Structural basis of long-range to short-range synaptic transition in NHEJ

Nature. 2021 May;593(7858):294-298. doi: 10.1038/s41586-021-03458-7. Epub 2021 Apr 14.

Abstract

DNA double-strand breaks (DSBs) are a highly cytotoxic form of DNA damage and the incorrect repair of DSBs is linked to carcinogenesis1,2. The conserved error-prone non-homologous end joining (NHEJ) pathway has a key role in determining the effects of DSB-inducing agents that are used to treat cancer as well as the generation of the diversity in antibodies and T cell receptors2,3. Here we applied single-particle cryo-electron microscopy to visualize two key DNA-protein complexes that are formed by human NHEJ factors. The Ku70/80 heterodimer (Ku), the catalytic subunit of the DNA-dependent protein kinase (DNA-PKcs), DNA ligase IV (LigIV), XRCC4 and XLF form a long-range synaptic complex, in which the DNA ends are held approximately 115 Å apart. Two DNA end-bound subcomplexes comprising Ku and DNA-PKcs are linked by interactions between the DNA-PKcs subunits and a scaffold comprising LigIV, XRCC4, XLF, XRCC4 and LigIV. The relative orientation of the DNA-PKcs molecules suggests a mechanism for autophosphorylation in trans, which leads to the dissociation of DNA-PKcs and the transition into the short-range synaptic complex. Within this complex, the Ku-bound DNA ends are aligned for processing and ligation by the XLF-anchored scaffold, and a single catalytic domain of LigIV is stably associated with a nick between the two Ku molecules, which suggests that the joining of both strands of a DSB involves both LigIV molecules.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Cryoelectron Microscopy*
  • DNA / chemistry
  • DNA / metabolism*
  • DNA / ultrastructure*
  • DNA Breaks, Double-Stranded*
  • DNA End-Joining Repair*
  • DNA Ligase ATP / metabolism
  • DNA Ligase ATP / ultrastructure
  • DNA Repair Enzymes / metabolism
  • DNA Repair Enzymes / ultrastructure
  • DNA-Activated Protein Kinase / metabolism
  • DNA-Activated Protein Kinase / ultrastructure
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / ultrastructure
  • Humans
  • Ku Autoantigen / metabolism
  • Ku Autoantigen / ultrastructure
  • Models, Molecular
  • Phosphorylation

Substances

  • DNA-Binding Proteins
  • NHEJ1 protein, human
  • XRCC4 protein, human
  • DNA
  • DNA-Activated Protein Kinase
  • XRCC5 protein, human
  • Ku Autoantigen
  • DNA Repair Enzymes
  • DNA Ligase ATP