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在大肠杆菌中抑制因子依赖性转录终止可能通过体内消除 H-NS-DNA 相互作用来缓解异种沉默。

Inhibition of factor-dependent transcription termination in Escherichia coli might relieve xenogene silencing by abrogating H-NS-DNA interactions in vivo.

机构信息

National Centre for Biological Sciences, Tata Institute of Fundamental Research, GKVK, Bellary Road, Bangalore 560 065, India.

出版信息

J Biosci. 2014 Mar;39(1):53-61. doi: 10.1007/s12038-014-9413-4.

Abstract

Many horizontally acquired genes (xenogenes) in the bacterium Escherichia coli are maintained in a silent transcriptional state by the nucleoid-associated transcription regulatory protein H-NS. Recent evidence has shown that antibiotic-mediated inhibition of the transcription terminator protein Rho leads to de-repression of horizontally acquired genes, akin to a deletion of hns. The mechanism behind this similarity in outcomes between the perturbations of two distinct processes remains unclear. Using ChIP-seq of H-NS in wild-type cells, in addition to that in cells treated with bicyclomycin--a specific inhibitor of Rho, we show that bicyclomycin treatment leads to a decrease in binding signal for H-NS to the E. coli chromosome. Rho inhibition leads to RNA polymerase readthrough, which in principle could displace H-NS from the DNA, thus leading to transcriptional derepression of H-NS-silenced genes. Other possible mediators of the effect of Rho on H-NS are discussed. A possible positive feedback between Rho and H-NS might help reinforce xenogene silencing.

摘要

许多在细菌大肠杆菌中水平获得的基因(异源基因)通过核体相关转录调控蛋白 H-NS 保持在沉默转录状态。最近的证据表明,抗生素介导的转录终止蛋白 Rho 的抑制导致水平获得的基因去抑制,类似于 hns 的缺失。这两种不同过程的扰动在结果上的相似性背后的机制尚不清楚。我们使用野生型细胞中的 H-NS 的 ChIP-seq,以及用双环霉素(Rho 的特异性抑制剂)处理的细胞中的 H-NS 的 ChIP-seq,表明双环霉素处理导致 H-NS 与大肠杆菌染色体结合信号减少。Rho 抑制导致 RNA 聚合酶通读,这在原则上可以将 H-NS 从 DNA 上置换出来,从而导致 H-NS 沉默基因的转录去抑制。还讨论了 Rho 对 H-NS 影响的其他可能介质。Rho 和 H-NS 之间的可能正反馈可能有助于加强异源基因沉默。

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