BRCA1-Dependent Translational Regulation in Breast Cancer Cells.

BRCA1 (Breast Cancer 1) has been implicated in a number of cellular processes, including transcription regulation, DNA damage repair and protein ubiquitination. We previously demonstrated that BRCA1 interacts with PABP1 (Poly(A)-Binding Protein 1) and that BRCA1 modulates protein synthesis through t...

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Main Authors: Estelle Dacheux, Anne Vincent, Nicolas Nazaret, Christophe Combet, Anne Wierinckx, Sylvie Mazoyer, Jean-Jacques Diaz, Joël Lachuer, Nicole Dalla Venezia
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3689694?pdf=render
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spelling doaj-dcc2bb5e219f423e9378db88e2347a892020-11-24T21:55:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0186e6731310.1371/journal.pone.0067313BRCA1-Dependent Translational Regulation in Breast Cancer Cells.Estelle DacheuxAnne VincentNicolas NazaretChristophe CombetAnne WierinckxSylvie MazoyerJean-Jacques DiazJoël LachuerNicole Dalla VeneziaBRCA1 (Breast Cancer 1) has been implicated in a number of cellular processes, including transcription regulation, DNA damage repair and protein ubiquitination. We previously demonstrated that BRCA1 interacts with PABP1 (Poly(A)-Binding Protein 1) and that BRCA1 modulates protein synthesis through this interaction. To identify the mRNAs that are translationally regulated by BRCA1, we used a microarray analysis of polysome-bound mRNAs in BRCA1-depleted and non-depleted MCF7 cells. Our findings show that BRCA1 modifies the translational efficiency of approximately 7% of the mRNAs expressed in these cells. Further analysis revealed that several processes contributing to cell surveillance such as cell cycle arrest, cell death, cellular growth and proliferation, DNA repair and gene expression, are largely enriched for the mRNAs whose translation is impacted by BRCA1. The BRCA1-dependent translation of these species of mRNAs therefore uncovers a novel mechanism through which BRCA1 exerts its onco-suppressive role. In addition, the BRCA1-dependent translation of mRNAs participating in unexpected functions such as cellular movement, nucleic acid metabolism or protein trafficking is indicative of novel functions for BRCA1. Finally, this study contributes to the identification of several markers associated with BRCA1 deficiency and to the discovery of new potential anti-neoplastic therapeutic targets.http://europepmc.org/articles/PMC3689694?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Estelle Dacheux
Anne Vincent
Nicolas Nazaret
Christophe Combet
Anne Wierinckx
Sylvie Mazoyer
Jean-Jacques Diaz
Joël Lachuer
Nicole Dalla Venezia
spellingShingle Estelle Dacheux
Anne Vincent
Nicolas Nazaret
Christophe Combet
Anne Wierinckx
Sylvie Mazoyer
Jean-Jacques Diaz
Joël Lachuer
Nicole Dalla Venezia
BRCA1-Dependent Translational Regulation in Breast Cancer Cells.
PLoS ONE
author_facet Estelle Dacheux
Anne Vincent
Nicolas Nazaret
Christophe Combet
Anne Wierinckx
Sylvie Mazoyer
Jean-Jacques Diaz
Joël Lachuer
Nicole Dalla Venezia
author_sort Estelle Dacheux
title BRCA1-Dependent Translational Regulation in Breast Cancer Cells.
title_short BRCA1-Dependent Translational Regulation in Breast Cancer Cells.
title_full BRCA1-Dependent Translational Regulation in Breast Cancer Cells.
title_fullStr BRCA1-Dependent Translational Regulation in Breast Cancer Cells.
title_full_unstemmed BRCA1-Dependent Translational Regulation in Breast Cancer Cells.
title_sort brca1-dependent translational regulation in breast cancer cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description BRCA1 (Breast Cancer 1) has been implicated in a number of cellular processes, including transcription regulation, DNA damage repair and protein ubiquitination. We previously demonstrated that BRCA1 interacts with PABP1 (Poly(A)-Binding Protein 1) and that BRCA1 modulates protein synthesis through this interaction. To identify the mRNAs that are translationally regulated by BRCA1, we used a microarray analysis of polysome-bound mRNAs in BRCA1-depleted and non-depleted MCF7 cells. Our findings show that BRCA1 modifies the translational efficiency of approximately 7% of the mRNAs expressed in these cells. Further analysis revealed that several processes contributing to cell surveillance such as cell cycle arrest, cell death, cellular growth and proliferation, DNA repair and gene expression, are largely enriched for the mRNAs whose translation is impacted by BRCA1. The BRCA1-dependent translation of these species of mRNAs therefore uncovers a novel mechanism through which BRCA1 exerts its onco-suppressive role. In addition, the BRCA1-dependent translation of mRNAs participating in unexpected functions such as cellular movement, nucleic acid metabolism or protein trafficking is indicative of novel functions for BRCA1. Finally, this study contributes to the identification of several markers associated with BRCA1 deficiency and to the discovery of new potential anti-neoplastic therapeutic targets.
url http://europepmc.org/articles/PMC3689694?pdf=render
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