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FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells
The chromatin regulator FACT (facilitates chromatin transcription) is essential for ensuring stable gene expression by promoting transcription. In a genetic screen using Caenorhabditis elegans, we identified that FACT maintains cell identities and acts as a barrier for transcription factor-mediated...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137076/ https://www.ncbi.nlm.nih.gov/pubmed/30078731 http://dx.doi.org/10.1016/j.devcel.2018.07.006 |
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author | Kolundzic, Ena Ofenbauer, Andreas Bulut, Selman I. Uyar, Bora Baytek, Gülkiz Sommermeier, Anne Seelk, Stefanie He, Mei Hirsekorn, Antje Vucicevic, Dubravka Akalin, Altuna Diecke, Sebastian Lacadie, Scott A. Tursun, Baris |
author_facet | Kolundzic, Ena Ofenbauer, Andreas Bulut, Selman I. Uyar, Bora Baytek, Gülkiz Sommermeier, Anne Seelk, Stefanie He, Mei Hirsekorn, Antje Vucicevic, Dubravka Akalin, Altuna Diecke, Sebastian Lacadie, Scott A. Tursun, Baris |
author_sort | Kolundzic, Ena |
collection | PubMed |
description | The chromatin regulator FACT (facilitates chromatin transcription) is essential for ensuring stable gene expression by promoting transcription. In a genetic screen using Caenorhabditis elegans, we identified that FACT maintains cell identities and acts as a barrier for transcription factor-mediated cell fate reprogramming. Strikingly, FACT’s role as a barrier to cell fate conversion is conserved in humans as we show that FACT depletion enhances reprogramming of fibroblasts. Such activity is unexpected because FACT is known as a positive regulator of gene expression, and previously described reprogramming barriers typically repress gene expression. While FACT depletion in human fibroblasts results in decreased expression of many genes, a number of FACT-occupied genes, including reprogramming-promoting factors, show increased expression upon FACT depletion, suggesting a repressive function of FACT. Our findings identify FACT as a cellular reprogramming barrier in C. elegans and humans, revealing an evolutionarily conserved mechanism for cell fate protection. |
format | Online Article Text |
id | pubmed-6137076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61370762018-09-19 FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells Kolundzic, Ena Ofenbauer, Andreas Bulut, Selman I. Uyar, Bora Baytek, Gülkiz Sommermeier, Anne Seelk, Stefanie He, Mei Hirsekorn, Antje Vucicevic, Dubravka Akalin, Altuna Diecke, Sebastian Lacadie, Scott A. Tursun, Baris Dev Cell Article The chromatin regulator FACT (facilitates chromatin transcription) is essential for ensuring stable gene expression by promoting transcription. In a genetic screen using Caenorhabditis elegans, we identified that FACT maintains cell identities and acts as a barrier for transcription factor-mediated cell fate reprogramming. Strikingly, FACT’s role as a barrier to cell fate conversion is conserved in humans as we show that FACT depletion enhances reprogramming of fibroblasts. Such activity is unexpected because FACT is known as a positive regulator of gene expression, and previously described reprogramming barriers typically repress gene expression. While FACT depletion in human fibroblasts results in decreased expression of many genes, a number of FACT-occupied genes, including reprogramming-promoting factors, show increased expression upon FACT depletion, suggesting a repressive function of FACT. Our findings identify FACT as a cellular reprogramming barrier in C. elegans and humans, revealing an evolutionarily conserved mechanism for cell fate protection. Cell Press 2018-09-10 /pmc/articles/PMC6137076/ /pubmed/30078731 http://dx.doi.org/10.1016/j.devcel.2018.07.006 Text en © 2018 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 | Article Kolundzic, Ena Ofenbauer, Andreas Bulut, Selman I. Uyar, Bora Baytek, Gülkiz Sommermeier, Anne Seelk, Stefanie He, Mei Hirsekorn, Antje Vucicevic, Dubravka Akalin, Altuna Diecke, Sebastian Lacadie, Scott A. Tursun, Baris FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells |
title | FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells |
title_full | FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells |
title_fullStr | FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells |
title_full_unstemmed | FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells |
title_short | FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells |
title_sort | fact sets a barrier for cell fate reprogramming in caenorhabditis elegans and human cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137076/ https://www.ncbi.nlm.nih.gov/pubmed/30078731 http://dx.doi.org/10.1016/j.devcel.2018.07.006 |
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