Evaluation of suitable reference genes for gene expression studies in bronchoalveolar lavage cells from horses with inflammatory airway disease

被引:51
作者
Beekman, Laura [1 ]
Tohver, Triin [1 ]
Dardari, Rkia [2 ]
Leguillette, Renaud [1 ]
机构
[1] Univ Calgary, Dept Vet Clin & Diagnost Sci, Fac Vet Med, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Fac Med, Dept Microbiol & Infect Dis, Calgary, AB T2N 4N1, Canada
关键词
MESSENGER-RNA EXPRESSION; TRANSCRIPTION-PCR DATA; TIME RT-PCR; REAL-TIME; HOUSEKEEPING GENE; ALVEOLAR MACROPHAGES; INTERNAL CONTROL; BETA-ACTIN; NORMALIZATION; SELECTION;
D O I
10.1186/1471-2199-12-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: The stability of reference genes has a tremendous effect on the results of relative quantification of genes expression by quantitative polymerase chain reaction. Equine Inflammatory Airway Disease (IAD) is a common condition often treated with corticosteroids. The diagnosis of IAD is based on clinical signs and bronchoalveolar lavage (BAL) fluid cytology. The aim of this study was to identify reference genes with the most stable mRNA expression in the BAL cells of horses with IAD irrespective of corticosteroids treatment. Results: The expression stability of seven candidate reference genes (B2M, HPRT, GAPDH, ACTB, UBB, RPL32, SDHA) was determined by qRT-PCR in BAL samples taken pre- and post-treatment with dexamethasone and fluticasone propionate for two weeks in 7 horses with IAD. Primers' efficiencies were calculated using LinRegPCR. NormFinder, GeNorm and qBasePlus softwares were used to rank the genes according to their stability. GeNorm was also used to determine both the ideal number and the best combination of reference genes. GAPDH was found to be the most stably expressed gene with the three softwares. GeNorm ranked B2M as the least stable gene. Based on the pair-wise variation cut-off value determined with GeNorm, the number of genes required for optimal normalization was four and included GAPDH, SDHA, HPRT and RPL32. Conclusion: The geometric mean of GAPDH, HPRT, SDHA and RPL32 is recommended for accurate normalization of quantitative PCR data in BAL cells of horses with IAD treated with corticosteroids. If only one reference gene can be used, then GAPDH is recommended.
引用
收藏
页数:10
相关论文
共 44 条
[11]   The effect of adding oral dexamethasone to feed alterations on the airway cell inflammatory gene expression in stabled horses affected with recurrent airway obstruction [J].
DeLuca, L. ;
Erb, H. N. ;
Young, J. C. ;
Perkins, G. A. ;
Ainsworth, D. M. .
JOURNAL OF VETERINARY INTERNAL MEDICINE, 2008, 22 (02) :427-435
[12]   The implications of using an inappropriate reference gene for real-time reverse transcription PCR data normalization [J].
Dheda, K ;
Huggett, JF ;
Chang, JS ;
Kim, LU ;
Bustin, SA ;
Johnson, MA ;
Rook, GAW ;
Zumla, A .
ANALYTICAL BIOCHEMISTRY, 2005, 344 (01) :141-143
[13]   Validation of a reliable set of primer pairs for measuring gene expression by real-time quantitative RT-PCR in equine leukocytes [J].
Figueiredo, M. D. ;
Salter, C. E. ;
Andrietti, A. L. P. ;
Vandenplas, M. L. ;
Hurley, D. J. ;
Moore, J. N. .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2009, 131 (1-2) :65-72
[14]   Suitable reference genes for real-time PCR in human HBV-related hepatocellular carcinoma with different clinical prognoses [J].
Fu, Li-Yun ;
Jia, Hu-Liang ;
Dong, Qiong-Zhu ;
Wu, Jin-Cai ;
Zhao, Yue ;
Zhou, Hai-Jun ;
Ren, Ning ;
Ye, Qin-Hai ;
Qin, Lun-Xiu .
BMC CANCER, 2009, 9
[15]   Quantitation of equine cytokine mRNA expression by reverse transcription competitive polymerase chain reaction [J].
Giguère, S ;
Prescott, JF .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1999, 67 (01) :1-15
[16]   Cytokine induction in pulmonary airways of horses with heaves and effect of therapy with inhaled fluticasone propionate [J].
Giguère, S ;
Viel, L ;
Lee, E ;
MacKay, EJ ;
Hernandez, J ;
Franchini, M .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2002, 85 (3-4) :147-158
[17]   β-actin and GAPDH housekeeping gene expression in asthmatic airways is variable and not suitable for normalising mRNA levels [J].
Glare, EM ;
Divjak, M ;
Bailey, MJ ;
Walters, EH .
THORAX, 2002, 57 (09) :765-770
[18]   qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data [J].
Hellemans, Jan ;
Mortier, Geert ;
De Paepe, Anne ;
Speleman, Frank ;
Vandesompele, Jo .
GENOME BIOLOGY, 2007, 8 (02)
[19]  
HOFFMAN A, 2002, P WORKSH INFL AIRW D
[20]   Real-time RT-PCR normalisation; strategies and considerations [J].
Huggett, J ;
Dheda, K ;
Bustin, S ;
Zumla, A .
GENES AND IMMUNITY, 2005, 6 (04) :279-284