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Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification

Ribosome heterogeneity is of increasing biological significance and several examples have been described for multicellular and single cells organisms. In here we show for the first time a variation in ribose methylation within the 18S rRNA of Saccharomyces cerevisiae. Using RNA-cleaving DNAzymes, we...

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Autores principales: Buchhaupt, Markus, Sharma, Sunny, Kellner, Stefanie, Oswald, Stefanie, Paetzold, Melanie, Peifer, Christian, Watzinger, Peter, Schrader, Jens, Helm, Mark, Entian, Karl-Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938493/
https://www.ncbi.nlm.nih.gov/pubmed/24586927
http://dx.doi.org/10.1371/journal.pone.0089640
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author Buchhaupt, Markus
Sharma, Sunny
Kellner, Stefanie
Oswald, Stefanie
Paetzold, Melanie
Peifer, Christian
Watzinger, Peter
Schrader, Jens
Helm, Mark
Entian, Karl-Dieter
author_facet Buchhaupt, Markus
Sharma, Sunny
Kellner, Stefanie
Oswald, Stefanie
Paetzold, Melanie
Peifer, Christian
Watzinger, Peter
Schrader, Jens
Helm, Mark
Entian, Karl-Dieter
author_sort Buchhaupt, Markus
collection PubMed
description Ribosome heterogeneity is of increasing biological significance and several examples have been described for multicellular and single cells organisms. In here we show for the first time a variation in ribose methylation within the 18S rRNA of Saccharomyces cerevisiae. Using RNA-cleaving DNAzymes, we could specifically demonstrate that a significant amount of S. cerevisiae ribosomes are not methylated at 2′-O-ribose of A100 residue in the 18S rRNA. Furthermore, using LC-UV-MS/MS of a respective 18S rRNA fragment, we could not only corroborate the partial methylation at A100, but could also quantify the methylated versus non-methylated A100 residue. Here, we exhibit that only 68% of A100 in the 18S rRNA of S.cerevisiae are methylated at 2′-O ribose sugar. Polysomes also contain a similar heterogeneity for methylated Am100, which shows that 40S ribosome subunits with and without Am100 participate in translation. Introduction of a multicopy plasmid containing the corresponding methylation guide snoRNA gene SNR51 led to an increased A100 methylation, suggesting the cellular snR51 level to limit the extent of this modification. Partial rRNA modification demonstrates a new level of ribosome heterogeneity in eukaryotic cells that might have substantial impact on regulation and fine-tuning of the translation process.
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spelling pubmed-39384932014-03-04 Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification Buchhaupt, Markus Sharma, Sunny Kellner, Stefanie Oswald, Stefanie Paetzold, Melanie Peifer, Christian Watzinger, Peter Schrader, Jens Helm, Mark Entian, Karl-Dieter PLoS One Research Article Ribosome heterogeneity is of increasing biological significance and several examples have been described for multicellular and single cells organisms. In here we show for the first time a variation in ribose methylation within the 18S rRNA of Saccharomyces cerevisiae. Using RNA-cleaving DNAzymes, we could specifically demonstrate that a significant amount of S. cerevisiae ribosomes are not methylated at 2′-O-ribose of A100 residue in the 18S rRNA. Furthermore, using LC-UV-MS/MS of a respective 18S rRNA fragment, we could not only corroborate the partial methylation at A100, but could also quantify the methylated versus non-methylated A100 residue. Here, we exhibit that only 68% of A100 in the 18S rRNA of S.cerevisiae are methylated at 2′-O ribose sugar. Polysomes also contain a similar heterogeneity for methylated Am100, which shows that 40S ribosome subunits with and without Am100 participate in translation. Introduction of a multicopy plasmid containing the corresponding methylation guide snoRNA gene SNR51 led to an increased A100 methylation, suggesting the cellular snR51 level to limit the extent of this modification. Partial rRNA modification demonstrates a new level of ribosome heterogeneity in eukaryotic cells that might have substantial impact on regulation and fine-tuning of the translation process. Public Library of Science 2014-02-28 /pmc/articles/PMC3938493/ /pubmed/24586927 http://dx.doi.org/10.1371/journal.pone.0089640 Text en © 2014 Buchhaupt et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Buchhaupt, Markus
Sharma, Sunny
Kellner, Stefanie
Oswald, Stefanie
Paetzold, Melanie
Peifer, Christian
Watzinger, Peter
Schrader, Jens
Helm, Mark
Entian, Karl-Dieter
Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification
title Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification
title_full Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification
title_fullStr Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification
title_full_unstemmed Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification
title_short Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification
title_sort partial methylation at am100 in 18s rrna of baker's yeast reveals ribosome heterogeneity on the level of eukaryotic rrna modification
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938493/
https://www.ncbi.nlm.nih.gov/pubmed/24586927
http://dx.doi.org/10.1371/journal.pone.0089640
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