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Zrf1 is required to establish and maintain neural progenitor identity
The molecular mechanisms underlying specification from embryonic stem cells (ESCs) and maintenance of neural progenitor cells (NPCs) are largely unknown. Recently, we reported that the Zuotin-related factor 1 (Zrf1) is necessary for chromatin displacement of the Polycomb-repressive complex 1 (PRC1)....
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909791/ https://www.ncbi.nlm.nih.gov/pubmed/24449271 http://dx.doi.org/10.1101/gad.228510.113 |
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author | Aloia, Luigi Di Stefano, Bruno Sessa, Alessandro Morey, Lluis Santanach, Alexandra Gutierrez, Arantxa Cozzuto, Luca Benitah, Salvador Aznar Graf, Thomas Broccoli, Vania Di Croce, Luciano |
author_facet | Aloia, Luigi Di Stefano, Bruno Sessa, Alessandro Morey, Lluis Santanach, Alexandra Gutierrez, Arantxa Cozzuto, Luca Benitah, Salvador Aznar Graf, Thomas Broccoli, Vania Di Croce, Luciano |
author_sort | Aloia, Luigi |
collection | PubMed |
description | The molecular mechanisms underlying specification from embryonic stem cells (ESCs) and maintenance of neural progenitor cells (NPCs) are largely unknown. Recently, we reported that the Zuotin-related factor 1 (Zrf1) is necessary for chromatin displacement of the Polycomb-repressive complex 1 (PRC1). We found that Zrf1 is required for NPC specification from ESCs and that it promotes the expression of NPC markers, including the key regulator Pax6. Moreover, Zrf1 is essential to establish and maintain Wnt ligand expression levels, which are necessary for NPC self-renewal. Reactivation of proper Wnt signaling in Zrf1-depleted NPCs restores Pax6 expression and the self-renewal capacity. ESC-derived NPCs in vitro resemble most of the characteristics of the self-renewing NPCs located in the developing embryonic cortex, which are termed radial glial cells (RGCs). Depletion of Zrf1 in vivo impairs the expression of key self-renewal regulators and Wnt ligand genes in RGCs. Thus, we demonstrate that Zrf1 plays an essential role in NPC generation and maintenance. |
format | Online Article Text |
id | pubmed-3909791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39097912014-07-15 Zrf1 is required to establish and maintain neural progenitor identity Aloia, Luigi Di Stefano, Bruno Sessa, Alessandro Morey, Lluis Santanach, Alexandra Gutierrez, Arantxa Cozzuto, Luca Benitah, Salvador Aznar Graf, Thomas Broccoli, Vania Di Croce, Luciano Genes Dev Research Paper The molecular mechanisms underlying specification from embryonic stem cells (ESCs) and maintenance of neural progenitor cells (NPCs) are largely unknown. Recently, we reported that the Zuotin-related factor 1 (Zrf1) is necessary for chromatin displacement of the Polycomb-repressive complex 1 (PRC1). We found that Zrf1 is required for NPC specification from ESCs and that it promotes the expression of NPC markers, including the key regulator Pax6. Moreover, Zrf1 is essential to establish and maintain Wnt ligand expression levels, which are necessary for NPC self-renewal. Reactivation of proper Wnt signaling in Zrf1-depleted NPCs restores Pax6 expression and the self-renewal capacity. ESC-derived NPCs in vitro resemble most of the characteristics of the self-renewing NPCs located in the developing embryonic cortex, which are termed radial glial cells (RGCs). Depletion of Zrf1 in vivo impairs the expression of key self-renewal regulators and Wnt ligand genes in RGCs. Thus, we demonstrate that Zrf1 plays an essential role in NPC generation and maintenance. Cold Spring Harbor Laboratory Press 2014-01-15 /pmc/articles/PMC3909791/ /pubmed/24449271 http://dx.doi.org/10.1101/gad.228510.113 Text en © 2014 Aloia et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported), as described at http://creativecommons.org/licenses/by-nc/3.0/. |
spellingShingle | Research Paper Aloia, Luigi Di Stefano, Bruno Sessa, Alessandro Morey, Lluis Santanach, Alexandra Gutierrez, Arantxa Cozzuto, Luca Benitah, Salvador Aznar Graf, Thomas Broccoli, Vania Di Croce, Luciano Zrf1 is required to establish and maintain neural progenitor identity |
title | Zrf1 is required to establish and maintain neural progenitor identity |
title_full | Zrf1 is required to establish and maintain neural progenitor identity |
title_fullStr | Zrf1 is required to establish and maintain neural progenitor identity |
title_full_unstemmed | Zrf1 is required to establish and maintain neural progenitor identity |
title_short | Zrf1 is required to establish and maintain neural progenitor identity |
title_sort | zrf1 is required to establish and maintain neural progenitor identity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909791/ https://www.ncbi.nlm.nih.gov/pubmed/24449271 http://dx.doi.org/10.1101/gad.228510.113 |
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