ORIGINAL RESEARCH article
Comprehensive Genomic Identification and Expression Analysis of the Phosphate Transporter (PHT) Gene Family in Apple
- State Key Laboratory of Crop Stress Biology for Arid Areas, College of Horticulture, Northwest A&F University, Yangling, China
Elemental phosphorus (Pi) is essential to plant growth and development. The family of phosphate transporters (PHTs) mediates the uptake and translocation of Pi inside the plants. Members include five sub-cellular phosphate transporters that play different roles in Pi uptake and transport. We searched the Genome Database for Rosaceae and identified five clusters of phosphate transporters in apple (Malus domestica), including 37 putative genes. The MdPHT1 family contains 14 genes while MdPHT2 has two, MdPHT3 has seven, MdPHT4 has 11, and MdPHT5 has three. Our overview of this gene family focused on structure, chromosomal distribution and localization, phylogenies, and motifs. These genes displayed differential expression patterns in various tissues. For example, expression was high for MdPHT1;12, MdPHT3;6, and MdPHT3;7 in the roots, and was also increased in response to low-phosphorus conditions. In contrast, MdPHT4;1, MdPHT4;4, and MdPHT4;10 were expressed only in the leaves while transcript levels of MdPHT1;4, MdPHT1;12, and MdPHT5;3 were highest in flowers. In general, these 37 genes were regulated significantly in either roots or leaves in response to the imposition of phosphorus and/or drought stress. The results suggest that members of the PHT family function in plant adaptations to adverse growing environments. Our study will lay a foundation for better understanding the PHT family evolution and exploring genes of interest for genetic improvement in apple.
Phosphorus (Pi) is a key nutrient for plant growth and development (Raghothama, 1999) and is also an essential component of fertilizers used to sustain modern agriculture. In plants, Pi is part of important biomolecules and, in the form of phosphate, pyrophosphate, adenosine triphosphate, adenosine diphosphate, or adenosine monophosphate, has a crucial role in energy transfer and metabolic regulation. Globally, many soils are deficient in Pi and levels of available-Pi seldom exceed 10 μM even in fertile soils (Bieleski, 1973). Meanwhile, the Pi concentration in plant cell cytoplasm is generally greater than 10 mM (Raghothama, 1999). Therefore, plants must have specialized transporters to move Pi from the soil into cells against a large concentration gradient at the root–soil interface. Genome sequence analyses and experimental evidence have indicated that plants contain numerous Pi transporter families, including PHT1, PHT2, PHT3, PHT4, and PHT5, which are distinguished by their protein sequences, structures, locations, and functions (Schachtman et al., 1998; Mimura, 1999; Rausch and Bucher, 2002; Knappe et al., 2003; Guo et al., 2008; Liu et al., 2011, 2016; Zhang et al., 2016).
The PHT1 family has been the most widely studied in plants, and PHT1 proteins represent a group of phosphate carriers usually found in the plasma membrane (Pao et al., 1998). The first high-H+/Pi phosphate transporter identified in higher plants was AtPT1 from Arabidopsis thaliana (Muchhal et al., 1996). This gene has significant roles in the uptake of phosphorus from the soil (Lopez-Arredondo et al., 2014). Analyses of expressed sequence tags (ESTs) and genome sequences have revealed nine genes in Arabidopsis that share similarity with AtPT1, among which PHT1;1 transcripts is the most abundant (Mudge et al., 2002). Its overexpression increases Pi uptake in Arabidopsis (Wang et al., 2014). Arabidopsis thaliana PHT2;1 was the first member of the PHT2 family to be identified. AtPHT2;1 is a chloroplast phosphate transporter (Ferro et al., 2002; Versaw and Harrison, 2002) and also a low-affinity Pi transporter (Daram et al., 1999). Its activity affects Pi allocations and translocation within the plant and modulates the expression of Pi-starvation response genes (Versaw and Harrison, 2002). It also is a positive control for light-induced expression (Rausch et al., 2004). The third family of plant Pi transporters is localized to the mitochondria and includes the highly conserved PHT3 (Laloi, 1999). Three PHT3 genes have been identified in Arabidopsis (Rausch and Bucher, 2002). Within the PHT4 family, six members have been described from Arabidopsis (Guo et al., 2008). These genes are expressed in both roots and leaves. In addition to AtPHT4;1, a candidate thylakoid membrane-localized transporter, other transporters may be found in that organelle (Miyaji et al., 2015). PHT4;2 contributes to Pi transport in isolated root plastids, and starch accumulations are reduced in the roots and leaves of mutant plants (Irigoyen et al., 2011). AtPHT4;4 is a chloroplast-localized ascorbate transporter (Miyaji et al., 2015) and is induced by light exposure (Wang et al., 2011). AtPHT4;6 transports Pi out of the Golgi lumenal space to be recycled after release from glycosylation (Cubero et al., 2009). Allocation of phosphate, as mediated by PHT4;6, is critical for preventing the onset of dark-induced senescence (Hassler et al., 2016; Sebastian et al., 2016). Three Arabidopsis SYG1, PHO81, and XPR1 (SPX)-Major Facility Superfamily (MFS) proteins residing in the tonoplast are thought to form the phosphate transporter 5 family (Liu et al., 2016). Plants that over-express PHT5s show diminished growth and greater accumulations of Pi in their vacuoles relative to the cytosol, indicating transient misregulation of Pi-starvation response genes (Liu et al., 2016). In particular, AtPHT5;1 plays a prominent role in Pi accumulation. Similar to those in Arabidopsis, SPX-MFS proteins in rice (Oryza sativa) are localized in the tonoplast (Wang et al., 2015). There, PHT5s in the vacuolar membranes regulate cytoplasmic Pi homeostasis and are required for fitness and plant growth.
Apple (Malus domestica) is the fourth most economically significant woody fruit plant after Citrus sp., Vitis vinifera, and Musa L. (Hummer and Janick, 2009). Phosphate is an important nutrient for apple crops because it helps drive flowering, as well as fruit set, quality, and yield. Because many soils around the world are phosphate-deficient, abundant phosphatic fertilizers are applied to fields each year (Goldstein, 1992). In production areas within China, drought is the most challenging stress for apple trees (Hayano-Kanashiro et al., 2009). Therefore, it is urgent that researchers develop plants with enhanced efficiency of soil phosphorus use under such conditions. In doing so, one can also begin to reduce the environmental pollution caused by over-fertilization. One main approach to these problems is to improve the capacity of apple roots to absorb phosphorus. Because Pi is moved from the soil into plant cells in response to excess phosphate, genomic analyses have been conducted with Pi transporter families in Arabidopsis and rice. However, little is known about that gene family in woody plant species such as apple, which has a larger genome when compared with Arabidopsis and rice. Online publication of that genome (Velasco et al., 2010) has provided new tools for accelerating the identification of genes and other functional elements in apple (Troggio et al., 2012). Here, we isolated 37 MdPHT genes in Malus. Our goals were to examine gene structures, predict chromosome localizations, study phylogeny, and monitor patterns of transcriptional expression in roots, stem, leaves, shoot tips, flowers, young fruits, and mature fruits and in response to various abiotic stresses. The objective was to present a foundation for further functional dissection of MdPHTs so that genetic engineering approaches can been applied in efforts to improve the efficiency of phosphate uptake by stressed apple plants.
Materials and Methods
Database Searches for the Identification and Chromosome Locations of PHT Family Members in Apple
Previously reported phosphate transporter proteins for Arabidopsis thaliana, Oryza sativa, and Populus trichocarpa were used as queries against the apple genome database (http://genomics.research.iasma.it/). After overlapping sequences were removed, the genome annotations of Malus domestica were downloaded from that database. The protein sequences were aligned by ClustalX (ftp://ftp-igbmc.u-strasbg.fr/pub/ClustalX/) with default parameters, and were submitted to the Conserved Domain Database (http://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi), Pfam (http://pfam.sanger.ac.uk/), and SMART (http://smart.emblheidelberg.de/).
To verify our findings, we screened the apple EST database at the National Center for Biotechnology Information (NCBI) database (http://www.ncbi.nlm.nih.gov/guide/). Coding sequences identified from those genomic data were inspected and revised according to information from a database of M. domestica ESTs in the NCBI webserver. To identify protein sequences, we used the tools of the ExPASY Molecular Biology Server (http://web.expasy.org/protparam/) and TMHMM Server v. 2.0 (http://www.cbs.dtu.dk/services/TMHMM-2.0/). Locational data for PHT genes were retrieved from the Genome Database for Rosaceae (http://www.rosaceae.org/).
Multiple Sequence Alignments, Phylogenetic Analysis, Exon/Intron Organization, and Localization of MdPHT Proteins
Multiple alignments were performed with default parameters in the DNAMAN program (Lynnon Biosoft, USA). Full-length protein sequences from Arabidopsis, rice, and P. trichocarpa were downloaded from the NCBI protein database to study their evolutionary relationships. Phylogenetic trees were drawn with the MEGA6 program (Testerink and Munnik, 2011), using the Neighbor-Joining (NJ) method (Saitou and Nei, 1987) with Poisson corrections and 1,000 replications for the bootstrap analysis. A map of exon/intron organization was obtained from the online Gene Structure Display Server (http://gsds.cbi.pku.edu.cn/), applying the method for coding sequences and genomic sequences. Localization of each PHT was predicted via WoLF PSORT (http://www.genscript.com/wolf-psort.html).
Plant Materials and Treatments
Malus hupehensis var. pingyiensis is tolerant of waterlogged conditions. Because of its strong tendency for apomixes, few differences occur among seedlings (Li, 2001). Therefore, we used 6-year-old plants, the spacing of apple trees were 2 × 4 m, grown in an orchard at the Horticulture Experimental Station of Northwest A&F University, Yangling, Shaanxi, China, to study tissue-specific expression. Before the experiments began, all trees were well watered weekly and were supplied with compound fertilizer. Healthy and uniform plants were selected for sampling. Samples were taken of new roots, young stem segments, mature leaves from the middle portion of shoots, flowers (5 days after blooming, DBA), shoot tips, young fruits (15 DAB) and mature fruits (122 DAB). Roots, stems, mature leaves and young fruits were sampled at 15 DAB. Flowers were taken from apple trees 5 DAB. All samples were harvested from the south side of the tree canopy between 10:00 a. m. and 11:00 a. m., under full sun exposure.
For the hydroponics experiments, seeds were stratified in sand at 0 to 4°C for 60 d. After germinating, they were planted in individual plastic pots (12 × 12 cm) filled with sand and then placed in a greenhouse for 60 d under natural lighting and temperature conditions. To ensure that the seedling responses were consistent when exposed to our phosphorus and/or drought treatments, we planted three times as many seeds as were needed for these trials. The pots were moved out to an experimental field for 60 d under natural lighting and temperature conditions. Beginning at the second-true-leaf stage, the seedlings were irrigated every 4 d with a 1/2-strength Hoagland nutrient solution (Hoagland and Arnon, 1950). After 60 days outdoors, selected seedlings of similar size (with 6–8 leaves) were transferred to black plastic basins (52 × 37 × 15 cm), each containing 13 L of a 1/2-strength Hoagland nutrient solution. The basins were placed in a greenhouse under natural light and at day/night temperatures of 23 to 25°C/15 to 18°C. The nutrient solution was aerated each hour with an air pump and the dissolved oxygen concentration was maintained at 8.0 to 8.5 mg L−1. The pH of the nutrient solution was adjusted to 6.0 ± 0.1 by adding diluted H2SO4, and the solution was refreshed every 4 d. After 10 d of such pre-cultivation, stress treatments were initiated. Seedlings of Malus hupehensis var. pingyiensis were randomly assigned to six groups (n = 54 plants per treatment) each stress treatment had three biological replicates, every replicates contains 18 plants: (1) Control, standard 1/2-strength Hoagland nutrient solution supplemented with 500 μM KH2PO4; (2) Low-P treatment, 1/2-strength Hoagland nutrient solution plus 5 μM KH2PO4; (3) High-P treatment, 1/2-strength Hoagland nutrient solution with 5 mM KH2PO4; (4) Mild drought stress, generated by adding PEG 6000 to the 1/2-strength Hoagland solution and adjusting the osmotic potential to −0.75 MPa; (5) Combination of low-P and drought stress, 1/2-strength Hoagland nutrient solution (5 μM KH2PO4) and the osmotic potential adjusted to −0.75 MPa; or (6) Combination of and high-P and drought stress, 1/2-strength Hoagland nutrient solution (5 mM KH2PO4) and the osmotic potential adjusted to −0.75 MPa. On Day 15 of the experimental period, roots and leaves were harvested respectively.
RNA Extraction and cDNA Synthesis
All tissue samples were quickly frozen in liquid nitrogen and stored at −80°C. Total RNA was extracted according to the cetyl trimethyl ammonium bromide method (Chang et al., 1993). Residual DNA was removed by treating with RNase-free DNase I (Invitrogen, USA). The concentration of RNA was accurately quantified after this DNase I treatment, and 5 μg of total RNA was separated via 1.2% agarose gel electrophoresis to assess its quality and integrity. The RNA concentration and purity were measured with a spectrophotometer (NANODROP 2000c; ThermoScientific, USA). First-strand cDNAs were synthesized with 1 μg of total RNA, using a SYBR Prime Script RT-PCR Kit II (TaKaRa, Japan). After reverse-transcription, the reaction product was diluted 10-fold with sterile water as backup.
Molecular Cloning of PHT Genes in Apple
Leaf cDNA was used as template for amplifying the MdPHT sequences. Specific primers (Table S1) for gene cloning were designed based on the revised putative sequences. Polymerase chain reactions (PCRs) were performed with PrimeSTAR® HS DNA Polymerase (TaKaRa), and amplification conditions were empirically optimized. The PCR products were added to the 3′-termini using TaqDNA Polymerase (Fermentas, USA) and cloned into the pMD19-T vector (TaKaRa). Afterward, positive clones were sequenced. Gene nomenclature was assigned based on chromosome orders.
Expression Analysis of Apple PHT Genes
To obtain expression profiles for MdPHTs in different tissues and in response to phosphorus and/or drought treatment, we performed quantitative real-time PCR (qRT-PCR) on an iQ5.0 instrument (Bio-Rad, USA), using SYBR Green qPCR kits (TaKaRa) according to the manufacturer's instructions. The Actin gene served as our standard. Gene-specific primers were designed for these amplifications (Table S1). All reactions included 10.0 μL of SYBR® Premix Ex Taq™ (TaKaRa), 1.0 μL of cDNA template, 0.4 μL of each specific primer, and 8.2 μL of ddH2O2, made up to a 20-μL volume. The PCR conditions involved an initial 95°C for 3 min; then 40 cycles of 95°C for 20 s, 56°C for 20 s, and 72°C for 20 s. Based on three separate RNA extracts from three biological replications samples, each qRT-PCR was conducted three times to minimize inherent errors. Means and standard deviations were calculated from the results of three biological replicates. The relative expression levels of all MdPHT genes were calculated by the 2−ΔΔCT method (Livak and Schmittgen, 2001).
Identification of MdPHT Genes and Chromosomal Distribution of Family Members in Apple
To confirm the existence of PHT genes in apple, we employed previously identified protein sequences for Arabidopsis and rice in a broad search against apple genomics databases. In all, 43 candidates were found in apple. These included MDP0000926667 and MDP0000197466 on chr1, MDP0000278249 and MDP0000315320 on chr5, MDP0000209897 and MDP0000156379 on chr6, MDP0000613331 and MDP0000190109 on chr7, MDP0000255882 and MDP0000794044 on chr8, and MDP0000214285 and MDP0000315710 on chr17. Because each of those six pairs was close together on their respective chromosomes and the protein sequences of each pairing were highly similar, we speculated that they were tandem-duplicated genes. Therefore, each pair was treated as a single complete PHT sequence. This resulted in 37 PHT genes being identified in apple. The MdPHT1 family accounted for 14 genes, MdPHT2 for two, MdPHT3 for seven, MdPHT4 for 11, and MdPHT5 for five. Our BLAST analysis against the Pfam database showed that all proteins belong to the MFS family. Table 1 presents each gene name, locus, genome position, length of the open reading frame (ORF), numbers of exons and amino acids, isoelectric point (PI), molecular weight (MW), and GenBank Accession Number.
In all, 36 MdPHT genes are distributed on 17 apple chromosomes while one gene is not anchored (Figure 1). Chromosomes 1, 5, 13, 15, 16, and 17 each contain two genes; chr 2 and 11 have three each; chr 3, 4, 8, 9, 12, and 14 have one each; and chr 6, 7, and 10 have four each (Figure 1).
The full-length cDNA sequences were compared with corresponding genomic DNA sequences to determine the numbers and positions of exons and introns within each MdPHT gene (Figures 2A,B). Of the 37 total coding sequences, 18 showed no intron while the other coding sequences were disrupted by one to 15 introns each.
Figure 2. (A) Phylogenetic analysis. Different colors and shapes indicate genes within individual clusters. (B) Schematic diagram of exon/intron structures for PHT genes in apple. Diagram was made via Gene Structure Display Server, applying method for coding sequences and corresponding genome sequences. Yellow boxes and gray lines represent exons and introns, respectively.
Values for PI ranged from 5.69 to 9.96, while the 37 putative proteins had molecular weights of 34.0 to 81.3 kDa. These MdPHT protein sequences contained seven to 13 the transmembrane domain (TMDs). While MdPHT1 members were approximately 520 to 540 aa long, lengths for MdPHT2s were approximately 590, 300, to 400 for MdPHT3s (i.e., the shortest proteins), 400 to 590 for MdPHT4s, and 670 to 730 for MdPHT5s. A search of the Transport Classification Database (http://www.tcdb.org/analyze.php) identified seven to 13 transmembrane segments (TMSs) in the apple PHT family.
Molecular Cloning of MdPHT Genes in Apple
We cloned 13 of the 37 putative MdPHT genes and provided to NCBI (Table 1). Comparison of the sequences with published apple gene predictions revealed four anomalies, including redundant fragments and deletions. Such redundancies were detected in the middle portions of MDP0000146063, MDP0000283990, and MDP0000181017. Moreover, the predicted sequences of MDP0000145529 lacked a sequence region compare with the cloned gene from M. hupehensis. Nevertheless, these cloned sequences shared high similarity with the predicted coding sequences (CDS) in the apple genome, regardless of improperly predicted, redundant, or absent fragments.
Multiple Sequence Alignments and Phylogenetic Analysis
To investigate the evolutionary and phylogenetic relationships among PHTs in apple and other species at the molecular level, we compared their full-length protein sequences. Phylogenetic trees constructed by the NJ method (Figure 3) indicated that these PHT proteins could be divided into five clusters (I, II, III, IV, and V). Cluster I contained 14 members; Cluster II, two members; Cluster III, seven; Cluster IV, 11; and Cluster V, three. Those five clusters resembled the grouping of PHT families (PHT1 through PHT5) in Arabidopsis (Rausch and Bucher, 2002; Guo et al., 2008; Liu et al., 2016). This tree demonstrated that the MdPHTs are more closely related to dicot Arabidopsis and P. trichocarpa than to the monocot rice. We also confirmed that apple has 10 sets of paralogous genes: MdPHT2;1/MdPHT2;2, MdPHT3;4/MdPHT3;2, MdPHT3;7/MdPHT3;6, MdPHT4;8/MdPHT4;4, MdPHT4;10/MdPHT4;1, MdPHT4;9/MdPHT4;6, MdPHT5;1/MdPHT5;2/MdPHT5;3, MdPHT1;11/MdPHT1;10, MdPHT1;13/MdPHT1;12, and MdPHT1;6/MdPHT1;1.
Figure 3. Phylogenetic analyses of PHT genes in Arabidopsis thaliana (At), Oryza sativa (Os), Malus domestica (Md), and Populus trichocarpa (Ptr). Unrooted phylogenetic tree was constructed by NJ method, using MEGA6.0 program.
Motif Analysis of MdPHTs
Based on the protein sequence alignments obtained via MEME software (http://alternate.meme-suite.org/), we identified 15 putative conserved motifs (6–200 aa long) in the MdPHT family (Figure 4). Motifs 1, 2, 3, 5, 10, and 11 were present in all Cluster-I proteins; Motifs 13 and 15 appeared in all Cluster-II proteins; and Motifs 4 and 12 were in all Cluster-III proteins. For Cluster IV, MdPHT4;2, MdPHT4;3, and MdPHT4;7 contained Motifs 6, 8, and 9; MdPHT4;1 and MdPHT4;10 had Motifs 2, 8, and 11; while the others contained Motifs 6 and 7. All Cluster-V proteins featured Motifs 11 and 14.
Expression Profiles of Apple PHT Genes in Different Tissues
The qRT-PCR analysis revealed ubiquitous expression for all 37 MdPHTs in the apple roots, stems, leaves, shoot tips, flowers, young fruits and mature fruits. For Cluster-I members (Figure 5A), expression for MdPHT1;12 was strongest in roots and flowers, and its transcript levels were approximately three- to 5-fold higher than those of other MdPHT1 genes. Expression was strongest for MdPHT1;3 in the roots and for MdPHT1;5 and MdPHT1;13 in the leaves. The expression of MdPHT1;1 and MdPHT1;11 was 7- to 5-flod than other MdPHT1s in shoot tips. Most of MdPHT1s showed downtrend in fruit ripening, especial MdPHT1;10 was expressed highly in young fruits than mature fruits. Genes in Cluster II (Figure 5B) were expressed in all tissue types, but MdPHT2;2 was most highly expressed in the roots, stems and young fruits. Although genes in Cluster III (Figure 5C) were expressed in almost all tissues, expression was particularly high for MdPHT3;2 and MdPHT3;3 in the roots, stems and young fruits. For Cluster IV (Figure 5D), MdPHT4;1, MdPHT4;4, and MdPHT4;10 were expressed only in the leaves, while transcripts of MdPHT4;11 were detected in the leaves and the roots. Four other genes – MdPHT4;3, MdPHT4;5, MdPHT4;6, and MdPHT4;9—showed the greatest expression in the roots. The expression of MdPHT4;5 and MdPHT4;7 was highly in the shoot tips. Within Cluster V (Figure 5E), MdPHT5;1 and MdPHT5;2 were most strongly expressed in the leaves and roots, respectively, while expression of MdPHT5;3 was highest in the flowers.
Figure 5. Quantitative real-time PCR analysis of selected apple MdPHT1 genes (A), MdPHT2 genes (B), MdPHT3 genes (C), MdPHT4 genes (D), MdPHT5 genes (E) expressed in roots, stems, leaves, shoot tips, flowers, young fruits and mature fruits from Malus hupehensis var. pingyiensis. Data were normalized to level of apple Actin expression. Value for each sample is mean of 3 replicates. Vertical bars indicate standard deviation.
Effects of Stress Treatment on MdPHT Expression
After plants were exposed to 15 d of low-P conditions, only two genes (MdPHT1;11 and MdPHT1;12) were up-regulated in the leaves (Figure 6). The expression of other genes either remained stable or decreased. Under high-P conditions, expression of MdPHT1;12 was increased in the leaves while that of MdPHT3;6, MdPHT3;7, and MdPHT4;1 was up-regulated in those samples. Expression of MdPHT1;7, MdPHT1;10, MdPHT4;10, and MdPHT5;1 was not significantly changed by such treatment while all other genes were down-regulated. Under drought stress, expression in the leaves increased for MdPHT3;6, MdPHT3;7, MdPHT4;5, MdPHT1;12 and MdPHT4;7 when compared with the control. In response to the combined stress of low-P and drought, MdPHT5;2 and MdPHT3;3 were significantly induced in the leaves. Under the double stress of high-P and drought, MdPHT1;12, MdPHT2;2, and MdPHT3;1-3;3 were obviously up-regulated. Other genes showed either stable or only slightly decreased expression when plants were exposed to that combined treatment.
Figure 6. The expression profiles of PHT genes in leaves of Malus hupehensis var. pingyiensis. Heatmap shows PHT gene expression across after 15 d of phosphorus treatment, samples were taken from leaves exposed to low-P (LLP), high-P (LHP), drought (LD), drought with low-P (LDLP), or drought with high-P (LDHP) conditions. All transcript levels were normalized to their respective corresponding levels in non-stressed control (LCK).
In the roots, P-starvation treatment led to 14 MdPHT genes were highly expressed in the roots of M. hupehensis, suggesting that most MdPHT genes might be involved in Pi uptake. Only eight genes were down-regulated (Figure 7). When excessive P was supplied, expression of MdPHT4;7, MdPHT1;1, MdPHT1;2, MdPHT3;6, MdPHT3;7, and MdPHT4;3-4;5 were induced over the control. Expression of other genes was unchanged or declined after 15 d of high Pi treatment. Under drought stress, the expression of 15 MdPHT genes was up-regulated in apple. Expression of MdPHT1;7 was obviously up-regulated by the combined drought and starvation treatment. All of the MdPHT2s and most of the MdPHT3 members were also induced under such conditions. When drought and high-P stresses were applied together, expression of only MdPHT1;8, MdPHT1;10, MdPHT1;14, MdPHT4;2, and MdPHT4;3 remained stable while that of most other genes was up-regulated. Quantitative real-time PCR analysis of selected apple PHT genes expressed in leaves and roots under different stress treatments showed in Images 1, 2.
Figure 7. The expression profiles of PHT genes in roots of Malus hupehensis var. pingyiensis. Heatmap shows PHT gene expression across after 15 d of phosphorus treatment, samples were taken from roots exposed to low-P (RLP), high-P (RHP), drought (RD), drought with low-P (RDLP), or drought with high-P (RDHP) conditions. All transcript levels were normalized to their respective corresponding levels in non-stressed control (RCK).
Phosphate is one of the most important nutrients that significantly affect plant growth and metabolism (Raghothama, 1999). Therefore, examining the relationship between PHT proteins and Pi uptake/translocation enables us to understand how plants adapt to different environments. Our research was the first to focus on such transporters in apple, and involved a genome-wide survey and characterization of those genes so that potential candidate PHTs can be utilized in future functional analyses.
PHT Genes in Apple
We identified 37 members of the apple PHT family based on sequence alignments with the Arabidopsis PHT family. These MdPHTs can be classified into five clusters. A BLAST of the NCBI database indicated that the PHT1 family comprises more than 100 proteins. They include 13 PHT1 genes in the genome of haploid rice (Paszkowski et al., 2002); plus eight in Hordeum vulgare (Rae et al., 2003); five each in Zea mays (Nagy et al., 2002), Lycopersicon esculentum, and Solanum tuberosum (Nagy et al., 2005); and four in Nicotiana tabacum (Kai et al., 2002).
The MdPHT1 family is larger in apple (14 genes) than in other plants. These PHT1 members exhibit high sequence similarity to each other and contain 12 putative transmembrane segments (Raghothama, 1999; Smith, 2001). In apple, 12 TMSs are conjectural in eight MdPHT1 proteins, while 13 are predicated in six MdPHT1 proteins. The MdPHT1 proteins have 517 to 554 amino acids, making them similar in size to AtPHT1 proteins in Arabidopsis (Saier, 2000).
One PHT2 family gene has been identified in Arabidopsis (Daram et al., 1999) while two (MdPHT2;1 and MdPHT2;2) occur in apple. The latter two genes are located on different chromosomes (chr13 and chr16), and their encoded proteins are shorter than the AtPHT2;1 protein, i.e., 59 vs. 61 kDa. The 12 TMSs in Cluster II of apple compare with the 11 each in PHT2;1 of Arabidopsis and PHT2 of rice (Liu et al., 2011).
Arabidopsis has at least three AtPHT3 genes (Rausch and Bucher, 2002), while apple has seven in that family. The number of TMSs also varies among species, with rice having four to seven and Arabidopsis having seven (Liu et al., 2011). We found that apple has seven to eight such transmembrane-domain structures.
Apple contains 11 MdPHT4 genes while Arabidopsis has six (Guo et al., 2008). Rice has 11 to 12 TMSs in that family while Arabidopsis and apple each have 12 (Liu et al., 2011). The three MdPHT5 family genes in apple (12 TMSs) show similarities to the PHT5 protein in Arabidopsis (Liu et al., 2016). Because most of these MdPHTs (Table 1) are the same length as those members in Arabidopsis and rice (Liu et al., 2011), we conclude that proteins within that family are highly conserved among species.
Among the 37 coding sequences for MdPHT proteins, 18 have no introns while the others are disrupted by 1 to 15 introns each. When compared with the gene structures for Arabidopsis and rice PHTs (Liu et al., 2011), MdPHT1s have the same number of exons (1-2) as AtPHT1s and OsPHT1s, while MdPHT2s have three exons. All of the MdPHT3s have one exon fewer than either AtPHT3s or OsPHT3s while both MdPHT4s and MdPHT5s have more exons than the other two species. This difference suggests that the gene structure in apple is more divergent than that in Arabidopsis or rice.
Transcript Profiles of MdPHT Genes in Different Tissues
Most AtPHT1 genes are strongly expressed in the roots but are also detected in leaves and pollen (Karthikeyan et al., 2002; Mudge et al., 2002; Schünmann et al., 2004). Eight of the nine PHT1 family genes in Arabidopsis are expressed in the roots (Bucher et al., 2001; Mudge et al., 2002). By comparison, eight PHT1 genes in tomato (Chen et al., 2014) and 10 of the 13 PHT1 genes in rice are expressed in the roots (Paszkowski et al., 2002). We also detected MdPHT1;1, MdPHT1;2, MdPHT1;7, MdPHT1;13, and MdPHT1;14 transcripts in both leaves and roots. Expression of MdPHT1;12 is strong in the roots, flowers and young fruits. Almost all of the proteins in this family are predicted to be localized to the plasma membrane and expressed in the roots, suggesting their role in Pi uptake at the root–soil interface.
The PHT2 family may be low-affinity Pi transporters (Daram et al., 1999). PHT2;1 is preferentially expressed in the shoots, especially in rosette leaves (Ferro et al., 2002; Versaw and Harrison, 2002). We cloned two MdPHT2 genes and found that both are expressed in roots, stems, leaves, shoot tips, flowers, young fruits and mature fruits. As also noted for AtPHT2;1, a chloroplast phosphate transporter (Ferro et al., 2002; Versaw and Harrison, 2002), proteins of MdPHT2 are localized to that organelle.
Plant PHT3s are highly conserved within the mitochondrial transporter family (Laloi, 1999). In apple, MdPHT3 proteins are also predicted to occur on the mitochondria. Their strong expression in the roots, stems, leaves, shoot tips, flowers, young fruits and mature fruits are evidence of their great importance for plant growth.
The six members of the PHT4 gene family in Arabidopsis are well-characterized, putative intracellular PHTs (Guo et al., 2008). Such genes are generally expressed in roots and leaves. In apple, MdPHT4;1, MdPHT4;4, and MdPHT4;10 are expressed predominantly in the leaves while MdPHT4;3, MdPHT4;5, MdPHT4;6, MdPHT4;9, and MdPHT4;11 are expressed predominantly in the roots. In particular, expression is approximately 30-fold greater for MdPHT4;11 than for other family members.
PHT5 is considered a vacuolar phosphate transporter. Whereas AtPHT5;1 from Arabidopsis is expressed in most tissue types, AtPHT5;2 expression is confined to the guard cells, vascular tissue, and pollen (Liu et al., 2016). In apple, MdPHT5s genes are expressed less in young fruits and mature fruits. The expression of MdPHT5;2 is high in the roots while that of MdPHT5;3 is detected mainly in the stems and flowers. Because MdPHT5 proteins are localized to the vacuoles, this implies that they have possible functions in Pi storage within different tissues.
Expression of PHT Genes in Response to Different Phosphate Levels and Drought in Apple
Transcription of MdPHT genes varies in response to changes in phosphate levels. We found that, upon Pi-starvation, expression of MdPHT1;1, MdPHT1;2, MdPHT1;7, MdPHT1;12, MdPHT3;6, MdPHT3;7, MdPHT4;7, and MdPHT5s is induced in the roots. Most PHT1 family genes expressed in Arabidopsis roots are up-regulated in phosphate-deprived plants (Mudge et al., 2002). We also found that starvation conditions led to increases in expression, MdPHT1;1 and MdPHT1;7 increasing greatly over the control. MdPHT1;7 in apple are homologous to AtPHT1;4, which have been shown to be strongly up-regulated during Pi starvation (Shin et al., 2004). Indicating that they are maybe high-affinity phosphate transports proteins that operate at low Pi concentration by moving Pi from the external medium to the cytosol. Three MdPHT5 genes, like AtPHT5s (Liu et al., 2016), all transporters in the vacuoles, are markedly up-regulated in the roots under low-Pi conditions, supporting their roles in storing or removing phosphate. Although most MdPHT genes are up-regulated in the roots, two of them – MdPHT1;11 and MdPHT1;12—are also induced in the leaves while expression of the others remains stable or decreases in those tissues. Thus, genes expressed in the roots may be more sensitive to a limited supply of P in the soil.
When plants are exposed to excess Pi, MdPHT3;6, MdPHT3;7, MdPHT4;5, and MdPHT4;7 are up-regulated in the roots, suggesting that their proteins are low-affinity transporters. This might also be true for other PHT4 family members, based on the relatively high levels of Pi reported in the cytosol and other subcellular compartments (Mimura, 1999). It is very interesting that MdPHT3;6 and MdPHT3;7 showed up-regulated in roots and leaves under high Pi condition. AtPHT3 was a mitochondrial phosphate transporter (Jia et al., 2015). Under adversity stress, faster respiration rate and more reactive oxygen species (ROS) were produced in the plants, MdPHT3;7 and MdPHT3;8, predicted located in mitochondrial, were induced to transport more Pi to utilize for the conversion of ADP to ATP.
In response to drought treatment, expression of MdPHT1.5, MdPHT1;7, and MdPHT4;7 is markedly up-regulated in stressed apple roots, while MdPHT3;7, and MdPHT4;3 are obviously induced in the leaves. The expression levels of PtPHT1;2, and PtPHO9 were up-regulated under drought condition in poplar (Zhang et al., 2016). This suggests that these genes are positively regulated by drought stress. In contrast, experiments involving low-P conditions, alone or in combination with drought, showed that expression of MdPHT1;7 are extremely response. When only drought is induced, expression of that gene remains stable. It just induced by low Pi treatment, indicating that the up regulation of MdPHT1;7 may contribute to a low level of Pi tolerance of apple plants. Regardless of Pi status, expression of MdPHT1;8, MdPHT1;12, MdPHT3;2-3;5, and MdPHT4;7 in the roots, and MdPHT2;2, MdPHT3;3, and MdPHT3;5 in the leaves, is up-regulated under drought conditions, implying that these genes are not influenced by phosphate levels. However, drought-related changes in expression of MdPHT1;1, MdPHT1;5, MdPHT1;7, MdPHT1;11, MdPHT4;7, and other genes are largely dependent upon the level of phosphate. These results suggest therefore that, under drought conditions, Pi uptake in plants is likely associated with alterations in PHT expression, and may reflect the degree of drought tolerance in those stressed plants.
Under the drought and low phosphorus condition, the expression of 23 MdPHT genes is up-regulation in the leaves, 12 genes are induced in the roots, suggesting that the plant of aerial parts are influenced greatly than the underground parts, the aboveground parts of plant are not only to fight drought, but also to strengthen reusing the phosphorus. Relative to the single stress, MdPHT genes response positively under the dual stresses, the mechanism of the deeper reason remains to be further research.
The expression of MdPHT4;10 is concentrate upon leaves and it has nothing to do with the stresses, the subcellular location predicted of MdPHT4;10 is on chloroplast, so we guess MdPHT4;10 like AtPHT4;4 may be a chloroplast-localized ascorbate transporter (Miyaji et al., 2015).
Numerous PHT family genes have been described for rice and Arabidopsis but not for apple. Our study is the first to screen and analyze that family in apple and investigate their expression in different tissues, as well as under drought stress or limited/excessive Pi. Additional research is necessary if we are to understand the biological functions and regulatory mechanisms by which plants adapt when exposed to adverse growing environments.
We identified and characterized 37 MdPHT genes and organized them into five clusters based on their distinct exon/intron structures, phylogeny, and distribution of conserved motifs. Our qRT-PCR results demonstrated that these genes are induced by both Pi-starvation and excessive phosphate levels, as well as under drought stress. Therefore, they are good candidates for further analysis of their activities and functions. Although the roles for such MdPHTs are not yet fully known, our findings provide evidence that they participate in plant adaptations to stress conditions. If they can then be exploited to improve the tolerance of apple to Pi-starvation stress, then our study will also serve as a framework for future functional studies of the PHT family in that crop.
FM and ML conceived and designed the experiments. TS and LY performed the experiments. TS, YS, and ML analyzed the data. TS, ML, and FM wrote the paper.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This work was supported by the National Natural Science Foundation of China (31171916) and the earmarked fund for China Agriculture Research System (CARS-28). The authors are grateful to Mr. Zhengwei Ma and Ms. Xueyan Shi for management of the apple trees.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fpls.2017.00426/full#supplementary-material
Image 1. Expression patterns for selected apple PHT genes in leaves of Malus hupehensis var. pingyiensis. After 15 d of phosphorus treatment, samples were taken from leaves exposed to low-P (LLP), high-P (LHP), drought (LD), drought with low-P (LDLP), or drought with high-P (LDHP) conditions. All transcript levels were normalized to their respective corresponding levels in non-stressed control (LCK). Apple Actin served as reference gene. Mean values were obtained from 3 replicates. Vertical bars indicate standard deviation.
Image 2. Expression patterns for selected apple PHT genes in roots of Malus hupehensis var. pingyiensis. After 15 d of phosphorus treatment, samples were taken from roots exposed to low-P (RLP), high-P (RHP), drought (RD), drought with low-P (RDLP), or drought with high-P (RDHP) conditions. All transcript levels were normalized to their respective corresponding levels in non-stressed control (RCK). Apple Actin served as reference gene. Mean values were obtained from 3 replicates. Vertical bars indicate standard deviation.
Table S1. Primers used for cloning of MdPHT genes and quantitative real-time PCR analyses.
EST, expressed sequence tag; PHT, phosphate transporter; qRT-PCR, quantitative real-time polymerase chain reaction; DAB, days after blooming.
Bucher, M., Rausch, C., and Daram, P. (2001). Molecular and biochemical mechanisms of phosphorus uptake into plants. J. Plant Nutr. Soil Sci. 164, 209–217. doi: 10.1002/1522-2624(200104)164:2<209::AID-JPLN209>3.0.CO;2-F
Chen, A., Chen, X., Wang, H., Liao, D., Gu, M., Qu, H., et al. (2014). Genome-wide investigation and expression analysis suggest diverse roles and genetic redundancy of Pht1 family genes in response to Pi deficiency in tomato. BMC Plant Biol. 14:61. doi: 10.1186/1471-2229-14-61
Cubero, B., Nakagawa, Y., Jiang, X. Y., Miura, K. J., Li, F., Raghothama, K. G., et al. (2009). The phosphate transporter PHT4;6 is a determinant of salt tolerance that is localized to the golgi apparatus of Arabidopsis. Mol. Plant 2, 535–552. doi: 10.1093/mp/ssp013
Daram, P., Brunner, S., Rausch, C., Steiner, C., Amrhein, N., and Bucher, M. (1999). Pht2;1 encodes a low-affinity phosphate transporter from Arabidopsis. Plant Cell 11, 2153–2166. doi: 10.1105/tpc.11.11.2153
Ferro, M., Salvi, D., Riviere-Rolland, H., Vermat, T., Seigneurin-Berny, D., Grunwald, D., et al. (2002). Integral membrane proteins of the chloroplast envelope: identification and subcellular localization of new transporters. Proc. Natl. Acad. Sci. U.S.A. 99, 11487–11492. doi: 10.1073/pnas.172390399
Goldstein, A. H. (1992). “Phosphate starvation inducible enzymes and proteins in higher plants,” in Society for Experimental Biology Seminar Series 49: Inducible Plant Proteins, ed J. L. Wray (Cambridge: Cambridge University Press), 25–44.
Guo, B., Jin, Y., Wussler, C., Blancaflor, E. B., Motes, C. M., and Versaw, W. K. (2008). Functional analysis of the Arabidopsis PHT4 family of intracellular phosphate transporters. New Phytol. 177, 889–898. doi: 10.1111/j.1469-8137.2007.02331.x
Hassler, S., Jung, B., Lemke, L., Novák, O., Strnad, M., Martinoia, E., et al. (2016). Function of the Golgi-located phosphate transporter PHT4;6 is critical for senescence-associated processes in Arabidopsis. Mol. Plant 2, 535–552. doi: 10.1093/jxb/erw249
Hayano-Kanashiro, C., Calderon-Vazquez, C., Ibarra-Laclette, E., Herrera-Estrella, L., and Simpson, J. (2009). Analysis of gene expression and physiological responses in three Mexican maize landraces under drought stress and recovery irrigation. PLoS ONE 4:e7531. doi: 10.1371/journal.pone.0007531
Irigoyen, S., Karlsson, P. M., Kuruvilla, J., Spetea, C., and Versaw, W. K. (2011). The sink-specific plastidic phosphate transporter PHT4;2 influences starch accumulation and leaf size in Arabidopsis. Plant Physiol. 157, 1765–1777. doi: 10.1104/pp.111.181925
Jia, F., Wan, X., Zhu, W., Sun, D., Zheng, C., Liu, P., et al. (2015). Overexpression of mitochondrial phosphate transporter 3 severely hampers plant development through regulating mitochondrial function in arabidopsis. PLoS ONE 10:e0129717. doi: 10.1371/journal.pone.0129717
Kai, M., Takazumi, K., Adachi, H., Wasaki, J., Shinano, T., and Osaki, M. (2002). Cloning and characterization of four phosphate transporter cDNAs in tobacco. Plant Sci. 163, 837–846. doi: 10.1016/S0168-9452(02)00233-9
Karthikeyan, A. S., Varadarajan, D. K., Mukatira, U. T., D'Urzo, M. P., Damsz, B., and Raghothama, K. G. (2002). Regulated expression of Arabidopsis phosphate transporters. Plant Physiol. 130, 221–233. doi: 10.1104/pp.020007
Knappe, S., Flügge, U. I., and Fischer, K. (2003). Analysis of the plastidic phosphate translocator gene family in Arabidopsis and identification of new phosphate translocator-homologous transporters, classified by their putative substrate-binding site. Plant Physiol. 131, 1178–1190. doi: 10.1104/pp.016519
Liu, F., Chang, X. J., Ye, Y., Xie, W. B., Wu, P., and Li, X. M. (2011). Comprehensive sequence and whole-life-cycle expression profile analysis of the phosphate transporter gene family in rice. Mol. Plant 4, 1105–1122. doi: 10.1093/mp/ssr058
Liu, T. Y., Huang, T. K., Yang, S. Y., Hong, Y. T., Huang, S. M., Wang, F. N., et al. (2016). Identification of plant vacuolar transporters mediating phosphate storage. Nat. Commun. 7:11095. doi: 10.1038/ncomms11095
Lopez-Arredondo, D. L., Leyva-González, M. A., González-Morales, S. I., López-Bucio, J., and Herrera-Estrella, L. (2014). Phosphate nutrition: improving low-phosphate tolerance in crops. Plant Biol. 65, 95–123. doi: 10.1146/annurev-arplant-050213-035949
Miyaji, T., Kuromori, T., Takeuchi, Y., Yamaji, N., Yokosho, K., Shimazawa, A., et al. (2015). AtPHT4;4 is a chloroplast-localized ascorbate transporter in Arabidopsis. Nat. Commun. 6:5928. doi: 10.1038/ncomms6928
Muchhal, U. S., Pardo, J. M., and Raghothama, K. G. (1996). Phosphate transporters from the higher plant Arabidopsis thaliana. Proc. Natl. Acad. Sci. U.S.A. 93, 10519–10523. doi: 10.1073/pnas.93.19.10519
Mudge, S. R., Rae, A. L., Diatloff, E., and Smith, F. W. (2002). Expression analysis suggests novel roles for members of the Pht1 family of phosphate transporters in Arabidopsis. Plant J. 31, 341–353. doi: 10.1046/j.1365-313X.2002.01356.x
Nagy, R., Karandashov, V., Chague, W., Kalinkevich, K., Tamasloukht, M., Xu, G. H., et al. (2005). The characterization of novel mycorrhiza specific phosphate transporters from Lycopersicon esculentum and Solanum tuberosum uncovers functional redundancy in symbiotic phosphate transport in Solanaceous species. Plant J. 42, 236–250. doi: 10.1111/j.1365-313X.2005.02364.x
Nagy, R., Vasconcelos, M. J. V., Zhao, S., McElver, J., Bruce, W., Amrhein, N., et al. (2002). Differential regulation of five Phtl phosphate transporters from maize (Zea mays L.). Plant Biol. 8, 186–197. doi: 10.1055/s-2005-873052
Paszkowski, U., Kroken, S., Roux, C., and Briggs, S. P. (2002). Rice phosphate transporters include an evolutionarily divergent gene specifically activated in arbuscular mycorrhizal symbiosis. Proc. Natl. Acad. Sci. U.S.A. 99, 13324–13329. doi: 10.1073/pnas.202474599
Rae, A. L., Cybinski, D. H., Jarmey, J. M., and Smith, F. W. (2003). Characterization of two phosphate transporters from barley; evidence for diverse function and kinetic properties among members of the Pht1 family. Plant Mol. Biol. 53, 27–36. doi: 10.1023/B:PLAN.0000009259.75314.15
Rausch, C., Zimmermann, P., Amrhein, N., and Bucher, M. (2004). Expression analysis suggests novel roles for the plastidic phosphate transporter Pht2;1 in auto- and heterotrophic tissues in potato and Arabidopsis. Plant J. 39, 13–28. doi: 10.1111/j.1365-313X.2004.02106.x
Schünmann, P., Richardson, A., Smith, F., and Delhaize, E. (2004). Characterization of promoter expression patterns derived from the Pht1 phosphate transporter genes of barley (Hordeum vulgare L.). J. Exp. Bot. 55, 855–865. doi: 10.1093/jxb/erh103
Sebastian, H., Benjamin, J., Lilia, L., Ondřej, N., Miroslav, S., Enrico, M., et al. (2016). Function of the Golgi-located phosphate transporter PHT4;6 is critical for senescence-associated processes in Arabidopsis. Mol. Plant 2, 535–552. doi: 10.1093/jxb/erw249
Shin, H., Shin, H. S., Dewbre, G. R., and Harrison, M. J. (2004). Phosphate transport in Arabidopsis: Pht1;1 and Pht1;4 play a major role in phosphate acquisition from both low- and high-phosphate environments. Plant J. 39, 629–642. doi: 10.1111/j.1365-313X.2004.02161.x
Velasco, R., Zharkikh, A., Affourtit, J., Dhingra, A., Cestaro, A., Kalyanaraman, A., et al. (2010). The genome of the domesticated apple (Malus×domestica Borkh.). Nat. Genet. 42, 833–839. doi: 10.1038/ng.654
Versaw, W. K., and Harrison, M. J. (2002). A chloroplast phosphate transporter PHT2;1 influences allocation of phosphate within the plant and phosphate-starvation responses. Plant Cell 14, 1751–1766. doi: 10.1105/tpc.002220
Wang, C., Yue, W., Ying, Y., Wang, S., Secco, D., Liu, Y., et al. (2015). OsSPX-MFS3, a vacuolar phosphate efflux transporter, is involved in maintaining Pi homeostasis in rice. Plant Physiol. 169, 2822–2831. doi: 10.1104/pp.15.01005
Wang, G. Y., Shi, J. L., Ng, G., Battle, S. L., Zhang, C., and Lu, H. (2011). Circadian clock-regulated phosphate transporter PHT4;1 plays an important role in Arabidopsis defense. Mol. Plant 4, 516–526. doi: 10.1093/mp/ssr016
Wang, H., Xu, Q., Kong, Y. H., Chen, Y., Duan, J. Y., Wu, W. H., et al. (2014). Arabidopsis WRKY45 transcription factor activates PHOSPHATE TRANSPORTER1;1 expression in response to phosphate starvation. Plant Physiol. 164, 2020–2029. doi: 10.1104/pp.113.235077
Keywords: apple, phosphate transporters, gene family, phosphorus stress, drought, expression
Citation: Sun T, Li M, Shao Y, Yu L and Ma F (2017) Comprehensive Genomic Identification and Expression Analysis of the Phosphate Transporter (PHT) Gene Family in Apple. Front. Plant Sci. 8:426. doi: 10.3389/fpls.2017.00426
Received: 10 December 2016; Accepted: 13 March 2017;
Published: 30 March 2017.
Edited by:Laurent Gentzbittel, Ecole Nationale Supérieure Agronomique de Toulouse, France
Reviewed by:Rosario Muleo, University of Tuscia, Italy
Ji-Hong Liu, Huazhong Agricultural University, China
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