Writing, erasing and reading histone lysine methylations

被引:758
作者
Hyun, Kwangbeom [1 ]
Jeon, Jongcheol [1 ]
Park, Kihyun [1 ]
Kim, Jaehoon [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Lab Eukaryot Transcript, 291 Daehak Ro, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
MIXED-LINEAGE LEUKEMIA; EMBRYONIC STEM-CELLS; RNA-POLYMERASE-II; LINKED MENTAL-RETARDATION; ACUTE MYELOID-LEUKEMIA; H3K9 METHYLTRANSFERASE G9A; RESISTANT PROSTATE-CANCER; POLYCOMB GROUP PROTEIN; CXXC FINGER PROTEIN-1; TUMOR-SUPPRESSOR GENE;
D O I
10.1038/emm.2017.11
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Histone modifications are key epigenetic regulatory features that have important roles in many cellular events. Lysine methylations mark various sites on the tail and globular domains of histones and their levels are precisely balanced by the action of methyltransferases ('writers') and demethylases ('erasers'). In addition, distinct effector proteins ('readers') recognize specific methyl-lysines in a manner that depends on the neighboring amino-acid sequence and methylation state. Misregulation of histone lysine methylation has been implicated in several cancers and developmental defects. Therefore, histone lysine methylation has been considered a potential therapeutic target, and clinical trials of several inhibitors of this process have shown promising results. A more detailed understanding of histone lysine methylation is necessary for elucidating complex biological processes and, ultimately, for developing and improving disease treatments. This review summarizes enzymes responsible for histone lysine methylation and demethylation and how histone lysine methylation contributes to various biological processes.
引用
收藏
页码:e324 / e324
页数:22
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