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The ribosomal RNA m(5)C methyltransferase NSUN-1 modulates healthspan and oogenesis in Caenorhabditis elegans
Our knowledge about the repertoire of ribosomal RNA modifications and the enzymes responsible for installing them is constantly expanding. Previously, we reported that NSUN-5 is responsible for depositing m(5)C at position C2381 on the 26S rRNA in Caenorhabditis elegans. Here, we show that NSUN-1 is...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746234/ https://www.ncbi.nlm.nih.gov/pubmed/33289480 http://dx.doi.org/10.7554/eLife.56205 |
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author | Heissenberger, Clemens Rollins, Jarod A Krammer, Teresa L Nagelreiter, Fabian Stocker, Isabella Wacheul, Ludivine Shpylovyi, Anton Tav, Koray Snow, Santina Grillari, Johannes Rogers, Aric N Lafontaine, Denis L J Schosserer, Markus |
author_facet | Heissenberger, Clemens Rollins, Jarod A Krammer, Teresa L Nagelreiter, Fabian Stocker, Isabella Wacheul, Ludivine Shpylovyi, Anton Tav, Koray Snow, Santina Grillari, Johannes Rogers, Aric N Lafontaine, Denis L J Schosserer, Markus |
author_sort | Heissenberger, Clemens |
collection | PubMed |
description | Our knowledge about the repertoire of ribosomal RNA modifications and the enzymes responsible for installing them is constantly expanding. Previously, we reported that NSUN-5 is responsible for depositing m(5)C at position C2381 on the 26S rRNA in Caenorhabditis elegans. Here, we show that NSUN-1 is writing the second known 26S rRNA m(5)C at position C2982. Depletion of nsun-1 or nsun-5 improved thermotolerance and slightly increased locomotion at midlife, however, only soma-specific knockdown of nsun-1 extended lifespan. Moreover, soma-specific knockdown of nsun-1 reduced body size and impaired fecundity, suggesting non-cell-autonomous effects. While ribosome biogenesis and global protein synthesis were unaffected by nsun-1 depletion, translation of specific mRNAs was remodeled leading to reduced production of collagens, loss of structural integrity of the cuticle, and impaired barrier function. We conclude that loss of a single enzyme required for rRNA methylation has profound and highly specific effects on organismal development and physiology. |
format | Online Article Text |
id | pubmed-7746234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-77462342020-12-21 The ribosomal RNA m(5)C methyltransferase NSUN-1 modulates healthspan and oogenesis in Caenorhabditis elegans Heissenberger, Clemens Rollins, Jarod A Krammer, Teresa L Nagelreiter, Fabian Stocker, Isabella Wacheul, Ludivine Shpylovyi, Anton Tav, Koray Snow, Santina Grillari, Johannes Rogers, Aric N Lafontaine, Denis L J Schosserer, Markus eLife Cell Biology Our knowledge about the repertoire of ribosomal RNA modifications and the enzymes responsible for installing them is constantly expanding. Previously, we reported that NSUN-5 is responsible for depositing m(5)C at position C2381 on the 26S rRNA in Caenorhabditis elegans. Here, we show that NSUN-1 is writing the second known 26S rRNA m(5)C at position C2982. Depletion of nsun-1 or nsun-5 improved thermotolerance and slightly increased locomotion at midlife, however, only soma-specific knockdown of nsun-1 extended lifespan. Moreover, soma-specific knockdown of nsun-1 reduced body size and impaired fecundity, suggesting non-cell-autonomous effects. While ribosome biogenesis and global protein synthesis were unaffected by nsun-1 depletion, translation of specific mRNAs was remodeled leading to reduced production of collagens, loss of structural integrity of the cuticle, and impaired barrier function. We conclude that loss of a single enzyme required for rRNA methylation has profound and highly specific effects on organismal development and physiology. eLife Sciences Publications, Ltd 2020-12-08 /pmc/articles/PMC7746234/ /pubmed/33289480 http://dx.doi.org/10.7554/eLife.56205 Text en © 2020, Heissenberger et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Heissenberger, Clemens Rollins, Jarod A Krammer, Teresa L Nagelreiter, Fabian Stocker, Isabella Wacheul, Ludivine Shpylovyi, Anton Tav, Koray Snow, Santina Grillari, Johannes Rogers, Aric N Lafontaine, Denis L J Schosserer, Markus The ribosomal RNA m(5)C methyltransferase NSUN-1 modulates healthspan and oogenesis in Caenorhabditis elegans |
title | The ribosomal RNA m(5)C methyltransferase NSUN-1 modulates healthspan and oogenesis in Caenorhabditis elegans |
title_full | The ribosomal RNA m(5)C methyltransferase NSUN-1 modulates healthspan and oogenesis in Caenorhabditis elegans |
title_fullStr | The ribosomal RNA m(5)C methyltransferase NSUN-1 modulates healthspan and oogenesis in Caenorhabditis elegans |
title_full_unstemmed | The ribosomal RNA m(5)C methyltransferase NSUN-1 modulates healthspan and oogenesis in Caenorhabditis elegans |
title_short | The ribosomal RNA m(5)C methyltransferase NSUN-1 modulates healthspan and oogenesis in Caenorhabditis elegans |
title_sort | ribosomal rna m(5)c methyltransferase nsun-1 modulates healthspan and oogenesis in caenorhabditis elegans |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746234/ https://www.ncbi.nlm.nih.gov/pubmed/33289480 http://dx.doi.org/10.7554/eLife.56205 |
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