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Micrografting Provides Evidence for Systemic Regulation of Sulfur Metabolism between Shoot and Root

The uptake of sulfate by roots and its reductive assimilation mainly in the leaves are not only essential for plant growth and development but also for defense responses against biotic and abiotic stresses. The latter functions result in stimulus-induced fluctuations of sulfur demand at the cellular...

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Autores principales: Forieri, Ilaria, Aref, Rasha, Wirtz, Markus, Hell, Rüdiger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402062/
https://www.ncbi.nlm.nih.gov/pubmed/34451773
http://dx.doi.org/10.3390/plants10081729
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author Forieri, Ilaria
Aref, Rasha
Wirtz, Markus
Hell, Rüdiger
author_facet Forieri, Ilaria
Aref, Rasha
Wirtz, Markus
Hell, Rüdiger
author_sort Forieri, Ilaria
collection PubMed
description The uptake of sulfate by roots and its reductive assimilation mainly in the leaves are not only essential for plant growth and development but also for defense responses against biotic and abiotic stresses. The latter functions result in stimulus-induced fluctuations of sulfur demand at the cellular level. However, the maintenance and acclimation of sulfur homeostasis at local and systemic levels is not fully understood. Previous research mostly focused on signaling in response to external sulfate supply to roots. Here we apply micrografting of Arabidopsis wildtype knock-down sir1-1 mutant plants that suffer from an internally lowered reductive sulfur assimilation and a concomitant slow growth phenotype. Homografts of wildtype and sir1-1 confirm the hallmarks of non-grafted sir1-1 mutants, displaying substantial induction of sulfate transporter genes in roots and sulfate accumulation in shoots. Heterografts of wildtype scions and sir1-1 rootstocks and vice versa, respectively, demonstrate a dominant role of the shoot over the root with respect to sulfur-related gene expression, sulfate accumulation and organic sulfur metabolites, including the regulatory compound O-acetylserine. The results provide evidence for demand-driven control of the shoot over the sulfate uptake system of roots under sulfur-sufficient conditions, allowing sulfur uptake and transport to the shoot for dynamic responses.
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spelling pubmed-84020622021-08-29 Micrografting Provides Evidence for Systemic Regulation of Sulfur Metabolism between Shoot and Root Forieri, Ilaria Aref, Rasha Wirtz, Markus Hell, Rüdiger Plants (Basel) Article The uptake of sulfate by roots and its reductive assimilation mainly in the leaves are not only essential for plant growth and development but also for defense responses against biotic and abiotic stresses. The latter functions result in stimulus-induced fluctuations of sulfur demand at the cellular level. However, the maintenance and acclimation of sulfur homeostasis at local and systemic levels is not fully understood. Previous research mostly focused on signaling in response to external sulfate supply to roots. Here we apply micrografting of Arabidopsis wildtype knock-down sir1-1 mutant plants that suffer from an internally lowered reductive sulfur assimilation and a concomitant slow growth phenotype. Homografts of wildtype and sir1-1 confirm the hallmarks of non-grafted sir1-1 mutants, displaying substantial induction of sulfate transporter genes in roots and sulfate accumulation in shoots. Heterografts of wildtype scions and sir1-1 rootstocks and vice versa, respectively, demonstrate a dominant role of the shoot over the root with respect to sulfur-related gene expression, sulfate accumulation and organic sulfur metabolites, including the regulatory compound O-acetylserine. The results provide evidence for demand-driven control of the shoot over the sulfate uptake system of roots under sulfur-sufficient conditions, allowing sulfur uptake and transport to the shoot for dynamic responses. MDPI 2021-08-20 /pmc/articles/PMC8402062/ /pubmed/34451773 http://dx.doi.org/10.3390/plants10081729 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Forieri, Ilaria
Aref, Rasha
Wirtz, Markus
Hell, Rüdiger
Micrografting Provides Evidence for Systemic Regulation of Sulfur Metabolism between Shoot and Root
title Micrografting Provides Evidence for Systemic Regulation of Sulfur Metabolism between Shoot and Root
title_full Micrografting Provides Evidence for Systemic Regulation of Sulfur Metabolism between Shoot and Root
title_fullStr Micrografting Provides Evidence for Systemic Regulation of Sulfur Metabolism between Shoot and Root
title_full_unstemmed Micrografting Provides Evidence for Systemic Regulation of Sulfur Metabolism between Shoot and Root
title_short Micrografting Provides Evidence for Systemic Regulation of Sulfur Metabolism between Shoot and Root
title_sort micrografting provides evidence for systemic regulation of sulfur metabolism between shoot and root
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402062/
https://www.ncbi.nlm.nih.gov/pubmed/34451773
http://dx.doi.org/10.3390/plants10081729
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