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Using siRNA to define functional interactions between melanopsin and multiple G Protein partners

Melanopsin expressing photosensitive retinal ganglion cells (pRGCs) represent a third class of ocular photoreceptors and mediate a range of non-image forming responses to light. Melanopsin is a G protein coupled receptor (GPCR) and existing data suggest that it employs a membrane bound signalling ca...

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Autores principales: Hughes, Steven, Jagannath, Aarti, Hickey, Doron, Gatti, Silvia, Wood, Matthew, Peirson, Stuart N., Foster, Russell G., Hankins, Mark W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Basel 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282707/
https://www.ncbi.nlm.nih.gov/pubmed/24958088
http://dx.doi.org/10.1007/s00018-014-1664-6
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author Hughes, Steven
Jagannath, Aarti
Hickey, Doron
Gatti, Silvia
Wood, Matthew
Peirson, Stuart N.
Foster, Russell G.
Hankins, Mark W.
author_facet Hughes, Steven
Jagannath, Aarti
Hickey, Doron
Gatti, Silvia
Wood, Matthew
Peirson, Stuart N.
Foster, Russell G.
Hankins, Mark W.
author_sort Hughes, Steven
collection PubMed
description Melanopsin expressing photosensitive retinal ganglion cells (pRGCs) represent a third class of ocular photoreceptors and mediate a range of non-image forming responses to light. Melanopsin is a G protein coupled receptor (GPCR) and existing data suggest that it employs a membrane bound signalling cascade involving Gnaq/11 type G proteins. However, to date the precise identity of the Gα subunits involved in melanopsin phototransduction remains poorly defined. Here we show that Gnaq, Gna11 and Gna14 are highly co-expressed in pRGCs of the mouse retina. Furthermore, using RNAi based gene silencing we show that melanopsin can signal via Gnaq, Gna11 or Gna14 in vitro, and demonstrate that multiple members of the Gnaq/11 subfamily, including Gna14 and at least Gnaq or Gna11, can participate in melanopsin phototransduction in vivo and contribute to the pupillary light responses of mice lacking rod and cone photoreceptors. This diversity of G protein interactions suggests additional complexity in the melanopsin phototransduction cascade and may provide a basis for generating the diversity of light responses observed from pRGC subtypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00018-014-1664-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-42827072015-01-08 Using siRNA to define functional interactions between melanopsin and multiple G Protein partners Hughes, Steven Jagannath, Aarti Hickey, Doron Gatti, Silvia Wood, Matthew Peirson, Stuart N. Foster, Russell G. Hankins, Mark W. Cell Mol Life Sci Research Article Melanopsin expressing photosensitive retinal ganglion cells (pRGCs) represent a third class of ocular photoreceptors and mediate a range of non-image forming responses to light. Melanopsin is a G protein coupled receptor (GPCR) and existing data suggest that it employs a membrane bound signalling cascade involving Gnaq/11 type G proteins. However, to date the precise identity of the Gα subunits involved in melanopsin phototransduction remains poorly defined. Here we show that Gnaq, Gna11 and Gna14 are highly co-expressed in pRGCs of the mouse retina. Furthermore, using RNAi based gene silencing we show that melanopsin can signal via Gnaq, Gna11 or Gna14 in vitro, and demonstrate that multiple members of the Gnaq/11 subfamily, including Gna14 and at least Gnaq or Gna11, can participate in melanopsin phototransduction in vivo and contribute to the pupillary light responses of mice lacking rod and cone photoreceptors. This diversity of G protein interactions suggests additional complexity in the melanopsin phototransduction cascade and may provide a basis for generating the diversity of light responses observed from pRGC subtypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00018-014-1664-6) contains supplementary material, which is available to authorized users. Springer Basel 2014-06-24 2015 /pmc/articles/PMC4282707/ /pubmed/24958088 http://dx.doi.org/10.1007/s00018-014-1664-6 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research Article
Hughes, Steven
Jagannath, Aarti
Hickey, Doron
Gatti, Silvia
Wood, Matthew
Peirson, Stuart N.
Foster, Russell G.
Hankins, Mark W.
Using siRNA to define functional interactions between melanopsin and multiple G Protein partners
title Using siRNA to define functional interactions between melanopsin and multiple G Protein partners
title_full Using siRNA to define functional interactions between melanopsin and multiple G Protein partners
title_fullStr Using siRNA to define functional interactions between melanopsin and multiple G Protein partners
title_full_unstemmed Using siRNA to define functional interactions between melanopsin and multiple G Protein partners
title_short Using siRNA to define functional interactions between melanopsin and multiple G Protein partners
title_sort using sirna to define functional interactions between melanopsin and multiple g protein partners
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282707/
https://www.ncbi.nlm.nih.gov/pubmed/24958088
http://dx.doi.org/10.1007/s00018-014-1664-6
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