Answering the Call: Coping with DNA Damage at the Most Inopportune Time
Open Access
- 1 January 2002
- journal article
- review article
- Published by Wiley in BioMed Research International
- Vol. 2 (2) , 66-74
- https://doi.org/10.1155/s1110724302202016
Abstract
DNA damage incurred during the process of chromosomal replication has a particularly high possibility of resulting in mutagenesis or lethality for the cell. The SOS response of Escherichia coli appears to be well adapted for this particular situation and involves the coordinated up‐regulation of genes whose products center upon the tasks of maintaining the integrity of the replication fork when it encounters DNA damage, delaying the replication process (a DNA damage checkpoint), repairing the DNA lesions or allowing replication to occur over these DNA lesions, and then restoring processive replication before the SOS response itself is turned off. Recent advances in the fields of genomics and biochemistry has given a much more comprehensive picture of the timing and coordination of events which allow cells to deal with potentially lethal or mutagenic DNA lesions at the time of chromosomal replication.Keywords
Funding Information
- National Natural Science Foundation of China (MCB0130486)
This publication has 75 references indexed in Scilit:
- FtsQ, FtsL and FtsI require FtsK, but not FtsN, for co‐localization with FtsZ during Escherichia coli cell divisionMolecular Microbiology, 2001
- Converting a DNA damage checkpoint effector (UmuD2C) into a lesion bypass polymerase (UmuD'2C)The EMBO Journal, 2001
- Role of the Escherichia coli Nucleotide Excision Repair Proteins in DNA ReplicationJournal of Bacteriology, 2000
- Modulation of RNA Polymerase by (p)ppGpp Reveals a RecG-Dependent Mechanism for Replication Fork ProgressionCell, 2000
- UmuD′ 2 C is an error-prone DNA polymerase, Escherichia coli pol VProceedings of the National Academy of Sciences, 1999
- RecA Protein: Structure, Function, and Role in Recombinational DNA RepairProgress in Nucleic Acid Research and Molecular Biology, 1997
- A Dominant Negative Allele of the Escherichia coli uvrD Gene Encoding DNA Helicase IIJournal of Molecular Biology, 1994
- Inducibility of a gene product required for UV and chemical mutagenesis in Escherichia coli.Proceedings of the National Academy of Sciences, 1981
- Expression of the E. coli uvrA gene is inducibleNature, 1981
- Degradation of Escherichia coli DNA: Evidence for limitation in vivo by protein X, the recA gene productMolecular Genetics and Genomics, 1979