Cargando…
Reorganization of the 3D chromatin architecture of rice genomes during heat stress
BACKGROUND: The three-dimensional spatial organization of the genome plays important roles in chromatin accessibility and gene expression in multiple biological processes and has been reported to be altered in response to environmental stress. However, the functional changes in spatial genome organi...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7977607/ https://www.ncbi.nlm.nih.gov/pubmed/33740972 http://dx.doi.org/10.1186/s12915-021-00996-4 |
_version_ | 1783667137996390400 |
---|---|
author | Liang, Zhe Zhang, Qian Ji, Changmian Hu, Guihua Zhang, Pingxian Wang, Yifan Yang, Liwen Gu, Xiaofeng |
author_facet | Liang, Zhe Zhang, Qian Ji, Changmian Hu, Guihua Zhang, Pingxian Wang, Yifan Yang, Liwen Gu, Xiaofeng |
author_sort | Liang, Zhe |
collection | PubMed |
description | BACKGROUND: The three-dimensional spatial organization of the genome plays important roles in chromatin accessibility and gene expression in multiple biological processes and has been reported to be altered in response to environmental stress. However, the functional changes in spatial genome organization during environmental changes in crop plants are poorly understood. RESULTS: Here we perform Hi-C, ATAC-seq, and RNA-seq in two agronomically important rice cultivars, Nipponbare (Nip; Japonica) and 93-11 (Indica), to report a comprehensive profile of nuclear dynamics during heat stress (HS). We show that heat stress affects different levels of chromosome organization, including A/B compartment transition, increase in the size of topologically associated domains, and loss of short-range interactions. The chromatin architectural changes were associated with chromatin accessibility and gene expression changes. Comparative analysis revealed that 93-11 exhibited more dynamic gene expression and chromatin accessibility changes, including HS-related genes, consistent with observed higher HS tolerance in this cultivar. CONCLUSIONS: Our data uncovered higher-order chromatin architecture as a new layer in understanding transcriptional regulation in response to heat stress in rice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-00996-4. |
format | Online Article Text |
id | pubmed-7977607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79776072021-03-22 Reorganization of the 3D chromatin architecture of rice genomes during heat stress Liang, Zhe Zhang, Qian Ji, Changmian Hu, Guihua Zhang, Pingxian Wang, Yifan Yang, Liwen Gu, Xiaofeng BMC Biol Research Article BACKGROUND: The three-dimensional spatial organization of the genome plays important roles in chromatin accessibility and gene expression in multiple biological processes and has been reported to be altered in response to environmental stress. However, the functional changes in spatial genome organization during environmental changes in crop plants are poorly understood. RESULTS: Here we perform Hi-C, ATAC-seq, and RNA-seq in two agronomically important rice cultivars, Nipponbare (Nip; Japonica) and 93-11 (Indica), to report a comprehensive profile of nuclear dynamics during heat stress (HS). We show that heat stress affects different levels of chromosome organization, including A/B compartment transition, increase in the size of topologically associated domains, and loss of short-range interactions. The chromatin architectural changes were associated with chromatin accessibility and gene expression changes. Comparative analysis revealed that 93-11 exhibited more dynamic gene expression and chromatin accessibility changes, including HS-related genes, consistent with observed higher HS tolerance in this cultivar. CONCLUSIONS: Our data uncovered higher-order chromatin architecture as a new layer in understanding transcriptional regulation in response to heat stress in rice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-00996-4. BioMed Central 2021-03-19 /pmc/articles/PMC7977607/ /pubmed/33740972 http://dx.doi.org/10.1186/s12915-021-00996-4 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Liang, Zhe Zhang, Qian Ji, Changmian Hu, Guihua Zhang, Pingxian Wang, Yifan Yang, Liwen Gu, Xiaofeng Reorganization of the 3D chromatin architecture of rice genomes during heat stress |
title | Reorganization of the 3D chromatin architecture of rice genomes during heat stress |
title_full | Reorganization of the 3D chromatin architecture of rice genomes during heat stress |
title_fullStr | Reorganization of the 3D chromatin architecture of rice genomes during heat stress |
title_full_unstemmed | Reorganization of the 3D chromatin architecture of rice genomes during heat stress |
title_short | Reorganization of the 3D chromatin architecture of rice genomes during heat stress |
title_sort | reorganization of the 3d chromatin architecture of rice genomes during heat stress |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7977607/ https://www.ncbi.nlm.nih.gov/pubmed/33740972 http://dx.doi.org/10.1186/s12915-021-00996-4 |
work_keys_str_mv | AT liangzhe reorganizationofthe3dchromatinarchitectureofricegenomesduringheatstress AT zhangqian reorganizationofthe3dchromatinarchitectureofricegenomesduringheatstress AT jichangmian reorganizationofthe3dchromatinarchitectureofricegenomesduringheatstress AT huguihua reorganizationofthe3dchromatinarchitectureofricegenomesduringheatstress AT zhangpingxian reorganizationofthe3dchromatinarchitectureofricegenomesduringheatstress AT wangyifan reorganizationofthe3dchromatinarchitectureofricegenomesduringheatstress AT yangliwen reorganizationofthe3dchromatinarchitectureofricegenomesduringheatstress AT guxiaofeng reorganizationofthe3dchromatinarchitectureofricegenomesduringheatstress |