DDK Has a Primary Role in Processing Stalled Replication Forks to Initiate Downstream Checkpoint Signaling

Nanda Kumar Sasi (1) , Flavie Coquel (2) , Yea-Lih Lin (2) , Jeffrey Mackeigan (3) , Philippe Pasero (2) , Michael Weinreich (4)

1 Michigan State University [East Lansing]
2 IGH - Institut de génétique humaine
3 Laboratory of Systems Biology
4 Van Andel Institute [Grand Rapids]

CDC7-DBF4 kinase (DDK) initiates DNA replication in eukaryotes by activating the replicative MCM helicase. DDK has diverse and apparently conflicting roles in the replication checkpoint response in various organisms, but the underlying mechanisms are far from settled. We show that human DDK promotes limited resection of newly synthesized DNA at stalled replication forks or sites of DNA damage to initiate replication checkpoint signaling. DDK is also required for efficient fork restart and G2/M cell cycle arrest. DDK exhibits genetic interactions with the ssDNA exonuclease EXO1 and phosphorylates EXO1 in vitro. EXO1 is also required for nascent strand degradation following exposure to HU, so DDK might regulate EXO1 directly. Lastly, sublethal DDK inhibition causes various mitotic abnormalities, which is consistent with a checkpoint deficiency. In summary, DDK has a primary and previously undescribed role in the replication checkpoint to promote ssDNA accumulation at stalled forks, which is required to initiate a robust checkpoint response and cell cycle arrest to maintain genome integrity.

Domaines: Sciences du Vivant [q-bio]; Génétique

Nanda Kumar Sasi, Flavie Coquel, Yea-Lih Lin, Jeffrey Mackeigan, Philippe Pasero, et al.. DDK Has a Primary Role in Processing Stalled Replication Forks to Initiate Downstream Checkpoint Signaling. Journal of Mammary Gland Biology and Neoplasia, 2018, 20 (10), pp.985 - 995. ⟨10.1016/j.neo.2018.08.001⟩. ⟨hal-01887535⟩