RT Journal Article
SR Electronic
T1 POLD replicates both strands of small kilobase-long replication bubbles initiated at a majority of human replication origins
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 174730
DO 10.1101/174730
A1 Artem V. Artemov
A1 Maria A. Andrianova
A1 Georgii A. Bazykin
A1 Vladimir B. Seplyarskiy
YR 2017
UL http://biorxiv.org/content/early/2017/08/10/174730.abstract
AB Error-prone mutants of polymerase epsilon (POLE*) or polymerase delta (POLD1*) induce a mutator phenotype in human cancers. Here we show that the rate of mutations introduced by POLD1* is elevated by 50%, while the rate of POLE*-induced mutations is decreased twofold, within one kilobase from replication origins. These results support a model in which POLD1 replicates both the leading and the lagging strands within a kilobase from an origin. The magnitude of the mutational bias suggests that the probability of an individual origin to initiate replication exceeds 50%, which is much higher than previous estimates. Using additional data from nascent DNA sequencing and Okazaki fragments sequencing (OK-seq) experiments, we showed that a majority of origins are firing at each replication round, but the initiated replication fork does not propagate further than 1Kb in both directions. Analyses based on mutational data and on OK-seq data concordantly suggest that only approximately a quarter of fired origins result in a processive replication fork. Taken together, our results provide a new model of replication initiation.