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Genotyping single nucleotide polymorphisms directly from genomic DNA by invasive cleavage reaction on microspheres

机译:通过微球上的侵入性裂解反应直接从基因组DNA中对单核苷酸多态性进行基因分型

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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.
机译:在这里,我们报告基于微球的基因分型检测的原理证明,该检测直接从人类基因组DNA样本中检测单核苷酸多态性(SNP)。该测定基于结构特异性切割反应,该反应可通过5'核酸酶实现单碱基识别,该酶识别靶DNA与探针和上游寡核苷酸杂交后形成的三方底物。该测定很简单,只需两个简单步骤:裂解反应,在微球表面产生荧光信号,然后对微球进行流式细胞仪分析。对载脂蛋白E基因第158位氨基酸上的SNP基因组DNA样本进行基因分型。该测定法成功地对野生型,杂合和纯合突变体进行了评分。据我们所知,这是首次直接从基因组DNA中检测SNP而无需PCR扩增靶标的固相支持检测方法的首次报道。

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