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编码大肠杆菌脂蛋白的osmB基因的转录受双重信号调节:渗透压应激和稳定期。

Transcription of osmB, a gene encoding an Escherichia coli lipoprotein, is regulated by dual signals. Osmotic stress and stationary phase.

作者信息

Jung J U, Gutierrez C, Martin F, Ardourel M, Villarejo M

机构信息

Department of Biochemistry and Biophysics, University of California, Davis 95616.

出版信息

J Biol Chem. 1990 Jun 25;265(18):10574-81.

PMID:1693921
Abstract

The osmB gene, which encodes an outer membrane lipoprotein, can be induced by both osmotic and growth phase signals. Construction of two transcriptional fusions, an osmB-lacZ fusion in single copy on the bacterial chromosome and an osmB-cat fusion carried on a multicopy plasmid, demonstrated that induction of osmB by hyperosmolarity and during the stationary phase of growth occurred at the level of transcription. Two transcription initiation sites were identified by RNase protection of in vivo message. The downstream P2 promoter is the primary site for regulation; the basal level of expression is initiated at P2 and transcription from P2 is induced by elevated osmolarity or upon reaching stationary phase. Transcription from the P1 promoter, 150 base pairs (bp) upstream of the P2 promoter, occurred only when both osmotic and growth phase signals were present simultaneously; that is, when cells growing in high osmolarity medium have reached stationary phase. Deletion analysis narrowed the sequences necessary for P2 regulation to the 42-bp region upstream from the transcription start site. A 7-bp sequence just upstream from the -35 region was identified as a cis-acting regulatory element essential for osmotic stimulation of osmB expression. A hexanucleotide sequence within this segment could form the left arm of a region of dyad symmetry, flanking the -35 region of the promoter. Stationary phase induction at P2 does not require the 7-bp element.

摘要

编码外膜脂蛋白的osmB基因可被渗透压和生长阶段信号诱导。构建了两个转录融合体,一个是细菌染色体上单拷贝的osmB - lacZ融合体,另一个是多拷贝质粒携带的osmB - cat融合体,结果表明高渗和生长稳定期对osmB的诱导发生在转录水平。通过对体内信息的RNase保护鉴定出两个转录起始位点。下游的P2启动子是调控的主要位点;基础表达水平从P2起始,P2的转录受渗透压升高或进入稳定期诱导。P1启动子位于P2启动子上游150个碱基对(bp)处,仅在渗透压和生长阶段信号同时存在时启动转录,即高渗培养基中生长的细胞进入稳定期时。缺失分析将P2调控所需序列缩小到转录起始位点上游42 bp区域。-35区域上游紧邻的一个7 bp序列被鉴定为对osmB表达的渗透压刺激至关重要的顺式作用调控元件。该片段内的一个六核苷酸序列可形成启动子-35区域两侧二元对称区域的左臂。P2处的稳定期诱导不需要7 bp元件。

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