Characterization of the multigene family TaHKT 2;1 in bread wheat and the role of gene members in plant Na+ and K+status
© Ariyarathna et al.; licensee BioMed Central Ltd. 2014
Received: 2 April 2014
Accepted: 4 June 2014
Published: 11 June 2014
A member of the TaHKT2;1 multigene family was previously identified as a Na+ transporter with a possible role in root Na+ uptake. In the present study, the existing full-length cDNA of this member was used as a basis to query the International Wheat Genome Survey Sequence to identify all members of the TaHKT2;1 family. Individual TaHKT2;1 genes were subsequently studied for gene and predicted protein structures, promoter variability, tissue expression and their role in Na+ and K+ status of wheat.
Six TaHKT2;1 genes were characterized which included four functional genes (TaHKT2;1 7AL-1, TaHKT2;1 7BL-1, TaHKT2;1 7BL-2 and TaHKT2;1 7DL-1) and two pseudogenes (TaHKT2;1 7AL-2 and TaHKT2;1 7AL-3), on chromosomes 7A, 7B and 7D of hexaploid wheat. Variability in protein domains for cation specificity and in cis-regulatory elements for salt response in gene promoters, were identified amongst the functional TaHKT2;1 members. The functional genes were expressed under low and high NaCl conditions in roots and leaf sheaths, but were down regulated in leaf blades. Alternative splicing events were evident in TaHKT2;1 7AL-1. Aneuploid lines null for each functional gene were grown in high NaCl nutrient solution culture to identify potential role of each TaHKT2;1 member. Aneuploid lines null for TaHKT2;1 7AL-1, TaHKT2;1 7BL-1 and TaHKT2;1 7BL-2 showed no difference in Na+ concentration between Chinese Spring except for higher Na+ in sheaths. The same aneuploid lines had lower K+ in roots, sheath and youngest fully expanded leaf but only under high (200 mM) NaCl in the external solution. There was no difference in Na+ or K+ concentration for any treatment between aneuploid line null for the TaHKT2;1 7DL-1 gene and Chinese Spring.
TaHKT2;1 is a complex family consisting of pseudogenes and functional members. TaHKT2;1 genes do not have an apparent role in controlling root Na+ uptake in bread wheat seedlings under experimental conditions in this study, contrary to existing hypotheses. However, TaHKT2;1 genes or, indeed other genes in the same chromosome region on 7AL, are candidates that may control Na+ transport from root to sheath and regulate K+ levels in different plant tissues.
Saline soils are a challenge to cereal production in many regions of the world. Osmotic and ion-specific damage that significantly reduces crop growth in saline soils is largely due to excess of Na+ and Cl− ions [1, 2]. In bread wheat, a balance between restricting Na+ net uptake at roots and subsequent transport into shoots and sub-cellular compartmentation to cope with unfavourable levels of Na+ is needed to maintain ion homeostasis for plant growth and development under saline conditions [3, 4]. The regulation of Na+ transport and its genetic basis is, therefore, of significant interest in order to assist in development of targeted strategies for enhanced salinity tolerance in crops.
A major portion of Na+ exclusion (>98%) in bread wheat is accomplished by restricting net Na+ uptake at the soil-root interface and net xylem loading in roots , yet a number of channels and transporters facilitate Na+ influx when Na+ concentration is high in the soil solution [5–8]. Channel and transporter proteins are potential targets to reduce Na+ net uptake by roots and have been a major focus to investigate their role in crop tolerance to salinity. Electrophysiological observations and pharmacology of 22Na+ tracer influxes in cereal roots support the hypothesis that the bulk of Na+ influx is mediated by voltage-independent, non-selective cation channels (VICs/NSCCs) [9–11]. In addition, two transporters LCT1[12, 13] and HKT2;1 can mediate high and/or low-affinity Na+ transport in wheat. While both VICs/NSCCs  and LCT1 facilitate Ca2+ dependant unidirectional influx of various cations, TaHKT2;1 mediates Ca2+ independent influx of Na+ and K+[16, 17]. Although, TaHKT2;1 is a Na+/K+ co-transporter, the protein has a minor significance in K+ nutrition as Na+ - coupled K+ uptake has limited physiological relevance in terrestrial species . Therefore, among the genes encoding candidate proteins involved in root Na+ influx, TaHKT2;1 is of particular interest in crop breeding because of its high specificity for Na+ and the potential to manipulate TaHKT2;1 genes without largely interfering with the homeostasis of nutritionally important ions (e.g., K+, Ca2+) in plants.
TaHKT2;1 has a Gly-Gly-Gly-Gly type K+/Na+ selectivity pore [19, 20] and when expressed in Xenopus oocytes and yeast heterologous systems, preferentially mediates high affinity K+ uptake when external Na+ is at sub-millimolar levels, but facilitates low-affinity Na+ influx when millimolar levels of external Na+ are in excess of K+[16, 21, 22]. The ion transport properties of TaHKT2;1 were determined when point mutations within the TaHKT2;1 gene improved K+ specificity and reduced Na+ influx in Xenopus oocytes and yeast [21, 23]. Down regulation of TaHKT2;1 in transgenic bread wheat by expressing anti-sense or truncated sense constructs reduced Na+ levels in K+ starved seedling roots . Since the gene is expressed in the cortical cells of roots, alongside in xylem parenchyma in leaves, it is possible that the protein encoded by TaHKT2;1 is associated with root Na+ uptake and translocation . Therefore, it appears that under saline conditions TaHKT2;1 is responsible for substantial Na+ influx into roots of bread wheat and transport to other parts of the plant.
TaHKT2;1 has been identified as a multi-gene family consisting of five individual members distributed across homeologous chromosome group 7 in bread wheat . Although previous studies identified the function of Na+ transport in one member of the TaHKT2;1 gene family in heterologous systems [21, 23] and in transgenic plants by down-regulation of one or more genes , the contribution of each member of the gene family and their interactions to control ion accumulation in wheat remains unknown. This study aimed to understand the organization and variability of each member of the TaHKT2;1 gene family, transcriptional regulation, their encoded proteins, and potential contributions to controlling Na+ and K+ status in bread wheat. The study used an existing full length cDNA (FL-cDNA) sequence (U16709) as a basis to select and characterize all members of the TaHKT2;1 gene family using the International Wheat Genome Survey Sequence (IWGSS) (http://www.wheatgenome.org).
Organization and structure of TaHKT2;1multi-gene family
Percent DNA sequence and amino acid (parentheses) identity between functional members of the TaHKT2;1 gene family
TaHKT2;1 7BL-1 and TaHKT2;1 7BL-2
Attributes of exons, introns and proteins of functional members of the TaHKT2;1 gene family
TaHKT2;1 7BL-1 TaHKT2;1 7BL-2
Exon 1 length (bp)
Exon 2 length (bp)
Exon 3 length (bp)
Total number of SNPs
Intron 1 length (bp)
Intron 2 length (bp)
Amino acid length
Amino acid substitutions
Salt induced cis– acting regulatory elements identified in the promoter regions of the functional TaHKT2;1 genes
Conserved sequence motif
Associated families of salt-stress activated TFs
AREB/ABF (ABA responsive element- binding proteins)
TaHKT2;1 7BL-2(1) TaHKT2;1 7DL-1(5)
TaHKT2;1 7AL-1(1) TaHKT2;1 7BL-1(2) TaHKT2;1 7BL-2(3) TaHKT2;1 7DL-1(5)
TaHKT2;1 7AL-1(1) TaHKT2;1 7BL-1(2) TaHKT2;1 7BL-2(1) TaHKT2;1 7DL-1(1)
CBF/DREB (C-repeat binding factor/dehydration- responsive element-binding proteins)
TaHKT2;1 7AL-1(3) TaHKT2;1 7BL-1(2) TaHKT2;1 7BL-2(3) TaHKT2;1 7DL-1(4)
plant specific family of TFs, NAC (No apical meristem)
TaHKT2;1 7BL-1(10) TaHKT2;1 7BL-2(4) TaHKT2;1 7DL-1(12)
Trihelix family, also known as GT factors
TaHKT2;1 7AL-1(12) TaHKT2;1 7BL-1(10) TaHKT2;1 7BL-2(10) TaHKT2;1 7DL-1(10)
WRKY transcription factors
Analysis of predicted proteins of TaHKT2;1multi-gene family
Promoter analysis of functional TaHKT2;1members
Promoter diversity was investigated in functional members of the TaHKT2;1 gene family by analysis of 2000 bp region up-stream of the predicted translation start site. The core promoter element, TATAA box (−69 bp) was conserved in all functional members of the TaHKT2;1 family. Although TaHKT2;1 7BL-1/-2 were identical in exon and intron sequences, they shared only 42.7% DNA sequence identity between promoters. The promoter region of TaHKT2;1 7AL-1, and TaHKT2;1 7DL-1 genes showed 65.8% and 43.5% DNA sequence identity, respectively, compared with TaHKT2;1 7BL-1/-2. Table 3 summarizes the number and type of cis-acting regulatory elements (CREs) identified in promoters of functional members of the TaHKT2;1 family using the PLANTcare and PLACE databases. Promoters of all functional TaHKT2;1 genes contained a number of CREs known to be involved in salt activated response in plants and each gene shared at least five CREs of different categories. Therefore, it appeared that salt stress-activated transcription factors (TFs) interact with CREs to regulate TaHKT2;1 genes.
Analysis of TaHKT2;1 pseudogenes in Triticumspecies
Gene specific PCR primers targeting INDELs and SNPs to amplify individual members of the TaHKT2;1 gene family
Primer location (bp)
Primer sequence 5′-3′
PCR and the annealing temperature (°C)
TaHKT2;1 7AL-2 and TaHKT2;1 7AL-3
Touch down PCR at 55-50
TaHKT2;1 7AL-2 and TaHKT2;1 7AL-3
Touch down PCR at 55-50
Touch down PCR at 55-50
Touch down PCR at 55-50
TaHKT2;1 7BL-1 and TaHKT2;1 7BL-2
Touch down PCR at 55-50
TaHKT2;1 7BL-1 and TaHKT2;1 7BL-2
Touch down PCR at 55-50
Touch down PCR at 55-50
Touch down PCR at 55-50
Standard PCR at 53
Standard PCR at 53
TaHKT2;1 7BL-1 and TaHKT2;1 7BL-2
Standard PCR at 53
TaHKT2;1 7BL-1 and TaHKT2;1 7BL-2
Standard PCR at 53
Standard PCR at 56
Standard PCR at 56
Expression of functional members of TaHKT2;1gene family
FL-cDNA transcripts of functional TaHKT2;1 genes expressed in root, sheath and leaf under low and high NaCl conditions were sequenced. The cDNA sequence for TaHKT2;1 7AL-1 [Genbank: KJ540616]; TaHKT2;1 7BL-1/-2 [Genbank: U16709] and TaHKT2;1 7DL-1 [Genbank: KJ540618] were identical from each tissue and were in perfect agreement with the predictions of gene structure in Figure 1 when aligned against the cognate genomic DNA sequence. Sequence analysis identified a 571 bp alternatively spliced transcript [Genbank: KJ540617] from TaHKT2;1 7AL-1 encoding a predicted protein of 133 amino acids. Alignment with genomic DNA identified a splice site within exon 1 resulting in the deleting of exon 2 and exon 3 and intervening introns relative to its larger cDNA counterpart [Genbank: KJ540616]. The alternatively spliced TaHKT2;1 7AL-1 sequence had the dinucleotide motif 5′-AT and AC-3′ at the exon-intron splice junction different to the conserved 5′GT and AG-3′ splice junction motifs in all other transcripts.
Tissue ion analyses of wheat aneuploid lines null for TaHKT2;1genes
The same aneuploid lines when exposed to an external solution containing 200 mM NaCl and 4 mM K+ showed no differences in K+ concentration in bulked leaf blades regardless of the genotype or the Na+ status (Figure 6B). However, K+ concentration was reduced by 23% in the roots and 19% in the youngest fully expanded leaf blade for Dt7BS compared to Chinese Spring, but only under 200 mM NaCl treatment (Figure 6B). Similarly, sheath K+ was reduced by 12% in the aneuploid line 7AL-1 in the 200 mM NaCl treatment (Figure 6B). Therefore, it appears that the chromosomal regions containing TaHKT2;1 7AL-1 and TaHKT2;1 7BL-1/-2 influence K+ status under high NaCl conditions in a tissue-specific manner. There was no significant difference in K+ between 7DL-2 and Chinese Spring (Figure 6B) indicating that TaHKT2;1 7DL-1 does not have a role in regulating K+ status in any tissue and treatments.
This study provides a detailed characterization of the TaHKT2;1 multigene family in bread wheat which included four functional members and two pseudogenes. Despite presence of salt induced stress responsive elements in the promoter region it was found that the functional members of the TaHKT2;1 family were expressed under low and high NaCl levels in roots and sheaths, but were down regulated in leaf blades. Wheat aneuploid lines were used to provide evidence for a potential role of individual TaHKT2;1 gene family members in Na+ and K+ homeostasis in seedlings under low and high NaCl hydroponic conditions.
Although all members of the TaHKT2;1 gene family contained three exons and two introns sharing the same gene structure as Group II HKT genes from other monocots , DNA sequence differences resulted in a degree of variability at the protein level. Variation amongst the TaHKT2;1 genes and their encoded proteins could be of functional relevance. TaHKT2;1 proteins potentially acting as K+/Na+ cotransporters have a conserved Gly-Gly-Gly-Gly signature in the selectivity filter, yet the filter signature alone does not necessarily predict ion selective properties and other domains responsible for ion specificity need to be considered [34, 35]. In this regard, induced mutations within the cytoplasmic (L149, E180) or P-loop (A240, L247, F463 and E464) domains affected selectivity and the rate of uptake of K+ and Na+ by the TaHKT2;1 7BL-1/-2 proteins in yeast and/or Xenopus oocytes heterologous systems [17, 19, 21, 23, 36, 37]. Interestingly, the majority of the amino acids that were mutated in previous experiments were conserved between the members of TaHKT2;1 family except for a A240S substitution in TaHKT2;1 7DL-1. In addition to A240S, five amino acid differences were identified within six base pair proximity to the filter glycine residues in the P-loops of TaHKT2;1 7AL-1, TaHKT2;1 7DL-1 compared to TaHKT2;1 7BL-1/-2. Therefore, it is reasonable to hypothesize that the amino acid differences between members of the TaHKT2;1 gene family in these regions may affect ion uptake properties (e.g. specificity and rate of ion transport). Since this study cloned FL-cDNAs of each member of the gene family, further investigations can be pursued using heterologous systems to evaluate the functional significance of the protein sequence variability for ion transport in the TaHKT2;1 gene family.
TaHKT2;1 7AL-2 and TaHKT2;1 7AL-3 shared typical characteristics of unprocessed pseudogenes, such as in-frame stop codons, location within close proximity to the functional genes on the same chromosome, and the absence of transcription . Pseudogenes have previously been reported in the HKT super-family but their functional relevance is unknown . Pseudogenes are thought to be an integral feature in evolution of polyploidy genomes, representing 12% of the genes in bread wheat  and may be of importance in gene or genome function. Pseudogenes in eukaryotes have been reported to have a regulatory role for genes from which they were derived, have non-coding functions or act as a source of genetic variability and were subjected to natural selection . Conservation across progenitor genomes indicated that the single base deletion in exon 1 that caused a pre-mature stop codon in TaHKT2;1 7AL-2 and TaHKT2;1 7AL-3 was an ancient event created during evolution of the A genome progenitor species prior to, and maintained during, polyploidization of the tetraploid and hexaploid genomes. The Ka/Ks between the functional genes was close to the average Ka/Ks ratio of 0.2 previously estimated for functional wheat genes , providing evidence that the functional members of the TaHKT2;1 gene family was subjected to resilient purifying selection. Although TaHKT2;1 7AL-2 and TaHKT2;1 7AL-3 had characteristics of pseudogenes the Ka/Ks value between these genes and TaHKT2;1 7AL-1 was less than the theoretical value of 1.0 for a bona-fide pseudogene , indicating a relaxed selective constraint during genome evolution. Furthermore, the fact that these pseudogenes were retained during evolution of the hexaploid wheat genome with gene structure conservation could indicate some functional importance.
Each member of the TaHKT2;1 gene family was variable for presence and frequency of salt induced CREs. Plant response to salinity is mediated by immediate and extensive reprogramming of the spatial and temporal gene transcription, instigated by the interaction of transcription factors with four major groups of CREs including ABA-independent CREs (CBF/DREB; NAC and ZF-HD) and ABA-dependent CREs (AREB/ABF; MYC/MYB) [42, 43], all of which were represented in TaHKT2;1 gene family. Interestingly, promoter diversity in AtHKT1;1 genes resulted in variable salt response in natural populations of Arabidopsis. Similarly, variability in CREs contributed to diverse expression patterns of TaHKT1;5 in bread wheat and wild relatives under salt stress , supporting the hypothesis that HKT genes are regulated by CREs mediated mechanisms. The presence of these elements with varying copies and combinations predict salt response with variable expression patterns of individual TaHKT2;1 members.
Given the CREs identified in this study, it was expected that each TaHKT2;1 gene would show diverse transcriptional regulation, yet, no obvious transcript differences were detected between low and high NaCl treated plants. Similar observations were reported  where saline treatments imposed with K+ deficient conditions did not induce differences in TaHKT2;1 gene expression in two week old wheat seedlings. However, expression of TaHKT2;1 7BL-1/-2 was up regulated by imposing K+ starved conditions in six day old wheat  indicating a rapid response of genes to external K+ in younger seedlings. In the present study, there was an obvious down regulation of TaHKT2;1 transcripts in leaf blades regardless of the NaCl concentration of the external solution, confirming adjustment of gene expression in this tissue. The extent of gene expression was further explored by mining wheat EST databases including NCBI, Transcriptome Shotgun Assembly and the TIGR Plant Transcript Assemblies, identifying a number of ESTs derived from pre-anthesis spikes and kernel tissue with 98-100% identity to members of the TaHKT2;1 gene family (data not shown). Further studies are needed to understand the expression of TaHKT2;1 gene family and how the various members influence ion homeostasis during different stages of plant development, various environmental conditions and variable salt levels.
An interesting feature of TaHKT2;1 gene expression was the level of complexity caused by alternative splicing of a 571 bp transcript unique to TaHKT2;1 7AL-1. Alternative splicing is evident in 25 to 42% of bread wheat genes whereby some forms are thought to play a role in regulating functional transcript levels . Alternative splicing at non-conventional–splice junctions has been reported in rice OsHKT1;5 resulting in a premature stop codon and non-functional transcripts as a possible means of regulating mRNA degradation . Similarly, alternative splicing event in TaHKT2;1 7AL-1 indicates a rare unstable splice-junction motif that may act as an embedded molecular switch for post-transcriptional regulation and mRNA turn-over processes, which presumably may then influence levels of protein production.
The use of wheat aneuploid lines null for specific members of the TaHKT2;1 family provided a system to analyse phenotypic effects of the genes on tissue ion concentrations. This approach provided evidence that a gene does not have a specific role when there was no significant difference between its corresponding aneuploid line and Chinese Spring (containing the full chromosome complement) whereas differences indicated that the gene would be a candidate controlling tissue Na+ and/or K+ status. The results, therefore, corroborate that TaHKT2;1 genes neither regulate root Na+ uptake nor Na+ accumulation in bulk leaf blades and youngest fully expanded leaf blade. Nevertheless, presence of transcripts for all TaHKT2;1 gene family members in these tissues under low and high NaCl conditions indicate alternative roles if they are translated into proteins. The higher sheath Na+ concentration in 7AL-1 and Dt7BS is likely from increased Na+ concentration in the xylem flow and being preferentially stored in sheaths. Wheat and other grasses do have mechanisms for withdrawal of Na+ from xylem in roots and sheath to reduce delivery of Na+ into the leaf blade . Therefore, TaHKT2;1 7AL-1 and TaHKT2;1 7BL-1/-2 genes are candidates regulating Na+ accumulation in sheaths, perhaps by modifying Na+ in the root xylem that affects the flow of Na+ into sheaths. The possibility of other genes in the same chromosomal region contributing to this phenotypic effect cannot be excluded and further studies are needed to confirm the function of TaHKT2;1 genes on 7AL and 7BL in controlling Na+ accumulation in the sheaths.
The TaHKT2;1 7AL-1 gene may also regulate K+ accumulation in the sheath but only under high NaCl conditions, whereas TaHKT2;1 7BL-1/-2 may serve a similar role in roots and the youngest fully expanded leaf blade, evident by the lower K+ in these tissues in the Dt7BS line. Since TaHKT2;1 genes are not involved in K+ uptake by roots under saline conditions [18, 49], the lower root K+ concentration observed for Dt7BS in this study would be due to a greater net K+ translocation from roots to shoots. Therefore, it is reasonable to assume that TaHKT2;1 7BL-1/ TaHKT2;1 7BL-2 genes control K+ translocation in specific tissues of salt stressed wheat. Extensive functional redundancy of K+ transport systems  can be a challenge in isolated studies on individual transporter proteins, yet evidence in the present study identified the importance of further investigating TaHKT2;1 7BL-1/TaHKT2;1 7BL-2 and TaHKT2;1 7AL-1 genes in controlling K+ homeostasis.
TaHKT2;1 genes has been of interest because the encoded proteins implement pathways for Na+ entry into wheat in saline conditions . However, previous studies do not recognize a role of individual members of the TaHKT2;1 gene family in controlling Na+ or indeed, of K+, during plant growth and development. The present study has highlighted diversity amongst the TaHKT2;1 gene family and predicted proteins, as well as promoter variability in salt signalling and presence of TaHKT2;1 transcripts in different tissues, under low and high levels of external Na+ and K+, gaining knowledge that TaHKT2;1 genes could assume multiple roles in bread wheat. The phenotypic effects when individual genes were deleted in bread wheat showed that TaHKT2;1 gene family are not involved in regulating root or leaf blade Na+ concentration but TaHKT2;1 7AL-1 and TaHKT2;1 7BL-1/-2 may be candidate genes controlling sheath Na+ concentration and K+ status in different tissues and experimental conditions. TaHKT2;1 7DL-1 had no apparent role in regulating Na+ and K+ status in different tissue and treatments in this study. In summary, the present findings from combined molecular and physiological studies provided a broader perspective of the role of the TaHKT2;1 family of genes in bread wheat.
Bread wheat variety Triticum aestivum L. cv. Chinese Spring, six nullisomic-tetrasomic lines (N7AT7B, N7AT7D, N7BT7A, N7BT7D, N7DT7A, N7DT7B), eight deletion lines (7AL-1, 7AS-8, 7BL-2, 7BL-7, 7DL-2, 7DL-3, 7DL-5, 7DS-5) and ditelosomic lines (Dt7BL and Dt7BS) were kindly provided by Dr John Raupp, Wheat Genetic and Genomic Resources Centre, Kansas State University, USA. Six hexaploid cultivated bread wheat varieties Calingiri, Ducula, Krichauff, Westonia, SARC-1 and a tetraploid variety (T. turgidum L.) Tamaroi were obtained from the germplasm collection at the Department of Agriculture and Food, Western Australia. DNA samples of the diploid species, T. monococcum (accession 4044) was provided by Dr Evans Lagudah, CSIRO Plant Industry, Canberra, Australia.
In-silico analysis of TaHKT2;1gene family
The TaHKT2;1 FL-cDNA, U16709, was used as the query sequence in BLASTN to search IWGSS database (http://www.wheatgenome.org) and retrieve coding and promoter regions of the individual members of TaHKT2;1 gene family. In-silico gene structure predictions for individual members of the TaHKT2;1 family were made using Spidey (http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/spidey/), GeneSeqer (http://www.plantgdb.org/cgi-bin/GeneSeqer/index.cg) and SIM4 (http://pbil.univ-lyon1.fr/sim4.php) software. Intron-exon structures for each member were confirmed by aligning retrieved genomic sequences with the FL-cDNA, U16709. DNA and protein sequence analysis and structure predictions were made using GENEIOUS 6.0.3  and phylogenetic analysis was performed in MEGA 5.05 .
The predicted proteins were analysed for structural and functional elements including hydrophobicity and membrane topology using TMHMM Server 2.0 (http://www.cbs.dtu.dk/services/TMHMM/) and MPEx 3.2  (http://blanco.biomol.uci.edu/mpex/) software suites. Three dimensional structures of the proteins were predicted by PHYRE 2 (http://www.sbg.bio.ic.ac.uk/phyre2/html/page.cgi?id=index). Protein sequence alignments, hydrophobicity plots and the 3-D structures were used to elucidate structural domains of the putative proteins.
DNA extraction and PCR amplification
Plant genomic DNA was extracted from leaves using a phenol-chloroform-based method as described in  and was used as a template for PCR to amplify individual members of the TaHKT2;1 family. Gene specific primer pairs were designed by targeting insertions and/or deletions (INDELs) and single nucleotide polymorphisms (SNPs) based on 3′ terminus mismatch described in . NetPrimer (http://www.premierbiosoft.com/netprimer/netprlaunch/netprlaunch.html) was used to confirm primer compatibility. Primer information is summarized in Table 1. PCR reactions contained 1.5 mM MgCl2, 0.2 mM of each deoxyribonucleotides, 10 μM of each primer, 1X PCR buffer, 0.1 U taq DNA polymerase (BIOTAQ™ DNA Polymerase, Bioline, Australia) and 50 ng of template DNA in a 20 μl reaction volume. Cycle conditions for standard PCR were 35 cycles of 94°C 30 sec, primer annealing temperature 30 sec, 72°C 30 sec and the final extension 7 min at 72°C; and for touchdown PCR were five cycles of 94°C 30 sec, 55-50°C 30 sec, 72°C 30 sec; and then 35 cycles of 94°C 30 sec, 50°C 30 sec, 72°C 30 sec and the final extension 7 min at 72°C. PCR products were separated on 1.5% agarose gel in 0.5X Tris-acetate EDTA at constant voltage (90 V) for 30 min and visualized under UV light using Gel Doc System (BioRad, Italy) after staining with ethidium bromide.
Hydroponic screening and tissue Na+ and K+ analysis of wheat aneuploid lines null for TaHKT2;1genes
Seeds of six selected wheat deletion and ditelosomic lines were washed in 0.04% sodium hypochlorite (42 g/L) for 30 sec, rinsed in deionized water, and placed on a mesh float on aerated 0.1 strength nutrient solution in the dark for three days. Seedlings were then transferred to 0.25 strength nutrient solution for one day. Nutrient composition at full strength was: (mM) K+, 3.95; Ca2+, 4; Mg2+, 0.4; NH4+, 0.625; NO3−, 4.375; SO42−, 1.9; HPO42−, 0.2; Fe-EDTA, 0.05; MES, 1.0; and micronutrients of one-quarter-concentration in Hoagland solution (pH was adjusted to 6.5 using Ca(OH)2). Four day old seedlings were then transferred to full strength nutrient solution in aerated, foil-covered, 4.5 L pots for 12 days. Each pot carried one individual of each of all six genotypes arranged randomly in each pot. There were four replicates of each genotype for each treatment in the experiment and the pots were arranged in a completely randomised design. Seedlings were held upright by a foam holder at the stem base inserted into individual holes in the pot lids. The experiment was carried out in a temperature controlled phytotron (20 ± 3°C/15 ± 2°C day/night) and the photosynthetically active radiation (PAR) recorded at midday was at ca. 1,400 - 1,500 μmol m−2 s−1. Solution levels in pots were maintained by topping up with deionized water.
In order to induce expression and study phenotypic effects of the TaHKT2;1 gene family, the plants were subjected to low K+ conditions prior to imposing salt treatments [24, 46]. As known TaHKT2;1 transporters might be involved with either Na+ and/or K+ transport [16, 21, 22] NaCl treatments were also imposed at the two K+ levels: low (0.2 mM) K+, where high affinity transport systems for K+ dominate and high (4 mM) K+, where K+ uptake kinetics was determined by low affinity systems . 12 day old seedlings were subjected to low K+ conditions for four days in a modified nutrient solution without added K+. The media contained (mM) Ca2+, 4; Mg2+, 0.4; NH4+, 0.825; NO3−, 4.375; SO42- , 0.4; HPO42-, 0.2; Fe-EDTA, 0.05; MES, 1.0; and micronutrients at one-quarter-concentrations in Hoagland solution (pH = 6.5, adjusted with Ca(OH)2) at a background Na+ and K+ concentrations of 0. 3 mM and 0.1 mM, respectively. After 4 days of low K+ level pre-treatment, 200 mM NaCl was applied to designated pots, so as to obtain four different Na+/K+ combinations: no added Na+/0.2 mM K+, no added Na+/4 mM K+, 200 mM Na+/0.2 mM K+ and 200 mM Na+/4 mM K+. The NaCl treatment was applied in 50 mM increments at 12 hour intervals and plants were maintained at the final 200 mM concentration for a full 3 days. The youngest fully expanded leaf blade, bulk leaf blades (all others), sheaths and roots of each plant were sampled. Prior to excision, roots were washed three times for 10 secs each in a solution containing 4 mM CaSO4 and 368 mM mannitol (200 mM treated plants) or in 4 mM CaSO4 (plants subjected to no added NaCl). Leaves and sheath samples were rinsed in deionized water. All tissue samples for ion analyses were oven-dried at 70°C, weighed and then ground to a powder. Samples of dried powdered tissue (100 mg) were extracted in 5 ml of 0.5 M HNO3 for 3 days on a mechanical shaker. Na+ and K+ were measured in technical triplicate using a flame photometer (Sherwood 410, Cambridge) and mean values represented each treatment replicate tissue sample. The reliability of the methods was confirmed by analyses of a reference tissue (broccoli, ASPAC Plant number 85) taken through the same procedures. Mean values from 4 treatment replicates of each genotype were analysed by ANOVA using SAS 9.4 (SAS Inc., USA) software.
RNA extraction and RT-PCR
T. aestivum var. Chinese Spring was grown in hydroponics and treated with NaCl as described above. Leaf blades (including youngest fully expanded leaf blade), sheaths and roots of plants treated with 4 mM K+ with no added Na+ and 4 mM K+ with 200 mM NaCl were harvested after treating the plants for three days, snap frozen in liquid nitrogen for RNA extraction and RT-PCR. Duplicate tissue samples were harvested for Na+ analysis (described above). Total RNA was isolated using RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). First strand cDNA was synthesised using RT Omniscript Kit (Qiagen, Hilden, Germany). Integrity of synthesised cDNA was verified by RT-PCR using primers (forward 5′-CGCCAGGGTTTTCCCAGTCACGAC −3′, reverse 5′-TCACACAGGAAACAGCTATGAC −3′) designed for glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene . FL- cDNA of individual members of the TaHKT2;1 gene family were amplified from cDNA preparations using primer pairs FL:A1 F and FL:A1 R, FL:A2/3 F and FL:A2/3R, FL:B1/2 F and FL:B1/2 R and FL:D1 F and FL:D1 R (Table 1).
FL-cDNA cloning and sequencing
RT-PCR amplicons were separated and excised from 1% agarose gels, purified using Wizard® SV Gel and PCR Clean-Up System (Promega, CA,USA), and cloned into pGEM®-T Easy Vector Systems (Promega, CA, USA). Three bacterial colonies containing cloned TaHKT2;1 FL-cDNA were selected and DNA templates were purified using Wizard® Plus SV Minipreps (Promega, CA, USA). The cloned fragments were sequenced using BigDye™ sequencing chemistry (Applied Biosystems, Perkin Elmer, Weiterstadt, Germany) and analysed using GENEIOUS 6.0.3 .
This work was partly funded by a Scholarship for International Research Fees (SIRF) and a University International Stipend (UIS) awarded to HACKA and a postdoctoral fellowship from the Higher Education Commission (HEC) of Pakistan awarded to TUH. The authors are grateful to Dr Klaus Oldach for critically reviewing the manuscript.
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