Rao Kakuturu V N, Stevens Priscilla Wilkins, Hall Jeff G, Lyamichev Victor, Neri Bruce P, Kelso David M
Department of Biomedical Engineering, Robert R. McCormick School of Engineering and Applied Science, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208-3107, USA.
Nucleic Acids Res. 2003 Jun 1;31(11):e66. doi: 10.1093/nar/gng066.
Here we report proof-of-principle for a microsphere-based genotyping assay that detects single nucleotide polymorphisms (SNPs) directly from human genomic DNA samples. This assay is based on a structure-specific cleavage reaction that achieves single base discrimination with a 5'-nuclease which recognizes a tripartite substrate formed upon hybridization of target DNA with probe and upstream oligonucleotides. The assay is simple with two easy steps: a cleavage reaction, which generates fluorescent signal on microsphere surfaces, followed by flow cytometry analysis of the microspheres. Genomic DNA samples were genotyped for the SNP in the Apolipoprotein E gene at amino acid position 158. The assay successfully scored wild type, heterozygous and homozygous mutants. To our knowledge, this is the first report of a solid-support assay for detection of SNPs directly from genomic DNA without PCR amplification of the target.
在此,我们报告了一种基于微球的基因分型检测方法的原理验证,该方法可直接从人类基因组DNA样本中检测单核苷酸多态性(SNP)。此检测基于一种结构特异性切割反应,该反应利用一种5'-核酸酶实现单碱基区分,该核酸酶识别靶DNA与探针及上游寡核苷酸杂交后形成的三方底物。该检测方法简单,只需两个步骤:一个切割反应,在微球表面产生荧光信号,随后对微球进行流式细胞术分析。对载脂蛋白E基因第158位氨基酸处的SNP进行了基因组DNA样本的基因分型。该检测成功区分了野生型、杂合子和纯合子突变体。据我们所知,这是首次报道无需对靶标进行PCR扩增即可直接从基因组DNA检测SNP的固相支持检测方法。