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Am J Physiol Endocrinol Metab 291: E429-E438, 2006. First published May 9, 2006; doi:10.1152/ajpendo.00124.2006
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INVITED REVIEW

Current and future approaches using genetically modified mice in endocrine research

Rachel A. Davey and Helen E. MacLean

Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria, Australia

Submitted 15 March 2006 ; accepted in final form 4 May 2006

Genetically modified mouse models have been used widely to advance our knowledge in the field of endocrinology and metabolism. A number of different approaches to generate genetically modified mice are now available, which provide the power to analyze the role of individual proteins in vivo. However, there are a number of points to be considered in the use and interpretation of these models. This review discusses the advantages and disadvantages involved in the generation and use of different genetically modified mouse models in endocrine research, including conventional techniques (e.g., overexpression, knockout, and knock-in models), tissue- and/or time-specific deletion of target genes [e.g., Cre-loxP and short interfering (si)RNA transgenic approaches], and gene-trap approaches to undertake functional genomics. This review also highlights the many factors that should be considered when assessing the phenotype of these mouse models, many of which are relevant to all murine physiological studies. These approaches are a powerful means by which to dissect the function of genes and are revolutionizing our understanding of endocrine physiology and metabolism.

transgenic; knockout; knock-in; cre-loxp; functional genomics; physiology



Address for reprint requests and other correspondence: H. E. MacLean, Dept. of Medicine, Univ. of Melbourne, Austin Health, Studley Rd., Heidelberg, VIC 3084, Australia (e-mail: hmaclean{at}unimelb.edu.au)




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