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CPK28-NLP7 module integrates cold-induced Ca(2+) signal and transcriptional reprogramming in Arabidopsis
Exposure to cold triggers a spike in cytosolic calcium (Ca(2+)) that often leads to transcriptional reprogramming in plants. However, how this Ca(2+) signal is perceived and relayed to the downstream cold signaling pathway remains unknown. Here, we show that the CALCIUM-DEPENDENT PROTEIN KINASE 28 (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242591/ https://www.ncbi.nlm.nih.gov/pubmed/35767615 http://dx.doi.org/10.1126/sciadv.abn7901 |
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author | Ding, Yanglin Yang, Hao Wu, Shifeng Fu, Diyi Li, Minze Gong, Zhizhong Yang, Shuhua |
author_facet | Ding, Yanglin Yang, Hao Wu, Shifeng Fu, Diyi Li, Minze Gong, Zhizhong Yang, Shuhua |
author_sort | Ding, Yanglin |
collection | PubMed |
description | Exposure to cold triggers a spike in cytosolic calcium (Ca(2+)) that often leads to transcriptional reprogramming in plants. However, how this Ca(2+) signal is perceived and relayed to the downstream cold signaling pathway remains unknown. Here, we show that the CALCIUM-DEPENDENT PROTEIN KINASE 28 (CPK28) initiates a phosphorylation cascade to specify transcriptional reprogramming downstream of cold-induced Ca(2+) signal. Plasma membrane (PM)–localized CPK28 is activated rapidly upon cold shock within 10 seconds in a Ca(2+)-dependent manner. CPK28 then phosphorylates and promotes the nuclear translocation of NIN-LIKE PROTEIN 7 (NLP7), a transcription factor that specifies the transcriptional reprogramming of cold-responsive gene sets in response to Ca(2+), thereby positively regulating plant response to cold stress. This study elucidates a previously unidentified mechanism by which the CPK28-NLP7 regulatory module integrates cold-evoked Ca(2+) signal and transcriptome and thus uncovers a key strategy for the rapid perception and transduction of cold signals from the PM to the nucleus. |
format | Online Article Text |
id | pubmed-9242591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-92425912022-07-13 CPK28-NLP7 module integrates cold-induced Ca(2+) signal and transcriptional reprogramming in Arabidopsis Ding, Yanglin Yang, Hao Wu, Shifeng Fu, Diyi Li, Minze Gong, Zhizhong Yang, Shuhua Sci Adv Biomedicine and Life Sciences Exposure to cold triggers a spike in cytosolic calcium (Ca(2+)) that often leads to transcriptional reprogramming in plants. However, how this Ca(2+) signal is perceived and relayed to the downstream cold signaling pathway remains unknown. Here, we show that the CALCIUM-DEPENDENT PROTEIN KINASE 28 (CPK28) initiates a phosphorylation cascade to specify transcriptional reprogramming downstream of cold-induced Ca(2+) signal. Plasma membrane (PM)–localized CPK28 is activated rapidly upon cold shock within 10 seconds in a Ca(2+)-dependent manner. CPK28 then phosphorylates and promotes the nuclear translocation of NIN-LIKE PROTEIN 7 (NLP7), a transcription factor that specifies the transcriptional reprogramming of cold-responsive gene sets in response to Ca(2+), thereby positively regulating plant response to cold stress. This study elucidates a previously unidentified mechanism by which the CPK28-NLP7 regulatory module integrates cold-evoked Ca(2+) signal and transcriptome and thus uncovers a key strategy for the rapid perception and transduction of cold signals from the PM to the nucleus. American Association for the Advancement of Science 2022-06-29 /pmc/articles/PMC9242591/ /pubmed/35767615 http://dx.doi.org/10.1126/sciadv.abn7901 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Ding, Yanglin Yang, Hao Wu, Shifeng Fu, Diyi Li, Minze Gong, Zhizhong Yang, Shuhua CPK28-NLP7 module integrates cold-induced Ca(2+) signal and transcriptional reprogramming in Arabidopsis |
title | CPK28-NLP7 module integrates cold-induced Ca(2+) signal and transcriptional reprogramming in Arabidopsis |
title_full | CPK28-NLP7 module integrates cold-induced Ca(2+) signal and transcriptional reprogramming in Arabidopsis |
title_fullStr | CPK28-NLP7 module integrates cold-induced Ca(2+) signal and transcriptional reprogramming in Arabidopsis |
title_full_unstemmed | CPK28-NLP7 module integrates cold-induced Ca(2+) signal and transcriptional reprogramming in Arabidopsis |
title_short | CPK28-NLP7 module integrates cold-induced Ca(2+) signal and transcriptional reprogramming in Arabidopsis |
title_sort | cpk28-nlp7 module integrates cold-induced ca(2+) signal and transcriptional reprogramming in arabidopsis |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242591/ https://www.ncbi.nlm.nih.gov/pubmed/35767615 http://dx.doi.org/10.1126/sciadv.abn7901 |
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