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Chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells

Stem and progenitor cells undergo a global elevation of nascent transcription, or hypertranscription, during key developmental transitions involving rapid cell proliferation. The chromatin remodeler Chd1 mediates hypertranscription in pluripotent cells but its mechanism of action remains poorly unde...

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Autores principales: Bulut-Karslioglu, Aydan, Jin, Hu, Kim, Yun-Kyo, Cho, Brandon, Guzman-Ayala, Marcela, Williamson, Andrew J. K., Hejna, Miroslav, Stötzel, Maximilian, Whetton, Anthony D., Song, Jun S., Ramalho-Santos, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357957/
https://www.ncbi.nlm.nih.gov/pubmed/34381042
http://dx.doi.org/10.1038/s41467-021-25088-3
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author Bulut-Karslioglu, Aydan
Jin, Hu
Kim, Yun-Kyo
Cho, Brandon
Guzman-Ayala, Marcela
Williamson, Andrew J. K.
Hejna, Miroslav
Stötzel, Maximilian
Whetton, Anthony D.
Song, Jun S.
Ramalho-Santos, Miguel
author_facet Bulut-Karslioglu, Aydan
Jin, Hu
Kim, Yun-Kyo
Cho, Brandon
Guzman-Ayala, Marcela
Williamson, Andrew J. K.
Hejna, Miroslav
Stötzel, Maximilian
Whetton, Anthony D.
Song, Jun S.
Ramalho-Santos, Miguel
author_sort Bulut-Karslioglu, Aydan
collection PubMed
description Stem and progenitor cells undergo a global elevation of nascent transcription, or hypertranscription, during key developmental transitions involving rapid cell proliferation. The chromatin remodeler Chd1 mediates hypertranscription in pluripotent cells but its mechanism of action remains poorly understood. Here we report a novel role for Chd1 in protecting genome integrity at promoter regions by preventing DNA double-stranded break (DSB) accumulation in ES cells. Chd1 interacts with several DNA repair factors including Atm, Parp1, Kap1 and Topoisomerase 2β and its absence leads to an accumulation of DSBs at Chd1-bound Pol II-transcribed genes and rDNA. Genes prone to DNA breaks in Chd1 KO ES cells are longer genes with GC-rich promoters, a more labile nucleosomal structure and roles in chromatin regulation, transcription and signaling. These results reveal a vulnerability of hypertranscribing stem cells to accumulation of endogenous DNA breaks, with important implications for developmental and cancer biology.
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spelling pubmed-83579572021-08-30 Chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells Bulut-Karslioglu, Aydan Jin, Hu Kim, Yun-Kyo Cho, Brandon Guzman-Ayala, Marcela Williamson, Andrew J. K. Hejna, Miroslav Stötzel, Maximilian Whetton, Anthony D. Song, Jun S. Ramalho-Santos, Miguel Nat Commun Article Stem and progenitor cells undergo a global elevation of nascent transcription, or hypertranscription, during key developmental transitions involving rapid cell proliferation. The chromatin remodeler Chd1 mediates hypertranscription in pluripotent cells but its mechanism of action remains poorly understood. Here we report a novel role for Chd1 in protecting genome integrity at promoter regions by preventing DNA double-stranded break (DSB) accumulation in ES cells. Chd1 interacts with several DNA repair factors including Atm, Parp1, Kap1 and Topoisomerase 2β and its absence leads to an accumulation of DSBs at Chd1-bound Pol II-transcribed genes and rDNA. Genes prone to DNA breaks in Chd1 KO ES cells are longer genes with GC-rich promoters, a more labile nucleosomal structure and roles in chromatin regulation, transcription and signaling. These results reveal a vulnerability of hypertranscribing stem cells to accumulation of endogenous DNA breaks, with important implications for developmental and cancer biology. Nature Publishing Group UK 2021-08-11 /pmc/articles/PMC8357957/ /pubmed/34381042 http://dx.doi.org/10.1038/s41467-021-25088-3 Text en © The Author(s) 2021 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
Bulut-Karslioglu, Aydan
Jin, Hu
Kim, Yun-Kyo
Cho, Brandon
Guzman-Ayala, Marcela
Williamson, Andrew J. K.
Hejna, Miroslav
Stötzel, Maximilian
Whetton, Anthony D.
Song, Jun S.
Ramalho-Santos, Miguel
Chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells
title Chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells
title_full Chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells
title_fullStr Chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells
title_full_unstemmed Chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells
title_short Chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells
title_sort chd1 protects genome integrity at promoters to sustain hypertranscription in embryonic stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357957/
https://www.ncbi.nlm.nih.gov/pubmed/34381042
http://dx.doi.org/10.1038/s41467-021-25088-3
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