Abstract

BackgroundTargeted 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.FindingsHere, 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.ConclusionsThe 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.

Highlights

  • Targeted genetic modification in the mouse becomes increasingly important in biomedical and basic science

  • 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

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Summary

Conclusions

This novel pink Cre-reporter mouse line represents a versatile tool in transgenic mouse research. A great advantage is the high expression level of the fluorescent protein mCherry, which allows easy recognition and separation of animals harboring the reporter allele from littermates without further analysis. The presence of two fluorescent proteins is useful for parallel in vivo monitoring of recombined and non-recombined cells, in vivo recordings, and analyses of cellular connectivity. This mouse line is well suited for teaching purposes. Its pink color can be used to demonstrate the power of transgenic technologies and crossed with an ubiquitously expressing Cre-driver, the color would disappear. All authors read and approved the final manuscript

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