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dc.contributor.authorSolís, María Teresaes_ES
dc.contributor.authorBerenguer, Eduardoes_ES
dc.contributor.authorRisueño, María Carmenes_ES
dc.contributor.authorTestillano, Pilar S.es_ES
dc.date.accessioned2016-09-15T10:37:29Z-
dc.date.available2016-09-15T10:37:29Z-
dc.date.issued2016-08-11-
dc.identifier.citationBMC Plant Biology 16: 176 (2016)es_ES
dc.identifier.issn1471-2229-
dc.identifier.urihttp://hdl.handle.net/10261/136820-
dc.description15 p.-9 fig.es_ES
dc.description.abstractBackground: Pectins are one of the main components of plant cell walls. They are secreted to the wall as highly methylesterified forms that can be de-esterified by pectin methylesterases (PMEs). The degree of methylesterification of pectins changes during development, PMEs are involved in the cell wall remodeling that occurs during diverse plant developmental processes. Nevertheless, the functional meaning of pectin-related wall remodeling in different cell types and processes remains unclear. In vivo, the microspore follows the gametophytic pathway and differentiates to form the pollen grain. In vitro, the microspore can be reprogrammed by stress treatments becoming a totipotent cell that starts to proliferate and follows the embryogenic pathway, a process known as microspore embryogenesis.es_ES
dc.description.abstractResults: To investigate if the change of developmental programme of the microspore towards embryogenesis involves changes in pectin esterification levels, which would cause the cell wall remodeling during the process, in the present study, dynamics of PME expression and degrees of pectin esterification have been analysed during microspore embryogenesis and compared with the gametophytic development, in Brassica napus. A multidisciplinary approach has been adopted including BnPME gene expression analysis by quantitative RT-PCR, fluorescence in situ hybridization, immuno-dot-blot and immunofluorescence with JIM5 and JIM7 antibodies to reveal low and highly-methylesterified pectins. The results showed that cell differentiation at advanced developmental stages involved induction of BnPME expression and pectin de-esterification, processes that were also detected in zygotic embryos, providing additional evidence that microspore embryogenesis mimics zygotic embryogenesis. By contrast, early microspore embryogenesis, totipotency and proliferation were associated with low expression of BnPME and high levels of esterified pectins.es_ES
dc.description.abstractConclusions: The results show that the change of developmental programme of the microspore involves changes in pectin esterification associated with proliferation and differentiation events, which may cause the cell wall remodeling during the process. The findings indicate pectin-related modifications in the cell wall during microspore embryogenesis,providing new insights into the role of pectin esterification and cell wall configuration in microspore totipotency,embryogenesis induction and progression.es_ES
dc.description.sponsorshipWork supported by projects (BFU2011-23752, AGL2014-52028-R) funded by the Spanish Ministry of Economy and Competitiveness (MINECO) and the European Regional Development Fund (ERDF/FEDER).es_ES
dc.description.sponsorshipWe acknowledge support by the CSIC Open Access Publication Initiative through its Unit of Information Resources for Research (URICI).-
dc.language.isoenges_ES
dc.publisherBioMed Centrales_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/AGL2014-52028-R-
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.subjectPectin methylesterase,es_ES
dc.subjectPectin esterification,es_ES
dc.subjectCell wall remodellinges_ES
dc.subjectCell reprogramminges_ES
dc.subjectMicrospore embryogenesises_ES
dc.subjectPollenes_ES
dc.subjectGametophytic developmentes_ES
dc.subjectTotipotencyes_ES
dc.subjectDifferentiationes_ES
dc.subjectProliferationes_ES
dc.titleBnPME is progressively induced after microspore reprogramming to embryogenesis, correlating with pectin de-esterification and cell differentiation in Brassica napuses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1186/s12870-016-0863-8-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/ 10.1186/s12870-016-0863-8es_ES
dc.identifier.e-issn1471-2229-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0/es_ES
dc.contributor.funderMinisterio de Economía y Competitividad (España)es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.contributor.funderCSIC - Unidad de Recursos de Información Científica para la Investigación (URICI)-
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.pmid27514748-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.languageiso639-1en-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairetypeartículo-
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