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Viral Z-RNA triggers ZBP1-dependent cell death

  • Emory University

Research output: Contribution to journalReview articlepeer-review

74 Scopus citations

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).

Original languageEnglish
Pages (from-to)134-140
Number of pages7
JournalCurrent Opinion in Virology
Volume51
DOIs
StatePublished - Dec 2021

Keywords

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

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