Moore M M, Clive D, Howard B E, Batson A G, Turner N T
Mutat Res. 1985 Aug;151(1):147-59. doi: 10.1016/0027-5107(85)90193-9.
TFTr mutants of L5178Y/TK+/- mouse lymphoma cells are analyzed as they appear in situ following cloning and incubation for 9-11 days in soft agar cloning medium. These TFTr mutants can be divided by colony size into sigma, small colony, and lambda, large colony, mutants. The use of a size discriminator on an automatic colony counter allows the production of histograms to evaluate the size distribution of colonies on a plate. The evaluation of these size distribution curves provides insight into the properties of sigma and lambda mutants. From these analyses several conclusions may be drawn. The sigma phenotype is preferentially associated with the TFTr subpopulation of a treated culture. The sigma phenotype is not an artifact of delayed toxicity following treatment. The frequency of quantifiable sigma mutants is not affected by agar concentrations between 0.20% and 0.45% in the cloning medium. TFTr sigma mutants are produced spontaneously and can be induced by a variety of mutagens. The decline in overall detectable mutants frequency observed for some mutagens with increasing time after treatment is due to the decline in sigma mutant frequency. The quantitation of both sigma and lambda mutants is thus useful in obtaining maximum utility of the information provided by the L5178Y/TK+/- mouse lymphoma assay.
对L5178Y/TK+/-小鼠淋巴瘤细胞的TFTr突变体进行分析,观察其在软琼脂克隆培养基中克隆并培养9至11天后的原位表现。这些TFTr突变体可根据集落大小分为σ(小集落)突变体和λ(大集落)突变体。在自动集落计数器上使用大小鉴别器可生成直方图,以评估平板上集落的大小分布。对这些大小分布曲线的评估有助于深入了解σ和λ突变体的特性。通过这些分析可得出几个结论。σ表型优先与经处理培养物中的TFTr亚群相关。σ表型不是处理后延迟毒性的假象。在克隆培养基中,0.20%至0.45%的琼脂浓度对可量化的σ突变体频率没有影响。TFTr σ突变体是自发产生的,可被多种诱变剂诱导。对于某些诱变剂,处理后随着时间的增加,总体可检测突变体频率的下降是由于σ突变体频率的下降。因此,对σ和λ突变体进行定量分析有助于充分利用L5178Y/TK+/-小鼠淋巴瘤试验提供的信息。