High-throughput screening of E3 ubiquitin ligases identifies TRIM48 as a novel negative regulator of RIG-I signaling

The retinoic acid-inducible gene-I (RIG-I) signaling is crucial for cell-intrinsic innate antiviral immunity. Upon cytosolic detection of virus-associated RNA, it triggers a cascade inducing production of potent cytokines, mainly type I and III interferons (IFNs). While effective, dysregulated respo...

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Hauptverfasser: Wu, Guandi (VerfasserIn) , Frankish, Jamie (VerfasserIn) , Willemsen, Joschka (VerfasserIn) , Ricken, Dominik (VerfasserIn) , Becker, Jonas (VerfasserIn) , Schweinoch, Darius (VerfasserIn) , Beneke, Jürgen (VerfasserIn) , Wüst, Sandra (VerfasserIn) , Beil, Nina (VerfasserIn) , Matula, Petr (VerfasserIn) , Rohr, Karl (VerfasserIn) , Erfle, Holger (VerfasserIn) , Kaderali, Lars (VerfasserIn) , Binder, Marco (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: October 2025
In: Cellular signalling
Year: 2025, Jahrgang: 134, Pages: 1-18
ISSN:1873-3913
DOI:10.1016/j.cellsig.2025.111973
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1016/j.cellsig.2025.111973
Verlag, kostenfrei, Volltext: https://www.sciencedirect.com/science/article/pii/S0898656825003882
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Verfasserangaben:Guandi Wu, Jamie Frankish, Joschka Willemsen, Dominik Ricken, Jonas Becker, Darius Schweinoch, Jürgen Beneke, Sandra Wüst, Nina Beil, Petr Matula, Karl Rohr, Holger Erfle, Lars Kaderali, Marco Binder

MARC

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520 |a The retinoic acid-inducible gene-I (RIG-I) signaling is crucial for cell-intrinsic innate antiviral immunity. Upon cytosolic detection of virus-associated RNA, it triggers a cascade inducing production of potent cytokines, mainly type I and III interferons (IFNs). While effective, dysregulated responses can harm the host, requiring tight pathway control. Here, we performed a comprehensive, systematic siRNA-based high-throughput screen across 616 established and putative E3 ubiquitin ligases for their impact on RIG-I signaling. We employed a fluorescence-based live-cell imaging assay in A549 cells to monitor nuclear translocation of IRF3 and NF-κB, two key transcription factors downstream of RIG-I. Candidate genes were validated in an orthogonal secondary screen, assessing their impact on the functional antiviral response to a Rift Valley Fever reporter virus. Fourteen hits showed consistent effects on RIG-I signaling across both screens. These genes were further validated and characterized by assessing IFN-β promoter reporter activity and IFNB1 mRNA levels upon dsRNA transfection. TRIM48 emerged as a highly robust negative regulator. Overexpression of TRIM48 suppressed RIG-I-mediated activation of IRF3 and NF-κB, reduced IFN and IFN-stimulated gene expression, and enhanced viral replication. Conversely, TRIM48 deficiency enhanced RIG-I signaling and inhibited viral replication. Notably, TRIM48 acts as an induced feedback regulator upon infection, and its effect depended on its enzymatic ubiquitin ligase activity. Our high-throughput screen provides an unbiased assessment of close to all E3 ubiquitin ligases for their regulatory effect in RIG-I signaling, and identified several interesting candidates for further investigation. TRIM48 was established as a negative feedback regulator of the RIG-I pathway. 
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