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参与DNA硫代磷酸酯修饰的DndE的体内突变特征分析。

In vivo mutational characterization of DndE involved in DNA phosphorothioate modification.

作者信息

Lai Chongde, Wu Xiaolin, Chen Chao, Huang Teng, Xiong Xiaolin, Wu Shuangju, Gu Meijia, Deng Zixin, Chen Xi, Chen Shi, Wang Lianrong

机构信息

Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, and School of Pharmaceutical Sciences, Wuhan University, Wuhan, China; College of Bioscience and Bioengineering, Jiangxi Agricultural University, Nanchang, China.

Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, and School of Pharmaceutical Sciences, Wuhan University, Wuhan, China; Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, China.

出版信息

PLoS One. 2014 Sep 30;9(9):e107981. doi: 10.1371/journal.pone.0107981. eCollection 2014.

Abstract

DNA phosphorothioate (PT) modification is a recently identified epigenetic modification that occurs in the sugar-phosphate backbone of prokaryotic DNA. Previous studies have demonstrated that DNA PT modification is governed by the five DndABCDE proteins in a sequence-selective and RP stereo-specific manner. Bacteria may have acquired this physiological modification along with dndFGH as a restriction-modification system. However, little is known about the biological function of Dnd proteins, especially the smallest protein, DndE, in the PT modification pathway. DndE was reported to be a DNA-binding protein with a preference for nicked dsDNA in vitro; the binding of DndE to DNA occurs via six positively charged lysine residues on its surface. The substitution of these key lysine residues significantly decreased the DNA binding affinities of DndE proteins to undetectable levels. In this study, we conducted site-directed mutagenesis of dndE on a plasmid and measured DNA PT modifications under physiological conditions by mass spectrometry. We observed distinctive differences from the in vitro binding assays. Several mutants with lysine residues mutated to alanine decreased the total frequency of PT modifications, but none of the mutants completely eliminated PT modification. Our results suggest that the nicked dsDNA-binding capacity of DndE may not be crucial for PT modification and/or that DndE may have other biological functions in addition to binding to dsDNA.

摘要

DNA硫代磷酸酯(PT)修饰是最近发现的一种表观遗传修饰,发生在原核生物DNA的糖磷酸骨架中。先前的研究表明,DNA PT修饰由五种DndABCDE蛋白以序列选择性和RP立体特异性方式控制。细菌可能已将这种生理修饰与dndFGH一起作为一种限制修饰系统获得。然而,对于Dnd蛋白的生物学功能,尤其是PT修饰途径中最小的蛋白DndE的生物学功能,人们了解甚少。据报道,DndE是一种DNA结合蛋白,在体外对带切口的双链DNA有偏好;DndE与DNA的结合通过其表面的六个带正电荷的赖氨酸残基发生。这些关键赖氨酸残基的取代显著降低了DndE蛋白与DNA的结合亲和力,使其降至无法检测的水平。在本研究中,我们对质粒上的dndE进行了定点诱变,并通过质谱法在生理条件下测量DNA PT修饰。我们观察到与体外结合试验有明显差异。几个赖氨酸残基突变为丙氨酸的突变体降低了PT修饰的总频率,但没有一个突变体完全消除PT修饰。我们的结果表明,DndE的带切口双链DNA结合能力可能对PT修饰并不关键,和/或DndE除了与双链DNA结合外可能还有其他生物学功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec9a/4182426/f370a3dfe7c4/pone.0107981.g001.jpg

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