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Systems genetics in diversity outbred mice inform BMD GWAS and identify determinants of bone strength

Genome-wide association studies (GWASs) for osteoporotic traits have identified over 1000 associations; however, their impact has been limited by the difficulties of causal gene identification and a strict focus on bone mineral density (BMD). Here, we use Diversity Outbred (DO) mice to directly addr...

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Detalles Bibliográficos
Autores principales: Al-Barghouthi, Basel M., Mesner, Larry D., Calabrese, Gina M., Brooks, Daniel, Tommasini, Steven M., Bouxsein, Mary L., Horowitz, Mark C., Rosen, Clifford J., Nguyen, Kevin, Haddox, Samuel, Farber, Emily A., Onengut-Gumuscu, Suna, Pomp, Daniel, Farber, Charles R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184749/
https://www.ncbi.nlm.nih.gov/pubmed/34099702
http://dx.doi.org/10.1038/s41467-021-23649-0
Descripción
Sumario:Genome-wide association studies (GWASs) for osteoporotic traits have identified over 1000 associations; however, their impact has been limited by the difficulties of causal gene identification and a strict focus on bone mineral density (BMD). Here, we use Diversity Outbred (DO) mice to directly address these limitations by performing a systems genetics analysis of 55 complex skeletal phenotypes. We apply a network approach to cortical bone RNA-seq data to discover 66 genes likely to be causal for human BMD GWAS associations, including the genes SERTAD4 and GLT8D2. We also perform GWAS in the DO for a wide-range of bone traits and identify Qsox1 as a gene influencing cortical bone accrual and bone strength. In this work, we advance our understanding of the genetics of osteoporosis and highlight the ability of the mouse to inform human genetics.