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The 5-methyl-deoxy-cytidine (5mdC) localization to reveal in situ the dynamics of DNA methylation chromatin pattern in a variety of plant organ and tissue cells during development

dc.contributor.authorSánchez Testillano, Pilar
dc.contributor.authorSolís González, María Teresa
dc.contributor.authorRisueño, María del Carmen
dc.date.accessioned2024-02-02T15:35:53Z
dc.date.available2024-02-02T15:35:53Z
dc.date.issued2012
dc.descriptionWork supported by projects granted by the Spanish Ministry of Science and Innovation (MICINN), BFU2011-23752, BFU2008-00203 and AGL2008-04255, and CSIC, PIE 201020E038.
dc.description.abstractDNA methylation of cytosine residues constitutes a prominent epigenetic modification of the chromatin fiber which is locked in a transcriptionally inactive conformation leading to gene silencing. Plant developmental processes, as differentiation and proliferation, are accompanied by chromatin remodeling and epigenetic reprogramming. Despite the increasing knowledge gained on the epigenetic mechanisms controlling plant developmental processes, the knowledge of the DNA methylation regulation during relevant developmental programs in flowering plants, such as gametogenesis or embryogenesis, is very limited. The analysis of global DNA methylation levels has been frequently conducted by high performance capillary electrophoresis, and more recently also by ELISA-based assays, which provided quantitative data of whole organs and tissues. Nevertheless, to investigate the DNA methylation dynamics during plant development in different cell types of the same organ, the analysis of spatial and temporal pattern of nuclear distribution of 5-methyl-deoxy-cytidine (5mdC) constitutes a potent approach. In this work, immunolocalization of 5mdC on sections and subsequent confocal laser microscopy analysis have been applied for in situ cellular analysis of a variety of plant cells, tissues and organs with different characteristics, e.g. hardness, heterogeneity, cell accessibility, tissue compactness, etc.; the results demonstrated the versatility and feasibility of the approach for different plant samples, and revealed defined DNA methylation nuclear patterns associated with differentiation and proliferation events of various plant cell types and developmental programs. Quantification of 5mdC immunofluorescence intensity by image analysis software also permitted to estimate differences in global DNA methylation levels among different cells types of the same organ during development.
dc.description.departmentDepto. de Genética, Fisiología y Microbiología
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (España)
dc.description.sponsorshipConsejo Superior de Investigaciones Científicas
dc.description.statuspub
dc.identifier.citationTestillano PS, Solís MT, Risueño MC. The 5-methyl-deoxy-cytidine (5mdC) localization to reveal in situ the dynamics of DNA methylation chromatin pattern in a variety of plant organ and tissue cells during development. Physiol Plant. 2013 Sep;149(1):104-13. doi: 10.1111/ppl.12015. Epub 2012 Dec 21. PMID: 23193951
dc.identifier.doi10.1111/PPL.12015
dc.identifier.essn1399-3054
dc.identifier.issn0031-9317
dc.identifier.officialurlhttps://doi.org/10.1111/ppl.12015
dc.identifier.pmid23193951
dc.identifier.urihttps://hdl.handle.net/20.500.14352/98401
dc.issue.number1
dc.journal.titlePhysiologia Plantarum
dc.language.isoeng
dc.page.final113
dc.page.initial104
dc.publisherWiley
dc.rights.accessRightsrestricted access
dc.subject.cdu576.32
dc.subject.cdu581.15
dc.subject.keywordEpigenetics
dc.subject.keywordPlant cell nucleus
dc.subject.keywordProliferation
dc.subject.keywordDifferentiation
dc.subject.keywordQuiescent cell
dc.subject.keywordCycling cell
dc.subject.keywordConfocal microscopy
dc.subject.keywordChromosomes
dc.subject.ucmBiología celular (Biología)
dc.subject.ucmBiotecnología
dc.subject.unesco2407 Biología Celular
dc.subject.unesco2417.12 Citología Vegetal
dc.titleThe 5-methyl-deoxy-cytidine (5mdC) localization to reveal in situ the dynamics of DNA methylation chromatin pattern in a variety of plant organ and tissue cells during development
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number149
dspace.entity.typePublication
relation.isAuthorOfPublication3da5e099-3087-4d19-8ed0-60a12692e004
relation.isAuthorOfPublication.latestForDiscovery3da5e099-3087-4d19-8ed0-60a12692e004

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