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大肠杆菌K-12 phoE基因启动子区域的分子分析。鉴定启动子上游一个对phoE蛋白高效表达所必需的元件。

Molecular analysis of the promoter region of the Escherichia coli K-12 phoE gene. Identification of an element, upstream from the promoter, required for efficient expression of phoE protein.

作者信息

Tommassen J, Koster M, Overduin P

机构信息

Department of Molecular Cell Biology, State University of Utrecht, The Netherlands.

出版信息

J Mol Biol. 1987 Dec 20;198(4):633-41. doi: 10.1016/0022-2836(87)90206-3.

Abstract

The phoE gene of Escherichia coli codes for an outer membrane pore protein whose expression is induced under phosphate limitation. The promoter of this gene contains a 17 base-pair fragment, designated a pho box, which is present also in other phosphate-controlled promoters. The mRNA start site was determined and found to be located downstream from the pho box, such that this element is located in the -35 region of the phoE promoter. A set of promoter deletions was generated in vitro and analysis of these deletions revealed that sequences upstream from the pho box are required for the efficient expression of phoE. The required upstream region is located (in part) between positions -106 and -121 relative to the mRNA start site, and contains sequences homologous to a pho box and a correctly spaced Pribnow box, but in the reversed orientation relative to the regular -35 and -10 regions. A proper spacing between this upstream region and the -35 region appears to be important, since an oligonucleotide insertion in the intervening region interferes with phoE expression. By cloning the upstream region in a lacZ operon fusion vector, a weak phosphate limitation-inducible promoter activity could be detected.

摘要

大肠杆菌的phoE基因编码一种外膜孔蛋白,其表达在磷酸盐限制条件下被诱导。该基因的启动子包含一个17个碱基对的片段,称为pho框,它也存在于其他受磷酸盐控制的启动子中。确定了mRNA起始位点,发现其位于pho框的下游,因此该元件位于phoE启动子的-35区域。在体外产生了一组启动子缺失,对这些缺失的分析表明,pho框上游的序列是phoE高效表达所必需的。所需的上游区域(部分)位于相对于mRNA起始位点的-106至-121位之间,并且包含与pho框和正确间隔的普里布诺框同源的序列,但相对于常规的-35和-10区域,其方向相反。该上游区域与-35区域之间的适当间距似乎很重要,因为在中间区域插入寡核苷酸会干扰phoE的表达。通过将上游区域克隆到lacZ操纵子融合载体中,可以检测到弱的磷酸盐限制诱导型启动子活性。

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