An optimistic view for quantifying mRNA in post-mortem human brain

被引:44
作者
Preece, P
Virley, DJ
Costandi, M
Coombes, R
Moss, SJ
Mudge, AW
Jazin, E
Cairns, NJ
机构
[1] Quantuum, Dept Neurol, Galicia 15177, Spain
[2] Glaxo SmithKline Pharmaceut, Dept Neurosci, Harlow CM19 5AW, Essex, England
[3] Guys Hosp, Kings Coll London, MRC Ctr Dev Neurobiol, London SE1 1UL, England
[4] UCL, MRC Lab Mol & Cellular Biol, London WC1E 6BT, England
[5] Uppsala Univ, Rudbeck Lab, Dept Med Genet, S-75185 Uppsala, Sweden
[6] Uppsala Univ, Rudbeck Lab, Dept Pathol, S-75185 Uppsala, Sweden
[7] Univ Penn, Ctr Neurodegenerat Dis Res, Sch Med, Philadelphia, PA 19104 USA
来源
MOLECULAR BRAIN RESEARCH | 2003年 / 116卷 / 1-2期
关键词
Alzheimer's disease; human brain; mRNA; quantification; TaqMan;
D O I
10.1016/S0169-328X(03)00208-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Quantitative human mRNA data are derived from post-mortem or biopsied tissue. RNA degradation, poor replication, a large mRNA variance and confounding factors such as brain pH and age of death are often cited, however, as objections to the data's reliability. A central question is whether post-mortem human mRNA can be treated as a statistically ordered system. TaqMan(TM) real-time RT-PCR was used to measure seven mRNAs in 513 cortical samples taken from 90 Alzheimer's disease and 81 control brains. Despite a high mRNA variance strong correlations were found between the mRNA transcripts in a single brain. Where a brain has a high/low level of one mRNA, the same brain invariably has a high/low level of other mRNAs; correlated order is present and allows removal of that source of variation common to all genes. Although levels of mRNA are highly variable between subjects (> 1000-fold), quantitative order is present in post-mortem human mRNA, allowing effects due to pathology or gender to be isolated and tested for significance. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 16
页数:10
相关论文
共 35 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   PREMORTEM AND POSTMORTEM INFLUENCES ON BRAIN-RNA [J].
BARTON, AJL ;
PEARSON, RCA ;
NAJLERAHIM, A ;
HARRISON, PJ .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (01) :1-11
[3]   The quantification of gene expression in an animal model of brain ischaemia using TaqMan™ real-time RT-PCR [J].
Bond, BC ;
Virley, DJ ;
Cairns, NJ ;
Hunter, AJ ;
Moore, GBT ;
Moss, SJ ;
Mudge, AW ;
Walsh, FS ;
Jazin, E ;
Preece, P .
MOLECULAR BRAIN RESEARCH, 2002, 106 (1-2) :101-116
[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]   ALTERED EXPRESSION OF GENES FOR AMYLOID AND CYTOSKELETAL PROTEINS IN ALZHEIMER CORTEX [J].
CLARK, AW ;
KREKOSKI, CA ;
PARHAD, IM ;
LISTON, D ;
JULIEN, JP ;
HOAR, DI .
ANNALS OF NEUROLOGY, 1989, 25 (04) :331-339
[6]  
Cochran W.G. G.M. Cox., 1957, Experimental Design
[7]   Recovery and expression of messenger RNA from postmortem human brain tissue [J].
Cummings, TJ ;
Strum, JC ;
Yoon, LW ;
Szymanski, MH ;
Hulette, CM .
MODERN PATHOLOGY, 2001, 14 (11) :1157-1161
[8]  
EHRLICH GD, 1994, PCR BASED DIAGNOSTIC, P6
[9]  
Gelfand DH, 1993, US Patent, Patent No. [5210015, 5,210,015]
[10]   A novel method for real time quantitative RT PCR [J].
Gibson, UEM ;
Heid, CA ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :995-1001