假尿苷
核糖核酸
RNA甲基化
N6-甲基腺苷
表观遗传学
甲基化
非编码RNA
核糖
生物
信使核糖核酸
计算生物学
小核RNA
核糖体RNA
转移RNA
甲基转移酶
DNA
遗传学
生物化学
基因
酶
作者
Yirong Wu,Siyao Zhan,Yizhou Xu,Xiangwei Gao
出处
期刊:Life Sciences
[Elsevier]
日期:2021-08-01
卷期号:278: 119565-119565
被引量:47
标识
DOI:10.1016/j.lfs.2021.119565
摘要
More than one hundred RNA modifications decorate the chemical and topological properties of these ribose nucleotides, thereby executing their biological functions through post-transcriptional regulation. In cardiovascular diseases, a wide range of RNA modifications including m6A (N6-adenosine methylation), m5C (5-methylcytidin), Nm (2′-O-ribose-methylation), Ψ (pseudouridine), m7G (N7-methylguanosine), and m1A (N1-adenosine methylation) have been found in tRNA, rRNA, mRNA and other noncoding RNA, which can function as a novel mechanism in metabolic syndrome, heart failure, coronary heart disease, and hypertension. In this review, we will summarize the current understanding of the regulatory roles and significance of several types of RNA modifications in CVDs (cardiovascular diseases) and the interplay between RNA modifications and noncoding RNA, epigenetics. Finally, we will focus on the potential therapeutic strategies by using RNA modifications.
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