AUTHOR=Li Linjing , Rao Kollu N. , Khanna Hemant 

TITLE=Structural but Not Functional Alterations in Cones in the Absence of the Retinal Disease Protein Retinitis Pigmentosa 2 (RP2) in a Cone-Only Retina

JOURNAL=Frontiers in Genetics

VOLUME=10

YEAR=2019

URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2019.00323

DOI=10.3389/fgene.2019.00323

ISSN=1664-8021

ABSTRACT=<p>X-linked retinitis pigmentosa 2 (XLRP2) patients and <italic>Rp2</italic><sup>null</sup> mice exhibit severe cone photoreceptor degeneration. However, due to the paucity of cones in mammalian model systems, it is not clear how cones respond to the loss of RP2. Here we have used the <italic>Nrl<sup>-/-</sup></italic> mice, which develop a rodless and short wavelength (S) opsin-containing cone-only retina, to generate <italic>Rp2</italic><sup>null</sup>::<italic>Nrl<sup>-/-</sup></italic> double knock out (<italic>Rp2</italic>-DKO) mice. We found that the ciliary axoneme and the outer segments (OSs) of the cones were significantly longer with disorganized membrane infoldings as compared to the <italic>Nrl<sup>-/-</sup></italic> mice. Additionally, we found misregulation in the expression of the genes related to ophthalmic disease, cell trafficking, and stress-response in the <italic>Rp2</italic>-DKO mice prior to the onset of cone degeneration. Surprisingly, the loss of RP2 did not affect progressive photoreceptor dysfunction of the <italic>Nrl<sup>-/-</sup></italic> mice and the trafficking of S opsin. Our data suggest that RP2 is a negative regulator of cone OS length but does not affect S-opsin trafficking and S-cone function. Our studies also provide a cone-only platform to design cone-targeted therapeutic strategies for X-linked RP2.</p>