Tian Weihua, Hao Xin, Nie Ruixue, Ling Yao, Zhang Bo, Zhang Hao, Wu Changxin
National Engineering Laboratory for Animal Breeding, Beijing Key Laboratory for Animal Genetic Improvement, College of Animal Science and Technology, China Agricultural University, Beijing 100193, China.
Animals (Basel). 2022 Apr 24;12(9):1099. doi: 10.3390/ani12091099.
Long non-coding RNAs (lncRNAs) are implicated in mammalian adipogenesis and obesity. However, their genome-wide distribution, expression profiles, and regulatory mechanisms during chicken adipogenesis remain rarely understood. In the present study, lncRNAs associated with adipogenesis were identified from chicken abdominal adipocytes at multiple differentiation stages using Ribo-Zero RNA-seq. A total of 15,179 lncRNAs were identified and characterized by stage-specific expression patterns. Of these, 840 differentially expressed lncRNAs were detected, and their - and -target genes were significantly enriched in multiple lipid-related pathways. Through weighted gene co-expression network analysis (WGCNA) and time-series expression profile clustering analysis, 14 key lncRNAs were identified as candidate regulatory lncRNAs in chicken adipogenic differentiation. The - and -regulatory interactions of key lncRNAs were constructed based on their differentially expressed - and -target genes, respectively. We also constructed a competing endogenous RNA (ceRNA) network based on the key lncRNAs, differentially expressed miRNAs, and differentially expressed mRNAs. MSTRG.25116.1 was identified as a potential regulator of chicken abdominal preadipocyte adipogenic differentiation by acting as a transcriptional -regulator of fatty acid amide hydrolase () gene expression and/or a ceRNA that post-transcriptionally mediates gene expression by sponging gga-miR-1635.
长链非编码RNA(lncRNAs)与哺乳动物脂肪生成和肥胖有关。然而,它们在鸡脂肪生成过程中的全基因组分布、表达谱和调控机制仍鲜为人知。在本研究中,使用Ribo-Zero RNA测序技术从鸡腹部脂肪细胞的多个分化阶段鉴定出与脂肪生成相关的lncRNAs。共鉴定出15179个lncRNAs,并根据阶段特异性表达模式对其进行了表征。其中,检测到840个差异表达的lncRNAs,它们的靶基因在多个脂质相关途径中显著富集。通过加权基因共表达网络分析(WGCNA)和时间序列表达谱聚类分析,确定了14个关键lncRNAs作为鸡脂肪生成分化中的候选调控lncRNAs。分别基于关键lncRNAs差异表达的靶基因构建了它们的调控相互作用。我们还基于关键lncRNAs、差异表达的miRNA和差异表达的mRNA构建了一个竞争性内源RNA(ceRNA)网络。MSTRG.25116.1被确定为鸡腹部前脂肪细胞脂肪生成分化的潜在调节因子,它通过作为脂肪酸酰胺水解酶(FAAH)基因表达的转录调节因子和/或通过海绵吸附gga-miR-1635转录后介导FAAH基因表达的ceRNA发挥作用。