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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,...
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/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. |
format | Online Article Text |
id | pubmed-8087716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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