Stetka D G, Bleicher W T, Brewen J G
Environ Mutagen. 1985;7(2):233-43. doi: 10.1002/em.2860070210.
It has been suggested not only that sister chromatid exchange (SCE) induction might serve as a qualitative indicator of mutagenesis, but also that induced SCE frequencies are linearly related to induced mutation frequencies. The consistency of the relationship between SCEs and mutations was tested in the present work. Confluent Chinese hamster ovary (CHO) cells were exposed to ethylnitrosourea (ENU) and then held at confluency for various times prior to initiation of SCE and mutation assays. Cells held at confluency are typically thought to be arrested in their progression through the cell cycle, so that "S-dependent" processes such as fixation of mutations and formation of SCEs will not occur, while DNA repair processes might continue to operate. If repair processes reduce the number of SCE-inducing lesions during the holding period and, hence, reduce the subsequently determined SCE frequencies, then mutation frequencies should similarly be reduced if SCEs and mutations are related. It was observed, however, that induced SCE frequencies decreased exponentially with holding time, while mutation frequencies remained constant. Qualitatively similar results were obtained in log-phase cells. Cell cycle analysis demonstrates that confluent CHO cells can cycle, and ways are considered in which this might affect SCE and mutation frequencies. It is concluded that the decline in SCE frequency (with time) cannot be attributed solely to the presence of cycling cells in confluent cultures. It appears, therefore, that at least some forms of ENU-induced DNA damage that can lead to SCE were repaired and as such are distinct from those forms that are mutagenic. Thus SCEs are not necessarily related to mutations, because the two events may represent manifestations of different forms of DNA damage. Whether or not this represents a universal phenomenon that would hold true for agents other than ENU remains to be determined.
有人提出,姐妹染色单体交换(SCE)诱导不仅可作为诱变的定性指标,而且诱导的SCE频率与诱导的突变频率呈线性相关。在本研究中测试了SCE与突变之间关系的一致性。将汇合的中国仓鼠卵巢(CHO)细胞暴露于乙基亚硝基脲(ENU),然后在开始SCE和突变测定之前在汇合状态下保持不同时间。通常认为处于汇合状态的细胞在其细胞周期进程中被阻滞,因此不会发生诸如突变固定和SCE形成等“S依赖”过程,而DNA修复过程可能会继续运行。如果修复过程在保持期内减少了诱导SCE的损伤数量,从而降低了随后测定的SCE频率,那么如果SCE与突变相关,则突变频率也应同样降低。然而观察到,诱导的SCE频率随保持时间呈指数下降,而突变频率保持不变。在对数期细胞中也获得了定性相似的结果。细胞周期分析表明汇合的CHO细胞可以循环,并考虑了这可能影响SCE和突变频率的方式。得出的结论是,SCE频率(随时间)的下降不能仅归因于汇合培养物中循环细胞的存在。因此,似乎至少某些形式的可导致SCE的ENU诱导的DNA损伤得到了修复,因此与那些具有诱变性的形式不同。因此,SCE不一定与突变相关,因为这两个事件可能代表不同形式的DNA损伤的表现。这是否代表一种对ENU以外的其他试剂也适用的普遍现象,仍有待确定。