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多顺反子信使核糖核酸的翻译偶联及有限降解调控质粒R1的parD稳定性系统中的差异基因表达。

Translational coupling and limited degradation of a polycistronic messenger modulate differential gene expression in the parD stability system of plasmid R1.

作者信息

Ruiz-Echevarría M J, de la Cueva G, Díaz-Orejas R

机构信息

Centro de Investigaciones Biológicas (CSIC), Madrid, Spain.

出版信息

Mol Gen Genet. 1995 Sep 20;248(5):599-609. doi: 10.1007/BF02423456.

Abstract

The parD stability system of plasmid R1 is an auto-regulated operon containing two genes, kis and kid, that code, respectively, for a killer protein (Kid) and for an antagonist of Kid action (Kis protein). A polycistronic transcript and a shorter mRNA, coding only for Kis and ending in a stem-loop sequence, have been identified as the main parD transcripts in cells carrying a derepressed parD operon. In this communication we show that both parD mRNAs have a half-life close to 1 min and are present in similar amounts. Using an assay based on cell-free extracts of Escherichia coli, we demonstrate that the short kis mRNA originates from limited degradation of the bicistronic parD transcript and that the stem-loop structure within the 5' end of the kid gene is specifically required for the formation of this short transcript. In vivo experiments show that synthesis of Kis is required for efficient synthesis of Kid. These data indicate that RNA processing and translational coupling are important mechanisms that modulate the differential expression of the two genes, kis and kid, in the bicistronic parD operon.

摘要

质粒R1的parD稳定性系统是一个自我调节的操纵子,包含两个基因,kis和kid,它们分别编码一种杀伤蛋白(Kid)和Kid作用的拮抗剂(Kis蛋白)。在携带去阻遏parD操纵子的细胞中,一个多顺反子转录本和一个仅编码Kis并以茎环序列结尾的较短mRNA已被鉴定为主要的parD转录本。在本通讯中,我们表明这两种parD mRNA的半衰期接近1分钟,且含量相似。使用基于大肠杆菌无细胞提取物的检测方法,我们证明短的kis mRNA源自双顺反子parD转录本的有限降解,并且kid基因5'端内的茎环结构是形成这种短转录本所特需的。体内实验表明,Kis的合成是Kid高效合成所必需的。这些数据表明,RNA加工和翻译偶联是调节双顺反子parD操纵子中kis和kid这两个基因差异表达的重要机制。

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