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Screening of Novel Epilepsy-Related Genes and Isolation and Identification of cDNAs
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作者 朱和明 朱长庚 +3 位作者 郝建东 孟祥文 王丽华 陈德权 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2000年第1期10-12,共3页
Summary: Twenty cDNA differential fragments were isolated from the hippocampus of rats in epileptic state. using mRNA differential display technique. Four fragments were sequenced and compared with the known sequences... Summary: Twenty cDNA differential fragments were isolated from the hippocampus of rats in epileptic state. using mRNA differential display technique. Four fragments were sequenced and compared with the known sequences in the Genebank, which showed that ERGS, ERG12, ERG12 had no significant identity to any known sequences; ERG14 had 64 %-69 % identity to micro- tubulin-associated protein of the rat. Because the differential expression of these genes was caused by epilepsy inducer coriaria lactone (CL) and anti-epilepsy drug MK-801 and ERGS might be a novel candidate epilepsy gene; ERG11 and ERG12 might be novel candidate anti-epilepsy genes. Since the microtubulin-associated protein is closely associated with the collateral sprouting of mossy.fibers in the hippocampus of seizured rat, the high expression of ERG14 in the early stage of epilepsy might predict the growth of axon and formation of synapse. 展开更多
关键词 mRNA differential display epilepsy-related gene molecular cloning
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Screening for glutamate-induced and dexamethasone-downregulated epilepsy-related genes in rats by mRNA differential display 被引量:3
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作者 MA Chun-ling ZHU Chang-geng +3 位作者 FAN Ming LIU Shu-hong LIU Qing-ying CONG Bin 《Chinese Medical Journal》 SCIE CAS CSCD 2006年第6期488-495,共8页
Background It is known that excessive release of glutamate can induce excitotoxicity in neurons and lead to seizure. Dexamethasone has anti-seizure function. The aim of this study was to investigate glutamatedexametha... Background It is known that excessive release of glutamate can induce excitotoxicity in neurons and lead to seizure. Dexamethasone has anti-seizure function. The aim of this study was to investigate glutamatedexamethasone interaction in the pathogenesis of epilepsy, identify differentially expressed genes in the hippocampus of glutamate-induced epileptic rats by mRNA differential display, and observe the effects of dexamethasone on these genes expression. Methods Seizure models were established by injecting 5μl (250 μg/μl) monosodium glutamate (MSG) into the lateral cerebral ventricle in rats. Dexamethasone (5 mg/kg) was injected intraperitoneally at 30 minutes after MSG inducing convulsion. The rats' behavior and electroencephalogram (EEG) were then recorded for 1 hour. The effects of dexamethasone on gene expression were observed in MSG-induced epileptic rats at 1 hour and 6 hours after the onset of seizure by mRNA differential display. The differentially expressed genes were confirmed by Dot blot. Results EEG and behaviors showed that MSG did induce seizure, and dexamethasone could clearly alleviate the symptom, mRNA differential display showed that MSG increased the expression of some genes in epileptic rats and dexamethasone could downregulate their expression. From more than 10 differentially expressed eDNA fragments, we identified a 226 bp eDNA fragment that was expressed higher in the hippocampus of epileptic rats than that in the control group. Its expression was reduced after the administration of dexamethasone. Sequence analysis and protein alignment showed that the predicted amino acid sequence of this cDNA fragment kept 43% identity to agmatinase, a member of the ureohydrolase superfamily. Conclusions The results of the current study suggest that the product of the 226 bp eDNA has a function similar to agmatinase. Dexamethasone might relax alleviate seizure by inhibiting expression of the gene. 展开更多
关键词 monosodium glutamate DEXAMETHASONE agmatinase mRNA differential display epilepsy-related gene
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