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Selective terminal methylation of a tRNA wobble base
Active tRNAs are extensively post-transcriptionally modified, particularly at the wobble position 34 and the position 37 on the 3′-side of the anticodon. The 5-carboxy-methoxy modification of U34 (cmo(5)U34) is present in Gram-negative tRNAs for six amino acids (Ala, Ser, Pro, Thr, Leu and Val), fou...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909439/ https://www.ncbi.nlm.nih.gov/pubmed/29361055 http://dx.doi.org/10.1093/nar/gky013 |
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author | Masuda, Isao Takase, Ryuichi Matsubara, Ryuma Paulines, Mellie June Gamper, Howard Limbach, Patrick A Hou, Ya-Ming |
author_facet | Masuda, Isao Takase, Ryuichi Matsubara, Ryuma Paulines, Mellie June Gamper, Howard Limbach, Patrick A Hou, Ya-Ming |
author_sort | Masuda, Isao |
collection | PubMed |
description | Active tRNAs are extensively post-transcriptionally modified, particularly at the wobble position 34 and the position 37 on the 3′-side of the anticodon. The 5-carboxy-methoxy modification of U34 (cmo(5)U34) is present in Gram-negative tRNAs for six amino acids (Ala, Ser, Pro, Thr, Leu and Val), four of which (Ala, Ser, Pro and Thr) have a terminal methyl group to form 5-methoxy-carbonyl-methoxy-uridine (mcmo(5)U34) for higher reading-frame accuracy. The molecular basis for the selective terminal methylation is not understood. Many cmo(5)U34-tRNAs are essential for growth and cannot be substituted for mutational analysis. We show here that, with a novel genetic approach, we have created and isolated mutants of Escherichia coli tRNA(Pro) and tRNA(Val) for analysis of the selective terminal methylation. We show that substitution of G35 in the anticodon of tRNA(Pro) inactivates the terminal methylation, whereas introduction of G35 to tRNA(Val) confers it, indicating that G35 is a major determinant for the selectivity. We also show that, in tRNA(Pro), the terminal methylation at U34 is dependent on the primary m(1)G methylation at position 37 but not vice versa, indicating a hierarchical ranking of modifications between positions 34 and 37. We suggest that this hierarchy provides a mechanism to ensure top performance of a tRNA inside of cells. |
format | Online Article Text |
id | pubmed-5909439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59094392018-04-24 Selective terminal methylation of a tRNA wobble base Masuda, Isao Takase, Ryuichi Matsubara, Ryuma Paulines, Mellie June Gamper, Howard Limbach, Patrick A Hou, Ya-Ming Nucleic Acids Res Methods Online Active tRNAs are extensively post-transcriptionally modified, particularly at the wobble position 34 and the position 37 on the 3′-side of the anticodon. The 5-carboxy-methoxy modification of U34 (cmo(5)U34) is present in Gram-negative tRNAs for six amino acids (Ala, Ser, Pro, Thr, Leu and Val), four of which (Ala, Ser, Pro and Thr) have a terminal methyl group to form 5-methoxy-carbonyl-methoxy-uridine (mcmo(5)U34) for higher reading-frame accuracy. The molecular basis for the selective terminal methylation is not understood. Many cmo(5)U34-tRNAs are essential for growth and cannot be substituted for mutational analysis. We show here that, with a novel genetic approach, we have created and isolated mutants of Escherichia coli tRNA(Pro) and tRNA(Val) for analysis of the selective terminal methylation. We show that substitution of G35 in the anticodon of tRNA(Pro) inactivates the terminal methylation, whereas introduction of G35 to tRNA(Val) confers it, indicating that G35 is a major determinant for the selectivity. We also show that, in tRNA(Pro), the terminal methylation at U34 is dependent on the primary m(1)G methylation at position 37 but not vice versa, indicating a hierarchical ranking of modifications between positions 34 and 37. We suggest that this hierarchy provides a mechanism to ensure top performance of a tRNA inside of cells. Oxford University Press 2018-04-20 2018-01-18 /pmc/articles/PMC5909439/ /pubmed/29361055 http://dx.doi.org/10.1093/nar/gky013 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Masuda, Isao Takase, Ryuichi Matsubara, Ryuma Paulines, Mellie June Gamper, Howard Limbach, Patrick A Hou, Ya-Ming Selective terminal methylation of a tRNA wobble base |
title | Selective terminal methylation of a tRNA wobble base |
title_full | Selective terminal methylation of a tRNA wobble base |
title_fullStr | Selective terminal methylation of a tRNA wobble base |
title_full_unstemmed | Selective terminal methylation of a tRNA wobble base |
title_short | Selective terminal methylation of a tRNA wobble base |
title_sort | selective terminal methylation of a trna wobble base |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909439/ https://www.ncbi.nlm.nih.gov/pubmed/29361055 http://dx.doi.org/10.1093/nar/gky013 |
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