The midbrain-hindbrain phenotype of Wnt-1-/Wnt-1- mice results from stepwise deletion of engrailed-expressing cells by 9.5 days postcoitum

Cell. 1992 May 15;69(4):581-95. doi: 10.1016/0092-8674(92)90222-x.

Abstract

Mice homozygous for null alleles of the putative signaling molecule Wnt-1 have a reproducible phenotype: loss of the midbrain and adjacent cerebellar component of the metencephalon. By examining embryonic expression of the mouse engrailed (En) genes, from 8.0 to 9.5 days postcoitum, we demonstrate that Wnt-1 primarily regulates midbrain development. The midbrain itself is required for normal development of the metencephalon. Thus, the observed neonatal phenotype is explained by a series of early events, within 48 hr of neural plate induction, that leads to a complete loss of En domains in the anterior central nervous system. Wnt-1 and a related gene, Wnt-3a, are coexpressed from early somite stages in dorsal aspects of the myelencephalon and spinal cord. We suggest that functional redundancy between these two genes accounts for the lack of a caudal central nervous system phenotype.

MeSH terms

  • Animals
  • Base Sequence
  • Brain / embryology*
  • Gene Expression
  • Genes
  • Mice / embryology*
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • Oligodeoxyribonucleotides / chemistry
  • Polymerase Chain Reaction
  • Proto-Oncogene Proteins / genetics*
  • RNA, Messenger / genetics
  • Spinal Cord / embryology*
  • Transcription Factors / genetics*
  • Wnt Proteins
  • Wnt1 Protein
  • Zebrafish Proteins*

Substances

  • Oligodeoxyribonucleotides
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Transcription Factors
  • Wnt Proteins
  • Wnt1 Protein
  • Wnt1 protein, mouse
  • Zebrafish Proteins