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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 (...

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Autores principales: Ding, Yanglin, Yang, Hao, Wu, Shifeng, Fu, Diyi, Li, Minze, Gong, Zhizhong, Yang, Shuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
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.
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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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