Global regulation of genome duplication in eukaryotes: an overview from the epifluorescence microscope

TL;DR

This paper reviews how eukaryotic cells globally regulate DNA replication initiation and elongation during S phase to ensure genome stability, emphasizing the roles of origin licensing, activation timing, and checkpoint controls.

Contribution

It provides a comprehensive overview of recent findings on the mechanisms coordinating replication origin activation and fork progression in eukaryotes.

Findings

Origin densities and fork rates are co-regulated.

ATM/ATR checkpoint influences replication coordination.

Proper regulation maintains genome stability.

Abstract

In eukaryotes, DNA replication is initiated along each chromosome at multiple sites called replication origins. Locally, each replication origin is "licensed", or specified, at the end of the M and the beginning of G1 phases of the cell cycle. During S phase when DNA synthesis takes place, origins are activated in stages corresponding to early and late replicating domains. The staged and progressive activation of replication origins reflects the need to maintain a strict balance between the number of active replication forks and the rate at which DNA synthesis procedes. This suggests that origin densities (frequency of intiation) and replication fork movement (rates of elongation) must be co-regulated in order to guarantee the efficient and complete duplication of each subchromosomal domain. Emerging evidence supports this proposal and suggests that the ATM/ATR intra-S phase checkpoint plays an important role in the co-regulation of initiation frequencies and rates of elongation. In the following, we review recent results concerning the mechanisms governing the global regulation of DNA replication and discuss the roles these mechanisms play in maintaining genome stability during both a normal and perturbed S phase.