TRIM25 predominately associates with anti-viral stress granules

Nat Commun. 2024 May 15;15(1):4127. doi: 10.1038/s41467-024-48596-4.

Abstract

Stress granules (SGs) are induced by various environmental stressors, resulting in their compositional and functional heterogeneity. SGs play a crucial role in the antiviral process, owing to their potent translational repressive effects and ability to trigger signal transduction; however, it is poorly understood how these antiviral SGs differ from SGs induced by other environmental stressors. Here we identify that TRIM25, a known driver of the ubiquitination-dependent antiviral innate immune response, is a potent and critical marker of the antiviral SGs. TRIM25 undergoes liquid-liquid phase separation (LLPS) and co-condenses with the SG core protein G3BP1 in a dsRNA-dependent manner. The co-condensation of TRIM25 and G3BP1 results in a significant enhancement of TRIM25's ubiquitination activity towards multiple antiviral proteins, which are mainly located in SGs. This co-condensation is critical in activating the RIG-I signaling pathway, thus restraining RNA virus infection. Our studies provide a conceptual framework for better understanding the heterogeneity of stress granule components and their response to distinct environmental stressors.

MeSH terms

  • Cytoplasmic Granules / metabolism
  • DEAD Box Protein 58 / metabolism
  • DNA Helicases / metabolism
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Immunity, Innate
  • Poly-ADP-Ribose Binding Proteins / genetics
  • Poly-ADP-Ribose Binding Proteins / metabolism
  • RNA Helicases / metabolism
  • RNA Recognition Motif Proteins / genetics
  • RNA Recognition Motif Proteins / metabolism
  • RNA Virus Infections* / immunology
  • RNA Virus Infections* / metabolism
  • RNA Virus Infections* / virology
  • RNA, Double-Stranded / metabolism
  • Receptors, Immunologic / metabolism
  • Signal Transduction
  • Stress Granules* / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Tripartite Motif Proteins* / genetics
  • Tripartite Motif Proteins* / metabolism
  • Ubiquitin-Protein Ligases* / genetics
  • Ubiquitin-Protein Ligases* / metabolism
  • Ubiquitination

Substances

  • DEAD Box Protein 58
  • DNA Helicases
  • Poly-ADP-Ribose Binding Proteins
  • Receptors, Immunologic
  • RNA Helicases
  • RNA Recognition Motif Proteins
  • RNA, Double-Stranded
  • Transcription Factors
  • Tripartite Motif Proteins
  • Ubiquitin-Protein Ligases
  • TRIM25 protein, human