A putative high affinity phosphate transporter, CmPT1, enhances tolerance to Pi deficiency of chrysanthemum
© Liu et al.; licensee BioMed Central Ltd. 2014
Received: 20 September 2013
Accepted: 6 January 2014
Published: 10 January 2014
Inorganic phosphate (Pi) is essential for plant growth, and phosphorus deficiency is a main limiting factor in plant development. Its acquisition is largely mediated by Pht1 transporters, a family of plasma membrane-located proteins. Chrysanthemum is one of the most important ornamental plants, its productivity is usually compromised when grown in phosphate deficient soils, but the study of phosphate transporters in chrysanthemum is limited.
We described the isolation from chrysanthemum of a homolog of the Phosphate Transporter 1 (PT1) family. Its predicted product is a protein with 12 transmembrane domains, highly homologous with other high affinity plant Pi transporters. Real-time quantitative PCR analysis revealed that the gene was transcribed strongly in the root, weakly in the stem and below the level of detection in the leaf of chrysanthemum plants growing in either sufficient or deficient Pi conditions. Transcript abundance was greatly enhanced in Pi-starved roots. A complementation assay in yeast showed that CmPT1 partially compensated for the absence of phosphate transporter activity in yeast strain MB192. The estimated K m of CmPT1 was 35.2 μM. Under both Pi sufficient and deficient conditions, transgenic plants constitutively expressing CmPT1 grew taller than the non-transformed wild type, produced a greater volume of roots, accumulated more biomass and took up more phosphate.
CmPT1 encodes a typical, root-expressed, high affinity phosphate transporter, plays an important role in coping Pi deficiency of chrysanthemum plants.
KeywordsChrysanthemum morifolium CmPT1 Functional characterization Complementation assay Transgenic plants
After nitrogen, phosphorus is the most frequently limiting plant macronutrient . Despite its abundance in the soil, most of it is present in a form which is not readily accessible to plants . The application of phosphate-based fertilizer can correct deficiency, but even when provided in a highly accessible form, as little as 10% of the phosphorus applied is recovered by plants , with the remainder either becoming immobilized or lost through run-off . The availability of economically viable sources of phosphate fertilizer is declining . There is thus some urgency associated with efforts to promote the efficiency with which crop plants are able to take up phosphate.
The concentration of inorganic phosphate (Pi) in plant tissues lies in the range 5–20 mM , whereas the level available in a typical soil is three orders of magnitude lower than this . Thus the acquisition of Pi occurs against a steep concentration gradient . Pi uptake by plants operates via both a low and a high affinity system [7, 9]. The high affinity route is largely mediated by plasma membrane-localized Pi transporters belonging to the PHOSPHATE TRANSPORTER1 (Pht1) family [8, 10]. Following the identification of Pi transporters in Arabidopsis thaliana, a large number of PT genes have been identified and characterized in a wide range of species such as Arabidopsis thaliana[3, 11, 12], rice [13–15], tomato , tobacco [17, 18], maize , barley , Medicago truncatula, Populus trichocarpa, and soybean .
The chrysanthemum (Chrysanthemum morifolium Ramat.) is a leading ornamental species. Its productivity is usually compromised when grown in phosphate deficient soils. Here, we describe the isolation of a Pht1 homolog present in the chrysanthemum variety ‘Nannongyinshan’, a cultivar which is relatively tolerant of phosphate deficiency . The gene’s transcription profile was characterized and the beneficial effect of its constitutive expression on the plant’s ability to cope with phosphate deficiency was demonstrated.
Plant material and growing conditions
Cuttings of the chrysanthemum cultivar ‘Nannongyinshan’ were obtained from the Chrysanthemum Germplasm Resource Preserving Centre, Nanjing Agricultural University, China, ‘Nannongyinshan’ was a low phosphorus tolerant cultivar in our privious study, and ‘Jinba’ is a low phosphorus intolerant cultivar compared to ‘Nannongyinshan’ . The cuttings were raised in a greenhouse in a 1:1 mixture of perlite and vermiculite, without any fertilizer supplementation. After two weeks, the plants were up-rooted, their roots were washed free of the rooting medium and the plants were transferred to a hydroponic solution consisting of a diluted (1:2) Hoagland’s solution . The phosphate treatments were initiated one week after the transfer, by removing three plants to an aerated hydroponic solution containing either 300 (+P) or 0 (−P) μM Pi. The nutrient solution was replaced every three days. Leaf, stem and root tissue was harvested after a further 11 days, snap-frozen in liquid nitrogen and stored at −80°C.
Isolation of CmPT1
Adaptor and primer sequences used
Oligo d (T)18
The open reading frame (ORF) of the full length cDNA isolated from ‘Nannongyinshan’ was identified using the ORF finder program (DNASTAR. Lasergene. v7.1). The location of hydrophobic and putative transmembrane domains was enabled through the software package mounted at http://expasy.org/tools/protscale.html. Multiple peptide alignments were carried out using DNAman software (v188.8.131.52; Lynnon Biosoft, St Louis, QC, Canada), and phylogenetic analyses using Clustal X and MEGA v4.0 software.
Total RNA was extracted from root, stem and leaf tissue of plants grown both in the + P and -P treatments using the RNAiso reagent, and was then used as the template for real-time quantitative PCR (qRT-PCR) assays, based on the SYBR Green master mix (SYBR Premix Ex Taq™ II, TaKaRa Bio) and the gene-specific primer pair qGSP-F/-R (sequences given in Table 1), which generated a 163 bp fragment. The reference sequence was a 151 bp fragment of EF-1a, amplified with the primers EF1a -F/-R (sequences given in Table 1). Each 20 μl RT-qPCR contained 10 μl SYBR Green master mix, 10 ng cDNA template and 0.2 μM of each primer. The PCR program comprised an initial denaturation step (95°C/60 s), followed by 40 cycles of 95°C/15 s, 60°C/15 s, 72°C/45 s. Relative transcription levels were estimated using the 2-ΔΔCt method .
Complementation of a yeast mutant strain defective for Pi uptake
The function of the chrysamthemum gene (denoted CmPT1) was studied by its heterologous expression in yeast strain MB192 (MATa pho3-1 Dpho84::HIS3 ade2 leu2-3.112 his3-532 trp1-289 ura3-1.2 can1) which lacks phosphate transporter activity. First, the CmPT1 ORF was amplified using a Phusion High-Fidelity PCR kit (New England Biolabs, lpswich, MA, USA) based on the primer pair CmPT1-EcoR-F/Not-R (sequences given in Table 1), and the resulting amplicon was digested with EcoRI and NotI and then introduced into the yeast expression vector p112A1NE. The structure of the resulting recombinant plasmid (p112A1NE-CmPT1) was confirmed by restriction enzyme digestion and DNA sequencing. MB192 cells were transformed with either p112A1NE-CmPT1 or with the empty p112A1NE vector. Transgenic cells were grown in a yeast nitrogen base (YNB) medium until up to the logarithmic phase, and the medium was then replaced with a range of Pi concentrations (20, 60 and 100 μM) and the cells left to grow for a further 20 h. Bromocresol Purple was used to indicate the pH of the medium, giving a color shift, from yellow to purple, during the acidification of the liquid medium: this change correlated well with the growth of the yeast cells . Thereafter, the cells were transferred into YNB medium containing 60 μM Pi for a further 40 h. The optical density of the yeast cultures was measured every 8 h. The pH dependence of Pi uptake was studied by growing the cells in a series of MES-based YNB buffers containing 60 μm Pi at a pH of between 4 and 8. The kinetic properties of CmPT1 were analysed by feeding the transformed yeast cells with 32P labelled Pi, following the methods described by . The K m value was calculated using GraphPad v4.0 software.
Construction of an constitutive expression vector and the development of transgenic plants
CmPT1 was inserted into the pBIG vector (offered by Professor Junping Gao, Department of Ornamental Horticulture, China Agricultural University) under the control of the CaMV 35S promoter. The structure of the resulting pBIG-CmPT1 recombinant plasmid was confirmed by restriction enzyme digestion and DNA sequencing, and was then transformed into Agrobacterium tumefaciens strain EHA105 via the heat shock method . The recipient of the transgene was the chrysanthemum cultivar ‘Jinba’, which is intolerant of phosphate deficiency . Transformation was effected using a slightly modified form of the procedure described by . Explants developing multiple shoots were transferred to a selective regeneration medium, with the addition of 1.0 mg · L-1 6-BA, 0.5 mg · L-1 NAA, 10 mg · L-1 kanamycin and 300 mg · L-1 carbenicillin. Regenerating shoots were then rooted by transferring the material to a half-strength Murashige and Skoog medium containing 7.5 mg · L-1 kanamycin and 200 mg · L-1 carbenicillin. After acclimation, kanamycin-resistant plants were transplanted to soil and grown on in a greenhouse.
The phenotype of transgenic lines constitutively expressing CmPT1
Verification of transformation was obtained by a PCR assay of genomic DNA isolated from both presumptively transformed rooted plants, primed with the oligonucleotide pair 35 s-F/-R (sequences given in Table 1) which targets the CaMV 35S promoter sequence. The PCR was initiated by a denaturation step (94°C/5 min, which was followed by 30 cycles of 94°C/45 s, 55°C/45 s, 72°C/30 s, and completed with a final elongation step of 72°C/10 min. Transcript abundance of CmPT1 in the confirmed primary transformants was obtained by qRT-PCR, as described above. Two independent transgenic plants (CmPT1-Oe1 and CmPT1-Oe2), along with non-transformed ‘Jinba’ plants were exposed to either Pi-sufficient (300 μM Pi; +P) and P-deficiency (15 μM Pi; -P) conditions for 20 days. Each assay involved three replicates of a set of ten plants per genotype. Plant height, root volume, total dry biomass and the phosphate concentration in the whole plant were measured. The root volume was obtained by displacement . Dry weight was obtained by weighing plants held at 80°C for three days. The whole plant phosphate concentration was estimated from a ~0.1 g sample of dry matter, following .
CmPT1encodes a Pht1 Pi transporter
Transcription of CmPT1
Complementation test in yeast
CmPT1constitutive expression in chrysanthemum enhances tolerance to Pi deficiency
The uptake of Pi from a heterogeneous, constantly fluctuating environment is a major challenge faced by all plants. The process is largely governed by Pht1 transporters . The predicted product of the chrysanthemum Pht1 homologue extracted from the cultivar ‘Nannongyinshan’ forms 12 transmembrane domains, separated into two groups of six by a charged hydrophilic loop (Figure 1). This structural arrangement is typical for Pht1 transporters . The CmPT1 sequence shares a high level of sequence identity to other known high affinity Pi transporters and includes the signature sequence GGDYPLSATIxSE. A number of members of the Pht1 family are strongly expressed in the root, and are induced by phosphate starvation [10, 13, 14, 16, 33], just as was the case for CmPT1 (Figure 3a, b). Nevertheless its pattern of transcription is not completely the same as that of certain high affinity Pi transporters, in particular those of LePT1, which is transcribed in both the root and the leaf of tomato , and OsPT8 which is also transcribed in the rice grain . CmPT1 transcript abundance was below the level of detection in the leaf, even in plants growing under phosphate deficient growing conditions, while its level in the stem was low but still discernible. The evidence as a whole strongly suggests that CmPT1 acts as a Pi transporter in chrysanthemum.
Several approaches have been used to investigate the Pi transport properties of the various PHT1 family members. In our study, CmPT1 was able to complement the loss of high affinity Pi transporter activity of the yeast mutant MB192 in the high affinity concentration range (Figure 4). Its estimated Km of 35.2 μM (Figure 4d) lies within the K m range of other plant high affinity phosphate transporters, measured by a similar method – the range being from 13 μM to 97 μM [13, 14, 21]. Heterologous expression in yeast provides an informative means of characterizing plant proteins, but the system does have some limitations with respect to assessing the kinetics of plant phosphate transporters, the yeast complementation only partially reflects the behavior of PHT1 proteins in plants [2, 20]. Estimates of K m obtained by transcription in suspension cultures are substantially lower: 3.1 μM for A. thaliana Pht1 when transcribed in tobacco cells ; 9.1 μM for the barley protein HORvu;Pht1;1 when expressed in rice cells . It may be possible to obtain a more accurate estimate of Km to CmPT1 by using a homologous system in the future.
Transcription of the gene encoding the primary transporter is often considered to be the control point in pathways of nutrient uptake . Many efforts have been made to research the function of the PT genes and the possibility of using the PT genes to improve the adaptability to Pi-deficient stress of crops. Overexpression of an Arabidopsis thaliana high-affinity phosphate transporter gene in tobacco cultured cells enhances cell growth under phosphate-limited conditions . Suspension cells of transgenic rice that over-expressed a high-affinity phosphate transporter HvPT1 were able to take up phosphate at a much higher rate than control cells , but over-expression of the same gene in transgenic barley plants does not enhance phosphate uptake rates at the whole plant level . Park transferred a high-affinity phosphate transporter gene from tobacco (NtPT1) to rice enhanced phosphate uptake and accumulation under low-P condition . Over-expressing low affinity phosphate transporter genes OsPT1 and OsPT2 in rice cannot bring significant differences to the transgenic plants under Pi-deficient supply [15, 38]. Here, a Pht1 transporter gene which cloned from a low P tolerant cultivar of cut chrysanthemum ‘Nannongyinshan’ transferred to ‘Jinba’, a low P sensitive cultivar, the growth of transgenic plants was significantly improved over that of the non-transformed ones under Pi deficient conditions (Figures 6 and 7). Considering the two cultivars sharing the same sequence of CmPT1 and the transgenic and non-transgenic plants having same genetic background, physiological and biochemical changes are direct results of the overexpression of CmPT1 gene. Two possibilities can be envisaged to explain mechanisms of these changes. More copies of the transporter protein are inserted into the plasma membrane in the overexpression transgenic lines. Evidence for the transcriptional control of PT activity has been shown by parallel increases in PT transcript and protein levels detected by high-affinity PT antibody in tomato . The CmPT1 gene may participate in the Pi-starvation signal transduction pathways, Overexpression of the CmPT1 gene directly or indirectly caused Pi-dependent root architecture alteration with enhanced root elongation and proliferated lateral root growth (Figures 6 and 7b), these responses enable the optimization of soil exploration and of the absorptive surface area of the root .
In conclusion, CmPT1 encodes a typical, root-expressed, high affinity phosphate transporter in chrysanthemum. Taking the flexible expression pattern into account, CmPT1 might function in a wide range of Pi environments and play a significant role in phosphate acquisition under natural conditions.
We thank Professor Guohua Xu (College of Resources and Environmental Sciences, Nanjing Agricultural University) for offer the yeast strains. The study was supported by the National Natural Science Foundation of China (31272202), the Program for New Century Excellent Talents in University of the Chinese Ministry of Education (NCET-10-0492, NCET-12-0890), the Program for Sci-Tech Support Research, Jiangsu, China, (BE2012350), the Fundamental Research Funds for the Central Universities (KYZ201147) from Nanjing Agricultural University and Youth Science and Technology Innovation Fund from Nanjing Agricultural University( KJ2011009).
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