DNA Phosphorothioate Modification Systems and Associated Phage Defense Systems

被引:3
作者
Wang, Lianrong [1 ,2 ,3 ]
Tang, Yaqian [2 ,3 ]
Deng, Zixin [2 ,3 ]
Chen, Shi [2 ,3 ,4 ]
机构
[1] Shenzhen Childrens Hosp, Inst Pediat, Dept Resp Dis, Shenzhen 518038, Peoples R China
[2] Wuhan Univ, Hubei Clin Ctr,Zhongnan Hosp, Sch Pharmaceut Sci, Dept Gastroenterol, Wuhan, Peoples R China
[3] Zhongnan Hosp Wuhan Univ, Wuhan Univ, Sch Pharmaceut Sci, Key Lab Intestinal & Colorectal Dis,Zhongnan Hosp, Wuhan, Peoples R China
[4] Shenzhen Univ Med Sch, Affiliated Hosp Shenzhen Univ 1,Shenzhen Inst Tran, Shenzhen Peoples Hosp 2, Dept Burn & Plast Surg,Key Lab Microbiol Genom Mod, Shenzhen, Peoples R China
关键词
DNA phosphorothioate modification; DNA PT modification; DndFGH; SspE; ScoMcrA; phage-resistant strains; sulfur-binding domain; RESTRICTION SYSTEM; EPIGENETICS; PROTEIN; BACTERIOPHAGE; RECOGNITION; PNEUMONIAE; STRATEGIES; CLEAVAGE; IMMUNITY; SULFUR;
D O I
10.1146/annurev-micro-041222-014330
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In contrast to the well-known DNA methylation of nucleobases, DNA phosphorothioate (PT) modification occurs in the DNA sugar-phosphate backbone. The non-bridging oxygen is replaced by a sulfur atom, which increases the nuclease tolerance of the DNA. In recent years, we have witnessed advances in understanding of PT modification enzymes, the features of PT modification across prokaryotic genomes, and PT-related physiological functions. Although only a small fraction of modifiable recognition sites across bacterial genomes undergo PT modification, enzymes such as DndFGH and SspE can use this modification as a recognition marker to differentiate between self- and non-self-DNA, thus destroying PT-lacking invasive DNA and preventing autoimmunity. We highlight the molecular mechanisms of PT modification-associated defense systems. We also describe notable applications of PT systems in the engineering of phage-resistant bacterial strains, RNA editing, and nucleic acid detection.
引用
收藏
页码:447 / 462
页数:16
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