Evidence map›Paper›PMID 41058318›Full record

ArticlePest management science2026

RNA degradomics and proteomics reveal the mechanism of dsProsβ1-mediated proteasome targeting in Psylliodes chrysocephala.

Doga Cedden, Gözde Güney, Michael Rostás, Stefan Scholten

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Article in Pest management science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Doga CeddenDepartment of Evolutionary Developmental Genetics, Johann-Friedrich-Blumenbach Institute, GZMB, University of Göttingen, Göttingen, Germany.ORCID https://orcid.org/0000-0001-9031-3710
Gözde GüneyAgricultural Entomology, Department of Crop Sciences, University of Göttingen, Göttingen, Germany.
Michael RostásAgricultural Entomology, Department of Crop Sciences, University of Göttingen, Göttingen, Germany.ORCID https://orcid.org/0000-0001-9722-6513
Stefan ScholtenDivision of Crop Plant Genetics, Department of Crop Sciences, University of Göttingen, Göttingen, Germany.

Funding

Deutscher Akademischer Austauschdienst
6 · The paper itself

Abstract

backgroundThe cabbage stem flea beetle (CSFB, Psylliodes chrysocephala) is a major threat to oilseed rape crops. Management of CSFB has become increasingly challenging owing to the European Union's ban on neonicotinoids and the emergence of pyrethroid-resistant populations. Recently, RNA interference (RNAi) has shown potential as an environmentally-friendly alternative for the management of CSFB, and proteasome subunits have been identified as very effective RNAi targets. However, the mode-of-action (MoA) of proteasome-targeting RNAi strategies remains to be fully characterized at the molecular level in CSFB and other pests. Here, we used CSFB to investigate the MoA of dsProsβ1, which is a double-stranded (ds)RNA targeting a proteasome subunit.

resultsRNA degradome sequencing identified small interfering (si)RNA-mediated cleavage events in the target transcript, with cleavage events occurring at higher rates between uracil-guanine and adenine-adenine pairs. RISC-bound small RNA sequencing (sRNA-seq) confirmed the presence of mature siRNAs guiding these cleavage events while revealing discrepancies between siRNA abundance and cleavage patterns. Proteomics analysis identified changes in protein levels caused by proteasome inhibition, including an increase in mitochondria- and cytoskeleton-related proteins and a decrease in proteins related to transcription and translation.

conclusionThis study demonstrates that combining RNA degradomics, RISC-bound sRNA-seq, and proteomics is an insightful approach to investigating the mechanism of RNAi-based pest control at the molecular level. The information gained from these methods can be used to enhance proteasome-targeting RNAi strategies against insect pests. © 2025 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Indexed as

HemipteraInsect ProteinsProteasome Endopeptidase ComplexRNA, Double-StrandedRNA InterferenceAnimalsProteomicsRNA, Small InterferingInsect ProteinsProteasome Endopeptidase ComplexRNA, Double-StrandedRNA, Small Interferingcabbage stem flea beetleMoApest controlproteasomeRNAitarget gene

Identifiers

PMID41058318
PMCPMC13665646

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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 OpenQuestion graph.