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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...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-10017677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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