CircRNA Profiling Reveals CircPPARγ Modulates Adipogenic Differentiation via Sponging miR-92a-3p.
Jiyao WuShaoli ZhangBinglin YueSihuan ZhangEnhui JiangHong ChenXianyong LanPublished in: Journal of agricultural and food chemistry (2022)
Adipogenesis describes the proliferation, differentiation, and apoptosis of mature adipocytes from primary adipocytes and is regulated by post-transcriptional modifications. Circular RNAs (circRNAs) play critical roles in mammalian development and physiology. However, the circRNA-mediated regulation of adipogenesis remains poorly understood. We profiled circRNA expression during bovine primary adipogenesis, detecting 16 circRNA candidates, including circPPARγ, which was abundant in the adipose tissue. Overexpression (overexpression plasmids) and interference (small interfering RNAs) with circPPARγ in bovine primary adipocytes, and proliferation, differentiation, and apoptosis were analyzed using EdU (5-ethynyl-2'-deoxyuridine) cell proliferation, cell counting kit-8, flow cytometry, TdT-mediated dUTP nick-end labeling apoptosis assay, Oil Red O staining, quantitative real-time PCR, and western blotting assays, which showed that circPPARγ facilitates adipocyte differentiation and inhibits proliferation and apoptosis. Dual-luciferase reporter assay and RNA immunoprecipitation assays indicated that circPPARγ binds miR-92a-3p and YinYang 1 (YY1). A novel regulatory pathway regulating adipogenesis and adipose deposition was revealed.
Keyphrases
- adipose tissue
- cell proliferation
- cell cycle arrest
- high fat diet induced
- oxidative stress
- endoplasmic reticulum stress
- insulin resistance
- flow cytometry
- high throughput
- cell death
- single cell
- transcription factor
- high fat diet
- pi k akt
- signaling pathway
- real time pcr
- poor prognosis
- stem cells
- type diabetes
- gene expression
- south africa
- fatty acid
- high resolution
- cell therapy
- long non coding rna
- binding protein
- mass spectrometry
- heat stress