首页 | 本学科首页   官方微博 | 高级检索  
     

中国汉族人ATM基因的单核苷酸多态与点突变
引用本文:汤洪伟,边建超,江峰,沈强,朱虔兮,张宏伟,吴毅. 中国汉族人ATM基因的单核苷酸多态与点突变[J]. 中华医学遗传学杂志, 2004, 21(6): 579-582
作者姓名:汤洪伟  边建超  江峰  沈强  朱虔兮  张宏伟  吴毅
作者单位:1. 200032,上海,复旦大学公共卫生学院流行病学教研室
2. 200032,上海,复旦大学附属肿瘤医院头颈肿瘤科
3. 200032,上海,复旦大学附属中山医院普通外科
基金项目:国家自然科学基金(30371236)~~
摘    要:目的研究中国汉族人共济失调性毛细血管扩张症(ataxiatelangiectasiamutated,ATM)基因的单核苷酸多态和点突变。方法首先用PCR扩增ATM基因第39、61和63外显子的靶片段,然后用单链构象多态性(singlestrandconformationpolymorphism,SSCP)技术进行筛选,选择典型带型经全自动DNA测序证实。结果在ATM基因第39外显子以及第61和63内含子发现6个新的单核苷酸多态,它们分别是第39外显子第5689位和第5691位的A/T多态,第61内含子第 69位的T/G多态、第 94位的A/G多态和第 99位的T/G多态,第63内含子第 17位的G/C多态。在ATM基因第61外显子、第62内含子和第63外显子发现5个新的点突变,它们分别是第61外显子第8618位的T/G颠换、第62内含子第-13位的T/G颠换、第63外显子第8793位的T/G颠换、第8816位和第8848位的G/A转换。证实了ATM基因第39外显子第5557位G/A、第61内含子第 104位T/C和第62内含子第-55位T/C多态在中国汉族人中的存在。结论中国汉族人ATM基因的单核苷酸多态与白人存在较大差异。

关 键 词:共济失调性毛细血管扩张症基因  单核苷酸多态  点突变
修稿时间:2003-11-19

Single nucleotide polymorphisms and point mutations of ataxia telangiectasia mutated gene in Chinese of Han ethnicity
TANG Hong-wei,BIAN Jian-chao,JIANG Feng,SHEN Qiang,ZHU Qian-xi,ZHANG Hong-wei,WU Yi. Single nucleotide polymorphisms and point mutations of ataxia telangiectasia mutated gene in Chinese of Han ethnicity[J]. Chinese journal of medical genetics, 2004, 21(6): 579-582
Authors:TANG Hong-wei  BIAN Jian-chao  JIANG Feng  SHEN Qiang  ZHU Qian-xi  ZHANG Hong-wei  WU Yi
Affiliation:Department of Epidemiology, School of Public Health, Zhongshan Hospital, Fudan University, Shanghai, 200032 P. R. China.
Abstract:Objective To explore the single nucleotide polymorphisms (SNPs) and point mutations of ataxia telangiectasia mutated ( ATM ) gene in Chinese of Han ethnicity. Methods The target fragments of the exon 39, exon 61 and exon 63 of ATM gene were first amplified using PCR technique, then screened for the SNPs and point mutations using single strand conformation polymorphism (SSCP) technique, finally the representive bands were sequenced for the verification of the new single neocleotide polymorphisms and point mutations using the automatic DNA sequencing technique. Results Six new SNPs were found in the exon 39, intron 61 and intron 63 of ATM gene. They are respectively the A/T polymorphisms at nucleotide 5689 and 5691 in exon 39,the T/G polymorphisms at nucleotide 69 and 99, the A/G polymorphism at nucleotide 94 in intron 61,the G/C polymorphism at nucleotide 17 in intron 63. Five new point mutations were found in the exon 61, intron 62 and exon 63 of ATM gene. They are respectively the T/G transversion at nucleotide 8618 in exon 61, the T/G transversion at nucleotide -13 in intron 62, the T/G transversion at nucleotide 8793, the G/A transitions at nucleotide 8816 and 8848 in exon 63. The known three SNPs, the G/A polymorphism at nucleotide 5557 in exon 39, the T/C polymorphism at nucleotide 104 in intron 61 and the T/C polymorphism at nucleotide -55 in intron 62, were verified in Chinese of Han ethnicity. Conclusion There are great differences in the SNPs of ATM gene between Chinese of Han ethnicity and Caucasian.
Keywords:ataxia telangiectasia mutated gene  single nucleotide polymorphism  point mutation
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号