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hal.structure.identifierBiologie du fruit et pathologie [BFP]
dc.contributor.authorPIRRELLO, Julien
hal.structure.identifierBiologie du fruit et pathologie [BFP]
dc.contributor.authorBOURDON, Matthieu
hal.structure.identifierBiologie du fruit et pathologie [BFP]
dc.contributor.authorCHENICLET, Catherine
hal.structure.identifierInstitut de Génétique, Environnement et Protection des Plantes [IGEPP]
dc.contributor.authorCORITON, Olivier
hal.structure.identifierLa plante et son environnement [PSE]
dc.contributor.authorBOURGE, Mickaël
hal.structure.identifierLa plante et son environnement [PSE]
dc.contributor.authorBROWN, Spencer
hal.structure.identifierBiologie du fruit et pathologie [BFP]
dc.contributor.authorRENAUDIN, Jean-Pierre
hal.structure.identifierBiologie du fruit et pathologie [BFP]
dc.contributor.authorFRANGNE, Nathalie
hal.structure.identifierBiologie du fruit et pathologie [BFP]
dc.contributor.authorCHEVALIER, Christian
dc.date.issued2013
dc.identifier.issn1342-4580
dc.description.abstractEnEndopolyploidy, i.e. the amplification of genomic DNA without mitosis, is a widespread process in plants. Cells from the tomato fruit pericarp are characterized by a wide range of ploidy levels (from 2C to 256C). Although various functional hypotheses have been attributed to endoreduplication according to the literature, evidence for a specific role of endoreduplication in transcription and metabolism control is still lacking. We have developed a new method based on bacterial artificial chromosome fluorescent in situ hybridization (BAC-FISH) that allows the in situ determination of DNA ploidy levels of individual nuclei. The advantage of this method is illustrated by the analysis of ploidy levels and cell sizes within the pericarp tissue from mature green tomato fruits. Using this cellular approach we established the ploidy map of the pericarp tissue. Based on this map, we performed a structural analysis of endoreduplicated nuclei at the level of chromatin organization, nuclear shape and relationship with mitochondria. We demonstrated a link between the ploidy level of nuclei, the complexity of their shape and the number of mitochondria at the vicinity of polyploid nuclei. The use of the DNA FISH method demonstrated that endopolyploidy leads to the formation of polytene chromosomes, whereas the use of a RNA FISH method demonstrated that the rDNA transcription was increased during polyploidization. Performing quantitative PCR (qPCR) and RT-qPCR on sorted nuclei respectively, we confirmed that endoreduplication did amplified exponentially loci for a set of specific genes allowing us to demonstrade that endoreduplication results in an increasing transcriptional activity.
dc.language.isoen
dc.publisherJapanese Society for Plant Cell and Molecular Biology
dc.rights.urihttp://creativecommons.org/licenses/by/
dc.subject.enendoreduplication
dc.subject.enkinase
dc.subject.enplant
dc.subject.enfish
dc.subject.encell size
dc.subject.engrowth
dc.subject.enarabidopsis
dc.subject.engenome
dc.subject.enanaphase promoting complex
dc.subject.enbac fish
dc.subject.entranscription
dc.subject.entomato fruit
dc.subject.enkaryoplasmic homeostasis
dc.title.enThe structural and molecular analysis of endoreduplicated nuclei in tomato (Solanum lycopersicum) fruit provides evidence for a ploidy-dependent increase in transcriptional activity
dc.typeArticle de revue
dc.identifier.doi10.5511/plantbiotechnology.13.0319b
dc.subject.halSciences du Vivant [q-bio]/Biologie végétale
bordeaux.journalPlant Biotechnology
bordeaux.page301-307
bordeaux.volume30
bordeaux.issue3
bordeaux.peerReviewedoui
hal.identifierhal-01208676
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01208676v1
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