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Calcium/calmodulin-mediated microbial symbiotic interactions in plants
Cytoplasmic calcium (Ca(2+)) transients and nuclear Ca(2+) oscillations act as hubs during root nodulation and arbuscular mycorrhizal symbioses. Plants perceive bacterial Nod factors or fungal signals to induce the Ca(2+) oscillation in the nucleus of root hair cells, and subsequently activate calmo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623113/ https://www.ncbi.nlm.nih.gov/pubmed/36330252 http://dx.doi.org/10.3389/fpls.2022.984909 |
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author | Yuan, Peiguo Luo, Feixiong Gleason, Cynthia Poovaiah, B. W. |
author_facet | Yuan, Peiguo Luo, Feixiong Gleason, Cynthia Poovaiah, B. W. |
author_sort | Yuan, Peiguo |
collection | PubMed |
description | Cytoplasmic calcium (Ca(2+)) transients and nuclear Ca(2+) oscillations act as hubs during root nodulation and arbuscular mycorrhizal symbioses. Plants perceive bacterial Nod factors or fungal signals to induce the Ca(2+) oscillation in the nucleus of root hair cells, and subsequently activate calmodulin (CaM) and Ca(2+)/CaM-dependent protein kinase (CCaMK). Ca(2+) and CaM-bound CCaMK phosphorylate transcription factors then initiate down-stream signaling events. In addition, distinct Ca(2+) signatures are activated at different symbiotic stages: microbial colonization and infection; nodule formation; and mycorrhizal development. Ca(2+) acts as a key signal that regulates a complex interplay of downstream responses in many biological processes. This short review focuses on advances in Ca(2+) signaling-regulated symbiotic events. It is meant to be an introduction to readers in and outside the field of bacterial and fungal symbioses. We summarize the molecular mechanisms underlying Ca(2+)/CaM-mediated signaling in fine-tuning both local and systemic symbiotic events. |
format | Online Article Text |
id | pubmed-9623113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96231132022-11-02 Calcium/calmodulin-mediated microbial symbiotic interactions in plants Yuan, Peiguo Luo, Feixiong Gleason, Cynthia Poovaiah, B. W. Front Plant Sci Plant Science Cytoplasmic calcium (Ca(2+)) transients and nuclear Ca(2+) oscillations act as hubs during root nodulation and arbuscular mycorrhizal symbioses. Plants perceive bacterial Nod factors or fungal signals to induce the Ca(2+) oscillation in the nucleus of root hair cells, and subsequently activate calmodulin (CaM) and Ca(2+)/CaM-dependent protein kinase (CCaMK). Ca(2+) and CaM-bound CCaMK phosphorylate transcription factors then initiate down-stream signaling events. In addition, distinct Ca(2+) signatures are activated at different symbiotic stages: microbial colonization and infection; nodule formation; and mycorrhizal development. Ca(2+) acts as a key signal that regulates a complex interplay of downstream responses in many biological processes. This short review focuses on advances in Ca(2+) signaling-regulated symbiotic events. It is meant to be an introduction to readers in and outside the field of bacterial and fungal symbioses. We summarize the molecular mechanisms underlying Ca(2+)/CaM-mediated signaling in fine-tuning both local and systemic symbiotic events. Frontiers Media S.A. 2022-10-18 /pmc/articles/PMC9623113/ /pubmed/36330252 http://dx.doi.org/10.3389/fpls.2022.984909 Text en Copyright © 2022 Yuan, Luo, Gleason and Poovaiah https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Yuan, Peiguo Luo, Feixiong Gleason, Cynthia Poovaiah, B. W. Calcium/calmodulin-mediated microbial symbiotic interactions in plants |
title | Calcium/calmodulin-mediated microbial symbiotic interactions in plants |
title_full | Calcium/calmodulin-mediated microbial symbiotic interactions in plants |
title_fullStr | Calcium/calmodulin-mediated microbial symbiotic interactions in plants |
title_full_unstemmed | Calcium/calmodulin-mediated microbial symbiotic interactions in plants |
title_short | Calcium/calmodulin-mediated microbial symbiotic interactions in plants |
title_sort | calcium/calmodulin-mediated microbial symbiotic interactions in plants |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623113/ https://www.ncbi.nlm.nih.gov/pubmed/36330252 http://dx.doi.org/10.3389/fpls.2022.984909 |
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