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在存在蛋白质合成抑制剂的情况下对转运RNA合成的控制。

Control of transfer RNA synthesis in the presence of inhibitors of protein synthesis.

作者信息

Westerberg U B, Bolcsfoldi G, Eliasson E

出版信息

Biochim Biophys Acta. 1976 Oct 4;447(2):203-13. doi: 10.1016/0005-2787(76)90343-9.

Abstract

The rate of synthesis of transfer RNA in suspension cultures of Chang's liver cells, has been examined in the presence of various inhibitors of protein synthesis with different modes of action. Inhibitors of polypeptide chain elongation such as cycloheximide and emetine stimulated the rate of synthesis of transfer RNA at concentrations that inhibited protein synthesis by 60-90%. Trichodermin, an inhibitor of the elongation and termination steps in protein synthesis, had as effect similar to that of cycloheximide and emetine. On the other hand verrucarin, an inhibitor of initiation, and puromycin, an analogue of the aminoacyl terminus of tRNA, had little effect of the synthesis of transfer RNA at low concentrations. At high concentrations these compounds inhibited transfer RNA synthesis. Inhibitors of protein synthesis can be divided in two groups based on their effect on the polysom pattern. The first group increased the number of large polysomes, while verrucarin and puromycin lead to a break down of large polysomes and to an accumulation of monosomes and small polysomes. Thus, there appears to be a correlation between the effect of these inhibitors of protein synthesis on the aggregational state of the polysomes and their effect on the rate of transfer RNA synthesis.

摘要

在存在具有不同作用模式的各种蛋白质合成抑制剂的情况下,对张氏肝癌细胞悬浮培养物中转录RNA的合成速率进行了检测。多肽链延伸抑制剂,如放线菌酮和吐根碱,在抑制蛋白质合成60%-90%的浓度下,刺激了转录RNA的合成速率。蛋白质合成延伸和终止步骤的抑制剂木霉菌素,具有与放线菌酮和吐根碱类似的作用。另一方面,起始抑制剂疣孢菌素和嘌呤霉素(一种tRNA氨酰基末端类似物),在低浓度时对转录RNA的合成几乎没有影响。在高浓度时,这些化合物抑制转录RNA的合成。根据蛋白质合成抑制剂对多聚核糖体模式的影响,可将其分为两组。第一组增加了大多聚核糖体的数量,而疣孢菌素和嘌呤霉素导致大多聚核糖体的解体,并导致单核糖体和小多聚核糖体的积累。因此,这些蛋白质合成抑制剂对多聚核糖体聚集状态的影响与其对转录RNA合成速率的影响之间似乎存在相关性。

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