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Tracking the embryonic stem cell transition from ground state pluripotency
Mouse embryonic stem (ES) cells are locked into self-renewal by shielding from inductive cues. Release from this ground state in minimal conditions offers a system for delineating developmental progression from naïve pluripotency. Here, we examine the initial transition process. The ES cell populati...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399622/ https://www.ncbi.nlm.nih.gov/pubmed/28174249 http://dx.doi.org/10.1242/dev.142711 |
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author | Kalkan, Tüzer Olova, Nelly Roode, Mila Mulas, Carla Lee, Heather J. Nett, Isabelle Marks, Hendrik Walker, Rachael Stunnenberg, Hendrik G. Lilley, Kathryn S. Nichols, Jennifer Reik, Wolf Bertone, Paul Smith, Austin |
author_facet | Kalkan, Tüzer Olova, Nelly Roode, Mila Mulas, Carla Lee, Heather J. Nett, Isabelle Marks, Hendrik Walker, Rachael Stunnenberg, Hendrik G. Lilley, Kathryn S. Nichols, Jennifer Reik, Wolf Bertone, Paul Smith, Austin |
author_sort | Kalkan, Tüzer |
collection | PubMed |
description | Mouse embryonic stem (ES) cells are locked into self-renewal by shielding from inductive cues. Release from this ground state in minimal conditions offers a system for delineating developmental progression from naïve pluripotency. Here, we examine the initial transition process. The ES cell population behaves asynchronously. We therefore exploited a short-half-life Rex1::GFP reporter to isolate cells either side of exit from naïve status. Extinction of ES cell identity in single cells is acute. It occurs only after near-complete elimination of naïve pluripotency factors, but precedes appearance of lineage specification markers. Cells newly departed from the ES cell state display features of early post-implantation epiblast and are distinct from primed epiblast. They also exhibit a genome-wide increase in DNA methylation, intermediate between early and late epiblast. These findings are consistent with the proposition that naïve cells transition to a distinct formative phase of pluripotency preparatory to lineage priming. |
format | Online Article Text |
id | pubmed-5399622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53996222017-05-16 Tracking the embryonic stem cell transition from ground state pluripotency Kalkan, Tüzer Olova, Nelly Roode, Mila Mulas, Carla Lee, Heather J. Nett, Isabelle Marks, Hendrik Walker, Rachael Stunnenberg, Hendrik G. Lilley, Kathryn S. Nichols, Jennifer Reik, Wolf Bertone, Paul Smith, Austin Development Stem Cells and Regeneration Mouse embryonic stem (ES) cells are locked into self-renewal by shielding from inductive cues. Release from this ground state in minimal conditions offers a system for delineating developmental progression from naïve pluripotency. Here, we examine the initial transition process. The ES cell population behaves asynchronously. We therefore exploited a short-half-life Rex1::GFP reporter to isolate cells either side of exit from naïve status. Extinction of ES cell identity in single cells is acute. It occurs only after near-complete elimination of naïve pluripotency factors, but precedes appearance of lineage specification markers. Cells newly departed from the ES cell state display features of early post-implantation epiblast and are distinct from primed epiblast. They also exhibit a genome-wide increase in DNA methylation, intermediate between early and late epiblast. These findings are consistent with the proposition that naïve cells transition to a distinct formative phase of pluripotency preparatory to lineage priming. The Company of Biologists Ltd 2017-04-01 /pmc/articles/PMC5399622/ /pubmed/28174249 http://dx.doi.org/10.1242/dev.142711 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Stem Cells and Regeneration Kalkan, Tüzer Olova, Nelly Roode, Mila Mulas, Carla Lee, Heather J. Nett, Isabelle Marks, Hendrik Walker, Rachael Stunnenberg, Hendrik G. Lilley, Kathryn S. Nichols, Jennifer Reik, Wolf Bertone, Paul Smith, Austin Tracking the embryonic stem cell transition from ground state pluripotency |
title | Tracking the embryonic stem cell transition from ground state pluripotency |
title_full | Tracking the embryonic stem cell transition from ground state pluripotency |
title_fullStr | Tracking the embryonic stem cell transition from ground state pluripotency |
title_full_unstemmed | Tracking the embryonic stem cell transition from ground state pluripotency |
title_short | Tracking the embryonic stem cell transition from ground state pluripotency |
title_sort | tracking the embryonic stem cell transition from ground state pluripotency |
topic | Stem Cells and Regeneration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399622/ https://www.ncbi.nlm.nih.gov/pubmed/28174249 http://dx.doi.org/10.1242/dev.142711 |
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