Loss of the JAK2 intramolecular auto-inhibition mechanism is predicted by structural modelling of a novel exon 12 insertion mutation in a case of idiopathic erythrocytosis

Br J Haematol. 2008 Sep;142(6):986-90. doi: 10.1111/j.1365-2141.2008.07180.x. Epub 2008 Jul 30.

Abstract

We report a novel gain-of-function JAK2 exon 12 insertion mutation in a patient with idiopathic erythrocytosis and low serum erythropoietin level. To date, only rare cases of such mutations have been reported in the JAK2 exon 12. Using computer-based structural modelling we propose that this mutation causes the loss of the JAK2 auto-inhibition step, leading to the constitutive activation of JAK2 tyrosine kinase-dependent activity. Our model-based hypothesis provides a useful approach for the investigation of the phenotype-genotype relationship in myeloproliferative disorders involving JAK2.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Exons / genetics
  • Humans
  • Janus Kinase 2 / genetics*
  • Janus Kinase 2 / physiology
  • Male
  • Middle Aged
  • Models, Molecular
  • Molecular Sequence Data
  • Mutagenesis, Insertional*
  • Polycythemia / genetics*
  • Polycythemia Vera / genetics
  • Protein Structure, Tertiary

Substances

  • JAK2 protein, human
  • Janus Kinase 2