Negative regulation of the RIG-I signaling by the ubiquitin ligase RNF125
Open Access
- 1 May 2007
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 104 (18), 7500-7505
- https://doi.org/10.1073/pnas.0611551104
Abstract
Retinoic acid-inducible gene I ( RIG-I ) plays a pivotal role in the regulation of cytokine production induced by pathogens. The RIG-I also augments the production of IFN and other cytokines via an amplification circuit. Because the production of cytokines is closely controlled, up- and down-regulation of RIG-I signaling also needs strict regulation. The mechanism of this regulation, however, remains elusive. Here, we found that RIG-I undergoes proteasomal degradation after conjugation to ubiquitin by RNF125. Further, RNF125 conjugates ubiquitin to MDA5, a family protein of RIG-I as well as IPS-1, which is also a downstream protein of RIG-I signaling that results in suppressing the functions of these proteins. Because RNF125 is enhanced by IFN, these functions constitute a negative regulatory loop circuit for IFN production.Keywords
This publication has 36 references indexed in Scilit:
- Staring, a Novel E3 Ubiquitin-Protein Ligase That Targets Syntaxin 1 for DegradationJournal of Biological Chemistry, 2002
- PIAS Proteins Modulate Transcription Factors by Functioning as SUMO-1 LigasesMolecular and Cellular Biology, 2002
- IRAK-M Is a Negative Regulator of Toll-like Receptor SignalingCell, 2002
- Links between innate and adaptive immunity via type I interferonCurrent Opinion in Immunology, 2002
- Efp targets 14-3-3σ for proteolysis and promotes breast tumour growthNature, 2002
- Innate Immune RecognitionAnnual Review of Immunology, 2002
- Toll-like receptors: critical proteins linking innate and acquired immunityNature Immunology, 2001
- Parkin is linked to the ubiquitin pathwayJournal of Molecular Medicine, 2001
- A Novel Centrosomal RING-Finger Protein, Dorfin, Mediates Ubiquitin Ligase ActivityBiochemical and Biophysical Research Communications, 2001
- Parkin functions as an E2-dependent ubiquitin– protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1Proceedings of the National Academy of Sciences, 2000