Unité 5-Luminy, Centre de Biochimie et de Biologie Moléculaire, Case 901, F-13288, Marseille Cedex 9, France.
Planta. 1984 Nov;162(5):434-40. doi: 10.1007/BF00393456.
Soybean cells were subcultured in the presence of 4 μM 2,4-dichlorophenoxyacetic acid (2,4-D;=stock cells), or transferred and subcultured in a culture medium depleted of 2,4-D (=control cells), then reincubated with 4 μM 2,4-D (=treated cells). Control cells responded to 2,4-D by resuming cell division and DNA, RNA and protein synthesis at levels which were comparable to those of stock cells. This study system was used to investigate auxin effects on RNA polymerases. Both activities of RNA polymerases and their absolute amounts in extracts from stock, control and treated cells were determined, using the in-vitro assy of transcription of denatured calf thymus DNA and the specific quantitative immunological method reported in Miassod and Got (1984, Planta 162, 427-434), respectively. The data showed that the levels of enzymes did not remain constant in the stock cells during the subculture cycle, that auxin treatment enhanced, by a factor of two to four, the amounts of RNA polymerase I and II, expressed as percents of total proteins of soybean cells, and that this increase was not necessarily reflected by a parallel increase of the activity measured in the in-vitro test.
在存在 4μM 2,4-二氯苯氧乙酸(2,4-D;= 原代细胞)的情况下对大豆细胞进行亚培养,或者在不含 2,4-D 的培养基中转代和亚培养(=对照细胞),然后用 4μM 2,4-D 再培养(=处理细胞)。对照细胞通过恢复细胞分裂以及 DNA、RNA 和蛋白质的合成来响应 2,4-D,其水平与原代细胞相当。本研究系统用于研究生长素对 RNA 聚合酶的影响。使用变性小牛胸腺 DNA 的体外转录测定和 Miassod 和 Got(1984,Planta 162, 427-434)中报道的特定定量免疫方法,分别确定了原代、对照和处理细胞提取物中 RNA 聚合酶的活性及其绝对数量。数据表明,在亚培养周期中,酶的水平在原代细胞中并不保持恒定,生长素处理将 RNA 聚合酶 I 和 II 的量分别提高了两到四倍,以大豆细胞总蛋白的百分比表示,并且这种增加并不一定反映在体外测试中测量的活性的平行增加。