Original Research ARTICLE
In-Depth Genomic and Transcriptomic Analysis of Five K+ Transporter Gene Families in Soybean Confirm Their Differential Expression for Nodulation
- 1Department of Biotechnology, Chonnam National University, Yeosu, South Korea
- 2Department of Arid Land Agriculture, King Abdul-Aziz University, Jeddah, Saudi Arabia
- 3Department of Biosciences, University of Wah, Wah Cantt, Pakistan
Plants have evolved a sophisticated network of K+ transport systems to regulate growth and development. Limited K+ resources are now forcing us to investigate how plant demand can be satisfied. To answer this complex question, we must understand the genomic and transcriptomic portfolio of K+ transporters in plants. Here, we have identified 70 putative K+ transporter genes from soybean, including 29 HAK/KT/KUP genes, 16 genes encoding voltage-gated K+ channels, 9 TPK/KCO genes, 4 HKT genes, and 12 KEA genes. To clarify the molecular evolution of each family in soybean, we analyzed their phylogeny, mode of duplication, exon structures and splice sites, and paralogs. Additionally, ortholog clustering and syntenic analysis across five other dicots further explored the evolution of these gene families and indicated that the soybean data is suitable as a model for all other legumes. Available microarray data sets from Genevestigator about nodulation was evaluated and further confirmed with the RNA sequencing data available by a web server. For each family, expression models were designed based on Transcripts Per Kilobase Million (TPM) values; the outcomes indicated differential expression linked to nodulation and confirmed the genes' putative roles. In-depth studies such as ours provides the basis for understanding K+ inventories in all other plants.
Potassium (K+) is the most widespread inorganic cation in plant cells, constituting up to 10% of plant dry matter, and plants have evolved a sophisticated network of K+ transport systems over millions of years (Leigh and Wyn Jones, 1984). Indeed, K+ deficiency symptoms reveal that the ion is vital to the regulation of plant growth and development, involved in many essential functions like protein biosynthesis, turgor-driven movement, osmoregulation, photosynthesis, and maintenance of plasma membrane potential. However, K+ resources have become limited, prompting an investigation of how to satisfy demand. This complex question can only be answered through understanding the genomic and transcriptomic portfolio of K+ transporters. Thus far, molecular knowledge of K+ transporters is available mainly from a few model species. This limited view on the dynamic involvement of K+ in diverse physiological processes can be misleading, but the massive data volume analyzed in modern approaches potentially address the problem. In this study, we therefore dissected all available genomic and transcriptomic data from wet-lab experiments and ran computational simulations to understand the five major K+-transport-related gene families in soybean (a model legume) and their role in nodulation. Moreover, we examined the transferability of our conclusions from model species to other plant species.
The five major K+ transporter families are as follows (Gomez-Porras et al., 2012; He et al., 2012): (1) the HAK/KT/KUP family of high-affinity transporters, (2) voltage-gated channels/shakers, (3) non-voltage-gated (tandem pore) TPK/KCO channels, (4) the HKT family of high-affinity transporters, and (5) the KEA family of efflux antiporters. Among them, the HAK/KT/KUP family is the largest and plays a critical role in plant growth and development, i.e., cell expansion, K+ acquisition and auxin distribution (Gierth et al., 2005; Gobert et al., 2007; He et al., 2012). To date, HAK/KT/KUP genes have been cloned from many plant species, including rice (Gupta et al., 2008; Yang et al., 2014; Chen et al., 2015), Arabidopsis (Gierth et al., 2005), tomato (Nieves-Cordones et al., 2007), pepper (Martinez-Cordero et al., 2004), lotus (Desbrosses et al., 2004), and grapevine (Davies et al., 2006). Respectively, 27, 13, and 31 HAK/KT/KUP genes have been identified in rice (Yang et al., 2009), Arabidopsis (Mäser et al., 2001), and poplar (He et al., 2012), based on genome-wide sequence analysis. Plant HAK/KT/KUP proteins possess 10–15 transmembrane domains (TMDs) with both the N- and the far longer C-termini on the intracellular side of the membrane (Gomez-Porras et al., 2012; Nieves-Cordones et al., 2016). This family exhibits considerable diversity in subcellular localization, ranging across the plasma membrane, tonoplast, and other endomembranes (Osakabe et al., 2013; Rigas et al., 2013). Furthermore, their expression patterns are diverse, observed in root meristems, vascular tissues, guard cells, fruits, and specialized organs such as flytraps (Osakabe et al., 2013; Scherzer et al., 2015). Functionally, some members contribute to root K+ uptake, notably through active K+ transport at low external concentrations (Nieves-Cordones et al., 2014).
Potassium channels from viruses to plants are characterized by a conserved amino acid motif (TVGYGD) in the narrowest stretch of the selectivity filter (Kuang et al., 2015). Three major categories of voltage-gated K+ channels exist in plants: (1) inward-rectifying (Kin) channels (AKT1, KAT1, KAT2, and SPIK) mediating K+ uptake and activated by membrane hyperpolarization; (2) weakly-inward-rectifying (Kweak) channels (AKT2/3) that mediate K+ uptake and release depending on local K electrochemical gradients; and (3) outward-rectifying (Kout) channels (SKOR and GORK) mediating K+ release from the cell and activated by membrane depolarization (Shabala and Pottosin, 2010; Gomez-Porras et al., 2012). Voltage-gated K+ channels genes are expressed ubiquitously in various plant tissues, providing a possibility for the rapid K+ redistribution between plant parts and cellular compartments. TPK/KCO channels participates in pollen tube growth, stomatal closure, and radical development; five members have been found in Arabidopsis (Czempinski et al., 2002; Wang and Wu, 2013). The first molecular analysis of K+ channels in plants involved the identification of AKT1 (Sentenac et al., 1992) and KAT1 (Anderson et al., 1992), two Arabidopsis K+ channel genes. Recently, an OsAKT1 gene was functionally characterized in rice (Ahmad et al., 2016).
The plant HKT family has been extensively studied since the discovery of TaHKT2;1 from bread wheat (Triticum aestivum), a gene that encodes Na+ and K+ co-transportation and also preferred Na+-selective low-affinity Na+ transport in the presence of a millimolar Na+ in Xenopus laevis oocytes and yeast (Horie et al., 2009). This group has been split into at least two subfamilies based on analysis of their structure and transport properties across multiple plant species (Platten et al., 2006). Class I HKT transporters generally exhibits Na+ selective transport with poor K+ permeability (Horie et al., 2009). Recently, an OsHKT1;4 gene from rice (Suzuki et al., 2016) and two genes from soybean named GmHKT1 and GmHKT1;4 were functionally characterized as being linked with salt tolerance (Chen H. et al., 2011; Chen J. et al., 2011; Chen et al., 2014). HKT genes are ubiquitously expressed in root and shoots (Almeida et al., 2013; Nieves-Cordones et al., 2016).
KEA proteins belong to the superfamily of monovalent cation proton antiporters (CPA) and several of its members are involved in chloroplast-envelope K+ transport in Arabidopsis and rice (Aranda-Sicilia et al., 2012; Kunz et al., 2014; Sheng et al., 2014). In addition, KEA antiporter systems have been detected in chloroplast and mitochondrial membranes, as well as tonoplast and plasma membranes (Song et al., 2004). For more detailed information about these five K+ transporter gene families, the author would like to recommend the extensive review papers by Rodriguez-Navarro and Rubio (2006), Dreyer and Uozumi (2011) and Hamamoto et al. (2015).
Here, we took advantage of publicly available genome and transcriptome data to prepare an inventory of K+ transporters in soybean as a resource and model for other dicots. We focused especially on HAK/KT/KUP, HKT, voltage- and non-voltage-gated K+ channels, HKT and KEA gene families. In this study, we first identified all members from each family in soybean. We next elucidated the evolutionary relationships of these K+ transporters with functional genomics: analyses of phylogeny, gene structure, splice sites, mode of duplication, paralogs, and orthologs. We associated the resultant data with root hair nodulation using microarray and RNA-seq-based transcriptome profiling of all K+ transporters. These in-depth genomic and transcriptomic investigations will provide more knowledge of the K+-transporter physiological complex in soybean and should contribute to an understanding of similar systems in other crops.
Genome-Wide Search for K+ Transporters
Putative K+ transporters were identified via screening with transporter-specific protein motifs in the conceptual proteome of Glycine max (Wm82.a2.v1). Screening was performed in the FUZZPRO program from EMBOSS (Rice et al., 2000; Gomez-Porras et al., 2012; Kuang et al., 2015), using the following 11 motifs. For HAK/KT/KUP genes: (1) [A,G] [D,S,G]-[V,L,I,M]-x-x[S,A]-P-L-Y; (2) [A,G]-[N,D,H,S]-[D,N]-x-G-[E,Q,D,N]-[A,G]; (3) [A,G,S]-[D,N] [G,S,A,C]-x-[L,I,V,F]-x-P-x-[V,I,L,M]-[A,S]; (4) G-[S,A,T,C]-E-[A,G]-x-[F,Y]-A-[D,N,E]-[L,I,V]-[G,C,S,A]x-F; (5) [Y,F]-x-x-x-x-x-[H,F,Y]-G-Y-x-[E,D]; for K+ channels: (6) [S,T]-x-xT-x-G-[Y,F,L]-G-[D,E], (7) R-[L,F]-x-R-[L,V,I,A,G]-x-[R,C,K][V,A,L,M], (8) [A,V,S]-Y-[L,I]-[I,L]-G-[N,I]-[M,I]-T-[N,A]-L[V,I]; for HKTs: (9) [S,T,A]-x-[F,Y,V,L,C]-x-[D,N,S]G, (10) [G,A]-[Y,F]-[G,A]-x-[V,A,I]-G-[L,M,Y,F]-[S,T]; and for KEA: (11) (G-x-G-x-x-G-x(n)-[DE].
New Motifs were also scanned with the MEME Suite web application (http://meme-suite.org/). Additionally, results were checked against BLASTP 2.2.28+ searches in the soybean genome, using known Arabidopsis and rice transporters of different classes as templates. To eliminate false-positives, the resultant raw data were curated semi-automatically. Sequences were discarded if they were <70% of the average length among the outermost motifs in corresponding Arabidopsis transporters. All genomic annotation data (e.g., chromosomal location, definition, and annotation) were obtained from Phytozome https://phytozome.jgi.doe.gov/pz/portal.html. The relative lengths and positions of all available domains in the five K+ transporter families were graphically depicted using information obtained with the Simple Modular Architecture Research Tool (SMART, http://smart.embl-heidelberg.de/). Data on protein molecular weight (kDa) (http://web.expasy.org/compute_pi/) and TMDs (http://hmmer.org) were also collected.
Phylogenetic Analyses of K+ Transporters in Soybean
To gain insight into the evolution of soybean K+ transporter families, the reference gene sequences were obtained from NCBI database by using their gene IDs (Gomez-Porras et al., 2012). Multiple amino-acid sequence alignments of K+ transporters were generated in ClustalW with the default settings. The bootstrap consensus (1,000 replicates) trees were constructed using theMaximum Likelihood using RAxML and 1,000 bootstrap replicates (Stamatakis, 2006).
Chromosomal Location and Expansion Patterns
To categorize K+ transporter gene family expansion, we examined the chromosomal locations of all members in soybean (JGI v1.0) and generated a map in MapChart. Segmental duplication, tandem duplication, and transposition events cause gene family expansion (He et al., 2012). In this study, we focused on segmental and tandem duplication. Paralogous segments were created through two whole-genome duplication events in the soybean, 59 and 13 million years ago (Schmutz et al., 2010). Segmental duplications were identified following He et al. (2012). The Ks values of duplicated genes are similar over time assuming a molecular clock (Shiu et al., 2004); hence, to estimate dates of segmental-duplication events, Ks values were cast off and their means calculated for each gene pair inside a duplicated block. The estimated date of the duplication event was then predicted with the mean Ks (T = Ks/2λ) values and assuming clock-like rates (λ) of 1.5 × 10−8 identical substitutions/synonymous site/year for 6.1 × 10−9 (Lynch and Conery, 2000). Syntenic relationships were determined among all paralogs in Circoletto (http://tools.bat.infspire.org/circoletto/) to check the pattern of evolution.
Genes Structure Analysis
Intron maps were constructed in accordance with a previously established method (Barvkar et al., 2012). Introns were classified based on their phase, length, and number in the genome. Diagrams of gene structures were drawn in Gene Structure Display Server (GSDS) (http://gsds.cbi.pku.edu.cn/). Exon boundaries within the coding regions of each tandem- or segmentally duplicated pairs were determined according to the thirty-first release of the Gramene database (http://www.gramene.org/). The nucleotide numbers (nt) for each exon as well as the phase of each splicing site were also determined. The potential domains of each K+ transporter family member were identified based on the Pfam database (He et al., 2012) to better understand its evolution within families.
Ortholog Identification and Clustering Pattern
Putative K+ transporters were searched against the NCBI Non-Redundant BLAST database with Blast2Go (E = 0.001) to identify orthologs in the genomic sequences of five dicots (Phaseolus vulgaris, Arabidopsis thaliana, Vitis vinifera, Populus trichocarpa, and Medicago truncatula), selected based on genome homologies. Sequences were considered orthologous at >80% similarity and their accession numbers were recorded. Orthologous peptide sequences were downloaded to investigate the clustering pattern of K+ transporter families in other genomes. Clustering analysis was performed in Orthovenn (Wang et al., 2015), and Venn gene clusters were generated for each family.
Differential Expression of K+ Transporters in Soybean
Microarray data of putative K+ transporters, obtained from the Genevestigator database (https://www.genevestigator.com/gv/), were used to detect expression in five developmental stages (flowering, fruit formation, germination, bean development, and main shoot growth) and 68 anatomical parts. Data collection focused on probe set used, developmental stage, and tissues in which putative genes were expressed. A heatmap was generated following published methods (Rehman et al., 2016).
Microarray data were further analyzed to clarify the possible roles of K+ transporters during nodulation. Although K+ transporters are widely expressed throughout plant tissues, this potential link to nodulation was deduced based on reports of LjKUP gene induction during nodule development in Lotus japonicas (Desbrosses et al., 2004) and the involvement of sulfate and histidine transporters in soybean nodulation (Libault et al., 2010). Perturbation analysis of the obtained microarray data was also performed using Genevestigator tool to generate heatmap on the basis of Bradyrhizobium-japonicum-treated and mock-treated William-82 root hair samples and the expression was examined at 6, 12, 18, 24, and 48 HAI (hours after inoculation).
RNA-Seq-Based Model Development for Nodulation
Nodulation-related differential expression of all K+ transporters was further confirmed with RNA-sequence data (Libault et al., 2010). The 78,773 soybean gene models were filtered with the RNA-seq browsing tool (http://18.104.22.168/SoyFN/). TPM values of zero to maximum in at least one of the seven stages (Root Hair 12HAI, Root hair_12HAImock, Root Hair 24 HAI, Root hair_24HAImock, Root Hair 48 HAI, Root hair_48HAImock) were calculated for all putative genes. On the basis of TPM values models were developed for each family and their responsible clades.
Identification and Phylogenetic Analyses
Our screenings putatively identified 29 HAK/KT/KUP genes, 16 genes encoding voltage-gated K+ channels, 9 genes encoding TPK/KCO channels, 4 HKT genes, and 12 KEA genes (Table S1). Together with previously reported sequences, 70 putative genes are possibly involved with K+ transport in soybean (Table S1). Phylogenetic trees were constructed from proteins with motifs and domains selected for screening (Figures S1, S2).
The number of genes identified in soybean (29) was greater than in rice (27) or Arabidopsis (13), and the same as in poplar (29). The length of HAK transporters in soybean ranged from 345 to 847 aa, and the exon number ranged from 1 to 10, with 12–14 TMDs (Table S1). The phylogenetic tree was constructed with 12 Arabidopsis genes, two rice genes, and one grape gene following previously described methods (Nieves-Cordones et al., 2016); five major clades were observed (I to V; Figure 1A), where I to IV followed previous numerations (Gomez-Porras et al., 2012; Very et al., 2014). Several subgroups were identified in clade I (Ia and Ib) and in clade II (IIa, IIb, and IIc) (Gupta et al., 2008; Nieves-Cordones et al., 2016). The HAK genes from each of the groups were found in all studied species of higher plants except Arabidopsis, where IV group is missing. Groups IIa and IIc constituted the largest clades, respectively containing five and seven soybean HAKs. Additionally, groups Ia and Ib clustered to form a larger clade, implying that they split from a common ancestor through subsequent gene duplications. The same clustering was observed for groups IIa and IIb.
Figure 1. Phylogenetic tree of putative HAK/KT/KUP transporters in soybean with their exon structure and splice sites. (A) Five clearly distinguished clades of HAK transporters are present in soybean. Each represents an independent group of paralogs. To construct the phylogenetic tree, reference genes were taken from Arabidopsis, rice, and grapes (indicated as dotted lines). Soybean genes were shown by bold lines (B) Exon structure (5′–3′) and splice-site analysis of each tandemly or segmentally duplicated soybean HAK/KT/KUP pair. Nucleotide lengths are given as numbers in boxes. Exons colored red are conserved in length among all soybean HAK/KT/KUP genes. Exons colored white are conserved in length between each duplicated pair. Black colored filled circles on the phylogenic tree are showing branch lengths.
The 16 voltage-gated K+ channel genes identified based on pore-forming regions were greater in number than orthologous Arabidopsis (9) or poplar genes (11). The length of these genes in soybean ranged from 424 to 879 aa, and the exon number ranged from 11 to 15, with 4–6 TMDs (Table S1). Based on established methods (Gomez-Porras et al., 2012), we divided the phylogenetic tree of voltage-gated K+ channel genes into four functional subgroups: (a) nine Kin genes, (b) two Ksilent genes, (c) two Kweak genes, (d) three Kout genes (Table S1 and Figure 2A).
Figure 2. Phylogenetic tree of putative Voltage-gated K+ channel and TPK/KCO genes in soybean, with exon structure and splice site analysis. (A) Evolutionary relationships among genes encoding voltage-gated and TPK/KCO channels. Extensive functional analysis identified Kin, Kout, Kweak, and Ksilent channel subunits in the voltage-gated family that modulates K+ uptake. The TPK/KCO family clearly splits into two main groups, shown in bright green and red. Reference genes for constructing the phylogenetic tree are indicated in dotted lines with their NCBI gene names. (B) Exons colored green and orange are conserved in length among all soybean voltage-gated and TPK/KCO channels, respectively.
Nine genes coding for TPK/KCO channel subunits were identified, a count that was greater than the TPK genes in Arabidopsis (6) and rice (3), but lower than poplar genes (10). Gene lengths in soybean ranged from 352 to 446 aa, and the exon number ranged from 2 to 5, with 4–5 TMDs (Table S1). The phylogenetic tree indicated that the soybean genes were divided into two clear groups, one containing the three KCO1 genes and the other with two and four genes from KCO2 and KCO3, respectively (Figure 2A).
Our screenings identified four HKT putative genes in soybean, more than in Arabidopsis (1) and poplar (1), but fewer than in rice (7). Gene lengths in soybean ranged from 410 to 574 aa, and the exon number ranged from 2 to 3, with 4–10 TMDs (Table S1). Phylogenetic analyses grouped all soybean HKTs into one group (Figure 3), indicating that the most recent common ancestor of these plants contained a single HKT-type protein. All four genes in soybean were part of the HKT subfamily 1 (Figure 3).
Figure 3. Phylogenetic tree of putative HKT genes in soybean. This family is represented by two subfamilies shown in green and blue. All soybean genes belong to HKT subfamily 1. Reference genes are shown in dotted lines with their NCBI gene names. No common splice site was found in the four soybean HKT genes.
Twelve putative KEA genes in soybean (more than the six in Arabidopsis) exhibited high percentage identity (Table S1). The exon number in the KEA gene family ranged from 19 to 21, coding for 576–1206 aa, with 9–12 TMDs. The phylogenetic tree revealed that the soybean KEA family split into three major clades: I (KEA3), II (KEA2 and KEA1), and III (KEA4, KEA5, and KEA6) (Figure 4A).
Figure 4. Phylogenetic tree of the putative KEA family in soybean, with exon structure and splice site analysis. (A) Three clearly distinguished clades are present in soybean. Referenced genes are indicated with dotted lines with their NCBI names. (B) Exons colored yellow are conserved in length among all soybean KEA genes.
Chromosomal Location and Expansion Pattern
K+-transporter-related genes were unevenly distributed in the soybean genome, located in 18 of the 20 chromosomes, with chromosome 8 containing the highest number (Figure 5).
Figure 5. Chromosomal distribution of all 70-putative K+ transporter genes and their duplication within genome. All chromosomes have K+ transporter related genes except Chr 10 and Chr 20. Black, red, blue, green, purple indicate genes belonging to HAK/KT/KUP, voltage-gated K+ channel, TPK/KCO, HKT, and KEA families respectively. Gray lines represent gene duplications in each chromosome.
Chromosomes 4, 6, 10, 14, 17, and 20 harbored no HAK/KT/KUP genes (Figure 5), while relatively high densities of HAKs (eight genes), with some apparent tandem duplications, were discovered in chromosome 8; chromosomes 1, 3, 7, 9, 11, and 13 each possessed a single HAK gene (Figure 5). Based on phylogenetic clusters, two pairs of tandemly duplicated paralogs were discovered (Glyma08g19120.1/Glyma08g07720.1 [HAK7], Glyma16g26470.1/Glyma16g05060.1 [KUP3]). Of the 29 genes, only three were located outside duplicate blocks. The remaining HAK/KT/KUP genes were segmentally duplicated. Overall, this family experienced three rounds of whole genome duplication (WGD) events in the soybean. Most were duplicated around 59 and 13 million years ago (mya), except Glyma19g01400.1, which was segmentally duplicated 198 mya from Glyma01g03850.1 (Table S2). Furthermore, syntenic analysis among paralogs confirmed the mode of duplicated regions within the gene pairs (Figure S3).
The 16 AKT genes were also unevenly distributed, found only in chromosomes 2, 4, 5, 6, 8, 13, 14, and 17 (Figure 5). One pair of tandemly duplicated paralogs (Glyma17g12740.1/Glyma17g31250.1 [AKT1]) was discovered. Of the 16 genes, only two were located outside duplicate blocks. Segmental duplication was dominant during the four rounds of WGD in this family, occurring to all pairs except two. Some genes were duplicated around 70–256 mya, indicating that these genes were duplicated individually and later became the part of the soybean genome (Table S2). Syntenic analysis confirmed the conserved regions during duplication (Figure S3).
The nine putative KCO genes were distributed only on chromosomes 2, 3, 5, 8, 14, 17, and 19, with approximately one to two genes per chromosome (Figure 5). This family was entirely duplicated through segmental duplication, rather than tandem or miss duplication, under one round of WGD (13–59 mya). However, two genes (Glyma17g01080.1 and Glyma02g46930.1) were duplicated around 120 mya (Table S2). Syntenic analysis among paralogs confirmed the mode of duplication in this family (Figure S3).
All four putative HKT genes were segmentally duplicated and distributed only on chromosomes 1, 6, 7, and 12 (Table S2 and Figure 5). This family experienced one round of WGD around 16–28 mya. The conserved regions remained the same during duplication (Figure S3).
The 12 KEA genes were distributed only on chromosomes 3, 1, 7, 8, 9, 12, 14, 16, 17, and 18 (Figure 5). Six pairs of segmentally duplicated paralogs were discovered in this family (Table S2). The KEA1 and KEA2 gene pairs were duplicated through three rounds of WGD around 8–36 mya (Table S2). The remaining genes (KEA3, KEA4, KEA5, and KEA6) were segmentally duplicated around 6–8 mya, suggesting an evolution from KEA1 and KEA2 (Table S2). Syntenic analysis revealed similarities between the coding regions within each KEA gene pair (Figure S3).
Gene Structure and Splice Site Analyses
Conserved exon structures (exons with the same nucleotide number and conserved intron phases) indicate similarities between genes (He et al., 2012; Tables S3, S4). Excluding those in HKT, a number of exons are conserved in length and possess nearly the same splice phases among HAK/KT/KUP, voltage-gated channels, TPK/KCO, and KEA families, respectively (Figures 1B, 2B, 4B). Intron phases were also highly conserved across all the segmentally and tandemly duplicated pairs of each family (Table S4 and Figure S4).
In the HAK/KT/KUP family, three exons (260, 52, and 254 nt) were highly conserved across all members except Glyma18g18822.1, Glyma02g39370.1, and Glyma11g27830.1, which do not have the 254-nt exon (Figure 1B). In addition to these three exons, each duplicated HAK pair shared several equal-length exons with the same splice phase. At least four conserved exon structures were shared by duplicated HAK pairs (Figure 1B).
All voltage-gated K+ channel genes possessed three highly conserved exons with lengths of 98, 57, and 185 nt, except Glyma08g20030.1 and Glyma12g29190.1, which lacked the 98-nt exon (green color in Figure 2B). Additionally, four to five exons of equal length, with the same splice and intron phases, were shared by each duplicated pair, again supporting the presence of a common ancestor (Figure 2B).
The TPK/KCO channel genes had two highly conserved, 150- and 147-nt exons (Figure 2B). Interestingly, no conserved exons were present across every member in this family, although each duplicated pair contained some conserved exons (Table S3). Intron phases remained conserved in this family, suggesting strong conservation throughout the family's evolutionary history (Table S4).
The KEA gene family also exhibited three highly conserved exons (68, 53, and 89 nt) (Figure 4B). The 53- and 89-nt exons were slightly variable among the duplicated KEA gene pairs. All gene pairs also contained 13–15 exons of equal length, with same splice site and intron phases (Tables S3, S4, and Figure 4B). The highly conserved exons support a common ancestor for the duplicated KEA genes.
Ortholog Identification and Clustering Pattern
In total, we identified 157 orthologs (>80% similarity) for 70 K+ transporter genes from five other legume proteomes (Table S5). Syntenic regions among the orthologs of five different families were identified in five separate dicots (Figure S5). Almost all annotated protein-coding genes in each family from these dicots were highly conserved (Figure S5).
We identified 66 orthologs with 2 clusters in the HAK/KT/KUP family, common across all five dicots (Figure S6). Arabidopsis had only one cluster for this family, suggesting that duplication expanded the HAK/KT/KUP family in the genomes of soybean and other dicots.
In voltage-gated K+ channel genes, a clustering pattern was observed among 33 identified orthologs, with one cluster in soybean and P. vulgaris, and two clusters in the other four dicots (Table S5 and Figure S6). This outcome implies that this family expanded in Medicago truncatula, Vitis vinifera, Populus trichocarpa, and Arabidopsis during evolution.
The remaining TPK/KCO, HKT, and KEA families had one cluster among all the orthologs, confirming their conservative mode of evolution through one common ancestor (Table S5 and Figure S6).
Differential Expression for Nodulation
Of the 70 K+ transporter genes, we found 26 genes that were unevenly expressed across five developmental stages (germination, main shoot growth, flowering, fruit formation) and 68 anatomical parts (Figures S7–S10). Anatomical tissues were further subdivided into five sub groups: (a) primary cell, (b) seedling, (c) inflorescence, (d) shoot, and (f) roots. In the HAK/KT/KUP family, 12 genes were highly expressed at germination, main shoot growth, and bean development (Figure S7A), but lowly expressed during flowering and fruit formation. The 12 genes were highly expressed in primary cells (paraveinal mesophyll cells and palisade parenchyma cells), seedlings (maturation zone and root hair), inflorescence (androecium, stamen, anther, and pollen), and roots (stele, pericycle, and root tip) (Figure S7B), but lowly expressed in shoots. Microarray data for HAK/KT/KUP genes revealed that Glyma19g45260.1 (HAK5), Glyma19g01400.1 (KUP6), and Glyma9g05830.1 (KUP10) were highly expressed across the B. japonicum-mock-treated William 82 root hair cells at 6, 12, 18, 24,36, 48 HAI (Figure S7C).
Six voltage-gated K+ channel genes were highly expressed during main shoot growth, flowering, and fruit formation (Figure S8A). Glyma14g39330.1 (SKOR type) was 100% expressed at flowering. These genes were maximally expressed at inflorescence (flower, androecium, stamen, anther, pollen), shoots (leaf, trifoliate leaf), and roots (pericycle and nodule) (Figure S8B). Microarray data revealed that Glyma17g12740.1 (AKT1) and Ghlyma14g39330.1 were 20% expressed in the B. japonicum-mock-treated root hair cells at 6 and 14 HAI (Figure S8C).
In the TPK/KCO family, we found two genes actively expressed at germination, main shoot growth, fruit formation, and bean development (Figure S9A). Glyma02g46930.1 (KCO1) was maximally expressed at germination, while Glyma14g01790 (KCO1) was consistently expressed across all five developmental stages. These two genes were highly expressed in seedlings (radical, maturation zone, and root hair), roots (primary root, root tip, stele, and pericycle), and inflorescence (shoot apical meristem, parenchyma) (Figure S9B). Glyma02g46930.1 and Glyma14g01790 (KCO1) were highly expressed in root hair cells mock-treated with B. japonicum at 6, 12, 18, 24, 36, and 48 HAI (Figure S9C). Interestingly, we did not find any HKT genes from the microarray data analysis.
The six KEA genes were actively expressed during main shoot growth, fruit formation, and bean development (Figure S10A). Glyma08g03320.1 (KEA4) was consistently expressed at all five stages of development. Moreover, these genes were highly expressed in the primary cell stage (leaf, mesophyll, paraveinal, and palisade parenchyma cells), inflorescence (seed, embryo, shoot apical meristem, and root apical meristem), shoots (leaf and trifoliate leaves), and roots (root tip and nodule) (Figure S10B). Glyma17g34780 (KEA6) was actively expressed in root hair cells mock-treated with B. japonicum at 6 and 12 HAI (Figure S10C).
RNA-Seq Based Transcriptome Profiling of K+ Transporters in Response to Nodulation
The differential expression of K+ transporter families was further confirmed by RNA-seq data (Table S6). We found 22 HAK/KT/KUP family genes that had TPM values >1. In phylogenetic groups Ia and Ib, Glyma19g45260.1 (HAK5) was maximally expressed at 24 and 48 HAI to B. japonicum, with average TPM values of 1,040.58 and 759.8, respectively (Figure 6A). Generally, HAK5 and KUP7 exhibited maximum TPM values in mock-treated root hair cells. In groups IIa, IIb, and IIc, Glyma19g01400 (KUP8) was maximally expressed at 24 HAI, with an TPM value of 108.45 (Figure 6B). In group III, Glyma15g1780.3 was maximally expressed at 24 and 48 HAI, with TPM values of 37.9 and 43.78, respectively (Figure 6B). Group IV did not exhibit absolute expression for nodulation. In group V, Glyma08g39840.1 (KUP12) was expressed at 24 and 48 HAI, with TPM values of 47.58 and 46.56, respectively (Figure 6B).
Figure 6. K+ transporter gene expression models derived from RNA-seq data for nodulation. Normalized TPM for all genes was recorded based on expression in B. japonicum-treated and mock-treated William 82 root hair samples at 6, 12, 18, 24, and 48 h after inoculation (HAI). Phylogeny-based models represent expression under at least one condition. (A,B) Clades 1a, Ib, IIa, IIb, IIc, III, and V genes from the HAK/KT/KUP family exhibit nodulation-related expression. (C) Expression of voltage-gated K+ channel genes in nodulation. (D) Expression of TPK/KCO genes in nodulation. (E) Expression of KEA family genes in nodulation. Arrows are showing the highest expression within a gene family.
Nine voltage-gated K+ channel genes exhibited medium-level expression for nodulation, ranging from 1 to 12 TPM. Two genes, Glyma14g39330.1 and Glyma02g41040.1 (Kout, SKOR type), were more highly expressed, with TPM values of 12.23 and 11.98 at 48 HAI (Figure 6C). Another gene expressed at 48 HAI was Glyma05g08230.1 (Kin, AKT1), with an TPM value of 9.05. These data reveal that voltage-gated K+ channel genes were mostly expressed at 48 HAI (Figure 6C).
Two TPK/KCO channel genes were expressed (TPM ~1–12) for nodulation; the highest expression for Glyma02g46930.1 (KCO1) and Glyma19g40890 (KCO3) occurred at 12 and 48 HAI (Figure 6D). Among the HKT family, Glyma12g16040.1 (HKT1;2) was the sole gene expressed only at 12 HAI (TPM = 4). In sum, this family was not found to be involved in soybean nodulation.
Nine KEA genes were dominantly expressed, with TPM values ranging from 1 to 45 (Figure 6E). Two genes, Glyma18g46420.1 (KEA2) and Glyma09g39770.1 (KEA2), were more highly expressed than the others at 48 HAI, with TPM values ranging from 39.38 to 19.32, respectively (Figure 6E). In general, KEA3, KEA4, and KEA6 were not expressed dominantly for nodulation.
HAK/KT/KUP Family in Soybean
Although only a relatively small number of HAK/KT/KUP transporters have established physiological roles, our present analyses allow us to draw some major conclusions regarding phylogenetically based evolution, gene structure, expansion pattern, and differential expression (based on microarray and RNA-seq data). With 29 genes, the HAK/KT/KUP family in soybean is the same size as in poplar (Gomez-Porras et al., 2012; Nieves-Cordones et al., 2016). In this study, the HAK/KT/KUP phylogenetic tree strictly followed the same distribution into five groups, corroborating data from Nieves-Cordones et al. (2016) (Figure 1A). The maximum number of genes was distributed into Groups IIb and IIc. Like other soybean genes, Glyma19g45260.1, Glyma03g42480.1, and Glyma07g04750.1 (HAK5) are all involved in root high-affinity K+ uptake and fall into clade Ia (Martinez-Cordero et al., 2004; Nieves-Cordones et al., 2007, 2016; Rubio et al., 2008; Aleman et al., 2009; Gomez-Porras et al., 2012). In rice, clade Ia genes OsHAK5 and OsHAK21 exhibited a more specialized function of transporting K+ to aerial parts during K+ deficiency and salt stress, respectively (Yang et al., 2014; Shen et al., 2015). The soybean putative genes in the same clades (IIb and IIc) likely have the putative function of K+ transportation to aerial parts under salt stress and K+ deficiency.
As seen in data from other plants, clade Ib HAK/KT/KUP transporters may contribute to high-affinity K+ uptake in digesting glandes of Venus flytrap and flowers and berry skin of, (grapevine) (Davies et al., 2006; Scherzer et al., 2015; Nieves-Cordones et al., 2016). Further characterization of clade Ib transporters will clarify whether they are specialized in tissue or root K+ transport. Therefore, group Ib genes could be considered to determine their putative role in high K+ uptake during flowering (Figure 1A).
The Arabidopsis clade IIa (AtKUP4/TRH1) gene contributes to the polar localization of auxin transporters in the root apex, a necessary process for both gravitropic responses and root hair formation (Rigas et al., 2013; Nieves-Cordones et al., 2016). In clade IIc, AtKUP2/6/8 negatively regulates plant growth and cell size via mediating K+ efflux rather than influx (Osakabe et al., 2013; Nieves-Cordones et al., 2016). Another clade IIb gene is AtKUP1/KT1, the first cloned HAK/KT/KUP transporter from Arabidopsis; however, its physiological role has not yet been determined (Kim et al., 1998). The role of clade III genes could potentially be discerned based on cotton (Gossypium hirsutum) GhKT1, which was specifically upregulated during cotton fiber elongation (Ruan et al., 2001; Nieves-Cordones et al., 2016). As for clade IV transporters, only one have been characterized so far in plants: LjKUP was highly expressed during late nodulation and complemented K+-uptake-deficient bacteria (Desbrosses et al., 2004). Finally, PpHAK1 from Physcomitrella patens provides insight into clade V function; it regulates steady K+ content and plant morphology under non-K+-limiting conditions, as well as contributing to high-affinity Rb+ and Cs+ uptake during K+ starvation (Garciadeblas et al., 2007; Nieves-Cordones et al., 2016). In future studies, In future studies, these genes can be functionally characterized for polar localization of auxin in root apex, K+ efflux, fiber development, nodule development and plant morphology from IIa, IIc, III, IV and V group members respectively (Figure 1A).
The gene structure and expansion patterns of soybean HAK/KT/KUP genes were highly similar with respect to conserved exon length (commonly 260, 52, and 254 nt), close to the lengths found in poplar (261, 53, and 254 nt) (Figure 1B; He et al., 2012). Segmental duplication was also dominant in both poplar and soybean. Moreover, three WGD events occurred in soybean HAK/KT/KUP evolution; the results were highly similar in poplar (He et al., 2012; Table S2). Ortholog clustering and syntenic analysis of the HAK/KT/KUP family in all five dicots revealed that their last common ancestor had two HAK transporters (Figures S5, S6), confirming the previous work (Gomez-Porras et al., 2012).
In-depth transcriptome profiling via microarray and RNA-seq established the differential expression of 22 HAK/KT/KUP genes for nodulation (Figures 6A,B, and Figure S7). In this family, Glyma19g45260.1 (HAK5), Glyma19g01400.1 (KUP8), Glyma08g39840.1 (KUP12), and Glyma15g17080.3 were maximally expressed for root hair nodulation (Figure 6). Our data corroborates a previous proposal of Glyma19g452601 (HAK5) being a strong candidate for soybean nodulation (De Carvalho et al., 2013), as well as other data describing the role of various transporters in nodulation as described by Collier and Tegeder (2012), Clarke et al. (2014) and Kryvoruchko et al. (2016). However, Glyma08g09720.1 from group IV was not highly expressed for nodulation in soybean, although it was highly similar to the LjKUP gene (in L. japonicus) responsible for late nodule development (Desbrosses et al., 2004).
Voltage-Gated K+ Channels in Soybean
The 16 genes encoding voltage-gated K+ channels in soybean were higher in number than the known genes in Arabidopsis (9), and poplar (11) (Gomez-Porras et al., 2012). The results of our phylogenetic analysis supported previous research (Gomez-Porras et al., 2012; Figure 2A). The maximum number of six Kin (AKT1) and three Kin (KAT1) putative genes in soybean confirmed the large K+ uptake range in soybean, allowing the plant to adjust K+ concentrations, especially when exposed to low K+ environments (Figure 2A). The recently characterized OsAKT1 from rice confirmed the previously reported, critical role of Kin type genes in K+ uptake, nutrition, and drought tolerance (Li et al., 2014; Ahmad et al., 2016). Hence, the genes in these clades could be a target for functional characterization, linking them to K+ uptake and drought tolerance in soybean and other legumes. Currently, AtKC1 is accepted to be involved in modulating AKT1 expression under low K+ stress responses in Arabidopsis (Wang et al., 2016). Therefore, we proposed that Glyma06g07840.1 and Glyma04g07750.1 (Ksilent) in soybean have a synergistic effect on AKT1 regulation under K+ deficient conditions.
The soybean genome harbors three Kout genes in the voltage-gated K+ channel family. Glyma05g33660.3 (GORK type) likely influences K+ efflux in stomatal closure, as its closest homolog in Arabidopsis has already been characterized for stomatal regulation (Hosy et al., 2003). The remaining two genes Glyma14g39330.1 and Glyma02g41040.1 (SKOR type) can be projected for their contribution to shoot-ward K+ secretion into the xylem sap (Gaymard et al., 1998). Glyma08g20030.1 and Glyma12g29190.1 (AKT2/3) were identified for weak K+ rectification. Functional characterization of the genes from this group has revealed enough functional plasticity to perform different roles in phloem tissue of source and sink organs. Moreover, they are also involved in drought tolerance and salt-induced depolarization of Arabidopsis roots (Lacombe et al., 2000; Salvador-Recatala, 2016).
The voltage-gated K+ channel family in soybean was observed to have highly conserved gene structure, with lengths of 57, 98, and 185 nt exons across all 16 genes (Figure 2B). Hence, this family probably evolved through these conserved exons. Segmental duplication was dominant during the expansion of this family (Table S2). Only two genes were tandemly duplicated. We also discovered that AKTC1, KAT1, AKT2/3, and GORK/SKOR genes evolved from AKT1 genes around 7–10 mya, a recent gene duplication event in soybean. AKT1 genes were duplicated 9–59 mya, whereas others were duplicated around 188–255 mya, only becoming part of soybean genome later (Table S2). Four rounds of WGD were involved in expanding this family in soybean. Ortholog clustering and syntenic analysis with other five dicots revealed that this family formed one cluster in both the common bean and soybean, while forming two clusters in the other species (Figures S5, S6).
Undoubtedly, voltage-gated K+ channels genes were widely expressed in shoots and roots. A detailed microarray and RNA-seq data confirmed their involvement in nodulation (Figure S8 and Figure 6C). Based on our analysis, we proposed that Glyma5g08230.1 (AKT1), Glyma14g39330.1, and Glyma02g41040.1 (SKOR type) are involved in nodule development (Figure 6C). Recently, a candidate gene from Medicago truncatula belonging to this family was proposed to affect cell membrane repolarization during the early electrical response to node factor, as well as being involved in stomatal movements and K+ secretion into the xylem sap (Damiani et al., 2016). Our microarray and RNA-seq results supported the link to nodule development.
TPK/KCO Family in Soybean
Functional TPK channels form dimers comprising two identical subunits; each subunit is characterized by a structure with four TMDs and tandem-pore-forming loops between the first, second, third, and fourth membrane-spanning domains (Maitrejean et al., 2011; Gomez-Porras et al., 2012). Soybean TPK/KCO channels are divided into KCO1, KCO2, and KCO3; these results are similar to Marcel et al. (2010) and Gomez-Porras et al. (2012) (Figure 2A). Findings on KCO1 genes in Arabidopsis confirmed that genes in this clade are related to vacuolar K+ conductance, salt stress adaptation, and K+ homeostasis (Latz et al., 2007; Maitrejean et al., 2011). KCO2 and KCO3 genes form homomeric ion channels in vivo; thus, the TPK/KCO genes can be functionally characterized as having such functions (Voelker et al., 2006; Rocchetti et al., 2012). Hence we proposed the putative functions of KCO1, KCO2, and KCO3 genes for vacuolar K+ conductance, salt stress adaption and K+ homeostasis respectively.
KCO1 genes in soybean did not exhibit any conserved exons and segmentally duplicated around 7 mya (Table S2). One conserved, 147-nt exon was observed in KCO2 and KCO3 genes, suggesting a common ancestor (Marcel et al., 2010; Figure 2B). Moreover, a recent duplication event of 11–14 mya was also found in soybean KCO2 and KCO3 genes (Marcel et al., 2010) (Table S2). Ortholog clustering and syntenic analysis among all five dicot TPK/KCO members revealed only one cluster, similar to results from Marcel et al. (2010) (Figures S5, S6).
Differential expression of Glyma02g46930.1 (KCO1) and Glyma19g40890.1 (KCO3) for nodulation was confirmed through microarray and RNA-seq (Figure S9 and Figure 6D). Until this study, KCO/TPK family had not been annotated for nodulation in any plant.
HKT Family in Soybean
The plant HKT family comprises transporters that mediate Na+ uptake in roots or in other plant organs. Phylogenetic analysis of HKT genes in soybean grouped them into HKT subfamily 1, highly similar to previous findings (Platten et al., 2006; Gomez-Porras et al., 2012; Figure 3). Recently, GmHKT1;4 in soybean was found to regulate the Na+/K+ ratio in roots under salt stress (Chen et al., 2014). Therefore, we propose that the three related genes in soybean are also functionally involved in salt stress response. Segmental duplication occurred around 16–28 mya in soybean HKT subfamily 1 (Table S2). Ortholog clustering and syntenic analysis with genes from five dicots showed that they had one common ancestor (one cluster) (Figures S5, S6). Interestingly, we did not find any HKT gene in soybean that was involved in nodulation. Hence, we concluded that this family only affects Na+/K+ regulation in soybean.
KEA Family in Soybean
The novel KEA family is responsible for active K+ accumulation and balance, as described by Aranda-Sicilia et al. (2012). Phylogenetic analysis of 12 KEA genes grouped them into three major clades, supporting Chanroj et al. (2012) (Figure 4). KEA1 and KEA2 represent very close homologs, most likely due to a gene-duplication event; thus, they are expected to perform the same transport function (Hohner et al., 2016). Genes KEA4 to KEA6 were all grouped into one clade, again similar to previous work (Chanroj et al., 2012). KEA family genes have been implicated in abiotic stresses, such as K+ deficiency, drought, and high salinity (Sheng et al., 2014). Recent studies with KEA1 and KEA2 mutants in Arabidopsis underscored their diverse influence in leaf growth and efficient photosynthesis rate (Kunz et al., 2014; Dana et al., 2016). Recently, an electro-neutral KEA3 gene from this family was identified in the thylakoid membrane, predominantly in the Arabidopsis stroma lamellae (Armbruster et al., 2014; Kunz et al., 2014). Hence, KEA genes in soybean likely have similar putative functions as their homologs in Arabidopsis.
Exon structure among all soybean KEA genes was highly conserved at lengths of 68 and 89 nt, indicating evolution from a common ancestor (Figure 4B). In particular, soybean KEA1 and KEA2 genes were segmentally duplicated 8–34 mya (Table S2) and exhibited similar patterns in phylogeny and gene structure. KEA3, KEA4, KEA5, and KEA6 evolved with a recent genome duplication around 6–7 mya in soybean. Ortholog clustering and syntenic analysis in all five dicots also confirmed that the KEA family was highly conserved throughout their expansion in dicots (Figures S5, S6).
Based on the differential expression observed during root hair inoculation with B. japonicum, we propose a new role for KEA2 genes in soybean nodulation (Figure 6E). Specifically, Glyma18g46420.1 and Glyma09g39770.1(KEA2) were differentially expressed in root hair cells 48 HAI mock treated (Figure 6E). RNA-seq data was similar with microarray data and confirmed the differential expression.
In the soybean genome, we identified 29 HAK/KT/KUP genes, 16 voltage-gated K+ channel genes, 9 TPK/KCO channel genes, 4 HKT genes, and 12 KEA genes. Based on phylogenetic analyses, expansion patterns, gene structures, splice sites, paralog analysis, and ortholog clustering, we were able to predict detailed functional properties for several genes (Figures 1–4 and Figures S4–S6). In addition, a microarray analysis clarified the genes' mode and place of expression in focusing on five developmental stages and 68 anatomical parts. Until this study, very little was known about the functional role of these genes in soybean nodulation. Hence, for each family, we proposed models of differential expression related to soybean nodulation, based on microarray and RNA-seq data (Figure 6 and Figures S7–S10).
HR and MN proposed and wrote the manuscript. ZS and SK managed the graphics. ID, SY, and GC refine and approved the manuscript.
Conflict of Interest Statement
This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF), funded by the Ministry of Education (NRF-2015R1D1A1A09060925).
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fpls.2017.00804/full#supplementary-material
AKT, Arabidopsis K+ transporter; ATKC, Arabidopsis thaliana K+ rectifying channel; BLAST, Basic local alignment search tool; CPA, Cation proton antiporters; GORK, Gated outward rectifying K+ channel; HAI, Hours after inoculation; HAK, High-affinity K+ transporter; HKT, High-affinity K+ transporter; KAT, K+ channel in Arabidopsis thaliana; KCO, K+ channel outward; kDa, Kilo Dalton; KEA, K+ efflux antiporters; KT, K+ transporter; KUP, + uptake permease; Mya, Million years ago; TPM, Transcripts Per Kilobase Million; SKOR, Stelar K+ outward rectifier; SPIK, Shaker pollen inward K+ channel; TMDs, Transmembrane domains; TPK, Tandem-pore K+ channel; WGD, Whole genome duplication.
Ahmad, I., Mian, A., and Maathuis, F. J. M. (2016). Overexpression of the rice AKT1 potassium channel affects potassium nutrition and rice drought tolerance. J. Exp. Bot. 67, 2689–2698. doi: 10.1093/jxb/erw103
Aleman, F., Nieves-Cordones, M., Martinez, V., and Rubio, F. (2009). Differential regulation of the HAK5 genes encoding the high-affinity K+ transporters of Thellungiella halophila and Arabidopsis thaliana. Environ. Exp. Bot. 65, 263–269. doi: 10.1016/j.envexpbot.2008.09.011
Anderson, J. A., Huprikar, S. S., Kochian, L. V., Lucas, W. J., and Gaber, R. F. (1992). Functional expression of a probable Arabidopsis thaliana potassium channel in Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. U.S.A. 89, 3736–3740. doi: 10.1073/pnas.89.9.3736
Aranda-Sicilia, M. N., Cagnac, O., Chanroj, S., Sze, H., Rodriguez-Rosales, M. P., and Venema, K. (2012). Arabidopsis KEA2, a homolog of bacterial KefC, encodes a K+/H+ antiporter with a chloroplast transit peptide. Biochim. Biophys. Acta 1818, 2362–2371. doi: 10.1016/j.bbamem.2012.04.011
Armbruster, U., Carrillo, L. R., Venema, K., Pavlovic, L., Schmidtmann, E., Kornfeld, A., et al. (2014). Ion antiport accelerates photosynthetic acclimation in fluctuating light environments. Nat. Commun. 5, 5439. doi: 10.1038/ncomms6439
Barvkar, V. T., Pardeshi, V. C., Kale, S. M., Kadoo, N. Y., and Gupta, V. S. (2012). Phylogenomic analysis of UDP glycosyltransferase 1 multigene family in Linum usitatissimum identified genes with varied expression patterns. BMC Genomics 13:175. doi: 10.1186/1471-2164-13-175
Chanroj, S., Wang, G., Venema, K., Zhang, M. W., Delwiche, C. F., and Sze, H. (2012). Conserved and diversified gene families of monovalent cation/H+ antiporters from algae to flowering plants. Front. Plant Sci. 3:25. doi: 10.3389/fpls.2012.00025
Chen, G., Hu, Q., Luo, L., Yang, T., Zhang, S., Hu, Y., et al. (2015). Rice potassium transporter OsHAK1 is essential for maintaining potassium-mediated growth and functions in salt tolerance over low and high potassium concentration ranges. Plant Cell Environ. 38, 2747–2765. doi: 10.1111/pce.12585
Chen, H., Chen, X., Gu, H., Wu, B., Zhang, H., Yuan, X., et al. (2014). GmHKT1;4, a novel soybean gene regulating Na+/K+ ratio in roots enhances salt tolerance in transgenic plants. Plant Growth Regul. 73, 299–308. doi: 10.1007/s10725-014-9890-3
Chen, H., He, H., and Yu, D. (2011). Overexpression of a novel soybean gene modulating Na+ and K+ transport enhances salt tolerance in transgenic tobacco plants. Physiol. Plant. 141, 11–18. doi: 10.1111/j.1399-3054.2010.01412.x
Chen, J., Wu, F. H., Wang, W. H., Zheng, C. J., Lin, G. H., Dong, X. J., et al. (2011). Hydrogen sulphide enhances photosynthesis through promoting chloroplast biogenesis, photosynthetic enzyme expression, and thiol redox modification in Spinacia oleracea seedlings. J. Exp. Bot. 62, 4481–4493. doi: 10.1093/jxb/err145
Czempinski, K., Frachisse, J. M., Maurel, C., Barbier-Brygoo, H., and Mueller-Roeber, B. (2002). Vacuolar membrane localization of the Arabidopsis “two-pore” K+ channel KCO1. Plant J. 29, 809–820. doi: 10.1046/j.1365-313X.2002.01260.x
Damiani, I., Drain, A., Guichard, M., Balzergue, S., Boscari, A., Boyer, J. C., et al. (2016). Nod Factor Effects on Root Hair-specific transcriptome of Medicago truncatula: focus on plasma membrane transport systems and reactive oxygen species networks. Front. Plant Sci. 7:794. doi: 10.3389/fpls.2016.00794
Dana, S., Herdean, A., Lundin, B., and Spetea, C. (2016). Each of the chloroplast potassium efflux antiporters affects photosynthesis and growth of fully developed Arabidopsis rosettes under short-day photoperiod. Physiol. Plant. 158, 483–491 doi: 10.1111/ppl.12452
Davies, C., Shin, R., Liu, W., Thomas, M. R., and Schachtman, D. P. (2006). Transporters expressed during grape berry (Vitis vinifera L.) development are associated with an increase in berry size and berry potassium accumulation. J. Exp. Bot. 57, 3209–3216. doi: 10.1093/jxb/erl091
De Carvalho, G. A. B., Batista, J. S. S., Marcelino-Guimarães, F. C., Do Nascimento, L. C., and Hungria, M. (2013). Transcriptional analysis of genes involved in nodulation in soybean roots inoculated with Bradyrhizobium japonicum strain CPAC 15. BMC Genomics 14:153. doi: 10.1186/1471-2164-14-153
Desbrosses, G., Kopka, C., Ott, T., and Udvardi, M. K. (2004). Lotus japonicus LjKUP is induced late during nodule development and encodes a potassium transporter of the plasma membrane. Mol. Plant. Microbe. Interact. 17, 789–797. doi: 10.1094/MPMI.2004.17.7.789
Garciadeblas, B., Barrero-Gil, J., Benito, B., and Rodriguez-Navarro, A. (2007). Potassium transport systems in the moss Physcomitrella patens: pphak1 plants reveal the complexity of potassium uptake. Plant J. 52, 1080–1093. doi: 10.1111/j.1365-313X.2007.03297.x
Gaymard, F., Pilot, G., Lacombe, B., Bouchez, D., Bruneau, D., Boucherez, J., et al. (1998). Identification and disruption of a plant shaker-like outward channel involved in K+ release into the xylem sap. Cell 94, 647–655. doi: 10.1016/S0092-8674(00)81606-2
Gierth, M., Maser, P., and Schroeder, J. I. (2005). The potassium transporter AtHAK5 functions in K+ deprivation-induced high-affinity K+ uptake and AKT1 K+ channel contribution to K+ uptake kinetics in Arabidopsis roots. Plant Physiol. 137, 1105–1114. doi: 10.1104/pp.104.057216
Gobert, A., Isayenkov, S., Voelker, C., Czempinski, K., and Maathuis, F. J. M. (2007). The two-pore channel TPK1 gene encodes the vacuolar K+ conductance and plays a role in K+ homeostasis. Proc. Natl. Acad. Sci. U.S.A. 104, 10726–10731. doi: 10.1073/pnas.0702595104
Gomez-Porras, J. L., Ria-o-Pachón, D. M., Benito, B., Haro, R., Sklodowski, K., Rodríguez-Navarro, A., et al. (2012). Phylogenetic analysis of K+ transporters in bryophytes, lycophytes, and flowering plants indicates a specialization of vascular plants. Front. Plant Sci. 3:167. doi: 10.3389/fpls.2012.00167
Gupta, M., Qiu, X., Wang, L., Xie, W., Zhang, C., Xiong, L., et al. (2008). KT/HAK/KUP potassium transporters gene family and their whole-life cycle expression profile in rice (Oryza sativa). Mol. Genet. Genomics 280, 437–452. doi: 10.1007/s00438-008-0377-7
Hamamoto, S., Horie, T., Hauser, F., Deinlein, U., Schroeder, J. I., and Uozumi, N. (2015). HKT transporters mediate salt stress resistance in plants: from structure and function to the field. Curr. Opin. Biotechnol. 32, 113–120. doi: 10.1016/j.copbio.2014.11.025
He, C., Cui, K., Duan, A., Zeng, Y., and Zhang, J. (2012). Genome-wide and molecular evolution analysis of the poplar KT/HAK/KUP potassium transporter gene family. Ecol. Evol. 2, 1996–2004. doi: 10.1002/ece3.299
Horie, T., Hauser, F., and Schroeder, J. I. (2009). HKT transporter-mediated salinity resistance mechanisms in Arabidopsis and monocot crop plants. Trends Plant Sci. 14, 660–668. doi: 10.1016/j.tplants.2009.08.009
Hosy, E., Vavasseur, A., Mouline, K., Dreyer, I., Gaymard, F., Poree, F., et al. (2003). The Arabidopsis outward K+ channel GORK is involved in regulation of stomatal movements and plant transpiration. Proc. Natl. Acad. Sci. U.S.A. 100, 5549–5554. doi: 10.1073/pnas.0733970100
Kryvoruchko, I. S., Sinharoy, S., Torres-Jerez, I., Sosso, D., Pislariu, C. I., Guan, D., et al. (2016). MtSWEET11, a nodule-specific sucrose transporter of Medicago truncatula. Plant Physiol. 171, 554–565. doi: 10.1104/pp.15.01910
Kunz, H. H., Gierth, M., Herdean, A., Satoh-Cruz, M., Kramer, D. M., Spetea, C., et al. (2014). Plastidial transporters KEA1, -2, and -3 are essential for chloroplast osmoregulation, integrity, and pH regulation in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 111, 7480–7485. doi: 10.1073/pnas.1323899111
Lacombe, B., Pilot, G., Michard, E., Gaymard, F., Sentenac, H., and Thibaud, J. B. (2000). A shaker-like K+ channel with weak rectification is expressed in both source and sink phloem tissues of Arabidopsis. Plant Cell 12, 837–851. doi: 10.1105/tpc.12.6.837
Latz, A., Becker, D., Hekman, M., Muller, T., Beyhl, D., Marten, I., et al. (2007). TPK1, a Ca2+-regulated Arabidopsis vacuole two-pore K+ channel is activated by 14-3-3 proteins. Plant J. 52, 449–459. doi: 10.1111/j.1365-313X.2007.03255.x
Leigh, R. A., and Wyn Jones, R. G. (1984). A hypothesis relating critical potassium concentrations for growth to the distribution and functions of this ion in the plant cell. New Phytol. 97, 1–13. doi: 10.1111/j.1469-8137.1984.tb04103.x
Li, J., Long, Y., Qi, G. N., Li, J., Xu, Z. J., Wu, W. H., et al. (2014). The Os-AKT1 channel is critical for K+ uptake in rice roots and is modulated by the rice CBL1-CIPK23 complex. Plant Cell 26, 3387–3402. doi: 10.1105/tpc.114.123455
Libault, M., Farmer, A., Brechenmacher, L., Drnevich, J., Langley, R. J., Bilgin, D. D., et al. (2010). Complete transcriptome of the soybean root hair cell, a single-cell model, and its alteration in response to Bradyrhizobium japonicum infection. Plant Physiol. 152, 541–552. doi: 10.1104/pp.109.148379
Maitrejean, M., Wudick, M. M., Voelker, C., Prinsi, B., Mueller-Roeber, B., Czempinski, K., et al. (2011). Assembly and sorting of the tonoplast potassium channel AtTPK1 and its turnover by internalization into the vacuole. Plant Physiol. 156, 1783–1796. doi: 10.1104/pp.111.177816
Marcel, D., Muller, T., Hedrich, R., and Geiger, D. (2010). K+ transport characteristics of the plasma membrane tandem-pore channel TPK4 and pore chimeras with its vacuolar homologs. FEBS Lett. 584, 2433–2439. doi: 10.1016/j.febslet.2010.04.038
Martinez-Cordero, M. A., Martinez, V., and Rubio, F. (2004). Cloning and functional characterization of the high-affinity K+ transporter HAK1 of pepper. Plant Mol. Biol. 56, 413–421. doi: 10.1007/s11103-004-3845-4
Mäser, P., Thomine, S., Schroeder, J. I., Ward, J. M., Hirschi, K., Sze, H., et al. (2001). Phylogenetic relationships within cation transporter families of Arabidopsis. Plant Physiol. 126, 1646–1667. doi: 10.1104/pp.126.4.1646
Nieves-Cordones, M., Aleman, F., Martinez, V., and Rubio, F. (2014). K+ uptake in plant roots. The systems involved, their regulation and parallels in other organisms. J. Plant Physiol. 171, 688–695. doi: 10.1016/j.jplph.2013.09.021
Nieves-Cordones, M., Martínez-Cordero, M. A., Martínez, V., and Rubio, F. (2007). An -sensitive component dominates high-affinity K+ uptake in tomato plants. Plant Sci. 172, 273–280. doi: 10.1016/j.plantsci.2006.09.003
Nieves-Cordones, M., Rodenas, R., Chavanieu, A., Rivero, R. M., Martinez, V., Gaillard, I., et al. (2016). Uneven HAK/KUP/KT protein diversity among angiosperms: species distribution and perspectives. Front. Plant Sci. 7:127. doi: 10.3389/fpls.2016.00127
Osakabe, Y., Arinaga, N., Umezawa, T., Katsura, S., Nagamachi, K., Tanaka, H., et al. (2013). Osmotic stress responses and plant growth controlled by potassium transporters in Arabidopsis. Plant Cell 25, 609–624. doi: 10.1105/tpc.112.105700
Platten, J. D., Cotsaftis, O., Berthomieu, P., Bohnert, H., Davenport, R. J., Fairbairn, D. J., et al. (2006). Nomenclature for HKT transporters, key determinants of plant salinity tolerance. Trends Plant Sci. 11, 372–374. doi: 10.1016/j.tplants.2006.06.001
Rehman, H. M., Nawaz, M. A., Bao, L., Shah, Z. H., Lee, J.-M., Ahmad, M. Q., et al. (2016). Genome-wide analysis of Family-1 UDP-glycosyltransferases in soybean confirms their abundance and varied expression during seed development. J. Plant Physiol. 206, 87–97. doi: 10.1016/j.jplph.2016.08.017
Rigas, S., Ditengou, F. A., Ljung, K., Daras, G., Tietz, O., Palme, K., et al. (2013). Root gravitropism and root hair development constitute coupled developmental responses regulated by auxin homeostasis in the Arabidopsis root apex. New Phytol. 197, 1130–1141. doi: 10.1111/nph.12092
Rocchetti, A., Sharma, T., Wulfetange, C., Scholz-Starke, J., Grippa, A., Carpaneto, A., et al. (2012). The putative K+ channel subunit AtKCO3 forms stable dimers in Arabidopsis. Front. Plant Sci. 3:251. doi: 10.3389/fpls.2012.00251
Ruan, Y. L., Llewellyn, D. J., and Furbank, R. T. (2001). The control of single-celled cotton fiber elongation by developmentally reversible gating of plasmodesmata and coordinated expression of sucrose and K+ transporters and expansin. Plant Cell 13, 47–60. doi: 10.1105/tpc.13.1.47
Rubio, F., Nieves-Cordones, M., Aleman, F., and Martinez, V. (2008). Relative contribution of AtHAK5 and AtAKT1 to K+ uptake in the high-affinity range of concentrations. Physiol. Plant. 134, 598–608. doi: 10.1111/j.1399-3054.2008.01168.x
Scherzer, S., Böhm, J., Krol, E., Shabala, L., Kreuzer, I., Larisch, C., et al. (2015). Calcium sensor kinase activates potassium uptake systems in gland cells of Venus flytraps. Proc. Natl. Acad. Sci. U.S.A. 112, 7309–7314. doi: 10.1073/pnas.1507810112
Sentenac, H., Bonneaud, N., Minet, M., Lacroute, F., Salmon, J., Gaymard, F., et al. (1992). Cloning and expression in yeast of a plant potassium-ion transport-system. Science 256, 663–665. doi: 10.1126/science.1585180
Shabala, S., and Pottosin, I. I. (2010). Potassium and potassium-permeable channels in plant salt tolerance, in Ion Channels and Plant Stress Responses, eds V. Demidchik and F. Maathuis (Berlin: Springer; Heidelberg), 87–110.
Shen, Y., Shen, L., Shen, Z., Jing, W., Ge, H., Zhao, J., et al. (2015). The potassium transporter OsHAK21 functions in the maintenance of ion homeostasis and tolerance to salt stress in rice. Plant Cell Environ. 38, 2766–2779. doi: 10.1111/pce.12586
Sheng, P., Tan, J., Jin, M., Wu, F., Zhou, K., Ma, W., et al. (2014). Albino midrib 1, encoding a putative potassium efflux antiporter, affects chloroplast development and drought tolerance in rice. Plant Cell Rep. 33, 1581–1594. doi: 10.1007/s00299-014-1639-y
Shiu, S. H., Karlowski, W. M., Pan, R., Tzeng, Y. H., Mayer, K. F., and Li, W. H. (2004). Comparative analysis of the receptor-like kinase family in Arabidopsis and rice. Plant Cell 16, 1220–1234. doi: 10.1105/tpc.020834
Song, C. P., Guo, Y., Qiu, Q., Lambert, G., Galbraith, D. W., Jagendorf, A., et al. (2004). A probable Na+(K+)/H+ exchanger on the chloroplast envelope functions in pH homeostasis and chloroplast development in Arabidopsis thaliana. Proc. Natl. Acad. Sci.U.S.A. 101, 10211–10216. doi: 10.1073/pnas.0403709101
Suzuki, K., Yamaji, N., Costa, A., Okuma, E., Kobayashi, N. I., Kashiwagi, T., et al. (2016). OsHKT1;4-mediated Na(+)transport in stems contributes to Na+ exclusion from leaf blades of rice at the reproductive growth stage upon salt stress. BMC Plant Biol. 16:22. doi: 10.1186/s12870-016-0709-4
Very, A. A., Nieves-Cordones, M., Daly, M., Khan, I., Fizames, C., and Sentenac, H. (2014). Molecular biology of K+ transport across the plant cell membrane: what do we learn from comparison between plant species? J. Plant Physiol. 171, 748–769. doi: 10.1016/j.jplph.2014.01.011
Voelker, C., Schmidt, D., Mueller-Roeber, B., and Czempinski, K. (2006). Members of the Arabidopsis AtTPK/KCO family form homomeric vacuolar channels in planta. Plant J. 48, 296–306. doi: 10.1111/j.1365-313X.2006.02868.x
Wang, X.-P., Chen, L.-M., Liu, W.-X., Shen, L., Wang, F.-L., Zhou, Y., et al. (2016). AtKC1 and CIPK23 synergistically modulate AKT1-mediated low potassium stress responses in Arabidopsis. Plant Physiol. 170, 2264–2277. doi: 10.1104/pp.15.01493
Wang, Y., Coleman-Derr, D., Chen, G., and Gu, Y. Q. (2015). OrthoVenn: a web server for genome wide comparison and annotation of orthologous clusters across multiple species. Nucleic Acids Res. 43, W78–W84. doi: 10.1093/nar/gkv487
Yang, T., Zhang, S., Hu, Y., Wu, F., Hu, Q., Chen, G., et al. (2014). The role of a potassium transporter OsHAK5 in potassium acquisition and transport from roots to shoots in rice at low potassium supply levels. Plant Physiol. 166, 945–959. doi: 10.1104/pp.114.246520
Keywords: K+ transporters, HAK/KT/KUP, voltage-gated K+ channel, TPK/KCO, HKT, KEA, soybean
Citation: Rehman HM, Nawaz MA, Shah ZH, Daur I, Khatoon S, Yang SH and Chung G (2017) In-Depth Genomic and Transcriptomic Analysis of Five K+ Transporter Gene Families in Soybean Confirm Their Differential Expression for Nodulation. Front. Plant Sci. 8:804. doi: 10.3389/fpls.2017.00804
Received: 10 January 2017; Accepted: 28 April 2017;
Published: 23 May 2017.
Edited by:Shrikant S. Mantri, National Agri-Food Biotechnology Institute, India
Reviewed by:Kira Vyatkina, St. Petersburg Academic University, Russia
Christopher Fields, University of Illinois at Urbana–Champaign, United States
Copyright © 2017 Rehman, Nawaz, Shah, Daur, Khatoon, Yang and Chung. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.