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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/112840
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dc.contributor.authorLopes, Fabricio R.-
dc.contributor.authorJjingo, Daudi-
dc.contributor.authorSilva, Carlos R. M. da-
dc.contributor.authorAndrade, Alan C.-
dc.contributor.authorMarraccini, Pierre-
dc.contributor.authorTeixeira, Joao B.-
dc.contributor.authorCarazzolle, Marcelo F.-
dc.contributor.authorPereira, Goncalo A. G.-
dc.contributor.authorPereira, Luiz Filipe P.-
dc.contributor.authorVanzela, Andre L. L.-
dc.contributor.authorWang, Lu-
dc.contributor.authorKing Jordan, I.-
dc.contributor.authorCarareto, Claudia M. A.-
dc.date.accessioned2014-12-03T13:11:05Z-
dc.date.accessioned2016-10-25T20:12:07Z-
dc.date.available2014-12-03T13:11:05Z-
dc.date.available2016-10-25T20:12:07Z-
dc.date.issued2013-11-11-
dc.identifierhttp://dx.doi.org/10.1371/journal.pone.0078931-
dc.identifier.citationPlos One. San Francisco: Public Library Science, v. 8, n. 11, 16 p., 2013.-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/11449/112840-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/112840-
dc.description.abstractPlant genomes are massively invaded by transposable elements (TEs), many of which are located near host genes and can thus impact gene expression. In flowering plants, TE expression can be activated (de-repressed) under certain stressful conditions, both biotic and abiotic, as well as by genome stress caused by hybridization. In this study, we examined the effects of these stress agents on TE expression in two diploid species of coffee, Coffea canephora and C. eugenioides, and their allotetraploid hybrid C. arabica. We also explored the relationship of TE repression mechanisms to host gene regulation via the effects of exonized TE sequences. Similar to what has been seen for other plants, overall TE expression levels are low in Coffea plant cultivars, consistent with the existence of effective TE repression mechanisms. TE expression patterns are highly dynamic across the species and conditions assayed here are unrelated to their classification at the level of TE class or family. In contrast to previous results, cell culture conditions per se do not lead to the de-repression of TE expression in C. arabica. Results obtained here indicate that differing plant drought stress levels relate strongly to TE repression mechanisms. TEs tend to be expressed at significantly higher levels in non-irrigated samples for the drought tolerant cultivars but in drought sensitive cultivars the opposite pattern was shown with irrigated samples showing significantly higher TE expression. Thus, TE genome repression mechanisms may be finely tuned to the ideal growth and/or regulatory conditions of the specific plant cultivars in which they are active. Analysis of TE expression levels in cell culture conditions underscored the importance of nonsense-mediated mRNA decay (NMD) pathways in the repression of Coffea TEs. These same NMD mechanisms can also regulate plant host gene expression via the repression of genes that bear exonized TE sequences.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipCentre de Cooperation Internationale en Recherche Agronomique pour le Developpement-
dc.format.extent16-
dc.language.isoeng-
dc.publisherPublic Library Science-
dc.sourceWeb of Science-
dc.titleTranscriptional Activity, Chromosomal Distribution and Expression Effects of Transposable Elements in Coffea Genomesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionGeorgia Inst Technol-
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)-
dc.contributor.institutionEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)-
dc.contributor.institutionCtr Cooperat Int Rech Agron Dev-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionPanAmer Bioinformat Inst-
dc.description.affiliationUniv Estadual Paulista, Univ Estadual Paulista Julio de Mesquita Filho, Dept Biol, Sao Jose do Rio Preto, Brazil-
dc.description.affiliationGeorgia Inst Technol, Sch Biol, Atlanta, GA 30332 USA-
dc.description.affiliationUniv Estadual Londrina, Dept Biol Geral, Londrina, Brazil-
dc.description.affiliationEmpresa Brasileira Pesquisa Agr Recursos Genet &, Brasilia, DF, Brazil-
dc.description.affiliationCtr Cooperat Int Rech Agron Dev, UMR AGAP, Montpellier, France-
dc.description.affiliationUniv Estadual Campinas, Dept Genet Evolucao & Bioagentes, Campinas, SP, Brazil-
dc.description.affiliationEmpresa Brasileira Pesquisa Agr Cafe, Brasilia, DF, Brazil-
dc.description.affiliationPanAmer Bioinformat Inst, Santa Marta, Magdalena, Colombia-
dc.description.affiliationUnespUniv Estadual Paulista, Univ Estadual Paulista Julio de Mesquita Filho, Dept Biol, Sao Jose do Rio Preto, Brazil-
dc.description.sponsorshipIdFAPESP: 08/05894-1-
dc.description.sponsorshipIdFAPESP: 07/55985-0-
dc.identifier.doi10.1371/journal.pone.0078931-
dc.identifier.wosWOS:000327221600081-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000327221600081.pdf-
dc.relation.ispartofPLOS ONE-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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