Misregulation of AUXIN RESPONSE FACTOR 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in Arabidopsis.

In Arabidopsis, micro (mi)RNAs and trans-acting (ta-si)RNAs synthesized directly or indirectly through the DICER-LIKE-1 (DCL1) ribonuclease have roles in patterning and hormonal responses, while DCL2,3,4-dependent small-interfering (si)RNAs are mainly involved in silencing of transposable elements a...

Full description

Bibliographic Details
Main Authors: Florence Jay, Yu Wang, Agnès Yu, Ludivine Taconnat, Sandra Pelletier, Vincent Colot, Jean-Pierre Renou, Olivier Voinnet
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-05-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC3093370?pdf=render
_version_ 1819236865521221632
author Florence Jay
Yu Wang
Agnès Yu
Ludivine Taconnat
Sandra Pelletier
Vincent Colot
Jean-Pierre Renou
Olivier Voinnet
author_facet Florence Jay
Yu Wang
Agnès Yu
Ludivine Taconnat
Sandra Pelletier
Vincent Colot
Jean-Pierre Renou
Olivier Voinnet
author_sort Florence Jay
collection DOAJ
description In Arabidopsis, micro (mi)RNAs and trans-acting (ta-si)RNAs synthesized directly or indirectly through the DICER-LIKE-1 (DCL1) ribonuclease have roles in patterning and hormonal responses, while DCL2,3,4-dependent small-interfering (si)RNAs are mainly involved in silencing of transposable elements and antiviral defense. Viral suppressors of RNA silencing (VSRs) produced by phytoviruses to counter plant defense may perturb plant developmental programs because of the collision of their inhibitory effects with the regulatory action of endogenous miRNAs and ta-siRNAs. This could explain the similar developmental aberrations displayed by Arabidopsis miRNA/ta-siRNA pathway mutants, including dcl1, and by some VSR-expressing plants. Nonetheless, the molecular bases for these morphological aberrations have remained mysterious, and their contribution to viral disease symptoms/virulence unexplored. The extent of VSR inhibitory actions to other types of endogenous small RNAs remains also unclear. Here, we present an in-depth analysis of transgenic Arabidopsis expressing constitutively HcPro, P19 and P15, three unrelated VSRs. We show that VSR expression has comparable, yet modest effects on known miRNA and ta-siRNA target RNA levels, similar to those observed using an hypomorphic dcl1 mutation. However, by combining results of transcriptome studies with deep-sequencing data from immuno-precipitated small RNAs, additional, novel endogenous targets of miRNA and ta-siRNA were identified, unraveling an unsuspected complexity in the origin and scope-of-action of these molecules. Other stringent analyses pinpointed misregulation of the miR167 target AUXIN RESPONSE FACTOR 8 (ARF8) as a major cause for the developmental aberrations exhibited by VSR transgenic plants, but also for the phenotypes induced during normal viral infection caused by the HcPro-encoding Turnip mosaic virus (TuMV). Neither RNA silencing, its suppression by VSRs, nor the virulence/accumulation of TuMV was altered by mutations in ARF8. These findings have important implications for our understanding of viral disease symptoms and small RNA-directed regulation of plant growth/development.
first_indexed 2024-12-23T13:11:14Z
format Article
id doaj.art-e82af17c62ff42da86d0f4a22900c7e2
institution Directory Open Access Journal
issn 1553-7366
1553-7374
language English
last_indexed 2024-12-23T13:11:14Z
publishDate 2011-05-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Pathogens
spelling doaj.art-e82af17c62ff42da86d0f4a22900c7e22022-12-21T17:45:44ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742011-05-0175e100203510.1371/journal.ppat.1002035Misregulation of AUXIN RESPONSE FACTOR 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in Arabidopsis.Florence JayYu WangAgnès YuLudivine TaconnatSandra PelletierVincent ColotJean-Pierre RenouOlivier VoinnetIn Arabidopsis, micro (mi)RNAs and trans-acting (ta-si)RNAs synthesized directly or indirectly through the DICER-LIKE-1 (DCL1) ribonuclease have roles in patterning and hormonal responses, while DCL2,3,4-dependent small-interfering (si)RNAs are mainly involved in silencing of transposable elements and antiviral defense. Viral suppressors of RNA silencing (VSRs) produced by phytoviruses to counter plant defense may perturb plant developmental programs because of the collision of their inhibitory effects with the regulatory action of endogenous miRNAs and ta-siRNAs. This could explain the similar developmental aberrations displayed by Arabidopsis miRNA/ta-siRNA pathway mutants, including dcl1, and by some VSR-expressing plants. Nonetheless, the molecular bases for these morphological aberrations have remained mysterious, and their contribution to viral disease symptoms/virulence unexplored. The extent of VSR inhibitory actions to other types of endogenous small RNAs remains also unclear. Here, we present an in-depth analysis of transgenic Arabidopsis expressing constitutively HcPro, P19 and P15, three unrelated VSRs. We show that VSR expression has comparable, yet modest effects on known miRNA and ta-siRNA target RNA levels, similar to those observed using an hypomorphic dcl1 mutation. However, by combining results of transcriptome studies with deep-sequencing data from immuno-precipitated small RNAs, additional, novel endogenous targets of miRNA and ta-siRNA were identified, unraveling an unsuspected complexity in the origin and scope-of-action of these molecules. Other stringent analyses pinpointed misregulation of the miR167 target AUXIN RESPONSE FACTOR 8 (ARF8) as a major cause for the developmental aberrations exhibited by VSR transgenic plants, but also for the phenotypes induced during normal viral infection caused by the HcPro-encoding Turnip mosaic virus (TuMV). Neither RNA silencing, its suppression by VSRs, nor the virulence/accumulation of TuMV was altered by mutations in ARF8. These findings have important implications for our understanding of viral disease symptoms and small RNA-directed regulation of plant growth/development.http://europepmc.org/articles/PMC3093370?pdf=render
spellingShingle Florence Jay
Yu Wang
Agnès Yu
Ludivine Taconnat
Sandra Pelletier
Vincent Colot
Jean-Pierre Renou
Olivier Voinnet
Misregulation of AUXIN RESPONSE FACTOR 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in Arabidopsis.
PLoS Pathogens
title Misregulation of AUXIN RESPONSE FACTOR 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in Arabidopsis.
title_full Misregulation of AUXIN RESPONSE FACTOR 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in Arabidopsis.
title_fullStr Misregulation of AUXIN RESPONSE FACTOR 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in Arabidopsis.
title_full_unstemmed Misregulation of AUXIN RESPONSE FACTOR 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in Arabidopsis.
title_short Misregulation of AUXIN RESPONSE FACTOR 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in Arabidopsis.
title_sort misregulation of auxin response factor 8 underlies the developmental abnormalities caused by three distinct viral silencing suppressors in arabidopsis
url http://europepmc.org/articles/PMC3093370?pdf=render
work_keys_str_mv AT florencejay misregulationofauxinresponsefactor8underliesthedevelopmentalabnormalitiescausedbythreedistinctviralsilencingsuppressorsinarabidopsis
AT yuwang misregulationofauxinresponsefactor8underliesthedevelopmentalabnormalitiescausedbythreedistinctviralsilencingsuppressorsinarabidopsis
AT agnesyu misregulationofauxinresponsefactor8underliesthedevelopmentalabnormalitiescausedbythreedistinctviralsilencingsuppressorsinarabidopsis
AT ludivinetaconnat misregulationofauxinresponsefactor8underliesthedevelopmentalabnormalitiescausedbythreedistinctviralsilencingsuppressorsinarabidopsis
AT sandrapelletier misregulationofauxinresponsefactor8underliesthedevelopmentalabnormalitiescausedbythreedistinctviralsilencingsuppressorsinarabidopsis
AT vincentcolot misregulationofauxinresponsefactor8underliesthedevelopmentalabnormalitiescausedbythreedistinctviralsilencingsuppressorsinarabidopsis
AT jeanpierrerenou misregulationofauxinresponsefactor8underliesthedevelopmentalabnormalitiescausedbythreedistinctviralsilencingsuppressorsinarabidopsis
AT oliviervoinnet misregulationofauxinresponsefactor8underliesthedevelopmentalabnormalitiescausedbythreedistinctviralsilencingsuppressorsinarabidopsis