Shaul Y, Ginzburg I, Aviv H
Eur J Biochem. 1981 Mar;114(3):591-5. doi: 10.1111/j.1432-1033.1981.tb05185.x.
Friend erythroleukemic cells were induced to differentiate by dimethylsulfoxide (Me2SO) in the absence or presence of the tumor promoter 12-O-tetradecanoyl-phorbol 13-acetate. The effects of the latter on the molecular parameters related to globin mRNA metabolism were examined. When differentiation was scored by benzidine staining, it had an inhibitory effect on Me2SO-treated cells. On the other hand, when differentiation was followed by determination of globin mRNA accumulation, it had a pleiotropic effect on Me2SO-treated cells. At the early phase of differentiation (2--3 days) the rate of globin mRNA accumulation was higher in the promoter-treated cells than in the control. This unexpectedly high level of accumulation was followed by a sharp reduction and most of the globin RNA sequences disappeared at later stages of differentiation (days 4--5). The reduction can be related to the effect of the promoter on the stability of globin RNA in the cytoplasm which was reduced from a half-life of 16 h to that of 8 h only. Other parameters, such as the rate of globin mRNA synthesis and its capability to serve as a template for cell-free protein synthesis were not affected by treatment with the promoter throughout the differentiation process.
在存在或不存在肿瘤启动子12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯的情况下,用二甲基亚砜(Me2SO)诱导Friend红白血病细胞分化。研究了后者对与珠蛋白mRNA代谢相关分子参数的影响。当通过联苯胺染色对分化进行评分时,它对经Me2SO处理的细胞有抑制作用。另一方面,当通过测定珠蛋白mRNA积累来跟踪分化时,它对经Me2SO处理的细胞有多种效应。在分化的早期阶段(2 - 3天),经启动子处理的细胞中珠蛋白mRNA积累速率高于对照。这种意外的高水平积累之后是急剧下降,并且在分化后期(第4 - 5天)大多数珠蛋白RNA序列消失。这种下降可能与启动子对细胞质中珠蛋白RNA稳定性的影响有关,其半衰期仅从16小时降至8小时。在整个分化过程中,其他参数,如珠蛋白mRNA合成速率及其作为无细胞蛋白质合成模板的能力,均不受启动子处理的影响。