Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Identification of a rice metal tolerance protein OsMTP11 as a manganese transporter

  • Mei Zhang ,

    Affiliation Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China

  • Baoxiu Liu

    Affiliations Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China, University of Chinese Academy of Sciences, Beijing, China

Identification of a rice metal tolerance protein OsMTP11 as a manganese transporter

  • Mei Zhang, 
  • Baoxiu Liu


Metal tolerance proteins (MTPs) are a gene family of cation efflux transporters that occur widely in plants and might serve an essential role in metal homeostasis and tolerance. Our research describes the identification, characterization, and localization of OsMTP11, a member of the MTP family from rice. OsMTP11 was expressed constitutively and universally in different tissues in rice plant. Heterologous expression in yeast showed that OsMTP11 complemented the hypersensitivity of mutant strains to Mn, and also complemented yeast mutants to other metals, including Co and Ni. Real time RT-PCR analysis demonstrated OsMTP11 expression was substantially enhanced following 4 h under Cd, Zn, Ni, and Mn treatments, suggesting possible roles of OsMTP11 involvement in heavy metal stress responses. Promoter analysis by transgenic assays with GUS as a reporter gene and mRNA in situ hybridization experiments showed that OsMTP11 was expressed specifically in conducting tissues in rice. DNA methylation assays of genomic DNA in rice treated with Cd, Zn, Ni, and Mn revealed that decreased DNA methylation levels were present in the OsMTP11 promoter region, which was consistent with OsMTP11 induced-expression patterns resulting from heavy metal stress. This result suggested that DNA methylation is one of major factors regulating expression of OsMTP11 through epigenetic mechanisms. OsMTP11 fused to green fluorescent protein (GFP) localized to the entire onion epidermal cell cytoplasm, while vacuolar membrane exhibited increased GFP signals, consistent with an OsMTP11 function in cation sequestration. Our results indicated that OsMTP11 might play vital roles in Mn and other heavy metal transportation in rice.


The rise of industrialism resulted in the beginning of long-term heavy metal pollution and led to serious environmental problems for modern agriculture and human health. Common heavy metals include Zn, Mn, Ni, Co, Cu, Cd, Pb and Hg, among others. Some of these metals are essential trace elements for numerous physiological processes in plants (Zn, Mn, Ni, Co and Cu), while others are non-essential elements, including Cd, Pb and Hg. However, in large amounts even these essential metals can inactive biomolecules, block functional proteins or displace other essential metal ions and therefore are toxic [1]. In nature, heavy metal stress severely affects plant growth and development, and consequently plants have developed chelation, excretion and subcellular compartmentalization mechanisms to alleviate heavy metal toxicity [2]. In these biological processes, several groups of cation transporters play vital roles in maintaining metal homeostasis and reducing ionic toxicity. In plants, divalent ion transporters include calcium antiporters, cation diffusion facilitator proteins, natural resistance-associated macrophage proteins (NRAMP), and Zn-regulated transporter Fe-regulated transporter like proteins [3]. Among these transporters, cation diffusion facilitator (CDF) family proteins are significant proteins responsible for metal ion homeostasis.

Proteins of the CDF family have been cloned from bacteria, fungi, plants, and animals [3], while in plants, these group proteins were renamed as metal tolerance proteins (MTPs). MTPs are one of the important groups of proteins that function in heavy metal homeostasis in plants and play a critical role in removing metals from the cytosol either by intracellular sequestration into vacuoles/vesicles or by cellular export to excellular region [4, 5]. In general, most of MTPs have the following features in common: an N-terminal signature sequence specific to this family (SLAILTDAAHLLSD); four to six putative transmembrane domains (TMDs); a histidine-rich cytoplasmic loop; a large cation efflux domain; and most of the cytoplasmic C-terminus [6, 7]. Protein sequence alignment and ion-binding specificities classified CDF members from three kingdoms of life (Archaea, Eubacteria, Eukaryotes) into three subgroups: Zn-CDF, Fe/Zn-CDF and Mn-CDF [8].

ZAT was the first identified plant cation diffusion facilitator (zinc transporter in Arabidopsis thaliana), which was identified as a crucial gene responsible for Zn tolerance by vacuolar Zn sequestration. ZAT was later renamed AtMTP1 (Metal Tolerance Protein 1 in Arabidopsis thaliana) [9]. AtMTP1 is expressed constitutively in both roots and shoots and confers a moderate increase in Zn tolerance when over-expressed. Two other metal tolerance protein genes in Arabidopsis, AtMTP3 [10] and AtMTP11 [11], were also identified. Among these proteins, AtMTP1 and AtMTP3 belong to Zn-CDFs, and AtMTP11 is allied with Mn-CDFs [8]. Function analysis demonstrated that AtMTP11 can specifically transfer Mn [11], and is involved in both Mn tolerance and homeostasis mechanisms in Arabidopsis. Another protein in Stylosanthes hamata, ShMTP1, is responsible for conferring Mn tolerance in yeast and plants [12]. Recently, several MTPs responsible for Mn transporting have been characterized. The first Mn-CDF member in rice, OsMTP8.1, was identified as tonoplast-localized membrane protein, and its over-expression was found to enhance Mn accumulation and tolerance in yeast and rice [13]. Another rice Mn-CDF member, OsMTP9, was found being involved in the uptake and translocation of manganese in rice plant [14]. Two Beta vulgaris Mn-CDF members, BmMTP10 and BmMTP11, and a cucumber CsMTP8, were also found as manganese transporters, and confer Mn tolerance in yeast [15, 16].

Initial analysis of the rice genome identified 10 genes that encode proteins belonging to the MTP family [8]. Among these, five of the putative proteins, similar to AtMTP11 and ShMTP1 (belonging to the Mn-CDF group), did not possess the N-terminal signature sequence (SLAILTDAAHLLSD) for the CDF family and lacked a His-rich region that is commonly found in eukaryotic members of the CDF family. Furthermore, the transmembrane prediction program (TMHMM, identified only four membrane-spanning regions in the Mn-CDF subfamily. However, the subfamily does exhibit the typical cation efflux domain in the C-terminus, which mediates metal transport. OsMTP11 has the highest homology with AtMTP11 in rice, and its expression is greatly induced by Mn and other heavy metals. Therefore, we propose that OsMTP11 might be integrally involved in Mn tolerance and other heavy metal homeostasis mechanisms in rice.

Manganese (Mn) is an essential trace element in plants, but it can exert phytotoxic effects at elevated concentrations. In our investigation, a rice cDNA encoding OsMTP11 was characterized at the molecular and biochemical levels. Our results showed that OsMTP11 complemented the hypersensitivity of a yeast mutant strain to Mn, and complemented partial yeast mutants to other metals, including Co and Ni. Cd, Zn, Ni and Mn treatments induced OsMTP11 expression. Bisulfite sequence assays showed that a DNA methylation promoter region might regulate the expression pattern of OsMTP11. Previously we have identified a new member of rice MTP family, OsMTP1, which is responsible for the Zn and Cd homeostasis/stress, and mediates the translocation of Zn and Cd from root to the aerial parts in rice [17]. Here in this paper, we characterized OsMTP11, and propose OsMTP11 as a new member of the rice MTP family that serves in Mn and other heavy metal tolerance and homeostasis. In addition, we also characterized the promoter of OsMTP11 as a heavy metal induced promoter, which could also drive the down-stream genes expressing in conducting tissues in rice.

Materials and methods

Phylogenetic and sequence analysis

MTP sequences from rice and Arabidopsis were identified through a BLAST search of the Arabidopsis Information Resource (TAIR; and Rice Genome Annotation ( or TIGR ( databases using AtMTP1 and Cation_efflux (PF01545) domains as queries. Data obtained were predicted amino acid sequences based on nucleotide sequence data. Phylogenetic trees were generated using MEGA 4.0.2. Sequences of OsMTP11, AtMTP11 and ShMTP1 were aligned using Clustal X 2.0. OsMTP11 exon prediction was identified in the Rice Genome Annotation Database ( The transmembrane prediction of OsMTP11, AtMTP11 and ShMTP1 was performed in the TMHMM program ( The OsMTP11 promoter regions were analyzed in the PlantCARE ( program.

Plant materials, growth conditions and stress treatments

Rice seeds (Oryza sativa L. ssp. japonica cv. Nipponbare) were sterilized and soaked in water at 28°C for 3 days without light, then transferred to 1/2 MS liquid medium to grow at 28°C in a 16 h / 8 h light cycle for 2 weeks. Different rice organs were harvested at different time periods to isolate total RNAs for OsMTP11 gene expression analysis. For heavy metal, salt and oxidative stresses, 2-week-old seedlings were transferred into half-strength Murashige Skoog liquid medium plus 0.5 mM CdCl2, 5 mM Zn(NO3)2, 1 mM NiCl2, 2 mM MnSO4, 300 mM NaCl and 100 μM methyl viologen (MV) respectively for different time periods, and the roots and leaves were subsequently collected to isolate total RNAs or stored at -70°C for further use. Experiments were performed following a completely randomized design with three replications and repeated at least twice. In the rice transgenic assay for OsMTP11’s promoter-derived GUS detection, Japonica rice (Zhonghua11) was used according to reference [17].

Gene expression analysis by real time RT-PCR

Total RNA was extracted with TRIzol Reagent (Invitrogen, USA) and reverse transcribed to cDNA with M-MLV reverse transcriptase (Promega, Shanghai) according to the manufacturer’s instructions. The cDNAs were further used for gene expression analysis. Real time RT-PCR was conducted using a model 7500 real-time PCR system (Applied Biosystems). To normalize the amount of total cDNA present in each reaction, the rice OsUBQ5 (AK061988) gene was used as an internal control. The primers used for cDNA cloning were as follows: OsMTP11RTF (5’- ACGCTCGTTGTTGTCTGATGGG-3’) and OsMTP11RTR (5’- GTCACTGCAAGCATGATGTCCAC-3’); OsUBQ5RTF (5’- CGCCGTGCTCCAGTTCTA-3’) and OsUBQ5RTR (5’- CGATTTCCTCCTCCTTCCTT-3’), designed according Arvidsson et al [18]. In brief, real-time RT-PCR was performed in a total volume of 20 μl reaction mixtures with gene-specific primers. Each reaction included 10 μl of SYBR green real-time PCR master mix (Bio labs), 0.5 μM (each) forward and reverse primers, and 2 μl of cDNA template (equivalent to 100 ng cDNA). The amplification was performed using the following cycle parameters: 94°C for 30 s, followed by 40 cycles of 94°C for 15 s, and 60°C for 40 s for plate reading. Three independent biological repeats were performed for each treatment. Gene expression levels were calculated from the threshold cycle (CT) according to the 2−ΔΔCT method.

mRNA in situ hybridization

mRNA in situ hybridization was performed as described by Yuan et al [17]. Briefly, the DNA fragment (414 bp) of OsMTP11 full length cDNA was chosen as a template to generate DIG-labeled probe, which was PCR-amplified with full length cDNA as template, and the primers were as follows: pM11RHF (5’-ATGGGGATGAGTTCAGCTTG-3’) and pM11RHR (5’-AGTAATGGGAGCCAAACGTG-3’). PCR products were then cloned into pGEM-T vector (Promega, Shanghai, China) to generate recombinant plasmid pGOsM11. Transverse sections (8 μm thick) were probed with a digoxigenin-labeled antisense probe or sense probe (control; DIG Northern starter kit; Roche). The slides were observed using a microscope and photographed.

Promoter cloning and GUS detection

The genomic DNA was isolated from rice leaf (japonica variety Zhonghua 11) with CTAB methods. The promoter region of OsMTP11 was cloned through standard PCR protocol with genomic DNA as template, and the primers are MTP11PF (5’-CGGAATTCTTATTTGGTTGCCTCCGTGT-3’) and MTP11PR (5’-AACTGCAGGCCATTATTCCACGAACCAG-3’). Then the 1,988 bp promoter fragments were digested with EcoRI and PstI, and inserted into the pCAMBIA1381z vector. After it was confirmed by sequencing, the construct was introduced into Agrobacterium strain EHA105 and transformed into wild-type Zhonghua 11 following a standard procedure [19]. Histochemical GUS analysis was performed. Briefly, after GUS staining, the rice roots and leaves were decolorized with 70% ethanol, and photographed using a microscope. Or the tissues were fixed with glutaraldehyde solution (0.1M PBS pH7.0, 2% glutaraldehyde, 2.5% PA), embedded with EP812 resin. Then the sections were photographed using a microscope.

Yeast strains, medium, and transformation

The yeast strains used in this study are summarized in Table 1. The yeast mutants used to derive the parental strain BY4741 were all obtained from Euroscarf ( Transformants were selected on uracil-deficient medium and grown in synthetic dropout medium containing 2% galactose (SDG medium), including 50 mM (NH4)2SO4, 0.7% yeast nitrogen base without amino acids (YNB, BD Difco, USA), and 0.3% appropriate amino acids, pH6.8. For metal tolerance assays, yeast was grown in liquid SDG medium (with 2% [w/v] galactose) until reaching OD600 to 1.0, and drop assays were performed on SDG plates under different concentrations of Mn, Zn, Cd, Co, Ni or Cu. The growth curve of yeast was measured based on the growth rate according to the OD600 values.

Table 1. List of S. cerevisiae mutant strains used in this research.

Euroscarf ( is a collection of single-deletion mutants in S. cerevisiae (Frankfurt).

The yeast expression vectors of OsMTP11 and AtMTP11 were constructed using two pairs of primers: MTP11YEF (5’- TTTCAGGGCGCCATGGATGGCGGCGGCGGTCGCGGG -3’) and MTP11YER (5’- TCATGCTAGACCATGGCTATTTTTCATGGGACAGAG -3’); and AtMTP11YEF (5’- TTTCAGGGCGCCATGGATGGTTGAGCCAGCTAGTCC -3’) and AtMTP11YER (5’- TCATGCTAGACCATGGCTAACAGTGGGATCTAGCGT -3’) were used to amplify the OsMTP11 and AtMTP11 open reading frame regions. The PCR fragments were subsequently subcloned into the NcoI sites of pYES260 (Euroscarf), following the GAL1 promoter with the in-fusion technique (BD In-Fusion PCR cloning Kit, Takara), yielding pYES260-OsMTP11 and pYES260-AtMTP11. The pYES260-OsMTP11, pYES260-AtMTP11 and pYES260 were then transformed into yeast cells following Gietz [20].

Measure of heavy-metal content in yeast

Yeast cells were grown for 36 h in 20 mL of culture (with different metals) and the OD value was measured until OD600 to 1.0 was reached. The yeast cultures were then diluted as 1:100 with fresh medium (with total volume of 500 ml medium for one sample). Under liquid-shaking culture for about 24 h (OD600 till 1.0), MnSO4, CoCl2, and NiCl2 was supplied separately until the final concentrations of Mn, Co and Ni reached at 3.5 mM, 0.2 mM and 0.15 mM, and yeast cells were allowed to grow for another 24 h to make sure absorbing sufficiently. The cells were collected and washed by centrifugation with double distilled water (ddH2O) for three times. Cell pellets were dried in the oven at 65°C for 3–5 days, and then the cell pellets were digested in in 6 mL of nitric acid at 80°C for 1 h following the instructions established by Li and Kaplan [21]. Following digestion, samples were diluted to 100 mL with deionized water and analyzed with Perkin-Elmer Inductively Coupled Plasma Atomic Absorption Spectrometer (ICP-AAS).

DNA methylation assay by the bisulfite sequence method

Two-week rice seedlings were rinsed separately with 0.5 mM CdCl2, 5 mM ZnSO4, 2 mM MnSO4, 1 mM NiCl2 and 300 mM NaCl for 72 hrs. The root genomic DNA was subsequently isolated using DNAeasy Plant Mini Kit (Qiagen, Germany). Untreated rice seedlings were used as controls. A total of 1 μg genomic DNA was subjected to bisulfate modification with the EpiTect Bisulfite Kit (Qiagen, Germany) following the manufacturer’s instructions. The OsMTP11 starting code (ATG) up stream sequence (-2,250 bp) was analyzed on the MethPrimer website ( The primers were designed based on this program, then used to amplify the OsMTP11 promoter region from -970 to -1216: P1-F: 5’- TGTATTTGAGTTTTATAGTTGTTTTTTT CGG-3’; and P1-R: 5’- AAAATTTTAACTACTTATTTACCATCCTTT -3’. The amplified fragments were subcloned into the pGEM-T Easy vector (Promega) and sequenced. In each sample, 30 clones in total were sequenced and analyzed on Kismeth ( to identify the DNA methylation status.

Transient expression of OsMTP11 in onion cells

DNA fragments containing an open reading frame region without an OsMTP11 stop codon were obtained via PCR with forward primer MTP11GL: 5’-CGGGATCCATGGCGGCGGCGGTCGCGGG-3’ and reverse primer MTP11GR: 5’-CGGGATCCTTTTTCATGGGACAGAGCGT-3’ (the BamHI site is underlined). The PCR fragment was then integrated into the BamHI site prior to the ATG start code of the Enhanced Green Fluorescent Protein (EGFP) using pUC18-EGFP [22]. The DNA constructs were introduced into onion (Allium cepa) epidermal cells as described previously [22]. After incubation at 22°C for 24 h, GFP fluorescence was observed using the confocal laser scanning microscope LSM5 PASAL (Carl Zeiss).


OsMTP11 is one of rice Mn-MTPs

The OsMTP11 gene (Os01g62070) encodes a protein of 415 amino acids (46.1 kDa) containing the cation efflux domain (PF01545, in its C-terminal region. Members of the cation efflux family are often integral membrane proteins which were found to increase tolerance to divalent metal ions such as Zn, Cd, Mn and Co. Rice genome sequencing results positioned OsMTP11 on chromosome 1 with six exons and five introns (Fig 1A).

Fig 1. Bioinformatics analyses of OsMTP11 nucleotide and amino acid sequences.

A. OsMTP11 gene structure analysis in the Rice Genome Annotation Database ( B. Phylogenetic tree of the MTP family from rice and Arabidopsis. The tree was constructed using MEGA 4.0.2 by the neighbor-joining method. Arabidopsis MTP amino acid sequences were obtained from AtMTP1, At2g46800; AtMTP2, At3g61940; AtMTP3, At3g58810; AtMTP4, At2g29410; AtMTP5, At3g12100; AtMTP6, At2g47830; AtMTP7, At1g51610; AtMTP8, At3g58060; AtMTP9, At1g79520; AtMTP10, At1g16310; AtMTP11, At2g39450; AtMTP12, At2g04620. Rice MTP amino acid sequences were downloaded from OsMTP11, Os01g62070; OsMTP1, Os05g03780; OsMTP5, Os02g58580; OsMTP6, Os03g22550; OsMTP7, Os04g23180; OsMTP8, Os02g53490; OsMTP8.1, Os03g12580; OsMTP9, Os01g03914; OsMTP11, Os01g62070; OsMTP11.1, Os05g38670; OsMTP12, Os08g32680. C. Amino acid alignment of OsMTP11, AtMTP11 [11] and ShMTP1 (AY181256) [12]. Amino acid sequences of four predicted transmembrane (TM) segments are boxed. Amino acid residues with dark shading indicate conserved sequences, and residues with light gray shading indicate those conserved in two protein sequences. D. The predicted transmembrane helices of OsMTP11. The transmembrane domains were estimated using TMHMM2: The peaks show the predicted transmembrane (TM) regions of proteins. These data indicate that OsMTP11 has four obvious TM regions.

In previous reports [5], OsMTP11 was grouped into the Mn-CDF group. In the present study, phylogeny reconstruction with 10 rice and 12 Arabidopsis MTPs showed that OsMTP11 has the highest homology with AtMTP11 [23] (Fig 1B). Furthermore, predicted sequence analysis from OsMTP11 protein showed 75.66% and 49.39% identity with AtMTP11 (Loci: At2g39450) and ShMTP1 (AY181256) at the amino acid level, respectively. We also perform OsMTP11 sequence alignment with AtMTP11 and ShMTP1. The results showed that OsMTP11, like AtMTP11 and ShMTP1, lacks the complete N-terminal signature sequence (SLAILTDAAHLLSD) for the CDF family and exhibits the absence of a His-rich region commonly found in eukaryotic members of the CDF family. Furthermore, the transmembrane prediction program identified models for the OsMTP11 consisting of four ( membrane-spanning regions (Fig 1C and 1D). These results indicated that OsMTP11 is a typical Mn-CDF in rice.

The expression of OsMTP11 was induced by several heavy metals

OsMTP11 spatial expression pattern was investigated by real time RT-PCR analysis. Our results demonstrated that OsMTP11 was expressed constitutively in most rice tissues (Fig 2A). The highest level of OsMTP11 transcript was detected in 2-week rice and 8-week roots and leaves. OsMTP11 was weakly expressed in 1-week rice tissues and 8-week stems, and there were some transcript accumulation in rice florets and immature seeds.

Fig 2. Expression pattern of OsMTP11 by real time RT-PCR.

A. Real time RT-PCR results of OsMTP11 expression in wild-type rice plants (Nipponbare) from different tissues or organs. The amplification of the rice OsUBQ5 (AK061988) gene was used as a control to normalize the transcript level of OsMTP11. B. Expression analysis of OsMTP11 under different heavy metal stresses (Mn, Cd, Zn and Ni) by real time RT-PCR. The expression of OsMTP11 is increased in rice roots and shoots treated with 0.5 mM CdCl2, 5 mM Zn(NO3)2, 1 mM NiCl2, 2 mM MnSO4, 300 mM NaCl and 100 μM methyl viologen (MV) for different time periods. C. Expression analysis of OsMTP11 under 300 mM NaCl and 100 μM methylviologen (MV) by real time RT-PCR.

To test if OsMTP11 expression was affected by heavy metal stresses, transcript accumulation in 2-week rice plants exposed to2 mM MnSO4, 0.5 mM CdCl2, 5 mM Zn(NO3)2 and 1 mM NiCl2 was assessed by real time RT-PCR analysis. Temporal induction of OsMTP11 transcripts in response to the above heavy metals was characterized by analyzing roots and leaves at various times following treatment. Fig 2B shows a rapid and marked increase in OsMTP11 expression following 4 h-stress by Cd, Zn, Ni and Mn, peaking at 24 h after stresses. OsMTP11 transcript induction was highest due to Mn and Zn treatment compared to Cd and Ni (Fig 2B). Meanwhile, we also checked the expression pattern of OsMTP11 under salt and MV treatments, our results showed that 300 mM NaCl hardly affected the transcript level of OsMTP11, while MV can slightly induce the OsMTP11’s expression (Fig 2C).

Heterogenous expression of OsMTP11 in yeast confers tolerance to Mn, Co and Ni but not Zn, Cd and Cu

The high sequence homology between OsMTP11 and AtMTP11 at the putative protein level, as well as the observation that OsMTP11 expression was indeed regulated by several heavy metals suggests that OsMTP11 might encode a functional cation efflux transporter. Previous reports revealed that AtMTP11 and ShMTP1 specifically transport Mn [11, 12, 23]. Here, OsMTP11 transport abilities for Mn and other divalent ions were also investigated using a series of yeast mutants defective in cation transport.

First, the Mn-transport ability of the OsMTP11 and AtMTP11 transporters were inferred from growth of S. cerevisiae Mn-sensitive mutant strain pmr1Δ on SDG medium supplemented with 1 mM Mn (Fig 3A). PMR1 is the yeast secretary pathway pump responsible for high-affinity transport of Mn and Ca into the Golgi and confers Mn tolerance by effectively removing Mn from the cytoplasm [24]. Heterologous expression of OsMTP11, as well as AtMTP11, restored the growth of the yeast mutant strain pmr1Δ on 1 mM Mn. The OsMTP11 and AtMTP11-transformed pmr1Δ mutant strain exhibited enhanced growth compared to the pmr1Δ mutant strain transformed with the empty vector (Fig 3A). Compared with the wild-type yeast, growth of the pmr1Δ yeast strain with OsMTP11 and AtMTP11 expression was slightly retarded, however the empty vector pmr1Δ yeast strain did not grow on 1 mM Mn (Fig 3A).

Fig 3. Complementation of yeast mutants on selective medium.

A. OsMTP11 and AtMTP11 genes complement the Mn-hypersensitive phenotype of a pmr1Δ yeast mutant on selective medium (SDG medium) without or with 1 mM Mn. B. OsMTP11 complemented the Co-hypersensitive phenotype of the cot1Δ yeast mutant and Ni-hypersensitive phenotype of the smf1Δ yeast mutant, but could not complement the Zn-hypersensitive phenotype of the zrc1Δ yeast mutant, the Cd-hypersensitive phenotype of the ycf1Δ yeast mutant and the Cu-hypersensitive phenotype of the cup2Δ yeast mutant. C. OsMTP11 is incapable of complementing the yeast vacuolar acidification mutants vph2Δ and vma8Δ.

In addition, we verified whether the OsMTP11 gene could complement yeast mutants defective in other divalent ion transport (Fig 3B). The cot1Δ mutant is hypersensitive to Co [21, 25], and we found that OsMTP11 partially complemented the cot1Δ mutant phenotype when grown on 0.3 mM Co, indicating that OsMTP11 can transport Co to a certain extent. The smf1Δ mutant is a Ni sensitive strain. The SMF1 gene that functions in cellular accumulation of Ni and Mn has been deleted [26]. OsMTP11 can, to a certain degree, complement the Ni-sensitive phenotype of the smf1Δ mutant, suggesting that OsMTP11 also transports Ni. The zrc1Δ yeast mutant is a Zn-sensitive strain. In this mutant, the ZRC1 gene-encoding transporter that sequesters Zn into the vacuole has been deleted [21]. Our results indicated OsMTP11 could not complement the zrc1Δ mutant Zn-sensitive phenotype. We further transformed the ycf1Δ, and cup2Δ mutant strains, which are unable to grow at the medium plus Cd and Cu, respectively. YCF1 is an ABC transporter that confers Cd tolerance through the transport of Cd conjugates into the vacuole [27]. CUP2 is a yeast copper-binding transcription factor, which can activate transcription of the metallothionein genes in response to elevated copper concentrations [28]. The results showed that OsMTP11 did not contribute to increased tolerance of ycf1Δ to Cd and cup2Δ to Cu (Fig 3B).

Two yeast vacuolar acidification mutants (vma8Δ and vph2Δ) were also chosen to determine if OsMTP11 could rescue the mutant Zn hypersensitive phenotype. The VMA8 gene encodes a subunit of the vacuolar-type H+-ATPase catalytic domain, and the VPH2 protein is required for functional vacuolar ATPase biogenesis [29, 30]. Yeast mutants vma8Δ and vph2Δ are unable to acidify their vacuoles and have increased sensitivity to some heavy metals, such as Zn (no growth at 0.25 mM Zn). Our results showed that OsMTP11 could not restore the growth of vma8Δ and vph2Δ under 0.25 mM Zn conditions (Fig 3C). This result indicated that OsMTP11 does not assist in the yeast proton gradient in the vacuole. The role of OsMTP11 is inconsistent with another MTP, PtdMTP1, which can partially rescue both acidification mutants [31].

The yeast growth curve was recorded under different heavy metal treatments. First, we evaluated mutant strain pmr1Δ under 0.1 mM Mn stress. Results showed that cell growth of pmr1Δ transformed with an empty vector was inhibited completely, whereas growth of pmr1Δ cells expressing OsMTP11 was nearly restored at 0.1 mM Mn, as same as AtMTP11 (Fig 4A). These data indicated that OsMTP11 complemented the Mn sensitivity of the pmr1Δ mutant yeast, acting as a Mn transporter on similar manners with AtMTP11. We also chose yeast mutant smf1Δ to investigate growth conditions under 3.5 mM Mn and 0.2 mM Ni stress. Our results showed that OsMTP11 partially restored the restrained growth condition of smf1Δ by Mn and Ni (Fig 4B). Similarly, OsMTP11 partially restored the restraining conditions of cot1Δ by 0.2 mM Co (Fig 4B), which indicated that OsMTP11 could transport Co and elevate the tolerance of Co in cot1Δ yeast.

Fig 4. Effect of OsMTP11 expression in wild yeast BY4741 and yeast mutants for heavy metal tolerance and cation content.

A. Yeast mutant (pmr1Δ) transformed with the empty plasmid vector (pYES260) or MTP genes in pYES260 (OsMTP11 and AtMTP11) were grown in either SDG liquid medium or SDG liquid medium supplemented with 0.1 mM Mn2+. Culture optical density at 600 nm (OD600) was determined at 12 h intervals. B. Yeast mutants (smf1Δ and cot1Δ) transformed with the empty plasmid vector (pYES260) or the OsMTP11 gene in pYES260 were grown in either SDG liquid medium or SDG liquid medium supplemented with 0.2 mM Ni2+ (smf1Δ), 3.5 mM Mn2+ (smf1Δ) and 0.2 mM Co2+ (cot1Δ). Culture optical density at 600 nm (OD600) was determined at 12 h intervals. C. Wild type yeast BY4741 transformed with the empty plasmid vector (pYES260) or the OsMTP11 gene in pYES260 was grown in either SDG liquid medium or SDG liquid medium supplemented with 3.5 mM Mn2+, 0.2 mM Co2+ and 0.15 mM Ni2+. Culture optical density at 600 nm (OD600) was determined at 12 h intervals. D. OsMTP11 expression affects heavy metal content in yeast. Wild type yeast BY4741 transformed with the empty plasmid vector (pYES260) or the OsMTP11 gene in pYES260 was grown in SDG liquid medium supplemented with 3.5 mM Mn2+, 0.2 mM Co2+ and 0.15 mM Ni2+. The yeast was harvested at an OD600 value as 1.5~1.8, then the heavy metal was measured with ICP-AAS. Results represent means ± standard error of three biological replicates. Single asterisk symbols (*) indicate significant differences between control (empty vector pYES260) and experimental samples (OsMTP11- pYES260) at an individual detection (0.01 < P < 0.05); Double asterisk symbols (**) indicate significant differences between control (empty vector pYES260) and experimental samples (OsMTP11- pYES260) at an individual detection (P < 0.01).

A previous study revealed that AtMTP1 actively transported Zn2+ into the vacuole using a pH gradient [32], and AtMTP3 conferred Zn tolerance in yeast cells through intracellular Zn sequestration [10]. We determined the basis of OsMTP11-mediated heavy metal tolerance by analyzing Mn, Co and Ni accumulation in the yeast transformants. First, we measured the growth curve of wild yeast strain BY4741 heterologous expression of OsMTP11 under Mn, Co and Ni treatments. Our results showed that all of the above metals inhibited yeast cell growth, and OsMTP11 partially restored yeast growth rates (Fig 4C). Subsequently, we analyzed Mn, Co and Ni accumulation in yeast (Fig 4D). Results showed that yeast transformed with pYES260-OsMTP11 accumulated lower levels of Mn, Co and Ni than yeast cells transformed with the empty vector pYES260. This suggests that OsMTP11-mediated Mn, Co and Ni tolerant yeast cells are derived from extracellular excretion of heavy metal cations.

DNA methylation of the OsMTP11 promoter region may regulate OsMTP11 induced-expression under heavy metal stresses

DNA methylation is an epigenetic regulatory mechanism of gene expression. Abiotic stresses, such as aluminum, heavy metals, and water are known to alter cytosine methylation throughout the genome and at specific loci [33]. In this study, OsMTP11 expression was induced by Cd, Zn, Ni and Mn and OsMTP11 promoter sequence (-2,250 bp) analysis indicated that five CpG islands exist in the promoter region (Fig 5A), which can mediate DNA methylation at cytosine and further affect gene expression. We investigated the epigenetic regulatory mechanism of OsMTP11 induced by heavy metals through performing DNA methylation detection assays using sodium bisulfate treatments and DNA sequencing. Our results showed a decreased methylation rate at CG, CHG, and CHH sites in the OsMTP11 promoter region under Cd, Zn, Ni and Mn treatments (Fig 5B), suggesting induced OsMTP11 expression by heavy metal stress might be regulated by promoter DNA methylation. While compared to salt treatment (300 mM NaCl), under which the expression level of OsMTP11 could not be affected (Fig 2B), accordingly, the DNA methylation status kept similar with the control (Fig 5B).

Fig 5. DNA methylation analysis of the OsMTP11 promoter region.

A. Schematic distribution of CpG sites and CpG islands in the OsMTP11 promoter region. Blue area indicates CpG islands. The scale bar indicates 100 bp. Red bar indicates the region analyzed by bisulfate sequencing. B. Comparison of percentages of cytosine methylation of three different types (CpG, CpHpG, and CpHpH) in rice seedling roots between control and under heavy metal stress (0.5 mM CdCl2, 5 mM ZnSO4, 2 mM MnSO4, 1 mM NiCl2) or salt treatment (300 mM NaCl) for 72 hours.

OsMTP11 functions as a cation transporter and is localized in the cytoplasm

The subcellular localization of OsMTP11 was determined by an in vivo targeting experiment in which OsMTP11-fused soluble enhanced fluorescent protein (EGFP) was transiently expressed in onion (Allium cepa L.) epidermal cells. The results localized OsMTP11-EGFP primarily to the entire cytoplasm (Fig 6, lower panels). However it was clearly absent in the vacuole, but the vacuolar membrane exhibited strong GFP signals. This was obviously distinguishable from the EGFP control, which was detected throughout the cell (Fig 6, upper panels). Based on these in vivo targeting results, we concluded that rice OsMTP11 is predominantly localized to the cytoplasm endomembrane system.

Fig 6. Transient expression of OsMTP11::EGFP in onion epidermal cells.

A. Localization of EGFP control. B. Bright-field and fluorescence merged image of A. C. Localization of OsMTP11::EGFP. D. Bright-field and fluorescence merged image of C.

The OsMTP11 subcellular localization results were verified by bioinformatics analysis with four different programs to predict the possible localization sites of OsMTP11 (Table 2). Predictions from WoLF PSORT ( showed that OsMTP11 localization at the plasma membrane, endoplasmic reticulum, endoplasmic reticulum vacuolar membrane and vacuolar membrane scored respectively 5, 4.5, 4.5 and 3.5, which indicated that OsMTP11 may evenly distribute at the plasma membrane and endomembrane systems, and coincided with our EGFP fusion protein assay results. Similarly, the Plant-Ploc ( program predicted OsMTP11 localized in the cytoplasm; and Target P ( predicted a low OsMTP11 score value for a chloroplast transit peptide (0.211, cTP), mitochondrial targeting peptide (0.053, mTP) and secretory pathway signal peptide (0.157, SP), with uncertain localization scores (0.715). ARAMEMNON ( predicted OsMTP11 distributed primarily in secretory pathways with a high absolute value (3.7). Cumulatively, the above program predictions indicated OsMTP11 with cytoplasmic localizations, primarily in the plasma membrane and endomembrane system, serving a role in transporting divalent ions extracellularly or into intracellular vacuoles.

Table 2. Subcellular localization of OsMTP11 was predicted using different databases and programs.

OsMTP11 was expressed mainly in conducting tissues in rice

Due to OsMTP11 as a transporter protein, we also detected the expression pattern of OsMTP11 through mRNA in situ hybridization and promoter derived- GUS staining assays. Our results indicated that OsMTP11 transcripts distributed mostly in conducting tissues in rice, and has a similar pattern with OsMTP1 [17]. In Fig 7, OsMTP11 mRNA accumulated specifically near vascular tissue (Fig 7A, 7B and 7C). The cross sections of leaf and sheath showed that the blue signals were distributed in specific sieve tube files (A and B), while the longitudinal leaf sheath sections showed that the signals were continuous (C). No positive reaction above background levels was detected on sections hybridized with sense RNA (Fig 7D).

Fig 7. mRNA in situ hybridization of OsMTP11 in rice leaves.

Blue or purple precipitates indicate positive OsMTP11 mRNA signals. A. Transverse sections of a mature leaf. B. Transverse sections of a young leaf bud. C. Longitudinal sections of a seedling leaf bud. D. Control with the transverse sections of leaf bud.

To further explore the expression pattern of OsMTP11, the putative promoter, about 2 kb DNA upstream of the OsMTP11 coding region sequence, was fused to the GUS reporter gene. Histochemical staining for GUS activity in transgenic rice plants showed that OsMTP11 was constitutively expressed, and the higher-intensity GUS staining was observed in conducting tissues in the rice leaves and roots (Fig 8).

Fig 8. OsMTP11 native promoter-drived GUS staining in rice leaves and roots.

Blue precipitates indicate positive GUS signals. A. Leaf with GUS staining in vein tissue. B. Root tip with GUS staining in conducting tissue. C.Transverse sections of A. D. Transverse sections of B.

The OsMTP11 promoter contains regulatory elements in response to environmental signals

In this study, Northern blot analysis characterized OsMTP11 as a heavy metal-induced gene. Therefore, analyzed the OsMTP11 promotor region (a 2,250 bp upstream genomic DNA region corresponding to the ATG start codon) to identify cis-acting regulatory elements, which can be regulated by heavy metal and other environmental stresses. The OsMTP11 promoter region (-2,250 bp to ATG) is shown in Fig 9. Analysis of the OsMTP11 promoter using PlantCARE ( indicated that a number of potential cis-acting elements that respond to environmental signals were present (Fig 9), and these elements are classified in Table 3. Two types of heavy metal-responsive elements (MREs) have been identified and their corresponding metal-induced transcription factors have been characterized in detail. One kind of MRE consists of a highly conserved heptanucleotide core (MRE1; 5’- TGCRCNC -3’, R = A, G; N = any residue) and less conserved flanking nucleotides [34]; the other is comprised of the consensus sequence 5’- HTHNNGCTGD -3’ (MRE2; D = A, G, or T; H = A, C, or T; N = any residue) [35]. We found 3-MRE1s and 1-MRE2 in the OsMTP11 promoter region. They were localized separately at -796 bp, -1,273 bp, -1,678 bp and -1,058 bp sites, which may be involved in heavy metal induced OsMTP11 expression. Seven putative abscisic acid-response element-like motifs (ABRE; 5’- ACGTG -3’) were present at -711 bp, -1,102 bp, -1,286 bp, -1,476 bp, -1,820 bp, -1,863 bp and -2,051 bp. These elements could be responsible for gene expression during dehydration and other stress [36]. Two I-box elements (5’- GATAAG -3’) thought to be involved in light response were also found [37] at -1,589 bp and -1,664 bp. Among others, there was also a vascular-specific expression cis-element (BS1EGCCR, 5’- AGCGGG -3’) [38] at -147 bp site, indicated that OsMTP11 was expressed in rice vascular tissue, and played a crutial role in ion transporting. These putative regulatory elements suggest that the promoter region of OsMTP11 may respond to a variety of environmental signals, including heavy metal and other forms of stresses.

Fig 9. The OsMTP11 putative promoter region (-2,250 bp) sequence.

The transcription start site is denoted +1, and the putative start codon is underlined. Diagram of the OsMTP11 promoter region using PlantCARE ( showed the presence of a number of potential cis-acting elements that respond to environmental signals. MRE, metal-response element [34, 35]; ABRE, abscisic acid-response element [36]; I-box, light-response element [37]; BS1EGCCR, "BS1 (binding site 1)" found in CCR gene promoter, which is a cis-element required for vascular expression of the cinnamoyl CoA reductase gene in E. gunnii [38]. MREs include MRE1: 5’-TGCRCNC-3’ (R = A or G; N = any residue) [34] and MRE2: 5’-HTHNNGCTGD-3’ (D = A, G, or T; H = A, C, or T; N = any residue) [35].

Table 3. The statistics for MREs (Metal Response Elements), ABREs (Abscisic acid-Response Elements), I-box elements (light response elements) and BS1EGCCR (cis-element required for vascular-specific expression, Binding Site 1 found in CCR gene) in OsMTP11 promoter (-2,250 bp upstream to translational start coden).


The aim of this study was to clarify the biochemical mechanisms of heavy metal transport, particularly Mn, by OsMTP11 and possibly elucidate the biological roles of OsMTP11, especially from the point of expression pattern affected by heavy metal. Rice is the primary grain crop in China and a large part of its planting area is polluted by heavy metals, including Cd, Ni, Mn, Cu, and Zn, among others. In recent years [4, 39], the mechanisms of heavy metal’s absorption, translocation and accumulation by plants has attracted much research interest and been studied comprehensively, especially in crop plants. Metal transporters are key factors which mediate the first step of plants responding to heavy metals, and then affect the physiological and biochemical mechanism of metal detoxification in plant. Cation diffusion facilitator (CDF), also renamed as metal tolerance protein (MTP) in plants, is a sort of key metal transporters and play pivotal roles in metal absorption and translocation [40]. Here in this paper, we described a rice metal tolerance protein gene, OsMTP11, using the following approaches: bioinformatics, expression pattern, yeast biochemical mechanisms, and protein subcellular localization analysis. These studies provided much needed data on the functions of OsMTP11 in heavy metal (especially Mn) sequestration in rice plants.

OsMTP11 is a Mn transporter but not specific

Sequence analysis revealed that OsMTP11 displayed many of the characteristic features of Mn-CDF ion transporters, such as AtMTP11 [23] and ShMTP1 [12], suggesting a similar molecular mechanism and physiological function among these genes. In this study, heterologous expression of OsMTP11 in S. cerevisiae cells provided a viable experimental system to evaluate OsMTP11 heavy metal transport function. Our results showed that OsMTP11, similar to AtMTP11, complemented Mn-sensitivity in the yeast mutant pmr1Δ, indicating that OsMTP11 had the capability of Mn-transport in yeast. In addition, OsMTP11 partially complemented Co- and Ni- sensitivity of the yeast mutants cot1Δ and smf1Δ, suggesting OsMTP11 could also transport these cations. However, its metal-specific transport feature in plant cells remains unclear and requires further investigation. When OsMTP11 was expressed heterologously in wild type yeast BY4741, it also increased yeast tolerance to Mn, Co and Ni. Accordingly, Mn, Co and Ni content was substantially reduced in yeast, which indicated that OsMTP11 might mediate cation excretion and consequently elevate heavy metal tolerance in yeast.

The cation diffusion facilitator (CDF) family is a ubiquitous family of heavy metal transporters and widely distribute in all three kingdoms of life (Archaea, Eubacteria, Eukaryotes) [8]. Based on sequence alignment and bioinformatics analysis, and coupled with the substrate specificities of some characterized CDF members, Montanini et al [8] classified the family members (273 proteins in total) into three major groups (Zn-, Fe/Zn- and Mn-CDF), and some members’ substrate specificity have been tested in yeast. Then Kolaj-Robin et al [40] further classified the CDF family (including 329 proteins in total) into 18 groups and uncovered novel clades (III and XII) with undefined substrate specificity (Ni2+ and Co2+). Studies have shown that the substrate specificities of CDF members usually depend on some conserved amino acid residues in transmembrane region [8, 23, 40]. Due to heavy metal cations often belong to transition metal elements and possess similar atomic structure, some CDF members might recognize and bind similar metal cations, and result in the non-specificity of substrate recognition.

The promoter of OsMTP11 is tissue-specific and metal-inducible

Real time RT-PCR analysis was used to examine the primary expression patterns of OsMTP11 and assess the possible roles of OsMTP11 during plant growth and development. Our results revealed that OsMTP11 was predominantly expressed in mature leaves, roots and stems. These results demonstrated that OsMTP11 mRNA was mainly distributed in actively transporting and vigorously metabolizing tissues during rice growth and development, and the expression pattern coincided with a possible function of cation transportation in plants. OsMTP11 was identified as a Mn/Ni transporter, and we didn’t find it could transport Zn and Cd in functional complementation assay by yeast mutants, while at the expression level in rice, the transcription of OsMTP11 was still induced by different metals including Mn, Cd, Zn and Ni. As to Mn, Zn and Ni, which are all essential trace elements for plant growth, while Cd as non-essential, toxic element, we performed the metal treatments with different concentration, such as relatively higher concentrations for Mn (5 mM), Zn (2 mM) and Ni (1 mM), and a lower concentration for Cd (0.5 mM). The expression of OsMTP11 was strongly up-regulated by heavy metal Cd, Zn, Ni and Mn stress, which indicated that OsMTP11 was involved in metal tolerance and homeostasis at the expression level in rice. We also analyzed the OsMTP11 promoter region sequence, with potential cis-acting elements to respond to heavy metal and environmental signals. Promoter derived GUS staining assay and mRNA in situ hybridization results showed that OsMTP11 was mainly expressed in conducting tissues in rice, and its expression pattern had obvious tissue-specific feature. Our results indicated that the native promoter of OsMTP11 was heavy metal inducible and vascular bundle specific. The expression pattern of OsMTP11 was coinciding with the biological role that OsMTP11 transport the metal ion intracellularly or intercellularly.

The promoter features of genes were greatly involved in the gene’s biological functions since the expression patterns were decided by the promoter region, and the recognition of plant promoters often occurs in specific tissues or under physiological stress conditions [41]. The results in this paper suggested that the promoter of OsMTP11 belongs to a metal induced promoter, linking heavy metal specific cellular responses in rice. Our results were consistent with previous reports regarding BjMTP1 [42] and BjCET2 [43]. Ni, Cd or Zn was shown to activate BjMTP1 expression and BjCET2 was strongly up-regulated by Cd and Zn stress, but not by low temperature, salt and drought.

The DNA methylation status of promoter region affected the metal-induced expression pattern of OsMTP11

Furthermore, we detected some DNA methylation sites (CpG islands) in OsMTP11 promoter regions. Our results showed that heavy metal stress (such as Cd, Zn, Ni and Mn) can reduce the DNA methylation rate in the promoter region, and DNA methylation in the OsMTP11 promoter may be one crucial epigenetic mechanism that regulates OsMTP11 gene expression.

DNA methylation is an important epigenetic factor and exists extensively in plant genomes. It has two major roles: defending the genome against invasive DNA and gene expression regulation [44]. Heavy metal stresses can affect gene expression in plants, and the promoter region is a key factor that influences expression patterns [45]. The epigenetic regulation of gene expression through cytosine methylation in the promoter region under stresses will supply significant evidence that plants respond to abiotic stress. In plants, DNA methylation patterns are sensitive to abiotic stress, and can contribute to heritable stress adaptation that correlates with changes in genome methylation [46]. There are three specific cytosine methylation types: CpG, CpHpG, and CpHpH (H = A, T, or G), which are often catalyzed by different DNA methyltransferases [47]. In Arabidopsis, stress-induced transgenerational responses can alter DNA methylation, and cause higher tolerance to stress in untreated progeny [46]. When Taraxacum plants were exposed to different ecological stresses, considerable methylation variation was observed throughout the genome, which resulted in increased epigenetic variation among offspring [48]. DNA methylation of promoter region is an epigenetic modification that plays an important role in gene regulation in response to abiotic stress, and growing evidences from recent studies have suggested that demethylation of promoter region could enhance the expression of genes when plants exposed to stresses [49]. TaGAPC1 is a multiple stress responding gene, and its’ expression were induced by salt and dehydration, along with the demethylation of promoter region of TaGAPC1 by the bisulfite sequencing PCR (BSP) detection [50] These studies revealed that in plants, DNA methylation is a type of gene expression regulation manner, and plays a pivotal role in response to abiotic stress.


In summary, our results indicate that OsMTP11 is a Mn-transport protein that drives the metal efflux to the yeast extracellular compartment, and might also be an important Mn transporter in rice. The expression pattern analysis indicated that OsMTP11 was induced by heavy metals (such as Mn, Cd, Zn, Ni), and the promoter region of OsMTP11 contains several metal response elements (MREs), which might play vital roles in regulating the metal inducible expression pattern. Combining that DNA methylation status detection of CpG island in promoter region, this research further proved the epigenetic regulation of OsMTP11 expression was metal-specific. A detailed biological function study of OsMTP11 should be conducted in future research by plant transgenic experiments. The results of the present study offer insights into a Mn molecular pathway and other heavy metal absorption, transport and reposition processes in rice.

Author Contributions

  1. Conceptualization: MZ.
  2. Data curation: MZ BXL.
  3. Formal analysis: MZ BXL.
  4. Funding acquisition: MZ.
  5. Investigation: MZ BXL.
  6. Methodology: MZ BXL.
  7. Project administration: MZ.
  8. Resources: MZ.
  9. Software: MZ.
  10. Supervision: MZ.
  11. Validation: MZ.
  12. Visualization: MZ.
  13. Writing – original draft: MZ.
  14. Writing – review & editing: MZ.


  1. 1. Goyer RA. Toxic and essential metal interactions. Annu Rev Nutr. 1997; 17: 37–50. pmid:9240918
  2. 2. Clemens CS. Molecular mechanisms of plant metal tolerance and homeostasis. Planta. 2001; 212: 475–486. pmid:11525504
  3. 3. Mäser P, Thomine S, Schroeder JI, Ward JM, Hirschi K, Sze H, Talke IN, Amtmann A, Maathuis FJ, Sanders D, Harper JF, Tchieu J, Gribskov M, Persans MW, Salt DE, Kim SA, Guerinot ML. Phylogenetic relationships within cation transporter families of Arabidopsis. Plant Physiol. 2001; 126: 1646–1667. pmid:11500563
  4. 4. Sharma SS, Dietz KJ, Mimura T. Vacuolar compartmentalization as indispensable component of heavy metal detoxification in plants. Plant Cell Environ. 2016; 39 (5):1112–1126. pmid:26729300
  5. 5. Gustin JL, Zanis MJ, Salt DE. Structure and evolution of the plant cation diffusion facilitator family of ion transporters. BMC Evol Biol. 2011; 24:76.
  6. 6. Paulsen IT, Saier MH Jr. A novel family of ubiquitous heavy metal ion transport proteins. J Membr Biol. 1997; 156: 99–103. pmid:9075641
  7. 7. Gaither LA, Eide DJ. Eukaryotic zinc transporters and their regulation. Biometals. 2001; 14: 251–270. pmid:11831460
  8. 8. Montanini B, Blaudez D, Jeandroz S, Sanders D, Chalot M. Phylogenetic and functional analysis of the Cation Diffusion Facilitator (CDF) family: improved signature and prediction of substrate specificity. BMC Genomics. 2007; 8: 107–122. pmid:17448255
  9. 9. Van der Zaal BJ, Neuteboom LW, Pinas JE, Chardonnens AN, Schat H, Verkleij JA, Hooykaas PJ. Overexpression of a novel Arabidopsis gene related to putative zinc-transporter genes from animals can lead to enhanced zinc resistance and accumulation. Plant Physiol. 1999; 119: 1047–1055. pmid:10069843
  10. 10. Arrivault S, Senger T, Krämer U. The Arabidopsis metal tolerance protein AtMTP3 maintains metal homeostasis by mediating Zn exclusion from the shoot under Fe deficiency and Zn oversupply. Plant J. 2006; 46: 861–879. pmid:16709200
  11. 11. Delhaize E, Gruber BD, Pittman JK, White RG, Leung H, Miao Y, Jiang L, Ryan PR, Richardson AE. A role for the AtMTP11 gene of Arabidopsis in manganese transport and tolerance. Plant J. 2007; 51: 198–210. pmid:17559518
  12. 12. Delhaize E., Kataoka T., Hebb D.M., White R.G., Ryan P.R., Genes encoding proteins of the cation diffusion facilitator family that confer manganese tolerance. Plant Cell. 2003; 15: 1131–1142. pmid:12724539
  13. 13. Chen Z, Fujii Y, Yamaji N, Masuda S, Takemoto Y, Kamiya T, Yusuyin Y, Iwasaki K, Kato S, Maeshima M, Ma JF, Ueno D. Mn tolerance in rice is mediated by MTP8.1, a member of the cation diffusion facilitator family. J Exp Bot. 2013; 64 (14): 4375–4387. pmid:23963678
  14. 14. Ueno D, Sasaki A, Yamaji N, Miyaji T, Fujii Y, Takemoto Y, Moriyama S, Che J, Moriyama Y, Iwasaki K, Ma JF. A polarly localized transporter for efficient manganese uptake in rice. Nat Plants. 2015; 1: 15170. pmid:27251715
  15. 15. Erbasol I, Bozdag GO, Koc A, Pedas P, Karakaya HC. Characterization of two genes encoding metal tolerance proteins from Beta vulgaris subspecies maritima that confers manganese tolerance in yeast. Biometals. 2013; 26 (5): 795–804. pmid:23864431
  16. 16. Migocka M, Papierniak A, Maciaszczyk-Dziubińska E, Poździk P, Posyniak E, Garbiec A, Filleur S. Cucumber metal transport protein MTP8 confers increased tolerance to manganese when expressed in yeast and Arabidopsis thaliana. J Exp Bot. 2014; 65 (18): 5367–5384. pmid:25039075
  17. 17. Yuan L, Yang S, Liu B, Zhang M, Wu K. Molecular characterization of a rice metal tolerance protein, OsMTP1. Plant Cell Rep. 2012; 31: 67–79. pmid:21892614
  18. 18. Arvidsson S, Kwasniewski M, Riaño-Pachón DM, Mueller-Roeber B. QuantPrime—a flexible tool for reliable high-throughput primer design for quantitative PCR. BMC Bioinformatics. 2008; 9: 465. pmid:18976492
  19. 19. Hiei Y, Ohta S, Komari T, Kumashiro T. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J. 1994; 6 (2): 271–282. pmid:7920717
  20. 20. Gietz RD. Transformation of yeast by the Liac/SS carrier DNA/PEG method. Methods Mol Biol. 2014; 1205: 1–12. pmid:25213235
  21. 21. Li L, Kaplan J. Defects in the yeast high affinity iron transport system result in increased metal sensitivity because of the increased expression of transporters with a broad transition metal specificity. J Biol Chem. 1998; 273: 22181–22187. pmid:9712830
  22. 22. Wang Y, Zhang M, Ke K, Lu YT. Cellular localization and biochemical characterization of a novel calcium-dependent protein kinase from tobacco. Cell Res. 2005; 15: 604–612. pmid:16117850
  23. 23. Peiter E, Montanini B, Gobert A, Pedas P, Husted S, Maathuis FJ, Blaudez D, Chalot M, Sanders D. A secretory pathway-localized cation diffusion facilitator confers plant manganese tolerance, Proc Natl Acad Sci USA. 2007; 104: 8532–8537. pmid:17494768
  24. 24. Ton VK, Mandal D, Vahadji C, Rao R. Functional expression in yeast of the human secretory pathway Ca2+, Mn2+-ATPase defective in Hailey-Hailey disease, J Biol Chem. 2002; 277: 6422–6427. pmid:11741891
  25. 25. Conklin DS, McMaster JA, Culbertson MR, Kung C. COT1, a gene involved in cobalt accumulation in Saccharomyces cerevisiae. Mol Cell Biol. 1992; 12: 3678–3688. pmid:1508175
  26. 26. Supek F, Supekova L, Nelson H, Nelson N. A yeast manganese transporter related to the macrophage protein involved in conferring resistance to mycobacteria. Proc Natl Acad Sci. U S A. 1996; 93: 5105–5110. pmid:8643535
  27. 27. Li ZS, Lu YP, Zhen RG, Szczypka M, Thiele DJ, Rea PA. A new pathway for vacuolar cadmium sequestration in Saccharomyces cerevisiae: YCF1-catalyzed transport of bis (glutathionato) cadmium. Proc Natl Acad Sci USA. 1997; 94: 42–47. pmid:8990158
  28. 28. Keller G, Bird A, Winge DR. Independent metalloregulation of Ace1 and Mac1 in Saccharomyces cerevisiae. Eukaryot Cell. 2005; 4: 1863–1871. pmid:16278453
  29. 29. Bachhawat AK, Manolson MF, Murdock DG, Garman JD, Jones EW. The VPH2 gene encodes a 25 kDa protein required for activity of the yeast vacuolar H+-ATPase. Yeast. 1993; 9: 175–184. pmid:8465604
  30. 30. Graham LA, Hill KJ, Stevens TH. VMA8 encodes a 32-kDa V1 subunit of the Saccharomyces cerevisiae vacuolar H+-ATPase required for function and assembly of the enzyme complex. J Biol Chem. 1995; 270: 15037–15044. pmid:7797485
  31. 31. Damien B, Annegret K, Francis M, Dale S, Michel C. Poplar metal tolerance protein 1 confers zinc tolerance and is an oligomeric vacuolar zinc transporter with an essential leucine zipper motif. Plant Cell. 2003; 15: 2911–2928. pmid:14630973
  32. 32. Kawachi M, Kobae Y, Mimura T, Maeshima M. Deletion of a histidine-rich loop of AtMTP1, a vacuolar Zn(2+)/H(+) antiporter of Arabidopsis thaliana, stimulates the transport activity. J Biol Chem. 2008; 28: 8374–8383.
  33. 33. Lukens LN, Zhan SH. The plant genome's methylation status and response to stress, implications for plant improvement. Curr Opin Plant Biol. 2007; 10: 317–322. pmid:17468039
  34. 34. Searle PF, Stuart GW, Palmiter RD. Metal regulatory elements of the mouse metallothionein-I gene. Experientia Suppl. 1987; 52: 407–414. pmid:2959530
  35. 35. Wimalarathna RN, Pan PY, Shen CH. Chromatin repositioning activity and transcription machinery are both recruited by Ace1p in yeast CUP1 activation. Biochem Biophys Res Commun. 2012; 422 (4): 658–663. pmid:22609398
  36. 36. Simpson SD, Nakashima K, Narusaka Y, Seki M, Shinozaki K, Yamaguchi-Shinozaki K. Two different novel cis-acting elements of erd1, a clpA homologous Arabidopsis gene function in induction by dehydration stress and dark-induced senescence. Plant J. 2003; 33: 259–270. pmid:12535340
  37. 37. Giuliano G, Pichersky E, Malik VS, Timko MP, Scolnik PA, Cashmore AR. An evolutionarily conserved protein binding sequence upstream of a plant light-regulated gene. Proc Natl Acad Sci U S A. 1988; 85: 7089–7093. pmid:2902624
  38. 38. Lacombe E, Van Doorsselaere J, Boerjan W, Boudet AM, Grima-Pettenati J. Characterization of cis-elements required for vascular expression of the cinnamoyl CoA reductase gene and for protein-DNA complex formation. Plant J. 2000; 23: 663–676. pmid:10972892
  39. 39. Singh S, Parihar P, Singh R, Singh VP, Prasad SM. Heavy metal tolerance in plants: role of transcriptomics, proteomics metabolomics, and ionomics. Front Plant Sci. 2015; 6.
  40. 40. Kolaj-Robin O, Russell D, Hayes KA, Pembroke JT, Soulimane T. Cation diffusion facilitator family: structure and function. FEBS Lett. 2015; 589 (12):1283–1295. pmid:25896018
  41. 41. Porto MS, Pinheiro MPN, Batista VGL, dos Santos RC, Filho Pde Albuquerque Melo, de Lima LM. Plant promoters: an approach of structure and function. Mol Biotechnol. 2014; 56 (1): 38–49. pmid:24122284
  42. 42. Muthukumar B, Yakubov B, Salt DE. Transcriptional activation and localization of expression of Brassica juncea putative metal transport protein BjMTP1. BMC Plant Biol. 2007; 7: 32–43. pmid:17577406
  43. 43. Xu J, Chai T, Zhang Y, Lang M, Han L. The cation-efflux transporter BjCET2 mediates zinc and cadmium accumulation in Brassica juncea L. leaves. Plant Cell Rep. 2009; 28: 1235–1242. pmid:19495770
  44. 44. Aichinger E, Köhler C. Bisulphite sequencing of plant genomic DNA. Methods Mol Biol. 2010; 655: 433–443. pmid:20734278
  45. 45. Qi X, Zhang Y, Chai T. Characterization of a novel plant promoter specifically induced by heavy metal and identification of the promoter regions conferring heavy metal responsiveness. Plant Physiol. 2007; 143: 50–59. pmid:16861574
  46. 46. Boyko A, Blevins T, Yao Y, Golubov A, Bilichak A, Ilnytskyy Y, Hollunder J, Meins F Jr, Kovalchuk I. Transgenerational adaptation of Arabidopsis to stress requires DNA methylation and the function of dicer-like proteins. PLoS One. 2010; 5: 9514–9525.
  47. 47. Meyer P. DNA methylation systems and targets in plants. FEBS Lett. 2011; 585: 2008–2015. pmid:20727353
  48. 48. Verhoeven KJ, Jansen JJ, van Dijk PJ, Biere A. Stress-induced DNA methylation changes and their heritability in asexual dandelions. New Phytol. 2010; 185: 1108–1118. pmid:20003072
  49. 49. Choi CS, Sano H. Abiotic-stress induces demethylation and transcriptional activation of a gene encoding a glycerophosphodiesterase-like protein in tobacco plants. Mol Genet Genomics. 2007; 277: 589–600. pmid:17273870
  50. 50. Fei Y, Xue Y, Du P, Yang S, Deng X. Expression analysis and promoter methylation under osmotic and salinity stress of TaGAPC1 in wheat (Triticum aestivum L). Protoplasma. 2016; Aug 3.