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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-7297541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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