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Chromosomal regions harboring genes for the work to femur failure in mice
Authors:Xinmin Li  Godfred Masinde  Weikuan Gu  Jon Wergedal  Melanie Hamilton-Ulland  Shizhong Xu  Subburaman Mohan  David J Baylink
Institution:(1) Molecular Genetics Division, Musculoskeletal Disease Center, JL Pettis VA Medical Center and Loma Linda University, 11201 Benton Street (151), Loma Linda, CA 92357, USA,;(2) Department of Botany and Plant Sciences, University of California, Riverside, CA 92521–0124, USA,
Abstract:The work to failure is defined as the maximum energy bone can absorb before breaking, and therefore is a direct test of the risk of fracture. To determine the genetic loci influencing work to failure, we have performed a high density genome-wide scan in 633 (MRL × SJL) F2 female mice. Five loci (P <0.005) with significant effects on work to failure were found on chromosomes 2, 7, 8, 9, and X, which collectively explained around 20% variance of work to femur failure in F2 mice. Of those, only the QTL on chromosome 9 was concordant with bone mineral density (BMD) QTLs. Eight significant interactions (P <0.01) between marker loci were identified, which accounted for an equivalent amount of F2 variance (23%) to combined single QTL effects. Our results demonstrate that most of the genetic loci regulating work to failure are different from those for BMD in the 7-week-old female mice. If this is also true in humans, this finding will challenge the predictive value of BMD for the risk of fracture. Electronic Publication
Keywords:Work to failure Bone mineral density Quantitative trait loci Instron
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