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Registro Completo |
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
19/10/2010 |
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Data da última atualização: |
19/05/2025 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
KULCHESKI, F. R.; MARCELINO-GUIMARAES, F. C.; NEPOMUCENO, A. L.; ABDELNOOR, R. V.; MARGIS, R. |
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Afiliação: |
FRANCELI RODRIGUES KULCHESKI, UFRGS; FRANCISMAR CORREA MARCELINO, CNPSO; ALEXANDRE LIMA NEPOMUCENO, CNPSO; RICARDO VILELA ABDELNOOR, CNPSO; ROGÉRIO MARGIS, UFRGS. |
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Título: |
The use of microRNAs as reference genes for quantitative polymerase chain reaction in soybean. |
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Ano de publicação: |
2010 |
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Fonte/Imprenta: |
Analytical Biochemistry, v. 406, n. 2, p. 185-192, nov. 2010. |
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DOI: |
10.1016/j.ab.2010.07.020 |
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Idioma: |
Inglês |
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Conteúdo: |
Reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) is a robust and widely applied technique used to investigate gene expression. However, for correct analysis and interpretation of results, the choice of a suitable gene to use as an internal control is a crucial factor. These genes, such as housekeeping genes, should have a constant expression level in different tissues and across different conditions. The advances in genome sequencing have provided high-throughput gene expression analysis and have contributed to the identification of new genes, including microRNAs (miRNAs). The miRNAs are fundamental regulatory genes of eukaryotic genomes, acting on several biological functions. In this study, miRNA expression stability was investigated in different soybean tissues and genotypes as well as after abiotic or biotic stress treatments. The present study represents the first investigation into the suitability of miRNAs as housekeeping genes in plants. The transcript stability of 10 miRNAs was compared to those of six previously reported housekeeping genes for the soybean. In this study, we provide evidence that the expression stabilities of miR156b and miR1520d were the highest across the soybean experiments. Furthermore, these miRNAs genes were more stable than the most commonly protein-coding genes used in soybean gene expression studies involving RT-qPCR. |
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Palavras-Chave: |
Reação em cadeia da polimerase. |
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Thesagro: |
Gene; RNA; Soja. |
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Thesaurus Nal: |
Genes; MicroRNA; Quantitative polymerase chain reaction; Soybeans. |
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Categoria do assunto: |
G Melhoramento Genético |
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Marc: |
LEADER 02232naa a2200277 a 4500 001 1864539 005 2025-05-19 008 2010 bl uuuu u00u1 u #d 024 7 $a10.1016/j.ab.2010.07.020$2DOI 100 1 $aKULCHESKI, F. R. 245 $aThe use of microRNAs as reference genes for quantitative polymerase chain reaction in soybean.$h[electronic resource] 260 $c2010 520 $aReverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) is a robust and widely applied technique used to investigate gene expression. However, for correct analysis and interpretation of results, the choice of a suitable gene to use as an internal control is a crucial factor. These genes, such as housekeeping genes, should have a constant expression level in different tissues and across different conditions. The advances in genome sequencing have provided high-throughput gene expression analysis and have contributed to the identification of new genes, including microRNAs (miRNAs). The miRNAs are fundamental regulatory genes of eukaryotic genomes, acting on several biological functions. In this study, miRNA expression stability was investigated in different soybean tissues and genotypes as well as after abiotic or biotic stress treatments. The present study represents the first investigation into the suitability of miRNAs as housekeeping genes in plants. The transcript stability of 10 miRNAs was compared to those of six previously reported housekeeping genes for the soybean. In this study, we provide evidence that the expression stabilities of miR156b and miR1520d were the highest across the soybean experiments. Furthermore, these miRNAs genes were more stable than the most commonly protein-coding genes used in soybean gene expression studies involving RT-qPCR. 650 $aGenes 650 $aMicroRNA 650 $aQuantitative polymerase chain reaction 650 $aSoybeans 650 $aGene 650 $aRNA 650 $aSoja 653 $aReação em cadeia da polimerase 700 1 $aMARCELINO-GUIMARAES, F. C. 700 1 $aNEPOMUCENO, A. L. 700 1 $aABDELNOOR, R. V. 700 1 $aMARGIS, R. 773 $tAnalytical Biochemistry$gv. 406, n. 2, p. 185-192, nov. 2010.
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Embrapa Soja (CNPSO) |
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| Registros recuperados : 8 | |
| 2. |  | MACEDO, M. A.; MALIANIO, M. R.; ROJAS, M. R.; SOUZA, J. O.; INOUE-NAGATA, A. K.; GILBERTSON, R. L. Urther evidence of local evolution of weed-infecting begomoviruses in Brazil: molecular characterization and production of infectious clones of a new species infecting sida sp. from the state of Piauí. Virus Reviews and Research, Belo Horizonte, v. 20, p. 211-212, Oct. 2015. Supplement 1, ref. PIV 404. Edição dos resumos do XXVI Brazilian Congress of Virology, X Mercosur Meeting of Virology, 2015, Florianópolis.| Tipo: Resumo em Anais de Congresso |
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| 6. |  | REIS, L. de N. A. dos; BOITEUX, L. S.; FONSECA, M. E. N.; ROJAS, M. R.; GILBERTSON, R. L.; CARVALHO, R. de C. P. Tomato golden net virus and tomato yellow net virus: two novel New World begomoviruses with monopartite genomes. Archives of Virology, v. 168, n. 2, article number 235, 2023.| Tipo: Artigo em Periódico Indexado | Circulação/Nível: B - 1 |
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| 8. |  | ROJAS, M. R.; MACEDO, M. A.; MALIANO, M. R.; SOTO-AGUILAR, M.; SOUZA, J. O.; BRIDDON, R. W.; KENYON, L.; BUSTAMANTE, R. F. R.; MURILO ZERBINI, F.; ADKINS, S.; LEGG, J. P.; KVARNHEDEN, A.; WINTERMANTEL, W. M.; SUDARSHANA, M. R.; PETERSCHMITT, M.; LAPIDOT, M.; MARTIN, D. P.; MORIONES, E.; INOUE-NAGATA, A. K.; GILBERTSON, R. L. World management of geminiviruses. Annual Review of Phytopathology, v. 56, p. 637-677, 2018.| Tipo: Artigo em Periódico Indexado | Circulação/Nível: A - 1 |
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| Registros recuperados : 8 | |
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| Nenhum registro encontrado para a expressão de busca informada. |
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