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Cell cycle-dependent regulation of the RNA-binding protein Staufen1

Staufen1 (Stau1) is a ribonucleic acid (RNA)-binding protein involved in the post-transcriptional regulation of gene expression. Recent studies indicate that Stau1-bound messenger RNAs (mRNAs) mainly code for proteins involved in transcription and cell cycle control. Consistently, we report here tha...

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Autores principales: Boulay, Karine, Ghram, Mehdi, Viranaicken, Wildriss, Trépanier, Véronique, Mollet, Stéphanie, Fréchina, Céline, DesGroseillers, Luc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081104/
https://www.ncbi.nlm.nih.gov/pubmed/24906885
http://dx.doi.org/10.1093/nar/gku506
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author Boulay, Karine
Ghram, Mehdi
Viranaicken, Wildriss
Trépanier, Véronique
Mollet, Stéphanie
Fréchina, Céline
DesGroseillers, Luc
author_facet Boulay, Karine
Ghram, Mehdi
Viranaicken, Wildriss
Trépanier, Véronique
Mollet, Stéphanie
Fréchina, Céline
DesGroseillers, Luc
author_sort Boulay, Karine
collection PubMed
description Staufen1 (Stau1) is a ribonucleic acid (RNA)-binding protein involved in the post-transcriptional regulation of gene expression. Recent studies indicate that Stau1-bound messenger RNAs (mRNAs) mainly code for proteins involved in transcription and cell cycle control. Consistently, we report here that Stau1 abundance fluctuates through the cell cycle in HCT116 and U2OS cells: it is high from the S phase to the onset of mitosis and rapidly decreases as cells transit through mitosis. Stau1 down-regulation is mediated by the ubiquitin-proteasome system and the E3 ubiquitin ligase anaphase promoting complex/cyclosome (APC/C). Stau1 interacts with the APC/C co-activators Cdh1 and Cdc20 via its first 88 N-terminal amino acids. The importance of controlling Stau1(55) levels is underscored by the observation that its overexpression affects mitosis entry and impairs proliferation of transformed cells. Microarray analyses identified 275 Stau1(55)-bound mRNAs in prometaphase cells, an early mitotic step that just precedes Stau1 degradation. Interestingly, several of these mRNAs are more abundant in Stau1(55)-containing complexes in cells arrested in prometaphase than in asynchronous cells. Our results point out for the first time to the possibility that Stau1 participates in a mechanism of post-transcriptional regulation of gene expression that is linked to cell cycle progression in cancer cells.
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spelling pubmed-40811042014-07-10 Cell cycle-dependent regulation of the RNA-binding protein Staufen1 Boulay, Karine Ghram, Mehdi Viranaicken, Wildriss Trépanier, Véronique Mollet, Stéphanie Fréchina, Céline DesGroseillers, Luc Nucleic Acids Res Molecular Biology Staufen1 (Stau1) is a ribonucleic acid (RNA)-binding protein involved in the post-transcriptional regulation of gene expression. Recent studies indicate that Stau1-bound messenger RNAs (mRNAs) mainly code for proteins involved in transcription and cell cycle control. Consistently, we report here that Stau1 abundance fluctuates through the cell cycle in HCT116 and U2OS cells: it is high from the S phase to the onset of mitosis and rapidly decreases as cells transit through mitosis. Stau1 down-regulation is mediated by the ubiquitin-proteasome system and the E3 ubiquitin ligase anaphase promoting complex/cyclosome (APC/C). Stau1 interacts with the APC/C co-activators Cdh1 and Cdc20 via its first 88 N-terminal amino acids. The importance of controlling Stau1(55) levels is underscored by the observation that its overexpression affects mitosis entry and impairs proliferation of transformed cells. Microarray analyses identified 275 Stau1(55)-bound mRNAs in prometaphase cells, an early mitotic step that just precedes Stau1 degradation. Interestingly, several of these mRNAs are more abundant in Stau1(55)-containing complexes in cells arrested in prometaphase than in asynchronous cells. Our results point out for the first time to the possibility that Stau1 participates in a mechanism of post-transcriptional regulation of gene expression that is linked to cell cycle progression in cancer cells. Oxford University Press 2014-08-01 2014-06-07 /pmc/articles/PMC4081104/ /pubmed/24906885 http://dx.doi.org/10.1093/nar/gku506 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Boulay, Karine
Ghram, Mehdi
Viranaicken, Wildriss
Trépanier, Véronique
Mollet, Stéphanie
Fréchina, Céline
DesGroseillers, Luc
Cell cycle-dependent regulation of the RNA-binding protein Staufen1
title Cell cycle-dependent regulation of the RNA-binding protein Staufen1
title_full Cell cycle-dependent regulation of the RNA-binding protein Staufen1
title_fullStr Cell cycle-dependent regulation of the RNA-binding protein Staufen1
title_full_unstemmed Cell cycle-dependent regulation of the RNA-binding protein Staufen1
title_short Cell cycle-dependent regulation of the RNA-binding protein Staufen1
title_sort cell cycle-dependent regulation of the rna-binding protein staufen1
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081104/
https://www.ncbi.nlm.nih.gov/pubmed/24906885
http://dx.doi.org/10.1093/nar/gku506
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