Author
Listed:
- Macarena Fernández-Chacón
(Centro Nacional de Investigaciones Cardiovasculares (CNIC))
- Verónica Casquero-García
(Centro Nacional de Investigaciones Cardiovasculares (CNIC))
- Wen Luo
(Centro Nacional de Investigaciones Cardiovasculares (CNIC))
- Federica Francesca Lunella
(Centro Nacional de Investigaciones Cardiovasculares (CNIC))
- Susana Ferreira Rocha
(Centro Nacional de Investigaciones Cardiovasculares (CNIC))
- Sergio Olmo-Cabrera
(Centro Nacional de Investigaciones Cardiovasculares (CNIC))
- Rui Benedito
(Centro Nacional de Investigaciones Cardiovasculares (CNIC))
Abstract
Most biomedical research aimed at understanding gene function uses the Cre-Lox system, which consists of the Cre recombinase-dependent deletion of genes containing LoxP sites. This system enables conditional genetic modifications because the expression and activity of the recombinase Cre/CreERT2 can be regulated in space by tissue-specific promoters and in time by the ligand tamoxifen. Since the precise Cre-Lox recombination event is invisible, methods were developed to report Cre activity and are widely used. However, numerous studies have shown that expression of a given Cre activity reporter cannot be assumed to indicate deletion of other LoxP-flanked genes of interest. Here, we report the generation of an inducible dual reporter-Cre mouse allele, iSuRe-Cre. By significantly increasing Cre activity in reporter-expressing cells, iSuRe-Cre provides certainty that these cells have completely recombined floxed alleles. This genetic tool increases the ease, efficiency, and reliability of conditional mutagenesis and gene function analysis.
Suggested Citation
Macarena Fernández-Chacón & Verónica Casquero-García & Wen Luo & Federica Francesca Lunella & Susana Ferreira Rocha & Sergio Olmo-Cabrera & Rui Benedito, 2019.
"iSuRe-Cre is a genetic tool to reliably induce and report Cre-dependent genetic modifications,"
Nature Communications, Nature, vol. 10(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10239-4
DOI: 10.1038/s41467-019-10239-4
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