A novel host-specific restriction system associated with DNA backbone S-modification in Salmonella

被引:116
作者
Xu, Tiegang
Yao, Fen
Zhou, Xiufen
Deng, Zixin
You, Delin [1 ]
机构
[1] Shanghai Jiao Tong Univ, Lab Microbial Metab, Shanghai 200030, Peoples R China
基金
美国国家科学基金会;
关键词
ESCHERICHIA-COLI; STREPTOMYCES-LIVIDANS; METHYLATION; ELECTROPHORESIS; DEGRADATION; SULFUR; GENES; BACTERIA; ENTERICA; VECTORS;
D O I
10.1093/nar/gkq610
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
A novel, site-specific, DNA backbone S-modification (phosphorothioation) has been discovered, but its in vivo function(s) have remained obscure. Here, we report that the enteropathogenic Salmonella enterica serovar Cerro 87, which possesses S-modified DNA, restricts DNA isolated from Escherichia coli, while protecting its own DNA by site-specific phosphorothioation. A cloned 15-kb gene cluster from S. enterica conferred both host-specific restriction and DNA S-modification on E. coli. Mutational analysis of the gene cluster proved unambiguously that the S-modification prevented host-specific restriction specified by the same gene cluster. Restriction activity required three genes in addition to at least four contiguous genes necessary for DNA S-modification. This functional overlap ensures that restriction of heterologous DNA occurs only when the host DNA is protected by phosphorothioation. Meanwhile, this novel type of host-specific restriction and modification system was identified in many diverse bacteria. As in the case of methylation-specific restriction systems, targeted inactivation of this gene cluster should facilitate genetic manipulation of these bacteria, as we demonstrate in Salmonella.
引用
收藏
页码:7133 / 7141
页数:9
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