首都医科大学学报 ›› 2010, Vol. 31 ›› Issue (6): 742-747.

• 帕金森病的发病机制与生物标志物 • 上一篇    下一篇

基于等位基因特异性引物延伸的高分辨率熔解曲线基因分型方法的建立

袁艳鹏, 林庆玲, 左晓虹, 蔡彦宁   

  1. 首都医科大学宣武医院北京老年病医疗研究中心神经生物学研究室
  • 收稿日期:2010-10-27 修回日期:1900-01-01 出版日期:2010-12-24 发布日期:2010-12-24
  • 通讯作者: 左晓虹

Establishment of a Modified High Resolution Melting Assay Based on Allele-specific-extension to Determine Single Nucleotide Polymorphism

YUAN Yan-peng, LIN Qing-ling, ZUO Xiao-hong, CAI Yan-ning   

  1. Department of Neurobiology, Beijing Institute of Geriatric, Xuanwu Hospital, Capital Medical University
  • Received:2010-10-27 Revised:1900-01-01 Online:2010-12-24 Published:2010-12-24

摘要: 目的 建立基于等位基因特异引物延伸的高分辨率熔解曲线法(allele-specific-extension high resolution melting curve analysis,ASE-HRM)。方法 ASE-HRM法是在普通高分辨率熔解曲线法(high resolution melting curve analysis,HRM)的PCR反应体系中加入一条等位基因特异性延伸引物(allele-specific-extension,ASE),该引物末端终止于单核苷酸多态性(single nucleotide polymorphism,SNP)位点,匹配一种等位基因。增加热循环次数,使等位基因特异性引物得以延伸。选取rs1869458位点,用ASE-HRM法和直接测序法对194个人源基因组DNA样品进行基因分型。结果 通过分析熔解曲线扩增峰,可区分杂合型和纯合型SNP;通过分析有无引物延伸峰,可区分2种纯合型;同时证明长度为11到13个碱基的ASE引物能得到较好的分型结果;使用锁定核酸(locked nucleic acid,LNA)修饰扩增引物可增加扩增产物和延伸产物的解链温度(melting temperature,Tm)差距,简化基因分型。2种方法对所选DNA样品基因分型所得结果完全吻合。结论 ASE-HRM是一种简单、廉价、闭管并能用于检测所有类型SNP的基因分型法。

关键词: 单核苷酸多态性, 高分辨率熔解曲线, 等位基因特异性引物延伸, 碱基对中性突变

Abstract: Objective To establish a modified high resolution melting assay based on allele-specific-extension(ASE-HRM)to determine single nucleotide polymorphisms(SNP).Methods The established ASE-HRM was designed as asymmetric polymerase chain reaction and melting curve analysis.An allele-specific-extension(ASE) primer which ends at the SNP site and matches one of the allele was added to the reaction system.Initially,asymmetric PCR was performed with undergoing additional thermal steps in order to get allele-specific-extension.A total of 194 human genomic DNA samples were genotyped with the developed assay and by direct sequencing.Results Heterozygotes could be discriminated from homozygotes according to their lower and broader melting transitions.Two different types of homozygote could be separated according to the presence or absence of an extension peak.Extension primers 11~13 bases long worked efficiently in an allele specific way.Modification of the limiting amplification primer with locked nucleic acid increased the Tm difference between extension and amplification peaks and facilitated subsequent genotyping.The 194 human genomic DNA samples were genotyped with the developed assay and by direct sequencing,with the different methods providing identical genotyping results.Conclusion ASE-HRM is a simple,inexpensive,closed-tube genotyping method that can be used to examine all types of SNP.

Key words: single nucleotide polymorphism, high resolution melting curve analysis, allele-specific-extension, base-pair neutral variant

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