Distinct Effects of p19 RNA Silencing Suppressor on Small RNA Mediated Pathways in Plants
Nicotiana
0301 basic medicine
570
QH301-705.5
Blotting, Western
Electrophoretic Mobility Shift Assay
630
Tombusvirus
Viral Proteins
03 medical and health sciences
Immunoprecipitation
Biology (General)
RNA, Small Interfering
Plant Diseases
Plant Proteins
Silencing
High-Throughput Nucleotide Sequencing
RC581-607
P19
Blotting, Northern
Plants, Genetically Modified
3. Good health
Q1 Science (General) / természettudomány általában
RNA, Plant
siRNA
RNAi
Immunologic diseases. Allergy
Research Article
DOI:
10.1371/journal.ppat.1005935
Publication Date:
2016-10-06T14:01:23Z
AUTHORS (10)
ABSTRACT
RNA silencing is one of the main defense mechanisms employed by plants to fight viruses. In change, viruses have evolved silencing suppressor proteins to neutralize antiviral silencing. Since the endogenous and antiviral functions of RNA silencing pathway rely on common components, it was suggested that viral suppressors interfere with endogenous silencing pathway contributing to viral symptom development. In this work, we aimed to understand the effects of the tombusviral p19 suppressor on endogenous and antiviral silencing during genuine virus infection. We showed that ectopically expressed p19 sequesters endogenous small RNAs (sRNAs) in the absence, but not in the presence of virus infection. Our presented data question the generalized model in which the sequestration of endogenous sRNAs by the viral suppressor contributes to the viral symptom development. We further showed that p19 preferentially binds the perfectly paired ds-viral small interfering RNAs (vsiRNAs) but does not select based on their sequence or the type of the 5' nucleotide. Finally, co-immunoprecipitation of sRNAs with AGO1 or AGO2 from virus-infected plants revealed that p19 specifically impairs vsiRNA loading into AGO1 but not AGO2. Our findings, coupled with the fact that p19-expressing wild type Cymbidium ringspot virus (CymRSV) overcomes the Nicotiana benthamiana silencing based defense killing the host, suggest that AGO1 is the main effector of antiviral silencing in this host-virus combination.
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