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dc.contributor.author | Abdollahi, M.R. | es_ES |
dc.contributor.author | Ghazanfari, P. | es_ES |
dc.contributor.author | Corral Martínez, Patricia | es_ES |
dc.contributor.author | Moieni, A. | es_ES |
dc.contributor.author | Seguí-Simarro, Jose M. | es_ES |
dc.date.accessioned | 2016-07-19T06:49:11Z | |
dc.date.available | 2016-07-19T06:49:11Z | |
dc.date.issued | 2012-08 | |
dc.identifier.issn | 0167-6857 | |
dc.identifier.uri | http://hdl.handle.net/10251/67777 | |
dc.description.abstract | Induction of secondary embryogenesis on transformed androgenic microspore-derived embryos (MDEs) is a convenient approach to avoid chimerism and hemizygosis for the introduced transgene. In this work, we improved two aspects related to secondary embryogenesis in rapeseed (Brassica napus L. cv. Topas) MDEs: the identification of the best source of secondary embryos in the germinated MDEs and the increase in the production of secondary embryos (SEs). We performed a ploidy analysis of the different organs of MDEs-derived plantlets by flow cytometry. Our results showed that 60 % of the MDEs-derived plantlets were mixoploid, with 60 % of them having different ploidies for different organs. We concluded that hypocotyl-derived SEs present in general higher levels of genome duplication, which makes them a source of SEs better than cotyledons in terms of genetic stability and avoidance of hemizygosis. In order to increase production of SEs, we used plant-derived aqueous smoke extracts. The aim was to verify whether these extracts have a positive effect on secondary embryogenesis and if so, to identify the most efficient conditions of use. We tested smoke extracts at different incubation times, concentrations and methods of application to MDEs. The use of smoke extract, either prior to or during germination of MDEs, markedly enhances secondary embryogenesis. The best results were obtained with the use of smoke extract as a pretreatment, incubating MDEs for no longer than 15 min with a 1:250 extract concentration. © 2012 Springer Science+Business Media B.V. | es_ES |
dc.description.sponsorship | This work was partially supported by a grant from Spanish MICINN AGL2010-17895 to J. M. Segui-Simarro. | en_EN |
dc.language | Inglés | es_ES |
dc.publisher | Springer Verlag (Germany) | es_ES |
dc.relation.ispartof | Plant Cell, Tissue and Organ Culture | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | Androgenesis | es_ES |
dc.subject | Germination | es_ES |
dc.subject | Microspore-derived embryo | es_ES |
dc.subject | Ploidy | es_ES |
dc.subject | Rapeseed | es_ES |
dc.subject | Smoke extract | es_ES |
dc.subject | Cultivation | es_ES |
dc.subject | Flow cytometry | es_ES |
dc.subject | Oilseeds | es_ES |
dc.subject | Smoke | es_ES |
dc.subject | Plant extracts | es_ES |
dc.subject | Brassica napus | es_ES |
dc.subject.classification | GENETICA | es_ES |
dc.title | Enhancing secondary embryogenesis in Brassica napus by selecting hypocotyl-derived embryos and using plant-derived smoke extract in culture medium | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1007/s11240-012-0152-7 | |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//AGL2010-17895/ES/GENERACION EFICIENTE DE DOBLE HAPLOIDES EN BERENJENA Y PIMIENTO MEDIANTE CULTIVO IN VITRO DE MICROSPORAS AISLADAS. ANALISIS CELULAR Y MOLECULAR DEL DESARROLLO ANDROGENICO/ | es_ES |
dc.rights.accessRights | Cerrado | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Instituto Universitario de Conservación y Mejora de la Agrodiversidad Valenciana - Institut Universitari de Conservació i Millora de l'Agrodiversitat Valenciana | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia | es_ES |
dc.description.bibliographicCitation | Abdollahi, M.; Ghazanfari, P.; Corral Martínez, P.; Moieni, A.; Seguí-Simarro, JM. (2012). Enhancing secondary embryogenesis in Brassica napus by selecting hypocotyl-derived embryos and using plant-derived smoke extract in culture medium. Plant Cell, Tissue and Organ Culture. 110(2):307-315. https://doi.org/10.1007/s11240-012-0152-7 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | http://dx.doi.org/10.1007/s11240-012-0152-7 | es_ES |
dc.description.upvformatpinicio | 307 | es_ES |
dc.description.upvformatpfin | 315 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 110 | es_ES |
dc.description.issue | 2 | es_ES |
dc.relation.senia | 223183 | es_ES |
dc.contributor.funder | Ministerio de Ciencia e Innovación | es_ES |
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