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Fis和H-NS对大肠杆菌dps启动子的选择性抑制作用

Selective repression by Fis and H-NS at the Escherichia coli dps promoter.

作者信息

Grainger David C, Goldberg Martin D, Lee David J, Busby Stephen J W

机构信息

School of Biosciences, University of Birmingham, Edgbaston, Birmingham, UK.

出版信息

Mol Microbiol. 2008 Jun;68(6):1366-77. doi: 10.1111/j.1365-2958.2008.06253.x. Epub 2008 Apr 28.

Abstract

Dps is a nucleoid-associated protein that plays a major role in condensation of the Escherichia coli chromosome in stationary phase. Here we show that two other nucleoid-associated proteins, Fis and H-NS, can bind at the dps gene promoter and downregulate its activity. Both Fis and H-NS selectively repress the dps promoter, preventing transcription initiation by RNA polymerase containing sigma(70), the housekeeping sigma factor, but not by RNA polymerase containing sigma(38), the stationary-phase sigma factor. Fis represses by trapping RNA polymerase containing sigma(70) at the promoter. In contrast, H-NS functions by displacing RNA polymerase containing sigma(70), but not RNA polymerase containing sigma(38). Dps levels are known to be very low in exponentially growing cells and rise sharply as cells enter stationary phase. Conversely, Fis levels are high in growing cells but fall to nearly zero in stationary-phase cells. Our data suggest a simple model to explain how the Dps-dependent super-compaction of the folded chromosome is triggered as cell growth ceases.

摘要

Dps是一种类核相关蛋白,在大肠杆菌染色体的稳定期凝聚过程中起主要作用。我们在此表明,另外两种类核相关蛋白Fis和H-NS能够结合到dps基因启动子上并下调其活性。Fis和H-NS均选择性地抑制dps启动子,阻止含有管家σ因子σ⁷⁰的RNA聚合酶起始转录,但不阻止含有稳定期σ因子σ³⁸的RNA聚合酶起始转录。Fis通过将含有σ⁷⁰的RNA聚合酶捕获在启动子上来实现抑制作用。相反,H-NS通过置换含有σ⁷⁰的RNA聚合酶起作用,但不置换含有σ³⁸的RNA聚合酶。已知在指数生长期细胞中Dps水平非常低,而随着细胞进入稳定期其水平急剧上升。相反,Fis在生长细胞中水平较高,但在稳定期细胞中降至几乎为零。我们的数据提示了一个简单模型,以解释细胞生长停止时如何触发依赖Dps的折叠染色体超凝聚。

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