Molecular and developmental mechanisms of anterior segment dysgenesis

Eye (Lond). 2007 Oct;21(10):1310-8. doi: 10.1038/sj.eye.6702852.

Abstract

Anterior segment dysgenesis (ASD) is a failure of the normal development of the tissues of the anterior segment of the eye. It leads to anomalies in the structure of the mature anterior segment, associated with an increased risk of glaucoma and corneal opacity. Several different gene mutations have been identified underlying these anomalies with the majority of ASD genes encoding transcriptional regulators. In this review, the role of the ASD genes, PITX2 and FOXC1, is considered in relation to the embryology of the anterior segment, the biochemical function of these proteins, and their role in development and disease aetiology. The emerging view is that these genes act in concert to specify a population of mesenchymal progenitor cells, mainly of neural crest origin, as they migrate anteriorly around the embryonic optic cup. These same genes then regulate mesenchymal cell differentiation to give rise to distinct anterior segment tissues. Development appears critically sensitive to gene dosage, and variation in the normal level of transcription factor activity causes a range of anterior segment anomalies. Interplay between PITX2 and FOXC1 in the development of different anterior segment tissues may partly explain the phenotypic variability and the genetic heterogeneity characteristic of ASD.

Publication types

  • Review

MeSH terms

  • Animals
  • Anterior Eye Segment / abnormalities*
  • Anterior Eye Segment / embryology
  • Fetal Development
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / physiology
  • Gene Expression Regulation, Developmental
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / physiology
  • Humans
  • Infant, Newborn
  • Mutation
  • Transcription Factors / genetics
  • Transcription Factors / physiology

Substances

  • FOXC1 protein, human
  • Forkhead Transcription Factors
  • Homeodomain Proteins
  • Transcription Factors
  • homeobox protein PITX2