December 2014
Volume 14, Issue 15
Free
OSA Fall Vision Meeting Abstract  |   December 2014
Basel exon skipping - a novel model of disease pathogenesis to explain CEP290-associated retinal degeneration and related ciliopathies
Author Affiliations
  • Adam Wojno
    Perelman School of Medicine, Cell and Molecular Biology Program, University of Pennsylvania
  • Theodore Drivas
    Perelman School of Medicine, Cell and Molecular Biology Program, University of Pennsylvania; Gene Therapy and Vaccines, Center for Advanced Retinal and Ocular Therapeutics
  • Budd Tucker
    Carver College of Medicine, University of Iowa
  • Edwin Stone
    Carver College of Medicine, University of Iowa
  • Jean Bennett
    F.M. Kirby Center for Molecular Ophthalmology, Perelman School of Medicine, Center for Advanced Retinal and Ocular Therapeutics, University of Pennsylvania
Journal of Vision December 2014, Vol.14, 85. doi:https://doi.org/10.1167/14.15.85
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      Adam Wojno, Theodore Drivas, Budd Tucker, Edwin Stone, Jean Bennett; Basel exon skipping - a novel model of disease pathogenesis to explain CEP290-associated retinal degeneration and related ciliopathies. Journal of Vision 2014;14(15):85. https://doi.org/10.1167/14.15.85.

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

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Abstract

Centrosomal Protein of 290 kDa (CEP290)-associated mutations are implicated in roughly 25% of cases of Leber congenital amaurosis (LCA), an inherited, retinal degenerative disease that leads to vision loss at an early age. In addition to LCA, the pleiotropic nature of CEP290 mutations manifest in a spectrum of more severe disease states such as Joubert syndrome, Senior-Løken Syndrome and Meckel syndrome. Despite knowing the location of many disease-causing mutations that have been shown to lead to CEP290-associated ciliopathies, explanations for the occurrence of CEP290-related pleiotropy, or that of many other genes, remain unknown. Here, we report that all human CEP290 samples tested demonstrated low levels of exon skipping. Using this observation, a model by which patient genotype can be used to accurately predict CEP290 protein levels as well as disease phenotype was generated. In addition, this model was validated using another unrelated disease gene, CC2D2A. Taken together, we report a novel model of disease pathogenesis that appears to explain, for the first time, the pleiotropic nature of CEP290 and CC2D2A-associated disease and which could potentially be extended to describe observed pleiotropy in other inherited conditions resulting from mutations in a single gene.

We would like to acknowledge the following funding sources for this work: The WyckGrosbeck Family Foundation, Foundation Fighting Blindness, Research to Prevent Blindness, Treatrush, NIH 8DP1EY023177

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