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鼠伤寒沙门氏菌metF基因受MetR蛋白的调控。

Regulation of the Salmonella typhimurium metF gene by the MetR protein.

作者信息

Cowan J M, Urbanowski M L, Talmi M, Stauffer G V

机构信息

Department of Microbiology, University of Iowa, Iowa City 52242.

出版信息

J Bacteriol. 1993 Sep;175(18):5862-6. doi: 10.1128/jb.175.18.5862-5866.1993.

Abstract

The metF gene in Escherichia coli and Salmonella typhimurium is under negative transcriptional control by the MetJ repressor. Expression of an S. typhimurium metF-lacZ gene fusion is repressed up to 10-fold by methionine addition to the growth medium in E. coli hosts encoding wild-type MetJ repressor; this repression is not seen in metJ mutants. metR mutations which eliminate the MetR activator protein result in two- to threefold-more-severe repression by the MetJ repressor. In a metJ metR double mutant, however, the level of metF-lacZ expression is the same as in a metJ mutant, suggesting that MetR antagonizes MetJ-mediated methionine repression of the metF promoter. A DNA footprint analysis showed that MetR binds to a DNA fragment carrying the metF promoter and protects two separate regions from DNase I digestion: a 46-bp region from position -50 to -95 upstream of the transcription initiation site and a 24-bp region from about position +62 to +85 downstream of the transcription initiation site and within the metF structural gene. Nucleotide changes in each of the MetR-binding sites away from the consensus sequence disrupt MetR-mediated regulation of the metF-lacZ fusion.

摘要

大肠杆菌和鼠伤寒沙门氏菌中的metF基因受到MetJ阻遏物的负转录调控。在编码野生型MetJ阻遏物的大肠杆菌宿主中,向生长培养基中添加甲硫氨酸可使鼠伤寒沙门氏菌metF - lacZ基因融合体的表达受到高达10倍的抑制;在metJ突变体中未观察到这种抑制作用。消除MetR激活蛋白的metR突变会导致MetJ阻遏物的抑制作用增强两到三倍。然而,在metJ metR双突变体中,metF - lacZ的表达水平与metJ突变体中的相同,这表明MetR拮抗MetJ介导的metF启动子的甲硫氨酸抑制作用。DNA足迹分析表明,MetR与携带metF启动子的DNA片段结合,并保护两个不同区域免受DNase I消化:一个位于转录起始位点上游 - 50至 - 95的46 bp区域,以及一个位于转录起始位点下游约 + 62至 + 85且在metF结构基因内的24 bp区域。每个MetR结合位点中远离共有序列的核苷酸变化会破坏MetR介导的metF - lacZ融合体的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ae/206665/d43dfe1d1a0d/jbacter00060-0128-a.jpg

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