Yamagishi M, de Boer H A, Nomura M
Department of Biological Chemistry, California College of Medicine, University of California, Irvine 92717.
J Mol Biol. 1987 Dec 5;198(3):547-50. doi: 10.1016/0022-2836(87)90299-3.
It was shown that induction of rRNA (and ribosome) synthesis from the lambda PL promoter/operator by temperature shift-up causes a repression of rRNA and tRNA synthesis from chromosomal genes. We have carried out experiments using a similar conditional rRNA gene expression system in which a mutational alteration was introduced in the anti-Shine-Dalgarno region at the 3'-end of the 16 S rRNA gene. It was found that the repression observed with the wild-type gene was largely abolished by the mutation. It appears that ribosomes inefficient in translational initiation are unable to cause feedback regulation of rRNA synthesis. It is suggested that the cell regulates rRNA (and tRNA) synthesis by monitoring the production of ribosomes, and that this monitoring is apparently carried out through their activity in the initiation (and perhaps subsequent steps) of translation.
研究表明,通过温度上调从λPL启动子/操纵子诱导rRNA(和核糖体)合成会导致染色体基因的rRNA和tRNA合成受到抑制。我们使用了类似的条件性rRNA基因表达系统进行实验,其中在16S rRNA基因3'端的反Shine-Dalgarno区域引入了突变。结果发现,该突变在很大程度上消除了野生型基因所观察到的抑制作用。似乎在翻译起始中效率低下的核糖体无法引起rRNA合成的反馈调节。这表明细胞通过监测核糖体的产生来调节rRNA(和tRNA)合成,并且这种监测显然是通过它们在翻译起始(也许还有后续步骤)中的活性来进行的。