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Thiol-based redox signaling in the nitrogen-fixing symbiosis
In nitrogen poor soils legumes establish a symbiotic interaction with rhizobia that results in the formation of root nodules. These are unique plant organs where bacteria differentiate into bacteroids, which express the nitrogenase enzyme complex that reduces atmospheric N (2) to ammonia. Nodule met...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783977/ https://www.ncbi.nlm.nih.gov/pubmed/24133498 http://dx.doi.org/10.3389/fpls.2013.00376 |
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author | Frendo, Pierre Matamoros, Manuel A. Alloing, Geneviève Becana, Manuel |
author_facet | Frendo, Pierre Matamoros, Manuel A. Alloing, Geneviève Becana, Manuel |
author_sort | Frendo, Pierre |
collection | PubMed |
description | In nitrogen poor soils legumes establish a symbiotic interaction with rhizobia that results in the formation of root nodules. These are unique plant organs where bacteria differentiate into bacteroids, which express the nitrogenase enzyme complex that reduces atmospheric N (2) to ammonia. Nodule metabolism requires a tight control of the concentrations of reactive oxygen and nitrogen species (RONS) so that they can perform useful signaling roles while avoiding nitro-oxidative damage. In nodules a thiol-dependent regulatory network that senses, transmits and responds to redox changes is starting to be elucidated. A combination of enzymatic, immunological, pharmacological and molecular analyses has allowed us to conclude that glutathione and its legume-specific homolog, homoglutathione, are abundant in meristematic and infected cells, that their spatio-temporally distribution is correlated with the corresponding (homo)glutathione synthetase activities, and that they are crucial for nodule development and function. Glutathione is at high concentrations in the bacteroids and at moderate amounts in the mitochondria, cytosol and nuclei. Less information is available on other components of the network. The expression of multiple isoforms of glutathione peroxidases, peroxiredoxins, thioredoxins, glutaredoxins and NADPH-thioredoxin reductases has been detected in nodule cells using antibodies and proteomics. Peroxiredoxins and thioredoxins are essential to regulate and in some cases to detoxify RONS in nodules. Further research is necessary to clarify the regulation of the expression and activity of thiol redox-active proteins in response to abiotic, biotic and developmental cues, their interactions with downstream targets by disulfide-exchange reactions, and their participation in signaling cascades. The availability of mutants and transgenic lines will be crucial to facilitate systematic investigations into the function of the various proteins in the legume-rhizobial symbiosis. |
format | Online Article Text |
id | pubmed-3783977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37839772013-10-16 Thiol-based redox signaling in the nitrogen-fixing symbiosis Frendo, Pierre Matamoros, Manuel A. Alloing, Geneviève Becana, Manuel Front Plant Sci Plant Science In nitrogen poor soils legumes establish a symbiotic interaction with rhizobia that results in the formation of root nodules. These are unique plant organs where bacteria differentiate into bacteroids, which express the nitrogenase enzyme complex that reduces atmospheric N (2) to ammonia. Nodule metabolism requires a tight control of the concentrations of reactive oxygen and nitrogen species (RONS) so that they can perform useful signaling roles while avoiding nitro-oxidative damage. In nodules a thiol-dependent regulatory network that senses, transmits and responds to redox changes is starting to be elucidated. A combination of enzymatic, immunological, pharmacological and molecular analyses has allowed us to conclude that glutathione and its legume-specific homolog, homoglutathione, are abundant in meristematic and infected cells, that their spatio-temporally distribution is correlated with the corresponding (homo)glutathione synthetase activities, and that they are crucial for nodule development and function. Glutathione is at high concentrations in the bacteroids and at moderate amounts in the mitochondria, cytosol and nuclei. Less information is available on other components of the network. The expression of multiple isoforms of glutathione peroxidases, peroxiredoxins, thioredoxins, glutaredoxins and NADPH-thioredoxin reductases has been detected in nodule cells using antibodies and proteomics. Peroxiredoxins and thioredoxins are essential to regulate and in some cases to detoxify RONS in nodules. Further research is necessary to clarify the regulation of the expression and activity of thiol redox-active proteins in response to abiotic, biotic and developmental cues, their interactions with downstream targets by disulfide-exchange reactions, and their participation in signaling cascades. The availability of mutants and transgenic lines will be crucial to facilitate systematic investigations into the function of the various proteins in the legume-rhizobial symbiosis. Frontiers Media S.A. 2013-09-26 /pmc/articles/PMC3783977/ /pubmed/24133498 http://dx.doi.org/10.3389/fpls.2013.00376 Text en Copyright © Frendo, Matamoros, Alloing and Becana. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Frendo, Pierre Matamoros, Manuel A. Alloing, Geneviève Becana, Manuel Thiol-based redox signaling in the nitrogen-fixing symbiosis |
title | Thiol-based redox signaling in the nitrogen-fixing symbiosis |
title_full | Thiol-based redox signaling in the nitrogen-fixing symbiosis |
title_fullStr | Thiol-based redox signaling in the nitrogen-fixing symbiosis |
title_full_unstemmed | Thiol-based redox signaling in the nitrogen-fixing symbiosis |
title_short | Thiol-based redox signaling in the nitrogen-fixing symbiosis |
title_sort | thiol-based redox signaling in the nitrogen-fixing symbiosis |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783977/ https://www.ncbi.nlm.nih.gov/pubmed/24133498 http://dx.doi.org/10.3389/fpls.2013.00376 |
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