Formation and removal of 1,N6-dimethyladenosine in mammalian transfer RNA

生物 RNA甲基化 核糖核酸 甲基化 转移RNA N6-甲基腺苷 腺苷 碱基 假尿苷 基因 生物化学 细胞生物学 遗传学 甲基转移酶 DNA
作者
Xue-Jiao You,Shan Zhang,Juanjuan Chen,Feng Tang,Jin-Gang He,Jie Wang,Changxing Qi,Yu‐Qi Feng,Bi-Feng Yuan
出处
期刊:Nucleic Acids Research [Oxford University Press]
卷期号:50 (17): 9858-9872 被引量:9
标识
DOI:10.1093/nar/gkac770
摘要

Abstract RNA molecules harbor diverse modifications that play important regulatory roles in a variety of biological processes. Over 150 modifications have been identified in RNA molecules. N6-methyladenosine (m6A) and 1-methyladenosine (m1A) are prevalent modifications occurring in various RNA species of mammals. Apart from the single methylation of adenosine (m6A and m1A), dual methylation modification occurring in the nucleobase of adenosine, such as N6,N6-dimethyladenosine (m6,6A), also has been reported to be present in RNA of mammals. Whether there are other forms of dual methylation modification occurring in the nucleobase of adenosine other than m6,6A remains elusive. Here, we reported the existence of a novel adenosine dual methylation modification, i.e. 1,N6-dimethyladenosine (m1,6A), in tRNAs of living organisms. We confirmed that m1,6A is located at position 58 of tRNAs and is prevalent in mammalian cells and tissues. The measured level of m1,6A ranged from 0.0049% to 0.047% in tRNAs. Furthermore, we demonstrated that TRMT6/61A could catalyze the formation of m1,6A in tRNAs and m1,6A could be demethylated by ALKBH3. Collectively, the discovery of m1,6A expands the diversity of RNA modifications and may elicit a new tRNA modification-mediated gene regulation pathway.
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