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Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways
The 5S ribonucleoprotein (RNP) is assembled from its three components (5S rRNA, Rpl5/uL18 and Rpl11/uL5) before being incorporated into the pre-60S subunit. However, when ribosome synthesis is disturbed, a free 5S RNP can enter the MDM2–p53 pathway to regulate cell cycle and apoptotic signaling. Her...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442235/ https://www.ncbi.nlm.nih.gov/pubmed/37291423 http://dx.doi.org/10.1038/s41594-023-01006-7 |
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author | Castillo Duque de Estrada, Nestor Miguel Thoms, Matthias Flemming, Dirk Hammaren, Henrik M. Buschauer, Robert Ameismeier, Michael Baßler, Jochen Beck, Martin Beckmann, Roland Hurt, Ed |
author_facet | Castillo Duque de Estrada, Nestor Miguel Thoms, Matthias Flemming, Dirk Hammaren, Henrik M. Buschauer, Robert Ameismeier, Michael Baßler, Jochen Beck, Martin Beckmann, Roland Hurt, Ed |
author_sort | Castillo Duque de Estrada, Nestor Miguel |
collection | PubMed |
description | The 5S ribonucleoprotein (RNP) is assembled from its three components (5S rRNA, Rpl5/uL18 and Rpl11/uL5) before being incorporated into the pre-60S subunit. However, when ribosome synthesis is disturbed, a free 5S RNP can enter the MDM2–p53 pathway to regulate cell cycle and apoptotic signaling. Here we reconstitute and determine the cryo-electron microscopy structure of the conserved hexameric 5S RNP with fungal or human factors. This reveals how the nascent 5S rRNA associates with the initial nuclear import complex Syo1–uL18–uL5 and, upon further recruitment of the nucleolar factors Rpf2 and Rrs1, develops into the 5S RNP precursor that can assemble into the pre-ribosome. In addition, we elucidate the structure of another 5S RNP intermediate, carrying the human ubiquitin ligase Mdm2, which unravels how this enzyme can be sequestered from its target substrate p53. Our data provide molecular insight into how the 5S RNP can mediate between ribosome biogenesis and cell proliferation. |
format | Online Article Text |
id | pubmed-10442235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-104422352023-08-23 Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways Castillo Duque de Estrada, Nestor Miguel Thoms, Matthias Flemming, Dirk Hammaren, Henrik M. Buschauer, Robert Ameismeier, Michael Baßler, Jochen Beck, Martin Beckmann, Roland Hurt, Ed Nat Struct Mol Biol Article The 5S ribonucleoprotein (RNP) is assembled from its three components (5S rRNA, Rpl5/uL18 and Rpl11/uL5) before being incorporated into the pre-60S subunit. However, when ribosome synthesis is disturbed, a free 5S RNP can enter the MDM2–p53 pathway to regulate cell cycle and apoptotic signaling. Here we reconstitute and determine the cryo-electron microscopy structure of the conserved hexameric 5S RNP with fungal or human factors. This reveals how the nascent 5S rRNA associates with the initial nuclear import complex Syo1–uL18–uL5 and, upon further recruitment of the nucleolar factors Rpf2 and Rrs1, develops into the 5S RNP precursor that can assemble into the pre-ribosome. In addition, we elucidate the structure of another 5S RNP intermediate, carrying the human ubiquitin ligase Mdm2, which unravels how this enzyme can be sequestered from its target substrate p53. Our data provide molecular insight into how the 5S RNP can mediate between ribosome biogenesis and cell proliferation. Nature Publishing Group US 2023-06-08 2023 /pmc/articles/PMC10442235/ /pubmed/37291423 http://dx.doi.org/10.1038/s41594-023-01006-7 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 Castillo Duque de Estrada, Nestor Miguel Thoms, Matthias Flemming, Dirk Hammaren, Henrik M. Buschauer, Robert Ameismeier, Michael Baßler, Jochen Beck, Martin Beckmann, Roland Hurt, Ed Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways |
title | Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways |
title_full | Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways |
title_fullStr | Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways |
title_full_unstemmed | Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways |
title_short | Structure of nascent 5S RNPs at the crossroad between ribosome assembly and MDM2–p53 pathways |
title_sort | structure of nascent 5s rnps at the crossroad between ribosome assembly and mdm2–p53 pathways |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442235/ https://www.ncbi.nlm.nih.gov/pubmed/37291423 http://dx.doi.org/10.1038/s41594-023-01006-7 |
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