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TARG1 protects against toxic DNA ADP-ribosylation.

Callum Tromans-CoiaAndrea SanchiGiuliana K MoellerGyula TiminszkyMassimo LopesIvan Ahel
Published in: Nucleic acids research (2021)
ADP-ribosylation is a modification that targets a variety of macromolecules and regulates a diverse array of important cellular processes. ADP-ribosylation is catalysed by ADP-ribosyltransferases and reversed by ADP-ribosylhydrolases. Recently, an ADP-ribosyltransferase toxin termed 'DarT' from bacteria, which is distantly related to human PARPs, was shown to modify thymidine in single-stranded DNA in a sequence specific manner. The antitoxin of DarT is the macrodomain containing ADP-ribosylhydrolase DarG, which shares striking structural homology with the human ADP-ribosylhydrolase TARG1. Here, we show that TARG1, like DarG, can reverse thymidine-linked DNA ADP-ribosylation. We find that TARG1-deficient human cells are extremely sensitive to DNA ADP-ribosylation. Furthermore, we also demonstrate the first detection of reversible ADP-ribosylation on genomic DNA in vivo from human cells. Collectively, our results elucidate the impact of DNA ADP-ribosylation in human cells and provides a molecular toolkit for future studies into this largely unknown facet of ADP-ribosylation.
Keyphrases
  • circulating tumor
  • single molecule
  • cell free
  • endothelial cells
  • escherichia coli
  • gene expression
  • mass spectrometry
  • high resolution
  • high throughput
  • dna methylation
  • real time pcr
  • circulating tumor cells