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Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence
During embryonic brain development, neural progenitor/stem cells (NPCs) sequentially give rise to different subtypes of neurons and glia via a highly orchestrated process. To accomplish the ordered generation of distinct progenies, NPCs go through multistep transitions of their developmental compete...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987727/ https://www.ncbi.nlm.nih.gov/pubmed/29666150 http://dx.doi.org/10.1083/jcb.201802117 |
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author | Yoon, Ki-Jun Vissers, Caroline Ming, Guo-li Song, Hongjun |
author_facet | Yoon, Ki-Jun Vissers, Caroline Ming, Guo-li Song, Hongjun |
author_sort | Yoon, Ki-Jun |
collection | PubMed |
description | During embryonic brain development, neural progenitor/stem cells (NPCs) sequentially give rise to different subtypes of neurons and glia via a highly orchestrated process. To accomplish the ordered generation of distinct progenies, NPCs go through multistep transitions of their developmental competence. The molecular mechanisms driving precise temporal coordination of these transitions remains enigmatic. Epigenetic regulation, including changes in chromatin structures, DNA methylation, and histone modifications, has been extensively investigated in the context of cortical neurogenesis. Recent studies of chemical modifications on RNA, termed epitranscriptomics, have also revealed their critical roles in neural development. In this review, we discuss advances in understanding molecular regulation of the sequential lineage specification of NPCs in the embryonic mammalian brain with a focus on epigenetic and epitranscriptomic mechanisms. In particular, the discovery of lineage-specific gene transcripts undergoing rapid turnover in NPCs suggests that NPC developmental fate competence is determined much earlier, before the final cell division, and is more tightly controlled than previously appreciated. We discuss how multiple regulatory systems work in harmony to coordinate NPC behavior and summarize recent findings in the context of a model of epigenetic and transcriptional prepatterning to explain NPC developmental competence. |
format | Online Article Text |
id | pubmed-5987727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59877272018-12-04 Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence Yoon, Ki-Jun Vissers, Caroline Ming, Guo-li Song, Hongjun J Cell Biol Reviews During embryonic brain development, neural progenitor/stem cells (NPCs) sequentially give rise to different subtypes of neurons and glia via a highly orchestrated process. To accomplish the ordered generation of distinct progenies, NPCs go through multistep transitions of their developmental competence. The molecular mechanisms driving precise temporal coordination of these transitions remains enigmatic. Epigenetic regulation, including changes in chromatin structures, DNA methylation, and histone modifications, has been extensively investigated in the context of cortical neurogenesis. Recent studies of chemical modifications on RNA, termed epitranscriptomics, have also revealed their critical roles in neural development. In this review, we discuss advances in understanding molecular regulation of the sequential lineage specification of NPCs in the embryonic mammalian brain with a focus on epigenetic and epitranscriptomic mechanisms. In particular, the discovery of lineage-specific gene transcripts undergoing rapid turnover in NPCs suggests that NPC developmental fate competence is determined much earlier, before the final cell division, and is more tightly controlled than previously appreciated. We discuss how multiple regulatory systems work in harmony to coordinate NPC behavior and summarize recent findings in the context of a model of epigenetic and transcriptional prepatterning to explain NPC developmental competence. Rockefeller University Press 2018-06-04 /pmc/articles/PMC5987727/ /pubmed/29666150 http://dx.doi.org/10.1083/jcb.201802117 Text en © 2018 Yoon et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Reviews Yoon, Ki-Jun Vissers, Caroline Ming, Guo-li Song, Hongjun Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence |
title | Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence |
title_full | Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence |
title_fullStr | Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence |
title_full_unstemmed | Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence |
title_short | Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence |
title_sort | epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987727/ https://www.ncbi.nlm.nih.gov/pubmed/29666150 http://dx.doi.org/10.1083/jcb.201802117 |
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