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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...

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Autores principales: Tye, Blake W, Commins, Nicoletta, Ryazanova, Lillia V, Wühr, Martin, Springer, Michael, Pincus, David, Churchman, L Stirling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
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.
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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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