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Transcriptional plasticity buffers genetic variation in zinc homeostasis

In roots of Arabidopsis thaliana, Zn can be either loaded into the xylem for translocation to the shoot or stored in vacuoles. Vacuolar storage is achieved through the action of the Zn/Cd transporter HMA3 (Heavy Metal Atpase 3). The Col-0 accession has an HMA3 loss-of-function allele resulting in hi...

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Autores principales: Pita-Barbosa, Alice, Ricachenevsky, Felipe K., Wilson, Michael, Dottorini, Tania, Salt, David E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925235/
https://www.ncbi.nlm.nih.gov/pubmed/31862901
http://dx.doi.org/10.1038/s41598-019-55736-0
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author Pita-Barbosa, Alice
Ricachenevsky, Felipe K.
Wilson, Michael
Dottorini, Tania
Salt, David E.
author_facet Pita-Barbosa, Alice
Ricachenevsky, Felipe K.
Wilson, Michael
Dottorini, Tania
Salt, David E.
author_sort Pita-Barbosa, Alice
collection PubMed
description In roots of Arabidopsis thaliana, Zn can be either loaded into the xylem for translocation to the shoot or stored in vacuoles. Vacuolar storage is achieved through the action of the Zn/Cd transporter HMA3 (Heavy Metal Atpase 3). The Col-0 accession has an HMA3 loss-of-function allele resulting in high shoot Cd, when compared to accession CSHL-5 which has a functional allele and low shoot Cd. Interestingly, both Col-0 and CSHL-5 have similar shoot Zn concentrations. We hypothesize that plants sense changes in cytosolic Zn that are due to variation in HMA3 function, and respond by altering expression of genes related to Zn uptake, transport and compartmentalisation, in order to maintain Zn homeostasis. The expression level of genes known to be involved in Zn homeostasis were quantified in both wild-type Col-0 and Col-0::HMA3(CSHL-5) plants transformed with the functional CSHL-5 allele of HMA3. We observed significant positive correlations between expression of HMA3 and of genes known to be involved in Zn homeostasis, including ZIP3, ZIP4, MTP1, and bZIP19. The results support our hypothesis that alteration in the level of function of HMA3 is counterbalanced by the fine regulation of the Zn homeostasis gene network in roots of A. thaliana.
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spelling pubmed-69252352019-12-24 Transcriptional plasticity buffers genetic variation in zinc homeostasis Pita-Barbosa, Alice Ricachenevsky, Felipe K. Wilson, Michael Dottorini, Tania Salt, David E. Sci Rep Article In roots of Arabidopsis thaliana, Zn can be either loaded into the xylem for translocation to the shoot or stored in vacuoles. Vacuolar storage is achieved through the action of the Zn/Cd transporter HMA3 (Heavy Metal Atpase 3). The Col-0 accession has an HMA3 loss-of-function allele resulting in high shoot Cd, when compared to accession CSHL-5 which has a functional allele and low shoot Cd. Interestingly, both Col-0 and CSHL-5 have similar shoot Zn concentrations. We hypothesize that plants sense changes in cytosolic Zn that are due to variation in HMA3 function, and respond by altering expression of genes related to Zn uptake, transport and compartmentalisation, in order to maintain Zn homeostasis. The expression level of genes known to be involved in Zn homeostasis were quantified in both wild-type Col-0 and Col-0::HMA3(CSHL-5) plants transformed with the functional CSHL-5 allele of HMA3. We observed significant positive correlations between expression of HMA3 and of genes known to be involved in Zn homeostasis, including ZIP3, ZIP4, MTP1, and bZIP19. The results support our hypothesis that alteration in the level of function of HMA3 is counterbalanced by the fine regulation of the Zn homeostasis gene network in roots of A. thaliana. Nature Publishing Group UK 2019-12-20 /pmc/articles/PMC6925235/ /pubmed/31862901 http://dx.doi.org/10.1038/s41598-019-55736-0 Text en © The Author(s) 2019 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
Pita-Barbosa, Alice
Ricachenevsky, Felipe K.
Wilson, Michael
Dottorini, Tania
Salt, David E.
Transcriptional plasticity buffers genetic variation in zinc homeostasis
title Transcriptional plasticity buffers genetic variation in zinc homeostasis
title_full Transcriptional plasticity buffers genetic variation in zinc homeostasis
title_fullStr Transcriptional plasticity buffers genetic variation in zinc homeostasis
title_full_unstemmed Transcriptional plasticity buffers genetic variation in zinc homeostasis
title_short Transcriptional plasticity buffers genetic variation in zinc homeostasis
title_sort transcriptional plasticity buffers genetic variation in zinc homeostasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925235/
https://www.ncbi.nlm.nih.gov/pubmed/31862901
http://dx.doi.org/10.1038/s41598-019-55736-0
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