The C-terminal domain of Cernunnos/XLF is dispensable for DNA repair in vivo

Mol Cell Biol. 2009 Mar;29(5):1116-22. doi: 10.1128/MCB.01521-08. Epub 2008 Dec 22.

Abstract

The core nonhomologous end-joining DNA repair pathway is composed of seven factors: Ku70, Ku80, DNA-PKcs, Artemis, XRCC4 (X4), DNA ligase IV (L4), and Cernunnos/XLF (Cernunnos). Although Cernunnos and X4 are structurally related and participate in the same complex together with L4, they have distinct functions during DNA repair. L4 relies on X4 but not on Cernunnos for its stability, and L4 is required for optimal interaction of Cernunnos with X4. We demonstrate here, using in vitro-generated Cernunnos mutants and a series of functional assays in vivo, that the C-terminal region of Cernunnos is dispensable for its activity during DNA repair.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • DNA Ligase ATP
  • DNA Ligases
  • DNA Repair Enzymes / chemistry
  • DNA Repair Enzymes / physiology*
  • DNA Repair*
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / physiology*
  • Humans
  • Multiprotein Complexes
  • Mutagenesis, Site-Directed
  • Mutant Proteins
  • Protein Structure, Tertiary

Substances

  • DNA-Binding Proteins
  • LIG4 protein, human
  • Multiprotein Complexes
  • Mutant Proteins
  • NHEJ1 protein, human
  • DNA Ligases
  • DNA Repair Enzymes
  • DNA Ligase ATP