Murugesan Gurunathan, Aboudola Samer, Szpurka Hadrian, Verbic Mary Ann, Maciejewski Jaroslaw P, Tubbs Raymond R, Hsi Eric D
Department of Clinical Pathology, Cleveland Clinic Foundation and the Cleveland Clinic, Lerner College of Medicine, Cleveland, OH 44195, USA.
Am J Clin Pathol. 2006 Apr;125(4):625-33. doi: 10.1309/TK0X-L917-XK2V-LRPQ.
We developed and validated a real-time polymerase chain reaction assay using fluorescent hybridization probes and melting curve analysis to identify the JAK2 V617F mutation, which is implicated in a substantial proportion of chronic myeloproliferative disorders (CMPDs). DNA from 161 samples was isolated from peripheral blood granulocytes and formalin-fixed bone marrow clot sections in patients with CMPDs and without myeloproliferative disorders previously genotyped for the JAK2 V617F (G-->T) mutation, which included 114 wild types (GG) and 47 mutants (GT and TT). Melting curve analysis of these samples yielded 114 wild types, 42 heterozygotes, and 5 homozygotes showing 100% concordance. Analytic sensitivity of the assay for mutant DNA was 5% for the LightTyper (Roche Applied Sciences, Indianapolis, IN) and 10% for the LightCycler (Roche Applied Sciences). Consistent with earlier reports, 78% of the non-chronic myelogenous leukemia CMPD patients and 8% of non-CMPD patients displayed this mutation. This study demonstrates that clinical genotyping of the JAK2 V617F mutation can be performed by melting analysis using both freshly isolated and formalin-fixed tissues.
我们开发并验证了一种使用荧光杂交探针和熔解曲线分析的实时聚合酶链反应检测方法,以鉴定JAK2 V617F突变,该突变与相当一部分慢性骨髓增殖性疾病(CMPD)有关。从CMPD患者和先前已对JAK2 V617F(G→T)突变进行基因分型的非骨髓增殖性疾病患者的外周血粒细胞和福尔马林固定的骨髓凝块切片中分离出161份样本的DNA,其中包括114份野生型(GG)和47份突变型(GT和TT)。对这些样本进行熔解曲线分析,得到114份野生型、42份杂合子和5份纯合子,结果显示一致性为100%。该检测方法对突变DNA的分析灵敏度,对于LightTyper(罗氏应用科学公司,印第安纳波利斯,印第安纳州)为5%,对于LightCycler(罗氏应用科学公司)为10%。与早期报告一致,78%的非慢性粒细胞白血病CMPD患者和8%的非CMPD患者显示出该突变。这项研究表明,JAK2 V617F突变的临床基因分型可以通过对新鲜分离组织和福尔马林固定组织进行熔解分析来进行。