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A Myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity
Stem cell identity depends on the integration of extrinsic and intrinsic signals, which directly influence the maintenance of their epigenetic state. Although Myc transcription factors play a major role in stem cell self-renewal and pluripotency, their integration with signalling pathways and epigen...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912626/ https://www.ncbi.nlm.nih.gov/pubmed/27301576 http://dx.doi.org/10.1038/ncomms11903 |
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author | Fagnocchi, Luca Cherubini, Alessandro Hatsuda, Hiroshi Fasciani, Alessandra Mazzoleni, Stefania Poli, Vittoria Berno, Valeria Rossi, Riccardo L. Reinbold, Rolland Endele, Max Schroeder, Timm Rocchigiani, Marina Szkarłat, Żaneta Oliviero, Salvatore Dalton, Stephen Zippo, Alessio |
author_facet | Fagnocchi, Luca Cherubini, Alessandro Hatsuda, Hiroshi Fasciani, Alessandra Mazzoleni, Stefania Poli, Vittoria Berno, Valeria Rossi, Riccardo L. Reinbold, Rolland Endele, Max Schroeder, Timm Rocchigiani, Marina Szkarłat, Żaneta Oliviero, Salvatore Dalton, Stephen Zippo, Alessio |
author_sort | Fagnocchi, Luca |
collection | PubMed |
description | Stem cell identity depends on the integration of extrinsic and intrinsic signals, which directly influence the maintenance of their epigenetic state. Although Myc transcription factors play a major role in stem cell self-renewal and pluripotency, their integration with signalling pathways and epigenetic regulators remains poorly defined. We addressed this point by profiling the gene expression and epigenetic pattern in ESCs whose growth depends on conditional Myc activity. Here we show that Myc potentiates the Wnt/β-catenin signalling pathway, which cooperates with the transcriptional regulatory network in sustaining ESC self-renewal. Myc activation results in the transcriptional repression of Wnt antagonists through the direct recruitment of PRC2 on these targets. The consequent potentiation of the autocrine Wnt/β-catenin signalling induces the transcriptional activation of the endogenous Myc family members, which in turn activates a Myc-driven self-reinforcing circuit. Thus, our data unravel a Myc-dependent self-propagating epigenetic memory in the maintenance of ESC self-renewal capacity. |
format | Online Article Text |
id | pubmed-4912626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49126262016-06-29 A Myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity Fagnocchi, Luca Cherubini, Alessandro Hatsuda, Hiroshi Fasciani, Alessandra Mazzoleni, Stefania Poli, Vittoria Berno, Valeria Rossi, Riccardo L. Reinbold, Rolland Endele, Max Schroeder, Timm Rocchigiani, Marina Szkarłat, Żaneta Oliviero, Salvatore Dalton, Stephen Zippo, Alessio Nat Commun Article Stem cell identity depends on the integration of extrinsic and intrinsic signals, which directly influence the maintenance of their epigenetic state. Although Myc transcription factors play a major role in stem cell self-renewal and pluripotency, their integration with signalling pathways and epigenetic regulators remains poorly defined. We addressed this point by profiling the gene expression and epigenetic pattern in ESCs whose growth depends on conditional Myc activity. Here we show that Myc potentiates the Wnt/β-catenin signalling pathway, which cooperates with the transcriptional regulatory network in sustaining ESC self-renewal. Myc activation results in the transcriptional repression of Wnt antagonists through the direct recruitment of PRC2 on these targets. The consequent potentiation of the autocrine Wnt/β-catenin signalling induces the transcriptional activation of the endogenous Myc family members, which in turn activates a Myc-driven self-reinforcing circuit. Thus, our data unravel a Myc-dependent self-propagating epigenetic memory in the maintenance of ESC self-renewal capacity. Nature Publishing Group 2016-06-15 /pmc/articles/PMC4912626/ /pubmed/27301576 http://dx.doi.org/10.1038/ncomms11903 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fagnocchi, Luca Cherubini, Alessandro Hatsuda, Hiroshi Fasciani, Alessandra Mazzoleni, Stefania Poli, Vittoria Berno, Valeria Rossi, Riccardo L. Reinbold, Rolland Endele, Max Schroeder, Timm Rocchigiani, Marina Szkarłat, Żaneta Oliviero, Salvatore Dalton, Stephen Zippo, Alessio A Myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity |
title | A Myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity |
title_full | A Myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity |
title_fullStr | A Myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity |
title_full_unstemmed | A Myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity |
title_short | A Myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity |
title_sort | myc-driven self-reinforcing regulatory network maintains mouse embryonic stem cell identity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912626/ https://www.ncbi.nlm.nih.gov/pubmed/27301576 http://dx.doi.org/10.1038/ncomms11903 |
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