Mitrokhin Iu I, Sizova S T, Gutnikova M N, Todorov I N
Biokhimiia. 1988 Dec;53(12):2033-41.
The biosynthesis of proteins, ribosomal RNA and other components of the rat liver protein-synthesizing system during the reparation and subsequent activation of translation inhibited by a sublethal dose cycloheximide (CHI, 3 mg/kg) was studied. It was found that the incorporation of labeled precursors into proteins and ribosomal rRNA isolated from free and membrane-bound polysomes is repaired already 3 hours after CHI injection. 6-9 hours thereafter, the level of component labeling reaches control values, whereas the total protein biosynthesis is retarded. After 12-24 hours, marked stimulation of ribosome biosynthesis and the integration of ribosomes into polysomes are observed together with an asymmetric accumulation of excessive amounts of newly synthesized 40S subunits into polysomes 12 hours after CHI infection. The putative mechanisms of the activation of expression of the part of the genome responsible for protein and ribosomal rRNA synthesis as well as for the synthesis of other components of the protein-synthesizing system are discussed.
研究了在亚致死剂量环己酰亚胺(CHI,3mg/kg)抑制翻译后,大鼠肝脏蛋白质合成系统修复及随后激活过程中蛋白质、核糖体RNA和其他组分的生物合成。发现注射CHI后3小时,标记前体掺入从游离和膜结合多核糖体分离的蛋白质和核糖体rRNA中的过程就已得到修复。此后6 - 9小时,组分标记水平达到对照值,而总蛋白质生物合成受到抑制。12 - 24小时后,观察到核糖体生物合成显著刺激以及核糖体整合到多核糖体中,同时在CHI感染后12小时多核糖体中过量新合成的40S亚基不对称积累。讨论了负责蛋白质和核糖体rRNA合成以及蛋白质合成系统其他组分合成的基因组部分表达激活的可能机制。