Oerum Stephanie, Dégut Clément, Barraud Pierre, Tisné Carine
Institut de Biologie Physico-chimique (IBPC), CNRS, UMR 8261 CNRS/Université Paris Diderot, 13 rue Pierre et Marie Curie, Paris 75005, France.
Biomolecules. 2017 Feb 21;7(1):20. doi: 10.3390/biom7010020.
To date, about 90 post-transcriptional modifications have been reported in tRNA expanding their chemical and functional diversity. Methylation is the most frequent post-transcriptional tRNA modification that can occur on almost all nitrogen sites of the nucleobases, on the C5 atom of pyrimidines, on the C2 and C8 atoms of adenosine and, additionally, on the oxygen of the ribose 2'-OH. The methylation on the N1 atom of adenosine to form 1-methyladenosine (m1A) has been identified at nucleotide position 9, 14, 22, 57, and 58 in different tRNAs. In some cases, these modifications have been shown to increase tRNA structural stability and induce correct tRNA folding. This review provides an overview of the currently known m1A modifications, the different m1A modification sites, the biological role of each modification, and the enzyme responsible for each methylation in different species. The review further describes, in detail, two enzyme families responsible for formation of m1A at nucleotide position 9 and 58 in tRNA with a focus on the tRNA binding, m1A mechanism, protein domain organisation and overall structures.
迄今为止,已报道tRNA中约有90种转录后修饰,这些修饰扩展了tRNA的化学和功能多样性。甲基化是最常见的tRNA转录后修饰,几乎可以发生在核碱基的所有氮位点、嘧啶的C5原子、腺苷的C2和C8原子上,此外,还可以发生在核糖2'-OH的氧原子上。腺苷N1原子甲基化形成1-甲基腺苷(m1A)已在不同tRNA的第9、14、22、57和58位核苷酸处被鉴定出来。在某些情况下,这些修饰已被证明可增加tRNA结构稳定性并诱导正确的tRNA折叠。本综述概述了目前已知的m1A修饰、不同的m1A修饰位点、每种修饰的生物学作用以及不同物种中每种甲基化所涉及的酶。该综述还详细描述了负责在tRNA的第9和58位核苷酸处形成m1A的两个酶家族,重点关注tRNA结合、m1A形成机制、蛋白质结构域组织和整体结构。