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大肠杆菌 udk 的过表达模拟了 T7 Gp2 功能的缺失,从而破坏了 T7 噬菌体的成功感染。

Overexpression of Escherichia coli udk mimics the absence of T7 Gp2 function and thereby abrogates successful infection by T7 phage.

机构信息

Section of Microbiology, Faculty of Medicine and MRC Centre for Molecular Bacteriology and Infection, Imperial College London, SW7 2AZ, UK.

Waksman Institute for Microbiology and Department of Molecular Biology and Biochemistry, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.

出版信息

Microbiology (Reading). 2013 Feb;159(Pt 2):269-274. doi: 10.1099/mic.0.064527-0. Epub 2012 Dec 14.

Abstract

Successful infection of Escherichia coli by bacteriophage T7 relies upon the transcription of the T7 genome by two different RNA polymerases (RNAps). The bacterial RNAp transcribes early T7 promoters, whereas middle and late T7 genes are transcribed by the T7 RNAp. Gp2, a T7-encoded transcription factor, is a 7 kDa product of an essential middle T7 gene 2, and is a potent inhibitor of the host RNAp. The essential biological role of Gp2 is to inhibit transcription of early T7 genes that fail to terminate efficiently in order to facilitate the coordinated usage of the T7 genome by both host and phage RNAps. Overexpression of the E. coli udk gene, which encodes a uridine/cytidine kinase, interferes with T7 infection. We demonstrate that overexpression of udk antagonizes Gp2 function in E. coli in the absence of T7 infection and thus independently of T7-encoded factors. It seems that overexpression of udk reduces Gp2 stability and functionality during T7 infection, which consequently results in inadequate inhibition of host RNAp and in the accumulation of early T7 transcripts. In other words, overexpression of udk mimics the absence of Gp2 during T7 infection. Our study suggests that the transcriptional regulation of the T7 genome is surprisingly complex and might potentially be affected at many levels by phage- and host-encoded factors.

摘要

噬菌体 T7 成功感染大肠杆菌依赖于两种不同的 RNA 聚合酶(RNAps)转录 T7 基因组。细菌 RNAp 转录早期 T7 启动子,而中间和晚期 T7 基因则由 T7 RNAp 转录。Gp2 是一种由 T7 编码的转录因子,是一个必需的中间 T7 基因 2 的 7 kDa 产物,是宿主 RNAp 的强抑制剂。Gp2 的基本生物学作用是抑制早期 T7 基因的转录,这些基因不能有效地终止,以促进宿主和噬菌体 RNAp 对 T7 基因组的协调使用。大肠杆菌 udk 基因的过度表达,该基因编码尿苷/胞苷激酶,会干扰 T7 感染。我们证明,在没有 T7 感染的情况下,udk 的过度表达会拮抗 Gp2 在大肠杆菌中的功能,因此独立于 T7 编码的因子。似乎在 T7 感染期间,udk 的过度表达会降低 Gp2 的稳定性和功能,从而导致宿主 RNAp 抑制不足,并积累早期 T7 转录本。换句话说,在 T7 感染期间,udk 的过度表达模拟了 Gp2 的缺失。我们的研究表明,T7 基因组的转录调控非常复杂,噬菌体和宿主编码的因子可能在多个层面上影响它。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e49c/3709561/a444c5baf7b3/064527-f1.jpg

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