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Photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment

Thioredoxins (Trxs) play a relevant role in thiol-dependent redox regulation, which allows the rapid adaptation of chloroplast metabolism to unpredictable environmental conditions. In chloroplasts, Trxs use reducing equivalents provided by photoreduced ferredoxin (Fdx) via the action of a ferredoxin...

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Autores principales: Ojeda, Valle, Nájera, Victoria A., González, Maricruz, Pérez-Ruiz, Juan M., Cejudo, Francisco J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640197/
https://www.ncbi.nlm.nih.gov/pubmed/28692378
http://dx.doi.org/10.1080/15592324.2017.1347244
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author Ojeda, Valle
Nájera, Victoria A.
González, Maricruz
Pérez-Ruiz, Juan M.
Cejudo, Francisco J.
author_facet Ojeda, Valle
Nájera, Victoria A.
González, Maricruz
Pérez-Ruiz, Juan M.
Cejudo, Francisco J.
author_sort Ojeda, Valle
collection PubMed
description Thioredoxins (Trxs) play a relevant role in thiol-dependent redox regulation, which allows the rapid adaptation of chloroplast metabolism to unpredictable environmental conditions. In chloroplasts, Trxs use reducing equivalents provided by photoreduced ferredoxin (Fdx) via the action of a ferredoxin-thioredoxin reductase (FTR), thus linking redox regulation to light. In addition, these organelles contain an NADPH-thioredoxin reductase, NTRC, with a Trx domain at the C-terminus. NTRC efficiently reduces 2-Cys peroxiredoxins (Prxs), hence having antioxidant function. However, NTRC also participates in the redox regulation of processes, such as starch and chlorophyll biosynthesis, which are known to be regulated by Trxs. Thus, the question arising is whether there is a cross-talk between the 2 redox systems. Arabidopsis mutants simultaneously devoid of NTRC and Trx x or Trxs f show a dramatic growth inhibition phenotype, indicating that NTRC is required for the function of these unrelated Trxs. Remarkably, both the ntrc-trxx double mutant and, to a higher extent, the ntrc-trxf1f2 triple mutant show high mortality at the seedling stage, which is rescued by sucrose. These findings show the relevant role of redox regulation for chloroplast performance and uncover the key function of cotyledons chloroplasts at the transition to autotrophic metabolism during seedling establishment.
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spelling pubmed-56401972017-10-23 Photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment Ojeda, Valle Nájera, Victoria A. González, Maricruz Pérez-Ruiz, Juan M. Cejudo, Francisco J. Plant Signal Behav Article Addendum Thioredoxins (Trxs) play a relevant role in thiol-dependent redox regulation, which allows the rapid adaptation of chloroplast metabolism to unpredictable environmental conditions. In chloroplasts, Trxs use reducing equivalents provided by photoreduced ferredoxin (Fdx) via the action of a ferredoxin-thioredoxin reductase (FTR), thus linking redox regulation to light. In addition, these organelles contain an NADPH-thioredoxin reductase, NTRC, with a Trx domain at the C-terminus. NTRC efficiently reduces 2-Cys peroxiredoxins (Prxs), hence having antioxidant function. However, NTRC also participates in the redox regulation of processes, such as starch and chlorophyll biosynthesis, which are known to be regulated by Trxs. Thus, the question arising is whether there is a cross-talk between the 2 redox systems. Arabidopsis mutants simultaneously devoid of NTRC and Trx x or Trxs f show a dramatic growth inhibition phenotype, indicating that NTRC is required for the function of these unrelated Trxs. Remarkably, both the ntrc-trxx double mutant and, to a higher extent, the ntrc-trxf1f2 triple mutant show high mortality at the seedling stage, which is rescued by sucrose. These findings show the relevant role of redox regulation for chloroplast performance and uncover the key function of cotyledons chloroplasts at the transition to autotrophic metabolism during seedling establishment. Taylor & Francis 2017-07-10 /pmc/articles/PMC5640197/ /pubmed/28692378 http://dx.doi.org/10.1080/15592324.2017.1347244 Text en © 2017 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Article Addendum
Ojeda, Valle
Nájera, Victoria A.
González, Maricruz
Pérez-Ruiz, Juan M.
Cejudo, Francisco J.
Photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment
title Photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment
title_full Photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment
title_fullStr Photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment
title_full_unstemmed Photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment
title_short Photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment
title_sort photosynthetic activity of cotyledons is critical during post-germinative growth and seedling establishment
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640197/
https://www.ncbi.nlm.nih.gov/pubmed/28692378
http://dx.doi.org/10.1080/15592324.2017.1347244
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