INRA, UMR1331, Toxalim, Research Centre in Food Toxicology, F-31027, Toulouse, France.
Cell Microbiol. 2013 Jan;15(1):1-15. doi: 10.1111/cmi.12028. Epub 2012 Oct 9.
The Cytolethal Distending Toxin (CDT) is a genotoxin produced by several pathogenic bacteria. It is generally admitted that CDT induces double-strand breaks (DSB) and cell cycle arrest in G2/M-phase, in an ATM-dependent manner. Most of these results were obtained at high dose (over 1 μg ml(-1) ) of CDT and late after treatment (8-24 h). We provide here evidence that the Escherichia coli CDT (EcCDT) - at low dose (50 pg ml(-1) or LD50) and early after treatment (3-6 h) - progressively induces DNA DSB, mostly in S-phase. DSB formation is related to the single-strand breaks induction by CDT, converted into DSB during the S-phase. We also show that homologous recombination is mobilized to these S-phase-associated DSB. This model unveils a new mechanism for CDT genotoxicity that may play a role in cells partly deficient in homologous recombination.
细胞致死膨胀毒素 (CDT) 是由几种致病性细菌产生的一种遗传毒素。一般认为,CDT 以依赖 ATM 的方式诱导双链断裂 (DSB) 和 G2/M 期细胞周期停滞。这些结果大多是在高剂量 (超过 1μg/ml) 的 CDT 和治疗后晚期 (8-24 小时) 获得的。我们在这里提供的证据表明,大肠杆菌 CDT (EcCDT) - 在低剂量 (50pg/ml 或 LD50) 和治疗后早期 (3-6 小时) - 逐渐诱导 DNA DSB,主要发生在 S 期。DSB 的形成与 CDT 诱导的单链断裂有关,在 S 期转化为 DSB。我们还表明,同源重组被动员到这些与 S 期相关的 DSB。该模型揭示了 CDT 遗传毒性的一种新机制,可能在同源重组部分缺陷的细胞中发挥作用。