首页> 外文OA文献 >The leucine-responsive regulatory protein of Escherichia coli negatively regulates transcription of ompC and micF and positively regulates translation of ompF.
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The leucine-responsive regulatory protein of Escherichia coli negatively regulates transcription of ompC and micF and positively regulates translation of ompF.

机译:大肠杆菌的亮氨酸反应性调节蛋白可负性调节ompC和micF的转录,并正性调节ompF的翻译。

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摘要

The two major porins of Escherichia coli K-12 strains, OmpC and OmpF, are inversely regulated with respect to one another. The expression of OmpC and OmpF has been shown to be influenced by the leucine-responsive regulatory protein (Lrp): two-dimensional gel electrophoresis of proteins from strains with and strains without a functional Lrp protein revealed that OmpC expression is increased in an lrp strain, while OmpF expression is decreased. In agreement with these findings, we now present evidence that transcriptional (operon) fusions of lacZ+ to ompC and micF are negatively regulated by Lrp. Lrp binds specifically to the intergenic region between micF and ompC, as indicated by mobility shift assays and by DNase I footprinting. The expression of an ompF'-lacZ+ gene (translational) fusion is increased 3.7-fold in an lrp+ background compared with an lrp background, but expression of an ompF-lacZ+ operon fusion is not. Studies of in vivo expression of the outer membrane porins during growth on glucose minimal medium showed that the OmpF/OmpC ratio is higher in lrp+ strains than it is in isogenic lrp strains. The effect of Lrp was not seen in a strain containing a deletion of micF. Our studies suggest that the positive effect of Lrp on OmpF expression stems from a negative effect of Lrp on the expression of micF, an antisense RNA that inhibits ompF translation.
机译:大肠杆菌K-12菌株的两个主要孔蛋白OmpC和OmpF相互反向调控。已证明OmpC和OmpF的表达受亮氨酸反应性调节蛋白(Lrp)的影响:带有和不带有功能性Lrp蛋白的菌株的蛋白质的二维凝胶电泳显示,在lrp菌株中OmpC的表达增加了,而OmpF表达减少。与这些发现一致,我们现在提供证据表明lacZ +与ompC和micF的转录(操纵子)融合受到Lrp的负调控。 Lrp特异性结合micF和ompC之间的基因间区域,如迁移率变动分析和DNase I足迹所示。与lrp背景相比,在lrp +背景中,ompF'-lacZ +基因(翻译)融合体的表达增加了3.7倍,而在orpF-lacZ +操纵子融合体中的表达则没有。对在葡萄糖基本培养基上生长期间外膜孔蛋白的体内表达的研究表明,在lrp +菌株中,OmpF / OmpC比在同基因lrp菌株中更高。在含有micF缺失的菌株中未观察到Lrp的作用。我们的研究表明,Lrp对OmpF表达的积极影响源于Lrp对micF表达的负面影响,而micF是一种抑制ompF翻译的反义RNA。

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