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Interplay of the two ancient metabolites auxin and MEcPP regulates adaptive growth

The ancient morphoregulatory hormone auxin dynamically realigns dedicated cellular processes that shape plant growth under prevailing environmental conditions. However, the nature of the stress-responsive signal altering auxin homeostasis remains elusive. Here we establish that the evolutionarily co...

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Autores principales: Jiang, Jishan, Rodriguez-Furlan, Cecilia, Wang, Jin-Zheng, de Souza, Amancio, Ke, Haiyan, Pasternak, Taras, Lasok, Hanna, Ditengou, Franck A., Palme, Klaus, Dehesh, Katayoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995930/
https://www.ncbi.nlm.nih.gov/pubmed/29891932
http://dx.doi.org/10.1038/s41467-018-04708-5
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author Jiang, Jishan
Rodriguez-Furlan, Cecilia
Wang, Jin-Zheng
de Souza, Amancio
Ke, Haiyan
Pasternak, Taras
Lasok, Hanna
Ditengou, Franck A.
Palme, Klaus
Dehesh, Katayoon
author_facet Jiang, Jishan
Rodriguez-Furlan, Cecilia
Wang, Jin-Zheng
de Souza, Amancio
Ke, Haiyan
Pasternak, Taras
Lasok, Hanna
Ditengou, Franck A.
Palme, Klaus
Dehesh, Katayoon
author_sort Jiang, Jishan
collection PubMed
description The ancient morphoregulatory hormone auxin dynamically realigns dedicated cellular processes that shape plant growth under prevailing environmental conditions. However, the nature of the stress-responsive signal altering auxin homeostasis remains elusive. Here we establish that the evolutionarily conserved plastidial retrograde signaling metabolite methylerythritol cyclodiphosphate (MEcPP) controls adaptive growth by dual transcriptional and post-translational regulatory inputs that modulate auxin levels and distribution patterns in response to stress. We demonstrate that in vivo accumulation or exogenous application of MEcPP alters the expression of two auxin reporters, DR5:GFP and DII-VENUS, and reduces the abundance of the auxin-efflux carrier PIN-FORMED1 (PIN1) at the plasma membrane. However, pharmacological intervention with clathrin-mediated endocytosis blocks the PIN1 reduction. This study provides insight into the interplay between these two indispensable signaling metabolites by establishing the mode of MEcPP action in altering auxin homeostasis, and as such, positioning plastidial function as the primary driver of adaptive growth.
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spelling pubmed-59959302018-06-13 Interplay of the two ancient metabolites auxin and MEcPP regulates adaptive growth Jiang, Jishan Rodriguez-Furlan, Cecilia Wang, Jin-Zheng de Souza, Amancio Ke, Haiyan Pasternak, Taras Lasok, Hanna Ditengou, Franck A. Palme, Klaus Dehesh, Katayoon Nat Commun Article The ancient morphoregulatory hormone auxin dynamically realigns dedicated cellular processes that shape plant growth under prevailing environmental conditions. However, the nature of the stress-responsive signal altering auxin homeostasis remains elusive. Here we establish that the evolutionarily conserved plastidial retrograde signaling metabolite methylerythritol cyclodiphosphate (MEcPP) controls adaptive growth by dual transcriptional and post-translational regulatory inputs that modulate auxin levels and distribution patterns in response to stress. We demonstrate that in vivo accumulation or exogenous application of MEcPP alters the expression of two auxin reporters, DR5:GFP and DII-VENUS, and reduces the abundance of the auxin-efflux carrier PIN-FORMED1 (PIN1) at the plasma membrane. However, pharmacological intervention with clathrin-mediated endocytosis blocks the PIN1 reduction. This study provides insight into the interplay between these two indispensable signaling metabolites by establishing the mode of MEcPP action in altering auxin homeostasis, and as such, positioning plastidial function as the primary driver of adaptive growth. Nature Publishing Group UK 2018-06-11 /pmc/articles/PMC5995930/ /pubmed/29891932 http://dx.doi.org/10.1038/s41467-018-04708-5 Text en © The Author(s) 2018 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
Jiang, Jishan
Rodriguez-Furlan, Cecilia
Wang, Jin-Zheng
de Souza, Amancio
Ke, Haiyan
Pasternak, Taras
Lasok, Hanna
Ditengou, Franck A.
Palme, Klaus
Dehesh, Katayoon
Interplay of the two ancient metabolites auxin and MEcPP regulates adaptive growth
title Interplay of the two ancient metabolites auxin and MEcPP regulates adaptive growth
title_full Interplay of the two ancient metabolites auxin and MEcPP regulates adaptive growth
title_fullStr Interplay of the two ancient metabolites auxin and MEcPP regulates adaptive growth
title_full_unstemmed Interplay of the two ancient metabolites auxin and MEcPP regulates adaptive growth
title_short Interplay of the two ancient metabolites auxin and MEcPP regulates adaptive growth
title_sort interplay of the two ancient metabolites auxin and mecpp regulates adaptive growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995930/
https://www.ncbi.nlm.nih.gov/pubmed/29891932
http://dx.doi.org/10.1038/s41467-018-04708-5
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