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dc.contributor.authorMartín-Pizarro, Carmen
dc.contributor.authorTriviño, Juan Carlos
dc.contributor.authorPosé-Padilla, David 
dc.date.accessioned2022-01-12T10:03:22Z
dc.date.available2022-01-12T10:03:22Z
dc.date.created2022
dc.date.issued2019-01
dc.identifier.urihttps://hdl.handle.net/10630/23593
dc.description.abstractThe B-class of MADS-box transcription factors has been studied in many plant species, but remains functionally unchar- acterized in Rosaceae. APETALA3 (AP3), a member of this class, controls petal and stamen identities in Arabidopsis. In this study, we identified two members of the AP3 lineage in cultivated strawberry, Fragaria × ananassa, namely FaAP3 and FaTM6. FaTM6, and not FaAP3, showed an expression pattern equivalent to that of AP3 in Arabidopsis. We used the CRISPR/Cas9 genome editing system for the first time in an octoploid species to characterize the function of TM6 in strawberry flower development. An analysis by high-throughput sequencing of the FaTM6 locus spanning the target sites showed highly efficient genome editing already present in the T0 generation. Phenotypic characterization of the mutant lines indicated that FaTM6 plays a key role in anther development in strawberry. Our results validate the use of the CRISPR/Cas9 system for gene functional analysis in F. × ananassa as an octoploid species, and offer new opportunities for engineering strawberry to improve traits of interest in breeding programs.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectFresases_ES
dc.subject.otherAP3es_ES
dc.subject.otherCRISPR/Cas9es_ES
dc.subject.otherFragaria x ananassaes_ES
dc.subject.otherFragaria vescaes_ES
dc.subject.otherGenome editinges_ES
dc.subject.otherTranscription Factores_ES
dc.subject.otherStrawberryes_ES
dc.subject.otherTM6es_ES
dc.subject.otherFlower developmentes_ES
dc.titleFunctional Analysis of TM6 MADS-box gene in the Octoploid Strawberry by CRISPR/Cas9 directed mutagenesises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.centroFacultad de Cienciases_ES
dc.identifier.doi10.1093/jxb/ery400
dc.rights.ccAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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