How to do successful gene expression analysis using real-time PCR

被引:556
作者
Derveaux, Stefaan
Vandesompele, Jo
Hellemans, Jan
机构
[1] Ghent Univ Hosp, Ctr Med Genet, B-9000 Ghent, Belgium
[2] Biogazelle, Ghent, Belgium
关键词
RT-qPCR; Quality control; Experiment design; Assay design; Reference gene validation; QUANTIFICATION; GUIDELINES;
D O I
10.1016/j.ymeth.2009.11.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Reverse transcription quantitative PCR (RT-qPCR) is considered today as the gold standard for accurate, sensitive and fast measurement of gene expression. Unfortunately, what many users fail to appreciate is that numerous critical issues in the workflow need to be addressed before biologically meaningful and trustworthy conclusions can be drawn. Here, we review the entire workflow from the planning and preparation phase, over the actual real-time PCR cycling experiments to data-analysis and reporting steps. This process can be captured with the appropriate acronym PCR: plan/prepare, cycle and report. The key message is that quality assurance and quality control are essential throughout the entire RT-qPCR workflow; from living cells, over extraction of nucleic acids, storage, various enzymatic steps such as DNase treatment, reverse transcription and PCR amplification, to data-analysis and finally reporting. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:227 / 230
页数:4
相关论文
共 19 条
[1]  
Aranyi Tamas, 2007, V402, P385
[2]   Gene expression profiling in single cells from the pancreatic islets of Langerhans reveals lognormal distribution of mRNA levels [J].
Bengtsson, M ;
Ståhlberg, A ;
Rorsman, P ;
Kubista, M .
GENOME RESEARCH, 2005, 15 (10) :1388-1392
[3]   The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments [J].
Bustin, Stephen A. ;
Benes, Vladimir ;
Garson, Jeremy A. ;
Hellemans, Jan ;
Huggett, Jim ;
Kubista, Mikael ;
Mueller, Reinhold ;
Nolan, Tania ;
Pfaffl, Michael W. ;
Shipley, Gregory L. ;
Vandesompele, Jo ;
Wittwer, Carl T. .
CLINICAL CHEMISTRY, 2009, 55 (04) :611-622
[4]  
Fleige Simone, 2006, Molecular Aspects of Medicine, V27, P126, DOI 10.1016/j.mam.2005.12.003
[5]   Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis [J].
Hellemans, J ;
Preobrazhenska, O ;
Willaert, A ;
Debeer, P ;
Verdonk, PCM ;
Costa, T ;
Janssens, K ;
Menten, B ;
Van Roy, N ;
Vermeulen, SJT ;
Savarirayan, R ;
Van Hul, W ;
Vanhoenacker, F ;
Huylebroeck, D ;
De Paepe, A ;
Naeyaert, JM ;
Vandesompele, J ;
Speleman, F ;
Verschueren, K ;
Coucke, PJ ;
Mortier, GR .
NATURE GENETICS, 2004, 36 (11) :1213-1218
[6]   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)
[7]   Rapid detection of VHL exon deletions using real-time quantitative PCR [J].
Hoebeeck, J ;
van der Luijt, R ;
Poppe, B ;
De Smet, E ;
Yigit, N ;
Claes, K ;
Zewald, R ;
de Jong, GJ ;
De Paepe, A ;
Speleman, F ;
Vandesompele, J .
LABORATORY INVESTIGATION, 2005, 85 (01) :24-33
[8]   RTPrimerDB: the portal for real-time PCR primers and probes [J].
Lefever, Steve ;
Vandesompele, Jo ;
Speleman, Frank ;
Pattyn, Filip .
NUCLEIC ACIDS RESEARCH, 2009, 37 :D942-D945
[9]   RDML: structured language and reporting guidelines for real-time quantitative PCR data [J].
Lefever, Steve ;
Hellemans, Jan ;
Pattyn, Filip ;
Przybylski, Daniel R. ;
Taylor, Chris ;
Geurts, Rene ;
Untergasser, Andreas ;
Vandesompele, Jo .
NUCLEIC ACIDS RESEARCH, 2009, 37 (07) :2065-2069
[10]  
Motulski H, 1995, INTUITIVE BIOSTATIST