Graubmann S, Dikomey E
Int J Radiat Biol Relat Stud Phys Chem Med. 1983 May;43(5):475-83. doi: 10.1080/09553008314550571.
Induction and repair of DNA strand breaks was investigated in synchronized CHO cells by using the alkaline DNA-unwinding technique followed by chromatography on hydroxyapatite. The velocity of DNA denaturation in an alkaline solution (pH 12.1) was found to be independent of the position in the cycle. In unirradiated cells the number of DNA strand breaks per 3.6 x 10(12) dalton was found to vary with age in cell cycle amounting to about 250 breaks per cell for G1, 400 for S, and 500 for G2 + M cells. The number of induced DNA strand breaks per unit dose was found to be the same in all phases; an average of 340 strand breaks were induced per Gy and per 3.6 x 10(12) dalton. Within the first hour after irradiation about 90 per cent of all radiation-induced strand breaks are rejoined.
通过使用碱性DNA解旋技术并随后在羟基磷灰石上进行色谱分析,研究了同步化的中国仓鼠卵巢(CHO)细胞中DNA链断裂的诱导和修复情况。发现在碱性溶液(pH 12.1)中DNA变性的速度与细胞周期中的位置无关。在未受辐照的细胞中,每3.6×10¹²道尔顿的DNA链断裂数随细胞周期中的年龄而变化,G1期细胞每细胞约250个断裂,S期细胞每细胞400个,G2 + M期细胞每细胞500个。发现每单位剂量诱导的DNA链断裂数在所有阶段均相同;每戈瑞(Gy)和每3.6×10¹²道尔顿平均诱导340个链断裂。在辐照后的第一小时内,所有辐射诱导的链断裂约90%会重新连接。