July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
TULP1 Missense Mutations Cause Variable Retinal Phenotypes
Author Affiliations & Notes
  • Satyabrata Sinha
    Ophthalmic Research, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio, United States
  • Gayle Pauer
    Ophthalmic Research, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio, United States
  • Neal S Peachey
    Ophthalmic Research, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio, United States
    Louis Stokes Cleveland VA Medical Center, Cleveland, Ohio, United States
  • Stephanie A Hagstrom
    Ophthalmic Research, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio, United States
  • Footnotes
    Commercial Relationships   Satyabrata Sinha, None; Gayle Pauer, None; Neal Peachey, None; Stephanie Hagstrom, None
  • Footnotes
    Support  Research to Prevent Blindness Challenge Grant
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 3983. doi:
  • Views
  • Share
  • Tools
    • Alerts
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Satyabrata Sinha, Gayle Pauer, Neal S Peachey, Stephanie A Hagstrom; TULP1 Missense Mutations Cause Variable Retinal Phenotypes. Invest. Ophthalmol. Vis. Sci. 2019;60(9):3983.

      Download citation file:

      © ARVO (1962-2015); The Authors (2016-present)

  • Supplements

Purpose : TULP1 is a photoreceptor-specific member of the Tubby-like protein family. Each member possesses a highly conserved C-terminal tubby domain while the N-terminus is divergent. We determined that mutations in TULP1 were a cause of autosomal recessive retinitis pigmentosa (RP). Interestingly, all but one of the pathogenic missense mutations are located in the C-terminus of the protein. To gain insights into the pathogenicity of the N-terminal missense mutation and a C-terminal missense mutation, we generated two knock-in mouse models each expressing a human RP-causing TULP1 mutation and compared the retinal phenotype to tulp1-/- and WT mice.

Methods : Tulp1 knock-in homozygous mutant mice were generated using CRISPR-Cas9 gene editing technology. The D94Y mutation was chosen because it is the only known missense mutation located outside of the tubby domain, whereas the F491L mutation was chosen because of its prevalence in patients with RP and location within the tubby domain. Phenotypic analyses of the retinas at several time points were evaluated by histology, immunohistochemistry, electroretinography, and in vivo imaging.

Results : Tulp1 localization in both tulp1D94Y and tulp1F491L retinas was expressed in the IS, CC and synapse of the photoreceptors, similar to WT. Characterization of the retinal morphology and function in tulp1D94Y mice revealed an absence of photoreceptor cell degeneration up to one year of age. However, phenotypic characterization of the retinas of tulp1F491L mice revealed a rapid and progressive photoreceptor degeneration, similar to the time course seen in tulp1-/- mice. Expression of endoplasmic reticulum (ER) stress markers in the retinas of tulp1F491 mice was detected early in the disease time course.

Conclusions : We generated two novel Tulp1 mouse strains. Our data indicate that the D94Y mutation protein does not cause photoreceptor degeneration in mice, questioning whether this variant is truly a pathological human mutation. In contrast, the F491L mutation produced an early-onset, progressive photoreceptor degeneration and triggered activation of ER stress markers. Further studies are ongoing to evaluate the activation of multiple cellular stress response pathways. Knock-in mice, harboring patient-specific mutations, provide additional animal models to study the pathological mechanism of TULP1-related RP and will be invaluable for the development of therapeutic interventions.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.


This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.