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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
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.
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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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