Differential Expression Analysis of tRNA-Derived Small RNAs from Subcutaneous Adipose Tissue of Obese and Lean Pigs.
Hao GuMailin GanLinghui WangYiting YangJinyong WangLei ChenShunhua ZhangYe ZhaoLili NiuDongmei JiangYiwu ChenAnan JiangLinyuan ShenLi ZhuPublished in: Animals : an open access journal from MDPI (2022)
Epigenetic factors, including non-coding RNA regulation, play a vital role in the development of obesity and have been well researched. Transfer RNA-derived small RNA (tsRNA) is a class of non-coding RNA proven to be involved in various aspects of mammalian biology. Here we take pigs as a model for obesity research and use tsRNA-seq to investigate the difference in tsRNA expression in the subcutaneous adipose tissue of obese and lean pigs to elucidate the role of tsRNA in obesity development. A total of 482 tsRNAs were identified in pig adipose tissue, of which 123 were significantly differentially accumulated tsRNAs compared with the control group. The tRF-5c was the main type of these tsRNAs. The largest number of tsRNAs produced was the Gly-carrying tRNA, which produced 81 tsRNAs. Functional enrichment analysis revealed that differential tsRNAs indirectly participated in MAPK, AMPK, insulin resistance, the TNF signaling pathway, adipocytokine signaling pathway, and other signaling pathways by interacting with target genes. These are involved in bioenergetic metabolic regulatory processes, suggesting that tsRNAs may influence these pathways to mediate the regulation of energy metabolism in porcine adipocytes to promote lipid deposition, thus contributing to obesity. Our findings suggest a potential function of tsRNA in regulating obesity development.
Keyphrases
- insulin resistance
- adipose tissue
- signaling pathway
- high fat diet induced
- metabolic syndrome
- high fat diet
- weight loss
- type diabetes
- polycystic ovary syndrome
- skeletal muscle
- pi k akt
- weight gain
- epithelial mesenchymal transition
- gene expression
- bariatric surgery
- single cell
- rheumatoid arthritis
- poor prognosis
- long non coding rna
- oxidative stress
- transcription factor
- climate change
- binding protein
- nucleic acid