4.5 Article

Oxidative DNA Damage and Repair in the Radioresistant Archaeon Thermococcus gammatolerans

Journal

CHEMICAL RESEARCH IN TOXICOLOGY
Volume 29, Issue 11, Pages 1796-1809

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrestox.6b00128

Keywords

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Funding

  1. Agence Nationale de la Recherche [ANR-12-BSV6-0012-01]
  2. Agence Nationale de la Recherche (ANR) [ANR-12-BSV6-0012] Funding Source: Agence Nationale de la Recherche (ANR)

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The hyperthermophilic archaeon Thermococcus gammatolerans can resist huge doses of gamma-irradiation, up to 5.0 kGy, without loss of viability. The potential to withstand such harsh conditions is probably due to complementary passive and active mechanisms, including repair of damaged chromosomes. In this work, we documented the formation and repair of oxidative DNA lesions in T. gammatolerans. The basal level of the oxidized nucleoside, 8-oxo-2'-deoxyguanosine (8-oxo-dGuo), was established at 9.2 (+/- 0.9) 8-oxo-dGuo per 10(6) nucleosides, a higher level than those usually measured in eukaryotic cells or bacteria. A significant increase in oxidative damage, i.e., up to 24.2 (+/- 8.0) 8-oxo-dGuo/10(6) nucleosides, was measured for T. gammatolerans exposed to a 5.0 kGy dose of gamma-rays. Surprisingly, the yield of radiation-induced modifications was lower than those previously observed for human cells exposed to doses corresponding to a few grays. One hour after irradiation, 8-oxo-dGuo levels were significantly reduced, indicating an efficient repair. Two putative base excision repair (BER) enzymes, TGAM_1277 and TGAM_1653, were demonstrated both by proteomics and transcriptomics to be present in the cells without exposure to ionizing radiation. Their transcripts were moderately upregulated after gamma irradiation. After heterologous production and purification of these enzymes, biochemical assays based on electrophoresis and MALDI-TOF (matrix-assisted laser desorption ionization time of flight) mass spectrometry indicated that both have a beta-elimination cleavage activity. TGAM_1653 repairs 8-oxo-dGuo, whereas TGAM_1277 is also able to remove lesions affecting pyrimidines (1-[2-deoxy-beta-n-erythro-pentofuranosyl]-5-hydroxyhydantoin (5-H-dHyd) and 1-[2-deoxy-beta-D-erythro-pentofuranosyl]-5-hydroxy-5-methylhydantoin (5-OH-5-Me-dHyd)). This work showed that in normal growth conditions or in the presence of a strong oxidative stress, T. gammatolerans has the potential to rapidly reduce the extent of DNA oxidation, with at least these two BER enzymes as bodyguards with distinct substrate ranges.

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