S Phase Progression in Human Cells Is Dictated by the Genetic Continuity of DNA Foci

DNA synthesis must be performed with extreme precision to maintain genomic integrity. In mammalian cells, different genomic regions are replicated at defined times, perhaps to preserve epigenetic information and cell differentiation status. However, the molecular principles that define this S phase program are unknown. By analyzing replication foci within discrete chromosome territories during interphase, we show that foci which are active during consecutive intervals of S phase are maintained as spatially adjacent neighbors throughout the cell cycle. Using extended DNA fibers, we demonstrate that this spatial continuity of replication foci correlates with the genetic continuity of adjacent replicon clusters along chromosomes. Finally, we used bioinformatic tools to compare the structure of DNA foci with DNA domains that are seen to replicate during discrete time intervals of S phase using genome-wide strategies. Data presented show that a major mechanism of S phase progression involves the sequential synthesis of regions of the genome because of their genetic continuity along the chromosomal fiber.

[1]  R. Drouin,et al.  Analysis of DNA replication during S-phase by means of dynamic chromosome banding at high resolution , 1990, Chromosoma.

[2]  M. DePamphilis,et al.  Regulating the licensing of DNA replication origins in metazoa. , 2006, Current opinion in cell biology.

[3]  A. Pombo,et al.  Mechanisms regulating S phase progression in mammalian cells. , 2009, Frontiers in bioscience.

[4]  Roy Riblet,et al.  Progressive activation of DNA replication initiation in large domains of the immunoglobulin heavy chain locus during B cell development. , 2005, Molecular cell.

[5]  Bernadett Papp,et al.  Genome-wide dynamics of replication timing revealed by in vitro models of mouse embryogenesis. , 2010, Genome research.

[6]  Mirit I. Aladjem,et al.  Replication in context: dynamic regulation of DNA replication patterns in metazoans , 2007, Nature Reviews Genetics.

[7]  R. Sclafani,et al.  Cell cycle regulation of DNA replication. , 2007, Annual review of genetics.

[8]  Laurent Duret,et al.  Genome-wide studies highlight indirect links between human replication origins and gene regulation , 2008, Proceedings of the National Academy of Sciences.

[9]  Olivier Hyrien,et al.  Paradoxes of eukaryotic DNA replication: MCM proteins and the random completion problem , 2003, BioEssays : news and reviews in molecular, cellular and developmental biology.

[10]  Michael O Dorschner,et al.  Sequencing newly replicated DNA reveals widespread plasticity in human replication timing , 2009, Proceedings of the National Academy of Sciences.

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

[12]  Jean Thierry-Mieg,et al.  Predictable dynamic program of timing of DNA replication in human cells. , 2009, Genome research.

[13]  H. Niida,et al.  Cyclin A–Cdk1 regulates the origin firing program in mammalian cells , 2009, Proceedings of the National Academy of Sciences.

[14]  Jan Koster,et al.  The Three-Dimensional Structure of Human Interphase Chromosomes Is Related to the Transcriptome Map , 2007, Molecular and Cellular Biology.

[15]  Heinrich Leonhardt,et al.  DNA polymerase clamp shows little turnover at established replication sites but sequential de novo assembly at adjacent origin clusters. , 2002, Molecular cell.

[16]  Dirk Schübeler,et al.  Global Reorganization of Replication Domains During Embryonic Stem Cell Differentiation , 2008, PLoS biology.

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

[18]  Alon Goren,et al.  Replicating by the clock , 2003, Nature Reviews Molecular Cell Biology.

[19]  Pedro Olivares-Chauvet,et al.  S-phase progression in mammalian cells: modelling the influence of nuclear organization , 2010, Chromosome Research.

[20]  Alain Verreault,et al.  Chromatin Challenges during DNA Replication and Repair , 2007, Cell.

[21]  Emily L. Crawford,et al.  Isolating apparently pure libraries of replication origins from complex genomes. , 2006, Molecular cell.

[22]  D. Gillespie,et al.  Chk1 regulates the density of active replication origins during the vertebrate S phase , 2007, The EMBO journal.

[23]  G J Brakenhoff,et al.  Dynamics of three-dimensional replication patterns during the S-phase, analysed by double labelling of DNA and confocal microscopy. , 1992, Journal of cell science.

[24]  D. Jackson Nuclear organization: uniting replication foci, chromatin domains and chromosome structure. , 1995, BioEssays : news and reviews in molecular, cellular and developmental biology.

[25]  T. Hashimshony,et al.  Establishment of transcriptional competence in early and late S phase , 2002, Nature.

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

[27]  T. Cremer,et al.  Quantitative motion analysis of subchromosomal foci in living cells using four-dimensional microscopy. , 1999, Biophysical journal.

[28]  Carol J. Bult,et al.  Folding and organization of a contiguous chromosome region according to the gene distribution pattern in primary genomic sequence , 2006, The Journal of cell biology.

[29]  D. Zink The temporal program of DNA replication: new insights into old questions , 2006, Chromosoma.

[30]  J. Weissenbach,et al.  DNA replication origin interference increases the spacing between initiation events in human cells. , 2006, Molecular biology of the cell.

[31]  T. Cremer,et al.  Chromosome territories, nuclear architecture and gene regulation in mammalian cells , 2001, Nature Reviews Genetics.

[32]  D. Jackson,et al.  Visualization of replication factories attached to a nucleoskeleton , 1993, Cell.

[33]  Zohar Yakhini,et al.  Global organization of replication time zones of the mouse genome. , 2008, Genome research.

[34]  Ramón Díaz-Uriarte,et al.  Transcription Initiation Activity Sets Replication Origin Efficiency in Mammalian Cells , 2009, PLoS genetics.

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

[36]  Owen T McCann,et al.  Replication timing of the human genome. , 2004, Human molecular genetics.

[37]  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.

[38]  Karl Rohr,et al.  Chromatin domains and the interchromatin compartment form structurally defined and functionally interacting nuclear networks , 2006, Chromosome Research.

[39]  D. Jackson,et al.  Replication and transcription sites are colocalized in human cells. , 1994, Journal of cell science.

[40]  D. Heermann,et al.  Spatially confined folding of chromatin in the interphase nucleus , 2009, Proceedings of the National Academy of Sciences.

[41]  Ronald Berezney,et al.  Spatial and Temporal Dynamics of DNA Replication Sites in Mammalian Cells , 1998, The Journal of cell biology.

[42]  H. Cedar,et al.  Shifts in replication timing actively affect histone acetylation during nucleosome reassembly. , 2009, Molecular cell.

[43]  J. Blow,et al.  Replication Origins in XenopusEgg Extract Are 5–15 Kilobases Apart and Are Activated in Clusters That Fire at Different Times , 2001, The Journal of cell biology.

[44]  S. Takebayashi,et al.  Regulation of replication at the R/G chromosomal band boundary and pericentromeric heterochromatin of mammalian cells. , 2005, Experimental cell research.