Quantitative RT-PCR analysis of uncoupling protein isoforms in mouse brain cortex: Methodological optimization and comparison of expression with brown adipose tissue and skeletal muscle

被引:67
作者
Lengacher, S [1 ]
Magistretti, PJ [1 ]
Pellerin, L [1 ]
机构
[1] Univ Lausanne, Inst Physiol, CH-1005 Lausanne, Switzerland
关键词
UCP polymerase chain reaction; thermogenesis mitochondria; free radicals; respiration; ATP synthesis;
D O I
10.1097/01.WCB.0000122743.72175.52
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Uncoupling proteins (UCPs) present in the inner mitochondrial membrane are involved in uncoupling respiration from ATP synthesis. Five UCP isoforms have been identified but information about their presence and level of expression in the central nervous system remains incomplete. To determine the nature and proportion of UCP isoform mRNAs present in brain cortex, we developed and optimized a specific quantitative reverse-transcription polymerase chain reaction procedure. Optimal range of RNA concentrations to be used in the reverse-transcriptase reaction was determined. Primer design and concentration were optimized for each target gene while polymerase chain reaction efficiency was assessed for a range of reverse-transcriptase dilutions. Genomic contribution to the quantitative signal was evaluated for each isoform and minimized. Three reference genes were tested for normalization, and beta-actin was found to be the most stable among tissues. Results indicate that brain cortex contains significant amounts of all UCP mRNAs, with UCP5 and UCP4 being the most abundant, as opposed to brown adipose tissue and skeletal muscle, which predominantly express UCP1 and UCP3, respectively. These data provide a first quantitative assessment of UCP mRNA expression in mouse brain, showing the presence of all five isoforms with distinct proportions, thus suggesting specific roles in the central nervous system.
引用
收藏
页码:780 / 788
页数:9
相关论文
共 29 条
[1]
Analysis of gene expression in the rat hippocampus using real time PCR reveals high inter-individual variation in mRNA expression levels [J].
Alfonso, J ;
Pollevick, GD ;
Castensson, A ;
Jazin, E ;
Frasch, ACC .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 67 (02) :225-234
[2]
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]
Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production [J].
Arsenijevic, D ;
Onuma, H ;
Pecqueur, C ;
Raimbault, S ;
Manning, BS ;
Miroux, B ;
Couplan, E ;
Alves-Guerra, MC ;
Goubern, M ;
Surwit, R ;
Bouillaud, F ;
Richard, D ;
Collins, S ;
Ricquier, D .
NATURE GENETICS, 2000, 26 (04) :435-439
[4]
Bastard JP, 2002, ANN BIOL CLIN-PARIS, V60, P513
[5]
Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays [J].
Bustin, SA .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2000, 25 (02) :169-193
[6]
Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems [J].
Bustin, SA .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2002, 29 (01) :23-39
[7]
The role of uncoupling proteins in the regulation of metabolism [J].
Erlanson-Albertsson, C .
ACTA PHYSIOLOGICA SCANDINAVICA, 2003, 178 (04) :405-412
[8]
A novel method for real time quantitative RT PCR [J].
Gibson, UEM ;
Heid, CA ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :995-1001
[9]
Uncoupling protein-3 is a mediator of thermogenesis regulated by thyroid hormone, beta 3-adrenergic agonists, and leptin [J].
Gong, DW ;
He, YF ;
Karas, M ;
Reitman, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (39) :24129-24132
[10]
Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408