The importance of repairing stalled replication forks
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- 2 March 2000
- journal article
- research article
- Published by Springer Nature in Nature
- Vol. 404 (6773) , 37-41
- https://doi.org/10.1038/35003501
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.Keywords
This publication has 63 references indexed in Scilit:
- sbcB sbcC null mutations allow RecF‐mediated repair of arrested replication forks in rep recBC mutantsMolecular Microbiology, 1999
- Analysis of DNA replication forks encountering a pyrimidine dimer in the template to the leading strandJournal of Molecular Biology, 1999
- RECOMBINATION AND RECOMBINATION-DEPENDENT DNA REPLICATION IN BACTERIOPHAGE T4Annual Review of Genetics, 1998
- The DNA replication protein PriA and the recombination protein RecG bind D-loopsJournal of Molecular Biology, 1997
- The Translocating RecBCD Enzyme Stimulates Recombination by Directing RecA Protein onto ssDNA in a χ-Regulated MannerCell, 1997
- An alternative pathway for yeast telomere maintenance rescues est1− senescencePublished by Elsevier ,1993
- PROKARYOTIC DNA REPLICATIONAnnual Review of Biochemistry, 1992
- Dissecting the functional role of PriA protein‐catalysed primosome assembly in Escherichia coli DNA replicationMolecular Microbiology, 1991
- Replication initiated at the origin (oriC) of the E. coli chromosome reconstituted with purified enzymesCell, 1984
- Mechanism of E. coli RecA protein directed strand exchanges in post-replication repair of DNANature, 1981