Alteration of mRNA 5-Methylcytosine Modification in Neurons After OGD/R and Potential Roles in Cell Stress Response and Apoptosis

• Published in: Frontiers in genetics Vol. 12; p. 633681
• Main Authors: Jian, Huan, Zhang, Chi, Qi, ZhangYang, Li, Xueying, Lou, Yongfu, Kang, Yi, Deng, Weimin, Lv, Yigang, Wang, Chaoyu, Wang, Wei, Shang, Shenghui, Hou, Mengfan, Zhou, Hengxing, Feng, Shiqing
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 03.02.2021
• Subjects: apoptosis; cell stress; epitranscriptome; Genetics; ischemia-reperfusion injury; m5C methylation; oxygen-glucose deprivation/reoxygenation; ischemia-reperfusion injury; apoptosis; oxygen-glucose deprivation/reoxygenation; epitranscriptome; m5C methylation; cell stress
• ISSN: 1664-8021; 1664-8021
• DOI: 10.3389/fgene.2021.633681

Epigenetic modifications play an important role in central nervous system disorders. As a widespread posttranscriptional RNA modification, the role of the m C modification in cerebral ischemia-reperfusion injury (IRI) remains poorly defined. Here, we successfully constructed a neuronal oxygen-glucose deprivation/reoxygenation (OGD/R) model and obtained an overview of the transcriptome-wide m C profiles using RNA-BS-seq. We discovered that the distribution of neuronal m C modifications was highly conserved, significantly enriched in CG-rich regions and concentrated in the mRNA translation initiation regions. After OGD/R, modification level of m C increased, whereas the number of methylated mRNA genes decreased. The amount of overlap of m C sites with the binding sites of most RNA-binding proteins increased significantly, except for that of the RBM3-binding protein. Moreover, hypermethylated genes in neurons were significantly enriched in pathological processes, and the hub hypermethylated genes RPL8 and RPS9 identified by the protein-protein interaction network were significantly related to cerebral injury. Furthermore, the upregulated transcripts with hypermethylated modification were enriched in the processes involved in response to stress and regulation of apoptosis, and these processes were not identified in hypomethylated transcripts. In final, we verified that OGD/R induced neuronal apoptosis using TUNEL and western blot assays. Our study identified novel m C mRNAs associated with ischemia-reperfusion in neurons, providing valuable perspectives for future studies on the role of the RNA methylation in cerebral IRI.