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 | Acesso ao texto completo restrito à biblioteca da Embrapa Recursos Genéticos e Biotecnologia. Para informações adicionais entre em contato com cenargen.biblioteca@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia. |
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Data corrente: |
14/09/2021 |
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Data da última atualização: |
14/01/2022 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
LEME, L. O.; MACHADO, G. M.; FIDELIS, A. A. G.; GUIMARÃES, A. L. S.; SPRÍCIGO, J. F. W.; CARVALHO, J. O.; PIVATO, I.; FRANCO, M. M.; DODE, M. A. N. |
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Afiliação: |
LIGIANE OLIVEIRA LEME, UFES; GRAZIELI MARINHEIRO MACHADO, UNB; ANDREI ANTONIONI GUEDES FIDELIS, UNB; ANA LUIZA SILVA GUIMARÃES, UNB; JOSÉ FELIPE WARMILING SPRÍCIGO, UNB; JOSÉ OLIVEIRA CARVALHO, UFES; I. PIVATO, UNB; MAURICIO MACHAIM FRANCO, Cenargen; MARGOT ALVES NUNES DODE, Cenargen. |
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Título: |
Transcriptome of D14 in vivo x in vitro bovine embryos: is there any difference? |
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Ano de publicação: |
2021 |
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Fonte/Imprenta: |
In Vitro Cellular & Developmental Biology - Animal, v. 57, p. 598-609, 2021. |
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DOI: |
https://doi.org/10.1007/s11626-021-00599-x |
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Idioma: |
Inglês |
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Palavras-Chave: |
Conceptus elongation; D14 bovine trophoblast; Trophoblast profile. |
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Thesaurus Nal: |
Gene expression; Trophoblast. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 00878naa a2200277 a 4500
001 2134312
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008 2021 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1007/s11626-021-00599-x$2DOI
100 1 $aLEME, L. O.
245 $aTranscriptome of D14 in vivo x in vitro bovine embryos$bis there any difference?$h[electronic resource]
260 $c2021
650 $aGene expression
650 $aTrophoblast
653 $aConceptus elongation
653 $aD14 bovine trophoblast
653 $aTrophoblast profile
700 1 $aMACHADO, G. M.
700 1 $aFIDELIS, A. A. G.
700 1 $aGUIMARÃES, A. L. S.
700 1 $aSPRÍCIGO, J. F. W.
700 1 $aCARVALHO, J. O.
700 1 $aPIVATO, I.
700 1 $aFRANCO, M. M.
700 1 $aDODE, M. A. N.
773 $tIn Vitro Cellular & Developmental Biology - Animal$gv. 57, p. 598-609, 2021.
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Embrapa Recursos Genéticos e Biotecnologia (CENARGEN) |
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Registro Completo
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Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
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Data corrente: |
14/10/2009 |
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Data da última atualização: |
02/02/2010 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
GARCIA, S. A. L.; TALEBI, R.; FERREIRA, C. F.; VROH, I.; PAIVA, L. V.; SOUZA JUNIOR, M. T.; KEMA, G. H. J. |
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Afiliação: |
S. A. L. Garcia, PRI/UFLA; R.T. ALEBI, PRI-Plant Research International; Cláudia Fortes Ferreira, CNPMF; I. VROH, IITA; Luciano Vilela Paiva, UFL; Manoel Teixeira Souza Junior, LABEX Europe; Gert H. J. Kema, PRI-Plant Research International. |
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Título: |
Identification and validation of EST-derived Molecular markers, TRAP and VNTR, for banana research. |
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Ano de publicação: |
2009 |
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Fonte/Imprenta: |
In: ISHS/PROMUSA BANANA SYMPOSIUM, 2009, Guangzhou, China. Global perspectives on asian challenges: programme and abstracts. Guangzhou: ISHS: Promusa, 2009. p. 10. |
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Idioma: |
Inglês |
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Conteúdo: |
The advent of high-throughput sequencing technology has generated abundant information on DNA sequences for the genomes of many plant species. Expressed Sequence Tag (EST), a unique DNA sequence derived from a cDNA library and therefore representing a gene which has been transcribed in a specific tissue or at some stage of development , is one type of DNA sequence made highly available lately for many important crop species. Molecular markers are used for bridging DNA sequence information with particular phenotypes and are useful tools for genotyping germplasm collections and also for tagging genes governing desirable agronomic traits. In this sense, there is always a strong demand for better marker techniques to better utilise the existing sequence information. A transcriptome database from banana (Musa spp.), DATAMusa, containing 42,724 ESTs from 11 different cDNA libraries and encompassing approximately 24 Mb of DNA sequence, was used in this study for the design of primers to PCR amplify txo types of EST-derived molecular markers, Variable Nucleotide Tandem Repeat (VNTR) and Target Region Amplification Polymorphism (TRAP). These primers were then validated against a panel of 14 Musa diploid genotypes and produced 33 (VNTR) and 119 (TRAP) alleles. Used separately or together, both types of markers were able to discriminate Musa genotypes from different genome background (A or B genomes). The TRAP alleles identified derived from only one unigene, while the VNTR derived from 12 unigenes. Based on the results from this study, it can be said that EST-derived markers are an important source of polymorphism to be used in genetic diversity and gene discovery studies in banana. MenosThe advent of high-throughput sequencing technology has generated abundant information on DNA sequences for the genomes of many plant species. Expressed Sequence Tag (EST), a unique DNA sequence derived from a cDNA library and therefore representing a gene which has been transcribed in a specific tissue or at some stage of development , is one type of DNA sequence made highly available lately for many important crop species. Molecular markers are used for bridging DNA sequence information with particular phenotypes and are useful tools for genotyping germplasm collections and also for tagging genes governing desirable agronomic traits. In this sense, there is always a strong demand for better marker techniques to better utilise the existing sequence information. A transcriptome database from banana (Musa spp.), DATAMusa, containing 42,724 ESTs from 11 different cDNA libraries and encompassing approximately 24 Mb of DNA sequence, was used in this study for the design of primers to PCR amplify txo types of EST-derived molecular markers, Variable Nucleotide Tandem Repeat (VNTR) and Target Region Amplification Polymorphism (TRAP). These primers were then validated against a panel of 14 Musa diploid genotypes and produced 33 (VNTR) and 119 (TRAP) alleles. Used separately or together, both types of markers were able to discriminate Musa genotypes from different genome background (A or B genomes). The TRAP alleles identified derived from only one unigene, while the VNTR derived fr... Mostrar Tudo |
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Thesagro: |
Banana; Marcador Molecular. |
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Thesaurus NAL: |
Musa. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02450naa a2200229 a 4500
001 1656060
005 2010-02-02
008 2009 bl uuuu u00u1 u #d
100 1 $aGARCIA, S. A. L.
245 $aIdentification and validation of EST-derived Molecular markers, TRAP and VNTR, for banana research.
260 $c2009
520 $aThe advent of high-throughput sequencing technology has generated abundant information on DNA sequences for the genomes of many plant species. Expressed Sequence Tag (EST), a unique DNA sequence derived from a cDNA library and therefore representing a gene which has been transcribed in a specific tissue or at some stage of development , is one type of DNA sequence made highly available lately for many important crop species. Molecular markers are used for bridging DNA sequence information with particular phenotypes and are useful tools for genotyping germplasm collections and also for tagging genes governing desirable agronomic traits. In this sense, there is always a strong demand for better marker techniques to better utilise the existing sequence information. A transcriptome database from banana (Musa spp.), DATAMusa, containing 42,724 ESTs from 11 different cDNA libraries and encompassing approximately 24 Mb of DNA sequence, was used in this study for the design of primers to PCR amplify txo types of EST-derived molecular markers, Variable Nucleotide Tandem Repeat (VNTR) and Target Region Amplification Polymorphism (TRAP). These primers were then validated against a panel of 14 Musa diploid genotypes and produced 33 (VNTR) and 119 (TRAP) alleles. Used separately or together, both types of markers were able to discriminate Musa genotypes from different genome background (A or B genomes). The TRAP alleles identified derived from only one unigene, while the VNTR derived from 12 unigenes. Based on the results from this study, it can be said that EST-derived markers are an important source of polymorphism to be used in genetic diversity and gene discovery studies in banana.
650 $aMusa
650 $aBanana
650 $aMarcador Molecular
700 1 $aTALEBI, R.
700 1 $aFERREIRA, C. F.
700 1 $aVROH, I.
700 1 $aPAIVA, L. V.
700 1 $aSOUZA JUNIOR, M. T.
700 1 $aKEMA, G. H. J.
773 $tIn: ISHS/PROMUSA BANANA SYMPOSIUM, 2009, Guangzhou, China. Global perspectives on asian challenges: programme and abstracts. Guangzhou: ISHS: Promusa, 2009. p. 10.
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