4.7 Article

An Essential Role for RAX Homeoprotein and NOTCH-HES Signaling in Otx2 Expression in Embryonic Retinal Photoreceptor Cell Fate Determination

Journal

JOURNAL OF NEUROSCIENCE
Volume 31, Issue 46, Pages 16792-16807

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.3109-11.2011

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Funding

  1. Japan Science and Technology Agency
  2. Ministry of Education, Culture, Sports, Science and Technology
  3. Takeda Science Foundation
  4. Uehara Memorial Foundation
  5. Naito Foundation
  6. Kato Memorial Bioscience Foundation
  7. Japan National Society for the Prevention of Blindness
  8. Grants-in-Aid for Scientific Research [23247037, 23390074] Funding Source: KAKEN

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The molecular mechanisms underlying cell fate determination from common progenitors in the vertebrate CNS remain elusive. We previously reported that the OTX2 homeoprotein regulates retinal photoreceptor cell fate determination. While Otx2 transactivation is a pivotal process for photoreceptor cell fate determination, its transactivation mechanism in the retina is unknown. Here, we identified an evolutionarily conserved Otx2 enhancer of similar to 500 bp, named embryonic enhancer locus for photoreceptor Otx2 transcription (EELPOT), which can recapitulate initial Otx2 expression in the embryonic mouse retina. We found that the RAX homeoprotein interacts with EELPOT to transactivate Otx2, mainly in the final cell cycle of retinal progenitors. Conditional inactivation of Rax results in downregulation of Otx2 expression in vivo. We also showed that NOTCH-HES signaling negatively regulates EELPOT to suppress Otx2 expression. These results suggest that the integrated activity of cell-intrinsic and -extrinsic factors on EELPOT underlies the molecular basis of photoreceptor cell fate determination in the embryonic retina.

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