Influence of PAX6 Gene Dosage on Development: Overexpression Causes Severe Eye Abnormalities

A Schedl, A Ross, Muriel Lee, D Engelkamp, P Rashbass, V van Heyningen, N D Hastie

Research output: Contribution to journalArticlepeer-review

Abstract

Aniridia in man and Small eye in mice are semidominant developmental disorders caused by mutations within the paired box gene PAX6. Whereas heterozygotes suffer from iris hypoplasia, homozygous mice lack eyes and nasal cavities and exhibit brain abnormalities. To investigate the role of gene dosage in more detail, we have generated yeast artificial chromosome transgenic mice carrying the human PAX6 locus. When crossed onto the Small eye background, the transgene rescues the mutant phenotype. Strikingly, mice carrying multiple copies on a wild-type background show specific developmental abnormalities of the eye, but not of other tissues expressing the gene. Thus, at least five different eye phenotypes are associated with changes in PAX6 expression. We provide evidence that not only reduced, but also increased levels of transcriptional regulators can cause developmental defects.
Original languageEnglish
Pages (from-to)71-82
Number of pages12
JournalCell
Volume86
Issue number1
DOIs
Publication statusPublished - 12 Jul 1996

Keywords

  • Animals
  • Base Sequence
  • DNA-Binding Proteins
  • Eye Abnormalities
  • Eye Proteins
  • Gene Dosage
  • Gene Expression Regulation, Developmental
  • Genetic Complementation Test
  • Homeodomain Proteins
  • Humans
  • In Situ Hybridization, Fluorescence
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Mice, Transgenic
  • Molecular Sequence Data
  • Paired Box Transcription Factors
  • Phenotype
  • Repressor Proteins
  • Transgenes

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