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dc.contributor.authorWaugh, Jeffrey L.
dc.contributor.authorCelver, Jeremy
dc.contributor.authorSharma, Meenakshi
dc.contributor.authorDufresne, Robert L.
dc.contributor.authorTerzi, Dimitra
dc.contributor.authorRisch, S. Craig
dc.contributor.authorFairbrother, William G.
dc.contributor.authorNeve, Rachael L.
dc.contributor.authorKane, John P.
dc.contributor.authorMalloy, Mary J.
dc.contributor.authorPullinger, Clive R.
dc.contributor.authorGu, Harvest F.
dc.contributor.authorTsatsanis, Christos
dc.contributor.authorHamilton, Steven P.
dc.contributor.authorGold, Stephen J.
dc.contributor.authorZachariou, Venetia
dc.contributor.authorKovoor, Abraham
dc.date.accessioned2012-02-23T19:12:42Z
dc.date.available2012-02-23T19:12:42Z
dc.date.issued2011-11
dc.date.submitted2011-09
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/69174
dc.description.abstractRegulator 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.en_US
dc.description.sponsorshipNational Institute of Mental Health (U.S.) (R41MH78570 award)en_US
dc.description.sponsorshipNational Center for Research Resources (U.S.) (Rhode Island IDeA Network of Biomedical Research Excellence (RI-INBRE) Award P20RR016457-10)en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0027984en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titleAssociation between Regulator of G Protein Signaling 9–2 and Body Weighten_US
dc.typeArticleen_US
dc.identifier.citationWaugh, Jeffrey L. et al. “Association Between Regulator of G Protein Signaling 9–2 and Body Weight.” Ed. Malú G. Tansey. PLoS ONE 6.11 (2011): e27984. Web. 23 Feb. 2012.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.approverNeve, Rachael L.
dc.contributor.mitauthorNeve, Rachael L.
dc.relation.journalPLoS ONEen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsWaugh, 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, Abrahamen
dc.identifier.orcidhttps://orcid.org/0000-0002-3854-5968
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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