A model for DNA replication showing how dormant origins safeguard against replication fork failure
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Xin Quan Ge | J Julian Blow | J. Blow | X. Ge | J. Blow
[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.