高等学校化学学报

高等学校化学学报

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一种基于磁性纳米粒子PCR的高通量SNP分型方法

刘洪娜1, 李松1, 2, 王志飞2, 何农跃2, 贺全国1   

    1. 湖南工业大学绿色包装与生物纳米技术应用湖南省重点实验室, 株洲 412008;
    2. 东南大学生物电子学国家重点实验室, 生物科学与医学工程系, 南京 210096
  • 收稿日期:2006-07-01 修回日期:1900-01-01 出版日期:2007-06-10 发布日期:2007-06-10
  • 通讯作者: 李松

High-throughput SNP Genotyping Method with PCR on Magnetic Nanoparticles

LIU Hong-Na1, LI Song1,2*, WANG Zhi-Fei2, HE Nong-Yue2, HE Quan-Guo1*   

    1. Key Laboratory of Green Packaging and Application of Biological Nanotechnology of Hunan Province, Hunan University of Technology, Zhuzhou 412008, China;
    2. State Key Laboratory of Bioelectronics, Department of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China
  • Received:2006-07-01 Revised:1900-01-01 Online:2007-06-10 Published:2007-06-10
  • Contact: LI Song

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被引次数

25

摘要： 利用磁性纳米粒子PCR扩增(MNPs-PCR)和等位基因特异性双色荧光探针(Cy3, Cy5)杂交, 建立了一种单核苷酸多态性(SNP)分型的新方法. 应用该方法对9个样本MTHFR基因的C677T多态进行检测, 野生和突变型样本正错配信号比大于9.0, 杂合型正错配信号比接近1.0, 分型结果经测序验证. 此方法无须产物纯化、浓缩, 扫描分型结果快速、直观, 是一种操作简单、快速、高通量、高灵敏度的分型方法.

关键词: 磁性纳米粒子, PCR, 双色荧光杂交, SNP分型

Abstract: Single nucleotide polymorphisms(SNPs) assay is important for elucidating the genetics of indivi-dual differences in drug response and disease susceptibility. This report described a novel high-throughput SNP genotyping method using magnetic nanoparticles as PCR primers carriers. PCR products were directly amplified on MNPs and interrogated by hybridization with a pair of dual-color fluorescence(Cy3, Cy5) probes to determine SNP, and then genotype of each sample can be simultaneously identified by scanning the microarray printed with the denatured fluorescent probes on an unmodified glass slide. As the results, the homozygous wild type, homozygous mutant type and heterozygote type yield strongly green, red and yellow fluorescent signals, respectively. The methylenetetrahydrofolate reductase(MTHFR) gene C677T polymorphism of nine di-fferent samples was detected and their fluorescent signals of the nine samples were quantified. The fluorescent ratios(match probe signal to mismatch probe signal) of homozygous samples were over 9.0, whereas heterozygous samples had ratios near 1.0. The genotyping results were additionally validated by sequencing. Without any purification and concentration of PCR products, the approach reported here should be a simple, sensitive, high-throughput and high accurate genotyping method.

Key words: Magnetic nanoparticles, PCR, Dual-color fluorescence hybridization, SNP genotyping

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