Department of Systems Biotechnology, Chung-Ang University, Anseong, Republic of Korea.
DOE Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Microbiome. 2022 Sep 28;10(1):157. doi: 10.1186/s40168-022-01340-w.
DNA methylation in prokaryotes is involved in many different cellular processes including cell cycle regulation and defense against viruses. To date, most prokaryotic methylation systems have been studied in culturable microorganisms, resulting in a limited understanding of DNA methylation from a microbial ecology perspective. Here, we analyze the distribution patterns of several microbial epigenetics marks in the ocean microbiome through genome-centric metagenomics across all domains of life.
We reconstructed 15,056 viral, 252 prokaryotic, 56 giant viral, and 6 eukaryotic metagenome-assembled genomes from northwest Pacific Ocean seawater samples using short- and long-read sequencing approaches. These metagenome-derived genomes mostly represented novel taxa, and recruited a majority of reads. Thanks to single-molecule real-time (SMRT) sequencing technology, base modification could also be detected for these genomes. This showed that DNA methylation can readily be detected across dominant oceanic bacterial, archaeal, and viral populations, and microbial epigenetic changes correlate with population differentiation. Furthermore, our genome-wide epigenetic analysis of Pelagibacter suggests that GANTC, a DNA methyltransferase target motif, is related to the cell cycle and is affected by environmental conditions. Yet, the presence of this motif also partitions the phylogeny of the Pelagibacter phages, possibly hinting at a competitive co-evolutionary history and multiple effects of a single methylation mark.
Overall, this study elucidates that DNA methylation patterns are associated with ecological changes and virus-host dynamics in the ocean microbiome. Video Abstract.
原核生物中的 DNA 甲基化参与了许多不同的细胞过程,包括细胞周期调控和抵御病毒。迄今为止,大多数原核甲基化系统已在可培养微生物中进行了研究,这导致从微生物生态学的角度对 DNA 甲基化的认识有限。在这里,我们通过对所有生命领域的基于基因组的宏基因组学分析,研究了海洋微生物组中几种微生物表观遗传标记的分布模式。
我们使用短读和长读测序方法,从西北太平洋海水样本中重建了 15056 个病毒、252 个原核生物、56 个巨型病毒和 6 个真核生物宏基因组组装基因组。这些宏基因组衍生的基因组主要代表新的分类群,并招募了大多数reads。由于单分子实时(SMRT)测序技术,这些基因组也可以检测到碱基修饰。这表明 DNA 甲基化可以在占主导地位的海洋细菌、古菌和病毒群体中很容易地被检测到,并且微生物表观遗传变化与种群分化相关。此外,我们对 Pelagibacter 的全基因组表观遗传分析表明,GANTC 是一种 DNA 甲基转移酶靶标基序,与细胞周期有关,并受环境条件影响。然而,该基序的存在也将 Pelagibacter 噬菌体的系统发育分开,这可能暗示着一种竞争的共同进化历史和单一甲基化标记的多种影响。
总的来说,这项研究阐明了 DNA 甲基化模式与海洋微生物组中的生态变化和病毒-宿主动态有关。