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Background <p>The longissimus dorsi muscle and backfat are important components of pork and complement each other in physiological function, significantly influencing key traits such as growth performance, carcass traits, and meat quality. While the transcriptomic atlas across different tissues in pigs has been widely studied, the underlying epigenetic regulatory mechanisms remain to be explored. In this study, we collected muscle and adipose tissues from hybrid offspring of lean-type (Western commercial pigs) and fat-type (Chinese indigenous pigs) pigs (<i>n</i> = 6) and performed integrated transcriptomic (RNA-seq) and DNA methylome (GM-seq) analysis to explore how DNA methylation coordinates tissue-specific differential gene expression. This has practical implications for optimizing breeding strategies and selecting superior breeds.</p> Results <p>Transcriptome sequencing identified 2,908 differentially expressed genes, which are primarily involved in collagen fibril organization, skeletal muscle contraction, and muscle organ development. Whole-genome DNA methylation sequencing identified 2,787 differentially methylated genes in the promoter region. Through integrative analysis, we found 571 genes that were shared, 390 of which showed a significant negative correlation between gene expression and promoter DNA methylation. These genes are mainly involved in cholesterol metabolism, PPAR signaling pathway, cytoskeleton in muscle cell, and calcium ion signaling pathways. Notably, we discovered that the differential expression of genes such as <i>APOE</i>, <i>FABP4</i>, <i>TNNI2</i>, and <i>TNNT3</i> between tissues is negatively regulated by promoter DNA methylation. In other words, low methylation of these gene promoters in one tissue was associated with high expression, while high methylation of the promoter in the opposite tissue suppressed expression.</p> Conclusions <p>These results suggest that DNA methylation plays an extensive and subtle regulatory role in tissue-specific gene expression, thereby facilitating different tissues to execute their specific physiological functions. This study further enriches our understanding of the integrative mechanisms between epigenetic regulation and transcriptomics in pigs and provides important theoretical foundations for precision molecular breeding.</p>

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Integrated analysis of DNA methylome and transcriptome of the backfat and longissimus dorsi muscle of Chinese-European hybrid pigs

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年1月24日

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  • Mei Ge,
  • Chenyu Li,
  • Tao Jiang,
  • Yani Huang,
  • Zhiyan Zhang

摘要

Background

The longissimus dorsi muscle and backfat are important components of pork and complement each other in physiological function, significantly influencing key traits such as growth performance, carcass traits, and meat quality. While the transcriptomic atlas across different tissues in pigs has been widely studied, the underlying epigenetic regulatory mechanisms remain to be explored. In this study, we collected muscle and adipose tissues from hybrid offspring of lean-type (Western commercial pigs) and fat-type (Chinese indigenous pigs) pigs (n = 6) and performed integrated transcriptomic (RNA-seq) and DNA methylome (GM-seq) analysis to explore how DNA methylation coordinates tissue-specific differential gene expression. This has practical implications for optimizing breeding strategies and selecting superior breeds.

Results

Transcriptome sequencing identified 2,908 differentially expressed genes, which are primarily involved in collagen fibril organization, skeletal muscle contraction, and muscle organ development. Whole-genome DNA methylation sequencing identified 2,787 differentially methylated genes in the promoter region. Through integrative analysis, we found 571 genes that were shared, 390 of which showed a significant negative correlation between gene expression and promoter DNA methylation. These genes are mainly involved in cholesterol metabolism, PPAR signaling pathway, cytoskeleton in muscle cell, and calcium ion signaling pathways. Notably, we discovered that the differential expression of genes such as APOE, FABP4, TNNI2, and TNNT3 between tissues is negatively regulated by promoter DNA methylation. In other words, low methylation of these gene promoters in one tissue was associated with high expression, while high methylation of the promoter in the opposite tissue suppressed expression.

Conclusions

These results suggest that DNA methylation plays an extensive and subtle regulatory role in tissue-specific gene expression, thereby facilitating different tissues to execute their specific physiological functions. This study further enriches our understanding of the integrative mechanisms between epigenetic regulation and transcriptomics in pigs and provides important theoretical foundations for precision molecular breeding.