A pink mouse reports the switch from red to green fluorescence upon Cre-mediated recombination

• Published in: BMC research notes 2012-06, Vol.5 (1), p.296-296, Article 296
• Main Authors: Hartwich, Heiner, Satheesh, Somisetty V, Nothwang, Hans Gerd
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Color; Color Perception; Fluorescence; Founder Effect; Gene Dosage; Gene Expression Regulation; Genes, Reporter; Genetic engineering; Genetic recombination; Genetically modified organisms; Genotype; Green Fluorescent Proteins - biosynthesis; Green Fluorescent Proteins - genetics; HEK293 Cells; Humans; Integrases - genetics; Integrases - metabolism; Journalists; Laboratory animals; Luminescent Proteins - biosynthesis; Luminescent Proteins - genetics; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microscopy, Fluorescence; Negotiation, mediation and arbitration; Phenotype; Promoter Regions, Genetic; Proteins; Recombination, Genetic; Red Fluorescent Protein; Skin - metabolism; Technical Note; Transfection; Zebrafish
• ISSN: 1756-0500; 1756-0500
• DOI: 10.1186/1756-0500-5-296

Targeted genetic modification in the mouse becomes increasingly important in biomedical and basic science. This goal is most often achieved by use of the Cre/loxP system and numerous Cre-driver mouse lines are currently generated. Their initial characterization requires reporter mouse lines to study the in vivo spatiotemporal activity of Cre. Here, we report a dual fluorescence reporter mouse line, which switches expression from the red fluorescent protein mCherry to eGFP after Cre-mediated recombination. Both fluorescent proteins are expressed from the ubiquitously active and strong CAGGS promoter. Among the founders, we noticed a pink mouse line, expressing high levels of the red fluorescent protein mCherry throughout the entire body. Presence of mCherry in the living animal as well as in almost all organs was clearly visible without optical equipment. Upon Cre-activity, mCherry expression was switched to eGFP, demonstrating functionality of this reporter mouse line. The pink mouse presented here is an attractive novel reporter line for fluorescence-based monitoring of Cre-activity. The high expression of mCherry, which is visible to the naked eye, facilitates breeding and crossing, as no genotyping is required to identify mice carrying the reporter allele. The presence of two fluorescent proteins allows in vivo monitoring of recombined and non-recombined cells. Finally, the pink mouse is an eye-catching animal model to demonstrate the power of transgenic techniques in teaching courses.