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dc.provenanceCONICET-
dc.creatorPombo, Marina Alejandra-
dc.creatorZheng, Yi-
dc.creatorFei, Zhangjun-
dc.creatorMartin, Gregory B.-
dc.creatorRosli, Hernan Guillermo-
dc.date2018-11-23T22:07:06Z-
dc.date2018-11-23T22:07:06Z-
dc.date2017-03-
dc.date2018-10-22T22:31:17Z-
dc.date.accessioned2019-04-29T15:44:36Z-
dc.date.available2019-04-29T15:44:36Z-
dc.date.issued2017-03-
dc.identifierPombo, Marina Alejandra; Zheng, Yi; Fei, Zhangjun; Martin, Gregory B.; Rosli, Hernan Guillermo; Use of RNA-seq data to identify and validate RT-qPCR reference genes for studying the tomato-Pseudomonas pathosystem; Nature Publishing Group; Scientific Reports; 7; 3-2017; 1-11; 44905-
dc.identifier2045-2322-
dc.identifierhttp://hdl.handle.net/11336/65099-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/300864-
dc.descriptionThe agronomical relevant tomato-Pseudomonas syringae pv. tomato pathosystem is widely used to explore and understand the underlying mechanisms of the plant immune response. Transcript abundance estimation, mainly through reverse transcription-quantitative PCR (RT-qPCR), is a common approach employed to investigate the possible role of a candidate gene in certain biological process under study. The accuracy of this technique relies heavily on the selection of adequate reference genes. Initially, genes derived from other techniques (such as Northern blots) were used as reference genes in RT-qPCR experiments, but recent studies in different systems suggest that many of these genes are not stably expressed. The development of high throughput transcriptomic techniques, such as RNA-seq, provides an opportunity for the identification of transcriptionally stable genes that can be adopted as novel and robust reference genes. Here we take advantage of a large set of RNA-seq data originating from tomato leaves infiltrated with different immunity inducers and bacterial strains. We assessed and validated 9 genes that are much more stable than two traditional reference genes. Specifically, ARD2 and VIN3 were the most stably expressed genes and consequently we propose they be adopted for RT-qPCR experiments involving this pathosystem.-
dc.descriptionFil: Pombo, Marina Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Fisiología Vegetal. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Instituto de Fisiología Vegetal; Argentina-
dc.descriptionFil: Zheng, Yi. Boyce Thompson Institute for Plant Research; Estados Unidos-
dc.descriptionFil: Fei, Zhangjun. Boyce Thompson Institute for Plant Research; Estados Unidos. United States Department of Agriculture; Estados Unidos-
dc.descriptionFil: Martin, Gregory B.. Boyce Thompson Institute for Plant Research; Estados Unidos. Cornell University; Estados Unidos-
dc.descriptionFil: Rosli, Hernan Guillermo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Fisiología Vegetal. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Instituto de Fisiología Vegetal; Argentina-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherNature Publishing Group-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1038/srep44905-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.nature.com/articles/srep44905-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.source.urihttp://hdl.handle.net/11336/65099-
dc.subjectRT-qPCR-
dc.subjectreference-
dc.subjectRNA-seq-
dc.subjecttomato-
dc.subjectPseudomonas syringae-
dc.subjectplant immunity-
dc.subjectOtras Ciencias Biológicas-
dc.subjectCiencias Biológicas-
dc.subjectCIENCIAS NATURALES Y EXACTAS-
dc.titleUse of RNA-seq data to identify and validate RT-qPCR reference genes for studying the tomato-Pseudomonas pathosystem-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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