File:Trans-kingdom-Cross-Talk-Small-RNAs-on-the-Move-pgen.1004602.g001.jpg

Trans-kingdom-Cross-Talk-Small-RNAs-on-the-Move-pgen.1004602.g001.jpg(739 × 346 pixels, file size: 68 KB, MIME type: image/jpeg)

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English: A,

Botrytis cinerea can transfer Bc-siRNA to its host. This process has been shown to be dependent on AGO1 in the host, Arabidopsis thaliana and on both Dcl1 and 2 in Botrytis cinerea [23]. B, Human miRNAs can be translocated to the malaria-parasite, P. falciparum, where they interfere with translation [16]. C, The nematode C. elegans has been shown to take up E. coli-produced ncRNAs that subsequently influence their foraging behavior. This is dependent on the C. elegans protein RDE-2, that is essential for RNAi [17]. D, The Chagas disease-causing parasite, T cruzi, produces tRNA-derived sRNAs (tsRNAs) that are exported from the cell in vesicles. These vesicles are shown to increase infectability of host cells, suggesting this might be caused by the tsRNAs. This has not been shown directly though [14]. E, The expression of sRNA-generating constructs to silence genes in pathogens, or other closely associated species, has now been demonstrated for many species combinations. This process is suggested to be dependent on Dcl1, since Dcl2, 3, and 4 seem to be dispensable to induce silencing by an Arabidopsis-expressed hairpin in the insect, Helicoverpa armigera

[24].
Date
Source Image file from Knip M, Constantin M, Thordal-Christensen H (2014). "Trans-kingdom Cross-Talk: Small RNAs on the Move". PLOS Genetics. DOI:10.1371/journal.pgen.1004602. PMID 25188222. PMC: 4154666.
Author Knip M, Constantin M, Thordal-Christensen H
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September 2014

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current10:08, 9 September 2014Thumbnail for version as of 10:08, 9 September 2014739 × 346 (68 KB)Recitation-botAutomatic upload of media from: doi:10.1371/journal.pgen.1004602

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