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大肠杆菌中核糖体蛋白基因表达的反馈调节

Feedback regulation of ribosomal protein gene expression in Escherichia coli.

作者信息

Dean D, Nomura M

出版信息

Proc Natl Acad Sci U S A. 1980 Jun;77(6):3590-4. doi: 10.1073/pnas.77.6.3590.

Abstract

The structural genes for Escherichia coli ribosomal protein (r-protein) genes L1, S4, and S11 were inserted into a plasmid vector containing the lac operator and promoter such that the synthesis of L1, S4, and S11 was controlled by lac regulatory elements. Synthesis of L1, S4, and S11 was stimulated by addition of an inducer of the lac operon (isopropyl thiogalactoside) to exponentially growing cells. Elevated synthesis of L1 caused a specific decrease in L11 synthesis, whereas overproduction of S4 resulted in lowered synthesis of S13 and L17. Stimulation of L1 or S4 synthesis also inhibited cell growth. Overproduction of S11 did not affect synthesis of other r-proteins or alter growth. These results confirm previous in vitro studies [Yates, J. L., Arfsten, A. E. & Nomura, M. (1980) Proc. Natl. Acad. Sci. USA 77, 1837-1841] and support the hypothesis that certain r-proteins have the capacity to selectively inhibit synthesis of r-proteins whose genes are in the same operon as their own.

摘要

将大肠杆菌核糖体蛋白(r蛋白)基因L1、S4和S11的结构基因插入到一个含有乳糖操纵子和启动子的质粒载体中,使得L1、S4和S11的合成受乳糖调节元件控制。向指数生长的细胞中添加乳糖操纵子的诱导剂(异丙基硫代半乳糖苷)可刺激L1、S4和S11的合成。L1合成的增加导致L11合成的特异性减少,而S4的过量产生导致S13和L17合成降低。L1或S4合成的刺激也会抑制细胞生长。S11的过量产生不影响其他r蛋白的合成,也不改变生长。这些结果证实了先前的体外研究[耶茨,J.L.,阿夫斯滕,A.E.和野村,M.(1980年)美国国家科学院院刊77,1837 - 1841],并支持了这样一种假说,即某些r蛋白有能力选择性抑制其基因与自身基因位于同一操纵子中的r蛋白的合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1bf/349663/4bdacab1f306/pnas00493-0533-a.jpg

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