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Methylated Nucleosides in TRNA and TRNA Methyltransferases

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Journal Front Genet
Date 2014 Jun 7
PMID 24904644
Citations 109
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Abstract

To date, more than 90 modified nucleosides have been found in tRNA and the biosynthetic pathways of the majority of tRNA modifications include a methylation step(s). Recent studies of the biosynthetic pathways have demonstrated that the availability of methyl group donors for the methylation in tRNA is important for correct and efficient protein synthesis. In this review, I focus on the methylated nucleosides and tRNA methyltransferases. The primary functions of tRNA methylations are linked to the different steps of protein synthesis, such as the stabilization of tRNA structure, reinforcement of the codon-anticodon interaction, regulation of wobble base pairing, and prevention of frameshift errors. However, beyond these basic functions, recent studies have demonstrated that tRNA methylations are also involved in the RNA quality control system and regulation of tRNA localization in the cell. In a thermophilic eubacterium, tRNA modifications and the modification enzymes form a network that responses to temperature changes. Furthermore, several modifications are involved in genetic diseases, infections, and the immune response. Moreover, structural, biochemical, and bioinformatics studies of tRNA methyltransferases have been clarifying the details of tRNA methyltransferases and have enabled these enzymes to be classified. In the final section, the evolution of modification enzymes is discussed.

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References
1.
de Crecy-Lagard V, Brochier-Armanet C, Urbonavicius J, Fernandez B, Phillips G, Lyons B . Biosynthesis of wyosine derivatives in tRNA: an ancient and highly diverse pathway in Archaea. Mol Biol Evol. 2010; 27(9):2062-77. PMC: 4481705. DOI: 10.1093/molbev/msq096. View

2.
Towns W, Begley T . Transfer RNA methytransferases and their corresponding modifications in budding yeast and humans: activities, predications, and potential roles in human health. DNA Cell Biol. 2011; 31(4):434-54. PMC: 3322404. DOI: 10.1089/dna.2011.1437. View

3.
Sakurai M, Ohtsuki T, Suzuki T, Watanabe K . Unusual usage of wobble modifications in mitochondrial tRNAs of the nematode Ascaris suum. FEBS Lett. 2005; 579(13):2767-72. DOI: 10.1016/j.febslet.2005.04.009. View

4.
Choudhury S, Asefa B, Kauler P, Chow T . Synergistic effect of TRM2/RNC1 and EXO1 in DNA double-strand break repair in Saccharomyces cerevisiae. Mol Cell Biochem. 2007; 304(1-2):127-34. DOI: 10.1007/s11010-007-9493-7. View

5.
Alian A, Lee T, Griner S, Stroud R, Finer-Moore J . Structure of a TrmA-RNA complex: A consensus RNA fold contributes to substrate selectivity and catalysis in m5U methyltransferases. Proc Natl Acad Sci U S A. 2008; 105(19):6876-81. PMC: 2383949. DOI: 10.1073/pnas.0802247105. View