The Biology of tRNA t6A Modification and Hypermodifications—Biogenesis and Disease Relevance

IF 4.5 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2025-08-15 Epub Date: 2025-03-27 DOI:10.1016/j.jmb.2025.169091
Wenhua Zhang , Eric Westhof
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Abstract

The structure and function of transfer RNAs (tRNAs) are highly dependent on post-transcriptional chemical modifications that attach distinct chemical groups to various nucleobase atoms at selected tRNA positions via enzymatic reactions. In all three domains of life, the greatest diversity of chemical modifications is concentrated at positions 34 and 37 of the tRNA anticodon loops. N6-threonylcarbamoyladenosine (t6A) is an essential and universal modification occurring at position 37 of tRNAs that decode codons beginning with an adenine. In a subset of tRNAs from specific organisms, t6A is converted into a variety of hypermodified forms, including cyclic N6-threonylcarbamoyladenosine (ct6A), hydroxy-N6-threonylcarbamoyladenosine (ht6A), N6-methyl-N6-threonylcarbamoyladenosine (m6t6A), 2-methylthio-N6-threonylcarbamoyladenosine (ms2t6A) and 2-methylthio-cyclic N6-threonylcarbamoyladenosine (ms2ct6A). The tRNAs carrying t6A or one of its hypermodified derivatives are dubbed as the t6A family. The t6A family modifications pre-organize the anticodon loop in a conformation that enhances binding to the cognate mRNA codons, thereby promoting translational fidelity. The dysfunctional installation of modifications in the tRNA t6A family leads to translation errors, compromises proteostasis and cell viability, interferes with the growth and development of higher eukaryotes and is implicated in several human diseases, such as neurological disorders, mitochondrial encephalomyopathies, type 2 diabetes and cancers. In addition, loss-of-function mutations in KEOPS complex–the tRNA t6A-modifying enzyme–are associated with shortened telomeres, defects in DNA damage response and transcriptional dysregulation in eukaryotes. The chemical structures, the molecular functions, the known cellular roles and the biosynthetic pathways of the t6A tRNA family are described by integrating and linking biochemical and structural data on these modifications to their biological functions.

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tRNA t6A修饰和超修饰的生物学-生物发生和疾病相关性。
转移rna (tRNA)的结构和功能高度依赖于转录后的化学修饰,这些修饰通过酶促反应将不同的化学基团附着在选定tRNA位置的各种核碱基原子上。在生命的所有三个领域中,化学修饰的最大多样性集中在tRNA反密码子环的第34和37位。n6 -苏酰基氨基腺苷(t6A)是一种重要的普遍修饰,发生在trna的第37位,解码以腺嘌呤开头的密码子。在来自特定生物体的trna子集中,t6A被转化为各种超修饰形式,包括环n6 -苏酰基氨酰基腺苷(ct6A)、羟基- n6 -苏酰基氨酰基腺苷(ht6A)、n6 -甲基- n6 -苏酰基氨酰基腺苷(m6t6A)、2-甲基硫代- n6 -苏酰基氨酰基腺苷(ms2t6A)和2-甲基硫代环n6 -苏酰基氨酰基腺苷(ms2ct6A)。携带t6A或其超修饰衍生物的trna被称为t6A家族。t6A家族修饰将反密码子环预先组织成一种增强与同源mRNA密码子结合的构象,从而提高翻译保真度。tRNA t6A家族中修饰的功能失调安装导致翻译错误,损害蛋白质平衡和细胞活力,干扰高等真核生物的生长和发育,并与几种人类疾病有关,如神经系统疾病、线粒体脑肌病、2型糖尿病和癌症。此外,KEOPS复合物(tRNA t6a修饰酶)的功能缺失突变与真核生物端粒缩短、DNA损伤反应缺陷和转录失调有关。t6A tRNA家族的化学结构、分子功能、已知的细胞作用和生物合成途径通过整合和连接这些修饰及其生物学功能的生化和结构数据来描述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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