Department of Plant & Microbial Biology, University of California, Berkeley, USA.
Department of Plant Sciences, University of California, Davis, USA.
Genome Biol. 2023 Oct 12;24(1):227. doi: 10.1186/s13059-023-03059-9.
In several eukaryotes, DNA methylation occurs within the coding regions of many genes, termed gene body methylation (GbM). Whereas the role of DNA methylation on the silencing of transposons and repetitive DNA is well understood, gene body methylation is not associated with transcriptional repression, and its biological importance remains unclear.
We report a newly discovered type of GbM in plants, which is under constitutive addition and removal by dynamic methylation modifiers in all cells, including the germline. Methylation at Dynamic GbM genes is removed by the DRDD demethylation pathway and added by an unknown source of de novo methylation, most likely the maintenance methyltransferase MET1. We show that the Dynamic GbM state is present at homologous genes across divergent lineages spanning over 100 million years, indicating evolutionary conservation. We demonstrate that Dynamic GbM is tightly associated with the presence of a promoter or regulatory chromatin state within the gene body, in contrast to other gene body methylated genes. We find Dynamic GbM is associated with enhanced gene expression plasticity across development and diverse physiological conditions, whereas stably methylated GbM genes exhibit reduced plasticity. Dynamic GbM genes exhibit reduced dynamic range in drdd mutants, indicating a causal link between DNA demethylation and enhanced gene expression plasticity.
We propose a new model for GbM in regulating gene expression plasticity, including a novel type of GbM in which increased gene expression plasticity is associated with the activity of DNA methylation writers and erasers and the enrichment of a regulatory chromatin state.
在几种真核生物中,DNA 甲基化发生在许多基因的编码区,称为基因体甲基化(GbM)。尽管 DNA 甲基化在转座子和重复 DNA 的沉默中起着重要作用,但基因体甲基化与转录抑制无关,其生物学重要性尚不清楚。
我们报告了一种在植物中发现的新型 GbM,它在所有细胞中(包括生殖细胞)都受到动态甲基化修饰剂的组成性添加和去除。动态 GbM 基因的甲基化由 DRDD 去甲基化途径去除,并由未知的从头甲基化来源添加,最有可能是维持甲基转移酶 MET1。我们表明,在跨越超过 1 亿年的不同进化枝的同源基因中存在动态 GbM 状态,表明其具有进化保守性。我们证明,与其他基因体甲基化基因相比,动态 GbM 状态与基因体中启动子或调节染色质状态的存在密切相关。我们发现,动态 GbM 与发育和多种生理条件下增强的基因表达可塑性密切相关,而稳定甲基化的 GbM 基因则表现出较低的可塑性。在 drdd 突变体中,动态 GbM 基因的动态范围减小,表明 DNA 去甲基化与增强的基因表达可塑性之间存在因果关系。
我们提出了一种新的 GbM 调节基因表达可塑性的模型,包括一种新型的 GbM,其中增加的基因表达可塑性与 DNA 甲基化写入器和擦除器的活性以及调节染色质状态的富集相关。