Quantitative polymerase chain reaction: Validation of microarray results from postmortem brain studies

被引:40
作者
Mimmack, ML
Brooking, J
Bahn, S [1 ]
机构
[1] Babraham Inst, Dept Neurobiol, Cambridge CB2 4AT, England
[2] Babraham Inst, Med Res Council Geneserv, Cambridge CB2 4AT, England
[3] Babraham Inst, Babraham Bioincubator, Cambridge CB2 4AT, England
[4] Univ Cambridge, Addenbrookes Hosp, Dept Psychiat, Cambridge CB2 1TN, England
关键词
quantitative polymerase chain reaction (Q-PCR); reverse transcription polymerase chain reaction (RT-PCR); minor groove binder; standard curve analysis; housekeeping genes; dissociation curve analysis;
D O I
10.1016/j.biopsych.2003.09.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Quantitative polymerase chain reaction (Q-PCR) is now considered the "technique of choice" for validating gene expression changes identified with ribonucleic acid-based expression profiling technologies (especially micro- and macroarray techniques). The identification of altered gene expression profiles with microarrays is best viewed as the first step in the determination of potential disease-associated genes; however, the false-positive rate can be high, particularly with small sample sets and in view of the typically small differences observed in brain expression studies. Quantitative PCR is a rapid and highly sensitive technique for accurate quantification of microarray results; however, careful consideration of experimental design, quality of primer/probe design, internal standards, and normalization procedures are pivotal, particularly when the work involves postmortem tissue.
引用
收藏
页码:337 / 345
页数:9
相关论文
共 28 条
[1]   Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder [J].
Afonina, I ;
Zivarts, M ;
Kutyavin, I ;
Lukhtanov, E ;
Gamper, H ;
Meyer, RB .
NUCLEIC ACIDS RESEARCH, 1997, 25 (13) :2657-2660
[2]   Gene expression profiling in the post-mortem human brain - no cause for dismay [J].
Bahn, S ;
Augood, S ;
Standaert, DG ;
Starkey, M ;
Emson, PC .
JOURNAL OF CHEMICAL NEUROANATOMY, 2001, 22 (1-2) :79-94
[3]   Gene expression in bipolar disorder and schizophrenia: new approaches to old problems [J].
Bahn, S .
BIPOLAR DISORDERS, 2002, 4 :70-72
[4]   High-resolution quantification of specific mRNA levels in human brain autopsies and biopsies [J].
Castensson, A ;
Emilsson, L ;
Preece, P ;
Jazin, E .
GENOME RESEARCH, 2000, 10 (08) :1219-1229
[5]   An overview of real-time quantitative PCR: Applications to quantify cytokine gene expression [J].
Giulietti, A ;
Overbergh, L ;
Valckx, D ;
Decallonne, B ;
Bouillon, R ;
Mathieu, C .
METHODS, 2001, 25 (04) :386-401
[6]   Identification and validation of endogenous reference genes for expression profiling of T helper cell differentiation by quantitative real-time RT-PCR [J].
Hamalainen, HK ;
Tubman, JC ;
Vikman, S ;
Kyrölä, T ;
Ylikoski, E ;
Warrington, JA ;
Lahesmaa, R .
ANALYTICAL BIOCHEMISTRY, 2001, 299 (01) :63-70
[7]   The relative importance of premortem acidosis and postmortem interval for human brain gene expression studies: Selective mRNA vulnerability and comparison with their encoded proteins [J].
Harrison, PJ ;
Heath, PR ;
Eastwood, SL ;
Burnet, PWJ ;
McDonald, B ;
Pearson, RCA .
NEUROSCIENCE LETTERS, 1995, 200 (03) :151-154
[8]   Gene expression profile for schizophrenia - Discrete neuron transcription patterns in the entorhinal cortex [J].
Hemby, SE ;
Ginsberg, SD ;
Brunk, B ;
Arnold, SE ;
Trojanowski, JQ ;
Eberwine, JH .
ARCHIVES OF GENERAL PSYCHIATRY, 2002, 59 (07) :631-640
[9]  
Herrler M, 2000, J MOL MED-JMM, V78, pB23
[10]   ORGANIZATION AND EXPRESSION OF THE HUMAN MYELIN BASIC-PROTEIN GENE [J].
KAMHOLZ, J ;
TOFFENETTI, J ;
LAZZARINI, RA .
JOURNAL OF NEUROSCIENCE RESEARCH, 1988, 21 (01) :62-70