Deletion of the mouse alpha-globin regulatory element (HS -26) has an unexpectedly mild phenotype

Blood. 2002 Nov 15;100(10):3450-6. doi: 10.1182/blood-2002-05-1409. Epub 2002 Jul 5.

Abstract

Natural deletions of the region upstream of the human alpha-globin gene cluster, together with expression studies in cell lines and transgenic mice, identified a single element (HS -40) as necessary and perhaps sufficient for high-level expression of the alpha-globin genes. A similar element occupies the corresponding position upstream of the mouse (m) alpha-globin genes (mHS -26) and was thought to have similar functional properties. We knocked out mHS -26 by homologous recombination and observed the surprising result that instead of the expected severe alpha-thalassemia phenotype, the mice had a mild disease. Transcription levels of the mouse genes were reduced by about 50%, but homozygotes were healthy, with normal hemoglobin levels and only mild decreases in mean corpuscular volume and mean corpuscular hemoglobin. These results may indicate differences in the regulation of the alpha-globin clusters in mice and humans or that additional cis-acting elements remain to be characterized in one or both clusters.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Chromosome Deletion*
  • Down-Regulation / genetics
  • Genes, Regulator / genetics
  • Genes, Regulator / physiology*
  • Globins / genetics*
  • Humans
  • Mice
  • Mice, Knockout
  • Multigene Family / genetics
  • Mutagenesis
  • Phenotype
  • RNA, Messenger / analysis
  • alpha-Thalassemia / genetics

Substances

  • RNA, Messenger
  • Globins