Cation Diffusion Facilitator proteins of Beta vulgaris reveal diversity of metal handling in dicotyledons.
Santiago AlejandroBastian MeierMinh Thi Thanh HoangEdgar PeiterPublished in: Plant, cell & environment (2023)
Manganese (Mn), iron (Fe), and zinc (Zn) are essential for diverse processes in plants, but their availability is often limiting or excessive. CATION DIFFUSION FACILITATOR (CDF) proteins have been implicated in the allocation of those metals in plants, whereby most of our mechanistic understanding has been obtained in Arabidopsis. It is unclear to what extent this can be generalized to other dicots. We characterized all CDFs/MTPs of sugar beet (Beta vulgaris spp. vulgaris), which is phylogenetically distant from Arabidopsis. Analysis of subcellular localization, substrate selectivities, and transcriptional regulation upon exposure to metal deficiencies and toxicities revealed unexpected deviations from their Arabidopsis counterparts. Localization and selectivity of some members were modulated by alternative splicing. Notably, unlike in Arabidopsis, Mn- and Zn-sequestrating members were not induced in Fe-deficient roots, pointing to differences in the Fe acquisition machinery. This was supported by low Zn and Mn accumulation under Fe deficiency and a strikingly increased Fe accumulation under Mn and Zn excess, coinciding an induction of BvIRT1. High Zn load caused a massive upregulation of Zn-BvMTPs. The results suggest that the employment of the CDF toolbox is highly diverse amongst dicots, which questions the general applicability of metal homeostasis models derived from Arabidopsis. This article is protected by copyright. All rights reserved.
Keyphrases
- metal organic framework
- transcription factor
- heavy metals
- room temperature
- cell wall
- plant growth
- ionic liquid
- aqueous solution
- lymph node
- transition metal
- health risk assessment
- poor prognosis
- body mass index
- visible light
- gene expression
- long non coding rna
- high glucose
- dna methylation
- oxidative stress
- climate change
- oxide nanoparticles
- endothelial cells
- wild type