Ogorek B, Bryant P E
Mutat Res. 1985 Jul;146(1):63-70. doi: 10.1016/0167-8817(85)90056-2.
The kinetics of disappearance of single-strand breaks (SSB) from the DNA of X-irradiated stationary yeast cells under liquid-holding conditions was found to proceed in a dose-independent manner up to a dose of at least 2400 Gy, and was found to be complete after incubation of cells for 1 h. This was deduced from data for a yeast wild-type (WT) haploid and diploid strain as well as for rad52 haploid cells defective in DNA double-strand break (DSB) repair. In all cases an initial fast repair component assumed to correspond to SSB repair was observed whereby about 80% of the induced 'unwinding points' disappeared from the DNA with a time constant of about 3 min. Following this fast component, a slower component of removal of 'unwinding points' occurred with a time constant estimated to be 20 min. The molecular nature of these two components of repair is not known. We could find no evidence for the induction of secondary (enzymatic) breaks in the DNA during post-irradiation incubation. Incubation of cells in growth medium after irradiation resulted in similar kinetics as those under liquid-holding conditions. In the absence of an energy source in the medium (i.e. when cells were incubated in buffer or distilled water after irradiation) only 60-80% of the SSB were removed from yeast DNA. Residual SSB disappeared from the DNA only when cells were transferred to a medium containing glucose. The relative mass of DNA unwound per induced strand break (i.e. represented by the slope of the dose-effect curve immediately after irradiation) was found to change slowly with the age of the cell culture under liquid-holding conditions. This effect had to be corrected for in the measurements of strand break repair under these conditions.
在液体保持条件下,发现X射线照射的静止酵母细胞DNA中单链断裂(SSB)的消失动力学在至少2400 Gy的剂量范围内以剂量独立的方式进行,并且在细胞孵育1小时后发现SSB完全消失。这是从酵母野生型(WT)单倍体和二倍体菌株以及DNA双链断裂(DSB)修复缺陷的rad52单倍体细胞的数据推导出来的。在所有情况下,都观察到一个初始的快速修复成分,假定其对应于SSB修复,由此约80%的诱导“解旋点”以约3分钟的时间常数从DNA中消失。在这个快速成分之后,“解旋点”的去除出现了一个较慢的成分,其时间常数估计为20分钟。这两个修复成分的分子性质尚不清楚。我们没有发现辐照后孵育期间DNA中诱导产生二级(酶促)断裂的证据。辐照后在生长培养基中孵育细胞产生的动力学与液体保持条件下的动力学相似。在培养基中没有能量源的情况下(即辐照后细胞在缓冲液或蒸馏水中孵育时),酵母DNA中仅60 - 80%的SSB被去除。只有当细胞转移到含有葡萄糖的培养基中时,残留的SSB才会从DNA中消失。发现每个诱导的链断裂解开的DNA相对质量(即由辐照后立即的剂量效应曲线斜率表示)在液体保持条件下随细胞培养物的年龄缓慢变化。在这些条件下测量链断裂修复时必须对此效应进行校正。