Fine-mapping alleles for body weight in LG/J x SM/J F 2 and F 34 advanced intercross lines
| dc.contributor.author | Parker , Clarissa C | |
| dc.contributor.author | Cheng, Riyan | |
| dc.contributor.author | Sokoloff, Greta | |
| dc.contributor.author | Lim, Jackie E | |
| dc.contributor.author | Skol, Andrew D | |
| dc.contributor.author | Abney, Mark | |
| dc.contributor.author | Palmer, Abraham A | |
| dc.date.accessioned | 2015-12-13T22:42:44Z | |
| dc.date.issued | 2011 | |
| dc.date.updated | 2016-02-24T09:35:06Z | |
| dc.description.abstract | The present study measured variation in body weight using a combined analysis in an F 2 intercross and an F 34 advanced intercross line (AIL). Both crosses were derived from inbred LG/J and SM/J mice, which were selected for large and small body size prior to inbreeding. Body weight was measured at 62 (±5) days of age. Using an integrated GWAS and forward model selection approach, we identified 11 significant QTLs that affected body weight on ten different chromosomes. With these results we developed a full model that explained over 18% of the phenotypic variance. The median 1.5-LOD support interval was 5.55 Mb, which is a significant improvement over most prior body weight QTLs. We identified nonsynonymous coding SNPs between LG/J and SM/J mice in order to further narrow the list of candidate genes. Three of the genes with nonsynonymous coding SNPs (Rad23b, Stk33, and Anks1b) have been associated with adiposity, waist circumference, and body mass index in human GWAS, thus providing evidence that these genes may underlie our QTLs. Our results demonstrate that a relatively small number of loci contribute significantly to the phenotypic variance in body weight, which is in marked contrast to the situation in humans. This difference is likely to be the result of strong selective pressure and the simplified genetic architecture, both of which are important advantages of our system. | |
| dc.identifier.issn | 0938-8990 | |
| dc.identifier.uri | http://hdl.handle.net/1885/78897 | |
| dc.publisher | Springer | |
| dc.source | Mammalian Genome | |
| dc.subject | Keywords: advanced intercross line; animal experiment; animal genetics; Anks1b gene; article; body mass; body weight; controlled study; female; gene; gene identification; gene mapping; genetic analysis; genetic association; genetic code; genetic variability; male; | |
| dc.title | Fine-mapping alleles for body weight in LG/J x SM/J F 2 and F 34 advanced intercross lines | |
| dc.type | Journal article | |
| local.bibliographicCitation.issue | 9-10 | |
| local.bibliographicCitation.lastpage | 571 | |
| local.bibliographicCitation.startpage | 563 | |
| local.contributor.affiliation | Parker , Clarissa C , The University of Chicago | |
| local.contributor.affiliation | Cheng, Riyan, College of Medicine, Biology and Environment, ANU | |
| local.contributor.affiliation | Sokoloff, Greta, University of Chicago | |
| local.contributor.affiliation | Lim, Jackie E , Duke University Medical Center | |
| local.contributor.affiliation | Skol, Andrew D, The University of Chicago | |
| local.contributor.affiliation | Abney, Mark, The University of Chicago | |
| local.contributor.affiliation | Palmer, Abraham A, The University of Chicago | |
| local.contributor.authoruid | Cheng, Riyan, u5264559 | |
| local.description.embargo | 2037-12-31 | |
| local.description.notes | Imported from ARIES | |
| local.identifier.absfor | 060412 - Quantitative Genetics (incl. Disease and Trait Mapping Genetics) | |
| local.identifier.absseo | 970106 - Expanding Knowledge in the Biological Sciences | |
| local.identifier.ariespublication | f5625xPUB7451 | |
| local.identifier.citationvolume | 22 | |
| local.identifier.doi | 10.1007/s00335-011-9349-z | |
| local.identifier.scopusID | 2-s2.0-80054756689 | |
| local.identifier.thomsonID | 000295130800007 | |
| local.type.status | Published Version |
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