Identification and characterization of the zinc-regulated transporters, iron-regulated transporter-like protein (ZIP) gene family in maize
- Suzhen Li†1, 2,
- Xiaojin Zhou†2,
- Yaqun Huang1,
- Liying Zhu1,
- Shaojun Zhang2,
- Yongfeng Zhao1,
- Jinjie Guo1,
- Jingtang Chen1Email author and
- Rumei Chen2Email author
© Li et al.; licensee BioMed Central Ltd. 2013
Received: 5 December 2012
Accepted: 1 August 2013
Published: 8 August 2013
Zinc (Zn) and iron (Fe) are essential micronutrients for plant growth and development, their deficiency or excess severely impaired physiological and biochemical reactions of plants. Therefore, a tightly controlled zinc and iron uptake and homeostasis network has been evolved in plants. The Zinc-regulated transporters, Iron-regulated transporter-like Proteins (ZIP) are capable of uptaking and transporting divalent metal ion and are suggested to play critical roles in balancing metal uptake and homeostasis, though a detailed analysis of ZIP gene family in maize is still lacking.
Nine ZIP-coding genes were identified in maize genome. It was revealed that the ZmZIP proteins share a conserved transmembrane domain and a variable region between TM-3 and TM-4. Transiently expression in onion epidermal cells revealed that all ZmZIP proteins were localized to the endoplasmic reticulum and plasma membrane. The yeast complementation analysis was performed to test the Zn or Fe transporter activity of ZmZIP proteins. Expression analysis showed that the ZmIRT1 transcripts were dramatically induced in response to Zn- and Fe-deficiency, though the expression profiles of other ZmZIP changed variously. The expression patterns of ZmZIP genes were observed in different stages of embryo and endosperm development. The accumulations of ZmIRT1 and ZmZIP6 were increased in the late developmental stages of embryo, while ZmZIP4 was up-regulated during the early development of embryo. In addition, the expression of ZmZIP5 was dramatically induced associated with middle stage development of embryo and endosperm.
These results suggest that ZmZIP genes encode functional Zn or Fe transporters that may be responsible for the uptake, translocation, detoxification and storage of divalent metal ion in plant cells. The various expression patterns of ZmZIP genes in embryo and endosperm indicates that they may be essential for ion translocation and storage during differential stages of embryo and endosperm development. The present study provides new insights into the evolutionary relationship and putative functional divergence of the ZmZIP gene family during the growth and development of maize.
KeywordsEmbryo Endosperm Expression profiling Zinc Iron Zinc-regulated transporters Iron-regulated transporter-like protein (ZIP) Subcellular localization Yeast complementation Maize
Zinc and iron are essential for plant metabolism and development . Zinc serves as a key structural motif in many proteins, including DNA-binding Zn-finger protein [2, 3], RING finger proteins and LIM domain containing proteins , which play vital roles in controlling cellular processes such as growth, development and differentiation. An adequate Zn content enhances crop productivity . Iron plays an important role in electron transfer in photosynthesis and respiration, though high concentration of intracellular iron may lead to elevated Fe3+/Fe2+ redox reactions and cause damage . The deficiency of Zn and Fe decreases plant growth and affecting cereal production and grain quality , but excess Zn and Fe may cause significant toxicity to biological systems [8, 9]. Therefore, plants have established a tightly controlled system to balance the uptake, utilization and storage of these metal ions [10, 11]. Because Zn cannot diffuse across cell membrane, specific zinc transporters are required to transport Zn into cytoplasm [12, 13]. In recent years, a number of metal transporters have been identified in plants, including the P1B-ATPase family, zinc-regulated transporter (ZRT), iron-regulated transporter (IRT)-like protein (ZIP), natural resistance-associated macrophage protein (NRAMP) family, and cation diffusion facilitator (CDF) family .
ZRT, IRT-like protein (ZIP) family has been characterized ubiquitously in organisms, including archaea, bacteria, fungi, plants and mammals, and has been demonstrated to be involved in metal uptake and transport . ZIP proteins generally contribute to metal ion homeostasis by transporting cations into the cytoplasm . Functional complementation in yeast indicated that ZIP proteins are able to transport various divalent cations, including Fe2+, Zn2+, Mn2+, and Cd2+. The ZIP proteins consist of 309-476 amino acid residues with eight potential transmembrane domains and a similar membrane topology. There is also a variable region between TM-3 and TM-4, in which the amino- and carboxyl-terminals located on the outside surface of plasma membrane. The variable region contains a potential metal-binding domain rich in conserved histidine residues . Several ZIP proteins have been identified in Arabidopsis. AtIRT1 (Iron-regulate transporter 1) was the first member to be identified through functional complementation of a yeast mutant defective in iron uptake, and it encodes a major Fe transporter at the root surface in Arabidopsis[17–20]. Further analysis showed that the irt1 mutant exhibited lethal chlorotic phenotypes [18–20], and had lower Ni accumulation under Fe-deficient conditions than the wild type plants. These results indicated that AtIRT1 mediates Fe and Ni translocation in Arabidopsis. Likewise, overexpressing AtIRT3 leads to increased accumulation of Zn in shoots and Fe in roots. Moreover, AtIRT3 could complement the Zn and Fe uptake double yeast mutants, indicating that AtIRT3 is involved in Zn and Fe translocation . Besides, expression analysis revealed that the transcripts of AtZIP1 to AtZIP5, AtZIP9 to AtZIP12, and AtIRT3 were increased in response to Zn-deficiency, suggesting that they may enhance Zn acquisition under deficient Zn status in Arabidopsis. In rice, overexpression of OsIRT1 leads to increased Fe and Zn accumulations in shoots, roots and mature seeds, suggesting OsIRT1 is a functional metal transporter for iron, and it is responsible for the absorption of iron from soil, especially under Fe-deficiency [24–26]. On the contrary, over accumulation of OsZIP4 and OsZIP5 cannot increase the Zn content in seeds, though the Zn concentration in roots were dramatically increased in transgenic plants [27, 28]. These results indicated that maintaining the endogenous expression pattern of ZIP genes may be essential for Zn translocation in plants. Likewise, overexpression of TdZIP1, a Zn transporter from wild emmer wheat, causes excess accumulation of Zn in cells, thus generating a toxic cytosolic environment . Therefore, increase Zn content by transgenic approaches may benefit from elucidating the expression pattern of ZIP genes.
Since ZIP is the key transporter for Zn and Fe uptake and translocation in plants, considerable progress has been achieved in cloning and characterizing its functions in crop plants, including soybean and maize [30, 31]. The soybean GmZIP1 is highly selective for Zn, and it might play a role in the symbiotic relationship between soybean and Bradyrhizobium japonicum. The ZmZLP1 (ZmZIP-like protein) was identified from a cDNA library of Zea mays L. (maize) pollen. It was reported that ZmZLP1 localized to the endoplasmic reticulum and may be responsible for transporting zinc from the ER to the cytoplasm, though its physiological function has not been characterized . The maize genome has been thoroughly sequenced and assembled. However, systematic analysis of the maize ZIP gene family is still limited. In the present study, we provide detailed information on the gene identification, chromosomal locations, subcellular localizations and expression patterns of nine ZmZIP genes. In addition, the transporter activities of ZmZIPs were tested by yeast complementation analysis. Our results suggest that ZmZIP genes may be responsible for the uptake and translocation of Zn or Fe and involve in detoxification and storage of metals in plant cells, as well as embryo and endosperm development.
Cloning of ZmZIPgenes and phylogenetic analysis
List of ZIP genes in the maize genome
Expression patterns of ZmZIPgenes in different tissues of maize
Under Fe-deficient conditions, the expression of ZmIRT1 was dramatically up-regulated in shoots and roots. In response to Fe-excess, the transcript level of ZmIRT1 was suppressed in shoots and roots, while that of ZmZIP4, 5, 7 and 8 were increased and reached to the maximum level at 96 h in both shoots and roots (Figure 3). These results indicated that ZmIRT1 and ZmZIP4, 5, 7, 8 are sensitive to environmental Fe conditions in shoots and roots. Under Cu- and Mn-deficient conditions, the expression patterns of ZmZIP genes showed no obvious change (Additional file 3).
Subcellular localization of ZmZIPs
Complementation in yeast cells
The ZIP genes have been reported in several plants, including Arabidopsis, rice, Medicago truncatula, wild emmer wheat, Vitis vinifera L and barley [18–22, 24–29, 32, 33, 35–45]. Most of these genes are found to function as Zn or Fe transporter, though some ZIPs have major roles in Mn transport [22, 33, 34]. Members of the ZIP family have eight predicted transmembrane (TM) domains and a variable region between TM-3 and TM-4 where contains a potential metal-binding domain . Although ZIPs have been characterized in many plants, to the best of our knowledge, there were few reports concerning the isolation and functional characterization of ZIPs in maize. Since, the maize genome sequencing project was completed, many gene families have been identified and characterized in maize [46–48]. In this study, nine cDNAs encoding ZmZIP genes were obtained from maize based on amino acids sequences similarity. In order to analyze the evolutionary relationship of the ZIP family, a phylogenetic tree consists of nine ZIPs and one ZLP1 from maize, 14 rice ZIPs (OsZIPs), 16 Arabidopsis ZIPs (AtZIPs), 5 Hordeum vulgare ZIPs (HvZIPs), 7 Medicago truncatula ZIPs (MtZIPs), Wild Emmer Wheat ZIP (TdZIP1), and Glycine max ZIP (GmZIP1) was generated (Figure 2). It was revealed that the predicted amino acid sequences of ZmZIPs were closely related to ZIPs from other plant species and they were existed as orthologs (ZmIRT1 and HvIRT1, ZmZIP1 and OsIAR1, ZmZIP2 and OsZIP2, ZmZIP3 and OsZIP3, ZmZIP4 and OsZIP4, ZmZIP6 and OsZIP6, ZmZIP7 and OsZIP7, ZmZIP8 and OsZIP8), indicating that those ZIPs from maize, rice and barley may share a common evolutionary ancestor. It has been reported that OsZIP4, OsZIP5 and OsZIP8 are functional zinc transporters and localized to the plasma membrane [27, 32, 36]. AtIRT2 is an iron transporter and localized to intracellular vesicles, suggesting an essential role in preventing metal toxicity through compartmentalization and remobilize iron stores from internal storage vesicles . All of these proteins are able to complement the growth of the yeast strain ZHY3 or DEY1453, which is sensitive to Zn or Fe deprivation due to the mutation in both high and low Zn or Fe affinity system. In this study, similar to the Arabidopsis and rice ZIPs, the maize ZIP proteins showed different degree of zinc or iron complementary capabilities (Figure 6A and 6B). Moreover, ZmZIPs were localized to the plasma membrane and endoplasmic reticulum (Figure 5), suggesting they may functional related to excessive ion detoxification. Hence, these results demonstrated that ZmZIP genes encode Zn or Fe transporters and have various functions associated with uptake and translocation, detoxification and storage of Zn or Fe in plant cells.
The expression patterns of ZmZIP genes reflect their diverse functions during Zn or Fe translocation. It has been reported that the ZIP genes displayed various expression profiles regarding tissue specificity and response to fluctuating environmental Zn and Fe conditions. For example, OsZIP7a was induced mainly in Fe-deficient roots, while OsZIP8 was stimulated in Zn-deficient shoots and roots . Histochemical localization analysis showed that the mRNA of OsZIP4 was accumulated in the vascular bundles of leaves and roots, phloem cells of the stem and the meristems . In the model legume Medicago truncatula, the expression of MtZIP2 was detected in roots and stems and was induced by Zn deficiency , likewise MtZIP1 was expressed in Zn-deficient roots and leaves . In our study, the expression of ZmIRT1 was remarkably up-regulated in roots and shoots under Fe-deficiency, and was induced in shoots at 96 h after Zn-deficiency (Figure 3). ZmZIP4, 5, 7 and 8 were induced and reached a peak in shoots and roots at 96 h after Fe-excess (Figure 3). These results suggested that ZmIRT1 may play essential roles in Fe and Zn uptake, especially under iron deficiency, while ZmZIP4, 5, 7 and 8 may associate with detoxification and storage of excessive Fe. Previous study showed that Arabidopsis thaliana transcription factors bZIP19 and bZIP23 regulate the adaptation to zinc deficiency by increase the transcription of ZIPs and other genes . Therefore, maize bZIP-like transcription factors may be essential for the regulation of ZmZIP expression under Zn deficient status.
It has been demonstrated that Zn play essential roles in embryo and endosperm development [2–4]. Therefore, the ZmZIP genes that preferentially expressed in embryo and endosperm may be important for translocation of Zn2+ into sink organs. The expression analysis showed that ZmIRT1, ZmZIP4 and ZmZIP6 were mainly expressed in embryo, while ZmZIP5 was expressed in both embryo and endosperm. The accumulations of ZmZIP4 and ZmZIP5 were up-regulated in the middle stages of embryo development and then they were repressed, suggesting that they may be essential for plumule and radicle growth. In contrast, ZmIRT1 and ZmZIP6 were stimulated in the late development stages of embryo, which indicates that they may associate with the maturation of embryo. Interestingly, it was observed that the accumulation of ZmZIP5 was dramatically up-regulated during the development of endosperm and reached a peak on 19 DAP, though its expression was decreased on 21 DAP, which suggests that ZmZIP5 may involve in the accumulation of nutrient substance at early grain filling stage. By the light of well assembled genome sequence of maize, an in silico promoter analysis was performed for those ZmZIP genes preferentially expressed in embryo and endosperm. The results showed that the ZmIRT1, ZmZIP4, ZmZIP5 and ZmZIP6 contain cis-elements for seed expression (Additional file 7). Considering that there was some correlation between the VvZIP3 expression profile and the Zn accumulation pattern during the development of reproductive organs , we assumed that ZmIRT1, ZmZIP4, ZmZIP5 and ZmZIP6 may play various roles in both embryo and endosperm development.
Enhancing the iron and zinc content in cereal grains is important for improving human nutrition. Since the amount of metal transporter is generally rate-limiting , manipulating the transporters involved in translocation of micro-essential metals into sink organs could be a way to increase mineral contents. For instance, overexpressing AtZIP1 in barley resulted in a rise in the short-term zinc uptake as well as higher seed Zn and Fe contents . Likewise, the iron and zinc contents were elevated in the shoots, roots and mature seeds of transgenic rice constitutively overexpressing OsIRT1. However, overexpressing OsZIP4 under the control of the cauliflower mosaic virus (CaMV) 35S promoter lead to Zn accumulation in roots, while the Zn concentration in seeds were four times lower than untransgenic controls . Moreover, overexpressing OsZIP5 and OsZIP8 in rice under the control of the maize ubiquitin promoter lead to increased Zn level in roots, though that in shoots and mature seeds were reduced in the transgenic plants [27, 32]. These results indicate that ectopic overexpression of ZIP proteins may have little effect on the enhancement of Zn content in seeds due to overproduction of ZIP in vegetative tissues. Therefore, increasing the accumulation of ZIP proteins and maintain their expression pattern may provide an alternative way to enhance Zn or Fe contents. Since it was revealed that the expression of ZmIRT1, ZmZIP4, ZmZIP5 and ZmZIP6 are associated with seed development, it can be assumed that overexpression of these ZIP genes in a seed specific manner may provide an alternative strategy for biofortification of crops with Zn and Fe.
Although zinc and iron are essential micronutrients for plant growth and development, functional analysis of ZIP family in maize is still limited. The present study provides relevant information concerning the identification and functional characterization of ZmZIP family, and suggests that they may involve in metal uptake and overall cell zinc homeostasis. It is also indicated that ZmZIPs may be essential for ion translocation and storage during differential stages of embryo and endosperm development. In the present study, we provided detailed information of the evolutionary relationship and putative functional divergence of the ZmZIP gene family during the growth and development of maize.
Zea mays seeds were cultured in vermiculite (irrigated with Hoagland nutrient solution) in climate chambers with a light/dark cycle of 16/8 h. The 13-day-old seedlings were transferred to the Hoagland nutrient solution grown for 6 days (The standard Hoagland nutrient solution contained 2.0 μM ZnSO4, 50 μM Fe(III)-EDTA, 0.5 μM CuSO4, and 2.0 μM MnSO4), then transferred to the standard Hoagland nutrient solution and Hoagland medium lacking ZnSO4 (Zn-deficient), Fe (III)-EDTA (Fe- deficient), and 200 μM ZnSO4 (Zn-excess), 500 μM Fe(III)-EDTA (Fe-excess). Shoots and roots were selected and detached at 0 h, 6 h, 12 h, 24 h, 48 h and 96 h after the different treatment for real-time RT-PCR assays.
The BLAST program at GenBank (http://www.ncbi.nlm.nih.gov/blast) was used to search the maize ZIP cDNAs and the acquired cDNAs were compared to the corresponding genome database from maizesequence (http://maizesequence.org/index.html). The putative amino acid sequences were aligned with the program Clustal X Version 2.0  and colored by BOXSHADE (http://www.ch.embnet.org/software/BOX_form.html). Potential transmembrane domains in protein sequences were identified using TMHMM . The phylogenetic tree of 54 members of the ZIP proteins from various species was constructed using MEGA version 4.0 . The accession numbers for the proteins are as follows: Arabidopsis thaliana (AtZIP1: AAC24197, AtZIP2: AAC24198, AtZIP3: AAC24199, AtZIP4: AAB65480, AtZIP5: AAL38432, AtZIP6: AAL38433, AtZIP7: AAL38434, AtZIP8: AAL83293, AtZIP9: AAL38435, AtZIP10: AAL38436, AtZIP11: AAL67953, AtZIP12: AAL38437, AtIRT1: AAB01678, AtIRT2: NP_001031670, AtIRT3: NP_564766, AtIAR1: AF216524); Oryza sativa (OsIAR1: NP_001062003, OsIRT1: AB070226, OsIRT2: AB126086, OsZIP1: AY302058, OsZIP2: AY302059, OsZIP3: AY323915, OsZIP4: AB126089, OsZIP5: AB126087, OsZIP6: AB126088, OsZIP7: AB126090, OsZIP7a: AY275180, OsZIP8: AY324148, OsZIP9: AY281300, OsZIP10: AK107681); Zea mays (ZmZIP1: NM_001137726, ZmZIP2: NM_001159169, ZmZIP3: NM_001155536, ZmZIP4: HM048832, ZmZIP5: NM_001154257, ZmZIP6: NM_001156151, ZmZIP7: NM_001157018, ZmZIP8: NM_001154769, ZmIRT1: NM_001158638, ZmZLP1: ACO50388); Hordeum vulgare (HvIRT1: EU545802, HvZIP3: FJ208991, HvZIP5: FJ208992, HvZIP7: AM182059, HvZIP8: FJ208993); Medicago truncatula (MtZIP1: AY339054, MtZIP2: AY007281, MtZIP3: AY339055, MtZIP4: AY339056, MtZIP5: AY339057, MtZIP6: AY339058, MtZIP7: AY339059); Wild Emmer Wheat (TdZIP1:AY864924); Glycine max (GmZIP1: AY029321).
RNA isolation and real-time RT-PCR
Total RNA was isolated from shoots and roots with TRIzol (Takara). For cDNA synthesis, we used 4 μg of total RNA as a template and M-MLV reverse transcriptase (Fermentas) by primering with oligo-d(T)18 in a 40-μL reaction mixture. Real-time RT-PCR was performed in a 20-μL solution containing a 5-μL aliquot of the cDNA, 0.4 μM of gene-specific primers (Additional file 8) and 10-μL SYBR Green I (Takara). The fragment was amplified by PCR in an ABI 7500 Real Time Thermal Cycler. The constitutively expressed ZmActin1 gene [GenBank: J01238.1] was amplified as the reference gene using the primers ZmActin1F and ZmActin1R (Additional file 8). Changes in expression were calculated via the ∆∆Ct method . For all real-time RT-PCR analysis, two biological replicates were used and three technical replicates were performed for each biological replicate. The sizes of the amplified fragments were confirmed by gel electrophoresis.
Cloning of target genes
The cDNA sequences of nine putative maize ZIP genes with a complete ORF were obtained from the MaizeSequence database (http://www.maizesequence.org/). The primers (Additional file 8) were designed for amplifying the ORFs of these nine ZmZIP genes. Total RNA was isolated from shoots with TRIzol (Takara), and was treated with DNaseI (NEB) before being reverse transcribed. For cDNA synthesis, we used 2 μg of total RNA as a template and M-MLV reverse transcriptase (Fermentas) by primering with oligo-d(T)18 in a 20-μL reaction mixture. PCR was performed in a 20-μL solution containing a 5-μL aliquot of the cDNA, 10 μM of gene-specific primers (Additional file 8), 0.5 U Ex Taq polymerase (Takara), 8 mM dNTPs, 10-μL of 2 × GCI buffer. PCR was performed on a DNA amplification machine (BIO RAD) for a denaturation of 4 min at 94°C, followed by 33 cycles of 1 min at 94°C, 1 min at 60°C, and 1 min at 72°C and a final extension of 10 min at 72°C. The PCR products were separated on a 1% agarose gel and purified with Gel DNA Purification Kit (Shenergy Biocolor) according to the manufacturer’s instruction. The purified product was then cloned into the pGEM-T easy vector (Promega, USA) and sequenced (Openlab, China).
For subcellular localization, a C-terminal GFP fusion expression vector pRTL2GFP was used . Gene-specific primers were designed and the stop codons were deleted (Additional file 8). The coding regions without the stop codon were cloned into pRTL2GFP, respectively. The plasmids were purified using the Wizard Plus Miniprep DNA Purification System (Promega). The ZmZIP-GFP fusion constructs and the mcherry labeled ER marker were co-transformed into Arabidopsis mesophyll protoplasts as described previously [55, 56]. After incubation in the dark at 26°C for 14 h, the fluorescence was examined using a confocal microscope (LSM700; Carl Zeiss). The GFP signal was excitated at 488 nm, and the emission was collected at 500-530 nm; the mcherry signal was excitated at 555 nm, and the fluorescence emission was collected at 610 nm; the 630 emission filter was used to observe the autofluorescence of chlorophyll.
The ORFs of ZmZIP genes were amplified with gene specific primers (Additional file 8), and the PCR fragments were purified from an agarose gel and subsequently ligated into the NotI site of the yeast expression vector pFL61 (provided from Dr. David Eide, University of Missouri-Columbia) . The resulting constructs were sequenced to ensure the correct orientations of the inserts and sequences. The yeast strains used in this experiment are zrt1zrt2 ZHY3 (MATα ade6 can1 his3 leu2 trp1 ura3 zrt1::LEU2 zrt2::HIS3), fet3fet4 DEY1453 (MATa/MATa ade2/+ can1/can1 his3/his3 leu2/leu2 trp1/trp1 ura3/ura3 fet3-2::HIS3/fet3-2::HIS3 fet4-1::LEU2/fet4-1::LEU2), and DY1455 (MATa ade6 can1 his3 leu2 trp1 ura3) (provided by Dr. David Eide) [58, 59]. The pFL61-ZmZIPs were transformed into the yeast strains ZHY3 and DEY1453 using the electroporation method. The empty vector pFL61was applied as a negative control, OsIRT1 was used as the positive control for iron transporter, OsZIP5 and OsZIP8 were applied as the positive control for zinc transporter, and the wild type strain DY1455 harbouring pFL61 was used as another positive control. The yeast complementation was performed as described previously  with slight modification. Transformed cells were selected on synthetic agar medium (SD) containing amino acid supplements without Uracil and 2% glucose. In growth-test experiments, 5-μL drops of yeast culture at an optical density of 1.0, 0.1, 0.01 and 0.001 were spotted onto medium. The yeast strain of zrt1zrt2 ZHY3 were grown on SD/–ura medium (pH 4.4) supplemented with 0.4 mM EDTA and 250 μM or 300 μM ZnSO4. The yeast strain of fet3fet4 were grown on SD/–ura medium (pH 5.5, 5.8 containing 50 mM 2-(N-morpholino) ethanesulfonic acid (MES) supplemented with 0, 50 or 100 μM FeCl3.
Cauliflower mosaic virus
Green fluorescent protein
Opening reading frame
Zinc-regulated transporters, iron-regulated transporter-like protein.
We thank Dr. David Eide (Nutritional Science Program, University of Missouri, Columbia, USA) for providing the yeast strains DEY1453, ZHY3 and yeast expression vector pFL61; Dr. Dongtao Ren (College of Biological Sciences, China Agricultural University) for providing the ER-marker. This work was supported by the National Special Program for GMO Development of China (grant number 2008ZX08003-002).
- Haydon MJ, Cobbett CS: Transporters of ligands for essential metal ions in plants. New Phytol. 2007, 174 (3): 499-506. 10.1111/j.1469-8137.2007.02051.x.PubMedView ArticleGoogle Scholar
- Rhodes D, Klug A: Zinc fingers. Sci Am. 1993, 268 (2): 56-59. 10.1038/scientificamerican0293-56. 62-55PubMedView ArticleGoogle Scholar
- Vallee BL, Auld DS: Zinc coordination, function, and structure of zinc enzymes and other proteins. Biochemistry. 1990, 29 (24): 5647-5659. 10.1021/bi00476a001.PubMedView ArticleGoogle Scholar
- Vallee BL, Falchuk KH: The biochemical basis of zinc physiology. Physiol Rev. 1993, 73 (1): 79-118. 10.2466/pr0.19220.127.116.11.PubMedGoogle Scholar
- Cakmak I: Enrichment of cereal grains with zinc: agronomic or genetic biofortification?. Plant Soil. 2008, 302 (1–2): 1-17.Google Scholar
- Briat JF, Lebrun M: Plant responses to metal toxicity. C R Acad Sci III. 1999, 322 (1): 43-54. 10.1016/S0764-4469(99)80016-X.PubMedView ArticleGoogle Scholar
- 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): 1966-1972.PubMedGoogle Scholar
- 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.View ArticleGoogle Scholar
- 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): 477-484. 10.1111/j.1365-3040.1991.tb01517.x.View ArticleGoogle Scholar
- Palmgren MG, Clemens S, Williams LE, Kramer U, Borg S, Schjorring JK, Sanders D: Zinc biofortification of cereals: problems and solutions. Trends Plant Sci. 2008, 13 (9): 464-473. 10.1016/j.tplants.2008.06.005.PubMedView ArticleGoogle Scholar
- Grotz N, Guerinot ML: Molecular aspects of Cu, Fe and Zn homeostasis in plants. Biochim Biophys Acta. 2006, 1763 (7): 595-608. 10.1016/j.bbamcr.2006.05.014.PubMedView ArticleGoogle Scholar
- Kambe T, Yamaguchi-Iwai Y, Sasaki R, Nagao M: Overview of mammalian zinc transporters. Cell Mol Life Sci. 2004, 61 (1): 49-68. 10.1007/s00018-003-3148-y.PubMedView ArticleGoogle Scholar
- Taylor KM, Morgan HE, Johnson A, Nicholson RI: Structure-function analysis of HKE4, a member of the new LIV-1 subfamily of zinc transporters. Biochem J. 2004, 377 (Pt 1): 131-139.PubMedPubMed CentralView ArticleGoogle Scholar
- Colangelo EP, Guerinot ML: Put the metal to the petal: metal uptake and transport throughout plants. Curr Opin Plant Biol. 2006, 9 (3): 322-330. 10.1016/j.pbi.2006.03.015.PubMedView ArticleGoogle Scholar
- Guerinot ML: The ZIP family of metal transporters. Biochim Biophys Acta. 2000, 1465 (1–2): 190-198.PubMedView ArticleGoogle Scholar
- Maser P, Thomine S, Schroeder JI, Ward JM, Hirschi K, Sze H, Talke IN, Amtmann A, Maathuis FJ, Sanders D, et al: Phylogenetic relationships within cation transporter families of Arabidopsis. Plant Physiol. 2001, 126 (4): 1646-1667. 10.1104/pp.126.4.1646.PubMedPubMed CentralView ArticleGoogle Scholar
- 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): 5624-5628. 10.1073/pnas.93.11.5624.PubMedPubMed CentralView ArticleGoogle Scholar
- Henriques R, Jasik J, Klein M, Martinoia E, Feller U, Schell J, Pais MS, Koncz C: Knock-out of Arabidopsis metal transporter gene IRT1 results in iron deficiency accompanied by cell differentiation defects. Plant Mol Biol. 2002, 50 (4–5): 587-597.PubMedView ArticleGoogle Scholar
- 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): 589-599. 10.1046/j.1365-313X.2002.01381.x.PubMedView ArticleGoogle Scholar
- Vert G, Grotz N, Dedaldechamp F, Gaymard F, Guerinot ML, Briat JF, Curie C: IRT1, an Arabidopsis transporter essential for iron uptake from the soil and for plant growth. Plant Cell. 2002, 14 (6): 1223-1233. 10.1105/tpc.001388.PubMedPubMed CentralView ArticleGoogle Scholar
- 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): 1433-1442. 10.1093/pcp/pcr089.PubMedView ArticleGoogle Scholar
- Lin YF, Liang HM, Yang SY, Boch A, Clemens S, Chen CC, Wu JF, Huang JL, Yeh KC: Arabidopsis IRT3 is a zinc-regulated and plasma membrane localized zinc/iron transporter. New Phytol. 2009, 182 (2): 392-404. 10.1111/j.1469-8137.2009.02766.x.PubMedView ArticleGoogle Scholar
- Kramer U, Talke IN, Hanikenne M: Transition metal transport. FEBS Lett. 2007, 581 (12): 2263-2272. 10.1016/j.febslet.2007.04.010.PubMedView ArticleGoogle Scholar
- Bughio N, Yamaguchi H, Nishizawa NK, Nakanishi H, Mori S: Cloning an iron-regulated metal transporter from rice. J Exp Bot. 2002, 53 (374): 1677-1682. 10.1093/jxb/erf004.PubMedView ArticleGoogle Scholar
- Ishimaru Y, Suzuki M, Tsukamoto T, Suzuki K, Nakazono M, Kobayashi T, Wada Y, Watanabe S, Matsuhashi S, Takahashi M, et al: Rice plants take up iron as an Fe3+-phytosiderophore and as Fe2+. Plant J. 2006, 45 (3): 335-346. 10.1111/j.1365-313X.2005.02624.x.PubMedView ArticleGoogle Scholar
- Lee S, An G: Over-expression of OsIRT1 leads to increased iron and zinc accumulations in rice. Plant Cell Environ. 2009, 32 (4): 408-416. 10.1111/j.1365-3040.2009.01935.x.PubMedView ArticleGoogle Scholar
- 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): 507-517.PubMedView ArticleGoogle Scholar
- Ishimaru Y, Masuda H, Suzuki M, Bashir K, Takahashi M, Nakanishi H, Mori S, Nishizawa NK: Overexpression of the OsZIP4 zinc transporter confers disarrangement of zinc distribution in rice plants. J Exp Bot. 2007, 58 (11): 2909-2915. 10.1093/jxb/erm147.PubMedView ArticleGoogle Scholar
- Durmaz E, Coruh C, Dinler G, Grusak M, Peleg Z, Saranga Y, Fahima T, Yazici A, Ozturk L, Cakmak I, et al: Expression and cellular localization of ZIP1 transporter under zinc deficiency in wild emmer wheat. Plant Molecular Biology Reporter. 2011, 29 (3): 582-596. 10.1007/s11105-010-0264-3.View ArticleGoogle Scholar
- Moreau S, Thomson RM, Kaiser BN, Trevaskis B, Guerinot ML, Udvardi MK, Puppo A, Day DA: GmZIP1 encodes a symbiosis-specific zinc transporter in soybean. J Biol Chem. 2002, 277 (7): 4738-4746. 10.1074/jbc.M106754200.PubMedView ArticleGoogle Scholar
- Xu Y, Wang B, Yu J, Ao G, Zhao Q: Cloning and characterisation of ZmZLP1, a gene encoding an endoplasmic reticulum-localised zinc transporter in Zea mays. Functional Plant Biology. 2010, 37 (3): 194-205. 10.1071/FP09045.View ArticleGoogle Scholar
- 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): 551-558. 10.1007/s10059-010-0069-0.PubMedView ArticleGoogle Scholar
- Vert G, Briat JF, Curie C: Arabidopsis IRT2 gene encodes a root-periphery iron transporter. Plant J. 2001, 26 (2): 181-189. 10.1046/j.1365-313x.2001.01018.x.PubMedView ArticleGoogle Scholar
- Milner MJ, Seamon J, Craft E, Kochian LV: Transport properties of members of the ZIP family in plants and their role in Zn and Mn homeostasis. J Exp Bot. 2013, 64 (1): 369-381. 10.1093/jxb/ers315.PubMedPubMed CentralView ArticleGoogle Scholar
- Ramesh SA, Shin R, Eide DJ, Schachtman DP: Differential metal selectivity and gene expression of two zinc transporters from rice. Plant Physiol. 2003, 133 (1): 126-134. 10.1104/pp.103.026815.PubMedPubMed CentralView ArticleGoogle Scholar
- Ishimaru Y, Suzuki M, Kobayashi T, Takahashi M, Nakanishi H, Mori S, Nishizawa NK: OsZIP4, a novel zinc-regulated zinc transporter in rice. J Exp Bot. 2005, 56 (422): 3207-3214. 10.1093/jxb/eri317.PubMedView ArticleGoogle Scholar
- Lopez-Millan AF, Ellis DR, Grusak MA: Identification and characterization of several new members of the ZIP family of metal ion transporters in Medicago truncatula. Plant Mol Biol. 2004, 54 (4): 583-596.PubMedView ArticleGoogle Scholar
- Stephens BW, Cook DR, Grusak MA: Characterization of zinc transport by divalent metal transporters of the ZIP family from the model legume Medicago truncatula. Biometals. 2011, 24 (1): 51-58. 10.1007/s10534-010-9373-6.PubMedView ArticleGoogle Scholar
- 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): 373-385.PubMedView ArticleGoogle Scholar
- Vert G, Barberon M, Zelazny E, Seguela M, Briat JF, Curie C: Arabidopsis IRT2 cooperates with the high-affinity iron uptake system to maintain iron homeostasis in root epidermal cells. Planta. 2009, 229 (6): 1171-1179. 10.1007/s00425-009-0904-8.PubMedView ArticleGoogle Scholar
- Yang X, Huang J, Jiang Y, Zhang HS: Cloning and functional identification of two members of the ZIP (Zrt, Irt-like protein) gene family in rice (Oryza sativa L.). Mol Biol Rep. 2009, 36 (2): 281-287. 10.1007/s11033-007-9177-0.PubMedView ArticleGoogle Scholar
- Gainza-Cortes F, Perez-Diaz R, Perez-Castro R, Tapia J, Casaretto JA, Gonzalez S, Pena-Cortes H, Ruiz-Lara S, Gonzalez E: Characterization of a putative grapevine Zn transporter, VvZIP3, suggests its involvement in early reproductive development in Vitis vinifera L. BMC Plant Biol. 2012, 12: 111-10.1186/1471-2229-12-111.PubMedPubMed CentralView ArticleGoogle Scholar
- Pedas P, Schjoerring JK, Husted S: Identification and characterization of zinc-starvation-induced ZIP transporters from barley roots. Plant Physiol Biochem. 2009, 47 (5): 377-383. 10.1016/j.plaphy.2009.01.006.PubMedView ArticleGoogle Scholar
- Narayanan NN, Vasconcelos MW, Grusak MA: Expression profiling of Oryza sativa metal homeostasis genes in different rice cultivars using a cDNA macroarray. Plant Physiol Biochem. 2007, 45 (5): 277-286. 10.1016/j.plaphy.2007.03.021.PubMedView ArticleGoogle Scholar
- Sperotto RA, Boff T, Duarte GL, Santos LS, Grusak MA, Fett JP: Identification of putative target genes to manipulate Fe and Zn concentrations in rice grains. J Plant Physiol. 2010, 167 (17): 1500-1506. 10.1016/j.jplph.2010.05.003.PubMedView ArticleGoogle Scholar
- Lin YX, Jiang HY, Chu ZX, Tang XL, Zhu SW, Cheng BJ: Genome-wide identification, classification and analysis of heat shock transcription factor family in maize. BMC Genomics. 2011, 12: 76-10.1186/1471-2164-12-76.PubMedPubMed CentralView ArticleGoogle Scholar
- Xing H, Pudake RN, Guo G, Xing G, Hu Z, Zhang Y, Sun Q, Ni Z: Genome-wide identification and expression profiling of auxin response factor (ARF) gene family in maize. BMC Genomics. 2011, 12: 178-10.1186/1471-2164-12-178.PubMedPubMed CentralView ArticleGoogle Scholar
- Zhou X, Li S, Zhao Q, Liu X, Zhang S, Sun C, Fan Y, Zhang C, Chen R: Genome-wide identification, classification and expression profiling of nicotianamine synthase (NAS) gene family in maize. BMC Genomics. 2013, 14 (1): 238-10.1186/1471-2164-14-238.PubMedPubMed CentralView ArticleGoogle Scholar
- Burleigh SH, Kristensen BK, Bechmann IE: A plasma membrane zinc transporter from Medicago truncatula is up-regulated in roots by Zn fertilization, yet down-regulated by arbuscular mycorrhizal colonization. Plant Mol Biol. 2003, 52 (5): 1077-1088. 10.1023/A:1025479701246.PubMedView ArticleGoogle Scholar
- Assuncao AG, Herrero E, Lin YF, Huettel B, Talukdar S, Smaczniak C, Immink RG, van Eldik M, Fiers M, Schat H, et al: Arabidopsis thaliana transcription factors bZIP19 and bZIP23 regulate the adaptation to zinc deficiency. Proc Natl Acad Sci U S A. 2010, 107 (22): 10296-10301. 10.1073/pnas.1004788107.PubMedPubMed CentralView ArticleGoogle Scholar
- Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997, 25 (24): 4876-4882. 10.1093/nar/25.24.4876.PubMedPubMed CentralView ArticleGoogle Scholar
- Krogh A, Larsson B, von Heijne G, Sonnhammer EL: Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J Mol Biol. 2001, 305 (3): 567-580. 10.1006/jmbi.2000.4315.PubMedView ArticleGoogle Scholar
- Tamura K, Dudley J, Nei M, Kumar S: MEGA4: Molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol. 2007, 24 (8): 1596-1599. 10.1093/molbev/msm092.PubMedView ArticleGoogle Scholar
- Han MJ, Jung KH, Yi G, Lee DY, An G: Rice Immature Pollen 1 (RIP1) is a regulator of late pollen development. Plant Cell Physiol. 2006, 47 (11): 1457-1472. 10.1093/pcp/pcl013.PubMedView ArticleGoogle Scholar
- 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): 1565-1572. 10.1038/nprot.2007.199.PubMedView ArticleGoogle Scholar
- 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): 1126-1136. 10.1111/j.1365-313X.2007.03212.x.PubMedView ArticleGoogle Scholar
- Minet M, Dufour ME, Lacroute F: Complementation of Saccharomyces cerevisiae auxotrophic mutants by Arabidopsis thaliana cDNAs. Plant J. 1992, 2 (3): 417-422.PubMedGoogle Scholar
- Zhao H, Eide D: The yeast ZRT1 gene encodes the zinc transporter protein of a high-affinity uptake system induced by zinc limitation. Proc Natl Acad Sci U S A. 1996, 93 (6): 2454-2458. 10.1073/pnas.93.6.2454.PubMedPubMed CentralView ArticleGoogle Scholar
- Zhao H, Eide D: The ZRT2 gene encodes the low affinity zinc transporter in Saccharomyces cerevisiae. J Biol Chem. 1996, 271 (38): 23203-23210. 10.1074/jbc.271.38.23203.PubMedView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.