Ring finger protein 5 mediates STING degradation through ubiquitinating K135 and K155 in a teleost fish

Stimulator of interferon genes (STING) is a key connector protein in interferon (IFN) signaling, crucial for IFN induction during the activation of antiviral innate immunity. In mammals, ring finger protein 5 (RNF5) functions as an E3 ubiquitin ligase, mediating STING regulation through K150 ubiquitylation to prevent excessive IFN production. However, the mechanisms underlying RNF5's regulation of STING in teleost fish remain unknown. This study investigated the regulatory role of the mandarin fish (<i>Siniperca chuatsi</i>) RNF5 (<i>sc</i>RNF5) in the STING-mediated antiviral immune response and identified the specific regulatory sites on <i>sc</i>STING. Furthermore, an examination of <i>sc</i>RNF5 expression patterns in virus-infected cells revealed its responsiveness to mandarin fish ranavirus (MRV) infection. The ectopic expression of <i>sc</i>RNF5 suppressed <i>sc</i>STING-mediated IFN signaling and facilitated MRV replication. Co-immunoprecipitation experiments indicated an interaction between <i>sc</i>RNF5 and <i>sc</i>STING. The further experiments demonstrated that <i>sc</i>RNF5 exerted its inhibitory effect by promoting the degradation of <i>sc</i>STING, which was observed to be blocked by MG132 treatment. Ubiquitination assays with various <i>sc</i>STING mutants showed that <i>sc</i>RNF5 catalyzed the ubiquitination of <i>sc</i>STING at K135 and K155 residues. Furthermore, we provided evidence that <i>sc</i>RNF5 significantly attenuated <i>sc</i>STING-dependent antiviral immunity by targeting negative regulators within the <i>sc</i>STING signaling cascade. This study underscored that RNF5 negatively regulated the STING-mediated IFN signaling pathway in mandarin fish, attenuated STING's antiviral activity, and facilitated STING degradation via the ubiquitin-proteasome pathway at two novel lysine sites (K135 and K155). Our work offered valuable insights into the regulatory mechanisms of STING-mediated signaling in teleost fish, paving the way for further research.

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Publication Details

Journal
Frontiers in Immunology
Published
2024-12-11
DOI
https://doi.org/10.3389/fimmu.2024.1525376
Citations
2
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
0.48

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article

Ring finger protein 5 mediates STING degradation through ubiquitinating K135 and K155 in a teleost fish

Xiao-Wei Qin, Z. Qian, Jianguo He, Yanlin You et al.
2 citations
Frontiers in Immunology
interferon and immune responses
0.48
article

Ring finger protein 5 mediates STING degradation through ubiquitinating K135 and K155 in a teleost fish

Xiao-Wei Qin, Z. Qian, Jianguo He, Yanlin You, Mincong Liang, Chang-Jun Guo, Shaoping Weng, Chuanrui Li
article en
2 citations

Abstract

Stimulator of interferon genes (STING) is a key connector protein in interferon (IFN) signaling, crucial for IFN induction during the activation of antiviral innate immunity. In mammals, ring finger protein 5 (RNF5) functions as an E3 ubiquitin ligase, mediating STING regulation through K150 ubiquitylation to prevent excessive IFN production. However, the mechanisms underlying RNF5's regulation of STING in teleost fish remain unknown. This study investigated the regulatory role of the mandarin fish (<i>Siniperca chuatsi</i>) RNF5 (<i>sc</i>RNF5) in the STING-mediated antiviral immune response and identified the specific regulatory sites on <i>sc</i>STING. Furthermore, an examination of <i>sc</i>RNF5 expression patterns in virus-infected cells revealed its responsiveness to mandarin fish ranavirus (MRV) infection. The ectopic expression of <i>sc</i>RNF5 suppressed <i>sc</i>STING-mediated IFN signaling and facilitated MRV replication. Co-immunoprecipitation experiments indicated an interaction between <i>sc</i>RNF5 and <i>sc</i>STING. The further experiments demonstrated that <i>sc</i>RNF5 exerted its inhibitory effect by promoting the degradation of <i>sc</i>STING, which was observed to be blocked by MG132 treatment. Ubiquitination assays with various <i>sc</i>STING mutants showed that <i>sc</i>RNF5 catalyzed the ubiquitination of <i>sc</i>STING at K135 and K155 residues. Furthermore, we provided evidence that <i>sc</i>RNF5 significantly attenuated <i>sc</i>STING-dependent antiviral immunity by targeting negative regulators within the <i>sc</i>STING signaling cascade. This study underscored that RNF5 negatively regulated the STING-mediated IFN signaling pathway in mandarin fish, attenuated STING's antiviral activity, and facilitated STING degradation via the ubiquitin-proteasome pathway at two novel lysine sites (K135 and K155). Our work offered valuable insights into the regulatory mechanisms of STING-mediated signaling in teleost fish, paving the way for further research.

Frontiers in ImmunologyVol. 15
Sun Yat-sen University (CN), Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (CN), Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai) (CN)
Earmarked Fund for China Agriculture Research System, National Key Research and Development Program of China, Special Project for Research and Development in Key areas of Guangdong Province
Life below water
Openalex Percentile: Top 33%
interferon and immune responses
0.48
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