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The Caenorhabditis elegans Protein FIC-1 Is an AMPylase That Covalently Modifies Heat-Shock 70 Family Proteins, Translation Elongation Factors and Histones.

Matthias C TruttmannVictor Emmanuel CruzXuanzong GuoChristoph EngertThomas U SchwartzHidde L Ploegh
Published in: PLoS genetics (2016)
Protein AMPylation by Fic domain-containing proteins (Fic proteins) is an ancient and conserved post-translational modification of mostly unexplored significance. Here we characterize the Caenorhabditis elegans Fic protein FIC-1 in vitro and in vivo. FIC-1 is an AMPylase that localizes to the nuclear surface and modifies core histones H2 and H3 as well as heat shock protein 70 family members and translation elongation factors. The three-dimensional structure of FIC-1 is similar to that of its human ortholog, HYPE, with 38% sequence identity. We identify a link between FIC-1-mediated AMPylation and susceptibility to the pathogen Pseudomonas aeruginosa, establishing a connection between AMPylation and innate immunity in C. elegans.
Keyphrases
  • heat shock protein
  • heat shock
  • pseudomonas aeruginosa
  • amino acid
  • endothelial cells
  • cystic fibrosis
  • heat stress
  • oxidative stress
  • escherichia coli
  • staphylococcus aureus
  • induced pluripotent stem cells