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Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research

Orphan G-protein-coupled receptors (oGPCRs) possess untapped potential for drug discovery. In the brain, oGPCRs are generally expressed at low abundance and their function is understudied. Expression profiling is an essential step to position oGPCRs in brain function and disease, however public data...

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Autores principales: Ehrlich, Aliza T., Maroteaux, Grégoire, Robe, Anne, Venteo, Lydie, Nasseef, Md. Taufiq, van Kempen, Leon C., Mechawar, Naguib, Turecki, Gustavo, Darcq, Emmanuel, Kieffer, Brigitte L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123746/
https://www.ncbi.nlm.nih.gov/pubmed/30271982
http://dx.doi.org/10.1038/s42003-018-0106-7
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author Ehrlich, Aliza T.
Maroteaux, Grégoire
Robe, Anne
Venteo, Lydie
Nasseef, Md. Taufiq
van Kempen, Leon C.
Mechawar, Naguib
Turecki, Gustavo
Darcq, Emmanuel
Kieffer, Brigitte L.
author_facet Ehrlich, Aliza T.
Maroteaux, Grégoire
Robe, Anne
Venteo, Lydie
Nasseef, Md. Taufiq
van Kempen, Leon C.
Mechawar, Naguib
Turecki, Gustavo
Darcq, Emmanuel
Kieffer, Brigitte L.
author_sort Ehrlich, Aliza T.
collection PubMed
description Orphan G-protein-coupled receptors (oGPCRs) possess untapped potential for drug discovery. In the brain, oGPCRs are generally expressed at low abundance and their function is understudied. Expression profiling is an essential step to position oGPCRs in brain function and disease, however public databases provide only partial information. Here, we fine-map expression of 78 brain-oGPCRs in the mouse, using customized probes in both standard and supersensitive in situ hybridization. Images are available at http://ogpcr-neuromap.douglas.qc.ca. This searchable database contains over 8000 coronal brain sections across 1350 slides, providing the first public mapping resource dedicated to oGPCRs. Analysis with public mouse (60 oGPCRs) and human (56 oGPCRs) genome-wide datasets identifies 25 oGPCRs with potential to address emotional and/or cognitive dimensions of psychiatric conditions. We probe their expression in postmortem human brains using nanoString, and included data in the resource. Correlating human with mouse datasets reveals excellent suitability of mouse models for oGPCRs in neuropsychiatric research.
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spelling pubmed-61237462018-09-28 Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research Ehrlich, Aliza T. Maroteaux, Grégoire Robe, Anne Venteo, Lydie Nasseef, Md. Taufiq van Kempen, Leon C. Mechawar, Naguib Turecki, Gustavo Darcq, Emmanuel Kieffer, Brigitte L. Commun Biol Article Orphan G-protein-coupled receptors (oGPCRs) possess untapped potential for drug discovery. In the brain, oGPCRs are generally expressed at low abundance and their function is understudied. Expression profiling is an essential step to position oGPCRs in brain function and disease, however public databases provide only partial information. Here, we fine-map expression of 78 brain-oGPCRs in the mouse, using customized probes in both standard and supersensitive in situ hybridization. Images are available at http://ogpcr-neuromap.douglas.qc.ca. This searchable database contains over 8000 coronal brain sections across 1350 slides, providing the first public mapping resource dedicated to oGPCRs. Analysis with public mouse (60 oGPCRs) and human (56 oGPCRs) genome-wide datasets identifies 25 oGPCRs with potential to address emotional and/or cognitive dimensions of psychiatric conditions. We probe their expression in postmortem human brains using nanoString, and included data in the resource. Correlating human with mouse datasets reveals excellent suitability of mouse models for oGPCRs in neuropsychiatric research. Nature Publishing Group UK 2018-08-06 /pmc/articles/PMC6123746/ /pubmed/30271982 http://dx.doi.org/10.1038/s42003-018-0106-7 Text en © The Author(s) 2018 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/.
spellingShingle Article
Ehrlich, Aliza T.
Maroteaux, Grégoire
Robe, Anne
Venteo, Lydie
Nasseef, Md. Taufiq
van Kempen, Leon C.
Mechawar, Naguib
Turecki, Gustavo
Darcq, Emmanuel
Kieffer, Brigitte L.
Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research
title Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research
title_full Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research
title_fullStr Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research
title_full_unstemmed Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research
title_short Expression map of 78 brain-expressed mouse orphan GPCRs provides a translational resource for neuropsychiatric research
title_sort expression map of 78 brain-expressed mouse orphan gpcrs provides a translational resource for neuropsychiatric research
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123746/
https://www.ncbi.nlm.nih.gov/pubmed/30271982
http://dx.doi.org/10.1038/s42003-018-0106-7
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