CcrM 的 DNA 甲基化有助于农杆菌植物病原体的基因组维护。

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Nucleic Acids Research Pub Date : 2024-09-04 DOI:10.1093/nar/gkae757
Sandra Martin, Florian Fournes, Giovanna Ambrosini, Christian Iseli, Karolina Bojkowska, Julien Marquis, Nicolas Guex, Justine Collier
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引用次数: 0

摘要

细胞周期调控的 DNA 甲基转移酶 CcrM 在大多数 Alphaproteobacteria 中都是保守的,但它在具有复杂或多中心基因组的细菌中的作用仍有待探索。在这里,我们比较了野生型和去除了 CcrM 的农杆菌细胞的甲基组、转录组和表型。我们发现,DNA 甲基化对细胞的运动性、生物膜的形成和活力有多方面的影响。值得注意的是,CcrM 可促进 repABCCh2 操作子的表达,该操作子编码在 ori2 处启动/分配复制所需的蛋白质,并抑制 gcrA 的表达,gcrA 编码一种保守的全球细胞周期调节因子。通过对活细胞中的 ori1 和 ori2 进行成像,我们发现在基因组甲基化过低的细胞中,ori2 的复制通常会延迟,而在基因组甲基化过高的细胞中,ori2 则会过度启动。进一步的分析表明,GcrA 很可能通过抑制 RepECh2 反义 RNA 促进 RepCCh2 启动子的表达。总之,我们认为在 ori1 处复制会导致 gcrA 启动子的瞬时半甲基化和激活,从而使 GcrA 激活 RepCCh2,并促进在 ori2 处的启动。这项研究揭示了 CcrM 依赖性 DNA 甲基化、一种保守的表观遗传调节因子与阿尔法蛋白细菌病原体基因组维护之间的新颖联系。
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DNA methylation by CcrM contributes to genome maintenance in the Agrobacterium tumefaciens plant pathogen.

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.

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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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