Strömqvist Meuzelaar Linda, Hopkins Katie, Liebana Ernesto, Brookes Anthony J
Department of Genetics, University of Leicester, University Rd., Leicester, LE1 7RH, UK.
J Mol Diagn. 2007 Feb;9(1):30-41. doi: 10.2353/jmoldx.2007.060057.
Melting-curve procedures track DNA denaturation in real time and so provide an effective way of assessing sequence variants. Dynamic allele-specific hybridization (DASH) is one such method, based on fluorescence, which uses heat to denature a single allele-specific probe away from one strand of a polymerase chain reaction product attached to a solid support. DASH is a proven system for research genotyping, but here we evaluate it for DNA diagnostics under two scenarios. First, for mutation scanning (resequencing), a human genomic sequence of 97 bp was interrogated with 15 probes tiled with 12-base overlaps, providing up to fourfold redundancy per base. This test sequence spanned three high-frequency single nucleotide polymorphisms, all of which were correctly revealed in 16 individuals. Second, to score multiple different mutations in parallel, 18 alterations in the gyrA gene of Salmonella were assessed in 62 strains by using wild-type- and mutation-specific probes. Both experiments were performed in a blinded manner, and all results were confirmed by sequencing. All DNA variants were unambiguously resolved in every sample, with no false-positive or false-negative signals across all of the investigations. In conclusion, DASH performs accurately and robustly when applied to DNA diagnostic challenges, including mutation scoring and mutation scanning.
熔解曲线程序可实时追踪DNA变性,因此提供了一种评估序列变异的有效方法。动态等位基因特异性杂交(DASH)就是这样一种基于荧光的方法,它利用加热使附着在固相支持物上的聚合酶链反应产物的一条链上的单个等位基因特异性探针变性。DASH是一种经过验证的研究基因分型系统,但在此我们在两种情况下对其进行DNA诊断评估。首先,对于突变扫描(重测序),用15个探针以12个碱基重叠的方式平铺检测97bp的人类基因组序列,每个碱基提供高达四倍的冗余度。该测试序列跨越三个高频单核苷酸多态性,在16个个体中均正确显示。其次,为了并行检测多个不同突变,通过使用野生型和突变特异性探针,在62株沙门氏菌中评估了gyrA基因的18个改变。两个实验均以盲法进行,所有结果均通过测序确认。在所有调查中,每个样本中的所有DNA变异均得到明确解析,无假阳性或假阴性信号。总之,当应用于DNA诊断挑战,包括突变评分和突变扫描时,DASH表现准确且稳健。