上海市崇明县热性惊厥与SCN1A基因热点多态性变异的相关性分析  

Analysis of the correlation between febrile seizure and hot-spot polymorphism variation in SCN1A gene in children from Chongming County,Shanghai

作　　者：叶桂云[1] 陈柳[1] 戴红[1] 刘晓青[1] 

机构地区：[1]上海交通大学医学院附属新华医院儿内科,上海200082

出　　处：《上海交通大学学报（医学版）》2016年第11期1643-1647,共5页Journal of Shanghai Jiao tong University:Medical Science

摘　　要：目的·了解上海市崇明县儿童热性惊厥(FS)与电压门控钠离子通道α1亚型(SCNIA)基因外显子25、26及3'UTR区域之间的相关性。方法·提取96例FS患儿[包括32例全面性癫痫伴热性惊厥附加症(GEFS+)患儿]和53例健康对照组儿童的外周静脉血基因组DNA,进行SCNIA基因E25、E26及3'UTR区域PCR扩增及测序分析。结果·病例组和对照组SCNIA基因E25、E26均未见突变。3'UTR区域1例GEFS+患儿存在c.310-311delGT变异,2例FS患儿存在c.589T>G变异,6例存在c.593T>G变异;对照组均未发现变异。病例组和对照组已报道的单核苷酸多态性(SNP)c.1025T>C发生频率分别为18.2%和24.5%,2组间差异无统计学意义。预测结果显示114种miRNA能与SCNIA基因3'UTR区结合。c.310-311delGT不位于miRNA与SCN1A基因3'UTR区的结合序列内,c.589T>G变异、c.589T>G变异均位于此序列中。结论·经检测SCNIA基因E25、E26均未见突变;3'UTR区域发现c.310-311de1GT、c.589T>G和c.593T>G变异;SNPc.1025T>C与FS无明显关联。Objective · To explore the correlation of febrile seizure （FS） with voltage-gated sodium channel alpha 1 subtype （SCN1A） gene exons 25, 26 and 3’UTR region in children from Shanghai chongming County. Methods · The genomic DNA in peripheral venous blood was extracted from 96 children with FS （including 32 cases of genetic epilepsy with febrile seizures plus [GEFS＋]） and 53 healthy controls. PCR amplification and sequencing analysis were performed for SCN1A gene exons 25, 26 and 3’UTR region. Results · No mutation in SCN1A gene exons E25, E26 was found in both groups. For 3’UTR region, c.310311 delgt GT variation was found in 1 case of GEFS＋, c.589 T〉 G variation in 2 cases of FS, and c.593 T〉G variation in 6 cases, while no mutation was found in the control group. Reported frequencies of single nucleotide polymorphism （SNP） c.1025T〉C were 18.2% （the case group） and 24.5% （the control group）. The difference between two groups was not statistically significant. Prediction results showed that 114 microRNAs could bind with the 3’UTR region of SCN1A gene. C.310-311 delGT was not located in the sequence where miRNAs bound with 3’UTR region of SCN1A gene, while c. 589 T〉G and c.593 T 〉 G variations were located in this sequence. Conclusion · No mutation was found in SCN1Agene exons E25, E26. The c. 310-311delGT, c.589 T 〉 G, and c. 593 T 〉 G variations were found in 3’UTR region. There is no obvious correlation between SNPc.1025T〉C and FS.

关 键 词：热性惊厥 SCN1A 全面性癫痫伴热性惊厥附加症 单核苷酸多态性 3＇UTR 

分 类 号：R720.597[医药卫生—急诊医学]