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A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation
Eukaryotic ribosome biogenesis involves ∼200 assembly factors, but how these contribute to ribosome maturation is poorly understood. Here, we identify a network of factors on the nascent 60S subunit that actively remodels preribosome structure. At its hub is Rsa4, a direct substrate of the force-gen...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242840/ https://www.ncbi.nlm.nih.gov/pubmed/25404745 http://dx.doi.org/10.1083/jcb.201408111 |
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author | Baßler, Jochen Paternoga, Helge Holdermann, Iris Thoms, Matthias Granneman, Sander Barrio-Garcia, Clara Nyarko, Afua Stier, Gunter Clark, Sarah A. Schraivogel, Daniel Kallas, Martina Beckmann, Roland Tollervey, David Barbar, Elisar Sinning, Irmi Hurt, Ed |
author_facet | Baßler, Jochen Paternoga, Helge Holdermann, Iris Thoms, Matthias Granneman, Sander Barrio-Garcia, Clara Nyarko, Afua Stier, Gunter Clark, Sarah A. Schraivogel, Daniel Kallas, Martina Beckmann, Roland Tollervey, David Barbar, Elisar Sinning, Irmi Hurt, Ed |
author_sort | Baßler, Jochen |
collection | PubMed |
description | Eukaryotic ribosome biogenesis involves ∼200 assembly factors, but how these contribute to ribosome maturation is poorly understood. Here, we identify a network of factors on the nascent 60S subunit that actively remodels preribosome structure. At its hub is Rsa4, a direct substrate of the force-generating ATPase Rea1. We show that Rsa4 is connected to the central protuberance by binding to Rpl5 and to ribosomal RNA (rRNA) helix 89 of the nascent peptidyl transferase center (PTC) through Nsa2. Importantly, Nsa2 binds to helix 89 before relocation of helix 89 to the PTC. Structure-based mutations of these factors reveal the functional importance of their interactions for ribosome assembly. Thus, Rsa4 is held tightly in the preribosome and can serve as a “distribution box,” transmitting remodeling energy from Rea1 into the developing ribosome. We suggest that a relay-like factor network coupled to a mechano-enzyme is strategically positioned to relocate rRNA elements during ribosome maturation. |
format | Online Article Text |
id | pubmed-4242840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42428402015-05-24 A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation Baßler, Jochen Paternoga, Helge Holdermann, Iris Thoms, Matthias Granneman, Sander Barrio-Garcia, Clara Nyarko, Afua Stier, Gunter Clark, Sarah A. Schraivogel, Daniel Kallas, Martina Beckmann, Roland Tollervey, David Barbar, Elisar Sinning, Irmi Hurt, Ed J Cell Biol Research Articles Eukaryotic ribosome biogenesis involves ∼200 assembly factors, but how these contribute to ribosome maturation is poorly understood. Here, we identify a network of factors on the nascent 60S subunit that actively remodels preribosome structure. At its hub is Rsa4, a direct substrate of the force-generating ATPase Rea1. We show that Rsa4 is connected to the central protuberance by binding to Rpl5 and to ribosomal RNA (rRNA) helix 89 of the nascent peptidyl transferase center (PTC) through Nsa2. Importantly, Nsa2 binds to helix 89 before relocation of helix 89 to the PTC. Structure-based mutations of these factors reveal the functional importance of their interactions for ribosome assembly. Thus, Rsa4 is held tightly in the preribosome and can serve as a “distribution box,” transmitting remodeling energy from Rea1 into the developing ribosome. We suggest that a relay-like factor network coupled to a mechano-enzyme is strategically positioned to relocate rRNA elements during ribosome maturation. The Rockefeller University Press 2014-11-24 /pmc/articles/PMC4242840/ /pubmed/25404745 http://dx.doi.org/10.1083/jcb.201408111 Text en © 2014 Baßler et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Baßler, Jochen Paternoga, Helge Holdermann, Iris Thoms, Matthias Granneman, Sander Barrio-Garcia, Clara Nyarko, Afua Stier, Gunter Clark, Sarah A. Schraivogel, Daniel Kallas, Martina Beckmann, Roland Tollervey, David Barbar, Elisar Sinning, Irmi Hurt, Ed A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation |
title | A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation |
title_full | A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation |
title_fullStr | A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation |
title_full_unstemmed | A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation |
title_short | A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation |
title_sort | network of assembly factors is involved in remodeling rrna elements during preribosome maturation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242840/ https://www.ncbi.nlm.nih.gov/pubmed/25404745 http://dx.doi.org/10.1083/jcb.201408111 |
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