Department of Biology, William & Mary , Williamsburg, Virginia, USA.
J Bacteriol. 2024 Jan 25;206(1):e0030923. doi: 10.1128/jb.00309-23. Epub 2024 Jan 5.
In addition to its role in genome protection, DNA methylation can regulate gene expression. In this study, we characterized the impact of acidity, phase variation, and the ArsRS TCS on the expression of the Type I m6A DNA methyltransferase HsdM1 (HP0463) of 26695 and their subsequent effects on the methylome. Transcription of 1 increases at least fourfold in the absence of the sensory histidine kinase ArsS, the major acid-sensing protein of 1 exists in the phase-variable operon 1-1. Phase-locking 1 (HP0464), the restriction endonuclease gene, has significant impacts on the transcription of 1. To determine the impacts of methyltransferase transcription patterns on the methylome, we conducted methylome sequencing on samples cultured at pH 7 or pH 5. We found differentially methylated motifs between these growth conditions and that deletions of and/or 1 interfere with the epigenetic acid response. Deletion of leads to altered activity of HsdM1 and multiple other methyltransferases under both pH conditions indicating that the ArsRS TCS, in addition to direct effects on regulon transcription during acid acclimation, may also indirectly impact gene expression regulation of the methylome. We determined the target motif of HsdM1 (HP0463) to be the complementary bipartite sequence pair 5'-TCAVNTGY-3' and 3'-AGTNGACA-5'. This complex regulation of DNA methyltransferases, and thus differential methylation patterns, may have implications for the decades-long persistent infection by . IMPORTANCE This study expands the possibilities for complex, epigenomic regulation in . We demonstrate that the methylome is plastic and acid sensitive the two-component system ArsRS and the DNA methyltransferase HsdM1. The control of a methyltransferase by ArsRS may allow for a layered response to changing acidity. Likely, an early response whereby ArsR~P affects regulon expression, including the methyltransferase 1. Then, a somewhat later effect as the altered methylome, due to altered HsdM1 expression, subsequently alters the expression of other genes involved in acclimation. The intermediate methylation of certain motifs supports the hypothesis that methyltransferases play a regulatory role. Untangling this additional web of regulation could play a key role in understanding colonization and persistence.
除了在基因组保护中的作用外,DNA 甲基化还可以调节基因表达。在这项研究中,我们描述了酸度、相位变化和 ArsRS TCS 对 26695 型 I m6A DNA 甲基转移酶 HsdM1(HP0463)表达的影响,以及它们对甲基组的后续影响。在不存在感应组氨酸激酶 ArsS 的情况下,1 的转录至少增加了四倍,主要的酸感应蛋白 1 存在于相位可变操纵子 1-1 中。相位锁定 1(HP0464),限制内切酶基因,对 1 的转录有显著影响。为了确定甲基转移酶转录模式对甲基组的影响,我们在 pH7 或 pH5 下培养的样品上进行了甲基组测序。我们发现这些生长条件之间存在差异甲基化基序,并且 和/或 1 的缺失会干扰表观遗传酸反应。 缺失导致 HsdM1 和其他几种甲基转移酶在两种 pH 条件下的活性改变,这表明 ArsRS TCS 除了在酸适应过程中直接影响调节子转录外,还可能间接影响甲基组的基因表达调控。我们确定 HsdM1(HP0463)的靶标基序为互补的二分序列对 5'-TCAVNTGY-3'和 3'-AGTNGACA-5'。这种 DNA 甲基转移酶的复杂调控,以及因此的差异甲基化模式,可能对 持续存在数十年的感染有影响。 重要性 这项研究扩展了 中复杂的、表观基因组调控的可能性。我们证明了 甲基组具有可塑性和对酸敏感——两个组件系统 ArsRS 和 DNA 甲基转移酶 HsdM1。ArsRS 对甲基转移酶的控制可能允许对不断变化的酸度进行分层反应。可能是 ArsR~P 首先影响调节子表达,包括甲基转移酶 1,然后是稍微晚一点的效应,因为 HsdM1 表达的改变,随后改变了参与适应的其他基因的表达。某些基序的中间甲基化支持了甲基转移酶起调节作用的假说。解开这一额外的调控网络可能是理解 定植和持续存在的关键。