Skolkovo Institute of Science and Technology, Moscow, Russia.
Moscow Institute of Physics and Technology, Moscow, Russia.
Nucleic Acids Res. 2024 May 22;52(9):5195-5208. doi: 10.1093/nar/gkae243.
Bacterial defence systems are tightly regulated to avoid autoimmunity. In Type I restriction-modification (R-M) systems, a specific mechanism called restriction alleviation (RA) controls the activity of the restriction module. In the case of the Escherichia coli Type I R-M system EcoKI, RA proceeds through ClpXP-mediated proteolysis of restriction complexes bound to non-methylated sites that appear after replication or reparation of host DNA. Here, we show that RA is also induced in the presence of plasmids carrying EcoKI recognition sites, a phenomenon we refer to as plasmid-induced RA. Further, we show that the anti-restriction behavior of plasmid-borne non-conjugative transposons such as Tn5053, previously attributed to their ardD loci, is due to plasmid-induced RA. Plasmids carrying both EcoKI and Chi sites induce RA in RecA- and RecBCD-dependent manner. However, inactivation of both RecA and RecBCD restores RA, indicating that there exists an alternative, RecA-independent, homologous recombination pathway that is blocked in the presence of RecBCD. Indeed, plasmid-induced RA in a RecBCD-deficient background does not depend on the presence of Chi sites. We propose that processing of random dsDNA breaks in plasmid DNA via homologous recombination generates non-methylated EcoKI sites, which attract EcoKI restriction complexes channeling them for ClpXP-mediated proteolysis.
细菌防御系统受到严格调控以避免自身免疫。在 I 型限制修饰(R-M)系统中,一种称为限制缓解(RA)的特定机制控制着限制模块的活性。在大肠杆菌 I 型 R-M 系统 EcoKI 的情况下,RA 通过 ClpXP 介导的对结合在非甲基化位点上的限制复合物的蛋白水解来进行,这些非甲基化位点在宿主 DNA 复制或修复后出现。在这里,我们表明,在携带 EcoKI 识别位点的质粒存在的情况下,也会诱导 RA,我们将这种现象称为质粒诱导的 RA。此外,我们表明,先前归因于其 ardD 基因座的非共轭转座子如 Tn5053 等质粒携带的抗限制行为,是由于质粒诱导的 RA。携带 EcoKI 和 Chi 位点的质粒以依赖 RecA 和 RecBCD 的方式诱导 RA。然而,RecA 和 RecBCD 的失活都恢复了 RA,这表明存在一种替代的、不依赖 RecA 的同源重组途径,该途径在 RecBCD 存在时被阻断。事实上,在 RecBCD 缺陷背景下的质粒诱导的 RA 并不依赖 Chi 位点的存在。我们提出,通过同源重组对质粒 DNA 中的随机 dsDNA 断裂进行加工,产生非甲基化的 EcoKI 位点,这些位点吸引 EcoKI 限制复合物,并将其引导至 ClpXP 介导的蛋白水解。