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A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei
Trypanosomes are protozoan parasites that cycle between insect and mammalian hosts and are the causative agent of sleeping sickness. Here, we describe the changes of pseudouridine (Ψ) modification on rRNA in the two life stages of the parasite using four different genome-wide approaches. CRISPR-Cas9...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662448/ https://www.ncbi.nlm.nih.gov/pubmed/37985661 http://dx.doi.org/10.1038/s41467-023-43263-6 |
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author | Rajan, K. Shanmugha Madmoni, Hava Bashan, Anat Taoka, Masato Aryal, Saurav Nobe, Yuko Doniger, Tirza Galili Kostin, Beathrice Blumberg, Amit Cohen-Chalamish, Smadar Schwartz, Schraga Rivalta, Andre Zimmerman, Ella Unger, Ron Isobe, Toshiaki Yonath, Ada Michaeli, Shulamit |
author_facet | Rajan, K. Shanmugha Madmoni, Hava Bashan, Anat Taoka, Masato Aryal, Saurav Nobe, Yuko Doniger, Tirza Galili Kostin, Beathrice Blumberg, Amit Cohen-Chalamish, Smadar Schwartz, Schraga Rivalta, Andre Zimmerman, Ella Unger, Ron Isobe, Toshiaki Yonath, Ada Michaeli, Shulamit |
author_sort | Rajan, K. Shanmugha |
collection | PubMed |
description | Trypanosomes are protozoan parasites that cycle between insect and mammalian hosts and are the causative agent of sleeping sickness. Here, we describe the changes of pseudouridine (Ψ) modification on rRNA in the two life stages of the parasite using four different genome-wide approaches. CRISPR-Cas9 knock-outs of all four snoRNAs guiding Ψ on helix 69 (H69) of the large rRNA subunit were lethal. A single knock-out of a snoRNA guiding Ψ530 on H69 altered the composition of the 80S monosome. These changes specifically affected the translation of only a subset of proteins. This study correlates a single site Ψ modification with changes in ribosomal protein stoichiometry, supported by a high-resolution cryo-EM structure. We propose that alteration in rRNA modifications could generate ribosomes preferentially translating state-beneficial proteins. |
format | Online Article Text |
id | pubmed-10662448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106624482023-11-20 A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei Rajan, K. Shanmugha Madmoni, Hava Bashan, Anat Taoka, Masato Aryal, Saurav Nobe, Yuko Doniger, Tirza Galili Kostin, Beathrice Blumberg, Amit Cohen-Chalamish, Smadar Schwartz, Schraga Rivalta, Andre Zimmerman, Ella Unger, Ron Isobe, Toshiaki Yonath, Ada Michaeli, Shulamit Nat Commun Article Trypanosomes are protozoan parasites that cycle between insect and mammalian hosts and are the causative agent of sleeping sickness. Here, we describe the changes of pseudouridine (Ψ) modification on rRNA in the two life stages of the parasite using four different genome-wide approaches. CRISPR-Cas9 knock-outs of all four snoRNAs guiding Ψ on helix 69 (H69) of the large rRNA subunit were lethal. A single knock-out of a snoRNA guiding Ψ530 on H69 altered the composition of the 80S monosome. These changes specifically affected the translation of only a subset of proteins. This study correlates a single site Ψ modification with changes in ribosomal protein stoichiometry, supported by a high-resolution cryo-EM structure. We propose that alteration in rRNA modifications could generate ribosomes preferentially translating state-beneficial proteins. Nature Publishing Group UK 2023-11-20 /pmc/articles/PMC10662448/ /pubmed/37985661 http://dx.doi.org/10.1038/s41467-023-43263-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Rajan, K. Shanmugha Madmoni, Hava Bashan, Anat Taoka, Masato Aryal, Saurav Nobe, Yuko Doniger, Tirza Galili Kostin, Beathrice Blumberg, Amit Cohen-Chalamish, Smadar Schwartz, Schraga Rivalta, Andre Zimmerman, Ella Unger, Ron Isobe, Toshiaki Yonath, Ada Michaeli, Shulamit A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei |
title | A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei |
title_full | A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei |
title_fullStr | A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei |
title_full_unstemmed | A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei |
title_short | A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei |
title_sort | single pseudouridine on rrna regulates ribosome structure and function in the mammalian parasite trypanosoma brucei |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10662448/ https://www.ncbi.nlm.nih.gov/pubmed/37985661 http://dx.doi.org/10.1038/s41467-023-43263-6 |
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