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A rare human variant that disrupts GPR10 signalling causes weight gain in mice

Disruption of brain-expressed G protein-coupled receptor-10 (GPR10) causes obesity in animals. Here, we identify multiple rare variants in GPR10 in people with severe obesity and in normal weight controls. These variants impair ligand binding and G protein-dependent signalling in cells. Transgenic m...

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Autores principales: Talbot, Fleur, Feetham, Claire H., Mokrosiński, Jacek, Lawler, Katherine, Keogh, Julia M., Henning, Elana, Mendes de Oliveira, Edson, Ayinampudi, Vikram, Saeed, Sadia, Bonnefond, Amélie, Arslan, Mohammed, Yeo, Giles S. H., Froguel, Philippe, Bechtold, David A., Adamson, Antony, Humphreys, Neil, Barroso, Inês, Luckman, Simon M., Farooqi, I. Sadaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017677/
https://www.ncbi.nlm.nih.gov/pubmed/36922513
http://dx.doi.org/10.1038/s41467-023-36966-3
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author Talbot, Fleur
Feetham, Claire H.
Mokrosiński, Jacek
Lawler, Katherine
Keogh, Julia M.
Henning, Elana
Mendes de Oliveira, Edson
Ayinampudi, Vikram
Saeed, Sadia
Bonnefond, Amélie
Arslan, Mohammed
Yeo, Giles S. H.
Froguel, Philippe
Bechtold, David A.
Adamson, Antony
Humphreys, Neil
Barroso, Inês
Luckman, Simon M.
Farooqi, I. Sadaf
author_facet Talbot, Fleur
Feetham, Claire H.
Mokrosiński, Jacek
Lawler, Katherine
Keogh, Julia M.
Henning, Elana
Mendes de Oliveira, Edson
Ayinampudi, Vikram
Saeed, Sadia
Bonnefond, Amélie
Arslan, Mohammed
Yeo, Giles S. H.
Froguel, Philippe
Bechtold, David A.
Adamson, Antony
Humphreys, Neil
Barroso, Inês
Luckman, Simon M.
Farooqi, I. Sadaf
author_sort Talbot, Fleur
collection PubMed
description Disruption of brain-expressed G protein-coupled receptor-10 (GPR10) causes obesity in animals. Here, we identify multiple rare variants in GPR10 in people with severe obesity and in normal weight controls. These variants impair ligand binding and G protein-dependent signalling in cells. Transgenic mice harbouring a loss of function GPR10 variant found in an individual with obesity, gain excessive weight due to decreased energy expenditure rather than increased food intake. This evidence supports a role for GPR10 in human energy homeostasis. Therapeutic targeting of GPR10 may represent an effective weight-loss strategy.
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spelling pubmed-100176772023-03-17 A rare human variant that disrupts GPR10 signalling causes weight gain in mice Talbot, Fleur Feetham, Claire H. Mokrosiński, Jacek Lawler, Katherine Keogh, Julia M. Henning, Elana Mendes de Oliveira, Edson Ayinampudi, Vikram Saeed, Sadia Bonnefond, Amélie Arslan, Mohammed Yeo, Giles S. H. Froguel, Philippe Bechtold, David A. Adamson, Antony Humphreys, Neil Barroso, Inês Luckman, Simon M. Farooqi, I. Sadaf Nat Commun Article Disruption of brain-expressed G protein-coupled receptor-10 (GPR10) causes obesity in animals. Here, we identify multiple rare variants in GPR10 in people with severe obesity and in normal weight controls. These variants impair ligand binding and G protein-dependent signalling in cells. Transgenic mice harbouring a loss of function GPR10 variant found in an individual with obesity, gain excessive weight due to decreased energy expenditure rather than increased food intake. This evidence supports a role for GPR10 in human energy homeostasis. Therapeutic targeting of GPR10 may represent an effective weight-loss strategy. Nature Publishing Group UK 2023-03-15 /pmc/articles/PMC10017677/ /pubmed/36922513 http://dx.doi.org/10.1038/s41467-023-36966-3 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
Talbot, Fleur
Feetham, Claire H.
Mokrosiński, Jacek
Lawler, Katherine
Keogh, Julia M.
Henning, Elana
Mendes de Oliveira, Edson
Ayinampudi, Vikram
Saeed, Sadia
Bonnefond, Amélie
Arslan, Mohammed
Yeo, Giles S. H.
Froguel, Philippe
Bechtold, David A.
Adamson, Antony
Humphreys, Neil
Barroso, Inês
Luckman, Simon M.
Farooqi, I. Sadaf
A rare human variant that disrupts GPR10 signalling causes weight gain in mice
title A rare human variant that disrupts GPR10 signalling causes weight gain in mice
title_full A rare human variant that disrupts GPR10 signalling causes weight gain in mice
title_fullStr A rare human variant that disrupts GPR10 signalling causes weight gain in mice
title_full_unstemmed A rare human variant that disrupts GPR10 signalling causes weight gain in mice
title_short A rare human variant that disrupts GPR10 signalling causes weight gain in mice
title_sort rare human variant that disrupts gpr10 signalling causes weight gain in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017677/
https://www.ncbi.nlm.nih.gov/pubmed/36922513
http://dx.doi.org/10.1038/s41467-023-36966-3
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