Zeng Sha, Li Ziqi, Li Xiaokai, Du Qinjiao, Zhang Yu, Zhong Zhining, Wang Haoming, Zhang Songling, Li Penghao, Li Haohuan, Chen Li, Jiang Anan, Shang Peng, Li Mingzhou, Long Keren
State Key Laboratory of Swine and Poultry Breeding Industry, Sichuan Agricultural University, Chengdu, China.
College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, China.
FASEB J. 2025 Jan 31;39(2):e70347. doi: 10.1096/fj.202401137R.
Triglyceride (TG) metabolism is a complex and highly coordinated biological process regulated by a series of genes, and its dysregulation can lead to the occurrence of disorders in lipid metabolism. However, the transcriptional regulatory mechanisms of crucial genes in TG metabolism mediated by enhancer-promoter interactions remain elusive. Here, we identified candidate enhancers regulating the Agpat2, Dgat1, Dgat2, Pnpla2, and Lipe genes in 3T3-L1 adipocytes by integrating epigenomic data (H3K27ac, H3K4me1, and DHS-seq) with chromatin three-dimensional interaction data. Luciferase reporter assays revealed that 11 enhancers exhibited fluorescence activity. The repression of enhancers using the dCas9-KRAB system revealed the functional roles of enhancers of Dgat2 and Pnpla2 in regulating their expression and TG metabolism. Furthermore, transcriptome analyses revealed that inhibition of Dgat2-En4 downregulated pathways associated with lipid metabolism, lipid biosynthesis, and adipocyte differentiation. Additionally, overexpression and motif mutation experiments of transcription factor found that two TFs, PPARG and RXRA, regulate the activity of Agpat2-En1, Dgat2-En4, and Pnpla2-En5. Our study identified functional enhancers regulating TG metabolism and elucidated potential regulatory mechanisms of TG deposition from enhancer-promoter interactions, providing insights into understanding lipid deposition.
甘油三酯(TG)代谢是一个由一系列基因调控的复杂且高度协调的生物学过程,其失调会导致脂质代谢紊乱的发生。然而,由增强子-启动子相互作用介导的TG代谢关键基因的转录调控机制仍不清楚。在这里,我们通过整合表观基因组数据(H3K27ac、H3K4me1和DHS-seq)与染色质三维相互作用数据,在3T3-L1脂肪细胞中鉴定出调控Agpat2、Dgat1、Dgat2、Pnpla2和Lipe基因的候选增强子。荧光素酶报告基因检测显示,11个增强子具有荧光活性。使用dCas9-KRAB系统抑制增强子揭示了Dgat2和Pnpla2增强子在调节其表达和TG代谢中的功能作用。此外,转录组分析表明,抑制Dgat2-En4会下调与脂质代谢、脂质生物合成和脂肪细胞分化相关的途径。此外,转录因子的过表达和基序突变实验发现,两个转录因子PPARG和RXRA调节Agpat2-En1、Dgat2-En4和Pnpla2-En5的活性。我们的研究鉴定了调节TG代谢的功能性增强子,并阐明了从增强子-启动子相互作用调控TG沉积的潜在机制,为理解脂质沉积提供了见解。