PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects

Tom Glaser, Lisa Jepeal, Janice G. Edwards, S. Robert Young, Jack Favor, Richard L. Maas

Research output: Contribution to journalArticle

Abstract

The human eye malformation aniridia results from haploinsufficiency of PAX6, a paired box DNA-binding protein. To study this dosage effect, we characterized two PAX6 mutations in a family segregating aniridia and a milder syndrome consisting of congenital cataracts and late onset corneal dystrophy. The nonsense mutations, at codons 103 and 353, truncate PAX6 within the N-terminal paired and C-terminal PST domains, respectively. The wild-type PST domain activates transcription autonomously and the mutant form has partial activity. A compound heterozygote had severe craniofacial and central nervous system defects and no eyes. The pattern of malformations is similar to that in homozygous Sey mice and suggests a critical role for PAX6 in controlling the migration and differentiation of specific neuronal progenitor cells in the brain.

Original languageEnglish (US)
JournalNature Genetics
Volume7
Issue number4
StatePublished - Aug 1994
Externally publishedYes

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Anophthalmos
Aniridia
Gene Dosage
Cataract
Central Nervous System
Haploinsufficiency
Nonsense Codon
DNA-Binding Proteins
Heterozygote
Codon
Stem Cells
Mutation
Brain

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. / Glaser, Tom; Jepeal, Lisa; Edwards, Janice G.; Young, S. Robert; Favor, Jack; Maas, Richard L.

In: Nature Genetics, Vol. 7, No. 4, 08.1994.

Research output: Contribution to journalArticle

Glaser, Tom ; Jepeal, Lisa ; Edwards, Janice G. ; Young, S. Robert ; Favor, Jack ; Maas, Richard L. / PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. In: Nature Genetics. 1994 ; Vol. 7, No. 4.
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