Seipp Michael T, Herrmann Mark, Wittwer Carl T
ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, Utah 84108, USA.
J Biomol Tech. 2010 Dec;21(4):163-6.
Genotyping by high-resolution amplicon melting uses only two PCR primers per locus and a generic, saturating DNA dye that detects heteroduplexes as well as homoduplexes. Heterozygous genotypes have a characteristic melting curve shape and a broader width than homozygous genotypes, which are usually differentiated by their melting temperature (T(m)). The H63D mutation, associated with hemochromatosis, is a single nucleotide polymorphism, which is impossible to genotype based on T(m), as the homozygous WT and mutant amplicons melt at the same temperature. To distinguish such homozygous variants, WT DNA can be added to controls and unknown samples to create artificial heterozygotes with all genotypes distinguished by quantitative heteroduplex analysis. By automating DNA extraction, quantification, and PCR preparation, a hands-off integrated solution for genotyping is possible. A custom Biomek® NX robot with an onboard spectrophotometer and custom programming was used to extract DNA from whole blood, dilute the DNA to appropriate concentrations, and add the sample DNA to preprepared PCR plates. Agencourt® Genfind™ v.2 chemistry was used for DNA extraction. PCR was performed on a plate thermocycler, high-resolution melting data collected on a LightScanner-96, followed by analysis and automatic genotyping using custom software. In a blinded study of 42 H63D samples, 41 of the 42 sample genotypes were concordant with dual hybridization probe genotyping. The incorrectly assigned genotype was a heterozygote that appeared to be a homozygous mutant as a result of a low sample DNA concentration. Automated DNA extraction from whole blood with quantification, dilution, and PCR preparation was demonstrated using quantitative heteroduplex analysis. Accuracy is critically dependent on DNA quantification.
高分辨率扩增子熔解基因分型每个位点仅使用两条PCR引物和一种通用的饱和DNA染料,该染料可检测异源双链体和同源双链体。杂合基因型具有特征性的熔解曲线形状,且比纯合基因型的宽度更宽,纯合基因型通常通过其熔解温度(T(m))来区分。与血色素沉着症相关的H63D突变是一种单核苷酸多态性,由于纯合野生型和突变型扩增子在相同温度下熔解,因此无法基于T(m)进行基因分型。为了区分此类纯合变体,可以将野生型DNA添加到对照和未知样品中,以创建人工杂合子,所有基因型均可通过定量异源双链分析来区分。通过自动化DNA提取、定量和PCR制备,可以实现一种无需人工干预的基因分型集成解决方案。使用配备内置分光光度计和定制程序的定制Biomek® NX机器人从全血中提取DNA,将DNA稀释至适当浓度,并将样品DNA添加到预先制备的PCR板中。使用Agencourt® Genfind™ v.2化学方法进行DNA提取。在平板热循环仪上进行PCR,在LightScanner-96上收集高分辨率熔解数据,然后使用定制软件进行分析和自动基因分型。在对42个H63D样品的盲法研究中,42个样品基因型中的41个与双重杂交探针基因分型结果一致。错误指定的基因型是一个杂合子,由于样品DNA浓度低,它看起来像是纯合突变体。使用定量异源双链分析证明了从全血中自动提取DNA并进行定量、稀释和PCR制备。准确性严重依赖于DNA定量。