Diamond L, Kruszewski F, Baird W M
Mutat Res. 1982 Aug;95(2-3):353-62. doi: 10.1016/0027-5107(82)90270-6.
The effect of expression time (the time between the end of the treatment period and the first exposure to selective medium) on the frequency of benzo[a]pyrene (BP)-induced mutations at the HGPRT (hypoxanthine-guanine phosphoribosyl transferase 2.4.2.8) locus was examined in the cell-mediated mutation assay in which V79 Chinese hamster cells are the targets and BP activation is mediated by Syrian hamster embryo cells. After the optimal expression time (4-5 days), the mutation frequency induced by exposure to 0.5 microgram BP/ml decreased logarithmically with increasing length of expression time until at 40 days there was a complete absence of mutant cells. The growth rates of three BP-induced 6-thioguanine-resistant clones were examined; each of these clones had a 30% longer lag time before reaching the period of logarithmic growth than the parent V79 cells. This suggests that the decay in mutation frequency with increasing expression time may be due to the slower reinitiation of growth by mutant than non-mutant cells after subcultivation into non-selective medium; this results in a loss of 25-40% of the mutant cells with each subculture. These findings show that optimal expression time in cell-mediated mutation assays may be of short duration and that this must be taken into account in the design and interpretation of such assays.
在细胞介导的突变试验中,以V79中国仓鼠细胞为靶细胞,叙利亚仓鼠胚胎细胞介导苯并[a]芘(BP)活化,研究了表达时间(治疗期结束至首次接触选择培养基之间的时间)对BP诱导的次黄嘌呤 - 鸟嘌呤磷酸核糖基转移酶(HGPRT,2.4.2.8)位点突变频率的影响。在最佳表达时间(4 - 5天)后,暴露于0.5微克BP/ml所诱导的突变频率随着表达时间的延长呈对数下降,直至40天时完全没有突变细胞。检测了三个BP诱导的6 - 硫鸟嘌呤抗性克隆的生长速率;与亲本V79细胞相比,这些克隆中的每一个在进入对数生长期之前都有30%更长的延迟期。这表明随着表达时间的增加突变频率的下降可能是由于突变细胞在传代培养到非选择培养基后比非突变细胞生长重新起始更慢;这导致每次传代时25 - 40%的突变细胞丢失。这些发现表明细胞介导的突变试验中的最佳表达时间可能较短,并且在设计和解释此类试验时必须考虑到这一点。