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dc.contributor.authorBurrage, Lindsay C.
dc.contributor.authorBaskin-Hill, Annie E.
dc.contributor.authorSinasac, David S.
dc.contributor.authorSinger, Jonathan B.
dc.contributor.authorCroniger, Colleen M.
dc.contributor.authorKirby, Andrew
dc.contributor.authorKulbokas, E. J.
dc.contributor.authorDaly, Mark J.
dc.contributor.authorBroman, Karl W.
dc.contributor.authorNadeau, Joseph H.
dc.contributor.authorLander, Eric Steven
dc.date.accessioned2014-01-31T18:37:56Z
dc.date.available2014-01-31T18:37:56Z
dc.date.issued2010-02
dc.date.submitted2009-09
dc.identifier.issn0938-8990
dc.identifier.issn1432-1777
dc.identifier.urihttp://hdl.handle.net/1721.1/84628
dc.description.abstractDiscovery of genes that confer resistance to diseases such as diet-induced obesity could have tremendous therapeutic impact. We previously demonstrated that the C57BL/6J-Chr[superscript A/J]/NaJ panel of chromosome substitution strains (CSSs) is a unique model for studying resistance to diet-induced obesity. In the present study, three replicate CSS surveys showed remarkable consistency, with 13 A/J-derived chromosomes reproducibly conferring resistance to high-fat-diet-induced obesity. Twenty CSS intercrosses, one derived from each of the 19 autosomes and chromosome X, were used to determine the number and location of quantitative trait loci (QTLs) on individual chromosomes and localized six QTLs. However, analyses of mean body weight in intercross progeny versus C57BL/6J provided strong evidence that many QTLs discovered in the CSS surveys eluded detection in these CSS intercrosses. Studies of the temporal effects of these QTLs suggest that obesity resistance was dynamic, with QTLs acting at different ages or after different durations of diet exposure. Thus, these studies provide insight into the genetic architecture of complex traits such as resistance to diet-induced obesity in the C57BL/6J-Chr[superscript A/J]/NaJ CSSs. Because some of the QTLs detected in the CSS intercrosses were not detected using a traditional C57BL/6J × A/J intercross, our results demonstrate that surveys of CSSs and congenic strains derived from them are useful complementary tools for analyzing complex traits.en_US
dc.description.sponsorshipNational Center for Research Resources (U.S.) (RR12305)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (U54CA116867)en_US
dc.description.sponsorshipCharles B. Wang Foundationen_US
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s00335-010-9247-9en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleGenetic resistance to diet-induced obesity in chromosome substitution strains of miceen_US
dc.typeArticleen_US
dc.identifier.citationBurrage, Lindsay C., Annie E. Baskin-Hill, David S. Sinasac, Jonathan B. Singer, Colleen M. Croniger, Andrew Kirby, E. J. Kulbokas, et al. “Genetic resistance to diet-induced obesity in chromosome substitution strains of mice.” Mammalian Genome 21, no. 3 4 (April 3, 2010): 115-129.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorLander, Eric S.en_US
dc.relation.journalMammalian Genomeen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsBurrage, Lindsay C.; Baskin-Hill, Annie E.; Sinasac, David S.; Singer, Jonathan B.; Croniger, Colleen M.; Kirby, Andrew; Kulbokas, E. J.; Daly, Mark J.; Lander, Eric S.; Broman, Karl W.; Nadeau, Joseph H.en_US
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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