The importance of repairing stalled replication forks
- PMID: 10716434
- DOI: 10.1038/35003501
The importance of repairing stalled replication forks
Abstract
The bacterial SOS response to unusual levels of DNA damage has been recognized and studied for several decades. Pathways for re-establishing inactivated replication forks under normal growth conditions have received far less attention. In bacteria growing aerobically in the absence of SOS-inducing conditions, many replication forks encounter DNA damage, leading to inactivation. The pathways for fork reactivation involve the homologous recombination systems, are nonmutagenic, and integrate almost every aspect of DNA metabolism. On a frequency-of-use basis, these pathways represent the main function of bacterial DNA recombination systems, as well as the main function of a number of other enzymatic systems that are associated with replication and site-specific recombination.
Similar articles
-
Recombinase and translesion DNA polymerase decrease the speed of replication fork progression during the DNA damage response in Escherichia coli cells.Nucleic Acids Res. 2015 Feb 18;43(3):1714-25. doi: 10.1093/nar/gkv044. Epub 2015 Jan 27. Nucleic Acids Res. 2015. PMID: 25628359 Free PMC article.
-
Recombinational DNA repair of damaged replication forks in Escherichia coli: questions.Annu Rev Genet. 2001;35:53-82. doi: 10.1146/annurev.genet.35.102401.090016. Annu Rev Genet. 2001. PMID: 11700277 Review.
-
Interplay between DNA replication and recombination in prokaryotes.Annu Rev Microbiol. 2005;59:43-67. doi: 10.1146/annurev.micro.59.030804.121255. Annu Rev Microbiol. 2005. PMID: 15792496
-
Phenotypes of dnaXE145A Mutant Cells Indicate that the Escherichia coli Clamp Loader Has a Role in the Restart of Stalled Replication Forks.J Bacteriol. 2017 Nov 14;199(24):e00412-17. doi: 10.1128/JB.00412-17. Print 2017 Dec 15. J Bacteriol. 2017. PMID: 28947673 Free PMC article.
-
[Recombinations occurring in the process of DNA replication in Escherichia coli].Genetika. 2006 Jul;42(7):869-78. Genetika. 2006. PMID: 16915915 Review. Russian.
Cited by
-
Recombinase and translesion DNA polymerase decrease the speed of replication fork progression during the DNA damage response in Escherichia coli cells.Nucleic Acids Res. 2015 Feb 18;43(3):1714-25. doi: 10.1093/nar/gkv044. Epub 2015 Jan 27. Nucleic Acids Res. 2015. PMID: 25628359 Free PMC article.
-
PARP inhibitor resistance in breast and gynecological cancer: Resistance mechanisms and combination therapy strategies.Front Pharmacol. 2022 Aug 25;13:967633. doi: 10.3389/fphar.2022.967633. eCollection 2022. Front Pharmacol. 2022. PMID: 36091750 Free PMC article. Review.
-
NER initiation factors, DDB2 and XPC, regulate UV radiation response by recruiting ATR and ATM kinases to DNA damage sites.DNA Repair (Amst). 2013 Apr 1;12(4):273-83. doi: 10.1016/j.dnarep.2013.01.003. Epub 2013 Feb 17. DNA Repair (Amst). 2013. PMID: 23422745 Free PMC article.
-
Directed Evolution of RecA Variants with Enhanced Capacity for Conjugational Recombination.PLoS Genet. 2015 Jun 5;11(6):e1005278. doi: 10.1371/journal.pgen.1005278. eCollection 2015 Jun. PLoS Genet. 2015. PMID: 26047498 Free PMC article.
-
Human PSF concentrates DNA and stimulates duplex capture in DMC1-mediated homologous pairing.Nucleic Acids Res. 2012 Apr;40(7):3031-41. doi: 10.1093/nar/gkr1229. Epub 2011 Dec 9. Nucleic Acids Res. 2012. PMID: 22156371 Free PMC article.
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
