PMID:15470496
| Citation |
Fujii, S and Fuchs, RP (2004) Defining the position of the switches between replicative and bypass DNA polymerases. EMBO J. 23:4342-52 |
|---|---|
| Abstract |
Cells contain specialized DNA polymerases that are able to copy past lesions with an associated risk of generating mutations, the major cause of cancer. Here, we reconstitute translesion synthesis (TLS) using the replicative (Pol III) and major bypass (Pol V) DNA polymerases from Escherichia coli in the presence of accessory factors. When the replicative polymerase disconnects from the template in the vicinity of a lesion, Pol V binds the blocked replication intermediate and forms a stable complex by means of a dual interaction with the tip of the RecA filament and the beta-clamp, the processivity factor donated by the blocked Pol III holoenzyme. Both interactions are required to confer to Pol V the processivity that will allow it synthesize, in a single binding event, a TLS patch long enough to support further extension by Pol III. In the absence of these accessory factors, the patch synthesized by Pol V is too short, being degraded by the Pol III-associated exonuclease activity that senses the distortion induced by the lesion, thus leading to an aborted bypass process. |
| Links |
PubMed PMC524402 Online version:10.1038/sj.emboj.7600438 |
| Keywords |
DNA Damage; DNA Polymerase III/metabolism; DNA Replication; DNA, Single-Stranded/metabolism; DNA-Directed DNA Polymerase/metabolism; Escherichia coli/genetics; Escherichia coli/metabolism; Escherichia coli Proteins/genetics; Escherichia coli Proteins/metabolism; Macromolecular Substances; Nucleic Acid Conformation; Rec A Recombinases/metabolism |
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