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The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis
In the developing retina, multipotent neural progenitors undergo unidirectional differentiation in a precise spatiotemporal order. Here we profile the epigenetic and transcriptional changes that occur during retinogenesis in mice and humans. Although some progenitor genes and cell cycle genes were e...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508517/ https://www.ncbi.nlm.nih.gov/pubmed/28472656 http://dx.doi.org/10.1016/j.neuron.2017.04.022 |
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author | Aldiri, Issam Xu, Beisi Wang, Lu Chen, Xiang Hiler, Daniel Griffiths, Lyra Valentine, Marc Shirinifard, Abbas Thiagarajan, Suresh Sablauer, Andras Barabas, Marie-Elizabeth Zhang, Jiakun Johnson, Dianna Frase, Sharon Zhou, Xin Easton, John Zhang, Jinghui Mardis, Elaine R. Wilson, Richard K. Downing, James R. Dyer, Michael A. |
author_facet | Aldiri, Issam Xu, Beisi Wang, Lu Chen, Xiang Hiler, Daniel Griffiths, Lyra Valentine, Marc Shirinifard, Abbas Thiagarajan, Suresh Sablauer, Andras Barabas, Marie-Elizabeth Zhang, Jiakun Johnson, Dianna Frase, Sharon Zhou, Xin Easton, John Zhang, Jinghui Mardis, Elaine R. Wilson, Richard K. Downing, James R. Dyer, Michael A. |
author_sort | Aldiri, Issam |
collection | PubMed |
description | In the developing retina, multipotent neural progenitors undergo unidirectional differentiation in a precise spatiotemporal order. Here we profile the epigenetic and transcriptional changes that occur during retinogenesis in mice and humans. Although some progenitor genes and cell cycle genes were epigenetically silenced during retinogenesis, the most dramatic change was derepression of cell type–specific differentiation programs. We identified developmental stage–specific super-enhancers and showed that most epigenetic changes are conserved in humans and mice. To determine how the epigenome changes during tumorigenesis and reprogramming, we performed integrated epigenetic analysis of murine and human retinoblastomas and induced pluripotent stem cells (iPSCs) derived from murine rod photoreceptors. The retinoblastoma epigenome mapped to the developmental stage when retinal progenitors switch from neurogenic to a terminal patterns of cell division. The epigenome of retinoblastomas was more similar to that of normal retina than was that of retina-derived iPSCs, and we identified retina-specific epigenetic memory. |
format | Online Article Text |
id | pubmed-5508517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-55085172018-05-03 The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis Aldiri, Issam Xu, Beisi Wang, Lu Chen, Xiang Hiler, Daniel Griffiths, Lyra Valentine, Marc Shirinifard, Abbas Thiagarajan, Suresh Sablauer, Andras Barabas, Marie-Elizabeth Zhang, Jiakun Johnson, Dianna Frase, Sharon Zhou, Xin Easton, John Zhang, Jinghui Mardis, Elaine R. Wilson, Richard K. Downing, James R. Dyer, Michael A. Neuron Article In the developing retina, multipotent neural progenitors undergo unidirectional differentiation in a precise spatiotemporal order. Here we profile the epigenetic and transcriptional changes that occur during retinogenesis in mice and humans. Although some progenitor genes and cell cycle genes were epigenetically silenced during retinogenesis, the most dramatic change was derepression of cell type–specific differentiation programs. We identified developmental stage–specific super-enhancers and showed that most epigenetic changes are conserved in humans and mice. To determine how the epigenome changes during tumorigenesis and reprogramming, we performed integrated epigenetic analysis of murine and human retinoblastomas and induced pluripotent stem cells (iPSCs) derived from murine rod photoreceptors. The retinoblastoma epigenome mapped to the developmental stage when retinal progenitors switch from neurogenic to a terminal patterns of cell division. The epigenome of retinoblastomas was more similar to that of normal retina than was that of retina-derived iPSCs, and we identified retina-specific epigenetic memory. 2017-05-03 /pmc/articles/PMC5508517/ /pubmed/28472656 http://dx.doi.org/10.1016/j.neuron.2017.04.022 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This manuscript version is made available under the CC BY-NC-ND 4.0 license. |
spellingShingle | Article Aldiri, Issam Xu, Beisi Wang, Lu Chen, Xiang Hiler, Daniel Griffiths, Lyra Valentine, Marc Shirinifard, Abbas Thiagarajan, Suresh Sablauer, Andras Barabas, Marie-Elizabeth Zhang, Jiakun Johnson, Dianna Frase, Sharon Zhou, Xin Easton, John Zhang, Jinghui Mardis, Elaine R. Wilson, Richard K. Downing, James R. Dyer, Michael A. The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis |
title | The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis |
title_full | The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis |
title_fullStr | The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis |
title_full_unstemmed | The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis |
title_short | The Dynamic Epigenetic Landscape of the Retina During Development, Reprogramming, and Tumorigenesis |
title_sort | dynamic epigenetic landscape of the retina during development, reprogramming, and tumorigenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508517/ https://www.ncbi.nlm.nih.gov/pubmed/28472656 http://dx.doi.org/10.1016/j.neuron.2017.04.022 |
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