Evaluation and selection of reliable reference genes for gene expression under abiotic stress in cotton (Gossypium hirsutum L.)

被引:95
作者
Wang, Min [1 ]
Wang, Qinglian [2 ]
Zhang, Baohong [3 ]
机构
[1] Beijing Technol & Business Univ, Sch Sci, Beijing Key Lab Plant Resources Res & Dev, Dept Biotechnol, Beijing, Peoples R China
[2] Henan Inst Sci & Technol, Xinxiang 453003, Henan, Peoples R China
[3] E Carolina Univ, Dept Biol, Greenville, NC 27858 USA
基金
中国国家自然科学基金;
关键词
Cotton; Gossypium hirsutum; Reference gene; Gene expression; Real time PCR; RT-PCR NORMALIZATION; REAL-TIME; WIDE IDENTIFICATION; HOUSEKEEPING GENES; VALIDATION;
D O I
10.1016/j.gene.2013.07.084
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Reference genes are critical for normalization of the gene expression level of target genes. The widely used housekeeping genes may change their expression levels at different tissue under different treatment or stress conditions. Therefore, systematical evaluation on the housekeeping genes is required for gene expression analysis. Up to date, no work was performed to evaluate the housekeeping genes in cotton under stress treatment. In this study, we chose 10 housekeeping genes to systematically assess their expression levels at two different tissues (leaves and roots) under two different abiotic stresses (salt and drought) with three different concentrations. Our results show that there is no best reference gene for all tissues at all stress conditions. The reliable reference gene should be selected based on a specific condition. For example, under salt stress, UBQ7, GAPDH and EF1A8 are better reference genes in leaves; TUA10, UBQ7, CYP1, GAPDH and EF1A8 were better in roots. Under drought stress, UBQ7, EF1A8, TUA10, and GAPDH showed less variety of expression level in leaves and roots. Thus, it is better to identify reliable reference genes first before performing any gene expression analysis. However, using a combination of housekeeping genes as reference gene may provide a new strategy for normalization of gene expression. In this study, we found that combination of four housekeeping genes worked well as reference genes under all the stress conditions. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:44 / 50
页数:7
相关论文
共 32 条
[1]  
Alves-Ferreira M., 2010, BMC PEDIAT, V10
[2]   Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets [J].
Andersen, CL ;
Jensen, JL ;
Orntoft, TF .
CANCER RESEARCH, 2004, 64 (15) :5245-5250
[3]   Reference Genes for High-Throughput Quantitative Reverse Transcription-PCR Analysis of Gene Expression in Organs and Tissues of Eucalyptus Grown in Various Environmental Conditions [J].
Cassan-Wang, Hua ;
Soler, Marcal ;
Yu, Hong ;
Camargo, Eduardo Leal O. ;
Carocha, Victor ;
Ladouce, Nathalie ;
Savelli, Bruno ;
Paiva, Jorge A. P. ;
Leple, Jean-Charles ;
Grima-Pettenati, Jacqueline .
PLANT AND CELL PHYSIOLOGY, 2012, 53 (12) :2101-2116
[4]   Development of real-time PCR method for the detection and the quantification of a new endogenous reference gene in sugar beet "Beta vulgaris L.": GMO application [J].
Chaouachi, Maher ;
Alaya, Akram ;
Ali, Imen Ben Haj ;
Ben Hafsa, Ahmed ;
Nabi, Nesrine ;
Berard, Aurelie ;
Romaniuk, Marcel ;
Skhiri, Fethia ;
Said, Khaled .
PLANT CELL REPORTS, 2013, 32 (01) :117-128
[5]   Evaluation and Identification of Reliable Reference Genes for Pharmacogenomics, Toxicogenomics, and Small RNA Expression Analysis [J].
Chen, Dongliang ;
Pan, Xiaoping ;
Xiao, Peng ;
Farwell, Mary A. ;
Zhang, Baohong .
JOURNAL OF CELLULAR PHYSIOLOGY, 2011, 226 (10) :2469-2477
[6]   Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis [J].
Czechowski, T ;
Stitt, M ;
Altmann, T ;
Udvardi, MK ;
Scheible, WR .
PLANT PHYSIOLOGY, 2005, 139 (01) :5-17
[7]   Reference gene selection for quantitative reverse transcription-polymerase chain reaction normalization during in vitro adventitious rooting in Eucalyptus globulus Labill [J].
de Almeida, Marcia R. ;
Ruedell, Carolina M. ;
Ricachenevsky, Felipe K. ;
Sperotto, Raul A. ;
Pasquali, Giancarlo ;
Fett-Neto, Arthur G. .
BMC MOLECULAR BIOLOGY, 2010, 11
[8]   Identification of Reference Genes for RT-qPCR Expression Analysis in Arabidopsis and Tomato Seeds [J].
Dekkers, Bas J. W. ;
Willems, Leo ;
Bassel, George W. ;
van Bolderen-Veldkamp, R. P. ;
Ligterink, Wilco ;
Hilhorst, Henk W. M. ;
Bentsink, Leonie .
PLANT AND CELL PHYSIOLOGY, 2012, 53 (01) :28-37
[9]   Salt and Drought Stresses Induce the Aberrant Expression of microRNA Genes in Tobacco [J].
Frazier, Taylor P. ;
Sun, Guiling ;
Burklew, Caitlin E. ;
Zhang, Baohong .
MOLECULAR BIOTECHNOLOGY, 2011, 49 (02) :159-165
[10]   Towards a systematic validation of references in real-time RT-PCR [J].
Gutierrez, Laurent ;
Mauriat, Melanie ;
Pelloux, Jerome ;
Bellini, Catherine ;
van Wuytswinkel, Olivier .
PLANT CELL, 2008, 20 (07) :1734-1735