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Updated: May 31, 2026

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
Published on: November 25, 2015
The DdmDE defense system eradicates plasmids by target-centered bidirectional ssDNA loop extrusion and site-specific
Hao Yang1, Xiaoxuan Song2, Jiazheng Zhao2
1State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China; School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
None:
Bacteria have evolved a myriad of host-defense systems that protect against invasive mobile genetic elements. The DdmDE module, which consists of a DNA-guided, DNA-targeting prokaryotic Argonaute (pAgo) DdmE and a helicase-nuclease enzyme DdmD, represents a model anti-plasmid system. Here, we demonstrate that a double-stranded DNA (dsDNA)-destabilizing force generates transient bubbles that provoke promiscuous binding by DNA-guided DdmE. The resulting nucleoprotein complex discriminates on-targets from off-targets primarily through differences in dissociation rates. Remarkably, DNA-bound DdmE recruits a DdmD dimer to drive dsDNA shortening against a resisting force. Further analysis attributes this shortening to target-centered, bidirectional dsDNA unwinding and single-stranded DNA (ssDNA) extrusion by DdmD, in which monomeric DdmD engages both unwound strands. During this process, free DdmD rapidly associates with the two extruded strands and catalyzes ssDNA digestion with a sequence preference for a 5' guanine. Our findings provide a dynamic perspective on how pAgos cooperate with accessory factors to achieve plasmid clearance.
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