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Chromatin sequesters pioneer transcription factor Sox2 from exerting force on DNA
Biomolecular condensation constitutes an emerging mechanism for transcriptional regulation. Recent studies suggest that the co-condensation between transcription factors (TFs) and DNA can generate mechanical forces driving genome rearrangements. However, the reported forces generated by protein-DNA...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271091/ https://www.ncbi.nlm.nih.gov/pubmed/35810158 http://dx.doi.org/10.1038/s41467-022-31738-x |
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author | Nguyen, Tuan Li, Sai Chang, Jeremy T-H Watters, John W. Ng, Htet Osunsade, Adewola David, Yael Liu, Shixin |
author_facet | Nguyen, Tuan Li, Sai Chang, Jeremy T-H Watters, John W. Ng, Htet Osunsade, Adewola David, Yael Liu, Shixin |
author_sort | Nguyen, Tuan |
collection | PubMed |
description | Biomolecular condensation constitutes an emerging mechanism for transcriptional regulation. Recent studies suggest that the co-condensation between transcription factors (TFs) and DNA can generate mechanical forces driving genome rearrangements. However, the reported forces generated by protein-DNA co-condensation are typically below one piconewton (pN), questioning its physiological significance. Moreover, the force-generating capacity of these condensates in the chromatin context remains unknown. Here, we show that Sox2, a nucleosome-binding pioneer TF, forms co-condensates with DNA and generates forces up to 7 pN, exerting considerable mechanical tension on DNA strands. We find that the disordered domains of Sox2 are required for maximum force generation but not for condensate formation. Furthermore, we show that nucleosomes dramatically attenuate the mechanical stress exerted by Sox2 by sequestering it from coalescing on bare DNA. Our findings reveal that TF-mediated DNA condensation can exert significant mechanical stress on the genome which can nonetheless be attenuated by the chromatin architecture. |
format | Online Article Text |
id | pubmed-9271091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92710912022-07-11 Chromatin sequesters pioneer transcription factor Sox2 from exerting force on DNA Nguyen, Tuan Li, Sai Chang, Jeremy T-H Watters, John W. Ng, Htet Osunsade, Adewola David, Yael Liu, Shixin Nat Commun Article Biomolecular condensation constitutes an emerging mechanism for transcriptional regulation. Recent studies suggest that the co-condensation between transcription factors (TFs) and DNA can generate mechanical forces driving genome rearrangements. However, the reported forces generated by protein-DNA co-condensation are typically below one piconewton (pN), questioning its physiological significance. Moreover, the force-generating capacity of these condensates in the chromatin context remains unknown. Here, we show that Sox2, a nucleosome-binding pioneer TF, forms co-condensates with DNA and generates forces up to 7 pN, exerting considerable mechanical tension on DNA strands. We find that the disordered domains of Sox2 are required for maximum force generation but not for condensate formation. Furthermore, we show that nucleosomes dramatically attenuate the mechanical stress exerted by Sox2 by sequestering it from coalescing on bare DNA. Our findings reveal that TF-mediated DNA condensation can exert significant mechanical stress on the genome which can nonetheless be attenuated by the chromatin architecture. Nature Publishing Group UK 2022-07-09 /pmc/articles/PMC9271091/ /pubmed/35810158 http://dx.doi.org/10.1038/s41467-022-31738-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Nguyen, Tuan Li, Sai Chang, Jeremy T-H Watters, John W. Ng, Htet Osunsade, Adewola David, Yael Liu, Shixin Chromatin sequesters pioneer transcription factor Sox2 from exerting force on DNA |
title | Chromatin sequesters pioneer transcription factor Sox2 from exerting force on DNA |
title_full | Chromatin sequesters pioneer transcription factor Sox2 from exerting force on DNA |
title_fullStr | Chromatin sequesters pioneer transcription factor Sox2 from exerting force on DNA |
title_full_unstemmed | Chromatin sequesters pioneer transcription factor Sox2 from exerting force on DNA |
title_short | Chromatin sequesters pioneer transcription factor Sox2 from exerting force on DNA |
title_sort | chromatin sequesters pioneer transcription factor sox2 from exerting force on dna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271091/ https://www.ncbi.nlm.nih.gov/pubmed/35810158 http://dx.doi.org/10.1038/s41467-022-31738-x |
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