Epigenomics and Computational Biology Lab, Fralin Life Sciences Institute, Virginia Tech, Blacksburg, VA 24061, USA; Genetics, Bioinformatics and Computational Biology Program, Virginia Tech, Blacksburg, VA 24061, USA.
Epigenomics and Computational Biology Lab, Fralin Life Sciences Institute, Virginia Tech, Blacksburg, VA 24061, USA; Department of Biological Sciences, College of Science, Virginia Tech, Blacksburg, VA 24061, USA; Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24061, USA.
Genomics. 2023 May;115(3):110604. doi: 10.1016/j.ygeno.2023.110604. Epub 2023 Mar 6.
Post-transcriptional RNA modifications have been recognized as key regulators of neuronal differentiation and synapse development in the mammalian brain. While distinct sets of 5-methylcytosine (mC) modified mRNAs have been detected in neuronal cells and brain tissues, no study has been performed to characterize methylated mRNA profiles in the developing brain. Here, together with regular RNA-seq, we performed transcriptome-wide bisulfite sequencing to compare RNA cytosine methylation patterns in neural stem cells (NSCs), cortical neuronal cultures, and brain tissues at three postnatal stages. Among 501 mC sites identified, approximately 6% are consistently methylated across all five conditions. Compared to mC sites identified in NSCs, 96% of them were hypermethylated in neurons and enriched for genes involved in positive transcriptional regulation and axon extension. In addition, brains at the early postnatal stage demonstrated substantial changes in both RNA cytosine methylation and gene expression of RNA cytosine methylation readers, writers, and erasers. Furthermore, differentially methylated transcripts were significantly enriched for genes regulating synaptic plasticity. Altogether, this study provides a brain epitranscriptomic dataset as a new resource and lays the foundation for further investigations into the role of RNA cytosine methylation during brain development.
转录后 RNA 修饰已被认为是哺乳动物大脑中神经元分化和突触发育的关键调节剂。虽然在神经元细胞和脑组织中已经检测到了不同的 5-甲基胞嘧啶(mC)修饰的 mRNA,但尚未有研究对发育中的大脑中的甲基化 mRNA 图谱进行特征描述。在这里,我们与常规 RNA-seq 一起,进行了全转录组亚硫酸氢盐测序,以比较神经干细胞(NSC)、皮质神经元培养物和三个出生后阶段的脑组织中的 RNA 胞嘧啶甲基化模式。在鉴定的 501 个 mC 位点中,约 6%在所有五种条件下均保持甲基化。与 NSCs 中鉴定的 mC 位点相比,它们中有 96%在神经元中呈超甲基化状态,并且富集了参与正转录调控和轴突延伸的基因。此外,在出生后早期阶段的大脑中,RNA 胞嘧啶甲基化和 RNA 胞嘧啶甲基化读码器、写码器和擦除器的基因表达都发生了实质性变化。此外,差异甲基化的转录本显著富集了调节突触可塑性的基因。总的来说,这项研究提供了一个大脑表观转录组数据集作为新的资源,并为进一步研究 RNA 胞嘧啶甲基化在大脑发育过程中的作用奠定了基础。