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SOX2 is a dose-dependent regulator of retinal neural progenitor competence.

Approximately 10% of humans with anophthalmia (absent eye) or severe microphthalmia (small eye) show haploid insufficiency due to mutations in SOX2, a SOXB1-HMG box transcription factor. However, at present, the molecular or cellular mechanisms responsible for these conditions are poorly understood. Here, we directly assessed the requirement for SOX2 during eye development by generating a gene-dosage allelic series of Sox2 mutations in the mouse. The Sox2 mutant mice display a range of eye phenotypes consistent with human syndromes and the severity of these phenotypes directly relates to the levels of SOX2 expression found in progenitor cells of the neural retina. Retinal progenitor cells with conditionally ablated Sox2 lose competence to both proliferate and terminally differentiate. In contrast, in Sox2 hypomorphic/null mice, a reduction of SOX2 expression to <40% of normal causes variable microphthalmia as a result of aberrant neural progenitor differentiation. Furthermore, we provide genetic and molecular evidence that SOX2 activity, in a concentration-dependent manner, plays a key role in the regulation of the NOTCH1 signaling pathway in retinal progenitor cells. Collectively, these results show that precise regulation of SOX2 dosage is critical for temporal and spatial regulation of retinal progenitor cell differentiation and provide a cellular and molecular model for understanding how hypomorphic levels of SOX2 cause retinal defects in humans.

Pubmed ID: 16651659

Authors

  • Taranova OV
  • Magness ST
  • Fagan BM
  • Wu Y
  • Surzenko N
  • Hutton SR
  • Pevny LH

Journal

Genes & development

Publication Data

May 1, 2006

Associated Grants

  • Agency: PHS HHS, Id: 64798-01
  • Agency: PHS HHS, Id: P30-S045892-02

Mesh Terms

  • Alleles
  • Animals
  • Anophthalmos
  • Cell Differentiation
  • Cell Proliferation
  • DNA-Binding Proteins
  • Gene Dosage
  • Mice
  • Mice, Knockout
  • Microphthalmos
  • Mutation
  • Neurons
  • Receptor, Notch1
  • Retina
  • SOXB1 Transcription Factors
  • Signal Transduction
  • Stem Cells
  • Trans-Activators