DdmDE eliminates plasmid invasion by DNA-guided DNA targeting

被引:6
作者
Yang, Xiao-Yuan [1 ,2 ,3 ,4 ]
Shen, Zhangfei [1 ,2 ,4 ]
Wang, Chen [1 ,2 ]
Nakanishi, Kotaro [3 ,4 ,5 ]
Fu, Tian-Min [1 ,2 ,3 ,4 ]
机构
[1] Ohio State Univ, Dept Biol Chem & Pharmacol, Columbus, OH 43210 USA
[2] Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA
[3] Ohio State Univ, Ohio State Biochem Program, Columbus, OH 43210 USA
[4] Ohio State Univ, Ctr RNA Biol, Columbus, OH 43210 USA
[5] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
关键词
Highlights; nicking; RNA; TRANSLOCATION; RECOGNITION; DIVERSITY; MECHANISM; HELICASES; CLEAVAGE; SYSTEM;
D O I
10.1016/j.cell.2024.07.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Horizontal gene transfer is a key driver of bacterial evolution, but it also presents severe risks to bacteria by introducing invasive mobile genetic elements. To counter these threats, bacteria have developed various defense systems, including prokaryotic Argonautes (pAgos) and the DNA defense module DdmDE system. Through biochemical analysis, structural determination, and in vivo plasmid clearance assays, we elucidate the assembly and activation mechanisms of DdmDE, which eliminates small, multicopy plasmids. We demonstrate that DdmE, a pAgo-like protein, acts as a catalytically inactive, DNA-guided, DNA-targeting defense module. In the presence of guide DNA, DdmE targets plasmids and recruits a dimeric DdmD, which contains nuclease and helicase domains. Upon binding to DNA substrates, DdmD transitions from an auto-inhibited dimer to an active monomer, which then translocates along and cleaves the plasmids. Together, our findings reveal the intricate mechanisms underlying DdmDE-mediated plasmid clearance, offering fundamental insights into bacterial defense systems against plasmid invasions.
引用
收藏
页码:5253 / 5266.e16
页数:31
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