Inactivation of mouse alpha-globin gene by homologous recombination: mouse model of hemoglobin H disease

Blood. 1996 Sep 1;88(5):1846-51.

Abstract

We have disrupted the 5' locus of the duplicated adult alpha-globin genes by gene targeting in the mouse embryonic stem cells and created mice with alpha-thalassemia syndromes. The heterozygous knockout mice (.alpha/alpha alpha) are asymptomatic like the silent carriers in humans whereas the homozygous knockout mice (.alpha/.alpha) show hemolytic anemia. Mice with three dysfunctional alpha-globin genes generated by breeding the 5' alpha-globin knockouts (.alpha/alpha alpha) and the deletion type alpha-thalassemia mice (../alpha alpha) produce severe hemoglobin H disease and they die in utero. These results indicate that the 5' alpha-globin gene is the predominant locus in mice, and suggest that it is even more dominant than its human homologue.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Crosses, Genetic
  • Disease Models, Animal*
  • Fetal Blood / cytology
  • Fetal Death / genetics
  • Gene Targeting*
  • Genes, Dominant
  • Genotype
  • Globins / genetics*
  • Humans
  • Mice / embryology
  • Mice / genetics*
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Multigene Family
  • Recombination, Genetic*
  • Sequence Deletion
  • Stem Cells
  • alpha-Thalassemia / embryology
  • alpha-Thalassemia / genetics*

Substances

  • Globins