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Photosynthesis-dependent H(2)O(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism

Chloroplasts communicate information by signalling to nuclei during acclimation to fluctuating light. Several potential operating signals originating from chloroplasts have been proposed, but none have been shown to move to nuclei to modulate gene expression. One proposed signal is hydrogen peroxide...

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Autores principales: Exposito-Rodriguez, Marino, Laissue, Pierre Philippe, Yvon-Durocher, Gabriel, Smirnoff, Nicholas, Mullineaux, Philip M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491514/
https://www.ncbi.nlm.nih.gov/pubmed/28663550
http://dx.doi.org/10.1038/s41467-017-00074-w
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author Exposito-Rodriguez, Marino
Laissue, Pierre Philippe
Yvon-Durocher, Gabriel
Smirnoff, Nicholas
Mullineaux, Philip M.
author_facet Exposito-Rodriguez, Marino
Laissue, Pierre Philippe
Yvon-Durocher, Gabriel
Smirnoff, Nicholas
Mullineaux, Philip M.
author_sort Exposito-Rodriguez, Marino
collection PubMed
description Chloroplasts communicate information by signalling to nuclei during acclimation to fluctuating light. Several potential operating signals originating from chloroplasts have been proposed, but none have been shown to move to nuclei to modulate gene expression. One proposed signal is hydrogen peroxide (H(2)O(2)) produced by chloroplasts in a light-dependent manner. Using HyPer2, a genetically encoded fluorescent H(2)O(2) sensor, we show that in photosynthetic Nicotiana benthamiana epidermal cells, exposure to high light increases H(2)O(2) production in chloroplast stroma, cytosol and nuclei. Critically, over-expression of stromal ascorbate peroxidase (H(2)O(2) scavenger) or treatment with DCMU (photosynthesis inhibitor) attenuates nuclear H(2)O(2) accumulation and high light-responsive gene expression. Cytosolic ascorbate peroxidase over-expression has little effect on nuclear H(2)O(2) accumulation and high light-responsive gene expression. This is because the H(2)O(2) derives from a sub-population of chloroplasts closely associated with nuclei. Therefore, direct H(2)O(2) transfer from chloroplasts to nuclei, avoiding the cytosol, enables photosynthetic control over gene expression.
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spelling pubmed-54915142017-07-11 Photosynthesis-dependent H(2)O(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism Exposito-Rodriguez, Marino Laissue, Pierre Philippe Yvon-Durocher, Gabriel Smirnoff, Nicholas Mullineaux, Philip M. Nat Commun Article Chloroplasts communicate information by signalling to nuclei during acclimation to fluctuating light. Several potential operating signals originating from chloroplasts have been proposed, but none have been shown to move to nuclei to modulate gene expression. One proposed signal is hydrogen peroxide (H(2)O(2)) produced by chloroplasts in a light-dependent manner. Using HyPer2, a genetically encoded fluorescent H(2)O(2) sensor, we show that in photosynthetic Nicotiana benthamiana epidermal cells, exposure to high light increases H(2)O(2) production in chloroplast stroma, cytosol and nuclei. Critically, over-expression of stromal ascorbate peroxidase (H(2)O(2) scavenger) or treatment with DCMU (photosynthesis inhibitor) attenuates nuclear H(2)O(2) accumulation and high light-responsive gene expression. Cytosolic ascorbate peroxidase over-expression has little effect on nuclear H(2)O(2) accumulation and high light-responsive gene expression. This is because the H(2)O(2) derives from a sub-population of chloroplasts closely associated with nuclei. Therefore, direct H(2)O(2) transfer from chloroplasts to nuclei, avoiding the cytosol, enables photosynthetic control over gene expression. Nature Publishing Group UK 2017-06-29 /pmc/articles/PMC5491514/ /pubmed/28663550 http://dx.doi.org/10.1038/s41467-017-00074-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Exposito-Rodriguez, Marino
Laissue, Pierre Philippe
Yvon-Durocher, Gabriel
Smirnoff, Nicholas
Mullineaux, Philip M.
Photosynthesis-dependent H(2)O(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism
title Photosynthesis-dependent H(2)O(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism
title_full Photosynthesis-dependent H(2)O(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism
title_fullStr Photosynthesis-dependent H(2)O(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism
title_full_unstemmed Photosynthesis-dependent H(2)O(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism
title_short Photosynthesis-dependent H(2)O(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism
title_sort photosynthesis-dependent h(2)o(2) transfer from chloroplasts to nuclei provides a high-light signalling mechanism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491514/
https://www.ncbi.nlm.nih.gov/pubmed/28663550
http://dx.doi.org/10.1038/s41467-017-00074-w
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