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55.2是一个噬菌体T4孤儿基因,编码大肠杆菌拓扑异构酶I的抑制剂并提高噬菌体适应性。

55.2, a phage T4 ORFan gene, encodes an inhibitor of Escherichia coli topoisomerase I and increases phage fitness.

作者信息

Mattenberger Yves, Silva Filo, Belin Dominique

机构信息

Department of Pathology and Immunology, University of Geneva, Geneva, Switzerland.

出版信息

PLoS One. 2015 Apr 14;10(4):e0124309. doi: 10.1371/journal.pone.0124309. eCollection 2015.

Abstract

Topoisomerases are enzymes that alter the topological properties of DNA. Phage T4 encodes its own topoisomerase but it can also utilize host-encoded topoisomerases. Here we characterized 55.2, a phage T4 predicted ORF of unknown function. High levels of expression of the cloned 55.2 gene are toxic in E. coli. This toxicity is suppressed either by increased topoisomerase I expression or by partial inactivation of the ATPase subunit of the DNA gyrase. Interestingly, very low-level expression of 55.2, which is non-lethal to wild type E. coli, prevents the growth of a deletion mutant of the topoisomerase I (topA) gene. In vitro, gp55.2 binds DNA and blocks specifically the relaxation of negatively supercoiled DNA by topoisomerase I. In vivo, expression of gp55.2 at low non-toxic levels alters the steady state DNA supercoiling of a reporter plasmid. Although 55.2 is not an essential gene, competition experiments indicate that it is required for optimal phage growth. We propose that the role of gp55.2 is to subtly modulate host topoisomerase I activity during infection to insure optimal T4 phage yield.

摘要

拓扑异构酶是能够改变DNA拓扑性质的酶。噬菌体T4编码自身的拓扑异构酶,但它也可以利用宿主编码的拓扑异构酶。在这里,我们对噬菌体T4预测的功能未知的开放阅读框55.2进行了表征。克隆的55.2基因的高表达水平在大肠杆菌中具有毒性。这种毒性可以通过增加拓扑异构酶I的表达或通过部分失活DNA促旋酶的ATP酶亚基来抑制。有趣的是,55.2的极低水平表达对野生型大肠杆菌无致死性,但会阻止拓扑异构酶I(topA)基因缺失突变体的生长。在体外,gp55.2结合DNA并特异性地阻断拓扑异构酶I对负超螺旋DNA的松弛作用。在体内,低无毒水平的gp55.2表达会改变报告质粒的稳态DNA超螺旋。虽然55.2不是必需基因,但竞争实验表明它是噬菌体最佳生长所必需的。我们提出,gp55.2的作用是在感染期间微调宿主拓扑异构酶I的活性,以确保噬菌体T4的最佳产量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23a7/4396842/c636ea28cf51/pone.0124309.g001.jpg

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