With increasing incidence of obesity, there is greater demand for suitable research and therapeutic models. The ob/ob mouse model develops obesity by 5 weeks of age. Previously, a method using DNA purification, PCR, and restriction digestion of products was devised to identify mice bearing the ob allele. Here, we describe a direct PCR method that requires no DNA purification. Wild-type and ob-specific primers are used under the same conditions in two separate and simultaneously run three-primer PCRs. Standard PCR using the wild-type primer mix produces 191 bp and 104 bp bands in / and ob/ and only the control 191 bp band in ob/ob animals. The ob-specific primer reaction produces 191 bp and 123 bp bands in ob/ and ob/ob and only the control 191 bp band in / animals. Phenotypic weight gain in offspring of heterozygous intercrosses was used to validate genotypes. This primer-specific PCR method allows simultaneous identification of /, ob/, and ob/ob genotypes prior to breeding age to facilitate breeding and research studies in an important model of clinical obesity. © 2008 The Obesity Society.
CITATION STYLE
Ellett, J. D., Evans, Z. P., Zhang, G., Chavin, K. D., & Spyropoulos, D. D. (2009). A rapid PCR-based method for the identification of ob mutant mice. Obesity, 17(2), 402–404. https://doi.org/10.1038/oby.2008.443
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