Fully automated and super-rapid system for the detection of JAK2V617F mutation

Leuk Res. 2008 Sep;32(9):1462-7. doi: 10.1016/j.leukres.2007.12.019. Epub 2008 Mar 6.

Abstract

JAK2V617F is a common mutation in chronic myeloproliferative diseases (CMPDs). We have developed a system utilizing JAK2V617F-specific guanine quenching probe (QP-system) to detect JAK2V617F. With QP-system, results can be obtained from 100 microl of blood within 90 min. We compared QP-system with direct sequencing using 42 CMPD patients' specimens. JAK2V617F was detected in 25 specimens by QP-system, while direct sequencing failed to detect JAK2V617F in 7 of those 25. The presence of JAK2V617F mutation in these 7 specimens was confirmed by allele-specific PCR. These findings indicate that QP-system is more sensitive and useful than direct sequencing for diagnoses of CMPDs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Automation
  • Chronic Disease
  • DNA Mutational Analysis
  • DNA Primers
  • Female
  • Humans
  • Janus Kinase 2 / blood
  • Janus Kinase 2 / genetics*
  • Male
  • Middle Aged
  • Myeloproliferative Disorders / blood
  • Myeloproliferative Disorders / genetics*
  • Point Mutation*
  • Polymerase Chain Reaction

Substances

  • DNA Primers
  • JAK2 protein, human
  • Janus Kinase 2