Detection of JAK2V617F mutation rate by real-time fluorescent quantitative PCR using allele specific primer and TaqMan-MGB probe for dual inhibiting amplification of wild type alleles.
- Author:
Guo-Wei LIANG
1
;
Dong-Hua SHAO
;
Mei-Ling HE
;
Qing-Yun CAO
Author Information
1. Department of Clinical Laboratory, Aerospace Center Hospital, Beijing 100049, China. LGW721@163.com
- Publication Type:Journal Article
- MeSH:
Adult;
Aged;
Alleles;
Case-Control Studies;
DNA Mutational Analysis;
DNA Primers;
genetics;
Genotype;
Humans;
Janus Kinase 2;
genetics;
Middle Aged;
Mutation;
Myeloproliferative Disorders;
genetics;
Real-Time Polymerase Chain Reaction
- From:
Journal of Experimental Hematology
2012;20(6):1486-1491
- CountryChina
- Language:Chinese
-
Abstract:
This study was purposed to develop a real-time PCR assay for sensitive quantification of JAK2V617F allele burden in peripheral blood and to evaluate the clinical value of this method. Both allele-specific mutant reverse primer and wild-type TaqMan-MGB probe were used for dual-inhibiting amplification of wild-type alleles in a real-time PCR, and then the JAK2V617F mutant alleles were amplified specially. The standard curve for quantification of JAK2V617F was established by percentages of JAK2V617F alleles with threshold cycle (Ct) values in a real-time PCR. Furthermore, 89 apparent healthy donors were tested by this method. The results showed that the quantitative lower limit of this method for JAK2V617F was 0.1%, and the intra- and inter-assay average variability for quantifying percentage of JAK2V617F in total DNA was 4.1% and 6.1%, respectively. Two JAK2V617F-positive individuals were identified (the percentage of JAK2V617F alleles were 0.64% and 0.98%, respectively) using this method in blood from 89 apparently healthy donors. It is concluded that the developed method with highly sensitive and reproducible quantification of JAK2V617F mutant burden can be used clinically for diagnosis and evaluation of disease prognosis and efficacy of therapy in patients with myeloproliferative neoplasms. Moreover, this technique can be also used for quantitative detection of variety of single nucleotide mutation.
