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<p>5-methylcytosine (m<sup>5</sup>C) is a prevalent RNA modification that has various impacts on mRNA fate. Here, we generated 30 single-base resolution RNA m<sup>5</sup>C methylomes and revealed the dynamic nature of m<sup>5</sup>C of heart, muscle, lung, esophagus, stomach, pancreas, colon, jejunum, and rectum from 7 adult human individuals using RNA-BisSeq. Based on clustering analysis, the heart and muscle formed one cluster, while the remaining tissues constituted another cluster. Intriguingly, we observed a discrepancy pattern between m<sup>5</sup>C levels and gene expression in these tissues when comparing the m<sup>5</sup>C methylome and transcriptome. Moreover, we identified differences in NSUN2-mediated m<sup>5</sup>C modifications between esophageal paracancerous tissues and healthy individual tissues. Notably, NSUN2 was found to interact with <Emphasis Type="BoldItalic">PLXNA1</Emphasis> mRNA, and silencing <Emphasis Type="BoldItalic">NSUN2</Emphasis> in esophageal squamous cell carcinoma (ESCC) cells resulted in the downregulation of <Emphasis Type="BoldItalic">PLXNA1</Emphasis> expression through an m<sup>5</sup>C-mediated mechanism. Overall, our study provides valuable insights into the m<sup>5</sup>C profile and the relationship between the methylome and transcriptome in human tissues, highlighting the potential role of m<sup>5</sup>C modification as an epitranscriptomic biomarker.</p>

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Dynamic landscape and regulation of m5C methylation in human tissues

  • 期刊论文

  • 发表日期：

    2025年6月23日

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  • Ke An,
  • Ruijuan Liu,
  • Han Yang,
  • Luyao Feng,
  • Xinhan Zhang,
  • Xuran Zhang,
  • Mingyang Hou,
  • Jingyao Wei,
  • Xiao Han,
  • Boyang Shi,
  • Huan Yao,
  • Xing Chen,
  • Han Wang,
  • Xin Tian

摘要

5-methylcytosine (m5C) is a prevalent RNA modification that has various impacts on mRNA fate. Here, we generated 30 single-base resolution RNA m5C methylomes and revealed the dynamic nature of m5C of heart, muscle, lung, esophagus, stomach, pancreas, colon, jejunum, and rectum from 7 adult human individuals using RNA-BisSeq. Based on clustering analysis, the heart and muscle formed one cluster, while the remaining tissues constituted another cluster. Intriguingly, we observed a discrepancy pattern between m5C levels and gene expression in these tissues when comparing the m5C methylome and transcriptome. Moreover, we identified differences in NSUN2-mediated m5C modifications between esophageal paracancerous tissues and healthy individual tissues. Notably, NSUN2 was found to interact with PLXNA1 mRNA, and silencing NSUN2 in esophageal squamous cell carcinoma (ESCC) cells resulted in the downregulation of PLXNA1 expression through an m5C-mediated mechanism. Overall, our study provides valuable insights into the m5C profile and the relationship between the methylome and transcriptome in human tissues, highlighting the potential role of m5C modification as an epitranscriptomic biomarker.