Cargando…
Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation
Root architecture responds to environmental stress. Stress-induced metabolic and nutritional changes affect the endogenous root development program. Transcriptional and translational changes realize the switch between stem cell proliferation and cell differentiation, lateral root or root hair format...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644957/ https://www.ncbi.nlm.nih.gov/pubmed/33193499 http://dx.doi.org/10.3389/fpls.2020.569687 |
_version_ | 1783606563211051008 |
---|---|
author | Kumar, Vijay Vogelsang, Lara Schmidt, Romy R. Sharma, Shanti S. Seidel, Thorsten Dietz, Karl-Josef |
author_facet | Kumar, Vijay Vogelsang, Lara Schmidt, Romy R. Sharma, Shanti S. Seidel, Thorsten Dietz, Karl-Josef |
author_sort | Kumar, Vijay |
collection | PubMed |
description | Root architecture responds to environmental stress. Stress-induced metabolic and nutritional changes affect the endogenous root development program. Transcriptional and translational changes realize the switch between stem cell proliferation and cell differentiation, lateral root or root hair formation and root functionality for stress acclimation. The current work explores the effects of stress combination of arsenic toxicity (As) and hypoxia (Hpx) on root development in Arabidopsis thaliana. As revealed previously, combined As and Hpx treatment leads to severe nutritional disorder evident from deregulation of root transcriptome and plant mineral contents. Both As and Hpx were identified to pose stress-specific constraints on root development that lead to unique root growth phenotype under their combination. Besides inhibition of root apical meristem (RAM) activity under all stresses, As induced lateral root growth while root hair density and lengths were strongly increased by Hpx and HpxAs-treatments. A dual stimulation of phosphate (Pi)-starvation response was observed for HpxAs-treated plant roots; however, the response under HpxAs aligned more with Hpx than As. Transcriptional evidence along with biochemical data suggests involvement of PHOSPHATE STARVATION RESPONSE 1; PHR1-dependent systemic signaling. Pi metabolism-related transcripts in close association with cellular iron homeostasis modulate root development under HpxAs. Early redox potential changes in meristematic cells, differential ROS accumulation in root hair zone cell layers and strong deregulation of NADPH oxidases, NADPH-dependent oxidoreductases and peroxidases signify a role of redox and ROS signaling in root architecture remodeling under HpxAs. Differential aquaporin expression suggests transmembrane ROS transport to regulate root hair induction and growth. Reorganization of energy metabolism through NO-dependent alternate oxidase, lactate fermentation, and phosphofructokinase seems crucial under HpxAs. TOR and SnRK-signaling network components were potentially involved in control of sustainable utilization of available energy reserves for root hair growth under combined stress as well as recovery on reaeration. Findings are discussed in context of combined stress-induced signaling in regulation of root development in contrast to As and Hpx alone. |
format | Online Article Text |
id | pubmed-7644957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76449572020-11-13 Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation Kumar, Vijay Vogelsang, Lara Schmidt, Romy R. Sharma, Shanti S. Seidel, Thorsten Dietz, Karl-Josef Front Plant Sci Plant Science Root architecture responds to environmental stress. Stress-induced metabolic and nutritional changes affect the endogenous root development program. Transcriptional and translational changes realize the switch between stem cell proliferation and cell differentiation, lateral root or root hair formation and root functionality for stress acclimation. The current work explores the effects of stress combination of arsenic toxicity (As) and hypoxia (Hpx) on root development in Arabidopsis thaliana. As revealed previously, combined As and Hpx treatment leads to severe nutritional disorder evident from deregulation of root transcriptome and plant mineral contents. Both As and Hpx were identified to pose stress-specific constraints on root development that lead to unique root growth phenotype under their combination. Besides inhibition of root apical meristem (RAM) activity under all stresses, As induced lateral root growth while root hair density and lengths were strongly increased by Hpx and HpxAs-treatments. A dual stimulation of phosphate (Pi)-starvation response was observed for HpxAs-treated plant roots; however, the response under HpxAs aligned more with Hpx than As. Transcriptional evidence along with biochemical data suggests involvement of PHOSPHATE STARVATION RESPONSE 1; PHR1-dependent systemic signaling. Pi metabolism-related transcripts in close association with cellular iron homeostasis modulate root development under HpxAs. Early redox potential changes in meristematic cells, differential ROS accumulation in root hair zone cell layers and strong deregulation of NADPH oxidases, NADPH-dependent oxidoreductases and peroxidases signify a role of redox and ROS signaling in root architecture remodeling under HpxAs. Differential aquaporin expression suggests transmembrane ROS transport to regulate root hair induction and growth. Reorganization of energy metabolism through NO-dependent alternate oxidase, lactate fermentation, and phosphofructokinase seems crucial under HpxAs. TOR and SnRK-signaling network components were potentially involved in control of sustainable utilization of available energy reserves for root hair growth under combined stress as well as recovery on reaeration. Findings are discussed in context of combined stress-induced signaling in regulation of root development in contrast to As and Hpx alone. Frontiers Media S.A. 2020-10-23 /pmc/articles/PMC7644957/ /pubmed/33193499 http://dx.doi.org/10.3389/fpls.2020.569687 Text en Copyright © 2020 Kumar, Vogelsang, Schmidt, Sharma, Seidel and Dietz. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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 Kumar, Vijay Vogelsang, Lara Schmidt, Romy R. Sharma, Shanti S. Seidel, Thorsten Dietz, Karl-Josef Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation |
title | Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation |
title_full | Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation |
title_fullStr | Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation |
title_full_unstemmed | Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation |
title_short | Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation |
title_sort | remodeling of root growth under combined arsenic and hypoxia stress is linked to nutrient deprivation |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644957/ https://www.ncbi.nlm.nih.gov/pubmed/33193499 http://dx.doi.org/10.3389/fpls.2020.569687 |
work_keys_str_mv | AT kumarvijay remodelingofrootgrowthundercombinedarsenicandhypoxiastressislinkedtonutrientdeprivation AT vogelsanglara remodelingofrootgrowthundercombinedarsenicandhypoxiastressislinkedtonutrientdeprivation AT schmidtromyr remodelingofrootgrowthundercombinedarsenicandhypoxiastressislinkedtonutrientdeprivation AT sharmashantis remodelingofrootgrowthundercombinedarsenicandhypoxiastressislinkedtonutrientdeprivation AT seidelthorsten remodelingofrootgrowthundercombinedarsenicandhypoxiastressislinkedtonutrientdeprivation AT dietzkarljosef remodelingofrootgrowthundercombinedarsenicandhypoxiastressislinkedtonutrientdeprivation |