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Tn1721编码的tetR信使核糖核酸中缺乏5'非编码区,这与大肠杆菌中的低翻译效率和短半衰期相关。

Lack of a 5' non-coding region in Tn1721 encoded tetR mRNA is associated with a low efficiency of translation and a short half-life in Escherichia coli.

作者信息

Baumeister R, Flache P, Melefors O, von Gabain A, Hillen W

机构信息

Lehrstuhl für Mikrobiologie, Friedrich-Alexander-Universität Erlangen/Nürnberg, FRG.

出版信息

Nucleic Acids Res. 1991 Sep 11;19(17):4595-600. doi: 10.1093/nar/19.17.4595.

Abstract

The repressor-encoding tetR gene from Tn1721 is expressed with a very low efficiency. Its mRNA lacks an untranslated leader sequence. We have constructed protein fusions with the lacZ gene which contain between 14 and 157 5' nucleotides from the tetR gene. Since they are all expressed with similar efficiencies we conclude that the sequence information for initiation of translation is contained within the first 14 bases of the tetR coding region. These fusion transcripts are about 20-fold less efficiently translated than the wild type lacZ transcript. A toeprint analysis confirms that the initiation complex is indistinguishable from those formed by regular transcripts with 5' untranslated regions but occurs in a very low amount in vitro. Thus, the absence of a 5' leader causes a poor rate of translation initiation. The half-lives of tetR and tetR-lacZ mRNAs are about 30 seconds, which is 3-times lower than that of the wt lacZ mRNA. Inactivation of the ams/rne locus in E. coli stabilizes the tetR transcript more than ten-fold. The influence of translation on the tetR half-life is discussed.

摘要

来自Tn1721的阻遏物编码tetR基因表达效率非常低。其mRNA缺乏非翻译前导序列。我们构建了与lacZ基因的蛋白融合体,其中包含tetR基因14至157个5'核苷酸。由于它们都以相似的效率表达,我们得出结论,翻译起始的序列信息包含在tetR编码区的前14个碱基内。这些融合转录本的翻译效率比野生型lacZ转录本低约20倍。足迹分析证实,起始复合物与由具有5'非翻译区的常规转录本形成的复合物没有区别,但在体外的量非常低。因此,5'前导序列的缺失导致翻译起始率很低。tetR和tetR-lacZ mRNA的半衰期约为30秒,比野生型lacZ mRNA低3倍。大肠杆菌中ams/rne位点的失活使tetR转录本的稳定性提高了十多倍。讨论了翻译对tetR半衰期的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd23/328697/89b5ca0911e9/nar00097-0020-a.jpg

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