Cited by 143Retinal Development and DisordersPhotoreceptor and optogenetics researchRetinal Diseases and Treatments

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa

Morimura, Hiroyuki, Saindelle-Ribeaudeau, Florence, Berson, Eliot L, Dryja, Thaddeus P·1999·Nature Genetics

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Crossref · 10.1038/70496

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  • In the RPE, an additional source of 11-cis-retinal is a pathway with retinal G protein-coupled receptor (RGR) as the key enzyme; RGR preferentially binds all-trans-retinal, and within RGR a photon of light converts all-trans-retinal to 11-cis-retinal.

    “In RPE, an additional source of 11-cis-retinal is also a pathway with retinal G protein-coupled receptor (RGR) as the key enzyme. RGR is a RHO homologue, which, contrary to RHO, preferentially binds all-trans-retinal. Within RGR, a photon of light converts all-trans-retinal to 11-cis-retinal, the chromophore of the visual pigments.”

    From The Role of Vitamin A in Retinal Diseases (2022) · cites this paper as [56]

  • RGR, together with RPE65, contributes to the regeneration of 11-cis-retinal.

    “Therefore, RGR, together with RPE65, contributes to the regeneration of 11-cis-retinal [55,56,57,58].”

    From The Role of Vitamin A in Retinal Diseases (2022) · cites this paper as [56]

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References 11 · Cited by 143

Authors
Morimura, H., Saindelle-Ribeaudeau, F., Berson, E. L., & Dryja, T. P.
Affiliations
Massachusetts Eye and Ear Infirmary (US)
Venue
Nature Genetics
Published
1999-12
Volume
23
Issue
4
Pages
393-394
ISSN
  • 1061-4036 (ISSN-L)
  • 1546-1718
OpenAlex
W1607116816
Cited by
143
References
11
Citations by year
2026: 3 · 2025: 6 · 2024: 4 · 2023: 3 · 2022: 5 · 2021: 4 · 2020: 5 · 2019: 4 · 2018: 5 · 2017: 4 · 2016: 7 · 2015: 3 · 2014: 3 · 2013: 2 · 2012: 6
FWCI
2.19
Type
journal article
Language
en
Open access
closed
Locations
  • Nature Genetics (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Eye Institute (R01EY008683, EY 08683, EY00169)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Photoreceptor and optogenetics research
  • Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
Keywords
retinitis pigmentosa, G protein-coupled receptors, all-trans-retinal, retinal pigment epithelium, Müller cells, photoreceptor degeneration, genetic mutations
MeSH terms
Aged, Eye Proteins, Female, Heterozygote, Homozygote, Humans, Male, Mutation, Pedigree, Receptors, Cell Surface, Retinitis Pigmentosa, Rod Opsins, Receptors, G-Protein-Coupled

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