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resumen

Resumen
The complexity of the sugarcane genome, the narrow genetic base of subtropical germplasm, and the extended breeding and selection cycle pose significant challenges to conventional breeding methods. In vitro mutagenesis offers an alternative approach to generating genetic variability by harnessing both somaclonal variation and induced mutations. An in vitro mutagenesis protocol, using the chemical mutagen ethyl methanesulfonate (EMS) in an elite Argentine [ver mas...]
dc.contributor.authorDi Pauli, Valentina
dc.contributor.authorFontana, Paola Daniela
dc.contributor.authorLewi, Dalia Marcela
dc.contributor.authorFelipe, Arturo
dc.contributor.authorErazzu, Luis Ernesto
dc.date.accessioned2025-07-28T16:09:29Z
dc.date.available2025-07-28T16:09:29Z
dc.date.issued2025-07
dc.identifier.issn3005-1207
dc.identifier.otherhttps://doi.org/10.1007/s44372-025-00298-x
dc.identifier.urihttp://hdl.handle.net/20.500.12123/23188
dc.identifier.urihttps://link.springer.com/article/10.1007/s44372-025-00298-x
dc.description.abstractThe complexity of the sugarcane genome, the narrow genetic base of subtropical germplasm, and the extended breeding and selection cycle pose significant challenges to conventional breeding methods. In vitro mutagenesis offers an alternative approach to generating genetic variability by harnessing both somaclonal variation and induced mutations. An in vitro mutagenesis protocol, using the chemical mutagen ethyl methanesulfonate (EMS) in an elite Argentine sugarcane cultivar, was developed. The resulting genetic variability was assessed in the field in plant and first ratoon crops. Six-week-old embryogenic calli were treated with 8, 16, 32, and 48 mM EMS. Plants were regenerated from treated calli and acclimatized in a greenhouse. The lethal dose LD50 for regeneration capacity was 31.68 mM EMS, whereas LD25 was 17.71 mM EMS. Based on these results, the plants from the 16 and 32 mM EMS treatments were phenotypically assessed in the field. These assessments showed that EMS treatments exhibited phenotypic variability due to genetic changes. Traits such as the number of stalks, stalk length, stalk weight, internode length, and Brix showed an increase in the population mean in the EMS treatments compared with the wild type. Some traits maintained changes from one year to the next, whereas others reverted to the wild-type genotype values in the second year. Mutagenic treatments generated greater and more stable genetic variation than somaclonal variation, supporting their use as effective tools for sugarcane improvement. Based on agronomic traits, 23 mutant plants were selected and advanced to subsequent generations.eng
dc.formatapplication/pdfes_AR
dc.language.isoenges_AR
dc.publisherSpringer Naturees_AR
dc.relationinfo:eu-repograntAgreement/INTA/2023-PD-L01-I071, Mejoramiento genético de los Cultivos Industriales y estrategias alternativas para la obtención de biotipos adaptados a los nuevos escenarios y al cambio climáticoes_AR
dc.relationinfo:eu-repograntAgreement/INTA/2023-PD-L01-I086, Edición génica, transgénesis y mutaciones inducidas como generadores de nueva variabilidad en especies de interés agropecuarioes_AR
dc.rightsinfo:eu-repo/semantics/openAccesses_AR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/es_AR
dc.sourceDiscover Plants 2 : article number 230. (July 2025)es_AR
dc.subjectCaña de Azúcares_AR
dc.subjectSugar Caneeng
dc.subjectGenotiposes_AR
dc.subjectGenotypeseng
dc.subjectVariación Genéticaes_AR
dc.subjectGenetic Variationeng
dc.subjectMutagenesiseng
dc.subjectEmses_AR
dc.subjectEMSeng
dc.subjectArgentinaes_AR
dc.subject.otherEtilmetanosulfonatoes_AR
dc.subject.otherEthylmethanesulphonateeng
dc.titleEthyl methanesulfonate-induced mutagenesis generates genetic and morphological variations in an elite Argentine sugarcane genotypees_AR
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articlees_AR
dc.typeinfo:eu-repo/semantics/publishedVersiones_AR
dc.rights.licenseCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)es_AR
dc.description.origenEEA Famailláes_AR
dc.description.filFil: Di Pauli, Valentina. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Famaillá; Argentinaes_AR
dc.description.filFil: Fontana, Paola Daniela. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Famaillá; Argentinaes_AR
dc.description.filFil: Lewi, Dalia Marcela. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Genética; Argentinaes_AR
dc.description.filFil: Felipe, Arturo. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Famaillá; Argentinaes_AR
dc.description.filFil: Erazzú, Luis E. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Famaillá; Argentina.es_AR
dc.subtypecientifico


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