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Dynamic 3D Chromatin Reorganization during Establishment and Maintenance of Pluripotency

Higher-order chromatin structure is tightly linked to gene expression and therefore cell identity. In recent years, the chromatin landscape of pluripotent stem cells has become better characterized, and unique features at various architectural levels have been revealed. However, the mechanisms that...

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Detalles Bibliográficos
Autores principales: Pelham-Webb, Bobbie, Murphy, Dylan, Apostolou, Effie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724465/
https://www.ncbi.nlm.nih.gov/pubmed/33242398
http://dx.doi.org/10.1016/j.stemcr.2020.10.012
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author Pelham-Webb, Bobbie
Murphy, Dylan
Apostolou, Effie
author_facet Pelham-Webb, Bobbie
Murphy, Dylan
Apostolou, Effie
author_sort Pelham-Webb, Bobbie
collection PubMed
description Higher-order chromatin structure is tightly linked to gene expression and therefore cell identity. In recent years, the chromatin landscape of pluripotent stem cells has become better characterized, and unique features at various architectural levels have been revealed. However, the mechanisms that govern establishment and maintenance of these topological characteristics and the temporal and functional relationships with transcriptional or epigenetic features are still areas of intense study. Here, we will discuss progress and limitations of our current understanding regarding how the 3D chromatin topology of pluripotent stem cells is established during somatic cell reprogramming and maintained during cell division. We will also discuss evidence and theories about the driving forces of topological reorganization and the functional links with key features and properties of pluripotent stem cell identity.
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spelling pubmed-77244652020-12-13 Dynamic 3D Chromatin Reorganization during Establishment and Maintenance of Pluripotency Pelham-Webb, Bobbie Murphy, Dylan Apostolou, Effie Stem Cell Reports Review Higher-order chromatin structure is tightly linked to gene expression and therefore cell identity. In recent years, the chromatin landscape of pluripotent stem cells has become better characterized, and unique features at various architectural levels have been revealed. However, the mechanisms that govern establishment and maintenance of these topological characteristics and the temporal and functional relationships with transcriptional or epigenetic features are still areas of intense study. Here, we will discuss progress and limitations of our current understanding regarding how the 3D chromatin topology of pluripotent stem cells is established during somatic cell reprogramming and maintained during cell division. We will also discuss evidence and theories about the driving forces of topological reorganization and the functional links with key features and properties of pluripotent stem cell identity. Elsevier 2020-11-25 /pmc/articles/PMC7724465/ /pubmed/33242398 http://dx.doi.org/10.1016/j.stemcr.2020.10.012 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Pelham-Webb, Bobbie
Murphy, Dylan
Apostolou, Effie
Dynamic 3D Chromatin Reorganization during Establishment and Maintenance of Pluripotency
title Dynamic 3D Chromatin Reorganization during Establishment and Maintenance of Pluripotency
title_full Dynamic 3D Chromatin Reorganization during Establishment and Maintenance of Pluripotency
title_fullStr Dynamic 3D Chromatin Reorganization during Establishment and Maintenance of Pluripotency
title_full_unstemmed Dynamic 3D Chromatin Reorganization during Establishment and Maintenance of Pluripotency
title_short Dynamic 3D Chromatin Reorganization during Establishment and Maintenance of Pluripotency
title_sort dynamic 3d chromatin reorganization during establishment and maintenance of pluripotency
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724465/
https://www.ncbi.nlm.nih.gov/pubmed/33242398
http://dx.doi.org/10.1016/j.stemcr.2020.10.012
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