Unifying the DNA end-processing roles of the artemis nuclease: Ku-dependent artemis resection at blunt DNA ends

J Biol Chem. 2015 Oct 2;290(40):24036-50. doi: 10.1074/jbc.M115.680900. Epub 2015 Aug 14.

Abstract

Artemis is a member of the metallo-β-lactamase protein family of nucleases. It is essential in vertebrates because, during V(D)J recombination, the RAG complex generates hairpins when it creates the double strand breaks at V, D, and J segments, and Artemis is required to open the hairpins so that they can be joined. Artemis is a diverse endo- and exonuclease, and creating a unified model for its wide range of nuclease properties has been challenging. Here we show that Artemis resects iteratively into blunt DNA ends with an efficiency that reflects the AT-richness of the DNA end. GC-rich ends are not cut by Artemis alone because of a requirement for DNA end breathing (and confirmed using fixed pseudo-Y structures). All DNA ends are cut when both the DNA-dependent protein kinase catalytic subunit and Ku accompany Artemis but not when Ku is omitted. These are the first biochemical data demonstrating a Ku dependence of Artemis action on DNA ends of any configuration. The action of Artemis at blunt DNA ends is slower than at overhangs, consistent with a requirement for a slow DNA end breathing step preceding the cut. The AT sequence dependence, the order of strand cutting, the length of the cuts, and the Ku-dependence of Artemis action at blunt ends can be reconciled with the other nucleolytic properties of both Artemis and Artemis·DNA-PKcs in a model incorporating DNA end breathing of blunt ends to form transient single to double strand boundaries that have structural similarities to hairpins and fixed 5' and 3' overhangs.

Keywords: DNA; DNA binding protein; DNA endonuclease; DNA enzyme; DNA repair; endonuclease.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / chemistry
  • Catalysis
  • DNA / chemistry*
  • DNA Damage
  • DNA Helicases / metabolism*
  • DNA Repair
  • DNA, Single-Stranded / chemistry
  • DNA-Activated Protein Kinase / genetics*
  • DNA-Activated Protein Kinase / metabolism*
  • DNA-Binding Proteins
  • Endonucleases / genetics
  • Endonucleases / metabolism*
  • Humans
  • Ku Autoantigen
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism*
  • Oligonucleotides / genetics
  • Protein Binding
  • V(D)J Recombination

Substances

  • DNA, Single-Stranded
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Oligonucleotides
  • Adenosine Triphosphate
  • DNA
  • DNA-Activated Protein Kinase
  • PRKDC protein, human
  • DCLRE1C protein, human
  • Endonucleases
  • DNA Helicases
  • XRCC5 protein, human
  • Ku Autoantigen