PELI2 is a negative regulator of STING signaling that is dynamically repressed during viral infection

Mol Cell. 2024 Jul 11;84(13):2423-2435.e5. doi: 10.1016/j.molcel.2024.06.001. Epub 2024 Jun 24.

Abstract

The innate immune cGAS-STING pathway is activated by cytosolic double-stranded DNA (dsDNA), a ubiquitous danger signal, to produce interferon, a potent anti-viral and anti-cancer cytokine. However, STING activation must be tightly controlled because aberrant interferon production leads to debilitating interferonopathies. Here, we discover PELI2 as a crucial negative regulator of STING. Mechanistically, PELI2 inhibits the transcription factor IRF3 by binding to phosphorylated Thr354 and Thr356 on the C-terminal tail of STING, leading to ubiquitination and inhibition of the kinase TBK1. PELI2 sets a threshold for STING activation that tolerates low levels of cytosolic dsDNA, such as that caused by silenced TREX1, RNASEH2B, BRCA1, or SETX. When this threshold is reached, such as during viral infection, STING-induced interferon production temporarily downregulates PELI2, creating a positive feedback loop allowing a robust immune response. Lupus patients have insufficient PELI2 levels and high basal interferon production, suggesting that PELI2 dysregulation may drive the onset of lupus and other interferonopathies.

Keywords: E3 ubiquitin ligase; FHA domain; PELI2; STING regulation; autoimmunity; dsDNA sensing; immunotransmitter; innate immunity; type I interferon; viral infection.

MeSH terms

  • Animals
  • Exodeoxyribonucleases
  • Feedback, Physiological
  • HEK293 Cells
  • Host-Pathogen Interactions
  • Humans
  • Immunity, Innate
  • Interferon Regulatory Factor-3* / genetics
  • Interferon Regulatory Factor-3* / metabolism
  • Interferons / genetics
  • Interferons / immunology
  • Interferons / metabolism
  • Lupus Erythematosus, Systemic / genetics
  • Lupus Erythematosus, Systemic / immunology
  • Lupus Erythematosus, Systemic / metabolism
  • Lupus Erythematosus, Systemic / virology
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Phosphoproteins
  • Phosphorylation
  • Protein Serine-Threonine Kinases* / genetics
  • Protein Serine-Threonine Kinases* / metabolism
  • Signal Transduction*
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination*

Substances

  • STING1 protein, human
  • Protein Serine-Threonine Kinases
  • Membrane Proteins
  • Interferon Regulatory Factor-3
  • TBK1 protein, human
  • IRF3 protein, human
  • Sting1 protein, mouse
  • Ubiquitin-Protein Ligases
  • Interferons
  • three prime repair exonuclease 1
  • Exodeoxyribonucleases
  • Phosphoproteins