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NSUN6 is a human RNA methyltransferase that catalyzes formation of m(5)C72 in specific tRNAs
Many cellular RNAs require modification of specific residues for their biogenesis, structure, and function. 5-methylcytosine (m(5)C) is a common chemical modification in DNA and RNA but in contrast to the DNA modifying enzymes, only little is known about the methyltransferases that establish m(5)C m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536315/ https://www.ncbi.nlm.nih.gov/pubmed/26160102 http://dx.doi.org/10.1261/rna.051524.115 |
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author | Haag, Sara Warda, Ahmed S. Kretschmer, Jens Günnigmann, Manuel A. Höbartner, Claudia Bohnsack, Markus T. |
author_facet | Haag, Sara Warda, Ahmed S. Kretschmer, Jens Günnigmann, Manuel A. Höbartner, Claudia Bohnsack, Markus T. |
author_sort | Haag, Sara |
collection | PubMed |
description | Many cellular RNAs require modification of specific residues for their biogenesis, structure, and function. 5-methylcytosine (m(5)C) is a common chemical modification in DNA and RNA but in contrast to the DNA modifying enzymes, only little is known about the methyltransferases that establish m(5)C modifications in RNA. The putative RNA methyltransferase NSUN6 belongs to the family of Nol1/Nop2/SUN domain (NSUN) proteins, but so far its cellular function has remained unknown. To reveal the target spectrum of human NSUN6, we applied UV crosslinking and analysis of cDNA (CRAC) as well as chemical crosslinking with 5-azacytidine. We found that human NSUN6 is associated with tRNAs and acts as a tRNA methyltransferase. Furthermore, we uncovered tRNA(Cys) and tRNA(Thr) as RNA substrates of NSUN6 and identified the cytosine C72 at the 3′ end of the tRNA acceptor stem as the target nucleoside. Interestingly, target recognition in vitro depends on the presence of the 3′-CCA tail. Together with the finding that NSUN6 localizes to the cytoplasm and largely colocalizes with marker proteins for the Golgi apparatus and pericentriolar matrix, our data suggest that NSUN6 modifies tRNAs in a late step in their biogenesis. |
format | Online Article Text |
id | pubmed-4536315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45363152015-09-01 NSUN6 is a human RNA methyltransferase that catalyzes formation of m(5)C72 in specific tRNAs Haag, Sara Warda, Ahmed S. Kretschmer, Jens Günnigmann, Manuel A. Höbartner, Claudia Bohnsack, Markus T. RNA Reports Many cellular RNAs require modification of specific residues for their biogenesis, structure, and function. 5-methylcytosine (m(5)C) is a common chemical modification in DNA and RNA but in contrast to the DNA modifying enzymes, only little is known about the methyltransferases that establish m(5)C modifications in RNA. The putative RNA methyltransferase NSUN6 belongs to the family of Nol1/Nop2/SUN domain (NSUN) proteins, but so far its cellular function has remained unknown. To reveal the target spectrum of human NSUN6, we applied UV crosslinking and analysis of cDNA (CRAC) as well as chemical crosslinking with 5-azacytidine. We found that human NSUN6 is associated with tRNAs and acts as a tRNA methyltransferase. Furthermore, we uncovered tRNA(Cys) and tRNA(Thr) as RNA substrates of NSUN6 and identified the cytosine C72 at the 3′ end of the tRNA acceptor stem as the target nucleoside. Interestingly, target recognition in vitro depends on the presence of the 3′-CCA tail. Together with the finding that NSUN6 localizes to the cytoplasm and largely colocalizes with marker proteins for the Golgi apparatus and pericentriolar matrix, our data suggest that NSUN6 modifies tRNAs in a late step in their biogenesis. Cold Spring Harbor Laboratory Press 2015-09 /pmc/articles/PMC4536315/ /pubmed/26160102 http://dx.doi.org/10.1261/rna.051524.115 Text en © 2015 Haag et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article, published in RNA, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Reports Haag, Sara Warda, Ahmed S. Kretschmer, Jens Günnigmann, Manuel A. Höbartner, Claudia Bohnsack, Markus T. NSUN6 is a human RNA methyltransferase that catalyzes formation of m(5)C72 in specific tRNAs |
title | NSUN6 is a human RNA methyltransferase that catalyzes formation of m(5)C72 in specific tRNAs |
title_full | NSUN6 is a human RNA methyltransferase that catalyzes formation of m(5)C72 in specific tRNAs |
title_fullStr | NSUN6 is a human RNA methyltransferase that catalyzes formation of m(5)C72 in specific tRNAs |
title_full_unstemmed | NSUN6 is a human RNA methyltransferase that catalyzes formation of m(5)C72 in specific tRNAs |
title_short | NSUN6 is a human RNA methyltransferase that catalyzes formation of m(5)C72 in specific tRNAs |
title_sort | nsun6 is a human rna methyltransferase that catalyzes formation of m(5)c72 in specific trnas |
topic | Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536315/ https://www.ncbi.nlm.nih.gov/pubmed/26160102 http://dx.doi.org/10.1261/rna.051524.115 |
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