Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions

Detalhes bibliográficos
Autor(a) principal: Nakayama, T.J.
Data de Publicação: 2014
Outros Autores: Rodrigues, F.A., Neumaie, N., Marcelino-Guimarães, F.C., Farias, J.R.B., Oliveira, M.C.N. de, Borém, A., Oliveira, A.C.B. de, Emygdio, B.M., Nepomuceno, A.L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: LOCUS Repositório Institucional da UFV
Texto Completo: http://dx.doi.org/10.4238/2014.February.13.4
http://www.locus.ufv.br/handle/123456789/12041
Resumo: Quantitative real-time polymerase chain reaction (RT-qPCR) is a powerful tool used to measure gene expression. However, because of its high sensitivity, the method is strongly influenced by the quality and concentration of the template cDNA and by the amplification efficiency. Relative quantification is an effective strategy for correcting random and systematic errors by using the expression level of reference gene(s) to normalize the expression level of the genes of interest. To identify soybean reference genes for use in studies of flooding stress, we compared 5 candidate reference genes (CRGs) with the NormFinder and GeNorm programs to select the best internal control. The expression stability of the CRGs was evaluated in root tissues from soybean plants subjected to hypoxic conditions. Elongation factor 1-beta and actin-11 were identified as the most appropriate genes for RT-qPCR normalization by both the NormFinder and GeNorm analyses. The expression profiles of the genes for alcohol dehydrogenase 1, sucrose synthase 4, and ascorbate peroxidase 2 were analyzed by comparing different normalizing combinations (including no normalization) of the selected reference genes. Here, we have identified potential genes for use as references for RT-qPCR normalization in experiments with soybean roots growing in O2-depleted environments, such as flooding-stressed plants.
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spelling Nakayama, T.J.Rodrigues, F.A.Neumaie, N.Marcelino-Guimarães, F.C.Farias, J.R.B.Oliveira, M.C.N. deBorém, A.Oliveira, A.C.B. deEmygdio, B.M.Nepomuceno, A.L.2017-10-11T18:01:57Z2017-10-11T18:01:57Z2014-02-1316765680http://dx.doi.org/10.4238/2014.February.13.4http://www.locus.ufv.br/handle/123456789/12041Quantitative real-time polymerase chain reaction (RT-qPCR) is a powerful tool used to measure gene expression. However, because of its high sensitivity, the method is strongly influenced by the quality and concentration of the template cDNA and by the amplification efficiency. Relative quantification is an effective strategy for correcting random and systematic errors by using the expression level of reference gene(s) to normalize the expression level of the genes of interest. To identify soybean reference genes for use in studies of flooding stress, we compared 5 candidate reference genes (CRGs) with the NormFinder and GeNorm programs to select the best internal control. The expression stability of the CRGs was evaluated in root tissues from soybean plants subjected to hypoxic conditions. Elongation factor 1-beta and actin-11 were identified as the most appropriate genes for RT-qPCR normalization by both the NormFinder and GeNorm analyses. The expression profiles of the genes for alcohol dehydrogenase 1, sucrose synthase 4, and ascorbate peroxidase 2 were analyzed by comparing different normalizing combinations (including no normalization) of the selected reference genes. Here, we have identified potential genes for use as references for RT-qPCR normalization in experiments with soybean roots growing in O2-depleted environments, such as flooding-stressed plants.engGenetics and Molecular Researchv.13 n.(1): p.860-871, february, 2014Endogenous genesInternal control genesFloodingHousekeeping genesGene expressionReference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditionsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfinfo:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFVORIGINALgmr2769.pdfgmr2769.pdftexto completoapplication/pdf590238https://locus.ufv.br//bitstream/123456789/12041/1/gmr2769.pdf02d7d25f0d4a7e7812faf0ba4143a7deMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://locus.ufv.br//bitstream/123456789/12041/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52THUMBNAILgmr2769.pdf.jpggmr2769.pdf.jpgIM Thumbnailimage/jpeg4379https://locus.ufv.br//bitstream/123456789/12041/3/gmr2769.pdf.jpg0bd9cd8979a3fec57824173c58b6e0d6MD53123456789/120412017-10-11 23:00:56.196oai:locus.ufv.br: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Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452017-10-12T02:00:56LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.en.fl_str_mv Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions
title Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions
spellingShingle Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions
Nakayama, T.J.
Endogenous genes
Internal control genes
Flooding
Housekeeping genes
Gene expression
title_short Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions
title_full Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions
title_fullStr Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions
title_full_unstemmed Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions
title_sort Reference genes for quantitative real-time polymerase chain reaction studies in soybean plants under hypoxic conditions
author Nakayama, T.J.
author_facet Nakayama, T.J.
Rodrigues, F.A.
Neumaie, N.
Marcelino-Guimarães, F.C.
Farias, J.R.B.
Oliveira, M.C.N. de
Borém, A.
Oliveira, A.C.B. de
Emygdio, B.M.
Nepomuceno, A.L.
author_role author
author2 Rodrigues, F.A.
Neumaie, N.
Marcelino-Guimarães, F.C.
Farias, J.R.B.
Oliveira, M.C.N. de
Borém, A.
Oliveira, A.C.B. de
Emygdio, B.M.
Nepomuceno, A.L.
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Nakayama, T.J.
Rodrigues, F.A.
Neumaie, N.
Marcelino-Guimarães, F.C.
Farias, J.R.B.
Oliveira, M.C.N. de
Borém, A.
Oliveira, A.C.B. de
Emygdio, B.M.
Nepomuceno, A.L.
dc.subject.pt-BR.fl_str_mv Endogenous genes
Internal control genes
Flooding
Housekeeping genes
Gene expression
topic Endogenous genes
Internal control genes
Flooding
Housekeeping genes
Gene expression
description Quantitative real-time polymerase chain reaction (RT-qPCR) is a powerful tool used to measure gene expression. However, because of its high sensitivity, the method is strongly influenced by the quality and concentration of the template cDNA and by the amplification efficiency. Relative quantification is an effective strategy for correcting random and systematic errors by using the expression level of reference gene(s) to normalize the expression level of the genes of interest. To identify soybean reference genes for use in studies of flooding stress, we compared 5 candidate reference genes (CRGs) with the NormFinder and GeNorm programs to select the best internal control. The expression stability of the CRGs was evaluated in root tissues from soybean plants subjected to hypoxic conditions. Elongation factor 1-beta and actin-11 were identified as the most appropriate genes for RT-qPCR normalization by both the NormFinder and GeNorm analyses. The expression profiles of the genes for alcohol dehydrogenase 1, sucrose synthase 4, and ascorbate peroxidase 2 were analyzed by comparing different normalizing combinations (including no normalization) of the selected reference genes. Here, we have identified potential genes for use as references for RT-qPCR normalization in experiments with soybean roots growing in O2-depleted environments, such as flooding-stressed plants.
publishDate 2014
dc.date.issued.fl_str_mv 2014-02-13
dc.date.accessioned.fl_str_mv 2017-10-11T18:01:57Z
dc.date.available.fl_str_mv 2017-10-11T18:01:57Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://dx.doi.org/10.4238/2014.February.13.4
http://www.locus.ufv.br/handle/123456789/12041
dc.identifier.issn.none.fl_str_mv 16765680
identifier_str_mv 16765680
url http://dx.doi.org/10.4238/2014.February.13.4
http://www.locus.ufv.br/handle/123456789/12041
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartofseries.pt-BR.fl_str_mv v.13 n.(1): p.860-871, february, 2014
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Genetics and Molecular Research
publisher.none.fl_str_mv Genetics and Molecular Research
dc.source.none.fl_str_mv reponame:LOCUS Repositório Institucional da UFV
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