A gain-of-function mutation in the HIF2A gene in familial erythrocytosis

N Engl J Med. 2008 Jan 10;358(2):162-8. doi: 10.1056/NEJMoa073123.

Abstract

Hypoxia-inducible factor (HIF) alpha, which has three isoforms, is central to the continuous balancing of the supply and demand of oxygen throughout the body. HIF-alpha is a transcription factor that modulates a wide range of processes, including erythropoiesis, angiogenesis, and cellular metabolism. We describe a family with erythrocytosis and a mutation in the HIF2A gene, which encodes the HIF-2alpha protein. Our functional studies indicate that this mutation leads to stabilization of the HIF-2alpha protein and suggest that wild-type HIF-2alpha regulates erythropoietin production in adults.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Basic Helix-Loop-Helix Transcription Factors / genetics*
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • DNA Mutational Analysis
  • Erythropoiesis / genetics*
  • Erythropoietin / biosynthesis*
  • Female
  • Genotype
  • Hematocrit
  • Hemoglobins / analysis
  • Humans
  • Male
  • Pedigree
  • Point Mutation*
  • Polycythemia / genetics*
  • Polycythemia / metabolism
  • Polymerase Chain Reaction

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Hemoglobins
  • Erythropoietin
  • endothelial PAS domain-containing protein 1