Liu Ximing, Bai Ying, Cui Ran, He Shuaihan, Zhao Xingbo, Wu Keliang, Fang Meiying
National Engineering Laboratory for Animal Breeding, MOA Laboratory of Animal Genetics and Breeding, Department of Animal Genetics and Breeding, College of Animal Science and Technology, China Agricultural University, Beijing 100193, China.
College of Life Sciences and Food Engineering, Hebei University of Engineering, Handan 056021, China.
Biomolecules. 2022 May 26;12(6):753. doi: 10.3390/biom12060753.
CircRNAs play an important role in fat deposition, and testosterone-deficient boars exhibit significantly increased fat deposition; however, the mechanism by which testosterone regulates fat deposition through circRNAs remains unclear. In this study, circRNA-seq of backfat and abdominal fat from castrated and intact full-sib Yorkshire pigs was performed. The GO and KEGG enrichment analyses revealed that the host genes of the dorsal DE circRNAs were mainly involved in fatty acid transport, while in abdominal tissues, these genes were mainly involved in adipogenesis and inflammation. The interaction among sus_circPAPPA2, ssc-miR-2366 and was verified by dual fluorescence experiments and in porcine preadipocytes. The overexpression of sus_circPAPPA2 significantly inhibited the differentiation of preadipocytes. The expression of sus_circPAPPA2 was increased after adding 100 nM of testosterone, and preadipocyte differentiation was significantly inhibited. Testosterone can affect preadipocyte differentiation by upregulating the expression of sus_circPAPPA2, sponging miR-2366 and regulating the expression of genes, such as . These results indicate that testosterone can regulate the expression of adipocyte differentiation- and lipid metabolism-related genes by regulating the expression of circRNA, and ceRNA networks are different in the testosterone regulation of adipose deposition in different parts. This study provides basic data enhancing the understanding of the interaction between the hormone environment and mir-2366/GK to regulate trait performance in pigs.
环状RNA在脂肪沉积中发挥重要作用,睾酮缺乏的公猪脂肪沉积显著增加;然而,睾酮通过环状RNA调节脂肪沉积的机制尚不清楚。本研究对去势和未去势的全同胞约克夏猪的背膘和腹部脂肪进行了环状RNA测序。基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析表明,背部差异表达环状RNA的宿主基因主要参与脂肪酸转运,而在腹部组织中,这些基因主要参与脂肪生成和炎症反应。通过双荧光实验在猪前体脂肪细胞中验证了猪环状PAPPA2(sus_circPAPPA2)、猪微小RNA-2366(ssc-miR-2366)和[此处原文缺失相关内容]之间的相互作用。sus_circPAPPA2的过表达显著抑制了前体脂肪细胞的分化。添加100 nM睾酮后,sus_circPAPPA2的表达增加,前体脂肪细胞分化受到显著抑制。睾酮可通过上调sus_circPAPPA2的表达、吸附miR-2366以及调节[此处原文缺失相关基因名称]等基因的表达来影响前体脂肪细胞的分化。这些结果表明,睾酮可通过调节环状RNA的表达来调控脂肪细胞分化和脂质代谢相关基因的表达,并且在睾酮对不同部位脂肪沉积的调控中,竞争性内源RNA(ceRNA)网络存在差异。本研究提供了基础数据,有助于加深对激素环境与mir-2366/糖原合成酶激酶(GK)之间相互作用以调控猪性状表现的理解。