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Cambrian origin of the CYP27C1-mediated vitamin A(1)-to-A(2) switch, a key mechanism of vertebrate sensory plasticity

The spectral composition of ambient light varies across both space and time. Many species of jawed vertebrates adapt to this variation by tuning the sensitivity of their photoreceptors via the expression of CYP27C1, an enzyme that converts vitamin A(1) into vitamin A(2), thereby shifting the ratio o...

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Autores principales: Morshedian, Ala, Toomey, Matthew B., Pollock, Gabriel E., Frederiksen, Rikard, Enright, Jennifer M., McCormick, Stephen D., Cornwall, M. Carter, Fain, Gordon L., Corbo, Joseph C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541561/
https://www.ncbi.nlm.nih.gov/pubmed/28791166
http://dx.doi.org/10.1098/rsos.170362
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author Morshedian, Ala
Toomey, Matthew B.
Pollock, Gabriel E.
Frederiksen, Rikard
Enright, Jennifer M.
McCormick, Stephen D.
Cornwall, M. Carter
Fain, Gordon L.
Corbo, Joseph C.
author_facet Morshedian, Ala
Toomey, Matthew B.
Pollock, Gabriel E.
Frederiksen, Rikard
Enright, Jennifer M.
McCormick, Stephen D.
Cornwall, M. Carter
Fain, Gordon L.
Corbo, Joseph C.
author_sort Morshedian, Ala
collection PubMed
description The spectral composition of ambient light varies across both space and time. Many species of jawed vertebrates adapt to this variation by tuning the sensitivity of their photoreceptors via the expression of CYP27C1, an enzyme that converts vitamin A(1) into vitamin A(2), thereby shifting the ratio of vitamin A(1)-based rhodopsin to red-shifted vitamin A(2)-based porphyropsin in the eye. Here, we show that the sea lamprey (Petromyzon marinus), a jawless vertebrate that diverged from jawed vertebrates during the Cambrian period (approx. 500 Ma), dynamically shifts its photoreceptor spectral sensitivity via vitamin A(1)-to-A(2) chromophore exchange as it transitions between photically divergent aquatic habitats. We further show that this shift correlates with high-level expression of the lamprey orthologue of CYP27C1, specifically in the retinal pigment epithelium as in jawed vertebrates. Our results suggest that the CYP27C1-mediated vitamin A(1)-to-A(2) switch is an evolutionarily ancient mechanism of sensory plasticity that appeared not long after the origin of vertebrates.
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spelling pubmed-55415612017-08-08 Cambrian origin of the CYP27C1-mediated vitamin A(1)-to-A(2) switch, a key mechanism of vertebrate sensory plasticity Morshedian, Ala Toomey, Matthew B. Pollock, Gabriel E. Frederiksen, Rikard Enright, Jennifer M. McCormick, Stephen D. Cornwall, M. Carter Fain, Gordon L. Corbo, Joseph C. R Soc Open Sci Biology (Whole Organism) The spectral composition of ambient light varies across both space and time. Many species of jawed vertebrates adapt to this variation by tuning the sensitivity of their photoreceptors via the expression of CYP27C1, an enzyme that converts vitamin A(1) into vitamin A(2), thereby shifting the ratio of vitamin A(1)-based rhodopsin to red-shifted vitamin A(2)-based porphyropsin in the eye. Here, we show that the sea lamprey (Petromyzon marinus), a jawless vertebrate that diverged from jawed vertebrates during the Cambrian period (approx. 500 Ma), dynamically shifts its photoreceptor spectral sensitivity via vitamin A(1)-to-A(2) chromophore exchange as it transitions between photically divergent aquatic habitats. We further show that this shift correlates with high-level expression of the lamprey orthologue of CYP27C1, specifically in the retinal pigment epithelium as in jawed vertebrates. Our results suggest that the CYP27C1-mediated vitamin A(1)-to-A(2) switch is an evolutionarily ancient mechanism of sensory plasticity that appeared not long after the origin of vertebrates. The Royal Society Publishing 2017-07-05 /pmc/articles/PMC5541561/ /pubmed/28791166 http://dx.doi.org/10.1098/rsos.170362 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biology (Whole Organism)
Morshedian, Ala
Toomey, Matthew B.
Pollock, Gabriel E.
Frederiksen, Rikard
Enright, Jennifer M.
McCormick, Stephen D.
Cornwall, M. Carter
Fain, Gordon L.
Corbo, Joseph C.
Cambrian origin of the CYP27C1-mediated vitamin A(1)-to-A(2) switch, a key mechanism of vertebrate sensory plasticity
title Cambrian origin of the CYP27C1-mediated vitamin A(1)-to-A(2) switch, a key mechanism of vertebrate sensory plasticity
title_full Cambrian origin of the CYP27C1-mediated vitamin A(1)-to-A(2) switch, a key mechanism of vertebrate sensory plasticity
title_fullStr Cambrian origin of the CYP27C1-mediated vitamin A(1)-to-A(2) switch, a key mechanism of vertebrate sensory plasticity
title_full_unstemmed Cambrian origin of the CYP27C1-mediated vitamin A(1)-to-A(2) switch, a key mechanism of vertebrate sensory plasticity
title_short Cambrian origin of the CYP27C1-mediated vitamin A(1)-to-A(2) switch, a key mechanism of vertebrate sensory plasticity
title_sort cambrian origin of the cyp27c1-mediated vitamin a(1)-to-a(2) switch, a key mechanism of vertebrate sensory plasticity
topic Biology (Whole Organism)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541561/
https://www.ncbi.nlm.nih.gov/pubmed/28791166
http://dx.doi.org/10.1098/rsos.170362
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