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Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence

The exchange of small RNAs (sRNAs) between hosts and pathogens can lead to gene silencing in the recipient organism, a mechanism termed cross-kingdom RNAi (ck-RNAi). While fungal sRNAs promoting virulence are established, the significance of ck-RNAi in distinct plant pathogens is not clear. Here, we...

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Autores principales: Dunker, Florian, Trutzenberg, Adriana, Rothenpieler, Jan S, Kuhn, Sarah, Pröls, Reinhard, Schreiber, Tom, Tissier, Alain, Kemen, Ariane, Kemen, Eric, Hückelhoven, Ralph, Weiberg, Arne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297541/
https://www.ncbi.nlm.nih.gov/pubmed/32441255
http://dx.doi.org/10.7554/eLife.56096
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author Dunker, Florian
Trutzenberg, Adriana
Rothenpieler, Jan S
Kuhn, Sarah
Pröls, Reinhard
Schreiber, Tom
Tissier, Alain
Kemen, Ariane
Kemen, Eric
Hückelhoven, Ralph
Weiberg, Arne
author_facet Dunker, Florian
Trutzenberg, Adriana
Rothenpieler, Jan S
Kuhn, Sarah
Pröls, Reinhard
Schreiber, Tom
Tissier, Alain
Kemen, Ariane
Kemen, Eric
Hückelhoven, Ralph
Weiberg, Arne
author_sort Dunker, Florian
collection PubMed
description The exchange of small RNAs (sRNAs) between hosts and pathogens can lead to gene silencing in the recipient organism, a mechanism termed cross-kingdom RNAi (ck-RNAi). While fungal sRNAs promoting virulence are established, the significance of ck-RNAi in distinct plant pathogens is not clear. Here, we describe that sRNAs of the pathogen Hyaloperonospora arabidopsidis, which represents the kingdom of oomycetes and is phylogenetically distant from fungi, employ the host plant’s Argonaute (AGO)/RNA-induced silencing complex for virulence. To demonstrate H. arabidopsidis sRNA (HpasRNA) functionality in ck-RNAi, we designed a novel CRISPR endoribonuclease Csy4/GUS reporter that enabled in situ visualization of HpasRNA-induced target suppression in Arabidopsis. The significant role of HpasRNAs together with AtAGO1 in virulence was revealed in plant atago1 mutants and by transgenic Arabidopsis expressing a short-tandem-target-mimic to block HpasRNAs, that both exhibited enhanced resistance. HpasRNA-targeted plant genes contributed to host immunity, as Arabidopsis gene knockout mutants displayed quantitatively enhanced susceptibility.
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spelling pubmed-72975412020-06-18 Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence Dunker, Florian Trutzenberg, Adriana Rothenpieler, Jan S Kuhn, Sarah Pröls, Reinhard Schreiber, Tom Tissier, Alain Kemen, Ariane Kemen, Eric Hückelhoven, Ralph Weiberg, Arne eLife Microbiology and Infectious Disease The exchange of small RNAs (sRNAs) between hosts and pathogens can lead to gene silencing in the recipient organism, a mechanism termed cross-kingdom RNAi (ck-RNAi). While fungal sRNAs promoting virulence are established, the significance of ck-RNAi in distinct plant pathogens is not clear. Here, we describe that sRNAs of the pathogen Hyaloperonospora arabidopsidis, which represents the kingdom of oomycetes and is phylogenetically distant from fungi, employ the host plant’s Argonaute (AGO)/RNA-induced silencing complex for virulence. To demonstrate H. arabidopsidis sRNA (HpasRNA) functionality in ck-RNAi, we designed a novel CRISPR endoribonuclease Csy4/GUS reporter that enabled in situ visualization of HpasRNA-induced target suppression in Arabidopsis. The significant role of HpasRNAs together with AtAGO1 in virulence was revealed in plant atago1 mutants and by transgenic Arabidopsis expressing a short-tandem-target-mimic to block HpasRNAs, that both exhibited enhanced resistance. HpasRNA-targeted plant genes contributed to host immunity, as Arabidopsis gene knockout mutants displayed quantitatively enhanced susceptibility. eLife Sciences Publications, Ltd 2020-05-22 /pmc/articles/PMC7297541/ /pubmed/32441255 http://dx.doi.org/10.7554/eLife.56096 Text en © 2020, Dunker et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
Dunker, Florian
Trutzenberg, Adriana
Rothenpieler, Jan S
Kuhn, Sarah
Pröls, Reinhard
Schreiber, Tom
Tissier, Alain
Kemen, Ariane
Kemen, Eric
Hückelhoven, Ralph
Weiberg, Arne
Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence
title Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence
title_full Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence
title_fullStr Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence
title_full_unstemmed Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence
title_short Oomycete small RNAs bind to the plant RNA-induced silencing complex for virulence
title_sort oomycete small rnas bind to the plant rna-induced silencing complex for virulence
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297541/
https://www.ncbi.nlm.nih.gov/pubmed/32441255
http://dx.doi.org/10.7554/eLife.56096
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