A model for DNA replication showing how dormant origins safeguard against replication fork failure

Replication origins are ‘licensed’ for a single initiation event before entry into S phase; however, many licensed replication origins are not used, but instead remain dormant. The use of these dormant origins helps cells to survive replication stresses that block replication fork movement. Here, we present a computer model of the replication of a typical metazoan origin cluster in which origins are assigned a certain initiation probability per unit time and are then activated stochastically during S phase. The output of this model is in good agreement with experimental data and shows how inefficient dormant origins can be activated when replication forks are inhibited. The model also shows how dormant origins can allow replication to complete even if some forks stall irreversibly. This provides a simple explanation for how replication origin firing is regulated, which simultaneously provides protection against replicative stress while minimizing the cost of using large numbers of replication forks.

[1]  J. H. Taylor Increase in DNA replication sites in cells held at the beginning of S phase , 1977, Chromosoma.

[2]  J. Diffley,et al.  Visualization of Altered Replication Dynamics after DNA Damage in Human Cells* , 2004, Journal of Biological Chemistry.

[3]  J. Blow,et al.  Replication forks, chromatin loops and dormant replication origins , 2008, Genome Biology.

[4]  M. Debatisse,et al.  Replication fork movement sets chromatin loop size and origin choice in mammalian cells , 2008, Nature.

[5]  D. Gilbert Replication origin plasticity, Taylor-made: inhibition vs recruitment of origins under conditions of replication stress , 2007, Chromosoma.

[6]  E. Schwob,et al.  Excess MCM proteins protect human cells from replicative stress by licensing backup origins of replication , 2008, Proceedings of the National Academy of Sciences.

[7]  Anindya Dutta,et al.  Right Place, Right Time, and Only Once: Replication Initiation in Metazoans , 2005, Cell.

[8]  L. Drury,et al.  Cdc6p-dependent loading of Mcm proteins onto pre-replicative chromatin in budding yeast. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[9]  P. Dijkwel,et al.  Initiation Sites Are Distributed at Frequent Intervals in the Chinese Hamster Dihydrofolate Reductase Origin of Replication but Are Used with Very Different Efficiencies , 2002, Molecular and Cellular Biology.

[10]  D. Gilbert,et al.  Spatial distribution and specification of mammalian replication origins during G1 phase , 2003, The Journal of cell biology.

[11]  R. Knippers,et al.  Interactions of human nuclear proteins P1Mcm3 and P1Cdc46. , 1995, European journal of biochemistry.

[12]  T. Prokhorova,et al.  MCM2–7 Complexes Bind Chromatin in a Distributed Pattern Surrounding the Origin Recognition Complex inXenopus Egg Extracts* , 2002, The Journal of Biological Chemistry.

[13]  Ronald Berezney,et al.  Heterogeneity of eukaryotic replicons, replicon clusters, and replication foci , 2000, Chromosoma.

[14]  J. Diffley,et al.  Regulation of DNA replication fork progression through damaged DNA by the Mec1/Rad53 checkpoint , 2001, Nature.

[15]  J. Walter,et al.  Strength in numbers: preventing rereplication via multiple mechanisms in eukaryotic cells. , 2007, Genes & development.

[16]  C. Newlon,et al.  Regulation of DNA replication fork progression through damaged DNA by the Mec 1 / Rad 53 checkpoint , 2022 .

[17]  J. Julian Blow,et al.  Preventing re-replication of chromosomal DNA , 2005, Nature Reviews Molecular Cell Biology.

[18]  J. Blow,et al.  Cell Cycle Regulation of the Replication Licensing System: Involvement of a Cdk-dependent Inhibitor , 1997, The Journal of cell biology.

[19]  A. Gartner,et al.  Excess Mcm2–7 license dormant origins of replication that can be used under conditions of replicative stress , 2006, The Journal of cell biology.

[20]  Xin Quan Ge,et al.  Dormant origins licensed by excess Mcm2-7 are required for human cells to survive replicative stress. , 2007, Genes & development.

[21]  D. Gilbert,et al.  Temporally coordinated assembly and disassembly of replication factories in the absence of DNA synthesis , 2000, Nature Cell Biology.

[22]  Aaron Bensimon,et al.  Dynamics of DNA Replication in Mammalian Somatic Cells Nucleotide Pool Modulates Origin Choice and Interorigin Spacing , 2003, Cell.

[23]  Ana Pombo,et al.  Replicon Clusters Are Stable Units of Chromosome Structure: Evidence That Nuclear Organization Contributes to the Efficient Activation and Propagation of S Phase in Human Cells , 1998, The Journal of cell biology.

[24]  M. DePamphilis Replication origins in metazoan chromosomes: fact or fiction? , 1999, BioEssays : news and reviews in molecular, cellular and developmental biology.

[25]  J. Diffley,et al.  Activation of dormant origins of DNA replication in budding yeast. , 1999, Genes & development.