MPN patients harbor recurrent truncating mutations in transcription factor NF-E2

نویسندگان

  • Jonas S. Jutzi
  • Ruzhica Bogeska
  • Gorica Nikoloski
  • Corina A. Schmid
  • Thalia S. Seeger
  • Frank Stegelmann
  • Sven Schwemmers
  • Albert Gründer
  • Jan C. Peeken
  • Monika Gothwal
  • Julius Wehrle
  • Konrad Aumann
  • Kamar Hamdi
  • Christine Dierks
  • Wei Wang
  • Konstanze Döhner
  • Joop H. Jansen
  • Heike L. Pahl
چکیده

The molecular etiology of myeloproliferative neoplasms (MPNs) remains incompletely understood, despite recent advances incurred through the discovery of several different mutations in MPN patients. We have recently described overexpression of the transcription factor NF-E2 in MPN patients and shown that elevated NF-E2 levels in vivo cause an MPN phenotype and predispose to leukemic transformation in transgenic mice. We report the presence of acquired insertion and deletion mutations in the NF-E2 gene in MPN patients. These result in truncated NF-E2 proteins that enhance wild-type (WT) NF-E2 function and cause erythrocytosis and thrombocytosis in a murine model. NF-E2 mutant cells acquire a proliferative advantage, witnessed by clonal dominance over WT NF-E2 cells in MPN patients. Our data underscore the role of increased NF-E2 activity in the pathophysiology of MPNs.

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عنوان ژورنال:

دوره 210  شماره 

صفحات  -

تاریخ انتشار 2013