Department of Biological Chemistry and Pharmacology, The Ohio State University, Columbus, OH 43210, USA; The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, USA; Ohio State Biochemistry Program, The Ohio State University, Columbus, OH 43210, USA; Center for RNA Biology, The Ohio State University, Columbus, OH 43210, USA.
Department of Biological Chemistry and Pharmacology, The Ohio State University, Columbus, OH 43210, USA; The Ohio State University Comprehensive Cancer Center, Columbus, OH 43210, USA; Center for RNA Biology, The Ohio State University, Columbus, OH 43210, USA.
Cell. 2024 Sep 19;187(19):5253-5266.e16. doi: 10.1016/j.cell.2024.07.028. Epub 2024 Aug 21.
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 autoinhibited 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.
水平基因转移是细菌进化的关键驱动力,但它也通过引入入侵性的移动遗传元件给细菌带来了严重的风险。为了应对这些威胁,细菌已经开发出了各种防御系统,包括原核 Argonautes(pAgos)和 DNA 防御模块 DdmDE 系统。通过生化分析、结构测定和体内质粒清除实验,我们阐明了 DdmDE 的组装和激活机制,该机制可以清除小的、多拷贝质粒。我们证明,DdmE 是一种类似 pAgo 的蛋白,作为一种无催化活性的、DNA 导向的、靶向 DNA 的防御模块发挥作用。在向导 DNA 的存在下,DdmE 靶向质粒并招募二聚体的 DdmD,后者含有核酸酶和解旋酶结构域。与 DNA 底物结合后,DdmD 从自动抑制的二聚体转变为活性单体,然后沿着质粒移动并切割质粒。总之,我们的研究结果揭示了 DdmDE 介导的质粒清除的复杂机制,为细菌防御系统抵御质粒入侵提供了基本的见解。