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Diet X Gene Interactions Control Femoral Bone Adaptation to Low Dietary Calcium
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Metadata
Document Title
Diet X Gene Interactions Control Femoral Bone Adaptation to Low Dietary Calcium
Author
Chanpaisaeng K, Reyes-Fernandez PC, Dilkes B, Fleet JC
Name from Authors Collection
Affiliations
National Science & Technology Development Agency - Thailand; National Center Genetic Engineering & Biotechnology (BIOTEC); Indiana University System; Indiana University-Purdue University Indianapolis; Purdue University System; Purdue University; Purdue University West Lafayette Campus; Purdue University System; Purdue University; Purdue University West Lafayette Campus; University of Texas System; University of Texas Austin; University of Texas System; University of Texas Austin
Type
Article
Source Title
JBMR PLUS
Year
2022
Volume
6
Issue
9
Open Access
Green Published, gold
Publisher
WILEY
DOI
10.1002/jbm4.10668
Format
Abstract
Genetics and dietary calcium (Ca) are each critical regulators of peak bone mass but it is unclear how genetics alters the physiologic response of bone to dietary Ca restriction (RCR). Here, we conducted genetic mapping in C57BL/6J x DBA/2J (BXD) recombinant inbred mouse lines to identify environmentally sensitive loci controlling whole-bone mass (bone mineral density [BMD], bone mineral content [BMC]), distal trabecular bone, and cortical bone midshaft of the femur. Mice were fed adequate (basal) or low Ca diets from 4-12 weeks of age. Femurs were then examined by dual-energy X-ray absorptiometry (DXA) and micro-computed tomography (mu CT). Body size-corrected residuals were used for statistical analysis, genetic mapping, and to estimate narrow sense heritability (h(2)). Genetics had a strong impact on femoral traits (eg, bone volume fraction [BV/TV] basal Ca, h(2) = 0.60) as well as their RCR (eg, BV/TV, h(2) = 0.32). Quantitative trait locus (QTL) mapping identified up to six loci affecting each bone trait. A subset of loci was detected in both diet groups, providing replication of environmentally robust genetic effects. Several loci control multiple bone phenotypes suggesting the existence of genetic pleiotropy. QTL controlling the bone RCR did not overlap with basal diet QTL, demonstrating genetic independence of those traits. Candidate genes underlying select multi-trait loci were prioritized by protein coding effects or gene expression differences in bone cells. These include candidate alleles in Rictor (chromosome [chr] 15) and Egfl7 (chr 2) at loci affecting bone in the basal or low Ca groups and in Msr1 (chr 8), Apc, and Camk4 (chr 18) at loci affecting RCR. By carefully controlling dietary Ca and measuring traits in age-matched mice we identified novel genetic loci determining bone mass/microarchitecture of the distal femur as well as their physiologic adaptation to inadequate dietary Ca intake. (c) 2022 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
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Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
Funding Sponsor
NIH [DK118036, ES019103]; Purdue Bone and Body Composition Core within the Indiana Clinical and Translational Sciences Institute (NIH, National Center for Advancing Translational Sciences, Clinical and Translational Sciences Award) [UL1TR001108]; Royal Thai Government Scholarship; CONACyT Mexico
License
CC BY
Rights
Authors
Publication Source
WOS