组蛋白
组蛋白密码
组蛋白H2A
组蛋白修饰酶
癌症表观遗传学
组蛋白甲基转移酶
表观遗传学
生物
染色质重塑
相扑蛋白
组蛋白甲基化
瓜氨酸化
细胞生物学
核小体
生物化学
泛素
DNA
DNA甲基化
基因表达
基因
氨基酸
精氨酸
瓜氨酸
作者
Ruilin Wang,Mei Xin,Yanjiao Li,Pingyu Zhang,Meixia Zhang
出处
期刊:Current Protein & Peptide Science
[Bentham Science]
日期:2016-01-27
卷期号:17 (5): 438-445
被引量:50
标识
DOI:10.2174/1389203717666160122120521
摘要
Posttranslational modifications of proteins critically regulate the function, localization, and stability of target proteins. Histone modification is one of the regulatory mechanisms that modulate the chromatin structure and thereby affect various DNA-templated processes, such as gene transcription, DNA replication, DNA recombination, and DNA repair in cells. These molecular processes contribute to basic cellular functions, including cell cycle, cell growth, and apoptosis. Histone modifications consist of acetylation, methylation, phosphorylation, ubiquitination, sumoylation biotination, citrullination, poly-ADPribosylation, and N-glycosylation. The modification status of histone is balanced by two enzyme families with opposing catalytic activities: histone modifying and de-modifying enzymes. Recent studies have shown that dysfunction of histone modification enzymes is a major cause for human cancer initiation and progression. In this review, we will summarize the functions of histone modification enzymes in cancer, and the mechanisms that histone modification enzymes use to drive or suppress human malignancies.
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