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ResearchIn-Press PreviewDevelopmentOphthalmology Open Access | 10.1172/JCI173892
1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
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1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
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1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
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1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
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1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
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1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
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1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
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1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
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1Institute for Vision Research, Carver College of Medicine, University of Iowa, Iowa City, United States of America
2Department of Ophthalmic Research, Cleveland Clinic, Cleveland, United States of America
Find articles by Tucker, B. in: JCI | PubMed | Google Scholar |
Published April 23, 2024 - More info
While dysfunction and death of light-detecting photoreceptor cells underlie most inherited retinal dystrophies, knowledge of the species-specific details of human rod and cone photoreceptor cell development remains limited. Here, we generate retinal organoids carrying retinal disease-causing variants in NR2E3, as well as isogenic and unrelated controls. Organoids were sampled using single-cell RNA sequencing across the developmental window encompassing photoreceptor specification, emergence, and maturation. Using scRNAseq data, we reconstruct the rod photoreceptor developmental lineage and identify a branchpoint unique to the disease state. We show that the rod-specific transcription factor NR2E3 is required for the proper expression of genes involved in phototransduction, including rhodopsin, which is absent in divergent rods. NR2E3-null rods additionally misexpress several cone-specific phototransduction genes. Using joint multimodal single-cell sequencing, we further identify putative regulatory sites where rod-specific factors act to steer photoreceptor cell development. Finally, we show that rod-committed photoreceptor cells form and persist throughout life in a patient with NR2E3-associated disease. Importantly, these findings are strikingly different than those observed in Nr2e3 rodent models. Together, these data provide a roadmap of human photoreceptor development and leverage patient iPSCs to define the specific roles of rod transcription factors in photoreceptor cell emergence and maturation in health and disease.