Human ANP32A/B are SUMOylated and utilized by avian influenza virus NS2 protein to overcome species-specific restriction

Nat Commun. 2024 Dec 30;15(1):10805. doi: 10.1038/s41467-024-55034-y.

Abstract

Human ANP32A/B (huANP32A/B) poorly support the polymerase activity of avian influenza viruses (AIVs), thereby limiting interspecies transmission of AIVs from birds to humans. The SUMO-interacting motif (SIM) within NS2 promotes the adaptation of AIV polymerase to huANP32A/B via a yet undisclosed mechanism. Here we show that huANP32A/B are SUMOylated by the E3 SUMO ligase PIAS2α, and deSUMOylated by SENP1. SUMO modification of huANP32A/B results in the recruitment of NS2, thereby facilitating huANP32A/B-supported AIV polymerase activity. Such a SUMO-dependent recruitment of NS2 is mediated by its association with huANP32A/B via the SIM-SUMO interaction module, where K68/K153-SUMO in huANP32A or K68/K116-SUMO in huANP32B interacts with the NS2-SIM. The SIM-SUMO-mediated interactions between NS2 and huANP32A/B function to promote AIV polymerase activity by positively regulating AIV vRNP-huANP32A/B interactions and AIV vRNP assembly. Our study offers insights into the mechanism of NS2-SIM in facilitating AIVs adaptation to mammals.

MeSH terms

  • Animals
  • Birds / virology
  • Cysteine Endopeptidases / genetics
  • Cysteine Endopeptidases / metabolism
  • HEK293 Cells
  • Humans
  • Influenza A virus* / genetics
  • Influenza A virus* / metabolism
  • Influenza A virus* / physiology
  • Influenza in Birds / metabolism
  • Influenza in Birds / virology
  • Influenza, Human / metabolism
  • Influenza, Human / virology
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism
  • Nuclear Proteins* / genetics
  • Nuclear Proteins* / metabolism
  • Protein Inhibitors of Activated STAT / genetics
  • Protein Inhibitors of Activated STAT / metabolism
  • RNA-Binding Proteins* / genetics
  • RNA-Binding Proteins* / metabolism
  • Species Specificity
  • Sumoylation*
  • Viral Nonstructural Proteins* / genetics
  • Viral Nonstructural Proteins* / metabolism

Substances

  • Viral Nonstructural Proteins
  • ANP32A protein, human
  • Nuclear Proteins
  • ANP32B protein, human
  • RNA-Binding Proteins
  • Cysteine Endopeptidases
  • Protein Inhibitors of Activated STAT
  • PIAS2 protein, human
  • SENP1 protein, human
  • NS2 protein, influenza virus A
  • Molecular Chaperones