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The active DNA-PK holoenzyme occupies a tensed state in a staggered synaptic complex

Authors :
Linda Lee
David C. Schriemer
Susan P. Lees-Miller
Natalie C. J. Strynadka
Morgan Hepburn
Shujuan Fang
Claire E. Atkinson
Andrej Sali
Daniel J. Saltzberg
Source :
Structure, Structure (London, England : 1993), vol 29, iss 5
Publication Year :
2020

Abstract

In the non-homologous end joining (NHEJ) of a DNA double strand break, DNA ends are bound and protected by a large heterotrimeric DNA-PK complex, which synapses across the break to tether the broken ends and initiate the repair program. There is a lack of clarity surrounding the nature of the synaptic complex and the mechanism governing the transition to repair. We report an integrative structure of the synaptic complex at a precision of 13.5A (using crosslinking data and available structures), revealing a symmetric head-to-head arrangement with a large offset in the DNA ends and an extensive end-protection mechanism involving a previously uncharacterized plug domain. Hydrogen/deuterium exchange mass spectrometry suggests an allosteric pathway connecting DNA end-binding with the kinase domain that places DNA-PK under tension in the kinase-active state. We present a model for the transition from end-protection to repair, in which the synaptic complex facilitates hierarchical processing of the ends and the assembly of a scaffold, supporting displacement of the catalytic subunit and tension release through kinase activity.

Details

ISSN :
18784186
Volume :
29
Issue :
5
Database :
OpenAIRE
Journal :
Structure (London, England : 1993)
Accession number :
edsair.doi.dedup.....4088d78931fc93363a73aec75a563855