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Chromatin accessibility and translational landscapes of tea plants under chilling stress

Plants have evolved regulatory mechanisms at multiple levels to regulate gene expression in order to improve their cold adaptability. However, limited information is available regarding the stress response at the chromatin and translational levels. Here, we characterize the chromatin accessibility,...

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Autores principales: Wang, Pengjie, Jin, Shan, Chen, Xuejin, Wu, Liangyu, Zheng, Yucheng, Yue, Chuan, Guo, Yongchun, Zhang, Xingtan, Yang, Jiangfan, Ye, Naixing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087716/
https://www.ncbi.nlm.nih.gov/pubmed/33931606
http://dx.doi.org/10.1038/s41438-021-00529-8
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author Wang, Pengjie
Jin, Shan
Chen, Xuejin
Wu, Liangyu
Zheng, Yucheng
Yue, Chuan
Guo, Yongchun
Zhang, Xingtan
Yang, Jiangfan
Ye, Naixing
author_facet Wang, Pengjie
Jin, Shan
Chen, Xuejin
Wu, Liangyu
Zheng, Yucheng
Yue, Chuan
Guo, Yongchun
Zhang, Xingtan
Yang, Jiangfan
Ye, Naixing
author_sort Wang, Pengjie
collection PubMed
description Plants have evolved regulatory mechanisms at multiple levels to regulate gene expression in order to improve their cold adaptability. However, limited information is available regarding the stress response at the chromatin and translational levels. Here, we characterize the chromatin accessibility, transcriptional, and translational landscapes of tea plants in vivo under chilling stress for the first time. Chilling stress significantly affected both the transcription and translation levels as well as the translation efficiency of tea plants. A total of 3010 genes that underwent rapid and independent translation under chilling stress were observed, and they were significantly enriched in the photosynthesis-antenna protein and phenylpropanoid biosynthesis pathways. A set of genes that were significantly responsive to cold at the transcription and translation levels, including four (+)-neomenthol dehydrogenases (MNDs) and two (E)-nerolidol synthases (NESs) arranged in tandem on the chromosomes, were also found. We detected potential upstream open reading frames (uORFs) on 3082 genes and found that tea plants may inhibit the overall expression of genes by enhancing the translation of uORFs under chilling stress. In addition, we identified distal transposase hypersensitive sites (THSs) and proximal THSs and constructed a transcriptional regulatory network for tea plants under chilling stress. We also identified 13 high-confidence transcription factors (TFs) that may play a crucial role in cold regulation. These results provide valuable information regarding the potential transcriptional regulatory network in plants and help to clarify how plants exhibit flexible responses to chilling stress.
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spelling pubmed-80877162021-05-05 Chromatin accessibility and translational landscapes of tea plants under chilling stress Wang, Pengjie Jin, Shan Chen, Xuejin Wu, Liangyu Zheng, Yucheng Yue, Chuan Guo, Yongchun Zhang, Xingtan Yang, Jiangfan Ye, Naixing Hortic Res Article Plants have evolved regulatory mechanisms at multiple levels to regulate gene expression in order to improve their cold adaptability. However, limited information is available regarding the stress response at the chromatin and translational levels. Here, we characterize the chromatin accessibility, transcriptional, and translational landscapes of tea plants in vivo under chilling stress for the first time. Chilling stress significantly affected both the transcription and translation levels as well as the translation efficiency of tea plants. A total of 3010 genes that underwent rapid and independent translation under chilling stress were observed, and they were significantly enriched in the photosynthesis-antenna protein and phenylpropanoid biosynthesis pathways. A set of genes that were significantly responsive to cold at the transcription and translation levels, including four (+)-neomenthol dehydrogenases (MNDs) and two (E)-nerolidol synthases (NESs) arranged in tandem on the chromosomes, were also found. We detected potential upstream open reading frames (uORFs) on 3082 genes and found that tea plants may inhibit the overall expression of genes by enhancing the translation of uORFs under chilling stress. In addition, we identified distal transposase hypersensitive sites (THSs) and proximal THSs and constructed a transcriptional regulatory network for tea plants under chilling stress. We also identified 13 high-confidence transcription factors (TFs) that may play a crucial role in cold regulation. These results provide valuable information regarding the potential transcriptional regulatory network in plants and help to clarify how plants exhibit flexible responses to chilling stress. Nature Publishing Group UK 2021-05-01 /pmc/articles/PMC8087716/ /pubmed/33931606 http://dx.doi.org/10.1038/s41438-021-00529-8 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
Wang, Pengjie
Jin, Shan
Chen, Xuejin
Wu, Liangyu
Zheng, Yucheng
Yue, Chuan
Guo, Yongchun
Zhang, Xingtan
Yang, Jiangfan
Ye, Naixing
Chromatin accessibility and translational landscapes of tea plants under chilling stress
title Chromatin accessibility and translational landscapes of tea plants under chilling stress
title_full Chromatin accessibility and translational landscapes of tea plants under chilling stress
title_fullStr Chromatin accessibility and translational landscapes of tea plants under chilling stress
title_full_unstemmed Chromatin accessibility and translational landscapes of tea plants under chilling stress
title_short Chromatin accessibility and translational landscapes of tea plants under chilling stress
title_sort chromatin accessibility and translational landscapes of tea plants under chilling stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087716/
https://www.ncbi.nlm.nih.gov/pubmed/33931606
http://dx.doi.org/10.1038/s41438-021-00529-8
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