Conserved biological function between Pax-2 and Pax-5 in midbrain and cerebellum development: evidence from targeted mutations

Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14518-23. doi: 10.1073/pnas.94.26.14518.

Abstract

The development of two major subdivisions of the vertebrate nervous system, the midbrain and the cerebellum, is controlled by signals emanating from a constriction in the neural primordium called the midbrain/hindbrain organizer (Joyner, A. L. (1996) Trends Genet. 12, 15-201). The closely related transcription factors Pax-2 and Pax-5 exhibit an overlapping expression pattern very early in the developing midbrain/hindbrain junction. Experiments carried out in fish (Krauss, S., Maden, M., Holder, N. & Wilson, S. W. (1992) Nature (London) 360, 87-89) with neutralizing antibodies against Pax-b, the orthologue of Pax-2 in mouse, placed this gene family in an regulatory cascade necessary for the development of the midbrain and the cerebellum. The targeted mutation of Pax-5 has been reported to have only slight effects in the development of structures derived from the isthmic constriction, whereas the Pax-2 null mutant mice show a background-dependent phenotype with varying penetrance. To test a possible redundant function between Pax-2 and Pax-5 we analyzed the brain phenotypes of mice expressing different dosages of both genes. Our results demonstrate a conserved biological function of both proteins in midbrain/hindbrain regionalization. Additionally, we show that one allele of Pax-2, but not Pax-5, is necessary and sufficient for midbrain and cerebellum development in C57BL/6 mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cerebellum / embryology*
  • Cerebellum / physiology*
  • DNA-Binding Proteins / physiology*
  • Embryonic and Fetal Development
  • Gene Targeting
  • Mesencephalon / embryology*
  • Mesencephalon / physiology*
  • Mice
  • Mice, Mutant Strains
  • Mutation*
  • Nuclear Proteins / physiology*
  • PAX2 Transcription Factor
  • PAX5 Transcription Factor
  • Transcription Factors / physiology*

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • PAX2 Transcription Factor
  • PAX5 Transcription Factor
  • Pax2 protein, mouse
  • Pax5 protein, mouse
  • Transcription Factors