Diverse RNA viral effectors converge on facilitation of AGO4 degradation to promote infection

ARGONAUTE4 (AGO4)-mediated RNA-directed DNA methylation (RdDM) defends against DNA viruses by methylating their genomes. However, there is limited information available regarding RNA viruses. Here, we show that OsAGO4 has antiviral immunity against two different types of RNA viruses, rice stripe virus (RSV, Tenuivirus) and Southern rice black streaked dwarf virus (SRBSDV, Fijivirus). To facilitate infection, the evolutionarily distinct viral effectors RSV P2 and SRBSDV SP8 both targeted OsAGO4 for degradation. These unrelated viral proteins both recruited the F-box protein OsFBX68 to promote their association with OsAGO4, resulting in enhanced OsAGO4 degradation. In summary, our findings elucidated OsAGO4-mediated antiviral defense and reveal new mechanisms by which diverse RNA viral effectors exploit OsAGO4 to promote infection using a common counter-defense strategy.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-11-13
DOI
https://doi.org/10.1093/nar/gkaf1277
Primary Topic
Plant Virus Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Diverse RNA viral effectors converge on facilitation of AGO4 degradation to promote infection

Zhongtian Xu, Wenkai Yan, Zongtao Sun, Xiaodi Hu et al.
Nucleic Acids Research
Plant Virus Research Studies
article

Diverse RNA viral effectors converge on facilitation of AGO4 degradation to promote infection

Zhongtian Xu, Wenkai Yan, Zongtao Sun, Xiaodi Hu, Qingling Qi, Kaili Xie, Hehong Zhang, Yanjun Li, Lulu Li, Jianping Chen
article en

Abstract

ARGONAUTE4 (AGO4)-mediated RNA-directed DNA methylation (RdDM) defends against DNA viruses by methylating their genomes. However, there is limited information available regarding RNA viruses. Here, we show that OsAGO4 has antiviral immunity against two different types of RNA viruses, rice stripe virus (RSV, Tenuivirus) and Southern rice black streaked dwarf virus (SRBSDV, Fijivirus). To facilitate infection, the evolutionarily distinct viral effectors RSV P2 and SRBSDV SP8 both targeted OsAGO4 for degradation. These unrelated viral proteins both recruited the F-box protein OsFBX68 to promote their association with OsAGO4, resulting in enhanced OsAGO4 degradation. In summary, our findings elucidated OsAGO4-mediated antiviral defense and reveal new mechanisms by which diverse RNA viral effectors exploit OsAGO4 to promote infection using a common counter-defense strategy.

Nucleic Acids ResearchVol. 53(21)
Ningbo University (CN), Ministry of Agriculture and Rural Affairs (CN)
National Natural Science Foundation of China, Natural Science Foundation of Ningbo, National Key Research and Development Program of China, Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 74%
Plant Virus Research Studies
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Diverse RNA viral effectors converge on facilitation of AGO4 degradation to promote infection — Zhongtian Xu, Wenkai Yan, et al. · Nucleic Acids Research (2025) | TGRS Research Map | TGRS