A retinitis pigmentosa GTPase regulator (RPGR)- deficient mouse model for X-linked retinitis pigmentosa (RP3)
A retinitis pigmentosa GTPase regulator (RPGR)- deficient mouse model for X-linked retinitis pigmentosa (RP3)
The X-linked RP3 locus codes for retinitis pigmentosa GTPase regulator (RPGR), a protein of unknown function with sequence homology to the guanine nucleotide exchange factor for Ran GTPase. We created an RPGR-deficient murine model by gene knockout. In the mutant mice, cone photoreceptors exhibit ectopic localization of cone opsins in the cell body and synapses and rod photoreceptors have a reduced level of rhodopsin. Subsequently, both cone and rod photoreceptors degenerate. RPGR was found normally localized to the connecting cilia of rod and cone photoreceptors. These data point to a role for RPGR in maintaining the polarized protein distribution across the connecting cilium by facilitating directional transport or restricting redistribution. The function of RPGR is essential for the long-term maintenance of photoreceptor viability.
- Harvard University United States
- Massachusetts Eye and Ear Infirmary United States
Male, X Chromosome, Base Sequence, Genetic Linkage, Mice, Inbred C57BL, Disease Models, Animal, Mice, Microscopy, Electron, Animals, Female, Carrier Proteins, Eye Proteins, Retinitis Pigmentosa, DNA Primers, Photoreceptor Cells, Vertebrate
Male, X Chromosome, Base Sequence, Genetic Linkage, Mice, Inbred C57BL, Disease Models, Animal, Mice, Microscopy, Electron, Animals, Female, Carrier Proteins, Eye Proteins, Retinitis Pigmentosa, DNA Primers, Photoreceptor Cells, Vertebrate
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