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大肠杆菌hns启动子下游区域的诱变

Mutagenesis of the downstream region of the Escherichia coli hns promoter.

作者信息

Giangrossi M, Gualerzi C O, Pon C L

机构信息

Laboratory of Genetics, Department of Biology MCA, University of Camerino, 62032 Camerino (MC), Italy.

出版信息

Biochimie. 2001 Feb;83(2):251-9. doi: 10.1016/s0300-9084(01)01233-0.

Abstract

The promoter of hns, the structural gene for the abundant nucleoid-associated protein H-NS of Escherichia coli, contains, downstream of the initiation site, two four bp-long 'CG clamps', one of which overlaps the potential target sequence (CCAAT) of CspA, the cold-shock transcriptional enhancer of this gene. To establish the role of these potential regulatory signals during the cold-shock activation of hns, the CCCCAAT sequence has been subjected to mutagenesis, weakening the strength of the CG clamp and scrambling or inverting the CCAAT sequence. The resulting mutated hns promoters were placed in front of a reporter gene (cat) and their activity was studied in cells subjected to cold-shock under conditions where the increase in the concentration of CspA is either large or small. Our results allow us to conclude that although not essential, the CCCCAAT sequence, mainly due to the presence of the CG clamp, may play an important role in the CspA-mediated regulation of hns expression at both transcriptional and translational levels.

摘要

hns的启动子是大肠杆菌中丰富的类核相关蛋白H-NS的结构基因,在起始位点下游包含两个4bp长的“CG钳”,其中一个与该基因的冷休克转录增强子CspA的潜在靶序列(CCAAT)重叠。为了确定这些潜在调控信号在hns冷休克激活过程中的作用,对CCCCAA序列进行了诱变,削弱了CG钳的强度,并打乱或颠倒了CCAAT序列。将得到的突变hns启动子置于报告基因(cat)之前,并在CspA浓度增加幅度大或小的条件下,对遭受冷休克的细胞中的启动子活性进行了研究。我们的结果使我们能够得出结论,尽管CCCCAA序列并非必不可少,但主要由于CG钳的存在,它可能在CspA介导的hns转录和翻译水平表达调控中发挥重要作用。

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