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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 |
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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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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.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1706332114</identifier><identifier>PMID: 28874556</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>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</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2017-10, Vol.114 (41), p.10882-10887</ispartof><rights>Volumes 1–89 and 106–114, copyright as a collective work only; author(s) retains copyright to individual articles</rights><rights>Copyright National Academy of Sciences Oct 10, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-f2652abfb31b7a0918c443b7812ab22e6140cde0ca8ac9f81b8ae5dcb76c94493</citedby><cites>FETCH-LOGICAL-c443t-f2652abfb31b7a0918c443b7812ab22e6140cde0ca8ac9f81b8ae5dcb76c94493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26488686$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26488686$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28874556$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shyam, Rajalekshmy</creatorcontrib><creatorcontrib>Gorusupudi, Aruna</creatorcontrib><creatorcontrib>Nelson, Kelly</creatorcontrib><creatorcontrib>Horvath, Martin P.</creatorcontrib><creatorcontrib>Bernstein, Paul S.</creatorcontrib><title>RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><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.</description><subject>Animals</subject><subject>Biological Sciences</subject><subject>Biosynthesis</subject><subject>Carotenoids</subject><subject>Cell culture</subject><subject>Chemical synthesis</subject><subject>Chick Embryo</subject><subject>Chickens</subject><subject>cis-trans-Isomerases - metabolism</subject><subject>Diet</subject><subject>Docking</subject><subject>Embryos</subject><subject>Epithelium</subject><subject>Esters</subject><subject>Eye</subject><subject>Fovea</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Inhibition</subject><subject>Iron</subject><subject>Isomerization</subject><subject>Lutein</subject><subject>Lutein - metabolism</subject><subject>Metabolism</subject><subject>Oxidative stress</subject><subject>Pharmacology</subject><subject>Plant protection</subject><subject>Plants</subject><subject>Retina</subject><subject>Retinal pigment epithelium</subject><subject>Retinal Pigment Epithelium - embryology</subject><subject>Retinal Pigment Epithelium - metabolism</subject><subject>Retinol isomerase</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Vertebrates</subject><subject>Vision, Ocular - physiology</subject><subject>Vitamin A</subject><subject>Zeaxanthin</subject><subject>Zeaxanthins - biosynthesis</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpdkUtv1DAUhS0EotPCmhXIEptu0tqO48cGqarKQ6oEQrC2bpwbJqMkHmynovx6HKa0wMrWOZ-P7vUh5AVnZ5zp-nw_Qzrjmqm6FpzLR2TDmeWVkpY9JhvGhK6MFPKIHKe0Y4zZxrCn5EgYo2XTqA2Bz5-uVEO3kCjMFLpuyEOYYaT9Mvv1SouTt0jHJeMw0xzohClUPxF-wJy3RRpSmDBCQrr6Bb3BmLGNkJHiLT4jT3oYEz6_O0_I17dXXy7fV9cf3324vLiuvJR1rnqhGgFt39a81VCWMKveasOLKgQqLpnvkHkw4G1veGsAm863Wnkrpa1PyJtD7n5pJ-w8zjnC6PZxmCDeugCD-9eZh637Fm5co6RQti4Bp3cBMXxfMGU3DcnjOMKMYUmO21oJpXXDC_r6P3QXlli-baU048o2v6nzA-VjSClifz8MZ26tz631uYf6yotXf-9wz__pqwAvD8Au5RAffCWNUUbVvwCqsKE9</recordid><startdate>20171010</startdate><enddate>20171010</enddate><creator>Shyam, Rajalekshmy</creator><creator>Gorusupudi, Aruna</creator><creator>Nelson, Kelly</creator><creator>Horvath, Martin P.</creator><creator>Bernstein, Paul S.</creator><general>National Academy of Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171010</creationdate><title>RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye</title><author>Shyam, Rajalekshmy ; 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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.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>28874556</pmid><doi>10.1073/pnas.1706332114</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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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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