Development of Molecular Beacon method to detect of JAK2 V617F mutation

A. Nazemi
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Abstract

V617F mutation of JAK2 gene is a point mutation of Somatic cells leading to permanent phosphorylation and protein kinase activity of the JAK2 protein. This mutation is a valuable marker in the diagnosis of myeloid neoplasms. Development of new techniques can be effective and highly sensitive for the detection of the mutation. The aim of this study is designing and executing a molecular beacon probe-based real-time PCR detect to V617F mutation. Test results were reviewed from a set of wild type and cloned JAK2 exon 12 mutated allele genes into plasmid vector and through amplification by Real-Time PCR system. The sensitivity and specificity of Molecular Beacon probes design were tested. The results showed that the Real-Time PCR system has %100 specificity and % 0.001 sensitivity. Based on the results obtained from the molecular beacon probe-based real-time PCR, it was proved that the system is able to detect normal and mutant alleles of JAK2 V617F position with high accuracy and a short time in a closed tube system
分子信标法检测JAK2 V617F突变的建立
JAK2基因的V617F突变是体细胞中导致JAK2蛋白永久磷酸化和蛋白激酶活性的点突变。这种突变是诊断髓系肿瘤的一个有价值的标志。新技术的发展可以有效和高灵敏度地检测突变。本研究的目的是设计并实现基于分子信标探针的实时PCR检测V617F突变。将野生型和克隆的JAK2外显子12突变等位基因导入质粒载体,并通过Real-Time PCR系统进行扩增。测试了分子信标探针设计的灵敏度和特异性。结果表明,Real-Time PCR系统特异性为%100,灵敏度为% 0.001。基于分子信标探针的实时PCR结果证明,该系统能够在封闭管系统中以较高的准确性和较短的时间检测JAK2 V617F的正常和突变等位基因的位置
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