Wilson病基因第18外显子多态及突变研究  

A Study on Polymorphism and Mutation of Exon 18 in ATP7B Gene of Wilson's Disease

作　　者：洪铭范[1] 琚双武[1] 任明山[1] 张志[1] 范玉新[2] 胡纪原[1] 韩咏竹[1] 杨任民[1] 

机构地区：[1]安徽中医学院神经病学研究所,230031 [2]复旦大学遗传学研究所,200433

出　　处：《中国临床神经科学》1999年第3期129-131,共3页Chinese Journal of Clinical Neurosciences

基　　金：本课题为安徽省科委自然科学基金资助项目(97412001)

摘　　要：目的:了解中国人肝豆状核变性患者ATP7B基因第18外显子的突变情况,以期为该病的基因诊断提供依据。方法:采用PCR-SSCP技术对患者及健康对照组的DNA扩增片断进行筛选,对其中异常的迁移带型行DNA测序。结果:30例对照组SSCP呈一种带型,122例患者中37例分别呈4种不同的异常迁移带型,泳动异常率为30.33%(37/122)。DNA测序结果表明SSCP呈I型的患者第3772位点C缺失而产生移码突变。结论:在中国人肝豆状核变性患者中发现一种新型移码突变。Aim: To investigate the mutation of exon 18 in ATP7B gene in Chinese patients with Wilson's disease. Methods: Exon 18 of ATP7B gene was amplified with PCR technique in patients and controls. Mutations were screened by single strand conformation polymorphism(SSCP)analysis and further confirmed by sequencing. Results: 30 controls showed the same migration bands in PCR-SSCP, but abnormal migration bands were observed in 37 patients. The abnormal migration frequency was 30. 33 %(37/122). Sequencing of PCR products with type I of abnormal bands revealed a C deletion mutation at nucleotide 3772, which produces a frameshift mutation. Conclusion: A new frameshift mutation of exon 18 in ATP7B gene was investigated in Chinese patients with Wilson's disease.

关 键 词：WILSON病 ATP7B基因 基因突变 第18外显子 

分 类 号：R742.402[医药卫生—神经病学与精神病学]