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大肠杆菌核糖体蛋白S8对spc操纵子的部分进行反馈调节。

Escherichia coli ribosomal protein S8 feedback regulates part of spc operon.

作者信息

Dean D, Yates J L, Nomura M

出版信息

Nature. 1981 Jan 1;289(5793):89-91. doi: 10.1038/289089a0.

Abstract

In Escherichia coli the genes coding for the 52 ribosomal proteins (r-proteins) are organized into a number of transcription units located at various regions on the bacterial genome. The expression of r-protein genes is balanced so that individual r-protein synthesis rates change coordinately in response to changing environmental conditions, and significant amounts of free r-proteins do not exist in the cellular pool. We have suggested a model for the balanced regulation of r-protein gene expression, namely that r-protein synthesis and ribosome assembly are coupled so that r-proteins not incorporated into ribosomes prevent the further translation of r-protein mRNA by a feedback regulatory mechanism. The model was tested in vitro by examining the effect of purified r-proteins on DNA directed r-protein synthesis, and in vivo by examining the effect of overproduction of certain r-proteins on the synthesis rates of other r-proteins. In vitro experiments have revealed that some r-proteins (L1, L4, L10, S4 and S8) can selectively inhibit the synthesis of r-proteins whose genes are in the same operon as their own, and that this specific feedback regulation occurs at the level of translation rather than at the level of transcription of mRNA. Regulatory roles for L1, S4 and L4 have also been established by in vivo experiments. We have studied further the feedback regulatory properties of S8 in vivo and in vitro, and report here that the protein regulates a part of the spc operon.

摘要

在大肠杆菌中,编码52种核糖体蛋白(r蛋白)的基因被组织成多个转录单元,位于细菌基因组的不同区域。r蛋白基因的表达是平衡的,因此单个r蛋白的合成速率会随着环境条件的变化而协同改变,并且细胞池中不存在大量游离的r蛋白。我们提出了一个r蛋白基因表达平衡调控的模型,即r蛋白的合成与核糖体组装相耦合,使得未掺入核糖体的r蛋白通过反馈调节机制阻止r蛋白mRNA的进一步翻译。该模型在体外通过检测纯化的r蛋白对DNA指导的r蛋白合成的影响进行了测试,在体内通过检测某些r蛋白的过量表达对其他r蛋白合成速率的影响进行了测试。体外实验表明,一些r蛋白(L1、L4、L10、S4和S8)可以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,并且这种特异性反馈调节发生在翻译水平而非mRNA转录水平。体内实验也证实了L1、S4和L4的调控作用。我们进一步研究了S8在体内和体外的反馈调节特性,在此报告该蛋白对spc操纵子的一部分具有调控作用。

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