Identification of the JAK2 V617F mutation in chronic myeloproliferative disorders using FRET probes and melting curve analysis

被引:57
作者
Murugesan, G
Aboudola, S
Szpurka, H
Verbic, MA
Maciejewski, JP
Tubbs, RR
Hsi, ED
机构
[1] Cleveland Clin Fdn, Dept Clin Pathol, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Taussig Canc Ctr, Cleveland, OH 44195 USA
[3] Cleveland Clin Lerner Coll Med, Cleveland, OH USA
关键词
JAK2; mutation; chronic myeloproliferative disorders; CMPD; fluorescence resonance energy transfer; FRET probes; melting curve; real-time PCR; LightCycler; LightTyper;
D O I
10.1309/TK0XL917XK2VLRPQ
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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 myeloprolative 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 Light Cycler (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 petformed by melting analysis using both freshly isolated and formalin-fixed tissues.
引用
收藏
页码:625 / 633
页数:9
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