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启动子上游激活序列是假单胞菌TOL质粒上xylS基因和上途径操纵子表达所必需的。

Promoter-upstream activator sequences are required for expression of the xylS gene and upper-pathway operon on the Pseudomonas TOL plasmid.

作者信息

Holtel A, Abril M A, Marques S, Timmis K N, Ramos J L

机构信息

C.S.I.C., Estación Experimental del Zaidin, Granada, Spain.

出版信息

Mol Microbiol. 1990 Sep;4(9):1551-6. doi: 10.1111/j.1365-2958.1990.tb02066.x.

Abstract

Stimulation of transcription from the Pseudomonas TOL plasmid xylS gene promoter (Ps) and the upper-pathway operon promoter (Pu) is dependent on the positive regulator protein XylR activated by an effector molecule such as 3-cholorotoluene, and on RpoN, an RNA polymerase sigma factor. Mutational analysis of the Ps and Pu promoters showed that upstream activator sequences located between -110 and -218bp upstream of the main transcription initiation point are required for regulated expression from these promoters. A search for homologous nucleotide sequences in the -110 to -218bp region in Pu and Ps revealed conserved sequences that may act as putative recognition sequences for the XylR protein. Ps and Pu exhibit another well-conserved region at around -50bp, which is homologous to corresponding sites in other RpoN-dependent promoters and may constitute a binding site for integration host factor (IHF).

摘要

假单胞菌TOL质粒木糖操纵子的木糖S基因启动子(Ps)和上途径操纵子启动子(Pu)的转录激活,依赖于由效应分子(如3-氯甲苯)激活的正调控蛋白XylR,以及RNA聚合酶σ因子RpoN。对Ps和Pu启动子的突变分析表明,主要转录起始点上游-110至-218bp之间的上游激活序列是这些启动子进行调控表达所必需的。在Pu和Ps的-110至-218bp区域中搜索同源核苷酸序列,发现了保守序列,这些序列可能作为XylR蛋白的假定识别序列。Ps和Pu在-50bp左右还表现出另一个保守区域,该区域与其他RpoN依赖型启动子中的相应位点同源,可能构成整合宿主因子(IHF)的结合位点。

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