Publication: iSuRe-Cre is a genetic tool to reliably induce and report Cre-dependent genetic modifications
| dc.contributor.author | Fernandez-Chacon, Macarena | |
| dc.contributor.author | Casquero-Garcia, Veronica | |
| dc.contributor.author | Luo, Wen | |
| dc.contributor.author | Lunella, Federica Francesca | |
| dc.contributor.author | Rocha, Susana | |
| dc.contributor.author | Del Olmo-Cabrera, Sergio | |
| dc.contributor.author | Benedito, Rui | |
| dc.contributor.funder | Ministerio de Economía, Industria y Competitividad (España) | |
| dc.contributor.funder | Unión Europea. Comisión Europea. European Research Council (ERC) | |
| dc.contributor.funder | Unión Europea. Comisión Europea | |
| dc.contributor.funder | Fundación La Caixa | |
| dc.contributor.funder | Fundación ProCNIC | |
| dc.date.accessioned | 2019-06-04T10:39:25Z | |
| dc.date.available | 2019-06-04T10:39:25Z | |
| dc.date.issued | 2019 | |
| dc.description.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. | es_ES |
| dc.description.peerreviewed | Sí | es_ES |
| dc.description.sponsorship | This study was supported by grants to the PI, R.B., from the Ministerio de Economía, Industría y Competitividad (MEIC: SAF2013-44329-P, SAF2013-42359-ERC and RYC- 2013-13209) and the European Research Council (ERC-2014-StG – 638028 AngioGenesHD). M.F. was supported by a PhD fellowship from Fundación La Caixa (CX_E-2015- 01) and W.L. by a FP7-PEOPLE-2012-COFUND GA600396 postdoctoral contract. We thank J.L. Pompa, G. Sabio, V. Andres, J.M. Redondo, F. Radtke, G. Breier, S. Martin, R.H. Adams, M. Torres, T. Schimmang and T. Honjo for sharing the Tie2-Cre, Alb-Cre, Ubc-CreERT2, MyHC-Cre, Dll4 and Notch1 floxed, Kdr floxed, Epas1 floxed, Cdh5(PAC)- CreERT2, Myc floxed, Mycn floxed and Rbpj floxed mice, respectively. We thank Simon Bartlett for English editing; Sofia Sanchez for help with the mouse colony; and all members of the CNIC gene targeting, transgenesis, cellomics, and microscopy units. The CNIC is supported by the Ministerio de Ciencia, Innovación y Universidades (MCNU) and the Pro CNIC Foundation, and is a Severo Ochoa Center of Excellence (SEV-2015-0505). | es_ES |
| dc.format.number | 1 | es_ES |
| dc.format.page | 2262 | es_ES |
| dc.format.volume | 10 | es_ES |
| dc.identifier.citation | Nat Commun. 2019; 10(1):2262 | es_ES |
| dc.identifier.doi | 10.1038/s41467-019-10239-4 | es_ES |
| dc.identifier.e-issn | 2041-1723 | es_ES |
| dc.identifier.issn | 2041-1723 | es_ES |
| dc.identifier.journal | Nature communications | es_ES |
| dc.identifier.pubmedID | 31118412 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/7719 | |
| dc.language.iso | eng | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/EC/H2020/638028/EU | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/SEV-2015-0505 | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/SAF2013-44329-P | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/SAF2013-42359-ERC | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/RYC-2013-13209 | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/EC/FP7/600396/EU | es_ES |
| dc.relation.publisherversion | https://doi.org/10.1038/s41467-019-10239-4 | es_ES |
| dc.repisalud.institucion | CNIC | es_ES |
| dc.repisalud.orgCNIC | CNIC::Grupos de investigación::Genética Molecular de la Angiogénesis | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Atribución 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.title | iSuRe-Cre is a genetic tool to reliably induce and report Cre-dependent genetic modifications | es_ES |
| dc.type | journal article | es_ES |
| dc.type.hasVersion | VoR | es_ES |
| dspace.entity.type | Publication | |
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| relation.isAuthorOfPublication | 924c4677-29f1-4917-92d2-765d534c2242 | |
| relation.isAuthorOfPublication.latestForDiscovery | 655524a2-7a61-4d4b-8334-2d5fdb9c2c96 |
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