Klaude M, von der Decken A
Arch Toxicol. 1983 Nov;54(3):215-25. doi: 10.1007/BF01239205.
The effect of dimethylnitrosamine on functional activities of liver chromatin was studied in mice. After a single dose of dimethylnitrosamine injected i.v. (25 mg/kg body wt, 45 min before sacrifice) liver nuclei were isolated and incubated with micrococcal nuclease (EC 3.1.4.7) to an acid-solubility of 2.5% of total DNA. Chromatin was fractionated into a 1,200 g pellet P1, 102,000 g pellet P2 and supernatant fraction S2. Chromatin-bound RNA polymerase I plus III activity decreased 15% in the P1 and 25% in the P2 fraction. No changes in activity were observed in the S2 fraction. Chromatin-bound RNA polymerase II activity decreased 19% in the P1, 49% in the P2 and 32% in the S2 fraction. Heparin stimulated RNA polymerase II activity decreased 10% in the P1 and 44% in the P2 fraction. Formation of initiation in nuclear lysates with RNA polymerase from Escherichia coli increased after administration of dimethylnitrosamine suggesting an increase in the number of sites available for the start of new RNA chains. The results show that limited digestion of nuclei with endonuclease cleaves chromatin regions which are more affected by dimethylnitrosamine than the total chromatin suggesting a non-random effect of the hepatotoxin on chromatin. Modifications of the DNA template by dimethylnitrosamine is indicated by the change in number of initiation complexes.
在小鼠中研究了二甲基亚硝胺对肝脏染色质功能活性的影响。静脉注射单剂量二甲基亚硝胺(25mg/kg体重,处死前45分钟)后,分离肝脏细胞核并用微球菌核酸酶(EC 3.1.4.7)孵育至总DNA酸溶性为2.5%。染色质被分离成1200g沉淀P1、102000g沉淀P2和上清液组分S2。染色质结合的RNA聚合酶I加III活性在P1组分中降低了15%,在P2组分中降低了25%。在S2组分中未观察到活性变化。染色质结合的RNA聚合酶II活性在P1组分中降低了19%,在P2组分中降低了49%,在S2组分中降低了32%。肝素刺激的RNA聚合酶II活性在P1组分中降低了10%,在P2组分中降低了44%。给予二甲基亚硝胺后,用来自大肠杆菌的RNA聚合酶在核裂解物中起始复合物的形成增加,这表明可用于新RNA链起始的位点数量增加。结果表明,用核酸内切酶对细胞核进行有限消化可切割染色质区域,这些区域比总染色质更受二甲基亚硝胺影响,提示肝毒素对染色质有非随机效应。起始复合物数量的变化表明二甲基亚硝胺对DNA模板有修饰作用。