Wolff Jonci N, Gemmell Neil J
School of Biological Sciences, University of Canterbury, Christchurch, New Zealand.
Biotechniques. 2008 Feb;44(2):193-4, 196, 199. doi: 10.2144/000112719.
TaqMan-nuclease assays are widely used for the qualitative detection of single nucleotide polymorphisms (SNPs) and the determination of biallelic states in pooled or heterozygous DNA samples. These assays are highly specific, reproducible, and suitable for high-throughput approaches. A crucial limitation of this method, and others, is the detection qf minor allele frequencies with detection limits of generally 3% to 9% for minor allele contributions. Here we describe the combination of customized TaqMan-nuclease assay and allele-specific restriction to increase the sensitivity of this method, allowing the qualitative detection of allele contributions as low as 0.05%.
TaqMan核酸酶分析广泛用于单核苷酸多态性(SNP)的定性检测以及混合或杂合DNA样本中双等位基因状态的测定。这些分析具有高度特异性、可重复性,适用于高通量方法。该方法以及其他方法的一个关键局限性在于检测次要等位基因频率,其检测限通常为次要等位基因贡献的3%至9%。在此,我们描述了定制的TaqMan核酸酶分析与等位基因特异性限制的结合,以提高该方法的灵敏度,从而能够定性检测低至0.05%的等位基因贡献。