Cryo-EM structure of a DNA-PK trimer: higher order oligomerisation in NHEJ
The ability of humans to maintain the integrity of the genome is imperative for cellular survival. DNA double-strand breaks (DSBs) are considered the most critical type of DNA lesion, which can ultimately lead to diseases including cancer. Non-homologous end joining (NHEJ) is one of two core mechanisms utilized to repair DSBs. DNA-PK is a key component in this process and has recently been shown to form alternate long-range synaptic dimers. This has led to the proposal that these complexes can be formed before transitioning to a short-range synaptic complex. Here we present cryo-EM data representing an NHEJ supercomplex consisting of a trimer of DNA-PK in complex with XLF, XRCC4, and DNA Ligase IV. This trimer represents a complex of both long-range synaptic dimers. We discuss the potential role of the trimeric structure, and possible higher order oligomers, as structural intermediates in the NHEJ mechanism, or as functional DNA repair centers.
Funding
Medical Research Council for the standard research grant (MR/X00029X/1)
Wellcome Trust for a Program Grant (O93167/Z/10/Z; 2011–2016)
Achieving Selectivity in Space and Time with DNA Double-Strand-Break Response and Repair: Molecular Stages and Scaffolds Come with Strings Attached
Wellcome Trust
Find out more...ANR-20-CE11-0026 and Infrastructure FRISBI ANR-10-INBS-05 for support
History
Author affiliation
Leicester Institute for Structural and Chemical Biology, Department of Molecular and Cell Biology, University of LeicesterVersion
- VoR (Version of Record)