TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa.

Abstract

Retinitis pigmentosa (RP) is the most common inherited retinal disease (IRD) and is characterized by photoreceptor degeneration and progressive loss of vision. We report here four patients who presented with RP from three unrelated families with variants in TBC1D32, which to date has never been associated with an IRD. To validate TBC1D32 as a putative RP causative gene, we combined Xenopus in vivo approaches and human iPSC-derived retinal models. Our data showed that TBC1D32 was expressed during retinal development and that it played an important role in retinal pigment epithelium (RPE) differentiation. Furthermore, we identified a role for TBC1D32 in ciliogenesis of the RPE. We demonstrated elongated ciliary defects that resulted in disrupted apical tight junctions, loss of functionality (delayed retinoid cycling and altered secretion balance), and the onset of an epithelial-mesenchymal transition-like phenotype. Lastly, our results also suggested photoreceptor differentiation defects, including connecting cilium anomalies, that resulted in impaired trafficking to the outer segment in both cones and rods in TBC1D32 iPSC-derived retinal organoids. Overall, our data not only highlight a critical role for TBC1D32 in the retina but demonstrate that TBC1D32 mutations lead to RP. We thus identify TBC1D32 as an IRD causative gene.