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Expression of distinct maternal and somatic 5.8S, 18S, and 28S rRNA types during zebrafish development

There is mounting evidence that the ribosome is not a static translation machinery, but a cell-specific, adaptive system. Ribosomal variations have mostly been studied at the protein level, even though the essential transcriptional functions are primarily performed by rRNAs. At the RNA level, oocyte...

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Autores principales: Locati, Mauro D., Pagano, Johanna F.B., Girard, Geneviève, Ensink, Wim A., van Olst, Marina, van Leeuwen, Selina, Nehrdich, Ulrike, Spaink, Herman P., Rauwerda, Han, Jonker, Martijs J., Dekker, Rob J., Breit, Timo M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513064/
https://www.ncbi.nlm.nih.gov/pubmed/28500251
http://dx.doi.org/10.1261/rna.061515.117
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author Locati, Mauro D.
Pagano, Johanna F.B.
Girard, Geneviève
Ensink, Wim A.
van Olst, Marina
van Leeuwen, Selina
Nehrdich, Ulrike
Spaink, Herman P.
Rauwerda, Han
Jonker, Martijs J.
Dekker, Rob J.
Breit, Timo M.
author_facet Locati, Mauro D.
Pagano, Johanna F.B.
Girard, Geneviève
Ensink, Wim A.
van Olst, Marina
van Leeuwen, Selina
Nehrdich, Ulrike
Spaink, Herman P.
Rauwerda, Han
Jonker, Martijs J.
Dekker, Rob J.
Breit, Timo M.
author_sort Locati, Mauro D.
collection PubMed
description There is mounting evidence that the ribosome is not a static translation machinery, but a cell-specific, adaptive system. Ribosomal variations have mostly been studied at the protein level, even though the essential transcriptional functions are primarily performed by rRNAs. At the RNA level, oocyte-specific 5S rRNAs are long known for Xenopus. Recently, we described for zebrafish a similar system in which the sole maternal-type 5S rRNA present in eggs is replaced completely during embryonic development by a somatic-type. Here, we report the discovery of an analogous system for the 45S rDNA elements: 5.8S, 18S, and 28S. The maternal-type 5.8S, 18S, and 28S rRNA sequences differ substantially from those of the somatic-type, plus the maternal-type rRNAs are also replaced by the somatic-type rRNAs during embryogenesis. We discuss the structural and functional implications of the observed sequence differences with respect to the translational functions of the 5.8S, 18S, and 28S rRNA elements. Finally, in silico evidence suggests that expansion segments (ES) in 18S rRNA, previously implicated in ribosome–mRNA interaction, may have a preference for interacting with specific mRNA genes. Taken together, our findings indicate that two distinct types of ribosomes exist in zebrafish during development, each likely conducting the translation machinery in a unique way.
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spelling pubmed-55130642017-08-02 Expression of distinct maternal and somatic 5.8S, 18S, and 28S rRNA types during zebrafish development Locati, Mauro D. Pagano, Johanna F.B. Girard, Geneviève Ensink, Wim A. van Olst, Marina van Leeuwen, Selina Nehrdich, Ulrike Spaink, Herman P. Rauwerda, Han Jonker, Martijs J. Dekker, Rob J. Breit, Timo M. RNA Report There is mounting evidence that the ribosome is not a static translation machinery, but a cell-specific, adaptive system. Ribosomal variations have mostly been studied at the protein level, even though the essential transcriptional functions are primarily performed by rRNAs. At the RNA level, oocyte-specific 5S rRNAs are long known for Xenopus. Recently, we described for zebrafish a similar system in which the sole maternal-type 5S rRNA present in eggs is replaced completely during embryonic development by a somatic-type. Here, we report the discovery of an analogous system for the 45S rDNA elements: 5.8S, 18S, and 28S. The maternal-type 5.8S, 18S, and 28S rRNA sequences differ substantially from those of the somatic-type, plus the maternal-type rRNAs are also replaced by the somatic-type rRNAs during embryogenesis. We discuss the structural and functional implications of the observed sequence differences with respect to the translational functions of the 5.8S, 18S, and 28S rRNA elements. Finally, in silico evidence suggests that expansion segments (ES) in 18S rRNA, previously implicated in ribosome–mRNA interaction, may have a preference for interacting with specific mRNA genes. Taken together, our findings indicate that two distinct types of ribosomes exist in zebrafish during development, each likely conducting the translation machinery in a unique way. Cold Spring Harbor Laboratory Press 2017-08 /pmc/articles/PMC5513064/ /pubmed/28500251 http://dx.doi.org/10.1261/rna.061515.117 Text en © 2017 Locati et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by/4.0/ This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Report
Locati, Mauro D.
Pagano, Johanna F.B.
Girard, Geneviève
Ensink, Wim A.
van Olst, Marina
van Leeuwen, Selina
Nehrdich, Ulrike
Spaink, Herman P.
Rauwerda, Han
Jonker, Martijs J.
Dekker, Rob J.
Breit, Timo M.
Expression of distinct maternal and somatic 5.8S, 18S, and 28S rRNA types during zebrafish development
title Expression of distinct maternal and somatic 5.8S, 18S, and 28S rRNA types during zebrafish development
title_full Expression of distinct maternal and somatic 5.8S, 18S, and 28S rRNA types during zebrafish development
title_fullStr Expression of distinct maternal and somatic 5.8S, 18S, and 28S rRNA types during zebrafish development
title_full_unstemmed Expression of distinct maternal and somatic 5.8S, 18S, and 28S rRNA types during zebrafish development
title_short Expression of distinct maternal and somatic 5.8S, 18S, and 28S rRNA types during zebrafish development
title_sort expression of distinct maternal and somatic 5.8s, 18s, and 28s rrna types during zebrafish development
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513064/
https://www.ncbi.nlm.nih.gov/pubmed/28500251
http://dx.doi.org/10.1261/rna.061515.117
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