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dc.rights.licenseopenen_US
hal.structure.identifierEcophysiologie et Génomique Fonctionnelle de la Vigne [UMR EGFV]
dc.contributor.authorCHAMBAUD, Clément
hal.structure.identifierEcophysiologie et Génomique Fonctionnelle de la Vigne [UMR EGFV]
dc.contributor.authorCOOKSON, Sarah J.
IDREF: 22161009X
hal.structure.identifierEcophysiologie et Génomique Fonctionnelle de la Vigne [UMR EGFV]
dc.contributor.authorOLLAT, Nathalie
IDREF: 126740062
hal.structure.identifierLaboratoire de biogenèse membranaire [LBM]
dc.contributor.authorBERNARD, Amélie
IDREF: 157438902
hal.structure.identifierBordeaux Imaging Center [BIC]
dc.contributor.authorBROCARD, Lysiane
dc.date.accessioned2024-01-31T14:07:04Z
dc.date.available2024-01-31T14:07:04Z
dc.date.issued2023-01-20
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/187708
dc.description.abstractEnCombining two different plants together through grafting is one of the oldest horticultural techniques. In order to survive, both partners must communicate via the formation of de novo connections between the scion and the rootstock. Despite the importance of grafting, the ultrastructural processes occurring at the graft interface remain elusive due to the difficulty of locating the exact interface at the ultrastructural level. To date, only studies with interfamily grafts showing enough ultrastructural differences were able to reliably localize the grafting interface at the ultrastructural level under electron microscopy. Thanks to the implementation of correlative light electron microscopy (CLEM) approaches where the grafted partners were tagged with fluorescent proteins of different colors, the graft interface was successfully and reliably targeted. Here, we describe a protocol for CLEM for the model plant Arabidopsis thaliana, which unambiguously targets the graft interface at the ultrastructural level. Moreover, this protocol is compatible with immunolocalization and electron tomography acquisition to achieve a three-dimensional view of the ultrastructural events of interest in plant tissues.
dc.language.isoENen_US
dc.subject.enArabidopsis Thaliana
dc.subject.enCorrelative Microscopy
dc.subject.enElectron Microscopy
dc.subject.enElectron Tomography
dc.subject.enPlant Grafting
dc.title.enTargeting Ultrastructural Events at the Graft Interface of Arabidopsis thaliana by A Correlative Light Electron Microscopy Approach
dc.typeArticle de revueen_US
dc.identifier.doi10.21769/BioProtoc.4590en_US
dc.subject.halSciences du Vivant [q-bio]/Biologie végétaleen_US
bordeaux.journalBio-protocolen_US
bordeaux.volume13en_US
bordeaux.hal.laboratoriesEcophysiologie et Génomique Fonctionnelle de la Vigne (EGFV) - UMR 1287en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux Sciences Agroen_US
bordeaux.institutionINRAEen_US
bordeaux.institutionCNRS
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Bio-protocol&rft.date=2023-01-20&rft.volume=13&rft.issue=2&rft.au=CHAMBAUD,%20Cl%C3%A9ment&COOKSON,%20Sarah%20J.&OLLAT,%20Nathalie&BERNARD,%20Am%C3%A9lie&BROCARD,%20Lysiane&rft.genre=article


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