Yu Jiangtao, Chen Haihua, Ma Haoli, Zhang Zhongxiang, Zhu Xiaolu, Wang Pengcheng, Liu Ruining, Jin Xiaoqing, Zhao Yan
Emergency Center, Zhongnan Hospital of Wuhan University, Wuhan, China.
Hubei Clinical Research Center for Emergency and Resuscitation, Zhongnan Hospital of Wuhan University, Wuhan, China.
Front Neurosci. 2022 May 30;16:848119. doi: 10.3389/fnins.2022.848119. eCollection 2022.
Recent studies showed that RNA N6-methyladenosine (m6A) plays an important role in neurological diseases. We used methylated RNA immunoprecipitation sequencing (MeRIP-Seq) technology to generate the m6A modification map after traumatic spinal cord injury (TSCI). A total of 2,609 differential m6A peaks were identified after TSCI. Our RNA sequencing results after TSCI showed 4,206 genes with significantly altered expression. Cross-link analysis of m6A sequencing results and RNA sequencing results showed that 141 hyper-methylated genes were upregulated, 53 hyper-methylated genes were downregulated, 57 hypo-methylated genes were upregulated, and 197 hypo-methylated genes were downregulated. Among these, the important inflammatory response factor and the important member of the neurotrophin family were both upregulated and hyper-methylated after TSCI. This study provides that in the future, the epigenetic modifications of the genes could be used as an indicator of TSCI.
最近的研究表明,RNA N6-甲基腺嘌呤(m6A)在神经疾病中起重要作用。我们使用甲基化RNA免疫沉淀测序(MeRIP-Seq)技术生成创伤性脊髓损伤(TSCI)后的m6A修饰图谱。TSCI后共鉴定出2609个差异m6A峰。我们TSCI后的RNA测序结果显示4206个基因表达有显著变化。m6A测序结果与RNA测序结果的交联分析表明,141个高甲基化基因上调,53个高甲基化基因下调,57个低甲基化基因上调,197个低甲基化基因下调。其中,重要的炎症反应因子和神经营养因子家族的重要成员在TSCI后均上调且高甲基化。本研究表明,未来基因的表观遗传修饰可作为TSCI的一个指标。