Clusters, factories and domains: The complex structure of S-phase comes into focus

Peter J. Gillespie, Julian Blow

Research output: Contribution to journalArticlepeer-review

41 Citations (Scopus)

Abstract

During S-phase of the cell cycle, chromosomal DNA is replicated according to a complex replication timing program, with megabase-sized domains replicating at different times. DNA fibre analysis reveals that clusters of adjacent replication origins fire near-synchronously. Analysis of replicating cells by light microscopy shows that DNA synthesis occurs in discrete foci or factories. The relationship between timing domains, origin clusters and replication foci is currently unclear. Recent work, using a hybrid Xenopus/hamster replication system, has shown that when CDK levels are manipulated during S-phase the activation of replication factories can be uncoupled from progression through the replication timing program. Here, we use data from this hybrid system to investigate potential relationships between timing domains, origin clusters and replication foci. We suggest that each timing domain typically comprises several replicon clusters, which are usually processed sequentially by replication factories. We discuss how replication might be regulated at different levels to create this complex organisation and the potential involvement of CDKs in this process.
Original languageEnglish
Pages (from-to)3238-3246
Number of pages9
JournalCell Cycle
Volume9
Issue number16
DOIs
Publication statusPublished - 15 Aug 2010

Keywords

  • DNA replication
  • CDKs
  • S-phase
  • replication timing
  • replicon clusters
  • replication foci
  • replication factories
  • chromosome domains
  • replication timing domains
  • CELL-CYCLE REGULATION
  • DNA-REPLICATION
  • CHROMOSOMAL DOMAINS
  • REPLICON CLUSTERS
  • DORMANT ORIGINS
  • EXCESS MCM2-7
  • G1 PHASE
  • XENOPUS
  • ORGANIZATION
  • CHROMATIN

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