Neuroscience Graduate Program, The University of Michigan, Ann Arbor, MI, 48109, USA.
Department of Molecular, Cellular and Developmental Biology, The University of Michigan, Ann Arbor, MI, 48109, USA.
Dev Biol. 2020 Jun 15;462(2):180-196. doi: 10.1016/j.ydbio.2020.03.013. Epub 2020 Mar 31.
Methylation of cytosine residues in DNA influences chromatin structure and gene transcription, and its regulation is crucial for brain development. There is mounting evidence that DNA methylation can be modulated by hormone signaling. We analyzed genome-wide changes in DNA methylation and their relationship to gene regulation in the brain of Xenopus tadpoles during metamorphosis, a thyroid hormone-dependent developmental process. We studied the region of the tadpole brain containing neurosecretory neurons that control pituitary hormone secretion, a region that is highly responsive to thyroid hormone action. Using Methylated DNA Capture sequencing (MethylCap-seq) we discovered a diverse landscape of DNA methylation across the tadpole neural cell genome, and pairwise stage comparisons identified several thousand differentially methylated regions (DMRs). During the pre-to pro-metamorphic period, the number of DMRs was lowest (1,163), with demethylation predominating. From pre-metamorphosis to metamorphic climax DMRs nearly doubled (2,204), with methylation predominating. The largest changes in DNA methylation were seen from metamorphic climax to the completion of metamorphosis (2960 DMRs), with 80% of the DMRs representing demethylation. Using RNA sequencing, we found negative correlations between differentially expressed genes and DMRs localized to gene bodies and regions upstream of transcription start sites. DNA demethylation at metamorphosis revealed by MethylCap-seq was corroborated by increased immunoreactivity for the DNA demethylation intermediates 5-hydroxymethylcytosine and 5-carboxymethylcytosine, and the methylcytosine dioxygenase ten eleven translocation 3 that catalyzes DNA demethylation. Our findings show that the genome of tadpole neural cells undergoes significant changes in DNA methylation during metamorphosis, and these changes likely influence chromatin architecture, and gene regulation programs occurring during this developmental period.
DNA 中胞嘧啶残基的甲基化影响染色质结构和基因转录,其调控对于大脑发育至关重要。越来越多的证据表明,DNA 甲基化可以通过激素信号来调节。我们分析了在变态过程中,即甲状腺激素依赖性发育过程中,非洲爪蟾蝌蚪大脑中 DNA 甲基化的全基因组变化及其与基因调控的关系。我们研究了包含控制脑垂体激素分泌的神经分泌神经元的蝌蚪大脑区域,该区域对甲状腺激素的作用高度敏感。使用甲基化 DNA 捕获测序(MethylCap-seq),我们在蝌蚪神经细胞基因组中发现了 DNA 甲基化的多样化景观,并且两两阶段比较鉴定了数千个差异甲基化区域(DMR)。在预变态到前变态期,DMR 的数量最少(1163 个),去甲基化占主导地位。从预变态到变态高峰期,DMR 几乎增加了一倍(2204 个),甲基化占主导地位。DNA 甲基化最大的变化发生在变态高峰期到变态完成期(2960 个 DMR),其中 80%的 DMR 代表去甲基化。使用 RNA 测序,我们发现差异表达基因与定位在基因体和转录起始位点上游区域的 DMR 之间存在负相关。MethylCap-seq 揭示的变态时的 DNA 去甲基化作用得到了 5-羟甲基胞嘧啶和 5-羧甲基胞嘧啶等 DNA 去甲基化中间产物以及催化 DNA 去甲基化的双加氧酶 ten eleven translocation 3 的免疫反应性增加的证实。我们的研究结果表明,在变态过程中,蝌蚪神经细胞的基因组经历了 DNA 甲基化的显著变化,这些变化可能影响染色质结构和发生在这个发育阶段的基因调控程序。