Figures
Abstract
Iron and zinc are important micronutrients for both the growth and nutrient availability of crop plants, and their absorption is tightly controlled by a metal uptake system. Zinc-regulated transporters, iron-regulated transporter-like proteins (ZIP), is considered an essential metal transporter for the acquisition of Fe and Zn in graminaceous plants. Several ZIPs have been identified in maize, although their physiological function remains unclear. In this report, ZmIRT1 was shown to be specifically expressed in silk and embryo, whereas ZmZIP3 was a leaf-specific gene. Both ZmIRT1 and ZmZIP3 were shown to be localized to the plasma membrane and endoplasmic reticulum. In addition, transgenic Arabidopsis plants overexpressing ZmIRT1 or ZmZIP3 were generated, and the metal contents in various tissues of transgenic and wild-type plants were examined based on ICP-OES and Zinpyr-1 staining. The Fe and Zn concentration increased in roots and seeds of ZmIRT1-overexpressing plants, while the Fe content in shoots decreased. Overexpressing ZmZIP3 enhanced Zn accumulation in the roots of transgenic plants, while that in shoots was repressed. In addition, the transgenic plants showed altered tolerance to various Fe and Zn conditions compared with wild-type plants. Furthermore, the genes associated with metal uptake were stimulated in ZmIRT1 transgenic plants, while those involved in intra- and inter- cellular translocation were suppressed. In conclusion, ZmIRT1 and ZmZIP3 are functional metal transporters with different ion selectivities. Ectopic overexpression of ZmIRT1 may stimulate endogenous Fe uptake mechanisms, which may facilitate metal uptake and homeostasis. Our results increase our understanding of the functions of ZIP family transporters in maize.
Citation: Li S, Zhou X, Li H, Liu Y, Zhu L, Guo J, et al. (2015) Overexpression of ZmIRT1 and ZmZIP3 Enhances Iron and Zinc Accumulation in Transgenic Arabidopsis. PLoS ONE 10(8): e0136647. https://doi.org/10.1371/journal.pone.0136647
Editor: Jin-Song Zhang, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, CHINA
Received: May 12, 2015; Accepted: August 6, 2015; Published: August 28, 2015
Copyright: © 2015 Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by the National Special Program for GMO Development of China (grant number 2014ZX08003-002) and by the National Natural Science Foundation of China (grant number 31101095).
Competing interests: The authors have declared that no competing interests exist.
Introduction
Micronutrients are essential for both plant growth and human health, and a deficiency in such nutrients may reduce the yield and quality of crop plants and lead to nutritional deficiency syndrome in mammals such as anaemia, hypophrenia, and stagnation of growth and development. It was reported that deficiencies in bio-available iron, zinc, and other essential minerals affect a large proportion of the global population [1–3]. Besides, zinc and iron are essential metal nutrient factors for plants since they play critical roles in the process of growth and development, including photosynthesis, respiration, and other biochemical reactions that require Zn or Fe as co-factors.
In plants, zinc deficiency leads to internode shortening, reduction in leaf size and other morphological changes [4–6], while iron deficiency can cause severe chlorosis and growth arrest. A deficiency in Zn and Fe repress plant growth and reduces the yield and quality [7], although too much Zn and Fe may result in considerable biochemical toxicity [8, 9]. To avoid excessive absorption and facilitate adequate intake, plants have created a balanced network to regulate the uptake, utilisation, and storage of these metal ions [10, 11]. Actually, such adjustments rely on genes that control ion homeostasis in plants. Recently, several metal transporters that contribute to metal-ion homeostasis in plants have been identified, including the zinc-regulated transporter (ZRT), iron-regulated transporter (IRT)-like protein (ZIP), natural resistance-associated macrophage protein (NRAMP), and yellow stripe-like protein (YSL).
Zn exhibits low solubility, and its solubilisation is thought to occur via acidification of rhizosphere and secretion of organic chelators such as nicotianamine (NA) and citric acid. Subsequently, as a free ion, zinc is uptake into the root cells by ZIPs [12]. Zn can then be transported into vacuoles and immobilised in the root symplast or it can be translocated into the vascular cylinder through plasmodesmata [12]. The translocation of Zn from roots to shoots requires the export of zinc from root cells and loading of zinc into the apoplastic xylem [13, 14]. Inside the xylem, zinc flux from roots to shoots is massflow driven and ionic zinc is chelated by low-molecular-weight ligands to avoid Zn retention. Then, Zn is taken up from the xylem of shoots and transported across the plasma membranes of adjacent cells via membrane zinc transporters [15]. Two different mechanisms are involved in iron acquisition in plants. Strategy I is specifically used by nongraminaceous plants, which contains the reduction of Fe3+ to Fe2+ on the root surface and the acquisition of Fe2+ into root cells by Fe2+ transporters, including ZIPs [12]. Furthermore, phenolics are secreted to facilitate iron acquisition during Fe starvation. These substances serve as iron chelators or electron donors for Fe3+ reduction during iron uptake [16]. Graminaceous plants such as rice and corn use strategy II, which involves the synthesis and secretion of phytosiderophores (PS) to facilitate iron uptake. The chelated Fe3+ is then translocated into roots cell by YS proteins. The transportation of iron in graminaceous plants is mediated by NA and YSL proteins. These results indicated that ZIPs play essential roles in both absorption and translocation of Zn and Fe in nongraminaceous plants, while their functions in graminaceous plants remain less understood.
ZIPs function in ion homeostasis as they can transport cations into the cytoplasm [17]. AtIRT1 was the first cloned member of ZIP family and encodes a major Fe transporter at the root surface [18–21]. Further studies showed that irt1 had lower Ni accumulation than the wild-type plants under Fe-deficiency status, indicating that AtIRT1 play essential roles in Fe and Ni translocation in Arabidopsis [22]. AtIRT2 localized to intracellular vesicles, suggesting it may play roles in compartmentalisation and remobilising of iron into internal storage vesicles to avoid metal toxicity [23]. Additionally, the accumulation of Zn in reproductive organs correlate with expression levels of VvZIP3 during the reproductive growth stage, indicating that ZIPs may be associated with Zn distribution in embryo and endosperm [6]. It has also been reported that overexpression of ZIPs may result in elevated metal ion content. Overexpressing AtZIP1 in Hordeum vulgare increases the Zn and Fe contents in seeds [24]. Similarly, Fe and Zn levels were increased in shoots, roots and seeds when overexpressing OsIRT1 in rice [25]. However, overaccumulating OsZIP4, result in increased Zn contents in roots, while Zn levels in seeds was significant lower than in non-transgenic plants [26]. Since it was reported that OsZIP4 was expressed in the phloem cells of stem, and vascular bundles of leaves and roots [27], it can be assumed that the endogenous expression profiles of ZIP genes may be critical for appropriate Zn and Fe distribution and metal homeostasis in plants.
The contribution of ZIP genes in the uptake and translocation of iron and zinc has been investigated extensively in Arabidopsis and rice. However, our understanding of the functions of ZIPs in maize remains limited. In this study, two ion transporters, ZmIRT1 and ZmZIP3, were cloned from maize and showed distinctive expression patterns. It was demonstrated that ZmIRT1 and ZmZIP3 showed different activity of yeast complementation, and the expression level of ZmIRT1 was induced by Fe deficiency [28]. To explore the physiological function of ZmIRT1 and ZmZIP3 in plants, transgenic Arabidopsis lines overexpressing ZmIRT1 and ZmZIP3 were generated. The contents of Zn and Fe in transgenic plants were then measured using ICP-OES and Zinpyr-1 staining. We analysed the phenotype of overexpression lines under excess and deficient Zn and Fe conditions, and detected the transcription levels of key genes that play a role in the uptake and translocation of Zn and Fe in transgenic Arabidopsis plants. It was shown that ZmIRT1 and ZmZIP3 are functional metal transporters, and ectopic overexpression of ZmIRT1 stimulated endogenous Fe uptake mechanisms, which may facilitate metal uptake and homeostasis.
Materials and Methods
Plant materials and growth conditions
The plants of maize (Zea mays L.) inbred line B73 were grown in the greenhouse. For expression analysis of ZmIRT1 and ZmZIP3, root, stem, leaf, and sheath samples were collected from the flare opening stage; tassel, anther, ear, cob, silk, and husk leaf were collected during the flowing period, and embryos and endosperms were sampled at 10, 15, and 20 d after pollination.
Seeds of Arabidopsis (Columbia wild-type and transgenic lines) were surface-sterilised with 75% ethanol for 10 min and grown on the standard Murashige and Skoog (MS) medium containing 30 μM ZnSO4, 100 μM Fe3+-EDTA, 0.1 μM CuSO4, and 10 μM MnSO4 as micronutrients [29]. For metal nutrition deficiency and excess analysis, seeds were germinated and grown for 13 d on standard MS and MS medium lacking ZnSO4 (Zn-deficient) or Fe3+-EDTA (Fe-deficient), and with 200 μM ZnSO4 (Zn-excess) or 300 μM Fe(III)-EDTA (Fe-excess). Surface-sterilised seeds were germinated on agar plates, and vernalisation was performed at 4°C for 2d. Seedlings were grown on MS medium for 10 d at 22°C under a light: dark cycle of 16 h: 8 h, after which the seedlings were transplanted to soil in a glasshouse.
To analyse the zinc and iron contents of wild-type and transgenic plants, the shoots and roots were sampled, respectively, at the bolting stage. To determine the zinc and iron levels in seeds, the same batch of seedlings was used.
Subcellular localization
For subcellular localization, the GFP-fusion expression vector was constructed as described in detail previously [28]. The ZmIRT1 and ZmZIP3-GFP fusion plasmid and the mcherry labelled ER marker were co-transformed into maize mesophyll protoplasts, respectively, following procedures described previously [30, 31]. After 14 h of incubation in the dark at 26°C, the GFP and ER fluorescence was determined by a confocal microscope (LSM700; Carl Zeiss).
Plasmid construction, Arabidopsis transformation, and overexpression plant confirmation
To construct ZmIRT1 and ZmZIP3-overexpressing vectors, the ZmIRT1 and ZmZIP3 coding sequences were amplified by PCR using the gene-specific primers IRT1oxF (with an added XbaI site) and IRT1oxR (with an added SnaBI site) for ZmIRT1, and ZIP3oxF (with an added SmaI site) and ZIP3oxR (with an added KpnI site) for ZmZIP3 (S1 Table), respectively. The PCR fragments were cloned into the corresponding site of the pBI121 vector to generate pBI121-ZmIRT1 and pBI121-ZmZIP3. Agrobacterium tumefaciens strains GV3101 harbouring the overexpression plasmids were used to transform Arabidopsis and generate the transgenic lines. Transformation was performed following the floral dip protocol [32]. Overexpression plants were confirmed by both PCR analysis and kanamycin selection.
Metal element analysis
For elemental analysis, leaves and roots were harvested, and the processing method as described in detail previously [33]. The tissues and seeds were air-dried for 6 d at room temperature. For elemental measurement, 0.5 g of plant material was digested in 2-mL HNO3 overnight, after which 2 mL of H2O2 were added, followed by microwave digestion. When digestion was completed, and the digests were diluted with Millipore water and filtered. The volume was then adjusted to 25 mL and analysed by ICP-OES on an iCAP 6000 Series spectrometer (Thermo-Fisher). For metal element analysis, three biological replicates were used, for each of which three technical replicates were performed. This experiment was performed at the Analysis and Testing Center of Tsinghua University.
Zinpyr-1 staining and quantification of fluorescence
The zinc concentration in various tissues of Arabidopsis was examined using Zinpyr-1, which is a cell-permeable and fluorescent probe that selectively detects free zinc in living cells, and propidium iodide was used to stain cell walls. The Zinpyr-1 and propidium iodide working solution were diluted to 20 μM and 75 μM, respectively. The 11 d old seedlings were collected and washed in deionised water, then immersed in Zinpyr-1 and propidium iodide to stain. Preparation and staining process of Zinpyr-1 and propidium iodide were performed as described in detail previously [33]. Images were obtained using a confocal microscope (LSM700; Carl Zeiss) with 488-nm excitation. To compare the signal intensity of transgenic and wild-type lines, all imaging parameters were fixed.
A method of signal quantification was developed using ZEN 2009 Light Edition software. For comparative analysis of zinc content in shoots, leaves and roots, the green and red fluorescence intensities in corresponding areas of the wild-type and transgenic plants were selected and calculated. The ratio of green-to-red fluorescence was used to normalize the results.
Reverse transcription (RT)-PCR and quantitative RT-PCR analysis
Total RNA was extracted using TRIzol (TransGen) from wild-type and transgenic lines, as well as various organs from the maize inbred line B73. For cDNA synthesis, 4 μg total RNA were reverse transcribed to cDNA in a 40-μL reaction volume using One-step gDNA Removal and cDNA Synthesis SuperMix (Transgen) and incubated at 42°C for 30 min in a H2O3-PRO drybath (Coyote Bioscience). The gene-specific primers (S1 Table) were used for RT-PCR and quantitative RT-PCR. The PCR mix and PCR conditions were performed as described in detail previously [28]. Data were analysed using the ABI7500 software (version 2.0.5) via the 2-ΔΔCT method, and the expression levels of ZmActin1 and AtUBP6 were used as references in maize and Arabidopsis, respectively. For quantitative RT-PCR analysis, three biological replicates were used, for each of which three technical replicates were performed.
Results
ZmIRT1 and ZmZIP3 show different gene expression patterns but similar subcellular localizations
In the present study, two ZmZIP genes were identified and showed distinctive expression patterns. Quantitative RT-PCR was applied to determine the transcript levels of ZmIRT1 and ZmZIP3 in various organs and developing seeds. ZmIRT1 was predominantly expressed in silk and embryo, while ZmZIP3 was expressed in a leaf-specific manner (Fig 1). The subcellular localization of ZmIRT1 and ZmZIP3 may be useful for inferring their functions in maize. Thus, the fusion construct was co-transferred with an ER marker and expressed transiently in maize protoplasts (S1 Fig). We found that ZmIRT1-GFP and ZmZIP3-GFP fusion proteins were localized to the plasma membrane and endoplasmic reticulum, as observed previously in Arabidopsis protoplasts.
The relative expression levels of ZmIRT1 and ZmZIP3 were normalised to that of ZmActin1. quantitative RT-PCR data were analysed following the 2-ΔΔCt method. Error bars indicate standard deviations.
Transgenic Arabidopsis ectopically expressing ZmIRT1 and ZmZIP3 respond differently to metal excess and deficiency conditions
It has been demonstrated that ZmIRT1 has a high selectivity for iron transportation, while ZmZIP3 is a zinc transporter. Additionally, ZmIRT1 and ZmZIP3 exhibited distinct expression patterns in response to excess and deficient metal conditions [28]. Since ZmIRT1 and ZmZIP3 have different spatial and temporal expression profiles, they were selected for further functional characterisation. The transgenic Arabidopsis ectopically overexpressing ZmIRT1 and ZmZIP3 were generated, respectively. To verify the expression of ZmIRT1 and ZmZIP3, their transcript levels were determined using RT-PCR in transgenic and wild-type plants (Figs 2A, 2B, 3A and 3B). ZmIRT1 lines OX9, OX10, and OX56 and ZmZIP3 lines OX1, OX10, and OX18 were chosen for further research. To examine the effect of ZmIRT1 or ZmZIP3 on plant growth and mineral nutrition status, we tested the phenotype of transgenic and wild-type Arabidopsis on medium with various metal compositions. No significant growth difference was observed between ZmIRT1-overexpressing and wild-type plants under sufficient and deficient metal nutritional conditions (Fig 2C, 2D, 2F and 2H). However, in response to Fe and Zn-excess, the roots of ZmIRT1 transgenic plants were longer than those of the wild-type (Fig 2E, 2G and 2H), suggesting that the overexpressing plants may tolerate excess metals. On the contrary, ZmZIP3-overexpressing transgenic plants were resistant to iron deficiency since their roots were longer than those of wild-type plants (Fig 3).
(A) Schematic diagram of pBI121-ZmIRT1 construct. (B) RT-PCR verifying the expression of ZmIRT1 in transgenic lines. AtUBP6 was used as an internal control. The growth trend of 2-week-old seedlings under (C) standard nutrient conditions (MS medium), (D) Zn, and (F) Fe-deficiency (Zn- and Fe-), as well as (E) 200 μM ZnSO4 (Zn++) and (G) 300 μM FeSO4 (Fe++) treatment. (H) The root lengths of the wild-type and transgenic plants were measured using the ImageJ software. Error bars represent standard errors. Asterisks denote significant differences: *P<0.05, **P<0.01.
(A) Schematic diagram of the pBI121-ZmZIP3 construct. (B) RT-PCR analysis of ZmZIP3 overexpression lines. AtUBP6 was amplified to show equal amounts of RNA in each sample. The growth trend of 2-week old seedlings under (C) standard nutrient condition (MS medium), (D) Zn, and (F) Fe-deficiency (Zn- and Fe-), as well as (E) 200 μM ZnSO4 (Zn++) and (G) 300 μM FeSO4 (Fe++) treatment. (H) The root lengths of the wild-type and transgenic plants were measured using the ImageJ software. Error bars represent standard errors. Asterisks denote significant differences: *P<0.05, **P<0.01.
Overexpression of ZmIRT1 and ZmZIP3 affects Fe and Zn distribution in plants
To assess whether overexpression of ZmIRT1 or ZmZIP3 affects metal distribution or accumulation, we measured the contents of zinc and iron in transgenic plants at the bolting stage and in mature seeds. When grown on a metal-sufficient medium, the ZmIRT1-overexpressing transgenic plants accumulated more iron (34.87–115.95%) and zinc (61.97–179.5%) in roots, as well as enhanced iron (49.29–172.57%) and zinc (35.69–51.7%) in seeds compared with wild-type plants (Fig 4A and 4E). However, the accumulation of iron in shoots was decreased and zinc content was almost unchanged in transgenic plants expressing ZmIRT1 (Fig 4C). In addition, Cu and Mn concentrations did not differ significantly between ZmIRT1-transgenic and wild-type plants (Fig 4A, 4C and 4E). These results indicated that ZmIRT1 facilitated Zn and Fe uptake in roots and may be involved in the translocation of Zn and Fe into seeds.
Plants were cultivated in nutrient soil. The Fe, Zn, Cu, and Mn contents of roots (A, B), shoots (C, D) and mature seeds (E, F) were analysed using ICP-OES. Values represent the means ± SD (n = 15). Asterisks indicate significant differences: *P<0.05, **P<0.01.
Compared with wild-type plants, ZmZIP3-overexpressing transgenic plants contained more Zn (45.13–92.14%) in roots and Mn (27.00–94.3%) in shoots, although the levels of Fe in roots and Zn in shoots were decreased (Fig 4B and 4D). Moreover, no obvious changes were detected in metal concentrations in the seeds of ZmZIP3-overexpressing lines (Fig 4F). These results indicated that ZmZIP3 may be associated with Zn uptake from soil to root, and ectopic over-accumulation of ZmZIP3 in the root may disrupt the local distribution of metal transporters and result in decreased Fe and Zn concentrations in roots and shoots, respectively.
Histological zinc accumulation patterns were examined in ZmIRT1- and ZmZIP3-overexpressing plants
To visualise the histological localization of Zn in roots and shoots, 11 d old seedlings of wild-type and transgenic plants were immersed in 20 μM Zinpyr-1 and 75 μM propidium iodide, and the signal was examined using a confocal laser-scanning microscope. The fluorescence intensity was calculated using the ZEN software, and the green/red ratio was applied to indicate the Zn relative quantities. In roots of transgenic plants, a high fluorescence signal level was observed in the xylem, while that in pericycle cells was relatively weak (Fig 5A, 5D and 5G). This result is consistent with previous reports [34]. In addition, the fluorescence signals in roots of wild-type plants were considerably weaker than that in transgenic lines (Fig 5J–5L). Moreover, the Zinpyr-1-dependent fluorescence signal in the meristem zone of lateral root and the root apical was significantly higher than that in the elongation region in both wild-type and overexpression lines (Fig 5), suggesting that Zn may be essential for the emergence and development of lateral roots. We also observed that fluorescence signals in the meristem of seedling, leaves, and petioles of overexpression plants were significantly higher than those in non-transgenics (Fig 6J and 6L). These results showed that transgenic plants accumulated more Zn than did the wild-type during seedling development. Moreover, Zn is concentrated in the xylem of roots and petiole of leaves where Zn flow is activated, as well as in the meristem of seedlings and roots where high levels of Zn may be required for bud development.
Roots of wild-type and overexpression plants were successively stained with Zinpyr-1 and propidium iodide to visualise Zn (green) and cell walls (red), respectively. (A-C) and (D-F) show ZmIRT1 (OXZmIRT1) and ZmZIP3 (OXZmZIP3) overexpression plants, respectively, and (G-I) show the wild-type. The boxed regions in (A, D, G) and circled regions in (B, C, E, F, H, I) show the regions used for quantifying average fluorescence intensity. Bars represent 100 μm. (J-L) show the fluorescence intensity of selected regions in the root-hair region, lateral root, and apical root, respectively. The signal ratio of Zinpyr-1/ propidium iodide represents the relative content of Zn. Values represent means ± SD (n = 6). x, xylem. p, pericycle. e, endodermis. c, cortex. ep, epidermis. Asterisks indicate significant differences from the wild-type mean: ***P < 0.001, *P < 0.05.
Shoots of wild-type and overexpression plants were consecutively stained with Zinpyr-1 and propidium iodide to visualise Zn (green) and cell walls (red), respectively. (A-C) and (D-F) show ZmIRT1 (OXZmIRT1) and ZmZIP3 (OXZmZIP3) overexpression plants, respectively, and (G-I) show the wild-type. The circled regions in (A-I) illustrate the regions used to quantify average fluorescence intensity. Bars represent 100 μm. (J-L) show the fluorescence intensity of selected regions of seedlings, leaves, and petioles, respectively. The signal ratio of Zinpyr-1/ propidium iodide represents the relative content of Zn. Values represent the means ± SD (n = 6). Asterisks indicate significant differences from the wild-type mean: ***P < 0.001.
Expression levels of key genes involved in metal uptake and transportation were altered in transgenic plants
Since the Zn accumulation patterns were affected and sensitivities to various Zn/Fe conditions were altered in the ZmIRT1 and ZmZIP3 overexpression lines, it can be assumed that the Zn and Fe homeostasis in the transgenic lines had changed. For genes involved in metal uptake and transportation, FRO2 (Ferric Reductase Oxidase) and IRT1 (Iron-Regulated Transporter), as well as several members of the NAS, YSL, and ZIP family were investigated. The results showed that the expression levels of these genes were changed in the transgenic lines. In ZmIRT1 overexpressing plants, the expression of FRO2, IRT1, and NAS family genes were enhanced (Fig 7), while the endogenous genes involved in metal transportation were repressed, including YSL1 and YSL2 among YSLs and ZIP2 and ZIP4 from the ZIP family (Fig 7). Unlike in the ZmIRT1 transgenic lines, the expression of the above genes was down regulated, excluding NAS1 in ZmZIP3-overexpressing plants (Fig 8).
RNA of wild-type and transgenic plants was prepared from 13 d old seedlings grown on standard MS medium. Relative mRNA abundance of each gene was normalised to that of AtUBP6. Data from quantitative RT-PCR were analyzed following the 2-ΔΔCt method. Error bars indicate standard deviations.
RNA of wild-type and transgenic plants was extracted from 13 d old seedlings grown on standard MS medium. Relative mRNA abundance of each gene was normalised to that of AtUBP6. Data from quantitative RT-PCR were analyzed following the 2-ΔΔCt method. Error bars indicate standard deviations.
For expression analysis of transcription regulators involved in metal uptake and other intracellular transporters, bHLH (basic-helix-loop-helix) and FIT (FER-like iron-deficiency-induced transcription factor), which control the expression of FRO2 and IRT1 [35–38], as well as NRAMP3 (natural resistance-associated macrophage protein) and NRAMP4 responsible for transporting Fe2+ from the vacuole to cytoplasm [39, 40] were examined. It was found that BHLH100 and FIT were induced (Fig 7), whereas the expression of NRAMP 2 and 3 was repressed (Fig 7). These results indicated that the Zn and Fe uptake system is activated in ZmIRT1 transgenic plants, while intracellular metal transportation is suppressed. In the ZmZIP3-overexpressing lines, expression of the above-mentioned genes was downregulated (Fig 8), suggesting that Zn/Fe uptake and intracellular transportation are inactivated.
Discussion
In this study, we demonstrated that ZmIRT1 and ZmZIP3 are involved in the uptake and translocation of metal ions in plants, and our results suggested that they might be associated with metal homeostasis by regulating the expression of genes involved in metal uptake and transportation.
It was reported that transgenic plants overexpressing OsIRT1 exhibited less chlorosis and had higher chlorophyll content than the wild-type under Fe-deficient conditions. Moreover, the Fe content was also increased in mature seeds of OsIRT1 overexpression plants [25]. In addition, overexpression of MxIRT1 enhanced Fe and Zn contents in rice seeds [41]. Likewise, overexpression of AtZIP1 in barley lead to an elevated level in the short-term Zn uptake, and enhanced Zn and Fe contents in seeds [24]. However, overexpression of OsZIP5 and OsZIP8 in rice leads to increased Zn levels in roots, although the Zn content was reduced in shoots and mature seeds of overexpression lines [29, 42]. These data suggested that the metal transportation activity of ZIP proteins may differ, or ectopic accumulation of ZIPs may disrupt the endogenous metal homeostasis due to incongruous in vivo ion transporter gradients. It was found that ZmIRT1 and ZmZIP3 showed strongly and relatively weaker reverse the yeast complement activity. Moreover, the expression of ZmIRT1 was significantly upregulated in roots and shoots under Fe-deficiency, and it was induced in shoots at 96 h after Zn-deficiency. These results suggested that ZmIRT1 might be essential for both uptake and translocation of Fe and Zn. On the contrary, ZmZIP3 was induced by Zn deficiency, indicating that ZmZIP3 may be important for Zn uptake [28]. In this study, we examined the expression pattern of ZmIRT1 and ZmZIP3 in various organs. ZmIRT1 was predominantly expressed in silk and embryo, while ZmZIP3 is a leaf-specific gene. The different expression pattern of ZmIRT1 and ZmZIP3 indicated that they might play distinct roles in metal uptake and translocation. To analyse the physiological roles of the ZmIRT1 and ZmZIP3 in plants, we generated transgenic Arabidopsis and examined whether ZmIRT1 and ZmZIP3 could transport Zn or Fe in plants. It was found that overexpression of ZmIRT1 in Arabidopsis enhanced Fe and Zn contents in both roots and seeds (Fig 4A and 4E), suggesting that ZmIRT1 is a functional Fe and Zn transporter, and it may be associated with the translocation of metals toward seeds. Additionally, we found that ZmIRT1-overexpressing plants grew longer roots than the wild-type under Zn- and Fe-excess conditions (Fig 2E and 2G), which indicates that the transgenic plants are more tolerant to excess zinc and iron. ZmIRT1 is localized to the plasma membrane and endoplasmic reticulum in maize (S1 Fig) and Arabidopsis mesophyll protoplasts [28]. Therefore, ZmIRT1 may function in translocating excess subcellular free Fe2+ and Zn2+ into the endoplasmic reticulum. Moreover, ZmIRT1 may play an essential role in storage and detoxification of Zn and Fe. On the contrary, ZmZIP3-overexpression plants developed more lateral roots and longer roots than wild-type under Fe-deficient conditions (Fig 3F), indicative of a stronger Fe deficiency response in transgenic plants. Consistently, the Fe content in roots was decreased in ZmZIP3-overexpressing plants, although Zn accumulated in roots (Fig 4B). It is noteworthy that the growth of ZmZIP3 transgenic plants was better than the wild-type, despite the Fe-deficiency response in roots (Fig 3F). This is probably because over-accumulation of ZmZIP3 facilitated the uptake of Zn in the roots, which alleviated the symptoms of Fe deficiency.
Besides the morphological changes, the expression of many genes associated with Fe/Zn deficiency and excess responses were also altered in the ZmIRT1- and ZmZIP3-overexpressing plants. It was reported that the expression profiles of genes associated with Fe and Zn uptake and translocation were regulated in accordance with the internal and environmental metal conditions. OsNAS3, OsNAAT1, and OsDMAS1 encode enzymes for the biosynthesis of NA and 2’-deoxymugineic acid (DMA), which plays important roles in chelating and distributing metal ions within plants. The expression of OsNAS3, OsNAAT1, and OsDMAS1 are enhanced in the overexpression lines under Zn-deficient conditions [29]. In addition, the activation of OsNAS3 resulted in increased Zn and Fe contents in rice grains, suggesting that OsNAS3 contributes to ion homeostasis [43]. In our study, the transcription levels of genes associated with Zn/Fe uptake and transportation may reflect the endogenous metal status; thus, we investigated the expression of 12 Arabidopsis genes known to be involved in the homeostasis of Zn and Fe (Fig 7). The results showed that the expressions of genes involved in the uptake of Fe and Zn were altered in both ZmIRT1 and ZmZIP3 transgenic lines. The transcript levels of AtNAS1, 2, which are associated with NA synthesis, AtFRO2 that plays a role in ferric reduction, and AtIRT1 that is related to ferrous uptake were up-regulated in ZmIRT1-overexpressing plants (Fig 7). The enhanced expression of these genes may be due to the root absorbed too much iron that stimulated the expression of NAS, FRO and IRT1, which associated with iron uptake. In contrast, AtFRO2 and AtIRT1 were reduced in the ZmZIP3 transgenic lines (Fig 8), possibly due to the iron content was decreased so suppressed the expression of these genes. These results suggest that ZmIRT1 and ZmZIP3 play different roles in metal homeostasis. The stimulation of these genes in ZmIRT1-overexpressing lines may be due to the increased expression of transcription factors that regulate ion homeostasis. It has been demonstrated that Fe homeostasis is controlled by conserved transcriptional networks in both grasses and non-grasses [44, 45]. Under Fe-deficiency, FIT (FER-like iron-deficiency-induced transcription factor) interacts with bHLH038 and bHLH039 to regulate the expression of IRT1 and FRO2 in Arabidopsis [37]. It was also reported that FIT, IRT1, FRO2, and BHLH100 are iron deficiency induced genes in roots [15]. Although there are no orthologs of FIT in rice, OsIRO2 is a regulator of the Fe deficiency-responsive gene, which is highly similar to bHLH38/39. OsIRO2 regulates the expression of Fe3+-PS translocation-related genes, with the exception of OsIRT1 [46]. Co-overexpression of FIT and bHLH38 or bHLH39 results in increased expression of NAS1 and NAS2, which enhanced NA accumulation and increased transport of Fe from roots to shoots [47]. We found that the expression of FIT was stimulated in the ZmIRT1 transgenic plants, indicating that a transcriptional cascade was activated as a result of ectopic accumulation of ZmIRT1. Besides, pleiotropic effects may also contribute to the activation of gene expression since a greater quantity of Fe and Zn was absorbed into the cytoplasm when ZmIRT1 was overexpressed. The expression of NRAMPs, YSLs, and endogenous ZIPs were suppressed in both ZmIRT1 and ZmZIP3 lines (Figs 7 and 8), suggesting that over-accumulation of ZIP proteins may inhibit the expression of endogenous genes that function in metal transportation. Taking this into consideration, our results suggested that overexpressing ZmIRT1 may facilitate Zn and Fe uptake by inducing genes associated with strategy I (ferric reduction and ferrous uptake) and strategy II (ion-chelator synthesis) iron uptake systems, although the expression of genes involved in intercellular ion transportation was suppressed.
Fe uptake mechanisms were classified into two strategies. Strategy I, a reduction-based strategy, is used by non-grasses such as Arabidopsis [44, 45]. It begins with acidification of the rhizosphere and increases the solubility of ferric in the soil [48–50]. The reduction of ferric irons then occurs on the membrane by a membrane-bound ferric-chelate reductase AtFRO2, and ferrous is taken into root epidermal cells by transmembrane transporters, such as AtIRT1 [21, 22]. On the contrary, strategy II, a chelation-based strategy is used by grasses such as barley, rice, and maize. Phytosiderophores are released into the rhizosphere to chelate ferric [51], and Fe3+-PS can be absorbed into root cells by YSLs [52, 53]. The main distinction between these two strategies is different oxidation and reduction forms of iron absorbed into the root cells, as non-grasses prefer ferrous and grasses absorb ferric. It is generally considered that the iron uptake mechanisms used by these two strategies do not overlap. The identification of two functional Fe2+ transporters, OsIRT1 and OsIRT2, indicates that strategy I may be used by graminaceous plants [54, 55]. It was proposed that rice uses a combined strategy including strategy II and partial strategy I to uptake Fe from the soil. TOM1/OsZIFL4 and OsYSL15 were reported to be involved in the release of PS and uptake of Fe3+-PS as strategy II, while OsIRT1 translocated Fe2+ into root cells through strategy I. However, the genes responsible for acidification and ferric reduction seemed to be lost in the rice genome [54, 56, 57]. As a graminaceous plant, maize was considered to apply strategy II for Fe uptake. However, ZmIRT1 was identified as a functional Fe2+ transporter in yeast and transgenic Arabidopsis. ZmIRT1 overexpression plants contain increased amounts of Zn and Fe in roots and seeds (Fig 4A and 4E), as well as elevated Zn levels in seedlings (Figs 5 and 6). In addition, ZmZIP3-overexpressing transgenic plants accumulated more Zn in roots. These results indicated that ZmIRT1 and ZmZIP3 are functional ion transporters. Moreover, we identified putative FRO and AHA genes in the maize genome (data not shown) using the reported AtFRO and AtAHA (H+-ATPase) as TBLASTN queries, and suggested that the ferric reducing and rhizosphere acidification capacities may be retained through evolution. Thus, further investigations are required to determine whether maize use strategy I as a complementary Fe uptake mechanism, and determine why it has been maintained during evolution.
It was previously reported that although AtIRT1 was expressed constitutively in 35S-IRT1 transgenic plants, the protein was present only in iron-limited roots. This result suggested that the accumulation of IRT1 is influenced by post-transcriptional regulation [58]. It was also reported that post-transcriptional regulation did not play a significant role in OsIRT1 overexpression rice, as both OsIRT1 and metals were accumulated under metal-sufficient conditions and the transgenic plants showed visible morphological changes when grown under standard conditions [25]. In this study, the ZmIRT1-overexpressing Arabidopsis exhibited increased levels of zinc and iron in different tissues, and the transgenic plants showed an enhanced resistance against excess-iron and zinc. These results indicated that ZmIRT1 might escape post-transcriptional control because ZmIRT1 is highly homologous with OsIRT1 (73.04% identity) and they share low sequence similarity with AtIRT1 (50.92% identity for ZmIRT1 and 48.93% identity for OsIRT1, respectively).
Conclusions
In conclusion, we generated transgenic Arabidopsis plants overexpressing ZmIRT1 or ZmZIP3 to explore the function of these genes in metal uptake, translocation, and homeostasis. As expected, the Fe and Zn contents were enhanced in roots and mature seeds of ZmIRT1 overexpression plants, while the Zn level was increased in roots of ZmZIP3-overexpressing lines. Likewise, zinc staining revealed that the Zn ions accumulated in the seedlings of both ZmIRT1 and ZmZIP3 transgenic plants. These results indicate that ZmIRT1 and ZmZIP3 are functional metal transporters, while they have different selectivity towards various metal ions. These results may be applied in molecular breeding and biofortification of maize with micro-essential metal nutrients.
Supporting Information
S1 Fig. Subcellular localization of ZmIRT1 and ZmZIP3 in maize mesophyll protoplasts.
Full-length cDNA without stop codon of the ZmIRT1 and ZmZIP3 genes were cloned into the pRTL2GFP vector and the resulting construct was transiently transformed into maize mesophyll protoplasts by the PEG method. The GFP signal is shown in green and the fluorescence of ER marker is indicated in red. The images were obtained by a confocal microscope. The scale bar represents 10 μm.
https://doi.org/10.1371/journal.pone.0136647.s001
(TIF)
S1 Table. Primers used for vector construction and quantitative RT-PCR analysis.
https://doi.org/10.1371/journal.pone.0136647.s002
(DOCX)
Acknowledgments
We thank Jie Li (College of Life Sciences, Beijing Normal University) for assisting in Arabidopsis culture.
Author Contributions
Conceived and designed the experiments: SZL XJZ JTC RMC. Performed the experiments: SZL XJZ HBL YFL LYZ JJG XQL. Analyzed the data: HBL YFL. Contributed reagents/materials/analysis tools: JJG XQL. Wrote the paper: SZL XJZ JTC RMC YLF.
References
- 1. Ghandilyan A, Vreugdenhil D, Aarts MGM. Progress in the genetic understanding of plant iron and zinc nutrition. Physiol Plant. 2006;126(3):407–17.
- 2. Stein A. Global impacts of human mineral malnutrition. Plant and Soil. 2010;335(1–2):133–54.
- 3. An P, Wu Q, Wang H, Guan Y, Mu M, Liao Y, et al. TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia. Hum Mol Genet. 2012;21(9):2124–31. Epub 2012/02/11. pmid:22323359.
- 4. Broadley MR, White PJ, Hammond JP, Zelko I, Lux A. Zinc in plants. New Phytol. 2007;173(4):677–702. pmid:17286818
- 5. Erikson KM, Syversen T, Steinnes E, Aschner M. Globus pallidus: a target brain region for divalent metal accumulation associated with dietary iron deficiency. J Nutr Biochem. 2004;15(6):335–41. Epub 2004/05/26. pmid:15157939.
- 6. Gainza-Cortes F, Perez-Diaz R, Perez-Castro R, Tapia J, Casaretto JA, Gonzalez S, et al. Characterization of a putative grapevine Zn transporter, VvZIP3, suggests its involvement in early reproductive development in Vitis vinifera L. BMC Plant Biol. 2012;12:111. Epub 2012/07/25. pmid:22824090; PubMed Central PMCID: PMC3432002.
- 7. Casterline JE, Allen LH, Ruel MT. Vitamin B-12 deficiency is very prevalent in lactating Guatemalan women and their infants at three months postpartum. J Nutr. 1997;127(10):1966–72. Epub 1997/10/06. pmid:9311952.
- 8. Påhlsson A-M. Toxicity of heavy metals (Zn, Cu, Cd, Pb) to vascular plants. Water, Air, and Soil Pollution. 1989;47(3–4):287–319.
- 9. Price AH, Hendry GAF. Iron-catalysed oxygen radical formation and its possible contribution to drought damage in nine native grasses and three cereals. Plant Cell Environ. 1991;14(5):477–84.
- 10. Palmgren MG, Clemens S, Williams LE, Kramer U, Borg S, Schjorring JK, et al. Zinc biofortification of cereals: problems and solutions. Trends Plant Sci. 2008;13(9):464–73. Epub 2008/08/15. pmid:18701340.
- 11. Grotz N, Guerinot ML. Molecular aspects of Cu, Fe and Zn homeostasis in plants. Biochim Biophys Acta. 2006;1763(7):595–608. Epub 2006/07/22. pmid:16857279.
- 12. Sinclair SA, Kramer U. The zinc homeostasis network of land plants. Biochim Biophys Acta. 2012;1823(9):1553–67. Epub 2012/05/26. pmid:22626733.
- 13. Hussain D, Haydon MJ, Wang Y, Wong E, Sherson SM, Young J, et al. P-type ATPase heavy metal transporters with roles in essential zinc homeostasis in Arabidopsis. Plant Cell. 2004;16(5):1327–39. Epub 2004/04/22. pmid:15100400; PubMed Central PMCID: PMC423219.
- 14. Hanikenne M, Talke IN, Haydon MJ, Lanz C, Nolte A, Motte P, et al. Evolution of metal hyperaccumulation required cis-regulatory changes and triplication of HMA4. Nature. 2008;453(7193):391–5. Epub 2008/04/22. pmid:18425111.
- 15. Klatte M, Schuler M, Wirtz M, Fink-Straube C, Hell R, Bauer P. The analysis of Arabidopsis nicotianamine synthase mutants reveals functions for nicotianamine in seed iron loading and iron deficiency responses. Plant Physiol. 2009;150(1):257–71. Epub 2009/03/24. pmid:19304929; PubMed Central PMCID: PMC2675739.
- 16. Kobayashi T, Nishizawa NK. Iron uptake, translocation, and regulation in higher plants. Annu Rev Plant Biol. 2012;63:131–52. Epub 2012/03/13. pmid:22404471.
- 17. Colangelo EP, Guerinot ML. Put the metal to the petal: metal uptake and transport throughout plants. Curr Opin Plant Biol. 2006;9(3):322–30. Epub 2006/04/18. pmid:16616607.
- 18. Eide D, Broderius M, Fett J, Guerinot ML. A novel iron-regulated metal transporter from plants identified by functional expression in yeast. Proc Natl Acad Sci U S A. 1996;93(11):5624–8. Epub 1996/05/28. pmid:8643627; PubMed Central PMCID: PMC39298.
- 19. Henriques R, Jasik J, Klein M, Martinoia E, Feller U, Schell J, et al. Knock-out of Arabidopsis metal transporter gene IRT1 results in iron deficiency accompanied by cell differentiation defects. Plant Mol Biol. 2002;50(4–5):587–97. Epub 2002/10/11. pmid:12374293.
- 20. Varotto C, Maiwald D, Pesaresi P, Jahns P, Salamini F, Leister D. The metal ion transporter IRT1 is necessary for iron homeostasis and efficient photosynthesis in Arabidopsis thaliana. Plant J. 2002;31(5):589–99. Epub 2002/09/05. pmid:12207649.
- 21. Vert G, Grotz N, Dedaldechamp F, Gaymard F, Guerinot ML, Briat JF, et al. IRT1, an Arabidopsis transporter essential for iron uptake from the soil and for plant growth. Plant Cell. 2002;14(6):1223–33. Epub 2002/06/27. pmid:12084823; PubMed Central PMCID: PMC150776.
- 22. Nishida S, Tsuzuki C, Kato A, Aisu A, Yoshida J, Mizuno T. AtIRT1, the primary iron uptake transporter in the root, mediates excess nickel accumulation in Arabidopsis thaliana. Plant Cell Physiol. 2011;52(8):1433–42. Epub 2011/07/12. pmid:21742768.
- 23. Vert G, Briat JF, Curie C. Arabidopsis IRT2 gene encodes a root-periphery iron transporter. Plant J. 2001;26(2):181–9. Epub 2001/06/08. pmid:11389759.
- 24. Ramesh SA, Choimes S, Schachtman DP. Over-expression of an Arabidopsis zinc transporter in hordeum vulgare increases short-term zinc uptake after zinc deprivation and seed zinc content. Plant Mol Biol. 2004;54(3):373–85. Epub 2004/07/31. pmid:15284493.
- 25. Lee S, An G. Over-expression of OsIRT1 leads to increased iron and zinc accumulations in rice. Plant Cell Environ. 2009;32(4):408–16. Epub 2009/02/03. pmid:19183299.
- 26. Ishimaru Y, Masuda H, Suzuki M, Bashir K, Takahashi M, Nakanishi H, et al. Overexpression of the OsZIP4 zinc transporter confers disarrangement of zinc distribution in rice plants. J Exp Bot. 2007;58(11):2909–15. Epub 2007/07/17. pmid:17630290.
- 27. Ishimaru Y, Suzuki M, Kobayashi T, Takahashi M, Nakanishi H, Mori S, et al. OsZIP4, a novel zinc-regulated zinc transporter in rice. J Exp Bot. 2005;56(422):3207–14. Epub 2005/11/03. pmid:16263903.
- 28. Li S, Zhou X, Huang Y, Zhu L, Zhang S, Zhao Y, et al. Identification and characterization of the zinc-regulated transporters, iron-regulated transporter-like protein (ZIP) gene family in maize. BMC Plant Biol. 2013;13:114. Epub 2013/08/09. pmid:23924433; PubMed Central PMCID: PMC3751942.
- 29. Lee S, Jeong HJ, Kim SA, Lee J, Guerinot ML, An G. OsZIP5 is a plasma membrane zinc transporter in rice. Plant Mol Biol. 2010;73(4–5):507–17. Epub 2010/04/27. pmid:20419467.
- 30. Yoo S-D, Cho Y-H, Sheen J. Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis. Nat Protocols. 2007;2(7):1565–72. pmid:17585298
- 31. Nelson BK, Cai X, Nebenfuhr A. A multicolored set of in vivo organelle markers for co-localization studies in Arabidopsis and other plants. Plant J. 2007;51(6):1126–36. Epub 2007/08/02. pmid:17666025.
- 32. Clough SJ, Bent AF. Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 1998;16(6):735–43. Epub 1999/03/09. pmid:10069079.
- 33. Deinlein U, Weber M, Schmidt H, Rensch S, Trampczynska A, Hansen TH, et al. Elevated nicotianamine levels in Arabidopsis halleri roots play a key role in zinc hyperaccumulation. Plant Cell. 2012;24(2):708–23. Epub 2012/03/01. pmid:22374395; PubMed Central PMCID: PMCPmc3315242.
- 34. Sinclair SA, Sherson SM, Jarvis R, Camakaris J, Cobbett CS. The use of the zinc-fluorophore, Zinpyr-1, in the study of zinc homeostasis in Arabidopsis roots. New Phytol. 2007;174(1):39–45. Epub 2007/03/06. pmid:17335495.
- 35. Colangelo EP, Guerinot ML. The essential basic helix-loop-helix protein FIT1 is required for the iron deficiency response. Plant Cell. 2004;16(12):3400–12. Epub 2004/11/13. pmid:15539473; PubMed Central PMCID: PMC535881.
- 36. Jakoby M, Wang HY, Reidt W, Weisshaar B, Bauer P. FRU (BHLH029) is required for induction of iron mobilization genes in Arabidopsis thaliana. FEBS Lett. 2004;577(3):528–34. Epub 2004/11/24. pmid:15556641.
- 37. Yuan Y, Wu H, Wang N, Li J, Zhao W, Du J, et al. FIT interacts with AtbHLH38 and AtbHLH39 in regulating iron uptake gene expression for iron homeostasis in Arabidopsis. Cell Res. 2008;18(3):385–97. Epub 2008/02/13. pmid:18268542.
- 38. Wang N, Cui Y, Liu Y, Fan H, Du J, Huang Z, et al. Requirement and functional redundancy of Ib subgroup bHLH proteins for iron deficiency responses and uptake in Arabidopsis thaliana. Mol Plant. 2013;6(2):503–13. Epub 2012/09/18. pmid:22983953.
- 39. Thomine S, Lelievre F, Debarbieux E, Schroeder JI, Barbier-Brygoo H. AtNRAMP3, a multispecific vacuolar metal transporter involved in plant responses to iron deficiency. Plant J. 2003;34(5):685–95. Epub 2003/06/06. pmid:12787249.
- 40. Lanquar V, Lelievre F, Bolte S, Hames C, Alcon C, Neumann D, et al. Mobilization of vacuolar iron by AtNRAMP3 and AtNRAMP4 is essential for seed germination on low iron. EMBO J. 2005;24(23):4041–51. Epub 2005/11/05. pmid:16270029; PubMed Central PMCID: PMC1356305.
- 41. Tan S, Han R, Li P, Yang G, Li S, Zhang P, et al. Over-expression of the MxIRT1 gene increases iron and zinc content in rice seeds. Transgenic Res. 2014. Epub 2014/08/08. pmid:25099285.
- 42. Lee S, Kim SA, Lee J, Guerinot ML, An G. Zinc deficiency-inducible OsZIP8 encodes a plasma membrane-localized zinc transporter in rice. Mol Cells. 2010;29(6):551–8. Epub 2010/05/25. pmid:20496122.
- 43. Lee S, Jeon US, Lee SJ, Kim YK, Persson DP, Husted S, et al. Iron fortification of rice seeds through activation of the nicotianamine synthase gene. Proc Natl Acad Sci U S A. 2009;106(51):22014–9. Epub 2010/01/19. pmid:20080803; PubMed Central PMCID: PMC2799860.
- 44. Hindt MN, Guerinot ML. Getting a sense for signals: regulation of the plant iron deficiency response. Biochim Biophys Acta. 2012;1823(9):1521–30. Epub 2012/04/10. pmid:22483849; PubMed Central PMCID: PMC4008143.
- 45. Ivanov R, Brumbarova T, Bauer P. Fitting into the harsh reality: regulation of iron-deficiency responses in dicotyledonous plants. Mol Plant. 2012;5(1):27–42. Epub 2011/08/30. pmid:21873619.
- 46. Ogo Y, Itai RN, Nakanishi H, Kobayashi T, Takahashi M, Mori S, et al. The rice bHLH protein OsIRO2 is an essential regulator of the genes involved in Fe uptake under Fe-deficient conditions. Plant J. 2007;51(3):366–77. Epub 2007/06/15. pmid:17559517.
- 47. Wu H, Chen C, Du J, Liu H, Cui Y, Zhang Y, et al. Co-overexpression FIT with AtbHLH38 or AtbHLH39 in Arabidopsis-enhanced cadmium tolerance via increased cadmium sequestration in roots and improved iron homeostasis of shoots. Plant Physiol. 2012;158(2):790–800. Epub 2011/12/21. pmid:22184655; PubMed Central PMCID: PMCPmc3271767.
- 48. Santi S, Cesco S, Varanini Z, Pinton R. Two plasma membrane H(+)-ATPase genes are differentially expressed in iron-deficient cucumber plants. Plant Physiol Biochem. 2005;43(3):287–92. Epub 2005/04/28. pmid:15854837.
- 49. Santi S, Schmidt W. Laser microdissection-assisted analysis of the functional fate of iron deficiency-induced root hairs in cucumber. J Exp Bot. 2008;59(3):697–704. Epub 2008/03/05. pmid:18316319.
- 50. Santi S, Schmidt W. Dissecting iron deficiency-induced proton extrusion in Arabidopsis roots. New Phytol. 2009;183(4):1072–84. Epub 2009/06/25. pmid:19549134.
- 51. Nozoye T, Nagasaka S, Kobayashi T, Takahashi M, Sato Y, Uozumi N, et al. Phytosiderophore efflux transporters are crucial for iron acquisition in graminaceous plants. J Biol Chem. 2011;286(7):5446–54. Epub 2010/12/16. pmid:21156806; PubMed Central PMCID: PMC3037657.
- 52. Curie C, Panaviene Z, Loulergue C, Dellaporta SL, Briat JF, Walker EL. Maize yellow stripe1 encodes a membrane protein directly involved in Fe(III) uptake. Nature. 2001;409(6818):346–9. Epub 2001/02/24. pmid:11201743.
- 53. Curie C, Cassin G, Couch D, Divol F, Higuchi K, Le Jean M, et al. Metal movement within the plant: contribution of nicotianamine and yellow stripe 1-like transporters. Ann Bot. 2009;103(1):1–11. Epub 2008/11/04. pmid:18977764; PubMed Central PMCID: PMC2707284.
- 54. Ishimaru Y, Suzuki M, Tsukamoto T, Suzuki K, Nakazono M, Kobayashi T, et al. Rice plants take up iron as an Fe3+-phytosiderophore and as Fe2+. Plant J. 2006;45(3):335–46. Epub 2006/01/18. pmid:16412081.
- 55. Walker EL, Connolly EL. Time to pump iron: iron-deficiency-signaling mechanisms of higher plants. Curr Opin Plant Biol. 2008;11(5):530–5. Epub 2008/08/30. pmid:18722804.
- 56. Inoue H, Kobayashi T, Nozoye T, Takahashi M, Kakei Y, Suzuki K, et al. Rice OsYSL15 is an iron-regulated iron(III)-deoxymugineic acid transporter expressed in the roots and is essential for iron uptake in early growth of the seedlings. J Biol Chem. 2009;284(6):3470–9. Epub 2008/12/04. pmid:19049971.
- 57. Lee S, Chiecko JC, Kim SA, Walker EL, Lee Y, Guerinot ML, et al. Disruption of OsYSL15 leads to iron inefficiency in rice plants. Plant Physiol. 2009;150(2):786–800. Epub 2009/04/21. pmid:19376836; PubMed Central PMCID: PMC2689993.
- 58. Connolly EL, Fett JP, Guerinot ML. Expression of the IRT1 metal transporter is controlled by metals at the levels of transcript and protein accumulation. Plant Cell. 2002;14(6):1347–57. Epub 2002/06/27. pmid:12084831; PubMed Central PMCID: PMC150784.