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Vaisman A, McDonald JP, Woodgate R. Translesion DNA Synthesis. EcoSal Plus. 2012;5(1)doi: 10.1128/ecosalplus.7.2.2.
Vaisman, A., McDonald, J. P., & Woodgate, R. (2012). Translesion DNA Synthesis. EcoSal Plus, 5(1), . https://doi.org/10.1128/ecosalplus.7.2.2
Vaisman, Alexandra, et al. "Translesion DNA Synthesis." EcoSal Plus vol. 5,1 (2012). doi: https://doi.org/10.1128/ecosalplus.7.2.2
Vaisman A, McDonald JP, Woodgate R. Translesion DNA Synthesis. EcoSal Plus. 2012 Nov;5(1). doi: 10.1128/ecosalplus.7.2.2. PMID: 26442823; PMCID: PMC4231548.
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EcoSal Plus. 2012 Nov;5(1). doi: 10.1128/ecosalplus.7.2.2.

Translesion DNA Synthesis.

EcoSal Plus

Alexandra Vaisman, John P McDonald, Roger Woodgate

PMID: 26442823 PMCID: PMC4231548 DOI: 10.1128/ecosalplus.7.2.2

Abstract

All living organisms are continually exposed to agents that damage their DNA, which threatens the integrity of their genome. As a consequence, cells are equipped with a plethora of DNA repair enzymes to remove the damaged DNA. Unfortunately, situations nevertheless arise where lesions persist, and these lesions block the progression of the cell's replicase. In these situations, cells are forced to choose between recombination-mediated "damage avoidance" pathways or a specialized DNA polymerase (pol) to traverse the blocking lesion. The latter process is referred to as Translesion DNA Synthesis (TLS). As inferred by its name, TLS not only results in bases being (mis)incorporated opposite DNA lesions but also bases being (mis)incorporated downstream of the replicase-blocking lesion, so as to ensure continued genome duplication and cell survival. Escherichia coli and Salmonella typhimurium possess five DNA polymerases, and while all have been shown to facilitate TLS under certain experimental conditions, it is clear that the LexA-regulated and damage-inducible pols II, IV, and V perform the vast majority of TLS under physiological conditions. Pol V can traverse a wide range of DNA lesions and performs the bulk of mutagenic TLS, whereas pol II and pol IV appear to be more specialized TLS polymerases.

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