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Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment
The temporal order of DNA replication is regulated during development and is highly correlated with gene expression, histone modifications and 3D genome architecture. We tracked changes in replication timing, gene expression, and chromatin conformation capture (Hi-C) A/B compartments over the first...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627004/ https://www.ncbi.nlm.nih.gov/pubmed/31231024 http://dx.doi.org/10.1016/j.stemcr.2019.05.021 |
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author | Dileep, Vishnu Wilson, Korey A. Marchal, Claire Lyu, Xiaowen Zhao, Peiyao A. Li, Ben Poulet, Axel Bartlett, Daniel A. Rivera-Mulia, Juan Carlos Qin, Zhaohui S. Robins, Allan J. Schulz, Thomas C. Kulik, Michael J. McCord, Rachel Patton Dekker, Job Dalton, Stephen Corces, Victor G. Gilbert, David M. |
author_facet | Dileep, Vishnu Wilson, Korey A. Marchal, Claire Lyu, Xiaowen Zhao, Peiyao A. Li, Ben Poulet, Axel Bartlett, Daniel A. Rivera-Mulia, Juan Carlos Qin, Zhaohui S. Robins, Allan J. Schulz, Thomas C. Kulik, Michael J. McCord, Rachel Patton Dekker, Job Dalton, Stephen Corces, Victor G. Gilbert, David M. |
author_sort | Dileep, Vishnu |
collection | PubMed |
description | The temporal order of DNA replication is regulated during development and is highly correlated with gene expression, histone modifications and 3D genome architecture. We tracked changes in replication timing, gene expression, and chromatin conformation capture (Hi-C) A/B compartments over the first two cell cycles during differentiation of human embryonic stem cells to definitive endoderm. Remarkably, transcriptional programs were irreversibly reprogrammed within the first cell cycle and were largely but not universally coordinated with replication timing changes. Moreover, changes in A/B compartment and several histone modifications that normally correlate strongly with replication timing showed weak correlation during the early cell cycles of differentiation but showed increased alignment in later differentiation stages and in terminally differentiated cell lines. Thus, epigenetic cell fate transitions during early differentiation can occur despite dynamic and discordant changes in otherwise highly correlated genomic properties. |
format | Online Article Text |
id | pubmed-6627004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-66270042019-07-23 Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment Dileep, Vishnu Wilson, Korey A. Marchal, Claire Lyu, Xiaowen Zhao, Peiyao A. Li, Ben Poulet, Axel Bartlett, Daniel A. Rivera-Mulia, Juan Carlos Qin, Zhaohui S. Robins, Allan J. Schulz, Thomas C. Kulik, Michael J. McCord, Rachel Patton Dekker, Job Dalton, Stephen Corces, Victor G. Gilbert, David M. Stem Cell Reports Article The temporal order of DNA replication is regulated during development and is highly correlated with gene expression, histone modifications and 3D genome architecture. We tracked changes in replication timing, gene expression, and chromatin conformation capture (Hi-C) A/B compartments over the first two cell cycles during differentiation of human embryonic stem cells to definitive endoderm. Remarkably, transcriptional programs were irreversibly reprogrammed within the first cell cycle and were largely but not universally coordinated with replication timing changes. Moreover, changes in A/B compartment and several histone modifications that normally correlate strongly with replication timing showed weak correlation during the early cell cycles of differentiation but showed increased alignment in later differentiation stages and in terminally differentiated cell lines. Thus, epigenetic cell fate transitions during early differentiation can occur despite dynamic and discordant changes in otherwise highly correlated genomic properties. Elsevier 2019-06-20 /pmc/articles/PMC6627004/ /pubmed/31231024 http://dx.doi.org/10.1016/j.stemcr.2019.05.021 Text en © 2019 The Author(s) 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 | Article Dileep, Vishnu Wilson, Korey A. Marchal, Claire Lyu, Xiaowen Zhao, Peiyao A. Li, Ben Poulet, Axel Bartlett, Daniel A. Rivera-Mulia, Juan Carlos Qin, Zhaohui S. Robins, Allan J. Schulz, Thomas C. Kulik, Michael J. McCord, Rachel Patton Dekker, Job Dalton, Stephen Corces, Victor G. Gilbert, David M. Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment |
title | Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment |
title_full | Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment |
title_fullStr | Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment |
title_full_unstemmed | Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment |
title_short | Rapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment |
title_sort | rapid irreversible transcriptional reprogramming in human stem cells accompanied by discordance between replication timing and chromatin compartment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627004/ https://www.ncbi.nlm.nih.gov/pubmed/31231024 http://dx.doi.org/10.1016/j.stemcr.2019.05.021 |
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