生物
竞争性内源性RNA
小RNA
核糖核酸
计算生物学
内生
长非编码RNA
基因
基因表达
差速器(机械装置)
遗传学
基因表达调控
生物信息学
内分泌学
工程类
航空航天工程
作者
Yahong Fu,Changbin Sun,Qi Li,Fengcui Qian,Chunquan Li,Xiangwen Xi,Desi Shang,Chuhan Wang,Xiang Peng,Minghui Piao,Wenbo Qu,Jinwei Tian,Bo Yu,Xia Gu,Jiangtian Tian
出处
期刊:Epigenomics
[Future Medicine]
日期:2021-01-01
卷期号:13 (2): 99-112
被引量:6
标识
DOI:10.2217/epi-2020-0252
摘要
Aim: To identify differential mRNA and ncRNA expression profiles and competing endogenous RNA-associated regulatory networks during the progression of atherosclerosis (AS). Materials & methods: We systematically analyzed whole-transcriptome sequencing of samples from different stages of AS to evaluate their long noncoding RNA (lncRNA), circular RNA (circRNA), miRNA and mRNA profiles. Results: We constructed three AS-related competing endogenous RNA regulatory networks of differentially expressed circRNAs, lncRNAs, miRNAs and mRNAs. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses revealed that the circRNAs in the network were enriched in lipid metabolic processes and participated in the PPAR signaling pathway. Furthermore, lncRNAs were related to receptor activity, myofibrils and cardiovascular system development. Conclusion: The current findings further clarified the regulatory mechanisms at different stages of AS and may provide new ideas and targets for AS.
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