Center for Host Defense against Enteropathogenic Bacteria Infection, Kwangju, 501-746, South Korea.
Mol Microbiol. 2012 Nov;86(3):707-19. doi: 10.1111/mmi.12012. Epub 2012 Sep 14.
In the modern concept of gene regulation, 'DNA looping' is the most common underlying mechanism in the interaction between RNA polymerase (RNAP) and transcription factors acting at a distance. This study demonstrates an additional mechanism by which DNA-bound proteins communicate with each other, by analysing the bacterial histone-like nucleoid-structuring protein (H-NS), a general transcriptional silencer. The LEE5 promoter (LEE5p) of enteropathogenic Escherichia coli was used as a model system to investigate the mechanism of H-NS-mediated transcription repression. We found that H-NS represses LEE5p by binding to a cluster of A tracks upstream of -114, followed by spreading to a site at the promoter through the oligomerization of H-NS molecules. At the promoter, the H-NS makes a specific contact with the carboxy terminal domain of the α subunit of RNAP, which prevents the processing of RNAP-promoter complexes into initiation-competent open promoter complexes, thereby regulating LEE5p from distance.
在现代基因调控概念中,“DNA 环化”是 RNA 聚合酶(RNAP)与远距离作用的转录因子相互作用的最常见潜在机制。本研究通过分析细菌组蛋白样核结构蛋白(H-NS),一种普遍的转录沉默因子,展示了 DNA 结合蛋白相互交流的另一种机制。我们发现 H-NS 通过与 -114 上游的 A 轨道簇结合来抑制 LEE5p,然后通过 H-NS 分子的寡聚化扩散到启动子处。在启动子处,H-NS 与 RNAP 的α亚基羧基末端结构域形成特异性接触,从而阻止 RNAP-启动子复合物转化为起始能力的开放启动子复合物,从而从远处调控 LEE5p。