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Association between Regulator of G Protein Signaling 9–2 and Body Weight

Regulator of G protein signaling 9–2 (RGS9–2) is a protein that is highly enriched in the striatum, a brain region that mediates motivation, movement and reward responses. We identified a naturally occurring 5 nucleotide deletion polymorphism in the human RGS9 gene and found that the mean body mass...

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Autores principales: Waugh, Jeffrey L., Celver, Jeremy, Sharma, Meenakshi, Dufresne, Robert L., Terzi, Dimitra, Risch, S. Craig, Fairbrother, William G., Neve, Rachael L., Kane, John P., Malloy, Mary J., Pullinger, Clive R., Gu, Harvest F., Tsatsanis, Christos, Hamilton, Steven P., Gold, Stephen J., Zachariou, Venetia, Kovoor, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223194/
https://www.ncbi.nlm.nih.gov/pubmed/22132185
http://dx.doi.org/10.1371/journal.pone.0027984
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author Waugh, Jeffrey L.
Celver, Jeremy
Sharma, Meenakshi
Dufresne, Robert L.
Terzi, Dimitra
Risch, S. Craig
Fairbrother, William G.
Neve, Rachael L.
Kane, John P.
Malloy, Mary J.
Pullinger, Clive R.
Gu, Harvest F.
Tsatsanis, Christos
Hamilton, Steven P.
Gold, Stephen J.
Zachariou, Venetia
Kovoor, Abraham
author_facet Waugh, Jeffrey L.
Celver, Jeremy
Sharma, Meenakshi
Dufresne, Robert L.
Terzi, Dimitra
Risch, S. Craig
Fairbrother, William G.
Neve, Rachael L.
Kane, John P.
Malloy, Mary J.
Pullinger, Clive R.
Gu, Harvest F.
Tsatsanis, Christos
Hamilton, Steven P.
Gold, Stephen J.
Zachariou, Venetia
Kovoor, Abraham
author_sort Waugh, Jeffrey L.
collection PubMed
description Regulator of G protein signaling 9–2 (RGS9–2) is a protein that is highly enriched in the striatum, a brain region that mediates motivation, movement and reward responses. We identified a naturally occurring 5 nucleotide deletion polymorphism in the human RGS9 gene and found that the mean body mass index (BMI) of individuals with the deletion was significantly higher than those without. A splicing reporter minigene assay demonstrated that the deletion had the potential to significantly decrease the levels of correctly spliced RGS9 gene product. We measured the weights of rats after virally transduced overexpression of RGS9–2 or the structurally related RGS proteins, RGS7, or RGS11, in the nucleus accumbens (NAc) and observed a reduction in body weight after overexpression of RGS9–2 but not RGS7 or 11. Conversely, we found that the RGS9 knockout mice were heavier than their wild-type littermates and had significantly higher percentages of abdominal fat. The constituent adipocytes were found to have a mean cross-sectional area that was more than double that of corresponding cells from wild-type mice. However, food intake and locomotion were not significantly different between the two strains. These studies with humans, rats and mice implicate RGS9–2 as a factor in regulating body weight.
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spelling pubmed-32231942011-11-30 Association between Regulator of G Protein Signaling 9–2 and Body Weight Waugh, Jeffrey L. Celver, Jeremy Sharma, Meenakshi Dufresne, Robert L. Terzi, Dimitra Risch, S. Craig Fairbrother, William G. Neve, Rachael L. Kane, John P. Malloy, Mary J. Pullinger, Clive R. Gu, Harvest F. Tsatsanis, Christos Hamilton, Steven P. Gold, Stephen J. Zachariou, Venetia Kovoor, Abraham PLoS One Research Article Regulator of G protein signaling 9–2 (RGS9–2) is a protein that is highly enriched in the striatum, a brain region that mediates motivation, movement and reward responses. We identified a naturally occurring 5 nucleotide deletion polymorphism in the human RGS9 gene and found that the mean body mass index (BMI) of individuals with the deletion was significantly higher than those without. A splicing reporter minigene assay demonstrated that the deletion had the potential to significantly decrease the levels of correctly spliced RGS9 gene product. We measured the weights of rats after virally transduced overexpression of RGS9–2 or the structurally related RGS proteins, RGS7, or RGS11, in the nucleus accumbens (NAc) and observed a reduction in body weight after overexpression of RGS9–2 but not RGS7 or 11. Conversely, we found that the RGS9 knockout mice were heavier than their wild-type littermates and had significantly higher percentages of abdominal fat. The constituent adipocytes were found to have a mean cross-sectional area that was more than double that of corresponding cells from wild-type mice. However, food intake and locomotion were not significantly different between the two strains. These studies with humans, rats and mice implicate RGS9–2 as a factor in regulating body weight. Public Library of Science 2011-11-23 /pmc/articles/PMC3223194/ /pubmed/22132185 http://dx.doi.org/10.1371/journal.pone.0027984 Text en Waugh et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Waugh, Jeffrey L.
Celver, Jeremy
Sharma, Meenakshi
Dufresne, Robert L.
Terzi, Dimitra
Risch, S. Craig
Fairbrother, William G.
Neve, Rachael L.
Kane, John P.
Malloy, Mary J.
Pullinger, Clive R.
Gu, Harvest F.
Tsatsanis, Christos
Hamilton, Steven P.
Gold, Stephen J.
Zachariou, Venetia
Kovoor, Abraham
Association between Regulator of G Protein Signaling 9–2 and Body Weight
title Association between Regulator of G Protein Signaling 9–2 and Body Weight
title_full Association between Regulator of G Protein Signaling 9–2 and Body Weight
title_fullStr Association between Regulator of G Protein Signaling 9–2 and Body Weight
title_full_unstemmed Association between Regulator of G Protein Signaling 9–2 and Body Weight
title_short Association between Regulator of G Protein Signaling 9–2 and Body Weight
title_sort association between regulator of g protein signaling 9–2 and body weight
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223194/
https://www.ncbi.nlm.nih.gov/pubmed/22132185
http://dx.doi.org/10.1371/journal.pone.0027984
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