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The Cell Cycle Regulator CCDC6 Is a Key Target of RNA-Binding Protein EWS

Genetic translocation of EWSR1 to ETS transcription factor coding region is considered as primary cause for Ewing sarcoma. Previous studies focused on the biology of chimeric transcription factors formed due to this translocation. However, the physiological consequences of heterozygous EWSR1 loss in...

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Autores principales: Duggimpudi, Sujitha, Larsson, Erik, Nabhani, Schafiq, Borkhardt, Arndt, Hoell, Jessica I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4353705/
https://www.ncbi.nlm.nih.gov/pubmed/25751255
http://dx.doi.org/10.1371/journal.pone.0119066
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author Duggimpudi, Sujitha
Larsson, Erik
Nabhani, Schafiq
Borkhardt, Arndt
Hoell, Jessica I
author_facet Duggimpudi, Sujitha
Larsson, Erik
Nabhani, Schafiq
Borkhardt, Arndt
Hoell, Jessica I
author_sort Duggimpudi, Sujitha
collection PubMed
description Genetic translocation of EWSR1 to ETS transcription factor coding region is considered as primary cause for Ewing sarcoma. Previous studies focused on the biology of chimeric transcription factors formed due to this translocation. However, the physiological consequences of heterozygous EWSR1 loss in these tumors have largely remained elusive. Previously, we have identified various mRNAs bound to EWS using PAR-CLIP. In this study, we demonstrate CCDC6, a known cell cycle regulator protein, as a novel target regulated by EWS. siRNA mediated down regulation of EWS caused an elevated apoptosis in cells in a CCDC6-dependant manner. This effect was rescued upon re-expression of CCDC6. This study provides evidence for a novel functional link through which wild-type EWS operates in a target-dependant manner in Ewing sarcoma.
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spelling pubmed-43537052015-03-17 The Cell Cycle Regulator CCDC6 Is a Key Target of RNA-Binding Protein EWS Duggimpudi, Sujitha Larsson, Erik Nabhani, Schafiq Borkhardt, Arndt Hoell, Jessica I PLoS One Research Article Genetic translocation of EWSR1 to ETS transcription factor coding region is considered as primary cause for Ewing sarcoma. Previous studies focused on the biology of chimeric transcription factors formed due to this translocation. However, the physiological consequences of heterozygous EWSR1 loss in these tumors have largely remained elusive. Previously, we have identified various mRNAs bound to EWS using PAR-CLIP. In this study, we demonstrate CCDC6, a known cell cycle regulator protein, as a novel target regulated by EWS. siRNA mediated down regulation of EWS caused an elevated apoptosis in cells in a CCDC6-dependant manner. This effect was rescued upon re-expression of CCDC6. This study provides evidence for a novel functional link through which wild-type EWS operates in a target-dependant manner in Ewing sarcoma. Public Library of Science 2015-03-09 /pmc/articles/PMC4353705/ /pubmed/25751255 http://dx.doi.org/10.1371/journal.pone.0119066 Text en © 2015 Duggimpudi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Duggimpudi, Sujitha
Larsson, Erik
Nabhani, Schafiq
Borkhardt, Arndt
Hoell, Jessica I
The Cell Cycle Regulator CCDC6 Is a Key Target of RNA-Binding Protein EWS
title The Cell Cycle Regulator CCDC6 Is a Key Target of RNA-Binding Protein EWS
title_full The Cell Cycle Regulator CCDC6 Is a Key Target of RNA-Binding Protein EWS
title_fullStr The Cell Cycle Regulator CCDC6 Is a Key Target of RNA-Binding Protein EWS
title_full_unstemmed The Cell Cycle Regulator CCDC6 Is a Key Target of RNA-Binding Protein EWS
title_short The Cell Cycle Regulator CCDC6 Is a Key Target of RNA-Binding Protein EWS
title_sort cell cycle regulator ccdc6 is a key target of rna-binding protein ews
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4353705/
https://www.ncbi.nlm.nih.gov/pubmed/25751255
http://dx.doi.org/10.1371/journal.pone.0119066
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