Viral Z-RNA triggers ZBP1-dependent cell death

Curr Opin Virol. 2021 Dec:51:134-140. doi: 10.1016/j.coviro.2021.10.004. Epub 2021 Oct 21.

Abstract

Z-DNA Binding protein 1 (ZBP1) activates Receptor Interacting Protein Kinase 3 (RIPK3) -dependent cell death during lytic infection by members of the orthomyxovirus, herpesvirus and poxvirus families. ZBP1 possesses two Zα domains capable of selective binding to Z-DNA, as well as to Z-RNA. We have now unveiled Z-RNA as the ligand that activates ZBP1 in cells infected with orthomyxoviruses (influenza A and B viruses) and the poxvirus vaccinia virus (VACV). Orthomyxovirus Z-RNA is sensed by ZBP1 in the nucleus of infected cells, resulting in nuclear activation of RIPK3, consequent rupture of the nucleus, and hyper-inflammatory 'nuclear necroptosis'. VACV-generated Z-RNA accumulates in the cytoplasm, where it is sequestered from ZBP1 by E3, the viral E3L gene product. In viruses where the E3 Zα domain has been mutated, ZBP1 senses Z-RNA and triggers RIPK3-dependent necroptosis in the cytoplasm. Z-RNA is thus a new viral pathogen-associated molecular pattern (PAMP).

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Humans
  • Influenza A virus*
  • Influenza B virus*
  • Necroptosis*
  • Nucleic Acid Conformation*
  • Pathogen-Associated Molecular Pattern Molecules / metabolism
  • RNA, Viral / chemistry*
  • RNA, Viral / metabolism*
  • RNA-Binding Proteins / metabolism*
  • Receptor-Interacting Protein Serine-Threonine Kinases / metabolism
  • Vaccinia virus*
  • Viral Proteins / metabolism

Substances

  • Pathogen-Associated Molecular Pattern Molecules
  • RNA, Viral
  • RNA-Binding Proteins
  • Viral Proteins
  • ZBP1 protein, human
  • RIPK3 protein, human
  • Receptor-Interacting Protein Serine-Threonine Kinases