Autophagy in Xenopus laevis rod photoreceptors is independently regulated by phototransduction and misfolded RHOP23H.

Abstract

We previously reported autophagic structures in rod photoreceptors expressing a misfolding RHO (rhodopsin) mutant (RHOP23H), suggesting that autophagy may play a role in degrading the mutant RHO and/or be involved in photoreceptor cell death. To further examine autophagy in normal and diseased rods, we generated transgenic Xenopus laevis tadpoles expressing the dually fluorescent autophagy marker mRFP-eGFP-LC3 in rods, which changes from green to yellow and finally red as autophagic structures develop and mature. Using transgenic lines with constitutive and inducible expression, we determined the time-course of autophagy in rod photoreceptors: autophagosomes last for 6 to 8 hours before fusing with lysosomes, and acidified autolysosomes last for about 28 hours before being degraded. Autophagy was diurnally regulated in normal rods, with more autophagic structures generated during periods of light, and this regulation was non-circadian. We also found that more autophagosomes were produced in rods expressing the misfolding RHOP23H mutant. The RHO chromophore absorbs photons to initiate phototransduction, and is consumed in this process; it also promotes RHO folding. To determine whether increased autophagy in light-exposed normal rods is caused by increased RHO misfolding or phototransduction, we used CRISPR/Cas9 to knock out the RPE65 and GNAT1 genes, which are essential for chromophore biosynthesis and phototransduction respectively. Both knockouts suppressed light-induced autophagy, indicating that although light and misfolded rhodopsin can both induce autophagy in rods, light-induced autophagy is not due to misfolding of RHO, but rather due to phototransduction. Abbreviations: CYCS: cytochrome c; bRHOP23H: bovine RHOP23H; Cas9: CRISPR associated protein 9; dpf: days post-fertilization; eGFP: enhanced green fluorescent protein; GNAT1: guanine nucleotide-binding protein G(t) subunit alpha-1 aka rod alpha-transducin; HSPA1A/hsp70: heat shock protein of 70 kilodaltons; LAMP1: lysosomal-associated membrane protein 1; LC3: microtubule-associated protein 1A/1B light chain 3; mRFP: monomeric red fluorescent protein; RHO: rhodopsin; RP: retinitis pigmentosa; RPE65: retinal pigment epithelium-specific 65 kDa protein: sfGFP: superfolding GFP; sgRNA: single guide RNA; WGA: wheat germ agglutinin; RHOp: the Xenopus laevis RHO.2.L promoter.

• Authors: Runxia H Wen, Paloma Stanar, Beatrice Tam, Orson L Moritz
• Journal: Autophagy (Autophagy) Vol. 15 Issue 11 Pg. 1970-1989 (11 2019) ISSN: 1554-8635 [Electronic] United States
• PMID: 30975014 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• enhanced green fluorescent protein
• Green Fluorescent Proteins
• Rhodopsin
• retinoid isomerohydrolase
• Heterotrimeric GTP-Binding Proteins
• cis-trans-Isomerases

Topics

• Animals
• Animals, Genetically Modified
• Autophagosomes (metabolism, radiation effects)
• Autophagy (genetics, radiation effects)
• Circadian Rhythm (genetics, radiation effects)
• Fluorescence
• Green Fluorescent Proteins (chemistry, genetics, metabolism)
• Heterotrimeric GTP-Binding Proteins (genetics, metabolism)
• Larva (genetics, metabolism, ultrastructure)
• Light Signal Transduction (genetics, radiation effects)
• Mutation
• Retinal Rod Photoreceptor Cells (cytology, metabolism, radiation effects, ultrastructure)
• Retinitis Pigmentosa (genetics, metabolism)
• Rhodopsin (chemistry, genetics, metabolism, radiation effects)
• Time Factors
• Xenopus laevis
• cis-trans-Isomerases (genetics, metabolism)