Evidence map›Paper›PMID 41708483›Full record

ArticleMolecular plant pathology2026

The Molecular Cochaperone NbSGT1 May Function as an Endogenous Suppressor of RNA Silencing That Is Recruited by a Potyvirus in Infection of Plants.

Wei Shi, Liwen Zhang, Na Li, Bei Gou, Li Qin, Wenping Qiu, Hongguang Cui, Hui Wang, Zhaoji Dai

Abstract read
In one paragraph

Article in Molecular plant pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Wei ShiKey Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests (Ministry of Education), School of Tropical Agriculture and Forestry, Hainan University, Haikou, Hainan, China.
Liwen ZhangKey Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests (Ministry of Education), School of Tropical Agriculture and Forestry, Hainan University, Haikou, Hainan, China.
Na LiKey Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests (Ministry of Education), School of Tropical Agriculture and Forestry, Hainan University, Haikou, Hainan, China.
Bei GouKey Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests (Ministry of Education), School of Tropical Agriculture and Forestry, Hainan University, Haikou, Hainan, China.
Li QinKey Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests (Ministry of Education), School of Tropical Agriculture and Forestry, Hainan University, Haikou, Hainan, China.
Wenping QiuSchool of Agriculture Science and Conservation, Missouri State University, Springfield, Missouri, USA.
Hongguang CuiKey Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests (Ministry of Education), School of Tropical Agriculture and Forestry, Hainan University, Haikou, Hainan, China.ORCID 0000-0001-9770-6621
Hui WangHainan Provincial Agricultural Machinery Appraisal and Extension Station, Haikou, Hainan, China.
Zhaoji DaiKey Laboratory of Green Prevention and Control of Tropical Plant Diseases and Pests (Ministry of Education), School of Tropical Agriculture and Forestry, Hainan University, Haikou, Hainan, China.ORCID 0000-0002-0001-6200

Funding

Graduate Innovation Research Project of Hainan Province Qhyb2023-84National Natural Science Foundation of China 32360651National Natural Science Foundation of China 32372484
6 · The paper itself

Abstract

Recent evidence indicates that plant cells contain specific endogenous suppressors of RNA silencing (ESRs) that plant viruses can exploit to counteract host defences. However, the underlying mechanisms are not yet fully understood. The helper component-proteinase (HC-Pro) of potyviruses is known to suppress RNA silencing and facilitate viral infection. Here, we used affinity purification followed by mass spectrometry to identify potential host proteins that interact with HC-Pro during telosma mosaic virus (TelMV, genus Potyvirus) infection in plants. We found that the molecular co-chaperone SGT1 (suppressor of the G2 allele of Skp1) interacts with HC-Pro via its SGS domain. Virus-induced gene silencing and RNAi-mediated knockdown of NbSGT1 resulted in decreased viral accumulation in Nicotiana benthamiana plants. Conversely, transient overexpression of NbSGT1 promoted TelMV multiplication. Through alanine-scanning mutagenesis, we identified three residues (K217, I227 and E332) in HC-Pro that are essential for its interaction with NbSGT1. Mutant viruses carrying these mutations exhibited reduced viral accumulation without affecting the RNA suppression of silencing (RSS) activity of HC-Pro. NbSGT1 enhanced the RSS activity of HC-Pro and increased the expression of foreign genes at both the protein and mRNA levels. Additionally, we demonstrated, through an Agrobacterium infiltratrion assay, that NbSGT1 may act as an ESR, inhibiting local but not systemic RNA silencing in plants. Finally, NbSGT1 significantly downregulated the expression of AGOs, DCLs, RDRs and SGS3, key genes of the RNA silencing pathway. Collectively, our findings provide evidence that the molecular co-chaperone SGT1 may act as a host ESR and is recruited by a potyvirus to facilitate viral infection.

Indexed as

Molecular ChaperonesNicotianaPlant DiseasesPlant ProteinsPotyvirusRNA InterferenceCysteine EndopeptidasesHost-Pathogen InteractionsViral ProteinsCysteine EndopeptidasesHC-Pro protein, potyvirusMolecular ChaperonesPlant ProteinsViral ProteinsESRHC‐PropotyvirusRNA silencingSGT1telosma mosaic virus

Identifiers

PMID41708483
PMCPMC12916245

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.