The genes involved in the morphogenesis of the eye

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

The two main ways to identify the genes involved in the process of morphogenesis are: 1) to analyze genetic causes in patients or animal models with developmental anomalies and 2) to elucidate patterns of the expression of genes by in situ hybridization during the normal development. In this report, these two methods were adopted to identify the genes involved in the morphogenesis of the eye. A unique mutation of the paired box (Pax)-6 gene (a kind of homeobox gene) was found in a new rat strain 'rSey' which showed no induction of both lens and nasal placodes in the homozygote. One base 'G' insertion in an exon of the genomic DNA gave rise to a new sequence, 'GT', which served as an abnormal 5' splice site to generate an internal deletion in the messenger RNA. The homozygote was also known to have impaired migration of neural crest cells from the anterior midbrain, indicating that the Pax-6 gene would play a role in conducting migration of these neural crest cells. Neural crest-derived mesenchymal cells located around the lens vesicle in the optic cup of mouse embryos were positive for the expression of retinoic acid receptor genes, showing that retinoic acids played a role in the formation of such eye structures composed of neural crest-derived cells as the primary vitreous, corneal, iris, and ciliary stroma. Transcripts of the fibroblast growth factor receptor type 1 were found mainly in neuroepithelium of the optic cup of chick embryos, whereas those of the type 2 receptor were detected in neural crest-derived mesenchymal cells surrounding the optic cup. In contrast, the type 3 receptor was expressed mainly in the lens vesicle, suggesting that altogether 3 types of the fibroblast growth factor receptor would be involved in signaling among different structures as the optic cup, lens vesicle, and neural crest-derived mesenchyme. Receptors for activin, a member of the transforming growth factor beta superfamily, were expressed in the neuroepithelium of the optic cup and in the lens vesicle. In the light of these molecular biological findings, the roles of neural crest-derived cells and epithelial-mesenchymal interactions as well as the concept of positional information in the morphogenesis of the eye were discussed.

Original languageEnglish
Pages (from-to)215-251
Number of pages37
JournalJapanese Journal of Ophthalmology
Volume37
Issue number3
Publication statusPublished - 1993

Fingerprint

Neural Crest
Morphogenesis
Lenses
Genes
Homozygote
Receptor, Fibroblast Growth Factor, Type 3
Activin Receptors
Receptor, Fibroblast Growth Factor, Type 1
RNA Splice Sites
Retinoic Acid Receptors
Homeobox Genes
Iris
Mesoderm
Chick Embryo
Mesencephalon
Tretinoin
Nose
Transforming Growth Factor beta
In Situ Hybridization
Exons

Keywords

  • Activin receptor
  • Fibroblast growth factor receptor
  • In situ hybridization
  • Morphogenesis of the eye
  • Neural crest cells
  • Pax-6 gene
  • Polymerase chain reaction
  • Retinoic acid receptor
  • rSey rat small eye phenotype

ASJC Scopus subject areas

  • Ophthalmology

Cite this

The genes involved in the morphogenesis of the eye. / Matsuo, Toshihiko.

In: Japanese Journal of Ophthalmology, Vol. 37, No. 3, 1993, p. 215-251.

Research output: Contribution to journalArticle

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