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条件上位相互作用图谱揭示了大肠杆菌中基因组完整性途径的全局功能重排。

Conditional Epistatic Interaction Maps Reveal Global Functional Rewiring of Genome Integrity Pathways in Escherichia coli.

作者信息

Kumar Ashwani, Beloglazova Natalia, Bundalovic-Torma Cedoljub, Phanse Sadhna, Deineko Viktor, Gagarinova Alla, Musso Gabriel, Vlasblom James, Lemak Sofia, Hooshyar Mohsen, Minic Zoran, Wagih Omar, Mosca Roberto, Aloy Patrick, Golshani Ashkan, Parkinson John, Emili Andrew, Yakunin Alexander F, Babu Mohan

机构信息

Department of Computer Science, University of Regina, Regina, SK S4S 0A2, Canada.

Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, ON M5S 3E5, Canada.

出版信息

Cell Rep. 2016 Jan 26;14(3):648-661. doi: 10.1016/j.celrep.2015.12.060. Epub 2016 Jan 8.

Abstract

As antibiotic resistance is increasingly becoming a public health concern, an improved understanding of the bacterial DNA damage response (DDR), which is commonly targeted by antibiotics, could be of tremendous therapeutic value. Although the genetic components of the bacterial DDR have been studied extensively in isolation, how the underlying biological pathways interact functionally remains unclear. Here, we address this by performing systematic, unbiased, quantitative synthetic genetic interaction (GI) screens and uncover widespread changes in the GI network of the entire genomic integrity apparatus of Escherichia coli under standard and DNA-damaging growth conditions. The GI patterns of untreated cultures implicated two previously uncharacterized proteins (YhbQ and YqgF) as nucleases, whereas reorganization of the GI network after DNA damage revealed DDR roles for both annotated and uncharacterized genes. Analyses of pan-bacterial conservation patterns suggest that DDR mechanisms and functional relationships are near universal, highlighting a modular and highly adaptive genomic stress response.

摘要

随着抗生素耐药性日益成为公共卫生问题,深入了解通常被抗生素靶向的细菌DNA损伤反应(DDR)可能具有巨大的治疗价值。尽管已经对细菌DDR的遗传成分进行了广泛的单独研究,但潜在的生物学途径如何在功能上相互作用仍不清楚。在这里,我们通过进行系统、无偏倚、定量的合成遗传相互作用(GI)筛选来解决这个问题,并揭示在标准和DNA损伤生长条件下大肠杆菌整个基因组完整性装置的GI网络中广泛的变化。未处理培养物的GI模式表明两种以前未被表征的蛋白质(YhbQ和YqgF)是核酸酶,而DNA损伤后GI网络的重组揭示了已注释和未表征基因在DDR中的作用。对泛细菌保守模式的分析表明,DDR机制和功能关系几乎是普遍存在的,突出了一种模块化且高度适应性的基因组应激反应。

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