Abstract

Plants, as sessile organisms, deploy transcriptional dynamics for adapting to extreme growth conditions such as cold stress. Emerging evidence suggests that chromatin architecture contributes to transcriptional regulation. However, the relationship between chromatin architectural dynamics and transcriptional reprogramming in response to cold stress remains unclear. Here, we apply a chemical-crosslinking assisted proximity capture (CAP-C) method to elucidate the fine-scale chromatin landscape, revealing chromatin interactions within gene bodies closely associated with RNA polymerase II (Pol II) densities across initiation, pausing, and termination sites. We observe dynamic changes in chromatin interactions alongside Pol II activity alterations during cold stress, suggesting local chromatin dynamics may regulate Pol II activity. Notably, cold stress does not affect large-scale chromatin conformations. We further identify a comprehensive promoter-promoter interaction (PPI) network across the genome, potentially facilitating co-regulation of gene expression in response to cold stress. Our study deepens the understanding of chromatin conformation-associated gene regulation in plant response to cold.

Plants utilize transcriptional dynamics to adapt to cold stress. Here, Zhang et al. describe a network of chromatin interactions between gene promoters across the Arabidopsis genome that could facilitate co-regulation of gene expression during cold stress.

Details

Title
A fine-scale Arabidopsis chromatin landscape reveals chromatin conformation-associated transcriptional dynamics
Author
Zhang, Yueying 1   VIAFID ORCID Logo  ; Dong, Qianli 2   VIAFID ORCID Logo  ; Wang, Zhen 3   VIAFID ORCID Logo  ; Liu, Qinzhe 4   VIAFID ORCID Logo  ; Yu, Haopeng 5   VIAFID ORCID Logo  ; Sun, Wenqing 2 ; Cheema, Jitender 5 ; You, Qiancheng 4 ; Ding, Ling 2 ; Cao, Xiaofeng 6   VIAFID ORCID Logo  ; He, Chuan 4   VIAFID ORCID Logo  ; Ding, Yiliang 5   VIAFID ORCID Logo  ; Zhang, Huakun 2   VIAFID ORCID Logo 

 Northeast Normal University, Key Laboratory of Molecular Epigenetics of Ministry of Education, Changchun, China (GRID:grid.27446.33) (ISNI:0000 0004 1789 9163); John Innes Centre, Department of Cell and Developmental Biology, Norwich, UK (GRID:grid.14830.3e) (ISNI:0000 0001 2175 7246) 
 Northeast Normal University, Key Laboratory of Molecular Epigenetics of Ministry of Education, Changchun, China (GRID:grid.27446.33) (ISNI:0000 0004 1789 9163) 
 John Innes Centre, Department of Cell and Developmental Biology, Norwich, UK (GRID:grid.14830.3e) (ISNI:0000 0001 2175 7246); Chinese Academy of Sciences, Institute of Genetics and Developmental Biology, Beijing, China (GRID:grid.9227.e) (ISNI:0000000119573309) 
 The University of Chicago, Howard Hughes Medical Institute, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); The University of Chicago, Department of Chemistry, Department of Biochemistry and Molecular Biology, Institute for Biophysical Dynamics, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822) 
 John Innes Centre, Department of Cell and Developmental Biology, Norwich, UK (GRID:grid.14830.3e) (ISNI:0000 0001 2175 7246) 
 Chinese Academy of Sciences, Institute of Genetics and Developmental Biology, Beijing, China (GRID:grid.9227.e) (ISNI:0000000119573309) 
Pages
3253
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3039629585
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.