Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12870-015-0625-z
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dc.titleDevelopment of marker-free transgenic Jatropha curcas producing curcin-deficient seeds through endosperm-specific RNAi-mediated gene silencing
dc.contributor.authorGu, K
dc.contributor.authorTian, D
dc.contributor.authorMao, H
dc.contributor.authorWu, L
dc.contributor.authorYin, Z
dc.date.accessioned2020-09-04T02:08:23Z
dc.date.available2020-09-04T02:08:23Z
dc.date.issued2015
dc.identifier.citationGu, K, Tian, D, Mao, H, Wu, L, Yin, Z (2015). Development of marker-free transgenic Jatropha curcas producing curcin-deficient seeds through endosperm-specific RNAi-mediated gene silencing. BMC Plant Biology 15 (1) : 242. ScholarBank@NUS Repository. https://doi.org/10.1186/s12870-015-0625-z
dc.identifier.issn14712229
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174278
dc.description.abstractBackground: Jatropha curcas L. is a potential biofuel plant and its seed oil is suitable for biodiesel production. Despite this promising application, jatropha seeds contain two major toxic components, namely phorbol esters and curcins. These compounds would reduce commercial value of seed cake and raise safety and environment concerns on jatropha plantation and processing. Curcins are Type I ribosome inactivating proteins. Several curcin genes have been identified in the jatropha genome. Among which, the Curcin 1 (C1) gene is identified to be specifically expressed in endosperm, whereas the Curcin 2A (C2A) is mainly expressed in young leaves. Results: A marker-free RNAi construct carrying a ?-estradiol-regulated Cre/loxP system and a C1 promoter-driven RNAi cassette for C1 gene was made and used to generate marker-free transgenic RNAi plants to specifically silence the C1 gene in the endosperm of J. curcas. Plants of transgenic line L1, derived from T0-1, carry two copies of marker-free RNAi cassette, whereas plants of L35, derived from T0-35, harbored one copy of marker-free RNAi cassette and three copies of closely linked and yet truncated Hpt genes. The C1 protein content in endosperm of L1 and L35 seeds was greatly reduced or undetectable, while the C2A proteins in young leaves of T0-1 and T0-35 plants were unaffected. In addition, the C1 mRNA transcripts were undetectable in the endosperm of T3 seeds of L1 and L35. The results demonstrated that the expression of the C1 gene was specifically down-regulated or silenced by the double-stranded RNA-mediated RNA interference generated from the RNAi cassette. Conclusion: The C1 promoter-driven RNAi cassette for the C1 gene in transgenic plants was functional and heritable. Both C1 transcripts and C1 proteins were greatly down-regulated or silenced in the endosperm of transgenic J. curcas. The marker-free transgenic plants and curcin-deficient seeds developed in this study provided a solution for the toxicity of curcins in jatropha seeds and addressed the safety concerns of the marker genes in transgenic plants on the environments. © 2015 Gu et al.
dc.publisherBioMed Central Ltd.
dc.sourceUnpaywall 20200831
dc.subjectbacterial DNA
dc.subjectcurcin protein, Jatropha curcas
dc.subjectgenetic marker
dc.subjectmessenger RNA
dc.subjectribosome inactivating protein 1
dc.subjectT-DNA
dc.subjectantibody specificity
dc.subjectbiosynthesis
dc.subjectendosperm
dc.subjectgene expression regulation
dc.subjectgenetic marker
dc.subjectgenetics
dc.subjectJatropha
dc.subjectmetabolism
dc.subjectNorthern blotting
dc.subjectplant seed
dc.subjectpolymerase chain reaction
dc.subjectRNA interference
dc.subjectSouthern blotting
dc.subjecttransgenic plant
dc.subjectWestern blotting
dc.subjectBlotting, Northern
dc.subjectBlotting, Southern
dc.subjectBlotting, Western
dc.subjectDNA, Bacterial
dc.subjectEndosperm
dc.subjectGene Expression Regulation, Plant
dc.subjectGenetic Markers
dc.subjectJatropha
dc.subjectOrgan Specificity
dc.subjectPlants, Genetically Modified
dc.subjectPolymerase Chain Reaction
dc.subjectRibosome Inactivating Proteins, Type 1
dc.subjectRNA Interference
dc.subjectRNA, Messenger
dc.subjectSeeds
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1186/s12870-015-0625-z
dc.description.sourcetitleBMC Plant Biology
dc.description.volume15
dc.description.issue1
dc.description.page242
dc.published.statePublished
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