3β-hydroxysteroid-Δ24 reductase dampens anti-viral innate immune responses by targeting K27 ubiquitination of MAVS and STING

J Virol. 2023 Dec 21;97(12):e0151323. doi: 10.1128/jvi.01513-23. Epub 2023 Nov 30.

Abstract

The precise regulation of the innate immune response is essential for the maintenance of homeostasis. MAVS and STING play key roles in immune signaling pathways activated by RNA and DNA viruses, respectively. Here, we showed that DHCR24 impaired the antiviral response by targeting MAVS and STING. Notably, DHCR24 interacts with MAVS and STING and inhibits TRIM21-triggered K27-linked ubiquitination of MAVS and AMFR-triggered K27-linked ubiquitination of STING, restraining the activation of MAVS and STING, respectively. Together, this study elucidates how one cholesterol key enzyme orchestrates two antiviral signal transduction pathways.

Keywords: AMFR; DHCR24; IFN; MAVS; STING; TRIM21; cholesterol metabolism; innate immunity; viral infection.

MeSH terms

  • Adaptor Proteins, Signal Transducing* / metabolism
  • Animals
  • Cell Line
  • Humans
  • Hydroxysteroids
  • Immunity, Innate*
  • Membrane Proteins* / metabolism
  • Mice
  • Oxidoreductases
  • Oxidoreductases Acting on CH-CH Group Donors* / genetics
  • Oxidoreductases Acting on CH-CH Group Donors* / metabolism
  • Ubiquitination

Substances

  • Adaptor Proteins, Signal Transducing
  • Dhcr24 protein, mouse
  • Hydroxysteroids
  • IPS-1 protein, mouse
  • Membrane Proteins
  • Oxidoreductases
  • Oxidoreductases Acting on CH-CH Group Donors
  • Sting1 protein, mouse