Shulman R W, Sripati C E, Warner J R
J Biol Chem. 1977 Feb 25;252(4):1344-9.
In the yeast Saccharomyces cerevisiae we have carried out a detailed study of the response of transcription to the inhibition of translation. Measurement of the incorporation of labeled bases and nucleosides into the nucleoside triphosphate pools revealed that amino acid deprivation brings about a 10- to 50-fold inhibition of such labeling. Therefore accurate comparisons of RNA synthesis using such precursors are difficult to obtain. To overcome this problem we have turned to the use of L-[methyl-3H] methionine as a precursor, because the labeling of the S-adenosylmethionine pool is relatively unaffected by the rate of protein synthesis. Using this precursor, we have observed that in the absence of protein synthesis the transcription of ribosomal RNA is reduced by 80%, the transcription of messenger RNA is reduced by about 25%, and the transcription of transfer RNA is reduced by less than 20%. These results are obtained when protein synthesis is inhibited either by deprivation of an amino acid or by the addition of cycloheximide. Ribosomal precursor RNA synthesized in the absence of protein synthesis is fully methylated. We conclude that the transcription of rRNA is the primary target of stringent control. Furthermore the inhibition of protein synthesis, itself, may be the trigger for this response.
在酿酒酵母中,我们对转录对翻译抑制的反应进行了详细研究。对标记碱基和核苷掺入核苷三磷酸池的测量表明,氨基酸缺乏会导致这种标记受到10至50倍的抑制。因此,使用此类前体难以准确比较RNA合成情况。为克服这一问题,我们转而使用L-[甲基-³H]甲硫氨酸作为前体,因为S-腺苷甲硫氨酸池的标记相对不受蛋白质合成速率的影响。使用这种前体,我们观察到在缺乏蛋白质合成的情况下,核糖体RNA的转录减少了80%,信使RNA的转录减少了约25%,转运RNA的转录减少了不到20%。当通过氨基酸缺乏或添加环己酰亚胺抑制蛋白质合成时,可得到这些结果。在缺乏蛋白质合成的情况下合成的核糖体前体RNA会被完全甲基化。我们得出结论,rRNA的转录是严格控制的主要靶点。此外,蛋白质合成的抑制本身可能是这种反应的触发因素。