Acta Veterinaria et Zootechnica Sinica ›› 2025, Vol. 56 ›› Issue (11): 5433-5448.doi: 10.11843/j.issn.0366-6964.2025.11.008

• Animal Genetics and Breeding • Previous Articles     Next Articles

Three-Dimensional Genome Architecture of Porcine White and Beige Adipocytes

JIANG Yifan1(), LI Haoxing2,3,4(), LIN Yu1, ZHANG Zhihua2,3,4, WANG Yanfang1,*()   

  1. 1. Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China
    2. China National Center for Bioinformation, Beijing 100101, China
    3. Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China
    4. College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China
  • Received:2025-04-08 Online:2025-11-23 Published:2025-11-27
  • Contact: WANG Yanfang E-mail:jiang092122@163.com;1076599497@qq.com;wangyanfang@caas.cn

Abstract:

This study aimed to investigate the differences between porcine white and beige adipocytes at the three-dimensional (3D) genome level, identify cell type-specific promoter-enhancer interactions (PEIs) in both adipocyte types, and screen for critical enhancers that promote the differentiation of porcine beige adipocytes. This study differentiated porcine white and beige adipocytes, and employed high-throughput chromosome conformation capture (Hi-C) to compare differences in chromatin compartments, topologically associating domains (TADs), and chromatin loops between the two adipocyte types. We comprehensively resolved the 3D genome architecture of porcine adipocytes. Using genome-wide H3K27ac and H3K4me3 ChIP-seq data, the study identified promoter-enhancer interactions (PEIs) in both adipocyte types and screened for potential enhancers that promote the differentiation of pig beige adipocytes. The activity of these enhancers was further validated through the construction of dual-luciferase reporter vectors. The Hi-C data revealed divergent 3D genome architectures between the two adipocyte types, with chromatin compartment switching occurring in 5% of genomic regions. A total of 1 923 white adipose-specific TADs (topologically associating domains) and 12 920 white adipose-specific loops were identified, while 2 010 beige adipose-specific TADs and 9 526 beige adipose-specific loops were also detected. ChIP-seq results revealed the identification of 795 white adipose-specific PEIs and 737 beige adipose-specific PEIs. By integrating transcriptomic data, we identified gene enhancers that are specifically highly expressed in beige adipocytes and exhibit cell type-specific PEIs, which were prioritized as critical enhancers promoting beige adipocyte differentiation. Furthermore, dual-luciferase reporter plasmids carrying 525 bp (TMEM100 gene) and 200 bp (AMCF-Ⅱ gene) candidate enhancer fragments were constructed. Luciferase activity assays demonstrated that these putative enhancers upregulated luciferase activity significantly (P < 0.05). This study constructed three-dimensional genome maps of porcine white and beige adipocytes, revealing differences in chromatin spatial structures between the two types of adipocytes. We validated the enhancer activity of the TMEM100 and AMCF-Ⅱ genes preliminarily, suggesting that the enhancers of both genes may promote the differentiation of porcine beige adipocytes through PEIs regulation.

Key words: pig, beige adipocyte, Hi-C, 3D genome, enhancer

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