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细菌Mfd蛋白通过一种不依赖核酸内切酶修复(NER)但依赖RecBC的途径,防止宿主氮免疫反应诱导的DNA损伤。

The Bacterial Mfd Protein Prevents DNA Damage Induced by the Host Nitrogen Immune Response in a NER-Independent but RecBC-Dependent Pathway.

作者信息

Darrigo Claire, Guillemet Elisabeth, Dervyn Rozenn, Ramarao Nalini

机构信息

Micalis Institute, INRA, AgroParisTech, Université Paris-Saclay, 78350 Jouy-en-Josas, France.

出版信息

PLoS One. 2016 Oct 6;11(10):e0163321. doi: 10.1371/journal.pone.0163321. eCollection 2016.

Abstract

Production of reactive nitrogen species is an important component of the host immune defence against bacteria. Here, we show that the bacterial protein Mfd (Mutation frequency decline), a highly conserved and ubiquitous bacterial protein involved in DNA repair, confers bacterial resistance to the eukaryotic nitrogen response produced by macrophage cells and during mice infection. In addition, we show that RecBC is also necessary to survive this stress. The inactivation of recBC and mfd genes is epistatic showing that Mfd follows the RecBC repair pathway to protect the bacteria against the genotoxic effect of nitrite. Surprisingly given the role of Mfd in transcription-coupled repair, UvrA is not necessary to survive the nitrite response. Taken together, our data reveal that during the eukaryotic nitrogen response, Mfd is required to maintain bacterial genome integrity in a NER-independent but RecBC-dependent pathway.

摘要

活性氮物质的产生是宿主针对细菌的免疫防御的重要组成部分。在此,我们表明细菌蛋白Mfd(突变频率下降),一种参与DNA修复的高度保守且普遍存在的细菌蛋白,赋予细菌对巨噬细胞产生的真核生物氮反应以及在小鼠感染期间的抗性。此外,我们表明RecBC对于在这种应激下存活也是必需的。recBC和mfd基因的失活表现为上位性,表明Mfd遵循RecBC修复途径来保护细菌免受亚硝酸盐的遗传毒性作用。鉴于Mfd在转录偶联修复中的作用,令人惊讶的是,UvrA对于在亚硝酸盐反应中存活并非必需。综上所述,我们的数据表明,在真核生物氮反应期间,需要Mfd以一种不依赖于核苷酸切除修复(NER)但依赖于RecBC的途径来维持细菌基因组的完整性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbdc/5053507/2168d9bdd5d2/pone.0163321.g001.jpg

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