Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep27085
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dc.titleDrosophila cells use nanotube-like structures to transfer dsRNA and RNAi machinery between cells
dc.contributor.authorKarlikow, M
dc.contributor.authorGoic, B
dc.contributor.authorMongelli, V
dc.contributor.authorSalles, A
dc.contributor.authorSchmitt, C
dc.contributor.authorBonne, I
dc.contributor.authorZurzolo, C
dc.contributor.authorSaleh, M.-C
dc.date.accessioned2020-10-31T11:33:18Z
dc.date.available2020-10-31T11:33:18Z
dc.date.issued2016
dc.identifier.citationKarlikow, M, Goic, B, Mongelli, V, Salles, A, Schmitt, C, Bonne, I, Zurzolo, C, Saleh, M.-C (2016). Drosophila cells use nanotube-like structures to transfer dsRNA and RNAi machinery between cells. Scientific Reports 6 : 27085. ScholarBank@NUS Repository. https://doi.org/10.1038/srep27085
dc.identifier.issn2045-2322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/182465
dc.description.abstractTunnelling nanotubes and cytonemes function as highways for the transport of organelles, cytosolic and membrane-bound molecules, and pathogens between cells. During viral infection in the model organism Drosophila melanogaster, a systemic RNAi antiviral response is established presumably through the transport of a silencing signal from one cell to another via an unknown mechanism. Because of their role in cell-cell communication, we investigated whether nanotube-like structures could be a mediator of the silencing signal. Here, we describe for the first time in the context of a viral infection the presence of nanotube-like structures in different Drosophila cell types. These tubules, made of actin and tubulin, were associated with components of the RNAi machinery, including Argonaute 2, double-stranded RNA, and CG4572. Moreover, they were more abundant during viral, but not bacterial, infection. Super resolution structured illumination microscopy showed that Argonaute 2 and tubulin reside inside the tubules. We propose that nanotube-like structures are one of the mechanisms by which Argonaute 2, as part of the antiviral RNAi machinery, is transported between infected and non-infected cells to trigger systemic antiviral immunity in Drosophila.
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectactin
dc.subjectAGO2 protein, Drosophila
dc.subjectargonaute protein
dc.subjectdouble stranded RNA
dc.subjectDrosophila protein
dc.subjectenhanced green fluorescent protein
dc.subjectfluorescent protein 583
dc.subjectgreen fluorescent protein
dc.subjectphotoprotein
dc.subjectRab protein
dc.subjectRab7 protein
dc.subjecttubulin
dc.subjectviral protein
dc.subjectanimal
dc.subjectantagonists and inhibitors
dc.subjectcell communication
dc.subjectcell line
dc.subjectcell organelle
dc.subjectDicistroviridae
dc.subjectDrosophila melanogaster
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjectgrowth, development and aging
dc.subjectmetabolism
dc.subjectmicrobiology
dc.subjectPectobacterium carotovorum
dc.subjectreporter gene
dc.subjectRNA interference
dc.subjecttransport at the cellular level
dc.subjectultrastructure
dc.subjectvirology
dc.subjectActins
dc.subjectAnimals
dc.subjectArgonaute Proteins
dc.subjectBiological Transport
dc.subjectCell Communication
dc.subjectCell Line
dc.subjectDicistroviridae
dc.subjectDrosophila melanogaster
dc.subjectDrosophila Proteins
dc.subjectGene Expression Regulation
dc.subjectGenes, Reporter
dc.subjectGreen Fluorescent Proteins
dc.subjectLuminescent Proteins
dc.subjectOrganelles
dc.subjectPectobacterium carotovorum
dc.subjectrab GTP-Binding Proteins
dc.subjectRNA Interference
dc.subjectRNA, Double-Stranded
dc.subjectTubulin
dc.subjectViral Proteins
dc.typeArticle
dc.contributor.departmentLIFE SCIENCES INSTITUTE
dc.description.doi10.1038/srep27085
dc.description.sourcetitleScientific Reports
dc.description.volume6
dc.description.page27085
dc.published.statepublished
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