RECQ5 Helicase Cooperates with MUS81 Endonuclease in Processing Stalled Replication Forks at Common Fragile Sites during Mitosis

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  • Stefano Di Marco
  • Zdenka Hasanova
  • Radhakrishnan Kanagaraj
  • Nagaraja Chappidi
  • Veronika Altmannova
  • Shruti Menon
  • Hana Sedlackova
  • Jana Langhoff
  • Kalpana Surendranath
  • Daniela Hühn
  • Bhowmick, Rahul
  • Victoria Marini
  • Stefano Ferrari
  • Hickson, Ian David
  • Lumir Krejci
  • Pavel Janscak

The MUS81-EME1 endonuclease cleaves late replication intermediates at common fragile sites (CFSs) during early mitosis to trigger DNA-repair synthesis that ensures faithful chromosome segregation. Here, we show that these DNA transactions are promoted by RECQ5 DNA helicase in a manner dependent on its Ser727 phosphorylation by CDK1. Upon replication stress, RECQ5 associates with CFSs in early mitosis through its physical interaction with MUS81 and promotes MUS81-dependent mitotic DNA synthesis. RECQ5 depletion or mutational inactivation of its ATP-binding site, RAD51-interacting domain, or phosphorylation site causes excessive binding of RAD51 to CFS loci and impairs CFS expression. This leads to defective chromosome segregation and accumulation of CFS-associated DNA damage in G1 cells. Biochemically, RECQ5 alleviates the inhibitory effect of RAD51 on 3'-flap DNA cleavage by MUS81-EME1 through its RAD51 filament disruption activity. These data suggest that RECQ5 removes RAD51 filaments stabilizing stalled replication forks at CFSs and hence facilitates CFS cleavage by MUS81-EME1.

OriginalsprogEngelsk
TidsskriftMolecular Cell
Vol/bind66
Udgave nummer5
Sider (fra-til)658-671.e8
ISSN1097-2765
DOI
StatusUdgivet - 1 jun. 2017

ID: 185901602