Tian Weihua, Zhang Bo, Zhong Haian, Nie Ruixue, Ling Yao, Zhang Hao, Wu Changxin
National Engineering Laboratory for Animal Breeding, College of Animal Science and Technology, China Agricultural University, Beijing, China.
Beijing Key Laboratory for Animal Genetic Improvement, College of Animal Science and Technology, China Agricultural University, Beijing, China.
Front Cell Dev Biol. 2021 Nov 12;9:761638. doi: 10.3389/fcell.2021.761638. eCollection 2021.
Circular RNA (circRNA), as a novel endogenous biomolecule, has been emergingly demonstrated to play crucial roles in mammalian lipid metabolism and obesity. However, little is known about their genome-wide identification, expression profile, and function in chicken adipogenesis. In present study, the adipogenic differentiation of chicken abdominal preadipocyte was successfully induced, and the regulatory functional circRNAs in chicken adipogenesis were identified from abdominal adipocytes at different differentiation stages using Ribo-Zero RNA-seq. A total of 1,068 circRNA candidates were identified and mostly derived from exons. Of these, 111 differentially expressed circRNAs (DE-circRNAs) were detected, characterized by stage-specific expression, and enriched in several lipid-related pathways, such as Hippo signaling pathway, mTOR signaling pathway. Through weighted gene co-expression network analyses (WGCNA) and K-means clustering analyses, two DE-circRNAs, Z:35565770|35568133 and Z:54674624|54755962, were identified as candidate regulatory circRNAs in chicken adipogenic differentiation. Z:35565770|35568133 might compete splicing with its parental gene, , owing to its strictly negative co-expression. We also constructed competing endogenous RNA (ceRNA) network based on DE-circRNA, DE-miRNA, DE-mRNAs, revealing that Z:54674624|54755962 might function as a ceRNA to regulate chicken adipogenic differentiation through the gga-miR-1635-//// and/or the novel_miR_232- axis. Translation activity analysis showed that Z:35565770|35568133 and Z:54674624|54755962 have no protein-coding potential. These findings provide valuable evidence for a better understanding of the specific functions and molecular mechanisms of circRNAs underlying avian adipogenesis.
环状RNA(circRNA)作为一种新型内源性生物分子,已逐渐被证明在哺乳动物脂质代谢和肥胖中发挥关键作用。然而,关于它们在鸡脂肪生成中的全基因组鉴定、表达谱和功能却知之甚少。在本研究中,成功诱导了鸡腹部前脂肪细胞的脂肪生成分化,并使用Ribo-Zero RNA测序从不同分化阶段的腹部脂肪细胞中鉴定出鸡脂肪生成中的调控功能性circRNA。共鉴定出1068个circRNA候选物,且大多来源于外显子。其中,检测到111个差异表达的circRNA(DE-circRNA),其具有阶段特异性表达特征,并富集于多个脂质相关途径,如Hippo信号通路、mTOR信号通路。通过加权基因共表达网络分析(WGCNA)和K均值聚类分析,鉴定出两个DE-circRNA,即Z:35565770|35568133和Z:54674624|54755962,作为鸡脂肪生成分化中的候选调控circRNA。Z:35565770|35568133由于其严格的负共表达,可能与其亲本基因竞争剪接。我们还基于DE-circRNA、DE-miRNA、DE-mRNA构建了竞争性内源RNA(ceRNA)网络,揭示Z:54674624|54755962可能作为ceRNA,通过gga-miR-1635-////和/或novel_miR_232-轴调节鸡脂肪生成分化。翻译活性分析表明,Z:35565770|35568133和Z:54674624|54755962没有蛋白质编码潜力。这些发现为更好地理解circRNA在禽类脂肪生成中的特定功能和分子机制提供了有价值的证据。