Ramagli L S, Holoubek V
Chem Biol Interact. 1984 Nov;52(1):51-66. doi: 10.1016/0009-2797(84)90082-6.
The effect of 3'-methyl-4-dimethylaminoazobenzene (3'-MeDAB) on the phosphorylation of the proteins of the nuclear ribonucleoprotein (RNP) particles was studied in liver of rats. Forty eight hours after the application of 4 mg of the hepatocarcinogen per 100 g of body wt. by stomach intubation the particle proteins contained only 7% as much phosphate per mg of protein as the proteins of the same particles isolated from liver of control animals. Determination of the protein kinase and protein phosphatase activities in the total fraction of the non-histone nuclear proteins 48 h after the application of the carcinogen have shown an increase (200% and 159%, respectively) in both enzymatic activities. These results suggest that the hepatocarcinogen could induce the observed high turnover of the phosphates on the proteins of the liver nuclear ribonucleoprotein particles and the resulting dephosphorylation of these particles by stimulation of nuclear protein kinases and phosphatases. Qualitatively the same, but quantitatively much smaller changes were also observed 48 h after the application of the non-carcinogenic p-aminoazobenzene (AB) by stomach intubation and in regenerating liver. After the application of AB phosphorylation of the proteins of rat liver nuclear ribonucleoprotein particles decreased to 70% and in regenerating liver to 61% of the phosphorylation of particle proteins in control liver. Since it is assumed that nuclear RNP particles are involved in the processing and transport of newly synthesized premessenger RNA it is possible that the drastic dephosphorylation of the particle proteins induced by the carcinogen could be connected with the distortion of RNA processing which is observed in liver of animals treated with hepatocarcinogens.
在大鼠肝脏中研究了3'-甲基-4-二甲基氨基偶氮苯(3'-MeDAB)对核糖核蛋白(RNP)颗粒蛋白磷酸化的影响。通过胃插管给每100克体重施用4毫克致癌剂48小时后,颗粒蛋白每毫克蛋白所含的磷酸盐量仅为从对照动物肝脏分离出的相同颗粒蛋白的7%。施用致癌剂48小时后,对非组蛋白核蛋白总组分中的蛋白激酶和蛋白磷酸酶活性进行测定,结果表明两种酶活性均有所增加(分别增加200%和159%)。这些结果表明,致癌剂可诱导观察到的肝核糖核蛋白颗粒蛋白上磷酸盐的高周转率,并通过刺激核蛋白激酶和磷酸酶导致这些颗粒的去磷酸化。通过胃插管施用非致癌性对氨基偶氮苯(AB)48小时后以及在再生肝脏中,也观察到了定性相同但定量上小得多的变化。施用AB后,大鼠肝核糖核蛋白颗粒蛋白的磷酸化降至对照肝脏中颗粒蛋白磷酸化的70%,在再生肝脏中降至61%。由于假定核RNP颗粒参与新合成的前体信使RNA的加工和运输,因此致癌剂诱导的颗粒蛋白的剧烈去磷酸化可能与在用致癌剂处理的动物肝脏中观察到的RNA加工畸变有关。