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Epistatic Effects Contribute to Variation in BMD in Fischer 344 × Lewis F2 Rats
Author(s) -
Koller Daniel L,
Liu Lixiang,
Alam Imranul,
Sun Qiwei,
Econs Michael J,
Foroud Tatiana,
Turner Charles H
Publication year - 2008
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1359/jbmr.071001
Subject(s) - epistasis , quantitative trait locus , genetic architecture , locus (genetics) , genetics , biology , genome wide association study , genome , microsatellite , genome scan , genotype , phenotype , allele , gene , single nucleotide polymorphism
To further delineate the factors underlying the complex genetic architecture of BMD in the rat model, a genome screen for epistatic interactions was conducted. Several significant interactions were identified, involving both previously identified and novel QTLs. Introduction : The variation in several of the risk factors for osteoporotic fracture, including BMD, has been shown to be caused largely by genetic differences. However, the genetic architecture of BMD is complex in both humans and in model organisms. We have previously reported quantitative trait locus (QTL) results for BMD from a genome screen of 595 female F 2 progeny of Fischer 344 and Lewis rats. These progeny also provide an excellent opportunity to search for epistatic effects, or interaction between genetic loci, that contribute to fracture risk. Materials and Methods : Microsatellite marker data from a 20‐cM genome screen was analyzed along with weight‐adjusted BMD (DXA and pQCT) phenotypic data using the R/qtl software package. Genotype and phenotype data were permuted to determine a genome‐wide significance threshold for the epistasis or interaction LOD score corresponding to an α level of 0.01. Results and Conclusions : Novel loci on chromosomes 12 and 15 showed a strong epistatic effect on total BMD at the femoral midshaft by pQCT (LOD = 5.4). A previously reported QTL on chromosome 7 was found to interact with a novel locus on chromosome 20 to affect whole lumbar BMD by pQCT (LOD = 6.2). These results provide new information regarding the mode of action of previously identified rat QTLs, as well as identifying novel loci that act in combination with known QTLs or with other novel loci to contribute to the risk factors for osteoporotic fracture.