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RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye

Carotenoids are plant-derived pigment molecules that vertebrates cannot synthesize de novo that protect the fovea of the primate retina from oxidative stress and light damage. meso-Zeaxanthin is an ocular-specific carotenoid for which there are no common dietary sources. It is one of the three major...

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Published in:Proceedings of the National Academy of Sciences - PNAS 2017-10, Vol.114 (41), p.10882-10887
Main Authors: Shyam, Rajalekshmy, Gorusupudi, Aruna, Nelson, Kelly, Horvath, Martin P., Bernstein, Paul S.
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description Carotenoids are plant-derived pigment molecules that vertebrates cannot synthesize de novo that protect the fovea of the primate retina from oxidative stress and light damage. meso-Zeaxanthin is an ocular-specific carotenoid for which there are no common dietary sources. It is one of the three major carotenoids present at the foveal center, but the mechanism by which it is produced in the eye is unknown. An isomerase enzyme is thought to be responsible for the transformation of lutein to meso-zeaxanthin by a double-bond shift mechanism, but its identity has been elusive. We previously found that meso-zeaxanthin is produced in a developmentally regulated manner in chicken embryonic retinal pigment epithelium (RPE)/choroid in the absence of light. In the present study, we show that RPE65, the isomerohydrolase enzyme of the vertebrate visual cycle that catalyzes the isomerization of all-trans-retinyl esters to 11-cis-retinol, is also the isomerase enzyme responsible for the production of meso-zeaxanthin in vertebrates. Its RNA is up-regulated 23-fold at the time of meso-zeaxanthin production during chicken eye development, and we present evidence that overexpression of either chicken or human RPE65 in cell culture leads to the production of meso-zeaxanthin from lutein. Pharmacologic inhibition of RPE65 function resulted in significant inhibition of meso-zeaxanthin biosynthesis during chicken eye development. Structural docking experiments revealed that the epsilon ring of lutein fits into the active site of RPE65 close to the nonheme iron center. This report describes a previously unrecognized additional activity of RPE65 in ocular carotenoid metabolism.
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subjects Animals
Biological Sciences
Biosynthesis
Carotenoids
Cell culture
Chemical synthesis
Chick Embryo
Chickens
cis-trans-Isomerases - metabolism
Diet
Docking
Embryos
Epithelium
Esters
Eye
Fovea
HEK293 Cells
Humans
Inhibition
Iron
Isomerization
Lutein
Lutein - metabolism
Metabolism
Oxidative stress
Pharmacology
Plant protection
Plants
Retina
Retinal pigment epithelium
Retinal Pigment Epithelium - embryology
Retinal Pigment Epithelium - metabolism
Retinol isomerase
Ribonucleic acid
RNA
Vertebrates
Vision, Ocular - physiology
Vitamin A
Zeaxanthin
Zeaxanthins - biosynthesis
title RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye
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