Clinopodium vulgare L. Extract Counteracts DNA Damaging Action of Radiomimetic Zeocin Accelerating DSBS Rejoining in Saccharomyces Cerevisiae

T. Todorova, Iviyana Ivanova, P. Parvanova, S. Chankova
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Abstract

The aim of the present work was to evaluate the potential of Clinopodium vulgare water leaves extract to decrease the DNA damaging action of zeocin and to throw more light on the mode of action. Single and combined treatments with 10, 100, and 1000 µg/ml plant extract and 100 µg/ml zeocin were performed on 551 (haploid) and D7ts1 (diploid) yeast strains. The protective potential, the magnitude of the repair capacity, and the role of incubation conditions were studied based on double strand breaks' (DSB) induction and rejoining. The results provided new evidence that despite the different ploidy both strains are DSBs repair proficient but differ in their repair capacity although comparable levels of initially induced DSBs were measured. The diploid strain D7ts1 was found to possess better-expressed repair capacity than the haploid strain 551. The combined treatment with Clinopodium vulgare L. extract at concentrations' range of 10—1000 µg/ml and zeocin resulted in a significant decrease in DSBs levels. It could be suggested that priming the cells with various concentrations of the extract results in an acceleration of DSBs rejoining when 30 min recovery time at optimal experimental conditions is given. When incubation is performed on ice the repair processes are impeded but not fully blocked. Such a study confirms that the difference in the repair capacity of the cells could be one of the possible mechanisms, participating in cell protection against different DNA damaging factors. The combined application of Clinopodium vulgare L. extract at concentrations range of 10—1000 µg/ml protects yeast DNA against zeocin-induced DSBs by acceleration of DSB rejoining.
Clinopodium vulgare L.提取物可抵消仿辐射沸石素对DNA的损伤作用,加速酿酒酵母中DSBS的重新连接
本研究的目的是评估clinopodium vulgare水叶提取物降低玉米素DNA损伤作用的潜力,并进一步揭示其作用模式。在 551(单倍体)和 D7ts1(二倍体)酵母菌株上分别用 10、100 和 1000 µg/ml 的植物提取物和 100 µg/ml 的玉米素进行单一处理和联合处理。根据双链断裂(DSB)的诱导和重接,研究了保护潜力、修复能力的大小以及培养条件的作用。研究结果提供了新的证据,表明尽管两株菌株的倍性不同,但它们都具有很强的DSB修复能力,只是在修复能力上有所不同,尽管测量到的最初诱导的DSB水平相当。研究发现,二倍体菌株D7ts1比单倍体菌株551具有更好的修复能力。用浓度范围为 10-1000 µg/ml 的 Clinopodium vulgare L. 提取物和 zeocin 联合处理后,DSBs 水平显著下降。这表明,在最佳实验条件下给细胞 30 分钟的恢复时间,用不同浓度的提取物处理细胞会加速 DSBs 的重新连接。在冰上培养时,修复过程会受到阻碍,但不会完全被阻断。这项研究证实,细胞修复能力的差异可能是参与细胞保护以抵御不同 DNA 损伤因子的可能机制之一。在 10-1000 µg/ml 的浓度范围内联合使用clinopodium vulgare L. 提取物,可通过加速 DSB 重接,保护酵母 DNA 免受玉米素诱导的 DSB 的损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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