Sato T, Ishikawa K, Ogata K
Biochim Biophys Acta. 1977 Feb 16;474(4):549-61. doi: 10.1016/0005-2787(77)90075-2.
Incubation medium II causes release of ribosomal subunits from isolated prelabeled nuclei of regenerating rat liver in vitro (Sato, T., Ishikawa, K. and Ogato, K. (1976) Biochim. Biophys. Acta 000, 000-000). The effects of individual components of this medium on release of subunits were studied and the following results were obtained. 1. Dialyzed cytosol was effective in causing release of total labeled RNA, but its effect on release of labeled ribosomal subunits was rather lower than that of low molecular yeast RNA. Spermidine inhibited the release of total labeled RNA as well as that of labeled ribosomal subunits. 2. Low molecular yeast RNA was the most effective component for inducing release of labeled ribosomal subunits. Homologous ribosomal RNA was as effective as yeast RNA. Cytoplasmic ribosomes, prepared by washing with solution of high salt concentration, and their subunits were also effective. 3. Transfer RNA was not so effective as yeast RNA and ribosomal RNA and even after heat treatment it had little effect. 4. Among the homopolyribonucleotides tested, polyuridylic acid had a strong effect but polyadenylic acid, polycytidylic acid and polyinosinic acid had no effect. 5. The effects of yeast RNA and polyuridylic acid in causing release of labeled ribosomal subunits were dependent upon their concentrations in the reaction mixture. The characteristics of the factors which cause release of labeled ribosomal subunits in vitro are discussed on the basis of the results.
培养液II可使体外培养的再生大鼠肝脏的预先标记的分离细胞核释放核糖体亚基(佐藤,T.,石川,K.和绪方,K.(1976年)《生物化学与生物物理学学报》000, 000 - 000)。研究了该培养液中各成分对亚基释放的影响,得到以下结果。1. 透析后的胞质溶胶可有效促使总标记RNA释放,但其对标记核糖体亚基释放的影响低于低分子酵母RNA。亚精胺抑制总标记RNA以及标记核糖体亚基的释放。2. 低分子酵母RNA是诱导标记核糖体亚基释放最有效的成分。同源核糖体RNA与酵母RNA效果相同。用高盐浓度溶液洗涤制备的细胞质核糖体及其亚基也有效。3. 转运RNA不如酵母RNA和核糖体RNA有效,即使经过热处理也几乎没有效果。4. 在测试的同聚核糖核苷酸中,聚尿苷酸有强烈作用,但聚腺苷酸、聚胞苷酸和聚肌苷酸没有作用。5. 酵母RNA和聚尿苷酸引起标记核糖体亚基释放的作用取决于它们在反应混合物中的浓度。根据这些结果讨论了体外引起标记核糖体亚基释放的因素的特征。