RT Journal Article
SR Electronic
T1 Disruption of origin chromatin structure by helicase activation in the absence of DNA replication
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2021.03.17.435814
DO 10.1101/2021.03.17.435814
A1 Rachel A. Hoffman
A1 David M. MacAlpine
YR 2021
UL http://biorxiv.org/content/early/2021/03/26/2021.03.17.435814.abstract
AB Prior to initiation of DNA replication, the eukaryotic helicase, Mcm2-7, must be activated to unwind DNA at replication start sites in early S-phase. To study helicase activation within origin chromatin, we constructed a conditional mutant of the polymerase α subunit Cdc17 (or Pol1) to prevent priming and block replication. Recovery of these cells at permissive conditions resulted in the generation of unreplicated gaps at origins, likely due to helicase activation prior to replication initiation. We used micrococcal nuclease (MNase)-based chromatin occupancy profiling under restrictive conditions to study chromatin dynamics associated with helicase activation. Helicase activation in the absence of DNA replication resulted in the disruption and disorganization of chromatin which extends up to one kilobase from early, efficient replication origins. The CMG holo-helicase complex also moves the same distance out from the origin, producing single-stranded DNA that activates the intra-S-phase checkpoint. Loss of the checkpoint did not regulate the progression and stalling of the CMG complex, but rather resulted in the disruption of chromatin at both early and late origins. Finally, we found that the local sequence context regulates helicase progression in the absence of DNA replication, suggesting that the helicase is intrinsically less processive when uncoupled from replication.Competing Interest StatementThe authors have declared no competing interest.