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Early rRNA processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity
The production of ribosomes is an energy-intensive process owing to the intricacy of these massive macromolecular machines. Each human ribosome contains 80 ribosomal proteins and four non-coding RNAs. Accurate assembly requires precise regulation of protein and RNA subunits. In response to stress, t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789083/ https://www.ncbi.nlm.nih.gov/pubmed/34928368 http://dx.doi.org/10.1093/nar/gkab1231 |
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author | Szaflarski, Witold Leśniczak-Staszak, Marta Sowiński, Mateusz Ojha, Sandeep Aulas, Anaïs Dave, Dhwani Malla, Sulochan Anderson, Paul Ivanov, Pavel Lyons, Shawn M |
author_facet | Szaflarski, Witold Leśniczak-Staszak, Marta Sowiński, Mateusz Ojha, Sandeep Aulas, Anaïs Dave, Dhwani Malla, Sulochan Anderson, Paul Ivanov, Pavel Lyons, Shawn M |
author_sort | Szaflarski, Witold |
collection | PubMed |
description | The production of ribosomes is an energy-intensive process owing to the intricacy of these massive macromolecular machines. Each human ribosome contains 80 ribosomal proteins and four non-coding RNAs. Accurate assembly requires precise regulation of protein and RNA subunits. In response to stress, the integrated stress response (ISR) rapidly inhibits global translation. How rRNA is coordinately regulated with the rapid inhibition of ribosomal protein synthesis is not known. Here, we show that stress specifically inhibits the first step of rRNA processing. Unprocessed rRNA is stored within the nucleolus, and when stress resolves, it re-enters the ribosome biogenesis pathway. Retention of unprocessed rRNA within the nucleolus aids in the maintenance of this organelle. This response is independent of the ISR or inhibition of cellular translation but is independently regulated. Failure to coordinately control ribosomal protein translation and rRNA production results in nucleolar fragmentation. Our study unveils how the rapid translational shut-off in response to stress coordinates with rRNA synthesis production to maintain nucleolar integrity. |
format | Online Article Text |
id | pubmed-8789083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87890832022-01-26 Early rRNA processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity Szaflarski, Witold Leśniczak-Staszak, Marta Sowiński, Mateusz Ojha, Sandeep Aulas, Anaïs Dave, Dhwani Malla, Sulochan Anderson, Paul Ivanov, Pavel Lyons, Shawn M Nucleic Acids Res RNA and RNA-protein complexes The production of ribosomes is an energy-intensive process owing to the intricacy of these massive macromolecular machines. Each human ribosome contains 80 ribosomal proteins and four non-coding RNAs. Accurate assembly requires precise regulation of protein and RNA subunits. In response to stress, the integrated stress response (ISR) rapidly inhibits global translation. How rRNA is coordinately regulated with the rapid inhibition of ribosomal protein synthesis is not known. Here, we show that stress specifically inhibits the first step of rRNA processing. Unprocessed rRNA is stored within the nucleolus, and when stress resolves, it re-enters the ribosome biogenesis pathway. Retention of unprocessed rRNA within the nucleolus aids in the maintenance of this organelle. This response is independent of the ISR or inhibition of cellular translation but is independently regulated. Failure to coordinately control ribosomal protein translation and rRNA production results in nucleolar fragmentation. Our study unveils how the rapid translational shut-off in response to stress coordinates with rRNA synthesis production to maintain nucleolar integrity. Oxford University Press 2021-12-20 /pmc/articles/PMC8789083/ /pubmed/34928368 http://dx.doi.org/10.1093/nar/gkab1231 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | RNA and RNA-protein complexes Szaflarski, Witold Leśniczak-Staszak, Marta Sowiński, Mateusz Ojha, Sandeep Aulas, Anaïs Dave, Dhwani Malla, Sulochan Anderson, Paul Ivanov, Pavel Lyons, Shawn M Early rRNA processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity |
title | Early rRNA processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity |
title_full | Early rRNA processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity |
title_fullStr | Early rRNA processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity |
title_full_unstemmed | Early rRNA processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity |
title_short | Early rRNA processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity |
title_sort | early rrna processing is a stress-dependent regulatory event whose inhibition maintains nucleolar integrity |
topic | RNA and RNA-protein complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789083/ https://www.ncbi.nlm.nih.gov/pubmed/34928368 http://dx.doi.org/10.1093/nar/gkab1231 |
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