DNA replication and progression through S phase
- PMID: 15838518
- DOI: 10.1038/sj.onc.1208616
DNA replication and progression through S phase
Abstract
Initiation and completion of DNA replication defines the beginning and ending of S phase of the cell cycle. Successful progression through S phase requires that replication be properly regulated and monitored to ensure that the entire genome is duplicated exactly once, without errors, in a timely fashion. Given the immense size and complexity of eukaryotic genomes, this presents a significant challenge for the cell. As a result, DNA replication has evolved into a tightly regulated process involving the coordinated action of numerous factors that function in all phases of the cell cycle. We will review our current understanding of these processes from the formation of prereplicative complexes in preparation for S phase to the series of events that culminate in the loading of DNA polymerases during S phase. We will incorporate structural data from archaeal and bacterial replication proteins and discuss their implications for understanding the mechanism of action of their corresponding eukaryotic homologues. We will also describe the concept of replication licensing which protects against genomic instability by limiting initiation events to once per cell cycle. Lastly, we will review our knowledge of checkpoint pathways that maintain the integrity of stalled forks and relay defects in replication to the rest of the cell cycle.
Similar articles
-
The DNA damage response during an unperturbed S-phase.DNA Repair (Amst). 2007 Jul 1;6(7):914-22. doi: 10.1016/j.dnarep.2007.02.005. Epub 2007 Mar 19. DNA Repair (Amst). 2007. PMID: 17374515 Review.
-
Maintenance of fork integrity at damaged DNA and natural pause sites.DNA Repair (Amst). 2007 Jul 1;6(7):900-13. doi: 10.1016/j.dnarep.2007.02.004. Epub 2007 Mar 26. DNA Repair (Amst). 2007. PMID: 17379579 Review.
-
G1 and S-phase checkpoints, chromosome instability, and cancer.Methods Mol Biol. 2004;280:3-49. doi: 10.1385/1-59259-788-2:003. Methods Mol Biol. 2004. PMID: 15187248 Review.
-
Replication fork movement sets chromatin loop size and origin choice in mammalian cells.Nature. 2008 Sep 25;455(7212):557-60. doi: 10.1038/nature07233. Epub 2008 Aug 17. Nature. 2008. PMID: 18716622
-
Mechanisms of dealing with DNA damage-induced replication problems.Cell Biochem Biophys. 2009;53(1):17-31. doi: 10.1007/s12013-008-9039-y. Epub 2008 Nov 26. Cell Biochem Biophys. 2009. PMID: 19034694 Review.
Cited by
-
Chronic p53-independent p21 expression causes genomic instability by deregulating replication licensing.Nat Cell Biol. 2016 Jul;18(7):777-89. doi: 10.1038/ncb3378. Epub 2016 Jun 20. Nat Cell Biol. 2016. PMID: 27323328 Free PMC article.
-
Functional cooperation between FACT and MCM is coordinated with cell cycle and differential complex formation.J Biomed Sci. 2010 Feb 16;17(1):11. doi: 10.1186/1423-0127-17-11. J Biomed Sci. 2010. PMID: 20156367 Free PMC article.
-
The midblastula transition defines the onset of Y RNA-dependent DNA replication in Xenopus laevis.Mol Cell Biol. 2011 Sep;31(18):3857-70. doi: 10.1128/MCB.05411-11. Epub 2011 Jul 26. Mol Cell Biol. 2011. PMID: 21791613 Free PMC article.
-
High expression of cell division cycle 7 protein correlates with poor prognosis in patients with diffuse large B-cell lymphoma.Med Oncol. 2012 Dec;29(5):3498-503. doi: 10.1007/s12032-012-0223-y. Epub 2012 Apr 19. Med Oncol. 2012. PMID: 22528513
-
DNA is a co-factor for its own replication in Xenopus egg extracts.Nucleic Acids Res. 2011 Jan;39(2):545-55. doi: 10.1093/nar/gkq739. Epub 2010 Sep 21. Nucleic Acids Res. 2011. PMID: 20861001 Free PMC article.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials