Nonhistone Lysine Methylation in the Regulation of Cancer Pathways

被引:95
作者
Carlson, Scott M. [1 ]
Gozani, Or [1 ]
机构
[1] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE | 2016年 / 6卷 / 11期
基金
美国国家卫生研究院;
关键词
G9A HISTONE METHYLTRANSFERASE; DOMAIN-CONTAINING PROTEINS; IN-VIVO; RECOMBINATION HOTSPOTS; MEIOTIC RECOMBINATION; CHROMATIN-STRUCTURE; DEMETHYLASE LSD1; GENE-EXPRESSION; BREAST CANCERS; CHEMICAL PROBE;
D O I
10.1101/cshperspect.a026435
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Proteins are regulated by an incredible array of posttranslational modifications (PTMs). Methylation of lysine residues on histone proteins is a PTM with well-established roles in regulating chromatin and epigenetic processes. The recent discovery that hundreds and likely thousands of nonhistone proteins are also methylated at lysine has opened a tremendous new area of research. Major cellular pathways involved in cancer, such as growth signaling and the DNA damage response, are regulated by lysine methylation. Although the field has developed quickly in recent years many fundamental questions remain to be addressed. We review the history and molecular functions of lysine methylation. We then discuss the enzymes that catalyze methylation of lysine residues, the enzymes that remove lysine methylation, and the cancer pathways known to be regulated by lysine methylation. The rest of the article focuses on two open questions that we suggest as a roadmap for future research. First is understanding the large number of candidate methyltransferase and demethylation enzymes whose enzymatic activity is not yet defined and which are potentially associated with cancer through genetic studies. Second is investigating the biological processes and cancer mechanisms potentially regulated by the multitude of lysine methylation sites that have been recently discovered.
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页数:16
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