Genetically Modified Animal Models As Tools for Studying Bone and Mineral Metabolism
Overview
Affiliations
Genetic modification of mice is a powerful tool for the study of bone development and metabolism. This review discusses the advantages and disadvantages of various approaches used in bone-related research and the contributions these studies have made to bone biology. Genetic modification of mice is a powerful tool for the study of bone development and metabolism. This review discusses the advantages and disadvantages of various approaches used in bone-related research and the contributions these studies have made to bone biology. The approaches to genetic modification included in this review are (1) overexpression of genes, (2) global gene knockouts, (3) tissue-specific gene deletion, and (4) gene knock-in models. This review also highlights issues that should be considered when using genetically modified animal models, including the rigorous control of genetic background, use of appropriate control lines, and confirmation of tissue specificity of gene expression where appropriate. This technology provides a unique and powerful way to probe the function of genes and is already revolutionizing our approach to understanding the physiology of bone development and metabolism.
Androgen Receptor Structure, Function and Biology: From Bench to Bedside.
Davey R, Grossmann M Clin Biochem Rev. 2016; 37(1):3-15.
PMID: 27057074 PMC: 4810760.
Chan J, Glass G, Ersek A, Freidin A, Williams G, Gowers K EMBO Mol Med. 2015; 7(5):547-61.
PMID: 25770819 PMC: 4492816. DOI: 10.15252/emmm.201404487.
Human androgen deficiency: insights gained from androgen receptor knockout mouse models.
Rana K, Davey R, Zajac J Asian J Androl. 2014; 16(2):169-77.
PMID: 24480924 PMC: 3955325. DOI: 10.4103/1008-682X.122590.
Ford J, Hajibeigi A, Long M, Hahner L, Gore C, Hsieh J J Bone Miner Res. 2010; 26(2):298-307.
PMID: 20734455 PMC: 3179349. DOI: 10.1002/jbmr.209.
Johnston J, Ramos-Valdes Y, Stanton L, Ladhani S, Beier F, DiMattia G Transgenic Res. 2010; 19(6):1017-39.
PMID: 20174869 DOI: 10.1007/s11248-010-9376-7.