A Novel Adipose-Specific Gene Deletion Model Demonstrates Potential Pitfalls of Existing Methods
Author(s) -
Shan E. Mullican,
Takuya Tomaru,
Christine A. Gaddis,
Lindsey C. Peed,
Anand Sundaram,
Mitchell A. Lazar
Publication year - 2012
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/me.2012-1267
Subject(s) - adipose tissue , biology , adipocyte , cre recombinase , gene targeting , gene , recombinase , function (biology) , in vivo , microbiology and biotechnology , genetics , computational biology , genetically modified mouse , endocrinology , transgene , recombination
Adipose-specific gene deletion in mice is crucial in determining gene function in adipocyte homeostasis and the development of obesity. We noted 100% mortality when the Hdac3 gene was conditionally deleted using Fabp4-Cre mice, the most commonly used model of adipose-targeted Cre recombinase. However, this surprising result was not reproduced using other models of adipose targeting of Cre, including a novel Retn-Cre mouse. These findings underscore the need for caution when interpreting data obtained using Fabp4-Cre mice and should encourage the use of additional or alternative adipose-targeting Cre mouse models before drawing conclusions about in vivo adipocyte-specific functions.
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