The JMJD family of histone demethylase and their intimate links to cardiovascular disease

脱甲基酶 表观遗传学 组蛋白 组蛋白甲基化 生物 DNA甲基化 疾病 组蛋白密码 遗传学 细胞生物学 生物信息学 医学 DNA 基因 核小体 基因表达 内科学
作者
Jiarun Xie,Haoyu Lin,Anna Zuo,Junqiao Shao,Wei Sun,Shao‐Ting Wang,Song Jianda,Yao Wang,Yanyu Luo,Jia Sun,Ming Wang
出处
期刊:Cellular Signalling [Elsevier BV]
卷期号:116: 111046-111046 被引量:1
标识
DOI:10.1016/j.cellsig.2024.111046
摘要

The incidence rate and mortality rate of cardiovascular disease rank first in the world. It is associated with various high-risk factors, and there is no single cause. Epigenetic modifications, such as DNA methylation or histone modification, actively participate in the initiation and development of cardiovascular diseases. Histone lysine methylation is a type of histone post-translational modification. The human Jumonji C domain (JMJD) protein family consists of more than 30 members. JMJD proteins participate in many key nuclear processes and play a key role in the specific regulation of gene expression, DNA damage and repair, and DNA replication. Importantly, increasing evidence shows that JMJD proteins are abnormally expressed in cardiovascular diseases, which may be a potential mechanism for the occurrence and development of these diseases. Here, we discuss the key roles of JMJD proteins in various common cardiovascular diseases. This includes histone lysine demethylase, which has been studied in depth, and less-studied JMJD members. Furthermore, we focus on the epigenetic changes induced by each JMJD member, summarize recent research progress, and evaluate their relationship with cardiovascular diseases and therapeutic potential.
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