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Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly

5S rRNA is an indispensable component of cytoplasmic ribosomes in all species. The functions of 5S rRNA and the reasons for its evolutionary preservation as an independent molecule remain unclear. Here we used ribosome engineering to investigate whether 5S rRNA autonomy is critical for ribosome func...

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Autores principales: Huang, Shijie, Aleksashin, Nikolay A., Loveland, Anna B., Klepacki, Dorota, Reier, Kaspar, Kefi, Amira, Szal, Teresa, Remme, Jaanus, Jaeger, Luc, Vázquez-Laslop, Nora, Korostelev, Andrei A., Mankin, Alexander S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283268/
https://www.ncbi.nlm.nih.gov/pubmed/32518240
http://dx.doi.org/10.1038/s41467-020-16694-8
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author Huang, Shijie
Aleksashin, Nikolay A.
Loveland, Anna B.
Klepacki, Dorota
Reier, Kaspar
Kefi, Amira
Szal, Teresa
Remme, Jaanus
Jaeger, Luc
Vázquez-Laslop, Nora
Korostelev, Andrei A.
Mankin, Alexander S.
author_facet Huang, Shijie
Aleksashin, Nikolay A.
Loveland, Anna B.
Klepacki, Dorota
Reier, Kaspar
Kefi, Amira
Szal, Teresa
Remme, Jaanus
Jaeger, Luc
Vázquez-Laslop, Nora
Korostelev, Andrei A.
Mankin, Alexander S.
author_sort Huang, Shijie
collection PubMed
description 5S rRNA is an indispensable component of cytoplasmic ribosomes in all species. The functions of 5S rRNA and the reasons for its evolutionary preservation as an independent molecule remain unclear. Here we used ribosome engineering to investigate whether 5S rRNA autonomy is critical for ribosome function and cell survival. By linking circularly permutated 5S rRNA with 23S rRNA we generated a bacterial strain devoid of free 5S rRNA. Viability of the engineered cells demonstrates that autonomous 5S rRNA is dispensable for cell growth under standard conditions and is unlikely to have essential functions outside the ribosome. The fully assembled ribosomes carrying 23S-5S rRNA are highly active in translation. However, the engineered cells accumulate aberrant 50S subunits unable to form stable 70S ribosomes. Cryo-EM analysis revealed a malformed peptidyl transferase center in the misassembled 50S subunits. Our results argue that the autonomy of 5S rRNA is preserved due to its role in ribosome biogenesis.
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spelling pubmed-72832682020-06-15 Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly Huang, Shijie Aleksashin, Nikolay A. Loveland, Anna B. Klepacki, Dorota Reier, Kaspar Kefi, Amira Szal, Teresa Remme, Jaanus Jaeger, Luc Vázquez-Laslop, Nora Korostelev, Andrei A. Mankin, Alexander S. Nat Commun Article 5S rRNA is an indispensable component of cytoplasmic ribosomes in all species. The functions of 5S rRNA and the reasons for its evolutionary preservation as an independent molecule remain unclear. Here we used ribosome engineering to investigate whether 5S rRNA autonomy is critical for ribosome function and cell survival. By linking circularly permutated 5S rRNA with 23S rRNA we generated a bacterial strain devoid of free 5S rRNA. Viability of the engineered cells demonstrates that autonomous 5S rRNA is dispensable for cell growth under standard conditions and is unlikely to have essential functions outside the ribosome. The fully assembled ribosomes carrying 23S-5S rRNA are highly active in translation. However, the engineered cells accumulate aberrant 50S subunits unable to form stable 70S ribosomes. Cryo-EM analysis revealed a malformed peptidyl transferase center in the misassembled 50S subunits. Our results argue that the autonomy of 5S rRNA is preserved due to its role in ribosome biogenesis. Nature Publishing Group UK 2020-06-09 /pmc/articles/PMC7283268/ /pubmed/32518240 http://dx.doi.org/10.1038/s41467-020-16694-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Huang, Shijie
Aleksashin, Nikolay A.
Loveland, Anna B.
Klepacki, Dorota
Reier, Kaspar
Kefi, Amira
Szal, Teresa
Remme, Jaanus
Jaeger, Luc
Vázquez-Laslop, Nora
Korostelev, Andrei A.
Mankin, Alexander S.
Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly
title Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly
title_full Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly
title_fullStr Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly
title_full_unstemmed Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly
title_short Ribosome engineering reveals the importance of 5S rRNA autonomy for ribosome assembly
title_sort ribosome engineering reveals the importance of 5s rrna autonomy for ribosome assembly
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283268/
https://www.ncbi.nlm.nih.gov/pubmed/32518240
http://dx.doi.org/10.1038/s41467-020-16694-8
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