Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2

Science. 1995 Aug 4;269(5224):679-82. doi: 10.1126/science.7624797.

Abstract

The related mouse Engrailed genes En-1 and En-2 are expressed from the one- and approximately five-somite stages, respectively, in a similar presumptive mid-hindbrain domain. However, mutations in En-1 and En-2 produce different phenotypes. En-1 mutant mice die at birth with a large mid-hindbrain deletion, whereas En-2 mutants are viable, with cerebellar defects. To determine whether these contrasting phenotypes reflect differences in temporal expression or biochemical activity of the En proteins, En-1 coding sequences were replaced with En-2 sequences by gene targeting. This rescued all En-1 mutant defects, demonstrating that the difference between En-1 and En-2 stems from their divergent expression patterns.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / abnormalities
  • Brain / embryology
  • Chimera
  • Crosses, Genetic
  • Female
  • Gene Expression Regulation, Developmental*
  • Gene Targeting*
  • Genes, Homeobox*
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / physiology
  • Limb Deformities, Congenital
  • Male
  • Mice
  • Mutation
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / physiology
  • Phenotype
  • Promoter Regions, Genetic
  • Recombination, Genetic
  • Stem Cells
  • Sternum / abnormalities

Substances

  • En1 protein, mouse
  • Homeodomain Proteins
  • Nerve Tissue Proteins
  • engrailed 2 protein