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A compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast
We herein employ in situ Hi-C with an auxin-inducible degron (AID) system to examine the effect of chromatin remodeling on 3D genome organization in yeast. Eight selected ATP-dependent chromatin remodelers representing various subfamilies contribute to 3D genome organization differently. Among the s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569116/ https://www.ncbi.nlm.nih.gov/pubmed/34737268 http://dx.doi.org/10.1038/s41467-021-26629-6 |
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author | Jo, Hyelim Kim, Taemook Chun, Yujin Jung, Inkyung Lee, Daeyoup |
author_facet | Jo, Hyelim Kim, Taemook Chun, Yujin Jung, Inkyung Lee, Daeyoup |
author_sort | Jo, Hyelim |
collection | PubMed |
description | We herein employ in situ Hi-C with an auxin-inducible degron (AID) system to examine the effect of chromatin remodeling on 3D genome organization in yeast. Eight selected ATP-dependent chromatin remodelers representing various subfamilies contribute to 3D genome organization differently. Among the studied remodelers, the temporary depletions of Chd1p, Swr1p, and Sth1p (a catalytic subunit of the Remodeling the Structure of Chromatin [RSC] complex) cause the most significant defects in intra-chromosomal contacts, and the regulatory roles of these three remodelers in 3D genome organization differ depending on the chromosomal context and cell cycle stage. Furthermore, even though Chd1p and Isw1p are known to share functional similarities/redundancies, their depletions lead to distinct effects on 3D structures. The RSC and cohesin complexes also differentially modulate 3D genome organization within chromosome arm regions, whereas RSC appears to support the function of cohesin in centromeric clustering at G(2) phase. Our work suggests that the ATP-dependent chromatin remodelers control the 3D genome organization of yeast through their chromatin-remodeling activities. |
format | Online Article Text |
id | pubmed-8569116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85691162021-11-15 A compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast Jo, Hyelim Kim, Taemook Chun, Yujin Jung, Inkyung Lee, Daeyoup Nat Commun Article We herein employ in situ Hi-C with an auxin-inducible degron (AID) system to examine the effect of chromatin remodeling on 3D genome organization in yeast. Eight selected ATP-dependent chromatin remodelers representing various subfamilies contribute to 3D genome organization differently. Among the studied remodelers, the temporary depletions of Chd1p, Swr1p, and Sth1p (a catalytic subunit of the Remodeling the Structure of Chromatin [RSC] complex) cause the most significant defects in intra-chromosomal contacts, and the regulatory roles of these three remodelers in 3D genome organization differ depending on the chromosomal context and cell cycle stage. Furthermore, even though Chd1p and Isw1p are known to share functional similarities/redundancies, their depletions lead to distinct effects on 3D structures. The RSC and cohesin complexes also differentially modulate 3D genome organization within chromosome arm regions, whereas RSC appears to support the function of cohesin in centromeric clustering at G(2) phase. Our work suggests that the ATP-dependent chromatin remodelers control the 3D genome organization of yeast through their chromatin-remodeling activities. Nature Publishing Group UK 2021-11-04 /pmc/articles/PMC8569116/ /pubmed/34737268 http://dx.doi.org/10.1038/s41467-021-26629-6 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 Jo, Hyelim Kim, Taemook Chun, Yujin Jung, Inkyung Lee, Daeyoup A compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast |
title | A compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast |
title_full | A compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast |
title_fullStr | A compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast |
title_full_unstemmed | A compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast |
title_short | A compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast |
title_sort | compendium of chromatin contact maps reflecting regulation by chromatin remodelers in budding yeast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569116/ https://www.ncbi.nlm.nih.gov/pubmed/34737268 http://dx.doi.org/10.1038/s41467-021-26629-6 |
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