Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1783481876915159040 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6925235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT pitabarbosaalice transcriptionalplasticitybuffersgeneticvariationinzinchomeostasis AT ricachenevskyfelipek transcriptionalplasticitybuffersgeneticvariationinzinchomeostasis AT wilsonmichael transcriptionalplasticitybuffersgeneticvariationinzinchomeostasis AT dottorinitania transcriptionalplasticitybuffersgeneticvariationinzinchomeostasis AT saltdavide transcriptionalplasticitybuffersgeneticvariationinzinchomeostasis |