Readshaw Jennifer J, Lee Yan-Jiun, Weigele Peter, Blower Tim R
Department of Biosciences, Durham University, Durham DH1 3LE, UK.
New England Biolabs, Ipswich, MA 01938, USA.
Philos Trans R Soc Lond B Biol Sci. 2025 Sep 4;380(1934):20240072. doi: 10.1098/rstb.2024.0072.
Bacteriophages (phages), viral predators of bacteria, generate selection pressure that causes bacteria to evolve defence systems. Type I, II and III restriction enzymes cleave incoming non-modified phage DNAs. Phages have evolved to defend against these restriction systems by modifying their DNA so that they are no longer suitable substrates. Type IV restriction enzymes have evolved to recognize and cleave modified DNA. We have recently characterized and solved the first structure for the Type IV GmrSD-family enzymes, using the BrxU homologue from . Though promiscuous in target modifications, little is known about BrxU substrate preference. We used modified DNAs in assays to characterize the substrate preferences of BrxU and investigate the impact of the GmrSD-inhibitor IPI* on BrxU activity. These data extend our knowledge of phage-host interactions and inform mechanistic studies on the reaction cycle of BrxU and GmrSD homologues.This article is part of the discussion meeting issue 'The ecology and evolution of bacterial immune systems'.
噬菌体作为细菌的病毒捕食者,会产生选择压力,促使细菌进化出防御系统。I型、II型和III型限制酶可切割进入的未修饰噬菌体DNA。噬菌体通过修饰自身DNA进行进化,以抵御这些限制系统,使其不再是合适的底物。IV型限制酶则进化到能够识别并切割修饰过的DNA。我们最近利用来自[具体来源未给出]的BrxU同源物,对IV型GmrSD家族酶进行了表征并解析了其首个结构。尽管BrxU在靶标修饰方面具有通用性,但对其底物偏好却知之甚少。我们在实验中使用修饰的DNA来表征BrxU的底物偏好,并研究GmrSD抑制剂IPI*对BrxU活性的影响。这些数据扩展了我们对噬菌体 - 宿主相互作用的认识,并为关于BrxU和GmrSD同源物反应周期的机制研究提供了信息。本文是“细菌免疫系统的生态学和进化”讨论会议论文集的一部分。