A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3)

DH Hong, BS Pawlyk, J Shang… - Proceedings of the …, 2000 - National Acad Sciences
DH Hong, BS Pawlyk, J Shang, MA Sandberg, EL Berson, T Li
Proceedings of the National Academy of Sciences, 2000National Acad Sciences
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 …
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.
National Acad Sciences