Department of Fundamental Microbiology, Faculty of Biology and Medicine, University of Lausanne, Lausanne CH-1015, Switzerland.
Bioinformatics Competence Center, University of Lausanne, Lausanne CH-1015, Switzerland.
Nucleic Acids Res. 2024 Oct 28;52(19):11519-11535. doi: 10.1093/nar/gkae757.
The cell cycle-regulated DNA methyltransferase CcrM is conserved in most Alphaproteobacteria, but its role in bacteria with complex or multicentric genomes remains unexplored. Here, we compare the methylome, the transcriptome and the phenotypes of wild-type and CcrM-depleted Agrobacterium tumefaciens cells with a dicentric chromosome with two essential replication origins. We find that DNA methylation has a pleiotropic impact on motility, biofilm formation and viability. Remarkably, CcrM promotes the expression of the repABCCh2 operon, encoding proteins required for replication initiation/partitioning at ori2, and represses gcrA, encoding a conserved global cell cycle regulator. Imaging ori1 and ori2 in live cells, we show that replication from ori2 is often delayed in cells with a hypo-methylated genome, while ori2 over-initiates in cells with a hyper-methylated genome. Further analyses show that GcrA promotes the expression of the RepCCh2 initiator, most likely through the repression of a RepECh2 anti-sense RNA. Altogether, we propose that replication at ori1 leads to a transient hemi-methylation and activation of the gcrA promoter, allowing repCCh2 activation by GcrA and contributing to initiation at ori2. This study then uncovers a novel and original connection between CcrM-dependent DNA methylation, a conserved epigenetic regulator and genome maintenance in an Alphaproteobacterial pathogen.
细胞周期调控的 DNA 甲基转移酶 CcrM 在大多数α变形菌中保守,但它在具有复杂或多中心基因组的细菌中的作用仍未被探索。在这里,我们比较了具有两个必需复制起点的二中心染色体的野生型和 CcrM 耗尽的根癌农杆菌细胞的甲基组、转录组和表型。我们发现 DNA 甲基化对运动性、生物膜形成和活力有多种影响。值得注意的是,CcrM 促进了 repABCCh2 操纵子的表达,该操纵子编码复制起始/分配所需的蛋白质 ori2,同时抑制了 gcrA,编码保守的全局细胞周期调节剂。在活细胞中对 ori1 和 ori2 进行成像,我们表明 ori2 的复制在基因组低甲基化的细胞中经常延迟,而在基因组高甲基化的细胞中 ori2 过度起始。进一步的分析表明,GcrA 促进了 RepCCh2 启动子的表达,这很可能是通过抑制 RepECh2 反义 RNA 来实现的。总的来说,我们提出了一种新的和原始的连接,即 ori1 处的复制导致瞬时半甲基化和 gcrA 启动子的激活,允许 GcrA 激活 repCCh2 并有助于 ori2 的起始。这项研究揭示了依赖 CcrM 的 DNA 甲基化、保守的表观遗传调节剂和α变形菌病原体中基因组维护之间的一种新的和原始的联系。