Structural Insights into N6-methyladenosine (m6A) Modification in the Transcriptome

被引:67
|
作者
Huang, Jinbo
Yin, Ping [1 ]
机构
[1] Huazhong Agr Univ, Natl Key Lab Crop Genet Improvement, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Epitranscriptomics; M(6)A modification; Writer; Reader; Eraser; MESSENGER-RNA METHYLATION; RESOLUTION MAPPING REVEALS; YTH DOMAIN; NUCLEAR-RNA; DEMETHYLASE ALKBH5; CRYSTAL-STRUCTURE; SEX DETERMINATION; GENE-EXPRESSION; REPAIR ENZYMES; BINDING MODE;
D O I
10.1016/j.gpb.2018.03.001
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
More than 100 types of chemical modifications in RNA have been well documented. Recently, several modifications, such as N-6-methyladenosine (m(6)A), have been detected in mRNA, opening the window into the realm of epitranscriptomics. The m(6)A modification is the most abundant modification in mRNA and non-coding RNA (ncRNA). At the molecular level, m(6)A affects almost all aspects of mRNA metabolism, including splicing, translation, and stability, as well as microRNA (miRNA) maturation, playing essential roles in a range of cellular processes. The m(6)A modification is regulated by three classes of proteins generally referred to as the "writer" (adenosine methyltransferase), "eraser" (m(6)A demethylating enzyme), and "reader" (m(6)A-binding protein). The m(6)A modification is reversibly installed and removed by writers and erasers, respectively. Readers, which are members of the YT521-B homology (YTH) family proteins, selectively bind to RNA and affect its fate in an m(6)A-dependent manner. In this review, we summarize the structures of the functional proteins that modulate the m(6)A modification, and provide our insights into the m(6)A-mediated gene regulation.
引用
收藏
页码:85 / 98
页数:14
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