Hazan N, McCauley R
Biochem J. 1976 Jun 15;156(3):665-70. doi: 10.1042/bj1560665.
The transport of nucleic acids from the nucleus to the cytoplasm is a potential site for modification of normal cellular processes by drugs and hormones. In this study the effect of phenobarbitone on nucleocytoplasmic transport of ribosomes was measured in an assay system in vitro. The transport of radioactive ribosomes from isolated rat hepatic nuclei to unlabelled post-microsomal supernatant was measured in rats treated with 80 mg of phenobarbitone/kg body wt. or saline 3h before death. With either treatment, transport was linear with time, and dependent on temperature and the presence of ATP. However, phenobarbitone treatment increased transport of ribonucleoproteins over saline-treated animals nearly twofold. The effect of phenobarbitone was mediated through the cytosol, but was not the result of altered stability of the RNA transported to the cytosol. Cycloheximide (5 mg/kg body wt.) given 3.5 h before death inhibited the stimulation of transport by phenobarbitone. The data indicate that phenobarbitone increased the transport of RNA by stimulating the synthesis of cytosol factors that regulate transport of RNA from the nucleus.
核酸从细胞核向细胞质的转运是药物和激素改变正常细胞过程的一个潜在作用位点。在本研究中,在体外分析系统中测定了苯巴比妥对核糖体核质转运的影响。在处死前3小时,给大鼠按80mg苯巴比妥/千克体重或生理盐水处理,然后测定放射性核糖体从分离的大鼠肝细胞核向未标记的微粒体后上清液的转运。无论哪种处理,转运均随时间呈线性,且依赖于温度和ATP的存在。然而,与生理盐水处理的动物相比,苯巴比妥处理使核糖核蛋白的转运增加了近两倍。苯巴比妥的作用是通过胞质溶胶介导的,但并非是转运至胞质溶胶的RNA稳定性改变的结果。在处死前3.5小时给予环己酰亚胺(5mg/千克体重)可抑制苯巴比妥对转运的刺激作用。数据表明,苯巴比妥通过刺激调节RNA从细胞核转运的胞质溶胶因子的合成来增加RNA的转运。