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Deep Sequencing Reveals Transcriptome Re-Programming of Cells to the Elicitation with Methyl Jasmonate

dc.contributor.authorSun, Guiling
dc.contributor.authorYang, Yanfang
dc.contributor.authorXie, Fuliang
dc.contributor.authorWen, Jian-Fan
dc.contributor.authorWu, Jianqiang
dc.contributor.authorWilson, Iain W.
dc.contributor.authorTang, Qi
dc.contributor.authorLiu, Hongwei
dc.contributor.authorQiu, Deyou
dc.date.accessioned2016-06-03T15:42:34Z
dc.date.available2016-06-03T15:42:34Z
dc.date.issued2013
dc.description.abstractBackground Plant cell culture represents an alternative source for producing high-value secondary metabolites including paclitaxel (Taxol®), which is mainly produced in Taxus and has been widely used in cancer chemotherapy. The phytohormone methyl jasmonate (MeJA) can significantly increase the production of paclitaxel, which is induced in plants as a secondary metabolite possibly in defense against herbivores and pathogens. In cell culture, MeJA also elicits the accumulation of paclitaxel; however, the mechanism is still largely unknown. Methodology/Principal Findings To obtain insight into the global regulation mechanism of MeJA in the steady state of paclitaxel production (7 days after MeJA addition), especially on paclitaxel biosynthesis, we sequenced the transcriptomes of MeJA-treated and untreated Taxus × media cells and obtained ∼ 32.5 M high quality reads, from which 40,348 unique sequences were obtained by de novo assembly. Expression level analysis indicated that a large number of genes were associated with transcriptional regulation, DNA and histone modification, and MeJA signaling network. All the 29 known genes involved in the biosynthesis of terpenoid backbone and paclitaxel were found with 18 genes showing increased transcript abundance following elicitation of MeJA. The significantly up-regulated changes of 9 genes in paclitaxel biosynthesis were validated by qRT-PCR assays. According to the expression changes and the previously proposed enzyme functions, multiple candidates for the unknown steps in paclitaxel biosynthesis were identified. We also found some genes putatively involved in the transport and degradation of paclitaxel. Potential target prediction of miRNAs indicated that miRNAs may play an important role in the gene expression regulation following the elicitation of MeJA. Conclusions/Significance Our results shed new light on the global regulation mechanism by which MeJA regulates the physiology of Taxus cells and is helpful to understand how MeJA elicits other plant species besides Taxus.en_US
dc.identifier.citationPLoS ONE; 8:4 p. 1-13en_US
dc.identifier.doi10.1371/journal.pone.0062865
dc.identifier.issn1932-6203
dc.identifier.pmidpmc3639896en_US
dc.identifier.urihttp://hdl.handle.net/10342/5448
dc.relation.urihttp://journals.plos.org/plosone/article?id=10.1371/journal.pone.0062865en_US
dc.subjectBiosynthesisen_US
dc.subjectGene expressionen_US
dc.subjectMicroRNAsen_US
dc.subjectTerpenesen_US
dc.titleDeep Sequencing Reveals Transcriptome Re-Programming of Cells to the Elicitation with Methyl Jasmonateen_US
dc.typeArticleen_US
ecu.journal.issue4en_US
ecu.journal.namePLoS ONEen_US
ecu.journal.pages1-13en_US
ecu.journal.volume8en_US

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