furthermore, the species helps with soil fertility and the restoration of degraded areas. However, A. pintoi has a limited number of molecular markers. The objective of this study was to create and characterize gene-derived microsatellite markers as well as to test their transferability to the peanut (Arachis hypogaea) and other six wild Arachis species. A total of 4461 putative simple sequence repeats (SSR) were identified, and PCR primer pairs were designed for 999 SSR regions after filtering out primers with the same annealing site and searching for sequences related to open reading frames (ORFs). The dinucleotide motif was the most common (628; 62.86%). For validation, 186 primer pairs were chosen at random, of which 63 (33.87%) were polymorphic, with an average of 7.37 alleles per locus. Polymorphic information content (PIC=0.70) and discriminatory power (D=0.80) were both high on average. The functional annotation discovered 120 sequences that were assigned to 87 gene ontology functional groups divided into three main categories: molecular function (27 sub-categories), cellular components (21 sub-categories), and biological process (39 sub-categories). Thirty-three SSRs were tested for transferability to peanut and six other wild Arachis species, resulting in variable cross-species amplification (63.64 to 100%). Here, we present the first gene-derived SSR for A. pintoi. These new informative microsatellites may be linked to agronomically important genes to be used in genetic studies.
650 $aArachis pintoi
650 $aGene transfer
650 $aGenetic markers
650 $aGenome
650 $aMicrosatellite repeats
650 $aPlant breeding
650 $aSpecies identification
650 $aTranscriptome
650 $aArachis Hypogaea
650 $aGenoma
650 $aIdentificação de Estirpe
650 $aMarcador Molecular
650 $aMelhoramento Genético Vegetal
653 $aAmendoim forrageiro
653 $aAnotação funcional
653 $aCacahuetes forrajeros
653 $aFitomejoramiento
653 $aForage peanut
653 $aIdentificación de especies
653 $aMarcadores genéticos
653 $aRepeticiones de microsatélite
653 $aRNA-Seq
653 $aTranscriptoma
653 $aTransferencia de genes
700 1 $aSILVA, A. L. D. da
700 1 $aSILVA, L. M. da
700 1 $aFORMIGHIERI, E. F.
700 1 $aPETERS, L. P.
700 1 $aASSIS, G. M. L. de
700 1 $aSILVA, C. C. da
700 1 $aSOUZA, A. P. de
700 1 $aCAMPOS, T. de
773 $tPlant Molecular Biology Reporter$gv. 42, p. 183-192, Mar. 2024.
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