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rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins

The structural constituents of the large eukaryotic ribosomal subunit are 3 ribosomal RNAs, namely the 25S, 5.8S and 5S rRNA and about 46 ribosomal proteins (r-proteins). They assemble and mature in a highly dynamic process that involves more than 150 proteins and 70 small RNAs. Ribosome biogenesis...

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Autores principales: Pöll, Gisela, Braun, Tobias, Jakovljevic, Jelena, Neueder, Andreas, Jakob, Steffen, Woolford, John L., Tschochner, Herbert, Milkereit, Philipp
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788216/
https://www.ncbi.nlm.nih.gov/pubmed/20011513
http://dx.doi.org/10.1371/journal.pone.0008249
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author Pöll, Gisela
Braun, Tobias
Jakovljevic, Jelena
Neueder, Andreas
Jakob, Steffen
Woolford, John L.
Tschochner, Herbert
Milkereit, Philipp
author_facet Pöll, Gisela
Braun, Tobias
Jakovljevic, Jelena
Neueder, Andreas
Jakob, Steffen
Woolford, John L.
Tschochner, Herbert
Milkereit, Philipp
author_sort Pöll, Gisela
collection PubMed
description The structural constituents of the large eukaryotic ribosomal subunit are 3 ribosomal RNAs, namely the 25S, 5.8S and 5S rRNA and about 46 ribosomal proteins (r-proteins). They assemble and mature in a highly dynamic process that involves more than 150 proteins and 70 small RNAs. Ribosome biogenesis starts in the nucleolus, continues in the nucleoplasm and is completed after nucleo-cytoplasmic translocation of the subunits in the cytoplasm. In this work we created 26 yeast strains, each of which conditionally expresses one of the large ribosomal subunit (LSU) proteins. In vivo depletion of the analysed LSU r-proteins was lethal and led to destabilisation and degradation of the LSU and/or its precursors. Detailed steady state and metabolic pulse labelling analyses of rRNA precursors in these mutant strains showed that LSU r-proteins can be grouped according to their requirement for efficient progression of different steps of large ribosomal subunit maturation. Comparative analyses of the observed phenotypes and the nature of r-protein – rRNA interactions as predicted by current atomic LSU structure models led us to discuss working hypotheses on i) how individual r-proteins control the productive processing of the major 5′ end of 5.8S rRNA precursors by exonucleases Rat1p and Xrn1p, and ii) the nature of structural characteristics of nascent LSUs that are required for cytoplasmic accumulation of nascent subunits but are nonessential for most of the nuclear LSU pre-rRNA processing events.
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spelling pubmed-27882162009-12-15 rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins Pöll, Gisela Braun, Tobias Jakovljevic, Jelena Neueder, Andreas Jakob, Steffen Woolford, John L. Tschochner, Herbert Milkereit, Philipp PLoS One Research Article The structural constituents of the large eukaryotic ribosomal subunit are 3 ribosomal RNAs, namely the 25S, 5.8S and 5S rRNA and about 46 ribosomal proteins (r-proteins). They assemble and mature in a highly dynamic process that involves more than 150 proteins and 70 small RNAs. Ribosome biogenesis starts in the nucleolus, continues in the nucleoplasm and is completed after nucleo-cytoplasmic translocation of the subunits in the cytoplasm. In this work we created 26 yeast strains, each of which conditionally expresses one of the large ribosomal subunit (LSU) proteins. In vivo depletion of the analysed LSU r-proteins was lethal and led to destabilisation and degradation of the LSU and/or its precursors. Detailed steady state and metabolic pulse labelling analyses of rRNA precursors in these mutant strains showed that LSU r-proteins can be grouped according to their requirement for efficient progression of different steps of large ribosomal subunit maturation. Comparative analyses of the observed phenotypes and the nature of r-protein – rRNA interactions as predicted by current atomic LSU structure models led us to discuss working hypotheses on i) how individual r-proteins control the productive processing of the major 5′ end of 5.8S rRNA precursors by exonucleases Rat1p and Xrn1p, and ii) the nature of structural characteristics of nascent LSUs that are required for cytoplasmic accumulation of nascent subunits but are nonessential for most of the nuclear LSU pre-rRNA processing events. Public Library of Science 2009-12-11 /pmc/articles/PMC2788216/ /pubmed/20011513 http://dx.doi.org/10.1371/journal.pone.0008249 Text en Pöll 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
Pöll, Gisela
Braun, Tobias
Jakovljevic, Jelena
Neueder, Andreas
Jakob, Steffen
Woolford, John L.
Tschochner, Herbert
Milkereit, Philipp
rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins
title rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins
title_full rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins
title_fullStr rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins
title_full_unstemmed rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins
title_short rRNA Maturation in Yeast Cells Depleted of Large Ribosomal Subunit Proteins
title_sort rrna maturation in yeast cells depleted of large ribosomal subunit proteins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788216/
https://www.ncbi.nlm.nih.gov/pubmed/20011513
http://dx.doi.org/10.1371/journal.pone.0008249
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