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Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness
To achieve maximal growth, cells must manage a massive economy of ribosomal proteins (r-proteins) and RNAs (rRNAs) to produce thousands of ribosomes every minute. Although ribosomes are essential in all cells, natural disruptions to ribosome biogenesis lead to heterogeneous phenotypes. Here, we mode...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453566/ https://www.ncbi.nlm.nih.gov/pubmed/30843788 http://dx.doi.org/10.7554/eLife.43002 |
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author | Tye, Blake W Commins, Nicoletta Ryazanova, Lillia V Wühr, Martin Springer, Michael Pincus, David Churchman, L Stirling |
author_facet | Tye, Blake W Commins, Nicoletta Ryazanova, Lillia V Wühr, Martin Springer, Michael Pincus, David Churchman, L Stirling |
author_sort | Tye, Blake W |
collection | PubMed |
description | To achieve maximal growth, cells must manage a massive economy of ribosomal proteins (r-proteins) and RNAs (rRNAs) to produce thousands of ribosomes every minute. Although ribosomes are essential in all cells, natural disruptions to ribosome biogenesis lead to heterogeneous phenotypes. Here, we model these perturbations in Saccharomyces cerevisiae and show that challenges to ribosome biogenesis result in acute loss of proteostasis. Imbalances in the synthesis of r-proteins and rRNAs lead to the rapid aggregation of newly synthesized orphan r-proteins and compromise essential cellular processes, which cells alleviate by activating proteostasis genes. Exogenously bolstering the proteostasis network increases cellular fitness in the face of challenges to ribosome assembly, demonstrating the direct contribution of orphan r-proteins to cellular phenotypes. We propose that ribosome assembly is a key vulnerability of proteostasis maintenance in proliferating cells that may be compromised by diverse genetic, environmental, and xenobiotic perturbations that generate orphan r-proteins. |
format | Online Article Text |
id | pubmed-6453566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-64535662019-04-10 Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness Tye, Blake W Commins, Nicoletta Ryazanova, Lillia V Wühr, Martin Springer, Michael Pincus, David Churchman, L Stirling eLife Biochemistry and Chemical Biology To achieve maximal growth, cells must manage a massive economy of ribosomal proteins (r-proteins) and RNAs (rRNAs) to produce thousands of ribosomes every minute. Although ribosomes are essential in all cells, natural disruptions to ribosome biogenesis lead to heterogeneous phenotypes. Here, we model these perturbations in Saccharomyces cerevisiae and show that challenges to ribosome biogenesis result in acute loss of proteostasis. Imbalances in the synthesis of r-proteins and rRNAs lead to the rapid aggregation of newly synthesized orphan r-proteins and compromise essential cellular processes, which cells alleviate by activating proteostasis genes. Exogenously bolstering the proteostasis network increases cellular fitness in the face of challenges to ribosome assembly, demonstrating the direct contribution of orphan r-proteins to cellular phenotypes. We propose that ribosome assembly is a key vulnerability of proteostasis maintenance in proliferating cells that may be compromised by diverse genetic, environmental, and xenobiotic perturbations that generate orphan r-proteins. eLife Sciences Publications, Ltd 2019-03-07 /pmc/articles/PMC6453566/ /pubmed/30843788 http://dx.doi.org/10.7554/eLife.43002 Text en © 2019, Tye 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 | Biochemistry and Chemical Biology Tye, Blake W Commins, Nicoletta Ryazanova, Lillia V Wühr, Martin Springer, Michael Pincus, David Churchman, L Stirling Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness |
title | Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness |
title_full | Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness |
title_fullStr | Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness |
title_full_unstemmed | Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness |
title_short | Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness |
title_sort | proteotoxicity from aberrant ribosome biogenesis compromises cell fitness |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453566/ https://www.ncbi.nlm.nih.gov/pubmed/30843788 http://dx.doi.org/10.7554/eLife.43002 |
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