Todorov I N, Shen R A, Zheliabovskaia S M, Galkin A P
Biokhimiia. 1976 Oct;41(10):1859-70.
A drastic inhibition of protein biosynthesis in rat liver in vivo by cycloheximide (CHI) (0.3 mg/100 g of body weight) first caused an increase of RNA synthesis (after 1 hour), which was then followed by its decrease. Partial gradual restoration of the protein synthesis level was shown to be accompanied by a repeated increase of RNA synthesis (12 hs) and its normalisation after 24 hs. The first maximum of RNA synthesis increase in the isolated nuclei system was AU-type RNA synthesis (sensitive to alpha-amanitine), the second one was due to GC-type RNA synthesis (resistant to this toxin). Purified chromatine template activity in the system with E. coli RNA polymerase (by 14%) an hour after CHI treatment, but 3 hrs later was decreased and subsequently restored (12 hrs after CHI injection). The changes of RNA biosynthesis induced by prolonged protein synthesis inhibition suggest the existence of continuous RNA synthesis control in nuclei. This control is realized by translation system using the feed back principle.
体内用环己酰亚胺(CHI)(0.3毫克/100克体重)强烈抑制大鼠肝脏中的蛋白质生物合成,首先导致RNA合成增加(1小时后),随后其减少。蛋白质合成水平的部分逐渐恢复伴随着RNA合成的再次增加(12小时),并在24小时后恢复正常。分离的细胞核系统中RNA合成增加的第一个峰值是AU型RNA合成(对α-鹅膏蕈碱敏感),第二个峰值是由于GC型RNA合成(对该毒素有抗性)。CHI处理1小时后,用大肠杆菌RNA聚合酶的系统中纯化染色质模板活性增加(14%),但3小时后降低,随后恢复(CHI注射后12小时)。长期蛋白质合成抑制诱导的RNA生物合成变化表明细胞核中存在连续的RNA合成控制。这种控制是通过翻译系统利用反馈原理实现的。