Central Laboratory, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China ; Department of Laboratory Medicine, Huashan Hospital North, Shanghai Medical College, Fudan University, Shanghai, China.
Department of Dermatology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Biomed Res Int. 2014;2014:458457. doi: 10.1155/2014/458457. Epub 2014 Mar 5.
A multiplex snapback primer system was developed for the simultaneous detection of JAK2 V617F and MPL W515L/K mutations in Philadelphia chromosome- (Ph-) negative myeloproliferative neoplasms (MPNs). The multiplex system comprises two snapback versus limiting primer sets for JAK2 and MPL mutation enrichment and detection, respectively. Linear-After exponential (LATE) PCR strategy was employed for the primer design to maximize the amplification efficiency of the system. Low ionic strength buffer and rapid PCR protocol allowed for selective amplification of the mutant alleles. Amplification products were analyzed by melting curve analysis for mutation identification. The multiplex system archived 0.1% mutation load sensitivity and <5% coefficient of variation inter-/intra-assay reproducibility. 120 clinical samples were tested by the multiplex snapback primer assay, and verified with amplification refractory system (ARMS), quantitative PCR (qPCR) and Sanger sequencing method. The multiplex system, with a favored versatility, provided the molecular diagnosis of Ph-negative MPNs with a suitable implement and simplified the genetic test process.
建立了一种用于同时检测费城染色体阴性骨髓增殖性肿瘤(MPN)中 JAK2 V617F 和 MPL W515L/K 突变的多重 snapback 引物系统。该多重系统包括用于 JAK2 和 MPL 突变富集和检测的两个 snapback 与限制引物对。线性后指数(LATE)PCR 策略用于引物设计,以最大化系统的扩增效率。低离子强度缓冲液和快速 PCR 方案允许选择性扩增突变等位基因。通过熔解曲线分析对扩增产物进行突变鉴定。该多重系统的突变载量灵敏度为 0.1%,批内/批间重现性的变异系数<5%。该多重 snapback 引物检测法检测了 120 例临床样本,并与扩增障碍系统(ARMS)、定量 PCR(qPCR)和 Sanger 测序法进行了验证。该多重系统具有较高的通用性,为 Ph 阴性 MPN 提供了合适的分子诊断方法,并简化了基因检测过程。