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

被引:41
作者
Tenea G.N. [1 ]
Peres Bota A. [1 ]
Cordeiro Raposo F. [1 ]
Maquet A. [1 ]
机构
[1] European Commission, Joint Research Centre (JRC), Institute for Reference Materials and Measurements (IRMM), 2440 Geel
关键词
Reference Gene; Winter Wheat; Candidate Reference Gene; Flag Leave; Stable Reference Gene;
D O I
10.1186/1756-0500-4-373
中图分类号
学科分类号
摘要
Background: 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 Triticum aestivum 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. Findings. 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: TaFNRII (ferredoxin-NADP(H) oxidoreductase; AJ457980.1), ACT2 (actin 2; TC234027), and rrn26 (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: CYP18-2 (Cyclophilin A, AY456122.1) and TaWIN1 (14-3-3 like protein, AB042193) were most consistently stably expressed. Furthermore, we showed that TaFNRII, ACT2, and CYP18-2 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. Conclusions: 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. © 2010 Maquet et al; licensee BioMed Central Ltd.
引用
收藏
相关论文
共 78 条
[1]  
Sun D.-W., Modern Techniques for Food Authentication, (2008)
[2]  
Weckwerth W., Integration of metabolomics and proteomics in molecular plant physiology - Coping with the complexity by data-dimensionality reduction, Physiol Plantarum, 132, 2, pp. 176-189, (2008)
[3]  
Bustin S.A., A-Z of Quantitative PCR, (2004)
[4]  
Vandesompele J., Kubista M., Pfaffl M.W., Reference gene validation software for improved normalization, Real-time PCR: Current Technology and Applications, (2009)
[5]  
Bustin S.A., Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): Trends and problems, Journal of Molecular Endocrinology, 29, 1, pp. 23-39, (2002)
[6]  
Huggett J., Dheda K., Bustin S., Zumla A., Real-time RT-PCR normalisation
[7]  
strategies and considerations, Genes and Immunity, 6, 4, pp. 279-284, (2005)
[8]  
Paolacci A., Tanzarella O., Porceddu E., Ciaffi M., Identification and validation of reference genes for quantitative RT-PCR normalization in wheat, BMC Mol Biol, 10, 1, (2009)
[9]  
Thellin O., Zorzi W., Lakaye B., De Borman B., Coumans B., Hennen G., Grisar T., Igout A., Heinen E., Housekeeping genes as internal standards: Use and limits, Journal of Biotechnology, 75, 2-3, pp. 291-295, (1999)
[10]  
Brunner A.M., Yakovlev I.A., Strauss S.H., Validating internal controls for quantitative plant gene expression studies, BMC Plant Biol, 4, 14, (2004)