Institute of Chemical Biology and Fundamental Medicine, Siberian Branch Russian Academy of Sciences, Novosibirsk, 630090, Russia.
LLC "BioLink", Novosibirsk, 630090, Russia.
Biochemistry (Mosc). 2024 Jul;89(7):1183-1191. doi: 10.1134/S0006297924070022.
Proteins of nucleotide excision repair system (NER) are responsible for detecting and removing a wide range of bulky DNA damages, thereby contributing significantly to the genome stability maintenance within mammalian cells. Evaluation of NER functional status in the cells is important for identifying pathological changes in the body and assessing effectiveness of chemotherapy. The following method, described herein, has been developed for better assessment of bulky DNA damages removal , based on qPCR. Using the developed method, NER activity was compared for the extracts of the cells from two mammals with different lifespans: a long-lived naked mole-rat () and a short-lived mouse (). Proteins of the cell extract have been shown to be 1.5 times more effective at removing bulky damage from the model DNA substrate than the proteins of the cell extract. These results are consistent with the experimental data previously obtained. The presented method could be applied not only in fundamental studies of DNA repair in mammalian cells, but also in clinical practice.
核苷酸切除修复系统 (NER) 的蛋白质负责检测和去除广泛的大体积 DNA 损伤,从而为哺乳动物细胞内的基因组稳定性维持做出重要贡献。评估细胞中的 NER 功能状态对于识别体内的病理变化和评估化疗效果非常重要。本文所述的方法是基于 qPCR 开发的,用于更好地评估大体积 DNA 损伤的去除。使用所开发的方法,比较了两种具有不同寿命的哺乳动物的细胞提取物中的 NER 活性:长寿的裸鼹鼠 () 和短命的小鼠 ()。结果表明,细胞提取物中的蛋白质去除模型 DNA 底物中大体积损伤的效率比细胞提取物中的蛋白质高 1.5 倍。这些结果与之前获得的实验数据一致。该方法不仅可以应用于哺乳动物细胞中 DNA 修复的基础研究,也可以应用于临床实践。