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Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.

Rhodopsin, the visual pigment mediating vision under dim light, is composed of the apoprotein opsin and the chromophore ligand 11-cis-retinal. A P23H mutation in the opsin gene is one of the most prevalent causes of the human blinding disease, autosomal dominant retinitis pigmentosa. Although P23H cultured cell and transgenic animal models have been developed, there remains controversy over whether they fully mimic the human phenotype; and the exact mechanism by which this mutation leads to photoreceptor cell degeneration remains unknown. By generating P23H opsin knock-in mice, we found that the P23H protein was inadequately glycosylated with levels 1-10% that of wild type opsin. Moreover, the P23H protein failed to accumulate in rod photoreceptor cell endoplasmic reticulum but instead disrupted rod photoreceptor disks. Genetically engineered P23H mice lacking the chromophore showed accelerated photoreceptor cell degeneration. These results indicate that most synthesized P23H protein is degraded, and its retinal cytotoxicity is enhanced by lack of the 11-cis-retinal chromophore during rod outer segment development.

Pubmed ID: 21224384 RIS Download

Mesh terms: Amino Acid Substitution | Animals | Cell Line | Disease Models, Animal | Endoplasmic Reticulum | Female | Gene Knock-In Techniques | Humans | Male | Mice | Mice, Knockout | Mutation, Missense | Retinal Rod Photoreceptor Cells | Retinitis Pigmentosa | Rod Opsins

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Associated grants

  • Agency: NEI NIH HHS, Id: K08 EY019031
  • Agency: NEI NIH HHS, Id: R01 EY009339
  • Agency: NEI NIH HHS, Id: P30 EY011373
  • Agency: NEI NIH HHS, Id: K08EY019880
  • Agency: NEI NIH HHS, Id: EY009339
  • Agency: NEI NIH HHS, Id: P30 EY11373
  • Agency: NEI NIH HHS, Id: K08 EY019880
  • Agency: NEI NIH HHS, Id: R24 EY021126
  • Agency: NEI NIH HHS, Id: EY019031

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