Expression profiling suggests underexpression of the GABAA receptor subunit δ in the fragile X knockout mouse model

被引:128
作者
Gantois, I
Vandesompele, J
Speleman, F
Reyniers, E
D'Hooge, R
Severijnen, LA
Willemsen, R
Tassone, F
Kooy, RF
机构
[1] Univ Antwerp, Dept Med Genet, B-2610 Antwerp, Belgium
[2] Ghent Univ Hosp, Dept Med Genet, Ghent, Belgium
[3] Univ Antwerp, Born Bunge Fdn, Dept Neurochem & Behav, B-2020 Antwerp, Belgium
[4] Erasmus MC, Dept Clin Genet, Rotterdam, Netherlands
[5] Univ Calif Davis, Sch Med, Dept Biol Chem, Sacramento, CA 95817 USA
关键词
fragile X syndrome; fragile X knockout mouse; GABA(A); receptor subunit delta; Rho guanine exchange factor 12;
D O I
10.1016/j.nbd.2005.07.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It is still unclear why absence of the fragile X protein (FMRP) leads to mental retardation and specific behavioral problems. In neurons, the protein transports specific mRNAs towards the actively translating ribosomes near the synapses. To unravel the mechanism leading to the disorder, we performed global gene expression analysis by means of the differential display method using the fragile X mouse model. To verify differential expression, we used microarray technology and real-time PCR. Three differentially expressed cDNAs showed consistent underexpression in the fragile X knockout mouse, including a GABA(A) receptor subunit 6, a Rho guanine exchange factor 12 and an EST BU563433. In addition, we identified 5 genes that showed differential expression dependent on the sample of RNA analysis. We consider their differential expression as provisional. It is possible that these differentially expressed genes play an important role in the cognitive and behavioral problems observed in the fragile X syndrome. 0 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:346 / 357
页数:12
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