Broccanello Chiara, Chiodi Claudia, Funk Andrew, McGrath J Mitchell, Panella Lee, Stevanato Piergiorgio
1DAFNAE, Università degli Studi di Padova, Legnaro, Italy.
2USDA-ARS Sugarbeet and Bean Research, East Lansing, MI USA.
Plant Methods. 2018 Mar 28;14:28. doi: 10.1186/s13007-018-0295-6. eCollection 2018.
PCR allelic discrimination technologies have broad applications in the detection of single nucleotide polymorphisms (SNPs) in genetics and genomics. The use of fluorescence-tagged probes is the leading method for targeted SNP detection, but assay costs and error rates could be improved to increase genotyping efficiency. A new assay, rhAmp, based on RNase H2-dependent PCR (rhPCR) combined with a universal reporter system attempts to reduce error rates from primer/primer and primer/probe dimers while lowering costs compared to existing technologies. Before rhAmp can be widely adopted, more experimentation is required to validate its effectiveness versus established methods.
The aim of this study was to compare the accuracy, sensitivity and costs of TaqMan, KASP, and rhAmp SNP genotyping methods in sugar beet ( L.). For each approach, assays were designed to genotype 33 SNPs in a set of 96 sugar beet individuals obtained from 12 parental lines. The assay sensitivity was tested using a series of dilutions from 100 to 0.1 ng per PCR reaction. PCR was carried out on the QuantStudio 12K Flex Real-Time PCR System (Thermo Fisher Scientific, USA). The call-rate, defined as the percentage of genotype calls relative to the possible number of calls, was 97.0, 97.6, and 98.1% for TaqMan, KASP, and rhAmp, respectively. For rhAmp SNP, 24 of the 33 SNPs demonstrated 100% concordance with other two technologies. The genotype concordance with either technologies for the other 9 targets was above 99% (99.34-99.89%).
The sensitivity test demonstrated that TaqMan and rhAmp were able to successfully determine SNP genotypes using as little as 0.2 ng DNA per reaction, while the KASP was unable to ascertain SNP states below 0.9 ng of DNA per reaction. Comparative cost per reaction was also analyzed with rhAmp SNP offering the lowest cost per reaction. In conclusion, rhAmp produced more calls than either TaqMan or KASP, higher signal to NTC data while offering the lowest cost per reaction.
聚合酶链式反应(PCR)等位基因鉴别技术在遗传学和基因组学中单核苷酸多态性(SNP)检测方面有广泛应用。使用荧光标记探针是靶向SNP检测的主要方法,但检测成本和错误率仍有待改进以提高基因分型效率。一种基于核糖核酸酶H2依赖性PCR(rhPCR)并结合通用报告系统的新检测方法rhAmp,试图降低引物/引物和引物/探针二聚体产生的错误率,同时与现有技术相比降低成本。在rhAmp能够被广泛采用之前,需要更多实验来验证其与既定方法相比的有效性。
本研究的目的是比较TaqMan、竞争性等位基因特异性PCR(KASP)和rhAmp SNP基因分型方法在甜菜(Beta vulgaris L.)中的准确性、灵敏度和成本。对于每种方法,设计检测以对从12个亲本系获得的一组96个甜菜个体中的33个SNP进行基因分型。使用每个PCR反应从100到0.1 ng的一系列稀释液测试检测灵敏度。在QuantStudio 12K Flex实时PCR系统(美国赛默飞世尔科技公司)上进行PCR。TaqMan、KASP和rhAmp的检出率(定义为基因型检出数相对于可能检出数的百分比)分别为97.0%、97.6%和98.1%。对于rhAmp SNP,33个SNP中的24个与其他两种技术显示出100%的一致性。其他9个靶点与任何一种技术的基因型一致性均高于99%(99.34 - 99.89%)。
灵敏度测试表明,TaqMan和rhAmp能够使用每个反应低至0.2 ng的DNA成功确定SNP基因型,而KASP在每个反应低于0.9 ng的DNA时无法确定SNP状态。还分析了每个反应的比较成本,rhAmp SNP每个反应的成本最低。总之,rhAmp比TaqMan或KASP产生更多的检出数,信号与无模板对照(NTC)数据的比值更高,同时每个反应的成本最低。