CRISPR/Cas9 editing of pectinase genes to reduce strawberry fruit softening.

dc.centroFacultad de Cienciases_ES
dc.contributor.authorMercado-Hornos, José Ángel
dc.contributor.authorRodríguez-Hiraldo, Claudia
dc.contributor.authorMuñoz-Blanco, Juan
dc.contributor.authorBlanco-Portales, Rosario
dc.contributor.authorPosé-Albacete, Sara
dc.contributor.authorMatas-Arroyo, Antonio Javier
dc.contributor.authorMercado-Carmona, José Ángel
dc.contributor.authorPaniagua, Candelas
dc.date.accessioned2025-02-07T12:35:04Z
dc.date.available2025-02-07T12:35:04Z
dc.date.issued2024
dc.departamentoBotánica y Fisiología Vegetal
dc.description.abstractStrawberry is a soft fruit characterized by undergoing extensive softening during its ripening. The disassembly of the parenchyma cell walls, the loss of cell-to-cell adhesion and the loss of cell turgor are the main determinant factors in strawberry fruit softening. Cell wall disassembly and the loss of middle lamella take place by the induction of ripening-related genes encoding enzymes on different cell wall components. In a previous study, Fragaria x ananassa knock-out plants for a polygalacturonase gene, FaPG1, were obtained. These plants produced fruits significantly firmer. De-methyl esterified homogalacturonan pectins are the target of polygacturonases. This pectin domain is also degraded by pectate lyases. In strawberry, this activity is mainly encoded by three ripening-induced genes that are expressed at similar levels in ripe fruits. In this research, CRISPR-Cas9 mutant strawberry plants for both polygalacturonase and pectate lyase genes were obtained. A FaPG1 mutant line previously obtained and characterized was introduced in vitro and re-transformed via A. tumefaciens with the plasmid pDe-CAS9-D10A containing a sgRNA guide specific for the pectate lyase genes FxaC_5g17410 and FxaC_6g23780. Nine kanamycin-resistant transgenic lines were obtained. The editing rate was determined by ICE software. Six out of the 9 lines obtained were successfully edited, ranging the editing efficiency from 60 to 95%. The most frequent editing events corresponded to the deletion of 1 or 2 bases, and the insertion of a single base. All the editing events induced frame-shifting and premature termination of protein transduction due to the introduction of stop codons. Transgenic plants were acclimated and transferred to the greenhouse for phenotypical evaluation. No significant alterations in the growth pattern of edited plants were observed. Experiments are currently underway to determine the effect of stacking mutations on fruit quality and postharvest shelf life.es_ES
dc.description.sponsorshipMCIN, grant PID2020-118468RB-C21 ERDF A way of making Europe Universidad de Málaga. Campus de Excelencia Internacional Andalucía Teches_ES
dc.identifier.citationMercado-Hornos JA, Rodríguez-Hiraldo C, Muñoz-Blanco J, Blanco-Portales R, Pose S, Matas AJ, Mercado JA, Paniagua C. 2024. CRISPR/Cas9 editing of pectinase genes to reduce strawberry fruit softening. XVII Meeting of Plant Molecular Biology. Castelló de la Plana, Book of abstract, p. 350es_ES
dc.identifier.urihttps://hdl.handle.net/10630/37745
dc.language.isoenges_ES
dc.relation.eventdate3-5 Julio 2024es_ES
dc.relation.eventplaceCastelló de la Planaes_ES
dc.relation.eventtitleXVII Meeting of Plant Molecular Biologyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectGlicosidasases_ES
dc.subjectFresases_ES
dc.subject.otherStrawberryes_ES
dc.subject.otherFragariaes_ES
dc.subject.otherFruit softeninges_ES
dc.subject.otherPectines_ES
dc.subject.otherCell wall dissasemblyes_ES
dc.subject.otherCRISPR/Cas9es_ES
dc.titleCRISPR/Cas9 editing of pectinase genes to reduce strawberry fruit softening.es_ES
dc.typeconference outputes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationfa0cce2a-bd19-44a2-9ebb-ec29420be654
relation.isAuthorOfPublication58608b24-b618-44c3-a2e4-42a8943b3d15
relation.isAuthorOfPublicationa17cd143-3a4b-4846-9f11-7f5cf2e9391b
relation.isAuthorOfPublication.latestForDiscoveryfa0cce2a-bd19-44a2-9ebb-ec29420be654

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