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New Prediction Model for Probe Specificity in an Allele-Specific Extension Reaction for Haplotype-Specific Extraction (HSE) of Y Chromosome Mixtures

机译:在等位基因特异性延长反应单体型的具体提取(HsE)的探针特异性的新预测模型的Y染色体混合物

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摘要

Allele-specific extension reactions (ASERs) use 3′ terminus-specific primers for the selective extension of completely annealed matches by polymerase. The ability of the polymerase to extend non-specific 3′ terminal mismatches leads to a failure of the reaction, a process that is only partly understood and predictable, and often requires time-consuming assay design. In our studies we investigated haplotype-specific extraction (HSE) for the separation of male DNA mixtures. HSE is an ASER and provides the ability to distinguish between diploid chromosomes from one or more individuals. Here, we show that the success of HSE and allele-specific extension depend strongly on the concentration difference between complete match and 3′ terminal mismatch. Using the oligonucleotide-modeling platform Visual Omp, we demonstrated the dependency of the discrimination power of the polymerase on match- and mismatch-target hybridization between different probe lengths. Therefore, the probe specificity in HSE could be predicted by performing a relative comparison of different probe designs with their simulated differences between the duplex concentration of target-probe match and mismatches. We tested this new model for probe design in more than 300 HSE reactions with 137 different probes and obtained an accordance of 88%.
机译:等位基因特异性延伸反应(ASER)使用3'末端特异性引物通过聚合酶选择性延伸完全退火的匹配。聚合酶扩展非特异性3'末端错配的能力导致反应失败,该过程只是部分被理解和可预测,并且通常需要耗时的测定设计。在我们的研究中,我们研究了用于分离雄性DNA混合物的单倍型特异性提取(HSE)。 HSE是一种ASER,可区分一个或多个个体的二倍体染色体。在这里,我们表明,HSE和等位基因特异性延伸的成功很大程度上取决于完全匹配和3'末端错配之间的浓度差异。使用寡核苷酸建模平台Visual Omp,我们证明了聚合酶的辨别力对不同探针长度之间的匹配和错配靶杂交的依赖性。因此,HSE中的探针特异性可以通过对不同探针设计及其靶-探针匹配和错配双链体浓度之间的模拟差异进行模拟比较来预测。我们用137种不同的探针在300多种HSE反应中测试了该新模型的探针设计,并获得了88%的一致性。

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