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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
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.
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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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