Publication:
iSuRe-Cre is a genetic tool to reliably induce and report Cre-dependent genetic modifications

dc.contributor.authorFernandez-Chacon, Macarena
dc.contributor.authorCasquero-Garcia, Veronica
dc.contributor.authorLuo, Wen
dc.contributor.authorLunella, Federica Francesca
dc.contributor.authorRocha, Susana
dc.contributor.authorDel Olmo-Cabrera, Sergio
dc.contributor.authorBenedito, Rui
dc.contributor.funderMinisterio de Economía, Industria y Competitividad (España)
dc.contributor.funderUnión Europea. Comisión Europea. European Research Council (ERC)
dc.contributor.funderUnión Europea. Comisión Europea
dc.contributor.funderFundación La Caixa
dc.contributor.funderFundación ProCNIC
dc.date.accessioned2019-06-04T10:39:25Z
dc.date.available2019-06-04T10:39:25Z
dc.date.issued2019
dc.description.abstractMost 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.peerreviewedes_ES
dc.description.sponsorshipThis 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.number1es_ES
dc.format.page2262es_ES
dc.format.volume10es_ES
dc.identifier.citationNat Commun. 2019; 10(1):2262es_ES
dc.identifier.doi10.1038/s41467-019-10239-4es_ES
dc.identifier.e-issn2041-1723es_ES
dc.identifier.issn2041-1723es_ES
dc.identifier.journalNature communicationses_ES
dc.identifier.pubmedID31118412es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/7719
dc.language.isoenges_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/638028/EUes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SEV-2015-0505es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SAF2013-44329-Pes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SAF2013-42359-ERCes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RYC-2013-13209es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/600396/EUes_ES
dc.relation.publisherversionhttps://doi.org/10.1038/s41467-019-10239-4es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Genética Molecular de la Angiogénesises_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleiSuRe-Cre is a genetic tool to reliably induce and report Cre-dependent genetic modificationses_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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