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Diurnal RNAPII-tethered chromatin interactions are associated with rhythmic gene expression in rice

BACKGROUND: The daily cycling of plant physiological processes is speculated to arise from the coordinated rhythms of gene expression. However, the dynamics of diurnal 3D genome architecture and their potential functions underlying the rhythmic gene expression remain unclear. RESULTS: Here, we revea...

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Autores principales: Deng, Li, Gao, Baibai, Zhao, Lun, Zhang, Ying, Zhang, Qing, Guo, Minrong, Yang, Yongqing, Wang, Shuangqi, Xie, Liang, Lou, Hao, Ma, Meng, Zhang, Wei, Cao, Zhilin, Zhang, Qinghua, McClung, C. Robertson, Li, Guoliang, Li, Xingwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734370/
https://www.ncbi.nlm.nih.gov/pubmed/34991658
http://dx.doi.org/10.1186/s13059-021-02594-7
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author Deng, Li
Gao, Baibai
Zhao, Lun
Zhang, Ying
Zhang, Qing
Guo, Minrong
Yang, Yongqing
Wang, Shuangqi
Xie, Liang
Lou, Hao
Ma, Meng
Zhang, Wei
Cao, Zhilin
Zhang, Qinghua
McClung, C. Robertson
Li, Guoliang
Li, Xingwang
author_facet Deng, Li
Gao, Baibai
Zhao, Lun
Zhang, Ying
Zhang, Qing
Guo, Minrong
Yang, Yongqing
Wang, Shuangqi
Xie, Liang
Lou, Hao
Ma, Meng
Zhang, Wei
Cao, Zhilin
Zhang, Qinghua
McClung, C. Robertson
Li, Guoliang
Li, Xingwang
author_sort Deng, Li
collection PubMed
description BACKGROUND: The daily cycling of plant physiological processes is speculated to arise from the coordinated rhythms of gene expression. However, the dynamics of diurnal 3D genome architecture and their potential functions underlying the rhythmic gene expression remain unclear. RESULTS: Here, we reveal the genome-wide rhythmic occupancy of RNA polymerase II (RNAPII), which precedes mRNA accumulation by approximately 2 h. Rhythmic RNAPII binding dynamically correlates with RNAPII-mediated chromatin architecture remodeling at the genomic level of chromatin interactions, spatial clusters, and chromatin connectivity maps, which are associated with the circadian rhythm of gene expression. Rhythmically expressed genes within the same peak phases of expression are preferentially tethered by RNAPII for coordinated transcription. RNAPII-associated chromatin spatial clusters (CSCs) show high plasticity during the circadian cycle, and rhythmically expressed genes in the morning phase and non-rhythmically expressed genes in the evening phase tend to be enriched in RNAPII-associated CSCs to orchestrate expression. Core circadian clock genes are associated with RNAPII-mediated highly connected chromatin connectivity networks in the morning in contrast to the scattered, sporadic spatial chromatin connectivity in the evening; this indicates that they are transcribed within physical proximity to each other during the AM circadian window and are located in discrete “transcriptional factory” foci in the evening, linking chromatin architecture to coordinated transcription outputs. CONCLUSION: Our findings uncover fundamental diurnal genome folding principles in plants and reveal a distinct higher-order chromosome organization that is crucial for coordinating diurnal dynamics of transcriptional regulation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02594-7.
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spelling pubmed-87343702022-01-07 Diurnal RNAPII-tethered chromatin interactions are associated with rhythmic gene expression in rice Deng, Li Gao, Baibai Zhao, Lun Zhang, Ying Zhang, Qing Guo, Minrong Yang, Yongqing Wang, Shuangqi Xie, Liang Lou, Hao Ma, Meng Zhang, Wei Cao, Zhilin Zhang, Qinghua McClung, C. Robertson Li, Guoliang Li, Xingwang Genome Biol Research BACKGROUND: The daily cycling of plant physiological processes is speculated to arise from the coordinated rhythms of gene expression. However, the dynamics of diurnal 3D genome architecture and their potential functions underlying the rhythmic gene expression remain unclear. RESULTS: Here, we reveal the genome-wide rhythmic occupancy of RNA polymerase II (RNAPII), which precedes mRNA accumulation by approximately 2 h. Rhythmic RNAPII binding dynamically correlates with RNAPII-mediated chromatin architecture remodeling at the genomic level of chromatin interactions, spatial clusters, and chromatin connectivity maps, which are associated with the circadian rhythm of gene expression. Rhythmically expressed genes within the same peak phases of expression are preferentially tethered by RNAPII for coordinated transcription. RNAPII-associated chromatin spatial clusters (CSCs) show high plasticity during the circadian cycle, and rhythmically expressed genes in the morning phase and non-rhythmically expressed genes in the evening phase tend to be enriched in RNAPII-associated CSCs to orchestrate expression. Core circadian clock genes are associated with RNAPII-mediated highly connected chromatin connectivity networks in the morning in contrast to the scattered, sporadic spatial chromatin connectivity in the evening; this indicates that they are transcribed within physical proximity to each other during the AM circadian window and are located in discrete “transcriptional factory” foci in the evening, linking chromatin architecture to coordinated transcription outputs. CONCLUSION: Our findings uncover fundamental diurnal genome folding principles in plants and reveal a distinct higher-order chromosome organization that is crucial for coordinating diurnal dynamics of transcriptional regulation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02594-7. BioMed Central 2022-01-06 /pmc/articles/PMC8734370/ /pubmed/34991658 http://dx.doi.org/10.1186/s13059-021-02594-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Deng, Li
Gao, Baibai
Zhao, Lun
Zhang, Ying
Zhang, Qing
Guo, Minrong
Yang, Yongqing
Wang, Shuangqi
Xie, Liang
Lou, Hao
Ma, Meng
Zhang, Wei
Cao, Zhilin
Zhang, Qinghua
McClung, C. Robertson
Li, Guoliang
Li, Xingwang
Diurnal RNAPII-tethered chromatin interactions are associated with rhythmic gene expression in rice
title Diurnal RNAPII-tethered chromatin interactions are associated with rhythmic gene expression in rice
title_full Diurnal RNAPII-tethered chromatin interactions are associated with rhythmic gene expression in rice
title_fullStr Diurnal RNAPII-tethered chromatin interactions are associated with rhythmic gene expression in rice
title_full_unstemmed Diurnal RNAPII-tethered chromatin interactions are associated with rhythmic gene expression in rice
title_short Diurnal RNAPII-tethered chromatin interactions are associated with rhythmic gene expression in rice
title_sort diurnal rnapii-tethered chromatin interactions are associated with rhythmic gene expression in rice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734370/
https://www.ncbi.nlm.nih.gov/pubmed/34991658
http://dx.doi.org/10.1186/s13059-021-02594-7
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