Liu Hongna, Li Song, Wang Zhifei, Ji Meiju, Nie Libo, He Nongyue
State Key Laboratory of Bioelectronics (Chien-Shiung Wu Laboratory), School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China.
J Biotechnol. 2007 Sep 15;131(3):217-22. doi: 10.1016/j.jbiotec.2007.06.023. Epub 2007 Jul 14.
Single-nucleotide polymorphisms (SNPs) are one-base variations in DNA sequence that can often be helpful when trying to find genes responsible for inherited diseases. In this paper, a microarray-based method for typing single nucleotide polymorphisms (SNPs) using solid-phase polymerase chain reaction (PCR) on magnetic nanoparticles (MNPs) was developed. One primer with biotin-label was captured by streptavidin coated magnetic nanoparticles (SA-MNPs), and PCR products were directly amplified on the surface of SA-MNPs in a 96-well plate. The samples were interrogated by hybridization with a pair of dual-color probes to determine SNP, and then genotype of each sample can be simultaneously identified by scanning the microarray printed with the denatured fluorescent probes. The C677T polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene from 126 samples were interrogated using this method. The results showed that three different genotypes were discriminated by three fluorescence patterns on the microarray. Without any purification and reduction procedure, and all reactions can be performed in the same vessel, this approach will be a simple and labor-saving method for SNP genotyping and can be applicable towards the automation system to achieve high-throughput SNP detection.
单核苷酸多态性(SNPs)是DNA序列中的单碱基变异,在寻找遗传性疾病相关基因时通常很有帮助。本文开发了一种基于微阵列的方法,用于在磁性纳米颗粒(MNPs)上通过固相聚合酶链反应(PCR)对单核苷酸多态性(SNPs)进行分型。一条生物素标记的引物被链霉亲和素包被的磁性纳米颗粒(SA-MNPs)捕获,PCR产物在96孔板中SA-MNPs的表面直接扩增。通过与一对双色探针杂交来检测样品以确定SNP,然后通过扫描印有变性荧光探针的微阵列可同时鉴定每个样品的基因型。使用该方法对126个样品的亚甲基四氢叶酸还原酶(MTHFR)基因的C677T多态性进行了检测。结果表明,微阵列上的三种荧光模式区分出了三种不同的基因型。无需任何纯化和还原步骤,且所有反应可在同一容器中进行,该方法将是一种用于SNP基因分型的简单省力的方法,并且可应用于自动化系统以实现高通量SNP检测。