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The intra-S phase checkpoint directly regulates replication elongation to preserve the integrity of stalled replisomes
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The intra-S phase checkpoint directly regulates replication elongation to preserve the integrity of stalled replisomes
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Journal Article
The intra-S phase checkpoint directly regulates replication elongation to preserve the integrity of stalled replisomes
2021
Overview
DNA replication is dramatically slowed down under replication stress. The regulation of replication speed is a conserved response in eukaryotes and, in fission yeast, requires the checkpoint kinases Rad3ATR and Cds1Chk2. However, the underlying mechanism of this checkpoint regulation remains unresolved. Here, we report that the Rad3ATR-Cds1Chk2 checkpoint directly targets the Cdc45-MCM-GINS (CMG) replicative helicase under replication stress. When replication forks stall, the Cds1Chk2 kinase directly phosphorylates Cdc45 on the S275, S322, and S397 residues, which significantly reduces CMG helicase activity. Furthermore, in cds1Chk2
-mutated cells, the CMG helicase and DNA polymerases are physically separated, potentially disrupting replisomes and collapsing replication forks. This study demonstrates that the intra-S phase checkpoint directly regulates replication elongation, reduces CMG helicase processivity, prevents CMG helicase delinking from DNA polymerases, and therefore helps preserve the integrity of stalled replisomes and replication forks.
Publisher
National Academy of Sciences
Subject
/ DNA
/ DNA Replication - drug effects
/ DNA-Directed DNA Polymerase - metabolism
/ Genetics
/ Kinases
/ Multienzyme Complexes - metabolism
/ Multiprotein Complexes - metabolism
/ Phosphorylation - drug effects
/ S phase
/ S Phase Cell Cycle Checkpoints - drug effects
/ Schizosaccharomyces - drug effects
/ Schizosaccharomyces - metabolism
/ Schizosaccharomyces pombe Proteins - genetics
/ Schizosaccharomyces pombe Proteins - metabolism
/ Yeast
