College of Lab Medicine, Hebei North University, Zhangjiakou 075000, China.
College of Animal Science and Technology, Hebei North University, Zhangjiakou 075000, China.
Genes (Basel). 2023 Mar 10;14(3):688. doi: 10.3390/genes14030688.
Obesity is a major risk factor for cardiovascular, cerebrovascular, metabolic, and respiratory diseases, and it has become an important social health problem affecting the health of the population. Obesity is affected by both genetic and environmental factors. In this study, we constructed a diet-induced obese C57BL/6J mouse model and performed deep RNA sequencing (RNA-seq) on liner-depleted RNA extracted from the liver tissues of the mice to explore the underlying mechanisms of obesity. A total of 7469 circular RNAs (circRNAs) were detected, and 21 were differentially expressed (DE) in the high-fat diet (HFD) and low-fat diet (LFD) groups. We then constructed a comprehensive circRNA-associated competing endogenous RNA (ceRNA) network. Bioinformatic analysis indicated that DE circRNAs associated with lipid metabolic-related pathways may act as miRNA sponges to modulate target gene expression. and may serve as new candidates to regulate the expression of . This study provides systematic circRNA-associated ceRNA profiling in HFD mouse liver, and the results can aid early diagnosis and the selection of treatment targets for obesity in the future.
肥胖是心血管、脑血管、代谢和呼吸系统疾病的一个主要危险因素,它已成为影响人口健康的一个重要社会健康问题。肥胖受遗传和环境因素的影响。在这项研究中,我们构建了一个饮食诱导肥胖的 C57BL/6J 小鼠模型,并对从肥胖小鼠肝脏组织中提取的线性耗尽 RNA 进行深度 RNA 测序(RNA-seq),以探讨肥胖的潜在机制。共检测到 7469 个环状 RNA(circRNA),其中 21 个在高脂肪饮食(HFD)和低脂肪饮食(LFD)组之间差异表达(DE)。然后,我们构建了一个全面的 circRNA 相关竞争性内源 RNA(ceRNA)网络。生物信息学分析表明,与脂质代谢相关途径相关的 DE circRNA 可能作为 miRNA 海绵调节靶基因表达。和可能作为新的候选物来调节的表达。这项研究提供了 HFD 小鼠肝脏中系统的 circRNA 相关 ceRNA 分析,结果可有助于肥胖的早期诊断和未来治疗靶点的选择。