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利用体外基因融合技术研究大肠杆菌K-12中的uxuR调控基因:转录方向及其表达调控

Use of in vitro gene fusions to study the uxuR regulatory gene in Escherichia coli K-12: direction of transcription and regulation of its expression.

作者信息

Ritzenthaler P, Mata-Gilsinger M

出版信息

J Bacteriol. 1982 Jun;150(3):1040-7. doi: 10.1128/jb.150.3.1040-1047.1982.

Abstract

The uxuAB operon is composed of two genes coding for enzymes involved in hexuronate degradation. This operon is negatively controlled by the uxuR and exuR regulatory gene products. Fusions that brought lac gene expression under the control of transcriptional and translational signals within the uxuR gene were used to study uxuR regulation. These fusions were formed on plasmid cloning vectors constructed by Casadaban et al. (J. Bacteriol. 143:971-980, 1980). The transcriptional direction of the uxuR gene was deduced from the restriction pattern and the phenotypic properties of the new plasmids. The gene is transcribed counterclockwise on the standard Escherichia coli map, as is the uxuAB operon. Introduction in trans of a compatible plasmid carrying a wild-type uxuR gene in the lac fusion plasmid containing strain resulted in a decrease of beta-galactosidase synthesis. It was concluded that expression of the uxuR gene itself is repressed by its own product. The two other types of regulation found in the uxuAB operon, i.e., induction by fructuronate and catabolite control, also apply to the uxuR gene, whereas repression by the exuR repressor does not seem to occur for the uxuR gene.

摘要

uxuAB操纵子由两个基因组成,这两个基因编码参与己糖醛酸降解的酶。该操纵子受uxuR和exuR调控基因产物的负调控。利用使lac基因表达受uxuR基因内转录和翻译信号控制的融合体来研究uxuR的调控。这些融合体构建在由卡萨达班等人(《细菌学杂志》143:971 - 980,1980年)构建的质粒克隆载体上。uxuR基因的转录方向是根据新质粒的限制酶切图谱和表型特性推导出来的。该基因在标准大肠杆菌图谱上是逆时针转录的,uxuAB操纵子也是如此。在含有lac融合质粒的菌株中反式导入携带野生型uxuR基因的相容质粒,导致β - 半乳糖苷酶合成减少。得出的结论是,uxuR基因自身的表达受其自身产物的抑制。在uxuAB操纵子中发现的另外两种调控类型,即由果糖醛酸诱导和分解代谢物控制,也适用于uxuR基因,而exuR阻遏物对uxuR基因的阻遏似乎并不发生。

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