Reference genes for gene expression studies in wheat flag leaves grown under different farming conditions

<p>Abstract</p> <p>Background</p> <p>Internal control genes with highly uniform expression throughout the experimental conditions are required for accurate gene expression analysis as no universal reference genes exists. In this study, the expression stability of 24 can...

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Main Authors: Cordeiro Raposo Fernando, Peres Bota Adrian, Tenea Gabriela N, Maquet Alain
Format: Article
Language:English
Published: BMC 2011-09-01
Series:BMC Research Notes
Online Access:http://www.biomedcentral.com/1756-0500/4/373
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spelling doaj-1530ea7f9ab44168a9f844ccc428c9c92020-11-25T02:08:35ZengBMCBMC Research Notes1756-05002011-09-014137310.1186/1756-0500-4-373Reference genes for gene expression studies in wheat flag leaves grown under different farming conditionsCordeiro Raposo FernandoPeres Bota AdrianTenea Gabriela NMaquet Alain<p>Abstract</p> <p>Background</p> <p>Internal control genes with highly uniform expression throughout the experimental conditions are required for accurate gene expression analysis as no universal reference genes exists. In this study, the expression stability of 24 candidate genes from <it>Triticum aestivum </it>cv. Cubus flag leaves grown under organic and conventional farming systems was evaluated in two locations in order to select suitable genes that can be used for normalization of real-time quantitative reverse-transcription PCR (RT-qPCR) reactions. The genes were selected among the most common used reference genes as well as genes encoding proteins involved in several metabolic pathways.</p> <p>Findings</p> <p>Individual genes displayed different expression rates across all samples assayed. Applying geNorm, a set of three potential reference genes were suitable for normalization of RT-qPCR reactions in winter wheat flag leaves cv. Cubus: <it>TaFNRII </it>(ferredoxin-NADP(H) oxidoreductase; AJ457980.1), <it>ACT2 </it>(actin 2; TC234027), and <it>rrn26 </it>(a putative homologue to RNA 26S gene; AL827977.1). In addition of these three genes that were also top-ranked by NormFinder, two extra genes: <it>CYP18-2 </it>(Cyclophilin A, AY456122.1) and <it>TaWIN1 </it>(14-3-3 like protein, AB042193) were most consistently stably expressed.</p> <p>Furthermore, we showed that <it>TaFNRII, ACT2</it>, and <it>CYP18-2 </it>are suitable for gene expression normalization in other two winter wheat varieties (Tommi and Centenaire) grown under three treatments (organic, conventional and no nitrogen) and a different environment than the one tested with cv. Cubus.</p> <p>Conclusions</p> <p>This study provides a new set of reference genes which should improve the accuracy of gene expression analyses when using wheat flag leaves as those related to the improvement of nitrogen use efficiency for cereal production.</p> http://www.biomedcentral.com/1756-0500/4/373
collection DOAJ
language English
format Article
sources DOAJ
author Cordeiro Raposo Fernando
Peres Bota Adrian
Tenea Gabriela N
Maquet Alain
spellingShingle Cordeiro Raposo Fernando
Peres Bota Adrian
Tenea Gabriela N
Maquet Alain
Reference genes for gene expression studies in wheat flag leaves grown under different farming conditions
BMC Research Notes
author_facet Cordeiro Raposo Fernando
Peres Bota Adrian
Tenea Gabriela N
Maquet Alain
author_sort Cordeiro Raposo Fernando
title Reference genes for gene expression studies in wheat flag leaves grown under different farming conditions
title_short Reference genes for gene expression studies in wheat flag leaves grown under different farming conditions
title_full Reference genes for gene expression studies in wheat flag leaves grown under different farming conditions
title_fullStr Reference genes for gene expression studies in wheat flag leaves grown under different farming conditions
title_full_unstemmed Reference genes for gene expression studies in wheat flag leaves grown under different farming conditions
title_sort reference genes for gene expression studies in wheat flag leaves grown under different farming conditions
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2011-09-01
description <p>Abstract</p> <p>Background</p> <p>Internal control genes with highly uniform expression throughout the experimental conditions are required for accurate gene expression analysis as no universal reference genes exists. In this study, the expression stability of 24 candidate genes from <it>Triticum aestivum </it>cv. Cubus flag leaves grown under organic and conventional farming systems was evaluated in two locations in order to select suitable genes that can be used for normalization of real-time quantitative reverse-transcription PCR (RT-qPCR) reactions. The genes were selected among the most common used reference genes as well as genes encoding proteins involved in several metabolic pathways.</p> <p>Findings</p> <p>Individual genes displayed different expression rates across all samples assayed. Applying geNorm, a set of three potential reference genes were suitable for normalization of RT-qPCR reactions in winter wheat flag leaves cv. Cubus: <it>TaFNRII </it>(ferredoxin-NADP(H) oxidoreductase; AJ457980.1), <it>ACT2 </it>(actin 2; TC234027), and <it>rrn26 </it>(a putative homologue to RNA 26S gene; AL827977.1). In addition of these three genes that were also top-ranked by NormFinder, two extra genes: <it>CYP18-2 </it>(Cyclophilin A, AY456122.1) and <it>TaWIN1 </it>(14-3-3 like protein, AB042193) were most consistently stably expressed.</p> <p>Furthermore, we showed that <it>TaFNRII, ACT2</it>, and <it>CYP18-2 </it>are suitable for gene expression normalization in other two winter wheat varieties (Tommi and Centenaire) grown under three treatments (organic, conventional and no nitrogen) and a different environment than the one tested with cv. Cubus.</p> <p>Conclusions</p> <p>This study provides a new set of reference genes which should improve the accuracy of gene expression analyses when using wheat flag leaves as those related to the improvement of nitrogen use efficiency for cereal production.</p>
url http://www.biomedcentral.com/1756-0500/4/373
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