A requirement for replication in activation of the ATR-dependent DNA damage checkpoint
A requirement for replication in activation of the ATR-dependent DNA damage checkpoint
Using the Xenopus egg extract system, we investigated the involvement of DNA replication in activation of the DNA damage checkpoint. We show here that DNA damage slows replication in a checkpoint-independent manner and is accompanied by replication-dependent recruitment of ATR and Rad1 to chromatin. We also find that the replication proteins RPA and Polα accumulate on chromatin following DNA damage. Finally, damage-induced Chk1 phosphorylation and checkpoint arrest are abrogated when replication is inhibited. These data indicate that replication is required for activation of the DNA damage checkpoint and suggest a unifying model for ATR activation by diverse lesions during S phase.
- Stanford University United States
DNA Replication, Ultraviolet Rays, Xenopus, Cell Cycle, Cell Cycle Proteins, Ataxia Telangiectasia Mutated Proteins, In Vitro Techniques, Protein Serine-Threonine Kinases, Xenopus Proteins, Endonucleases, Methyl Methanesulfonate, Models, Biological, Recombinant Proteins, DNA-Binding Proteins, Checkpoint Kinase 1, Oocytes, Animals, Female, Protein Kinases, DNA Damage
DNA Replication, Ultraviolet Rays, Xenopus, Cell Cycle, Cell Cycle Proteins, Ataxia Telangiectasia Mutated Proteins, In Vitro Techniques, Protein Serine-Threonine Kinases, Xenopus Proteins, Endonucleases, Methyl Methanesulfonate, Models, Biological, Recombinant Proteins, DNA-Binding Proteins, Checkpoint Kinase 1, Oocytes, Animals, Female, Protein Kinases, DNA Damage
7 Research products, page 1 of 1
- 2009IsAmongTopNSimilarDocuments
- 2001IsAmongTopNSimilarDocuments
- 1998IsAmongTopNSimilarDocuments
- 2018IsRelatedTo
- 2010IsAmongTopNSimilarDocuments
- 2018IsRelatedTo
- 2017IsRelatedTo
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).154 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 1% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 1%
