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Transfer RNA Methyltransferases from Thermoplasma acidophilum, a Thermoacidophilic Archaeon
We investigated tRNA methyltransferase activities in crude cell extracts from the thermoacidophilic archaeon Thermoplasma acidophilum. We analyzed the modified nucleosides in native initiator and elongator tRNA(Met), predicted the candidate genes for the tRNA methyltransferases on the basis of the t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307237/ https://www.ncbi.nlm.nih.gov/pubmed/25546389 http://dx.doi.org/10.3390/ijms16010091 |
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author | Kawamura, Takuya Anraku, Ryou Hasegawa, Takahiro Tomikawa, Chie Hori, Hiroyuki |
author_facet | Kawamura, Takuya Anraku, Ryou Hasegawa, Takahiro Tomikawa, Chie Hori, Hiroyuki |
author_sort | Kawamura, Takuya |
collection | PubMed |
description | We investigated tRNA methyltransferase activities in crude cell extracts from the thermoacidophilic archaeon Thermoplasma acidophilum. We analyzed the modified nucleosides in native initiator and elongator tRNA(Met), predicted the candidate genes for the tRNA methyltransferases on the basis of the tRNA(Met) and tRNA(Leu) sequences, and characterized Trm5, Trm1 and Trm56 by purifying recombinant proteins. We found that the Ta0997, Ta0931, and Ta0836 genes of T. acidophilum encode Trm1, Trm56 and Trm5, respectively. Initiator tRNA(Met) from T. acidophilum strain HO-62 contained G(+), m(1)I, and m(2)(2)G, which were not reported previously in this tRNA, and the m(2)G26 and m(2)(2)G26 were formed by Trm1. In the case of elongator tRNA(Met), our analysis showed that the previously unidentified G modification at position 26 was a mixture of m(2)G and m(2)(2)G, and that they were also generated by Trm1. Furthermore, purified Trm1 and Trm56 could methylate the precursor of elongator tRNA(Met), which has an intron at the canonical position. However, the speed of methyl-transfer by Trm56 to the precursor RNA was considerably slower than that to the mature transcript, which suggests that Trm56 acts mainly on the transcript after the intron has been removed. Moreover, cellular arrangements of the tRNA methyltransferases in T. acidophilum are discussed. |
format | Online Article Text |
id | pubmed-4307237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43072372015-02-02 Transfer RNA Methyltransferases from Thermoplasma acidophilum, a Thermoacidophilic Archaeon Kawamura, Takuya Anraku, Ryou Hasegawa, Takahiro Tomikawa, Chie Hori, Hiroyuki Int J Mol Sci Article We investigated tRNA methyltransferase activities in crude cell extracts from the thermoacidophilic archaeon Thermoplasma acidophilum. We analyzed the modified nucleosides in native initiator and elongator tRNA(Met), predicted the candidate genes for the tRNA methyltransferases on the basis of the tRNA(Met) and tRNA(Leu) sequences, and characterized Trm5, Trm1 and Trm56 by purifying recombinant proteins. We found that the Ta0997, Ta0931, and Ta0836 genes of T. acidophilum encode Trm1, Trm56 and Trm5, respectively. Initiator tRNA(Met) from T. acidophilum strain HO-62 contained G(+), m(1)I, and m(2)(2)G, which were not reported previously in this tRNA, and the m(2)G26 and m(2)(2)G26 were formed by Trm1. In the case of elongator tRNA(Met), our analysis showed that the previously unidentified G modification at position 26 was a mixture of m(2)G and m(2)(2)G, and that they were also generated by Trm1. Furthermore, purified Trm1 and Trm56 could methylate the precursor of elongator tRNA(Met), which has an intron at the canonical position. However, the speed of methyl-transfer by Trm56 to the precursor RNA was considerably slower than that to the mature transcript, which suggests that Trm56 acts mainly on the transcript after the intron has been removed. Moreover, cellular arrangements of the tRNA methyltransferases in T. acidophilum are discussed. MDPI 2014-12-23 /pmc/articles/PMC4307237/ /pubmed/25546389 http://dx.doi.org/10.3390/ijms16010091 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kawamura, Takuya Anraku, Ryou Hasegawa, Takahiro Tomikawa, Chie Hori, Hiroyuki Transfer RNA Methyltransferases from Thermoplasma acidophilum, a Thermoacidophilic Archaeon |
title | Transfer RNA Methyltransferases from Thermoplasma acidophilum, a Thermoacidophilic Archaeon |
title_full | Transfer RNA Methyltransferases from Thermoplasma acidophilum, a Thermoacidophilic Archaeon |
title_fullStr | Transfer RNA Methyltransferases from Thermoplasma acidophilum, a Thermoacidophilic Archaeon |
title_full_unstemmed | Transfer RNA Methyltransferases from Thermoplasma acidophilum, a Thermoacidophilic Archaeon |
title_short | Transfer RNA Methyltransferases from Thermoplasma acidophilum, a Thermoacidophilic Archaeon |
title_sort | transfer rna methyltransferases from thermoplasma acidophilum, a thermoacidophilic archaeon |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307237/ https://www.ncbi.nlm.nih.gov/pubmed/25546389 http://dx.doi.org/10.3390/ijms16010091 |
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