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A visual opsin from jellyfish enables precise temporal control of G protein signalling

Phototransduction is mediated by distinct types of G protein cascades in different animal taxa: bilateral invertebrates typically utilise the Gαq pathway whereas vertebrates typically utilise the Gαt(i/o) pathway. By contrast, photoreceptors in jellyfish (Cnidaria) utilise the Gαs intracellular path...

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Autores principales: van Wyk, Michiel, Kleinlogel, Sonja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147646/
https://www.ncbi.nlm.nih.gov/pubmed/37117224
http://dx.doi.org/10.1038/s41467-023-38231-z
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author van Wyk, Michiel
Kleinlogel, Sonja
author_facet van Wyk, Michiel
Kleinlogel, Sonja
author_sort van Wyk, Michiel
collection PubMed
description Phototransduction is mediated by distinct types of G protein cascades in different animal taxa: bilateral invertebrates typically utilise the Gαq pathway whereas vertebrates typically utilise the Gαt(i/o) pathway. By contrast, photoreceptors in jellyfish (Cnidaria) utilise the Gαs intracellular pathway, similar to olfactory transduction in mammals(1). How this habitually slow pathway has adapted to support dynamic vision in jellyfish remains unknown. Here we study a light-sensing protein (rhodopsin) from the box jellyfish Carybdea rastonii and uncover a mechanism that dramatically speeds up phototransduction: an uninterrupted G protein-coupled receptor – G protein complex. Unlike known G protein-coupled receptors (GPCRs), this rhodopsin constitutively binds a single downstream Gαs partner to enable G-protein activation and inactivation within tens of milliseconds. We use this GPCR in a viral gene therapy to restore light responses in blind mice.
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spelling pubmed-101476462023-04-30 A visual opsin from jellyfish enables precise temporal control of G protein signalling van Wyk, Michiel Kleinlogel, Sonja Nat Commun Article Phototransduction is mediated by distinct types of G protein cascades in different animal taxa: bilateral invertebrates typically utilise the Gαq pathway whereas vertebrates typically utilise the Gαt(i/o) pathway. By contrast, photoreceptors in jellyfish (Cnidaria) utilise the Gαs intracellular pathway, similar to olfactory transduction in mammals(1). How this habitually slow pathway has adapted to support dynamic vision in jellyfish remains unknown. Here we study a light-sensing protein (rhodopsin) from the box jellyfish Carybdea rastonii and uncover a mechanism that dramatically speeds up phototransduction: an uninterrupted G protein-coupled receptor – G protein complex. Unlike known G protein-coupled receptors (GPCRs), this rhodopsin constitutively binds a single downstream Gαs partner to enable G-protein activation and inactivation within tens of milliseconds. We use this GPCR in a viral gene therapy to restore light responses in blind mice. Nature Publishing Group UK 2023-04-28 /pmc/articles/PMC10147646/ /pubmed/37117224 http://dx.doi.org/10.1038/s41467-023-38231-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
van Wyk, Michiel
Kleinlogel, Sonja
A visual opsin from jellyfish enables precise temporal control of G protein signalling
title A visual opsin from jellyfish enables precise temporal control of G protein signalling
title_full A visual opsin from jellyfish enables precise temporal control of G protein signalling
title_fullStr A visual opsin from jellyfish enables precise temporal control of G protein signalling
title_full_unstemmed A visual opsin from jellyfish enables precise temporal control of G protein signalling
title_short A visual opsin from jellyfish enables precise temporal control of G protein signalling
title_sort visual opsin from jellyfish enables precise temporal control of g protein signalling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147646/
https://www.ncbi.nlm.nih.gov/pubmed/37117224
http://dx.doi.org/10.1038/s41467-023-38231-z
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