Ogorek B, Bryant P E
Mutat Res. 1985 Jul;146(1):55-61. doi: 10.1016/0167-8817(85)90055-0.
The DNA-unwinding method developed by Ahnström and his coworkers to measure DNA strand breaks in mammalian cells was used to measure single-strand breaks (SSB) in the DNA of intact yeast cells. DNA unwinding, which took place inside the rigid cell wall of yeast, was investigated as a function of time, radiation dose, and of pH and salt concentration of the alkaline solution. After DNA unwinding had taken place, the cell wall was destroyed by partial enzymatic digestion and sonication in the presence of detergents. Fragments of single- and double-stranded DNA were separated using hydroxylapatite chromatography. In this way the most suitable conditions for DNA unwinding within the cell wall were established. The results show that SSB and double-strand breaks (DSB) give rise to different kinetics of DNA unwinding.
安斯特伦及其同事开发的用于测量哺乳动物细胞中DNA链断裂的DNA解旋方法,被用于测量完整酵母细胞DNA中的单链断裂(SSB)。在酵母坚硬的细胞壁内发生的DNA解旋,被作为时间、辐射剂量以及碱性溶液的pH值和盐浓度的函数进行研究。DNA解旋发生后,在存在去污剂的情况下,通过部分酶消化和超声处理破坏细胞壁。使用羟基磷灰石色谱法分离单链和双链DNA片段。通过这种方式确定了细胞壁内DNA解旋的最合适条件。结果表明,单链断裂和双链断裂(DSB)导致不同的DNA解旋动力学。