Costa N D, Bryant P E
Department of Biology and Preclinical Medicine, University of St. Andrews, Fife, Great Britain.
Mutat Res. 1988 Sep;194(2):93-9. doi: 10.1016/0167-8817(88)90011-9.
The DNA unwinding technique has been used to measure the induction and repair of DNA strand breaks by X-rays in the X-ray-sensitive (xrs 5) mutant and its parent CHO K1 line of Chinese hamster cells. Results show that frequency of induction of DNA strand breaks was the same for both cell lines. The repair of single-strand breaks was found to be slightly slower in xrs 5 over the first 20 min after X-ray exposure, but the level of repair of ssb reached after an incubation of 1h following X-ray exposure in xrs 5 was the same as in CHO K1. Our results also show that the rate of repair of DNA double-strand breaks in xrs 5 cells was clearly slower than that in CHO K1, supporting the conclusion of Kemp et al. (1984) who used the neutral elution technique, that xrs 5 is defective in the repair pathway of DNA double-strand breaks.
DNA解旋技术已被用于测量X射线敏感(xrs 5)突变体及其亲本中国仓鼠细胞系CHO K1中X射线诱导和修复DNA链断裂的情况。结果表明,两种细胞系中DNA链断裂的诱导频率相同。发现xrs 5在X射线照射后的前20分钟内单链断裂的修复略慢,但在X射线照射后孵育1小时后,xrs 5中达到的单链断裂修复水平与CHO K1相同。我们的结果还表明,xrs 5细胞中DNA双链断裂的修复速率明显慢于CHO K1,支持了Kemp等人(1984年)使用中性洗脱技术得出的结论,即xrs 5在DNA双链断裂的修复途径中存在缺陷。