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哺乳动物体内蛋白质合成的调控。环己酰亚胺处理后体内肝脏核糖核酸合成受到刺激。

Regulation of mammalian protein synthesis in vivo. Stimulated liver ribonucleic acid synthesis in vivo after cycloheximide treatment.

作者信息

Ch'ih J J, Pike L M, Devlin T M

出版信息

Biochem J. 1977 Oct 15;168(1):57-63. doi: 10.1042/bj1680057.

Abstract
  1. As shown by a double-radioisotope technique in vivo, at a non-lethal dose of cycloheximide, a stimulation of nuclear RNA synthesis occurred by 12 h after the treatment; the stimulation lasted over 48 h. Analysis of radioactive nuclear RNA by gel electrophoresis demonstrated that most of the cycloheximide-stimulated synthesis could be accounted for by known rRNA precursors (45 S, 41 S, 32 S and 28 S). 2. During the inhibitory phase of protein synthesis, 2 h after cycloheximide treatment, synthesis of the poly(A)-containing mRNA isolated from the cytoplasmic ribonucleoprotein complexes with an oligo(dT)-cellulose column was stimulated, whereas the synthesis of rRNA was slightly inhibited. However, during the stimulatory phase of protein synthesis, 24 h after cycloheximide treatment, the syntheses of both poly(A)-containing mRNA and rRNA were enhanced. 3. Kinetic studies revealed that the newly synthesized RNA species were transported from the nuclei, integrated into the ribonucleoprotein complexes, and associated with both free and membrane-bound polyribosomes. 4. These data corroborate our proposal that the stimulated protein synthesis after cycloheximide administration involves gene transcription.
摘要
  1. 体内双放射性同位素技术显示,在使用非致死剂量的环己酰亚胺时,处理后12小时核RNA合成受到刺激;这种刺激持续超过48小时。通过凝胶电泳对放射性核RNA进行分析表明,环己酰亚胺刺激的合成大部分可由已知的rRNA前体(45S、41S、32S和28S)来解释。2. 在蛋白质合成的抑制阶段,即环己酰亚胺处理后2小时,用寡聚(dT)-纤维素柱从细胞质核糖核蛋白复合物中分离出的含多聚(A)的mRNA的合成受到刺激,而rRNA的合成略有抑制。然而,在蛋白质合成的刺激阶段,即环己酰亚胺处理后24小时,含多聚(A)的mRNA和rRNA的合成均增强。3. 动力学研究表明,新合成的RNA种类从细胞核转运出来,整合到核糖核蛋白复合物中,并与游离的和膜结合的多核糖体相关联。4. 这些数据证实了我们的提议,即环己酰亚胺给药后刺激的蛋白质合成涉及基因转录。

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本文引用的文献

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Evidence for a nonrandom reading of the genome.基因组非随机读取的证据。
Proc Natl Acad Sci U S A. 1962 Nov 15;48(11):1942-9. doi: 10.1073/pnas.48.11.1942.
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