Cargando…
The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles
Ribosome biogenesis takes place successively in the nucleolar, nucleoplasmic, and cytoplasmic compartments. Numerous nonribosomal factors transiently associate with the nascent ribosomes, but the mechanisms driving ribosome formation are mostly unknown. Here, we show that an energy-consuming enzyme,...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426938/ https://www.ncbi.nlm.nih.gov/pubmed/18559667 http://dx.doi.org/10.1083/jcb.200801181 |
_version_ | 1782156306879086592 |
---|---|
author | Kressler, Dieter Roser, Daniela Pertschy, Brigitte Hurt, Ed |
author_facet | Kressler, Dieter Roser, Daniela Pertschy, Brigitte Hurt, Ed |
author_sort | Kressler, Dieter |
collection | PubMed |
description | Ribosome biogenesis takes place successively in the nucleolar, nucleoplasmic, and cytoplasmic compartments. Numerous nonribosomal factors transiently associate with the nascent ribosomes, but the mechanisms driving ribosome formation are mostly unknown. Here, we show that an energy-consuming enzyme, the AAA-type (ATPases associated with various cellular activities) ATPase Rix7, restructures a novel pre-60S particle at the transition from the nucleolus to nucleoplasm. Rix7 interacts genetically with Nsa1 and is targeted to the Nsa1-defined preribosomal particle. In vivo, Nsa1 cannot dissociate from pre-60S particles in rix7 mutants, causing nucleolar Nsa1 to escape to the cytoplasm, where it remains associated with aberrant 60S subunits. Altogether, our data suggest that Rix7 is required for the release of Nsa1 from a discrete preribosomal particle, thereby triggering the progression of 60S ribosome biogenesis. |
format | Text |
id | pubmed-2426938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24269382008-12-16 The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles Kressler, Dieter Roser, Daniela Pertschy, Brigitte Hurt, Ed J Cell Biol Research Articles Ribosome biogenesis takes place successively in the nucleolar, nucleoplasmic, and cytoplasmic compartments. Numerous nonribosomal factors transiently associate with the nascent ribosomes, but the mechanisms driving ribosome formation are mostly unknown. Here, we show that an energy-consuming enzyme, the AAA-type (ATPases associated with various cellular activities) ATPase Rix7, restructures a novel pre-60S particle at the transition from the nucleolus to nucleoplasm. Rix7 interacts genetically with Nsa1 and is targeted to the Nsa1-defined preribosomal particle. In vivo, Nsa1 cannot dissociate from pre-60S particles in rix7 mutants, causing nucleolar Nsa1 to escape to the cytoplasm, where it remains associated with aberrant 60S subunits. Altogether, our data suggest that Rix7 is required for the release of Nsa1 from a discrete preribosomal particle, thereby triggering the progression of 60S ribosome biogenesis. The Rockefeller University Press 2008-06-16 /pmc/articles/PMC2426938/ /pubmed/18559667 http://dx.doi.org/10.1083/jcb.200801181 Text en © 2008 Kressler 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.jcb.org/misc/terms.shtml). 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 Kressler, Dieter Roser, Daniela Pertschy, Brigitte Hurt, Ed The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles |
title | The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles |
title_full | The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles |
title_fullStr | The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles |
title_full_unstemmed | The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles |
title_short | The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles |
title_sort | aaa atpase rix7 powers progression of ribosome biogenesis by stripping nsa1 from pre-60s particles |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426938/ https://www.ncbi.nlm.nih.gov/pubmed/18559667 http://dx.doi.org/10.1083/jcb.200801181 |
work_keys_str_mv | AT kresslerdieter theaaaatpaserix7powersprogressionofribosomebiogenesisbystrippingnsa1frompre60sparticles AT roserdaniela theaaaatpaserix7powersprogressionofribosomebiogenesisbystrippingnsa1frompre60sparticles AT pertschybrigitte theaaaatpaserix7powersprogressionofribosomebiogenesisbystrippingnsa1frompre60sparticles AT hurted theaaaatpaserix7powersprogressionofribosomebiogenesisbystrippingnsa1frompre60sparticles AT kresslerdieter aaaatpaserix7powersprogressionofribosomebiogenesisbystrippingnsa1frompre60sparticles AT roserdaniela aaaatpaserix7powersprogressionofribosomebiogenesisbystrippingnsa1frompre60sparticles AT pertschybrigitte aaaatpaserix7powersprogressionofribosomebiogenesisbystrippingnsa1frompre60sparticles AT hurted aaaatpaserix7powersprogressionofribosomebiogenesisbystrippingnsa1frompre60sparticles |