- Research article
- Open Access
Genome-wide identification and characterisation of Aquaporins in Nicotiana tabacum and their relationships with other Solanaceae species
BMC Plant Biology volume 20, Article number: 266 (2020)
Cellular membranes are dynamic structures, continuously adjusting their composition, allowing plants to respond to developmental signals, stresses, and changing environments. To facilitate transmembrane transport of substrates, plant membranes are embedded with both active and passive transporters. Aquaporins (AQPs) constitute a major family of membrane spanning channel proteins that selectively facilitate the passive bidirectional passage of substrates across biological membranes at an astonishing 108 molecules per second. AQPs are the most diversified in the plant kingdom, comprising of five major subfamilies that differ in temporal and spatial gene expression, subcellular protein localisation, substrate specificity, and post-translational regulatory mechanisms; collectively providing a dynamic transportation network spanning the entire plant. Plant AQPs can transport a range of solutes essential for numerous plant processes including, water relations, growth and development, stress responses, root nutrient uptake, and photosynthesis. The ability to manipulate AQPs towards improving plant productivity, is reliant on expanding our insight into the diversity and functional roles of AQPs.
We characterised the AQP family from Nicotiana tabacum (NtAQPs; tobacco), a popular model system capable of scaling from the laboratory to the field. Tobacco is closely related to major economic crops (e.g. tomato, potato, eggplant and peppers) and itself has new commercial applications. Tobacco harbours 76 AQPs making it the second largest characterised AQP family. These fall into five distinct subfamilies, for which we characterised phylogenetic relationships, gene structures, protein sequences, selectivity filter compositions, sub-cellular localisation, and tissue-specific expression. We also identified the AQPs from tobacco’s parental genomes (N. sylvestris and N. tomentosiformis), allowing us to characterise the evolutionary history of the NtAQP family. Assigning orthology to tomato and potato AQPs allowed for cross-species comparisons of conservation in protein structures, gene expression, and potential physiological roles.
This study provides a comprehensive characterisation of the tobacco AQP family, and strengthens the current knowledge of AQP biology. The refined gene/protein models, tissue-specific expression analysis, and cross-species comparisons, provide valuable insight into the evolutionary history and likely physiological roles of NtAQPs and their Solanaceae orthologs. Collectively, these results will support future functional studies and help transfer basic research to applied agriculture.
Cellular membranes are dynamic structures, continuously adjusting their composition in order to allow plants to respond to developmental signals, stresses, and changing environments . The biological function of cell membranes is conferred by its protein composition, with the lipid bilayer providing a basic structure and permeability barrier, and integral transmembrane proteins facilitating diffusion of selected substrates . Cell membrane diffusion is a fundamental process of plant biology and one of the oldest subjects studied in plant physiology . Diffusional events at the cellular level eventuate in the coordinated transport of substrates throughout the plant to support development and growth.
Plant membranes contain three major classes of transport proteins known as ATP-powered pumps, Transporters, and Channel proteins . Pumps, are active transporters that use the energy of ATP hydrolysis to move substrates across the membrane against a concentration gradient or electrical potential. Transporters move a variety of molecules across a membrane along or against a gradient at rates of 102 to 104 molecules per second. Unlike the first two classes, channel proteins are bidirectional and increase membrane permeability to a particular molecule. Channel proteins are permeable to a wide range of substrates and can pass up to 108 molecules per second. In plants, aquaporins (AQPs) constitute a major family of such channel proteins that facilitate selective transport of substrates for numerous biological processes including, water relations, plant development, stress responses, and photosynthesis [4, 5].
The AQP monomer forms a characteristic hour-glass membrane-spanning pore that assembles as tetrameric complexes in cell membranes. The union of the four monomers, creates a fifth pore at the centre of the tetramer which may provide an additional diffusional path . The substrate specificity of a given AQP is conferred by the complement of pore lining residues which achieve specificity through a combination of size exclusion and biochemical interactions with substrates . Key identified specificity residues include the dual Asn-Pro-Ala (NPA) motifs, the aromatic/Arginine filter (ar/R filter) and Froger’s positions (P1-P5) [8,9,10]. However, other pore-lining residues and lengths of the various transmembrane and loop domains of the AQP monomer are also known to influence substrate specificity through conformational changes of the pore size and accessibility [7, 11]. It is likely that other residues that determine specificity and transport efficiency remain to be elucidated.
Aquaporins, which are members of the major intrinsic proteins (MIP) superfamily, are found across all taxonomic kingdoms . While mammals usually have only 15 isoforms, plants have vastly larger AQP families commonly ranging from 30 to 121 members [5, 13,14,15]. This impressive diversification has been facilitated by the propensity of gene duplication events, especially prevalent in the angiosperms, and likely by the adaptive potential provided by AQPs. Based on sequence homology and subcellular localisation, up to thirteen AQP subfamilies are now recognised in the plant kingdom [13, 16,17,18,19]. Eight of these AQP subfamilies occur in more ancestral plant lineages and include, the GlpF-like Intrinsic Proteins (GIPs) and Hybrid Intrinsic Proteins (HIPs) in mosses, the MIPs A to E of green algae, and the Large Intrinsic Proteins (LIPs) in diatoms. The remaining five subfamilies are prevalent across higher plants and have extensively diversified into sub-groups and include the Plasma membrane Intrinsic Proteins (PIPs; subgroups PIP1 and PIP2), Tonoplast Intrinsic Proteins (TIPs; subgroups TIP1 to TIP5), Small basic Intrinsic Proteins (SIPs; subgroups SIP1 and SIP2), Nodulin 26-like Intrinsic Proteins (NIPs; subgroups NIP1 to NIP5), and X Intrinsic Proteins (XIPs; subgroups XIP1 to XIP3). The XIPs are present in many eudicot species, but are absent in the Brassicaceae and monocots .
The AQP subfamilies differ to some degree in substrate specificity and integrate into different cellular membranes, providing plants with a versatile system for both sub-cellular compartmentalisation and intercellular transport. In plants, AQPs are by far the most extensively diversified, capable of transporting a wide variety of substrates including water, ammonia, urea, carbon dioxide, hydrogen peroxide, boron, silicon and other metalloids [7, 20, 21]. More recently, lactic acid, oxygen, and cations have been identified as permeating substrates [22,23,24,25], with RNA molecules also implicated as a possible transported substrate . Further versatility is achieved through tightly regulated spatial and temporal tissue-specific expression of different AQP genes, as well as post-translational modification of AQP proteins (e.g. phosphorylation) that controls membrane trafficking and channel activity [27, 28].
Given their diverse complement of transported substrates and growing involvement in many developmental and stress responsive physiological roles, AQPs are targets for engineering more resilient and productive plants [5, 29]. For example, CO2-permeable AQP are being targeted to enhance photosynthetic efficiency and yield increases [5, 30, 31], while AQPs responsive to drought stress are being used to improve tolerance to water-limited conditions [32, 33], and manipulations of boron-permeable AQPs are being pursued to improve crop tolerance to soils with either toxic or sub-optimal levels of boron [15, 34, 35]. The genomic era of plant biology has provided unprecedented opportunity to query AQP biology by exploring sequence conservation and diversity between isoforms in many species. This is reflected in the increasing number of plant AQP family studies being reported in recent years. Almost exclusively, these studies focus on the species of interest with no direct evaluation with AQPs from other plant species. However, extending an AQP family characterisation to closely related species (e.g. within the same taxonomic family) can be especially informative, with comparisons of close orthologous AQPs helping to better elucidate the evolutionary history and physiological roles of different AQPs. Comparisons between closely related species can also improve the translation of basic AQP research to applied agriculture, especially if the analysis involves crop species.
To improve our current knowledge on AQP biology and aid in their potential use towards improving plant resilience and productivity, we have characterised the AQP family from Nicotiana tabacum (NtAQPs; tobacco). Tobacco is a fitting candidate species to explore unknowns of AQP biology as it is a popular model system for studying fundamental physiological processes that is capable of scaling from the laboratory to the field. Tobacco is part of the large Solanaceae family, which includes species of major economic importance such as tomato, potato, eggplant and peppers , and itself has renewed commercial applications in the biofuel and plant-based pharmaceutical sectors [37,38,39]. We found that tobacco harbours 76 AQPs, making it the second largest family characterised to date. Tobacco is a recent allotetraploid, which accounts for its large AQP family size. Phylogenetic relationships, gene structures, protein sequences, selectivity filter compositions, sub-cellular localisation, and tissue-specific expression profiles were used to characterise NtAQP family members. We also identified the AQPs of the tobacco parental genomes (Nicotiana sylvestris and Nicotiana tomentosiformis), allowing us to characterise the recent evolutionary history of the NtAQP family. Furthermore, using the already defined AQP families of tomato (Solanum lycopersicum) and potato (Solanum tuberosum) [40, 41], we made cross-species comparisons of gene structures, protein sequences and expression profiles, to provide insight into conservation and diversification of protein function and physiological roles for future studies and engineering efforts.
Identification and classification of NtAQP genes
A homology search, using tomato and potato AQP protein sequences as queries, identified 85 loci putatively encoding AQP-like genes in the genome of the TN90 tobacco cultivar . Nine of these genes encode for severely truncated proteins and were classified as pseudogenes (Additional file 1: Table S1). The remaining 76 genes had a level of homology to tomato and potato AQPs to be considered ‘bona fide’ tobacco AQPs (NtAQPs; Table 1). Seventy-three of these 76 tobacco AQP genes were also identified in the genome of the more recently sequenced K326 cultivar (Nitab4.5v)  (Table 1). To determine the precise protein sequences and gene structures of the tobacco AQPs, the surrounding genomic region of the identified coding sequences were examined in all forward translated frames. The likely protein products and associated intron/exon structures were curated through alignments with respective Solanaceae homologues. Our gene models were then independently validated and supported by alignments against tobacco whole transcriptome mRNA-seq data (obtained from Edwards et al., 2017), which also aided in defining the 5′ and 3′ UTRs. A comparison between our manually curated AQP protein and gene models against the computational predictions for the TN90 and K326 cultivars [42, 43] revealed that 15% of TN90 and 50% of K326 computed AQP models were incorrectly annotated (Table 1). Errors in the computed gene models were encountered across all NtAQP subfamilies and consisted of either missing or truncated 5′ and 3’UTRs, absent exons, truncated exons (ranging from 4 to 87 amino acids), and exon insertions (16–57 amino acids) due to inclusion of adjacent intron sequence (Fig. 1, Additional file 2: Figure S1). A summary of our NtAQP gene models, identifiers and genomic locations for the TN90 and K326 cultivars are available in Additional file 1: Table S2. FASTA sequencing files of coding DNA sequence (CDS), protein, and genomic sequence can be found in Additional file 3. Sequences of these high confidence NtAQP protein and gene models have been submitted to NCBI (Table 1).
Through the process of curating the tobacco AQP gene and protein sequences, we have made correction to several previously mis-annotated AQP genes of tomato and potato namely, StXIP3;1, StXIP4;1, SlXIP1;6, SlPIP2;1, and SlTIP2;2 (Additional file 1; Table S3). We also identified through our tobacco genome sequence analysis an erroneous non-synonymous single nucleotide mutation (C > T, CDS position 619) in the reported mRNA sequence of the frequently studied tobacco AQP1 gene (NtAQP1; assigned as NtPIP1;5 s in this study). The mutation results in a Histidine (H) to Tyrosine (Y) substitution at amino acid position 207 being incorrectly reported in the initial cloning of this gene and subsequent use ( ; NCBI AF024511 and AJ001416). This substitution is notable since His207, which corresponds to the His193 position of the well-studied crystal structures of Spinach PIP2;1 [6, 45, 46], is highly conserved across all angiosperm PIP AQPs and is a key regulator in the gating and therefore transport capacity of the AQP channel [6, 45, 47]. The inadvertent use of this H207Y NtAQP1 mutant in functional characterisation studies may have implication on the conclusions drawn for this frequently studied plant AQP. In support of His207 being the correct residue in NtAQP1, we found that independently generated gDNA-seq assemblies as well as RNA-seq mapped reads from both the TN90 and K326 cultivars had the His207 residue (Additional file 2: Figure S2). Furthermore, several closely related NtAQP1 orthologues across several Solanaceae species, including 3 additional Nicotiana species, all had the His207 residue (Additional file 2: Figure S2).
Gene structures and phylogenetic analysis of tobacco AQPs
To place the 76 curated NtAQP protein sequences into their respective subfamilies, we used phylogenetic analyses incorporating characterised AQP isoforms from a diverse set of angiosperms: Arabidopsis (Arabidopsis thaliana, Brassicales), tomato (Solanum lycopersicum, Solanales), rubber tree (Hevea brasiliensis, Malpighiales), rice (Oryza sativa, Poales) and soy bean (Glycine max, Fabales) (Additional file 4: Figure S3). The NtAQPs segregated into five distinct subfamilies that commonly occur in higher plants, namely the NIPs , SIPs , XIPs , PIPs  and TIPs  (Fig. 2, Additional file 4: Figure S3). An emerging problem among the increasing number of studies characterising plant AQP families across species is the confusion in nomenclature that either misses or incorrectly assigns orthology between AQP genes. Such confusion is seen in the nomenclature between tomato and potato AQPs. At least in this case, the naming inconsistency is predominantly a result of the two family characterisations being published concurrently by different groups [40, 41]. Towards contributing to a more congruent naming structure of AQPs between species, especially within a single family of angiosperms, we aligned our NtAQP naming convention with that of tomato AQPs, given their more consistent nomenclature to likely Arabidopsis AQP orthologues. Additional file 1: Table S2 lists the tobacco AQPs with their corresponding tomato and potato orthologous genes.
Sixty five of the 76 NtAQP genes had clear orthologs in tomato which directed their naming (Additional file 2: Figure S4 and Additional file 1: Table S2). The 11 tobacco AQPs with no apparent tomato or potato ortholog were allocated designations unique to tobacco (denoted by black stars in Additional file 2: Figure S4). Gene lengths varied between NtAQPs from 1091 bp to 6627 bp, with a single extreme instance of 17,278 bp (NtPIP2;11 s) due to a large intron insertion (Fig. 2). The exon-intron patterning of NtAQP genes were highly conserved with that of their tomato and potato orthologs (Additional file 1: Table S2) [40, 41]. Individual AQPs within the PIP, TIP, NIP and SIP subfamilies were well conserved across the three Solanaceae species (Additional file 2: Figure S4). The XIPs were an exception as they predominantly phylogenetically clustered within each separate species, pointing to a high degree of intra-species XIP diversification within the Solanaceae (Additional file 2: Figure S4).
A distinctive feature in the phylogeny was that most NtAQPs reside as pairs, supported by high bootstrap values (Fig. 2). The high homology in protein sequences between members of these phylogenetic pairs also extended to highly similar nucleotide sequences and gene structures (Fig. 2).
Tobacco AQP protein sequence comparisons
General structural features of NtAQP proteins
Topological analysis using TOPCON (see materials and methods), predicted that all NtAQP proteins consist of six transmembrane helical domains, five intervening loop regions and cytoplasmic localised N- and C- terminal tails, which is consistent with the typical structure of AQPs (Fig. 3). The size of the transmembrane helical domains appear to be an integral property of the AQP structure given their remarkably conserved lengths across the subfamilies (Fig. 3a). Conversely, the length of the loop regions showed substantial variability between subfamilies (Fig. 3a). The most pronounced was Loop A, which is prominently longer and apoplastically exposed in the PIP2s (18aa) and shorter in the NIPs (8aa) compared to the average length of TIPs, SIPs, and XIPs (14aa). The cytoplasmic Loop B, is shorter in XIPs (20aa vs. 24aa). Loop C is nearly double the length in the XIPs (38aa) compared to the other subfamilies (20aa). Loop D is slightly longer in the PIPs (12aa) and shorter in the SIPs (7aa), while Loop E is substantially longer in the XIPs (32aa) and shorter in the NIPs (20aa) (Fig. 3a). The cytoplasmically localised N- and C-terminal tails are the most varied in size of any of the AQP domains (Fig. 3a). The N-terminal tail ranges from 59aa in the NIPs to just 7aa in the SIPs and the C-terminal tail from 30aa in the NIPs to 14aa in the PIPs.
Examining sequence conservation of the different protein domains across the subfamilies, revealed that the transmembrane helices are generally the more highly conserved feature of the AQP (Fig. 3b). Loop B and E are also highly conserved relative to the other domains, which is likely owing to their direct role in forming the transmembrane pore. Conversely, Loops A and C, along with the two terminal tails were found to be the least conserved domains within each NtAQP sub-family (Fig. 3b).
To learn more about the putative functional characteristics of the different NtAQPs, we used multiple protein sequence alignments to report residue compositions at key positions in the protein known to regulate AQP function (Table 2). Included are the dual Asn-Pro-Ala (NPA) motifs, the five Froger’s position residues (P1-P5), and the residues of the aromatic/Arginine filter (ar/R filter), all of which are specific pore lining residues that contribute to determining which substrates permeate though the AQP pore. We also reported on several other sites known to be post-translationally modified, which influence channel activity and membrane localisation (Table 2).
The NtPIPs represent the largest NtAQP subfamily with 29 members that are phylogenetically divided into PIP1 and PIP2 subgroups. Despite being the largest subfamily, the NtPIPs were among the most conserved in protein sequence (> 50%; Fig. 3b). The apoplastic exposed Loops A and Loop C were the exceptions having only ~ 20% sequence identity and varying in size between PIP1 and PIP2 proteins (Fig. 3). This sequence diversification could be of functional importance given Loop A is involved in PIP-PIP dimerization mediated primarily through a conserved cysteine residue, which is present in all NtPIPs [48, 49]. The generally high sequence similarity across most of the PIP protein domains was also reflected in both PIP1s and PIP2s having identical configuration of residues across the NPA and ar/R motifs; which were predominantly hydrophilic residues (Table 2). Only Froger’s position 2 showed variation with amino acids of different properties (G, M or Q) occupying this position (Table 2). The NtPIP1s are predominantly distinguished from NtPIP2s by having longer N-terminal and shorter C-terminal tail sequences. The N-terminal tail is involved in calcium-dependent gating of the pore which occurs through interactions involving two acidic residues (Asp28 and Glu31, Table 2) . Pore gating is also triggered by pH involving protonation of a Loop D histidine (His-193, Table 2) and phosphorylation of a Loop B serine (Ser115, Table 2) [45, 47]. These four residues were identified in each NtPIPs indicating the entire subfamily retains these modes of regulation (Table 2). The Loop B serine (Ser115), or phosphorylatable threonine, was also conserved in members of XIPs, TIPs and SIPs (but not NIPs), suggesting a shared mechanism of gating regulation between different NtAQPs (Table 2). Two commonly phosphorylated serine sites were found conserved in the longer C-terminal tail of NtPIP2s (Ser274 and Ser277; Table 2, Additional file 2: Figure S5). The phosphorylation status of these serine residues are known to facilitate protein-protein interactions, influence trafficking to and from the plasma membrane, and alter the transport capacity of the pore [5, 50]. NtPIP1 proteins have the second of these serine residues (Ser277), but are not predicted to be phosphorylated (Table 2; Additional file 2: Figure S5). A strongly conserved positively charged lysine or arginine directly preceding the second phosphorylated serine is found across all NtPIPs, and also more broadly across PIPs from other plant species (data not shown), with the exception of NtPIP1;5 and PIP2;11 which have a histidine (Additional file 2: Figure S5). Histidine can achieve a positive charge through protonation, indicating a possible pH regulated functional state of the C-terminal tail in these NtPIPs.
NIPs were found to have the lowest overall sequence identity sites (~ 10%), suggesting a highly divergent subfamily at the sequence level (Fig. 3b). The sequence variation was evenly distributed across all AQP domains, with only Loop B and Loop E retaining modest conservation with > 30% identical residues per site. This comparatively higher conservation likely reflects these two loops being directly involved in forming the main pore structure and controlling substrate selectivity. Loops B and E each contain a NPA motif, and Loop E also contains ar/R and Froger’s residues (Table 2). Across the NtNIPs, there was substantial variation in the residues constituting the dual NPA motifs (NPA/S/V) and across all 5 Froger’s positions (Table 2). And all but LE2 of the ar/R residues were variable, although the residue that were present tended to be more hydrophobic (Table 2). Also notable in the NtNIPs, were their distinctively longer N and C terminals (~ 57-30aa) compared to those in other subfamilies (Fig. 3a). The extended C-terminal tail contains numerous serine residues, many of which were predicted to be phosphorylated (Additional file 2: Figure S5). Included were serine residues at homologous positions to the confirmed phosphorylated sites of Ser262 in GmNOD26 (a soybean NIP) and Ser277 in PIPs (Table 2). The Ser115 phosphorylation site that controls aspects of pore gating in PIPs was conserved and predicted to be phosphorylated in only NtNIP4;3 s, with all other NtNIPs having a structurally rigid proline residue at this position (Table 2).
Conservation among the NtTIPs was ~ 22% sequence identity (Fig. 3b). Similar to the NIPs, the highest sequence conservation occurred in Loops B and E (> 40%). The dual NPA motif, ar/R H2 and Froger’s P3 to P5 are well conserved among the different TIP subgroups. The exceptions being NtTIP2;1 s with a NPD configuration of the first NPA motif, and the NtTIP5;1 proteins which have a H > N substitution at ar/R H2 (Table 2). The other ar/R and Froger’s sites are rather variable among the NtTIPs, especially ar/R LE2 which varies between amino acids of quite differing properties (V, R or Y; Table 2). A histidine opposed to phenylalanine located at ar/R LC of NtTIP2s, TIP4s and TIP5s (Table 2), suggests an enhanced capacity to transport ammonia . The Ser115 phosphorylation site that controls pore gating in PIPs was identified in 5 of the 22 NtTIPs, with the remaining NtTIPs possessing a threonine which is also a potentially phosphorylatable residue. NtTIP2 and NtTIP5 proteins have a conserved histidine (His131) in Loop C that is involved in a similar pH regulated gating of the pore to that of His193 in Loop D of PIPs and NIPs [52, 53]. The C-terminal tail of NtTIPs contained on average less than 2 serine residues, none of which were predicted to be phosphorylation targets (data not shown).
While only comprising of 5 genes, the NtSIP subfamily had low sequence conservation, with Loop A the least conserved (Fig. 3b). The first NPA motif varied with NPA/T/L combinations (Table 2). Substantial variation was also was found in other key residues with completely different configuration of residues in the ar/R and Froger’s P1-P2 between NtSIP1 and NtSIP2 proteins (Table 2). The N- terminal tail of NtSIPs were distinctly shorter than other subfamilies (~7aa) (Fig. 3a).
The XIPs are a small sub-family with high sequence identity (~ 75%). The first NPA motif is replaced by a NPV motif in all four NtXIP proteins (Table 2). There is a strong consensus in the residues residing in the Froger’s and dual NPA motifs, with the only variation being I/A at ar/R H2 (Table 2). Concordant with other studies of XIPs, the loop C of NtXIP is substantially longer (~38aa) compared to that of other subfamilies . NtXIPs have the conserved phosphorylated Ser115, although it was not a predicted phosphorylation target (Table 2). The C-terminal tail of NtXIPs contained a single serine residue which was not predicted to be phosphorylated (data not shown).
Subcellular localisation of tobacco AQPs in planta
AQPs can facilitate diffusion of a range of substrates across various plant membranes and the specific membrane localisation can vary between the different subfamilies, which ultimately influences sub-cellular flow and compartmentalisation of solutes. Computational prediction programs can be used as an initial inference of subcellular localisation to further help elucidate putative biological activities and physiological functions of candidate proteins . We conducted subcellular prediction analyses using three commonly used software programs, Plant-mPLoc, Wolf Psort and YLoc (see materials and methods). Consistency in prediction across the three programs was found for 35 (46%) of NtAQPs (Table 2). Consensus in predicted localisation was mainly observed for the PIP2s and the NIPs, which were generally predicted to be plasma membrane (PM) localised. The TIPs and SIPs appeared to have the most contrasting predictions in subcellular localisation results, with TIP localisations ranging between tonoplast, PM, peroxisome, cytoplasmic and extra cellular localisation; and SIPs having PM, tonoplast, chloroplast, ER and extra cellular localisations across the 3 prediction tools (Table 2).
To complement the predictions, representative tobacco AQPs from the larger PIP, TIP and NIP subfamilies were visualised in planta using GFP:NtAQP fusions. NtSIPs were not included in this analysis as they are a smaller AQP subfamily, while NtXIPs are already established as localising to the PM . Plant AQPs retain their capacity for faithful subcellular localisations between tissues, even when translocated across plant species, as evident from numerous studies examining subcellular localisation or physiological manipulation using transgenic AQPs foreign to the host species [5, 57,58,59,60,61,62]. As such, we introduced our tobacco GFP:AQP transgenes into Arabidopsis, to be able to utilise established GFP marker lines that delineate specific subcellular compartments . Such marker lines are crucial in guiding the correct interpretations of subcellular locations, given the close proximity of certain subcellular structures occupied by AQPs. For example, both the PM and ER are possible locations, but parts of the ER network lay immediately adjacent to the PM, making it difficult to discern between ER, PM, or co-localisation. Interpretations are further compounded by the large vacuoles of most plant cells that occupy much of the internal volume, pushing the cytoplasm and its contents to the periphery. This can give the illusion of PM localisation even for cytosolic proteins such as ‘free’ GFP, especially if only examined as a 2D-optical slice at the whole cell level (Fig. 4ai).
We used confocal microscopy to visualise the subcellular localisation of GFP:NtAQP and GFP marker lines using both 2-D slices and 3-D optical stacks. To avoid signal contamination from chlorophyll auto-fluorescence, which excites and emits at wavelengths close to GFP, we examined root cells. GFP marker lines localising to the cytoplasm, plasma membrane (PM), ER, and tonoplast (tono), were used as these are the expected possible locations of the PIPs, TIPs, or NIPs (Fig. 4). Key differences between the four sub-cellular features were clearly discernible in the vicinity of the nucleus, the topography of the signal, and 3D renders of serial Z-stack images of the cells (Fig. 4b-g). The PM:GFP marker localised exclusively to the periphery of the cell when adjacent to the nucleus (Fig. 4bii), the ER:GFP wrapped around the nucleus (Fig. 4dii), and Tono:GFP localised internally to the nucleus leaving a signal void on the side adjacent to the PM (Fig. 4fii). PM:GFP produced a sharp defined integration with the cell margin (Fig. 4biii), featuring as an outer shell in the 3D render (Fig. 4biv). The ER:GFP peripheral signal was mottled in appearance (Fig. 4di), consisting of localised bright specks with distinct regions of no signal (Fig. 4diii), that appeared as a ‘web’ in the 3D render (Fig. 4div). Tono:GFP was present as large undulating ‘sheets’ of signal associated with the trans-vacuolar strands (tonoplast-delimited cytoplasmic tunnels) and folds of vacuole membrane (tonoplast) (Fig. 4fi-iv), which had a distinct ‘wavy’ topography (Fig. 4fiii).
Having established the defining features of the marker lines, we moved to examining the representative NtAQPs. Distinct in planta subcellular localisation patterns were observed for the PIP, TIP and NIP NtAQPs, consistent with the known membrane targeting properties of these different AQP subfamilies (Fig. 4c,e,g). The GFP signal of the representative PIP (NtPIP2;5 t) appeared sharp and uniformed around the cell periphery, with signal running external to the nucleus and forming a smooth outer shell in the 3D render with no discernible signal in any internal structures (Fig. 4c). This pattern was concordant with a PM:GFP marker (Fig. 4b), indicating a strong integration of NtPIP2;5 t into the PM.
The representative NtNIP (NtNIP2;1 s), had features indicating it co-localises to the PM and ER. The peripheral localised NtNIP GFP signal was mottled in appearance with distinct specks of intense bright signal similar to the ER marker. However, unlike the ER marker, these specks were dispersed along a consistent basal signal continuous around the cell periphery, indicative of PM localisation (Fig. 4ei-iii). The 3D render further demonstrated the shared shell-like PM signal overlapping the mottled web-like ER patterned signal (Fig. 4eiv).
The localisation of the representative NtTIP (NtTIP1;1 s) is consistent with integration into the tonoplast. The NtTIP GFP signal showed a uniform yet diffuse localisation within the cell consistent with tonoplast labelling. The NtTIP GFP signal surrounded the nucleus on the cytosolic but not plasma membrane side (Fig. 4gi-ii), and the labelled membrane had a wavy topography with the occurrence of internal membranes resembling transvacuolar strands (Fig. 4giii-iv).
The PM integration of NtPIP2;5 was predicted by all 3 software programs, whereas the tonoplast localisation of NtTIP1;1 s was only predicted by Plant-mPLoc. Lastly, the PM localisation of NtNIP2;5 s was anticipated in all 3 programs, but none predicted its co-localisation with the ER (Table 2).
Parental association and recent evolutionary history of tobacco AQPs
The distinctive phylogenetic pairing of most NtAQPs in our initial phylogenetic characterisation, is likely characteristic of the recent evolutionary origin of tobacco, which arose from an allotetraploid hybridisation event between N. sylvestris and N. tomentosiformis only ~ 0.2 M years ago [42, 43]. To explore the evolution of the tobacco AQP family, we identified the AQP gene families in the two parental lines using NtAQP nucleotide coding sequences as queries in BLAST searches. Initially, 40 and 41 AQPs were identified in both N. sylvestris and N. tomentosiformis respectively, which is comparable to the number of AQP genes found in the related diploid species of tomato and potato (Table 3). As shown in this work, tobacco has 76 AQPs, almost a full set from each parental species (40 N.sylvestris, and 42 N.tomentosiformis), being consistent with a recent allotetraploid hybridisation event. The introduction of the parental N. sylvestris and N. tomentosiformis AQPs into the NtAQP phylogeny, transformed the majority of the distinct NtAQP phylogenetic pairs into small clades of four genes where each of the paired NtAQPs was now clearly associated with an AQP from one of the two parents (e.g. NtPIP1;1 sub-clade, Fig. 5). This phylogenetic relationship confirmed that the distinctive phylogenetic pairing of NtAQPs corresponds to orthologous ‘sister’ genes arising from hybridisation, with both parental genomes having contributed one AQP gene to each tobacco sister pair (Fig. 5). Initially 30 sister gene pairs were identified that had a clear match to an orthologous gene from both N. sylvestris and N. tomentosiformis (Fig. 5). The ancestral origin of the NtAQP genes were denoted in the nomenclature by the addition of a suffix ‘s’ or ‘t’ (e.g. NtPIP1;1 s and NtPIP1;1 t), to indicate a N. sylvestris or N. tomentosiformis lineage, respectively.
One NtAQP gene had no resolved match to a N. sylvestris or N. tomentosiformis parental AQP and was assigned a suffix ‘x’ (NtPIP2;1x). The lack of a clear parental match to NtPIP2;1x likely means that the orthologous gene has been lost in the parental genome post tobacco emergence, or the orthologous parental AQP was not identified due to incomplete coverage of sequencing data. Either way, the presence of this gene in the tobacco genome allows us to infer its presence in a parental genome at the time of hybridisation. We predict that NtPIP2;1x was inherited from N. tomentosiformis, as it occurs in a distinct clade with a tobacco sister gene (NtPIP2;1 s) and an orthologous N. sylvestris AQP (N.sylPIP2;1), but lacks a N. tomentosiformis progenitor ortholog (orange box, Fig. 5). As such, assigning NtPIP2;1x as a N. tomentosiformis descendant, brings the total number of AQPs in the parental genomes to 40 in N. sylvestris and 42 in N. tomentosiformis, with the total number of genes within the PIP, NIP and TIP subfamilies being very similar to those of tomato and potato (Table 3).
The phylogenetic analysis also revealed recent evolutionary events in the tobacco, N. sylvestris and N. tomentosiformis AQP families. These events were recognised by deviations from the conventional four-gene small sub-clade groupings comprised of the tobacco sister genes and their respective parental orthologs. Seven AQP gene loss events were recognised in N. sylvestris, six of which occurred prior to the tobacco hybridisation event as the given AQP was absent in both N. sylvestris and tobacco (blue stars, Fig. 5). In several cases, the remnants of the eroding N. sylvestris pseudo gene were also inherited and identifiable in the tobacco genome (e.g. SIP1;1 and PIP2;7; Fig. 5). Two gene loss event was recognised in N. tomentosiformis, with no representative NIP1;1 or NIP2;1 orthologs identified in either N. tomentosiformis or tobacco (red star, Fig. 5). Five parental AQP genes have been lost in tobacco, three from N. tomentosiformis and two from N. sylvestris origins (green stars, Fig. 5). Instances of gene gains were also evident in both parental species prior to the tobacco hybridisation event (purple and orange stars, Fig. 5). These gained genes were distinct in the phylogenies as they did not uniquely match a specific Solanaceae gene ortholog, appearing instead as a duplicate copy of an existing AQP gene within the tobacco parental species (Additional file 2; Figure S4). Four AQP gene gain events occurred in N. sylvestris, two of which (N.sylNIP3;1 and N.sylPIP1;2), began redundant gene erosion prior to tobacco hybridization (purple stars, Fig. 5). The third, N.sylPIP2;11b, is retained as a functional unit in N. sylvestris but has eroded in tobacco; hence the designation ‘b’ as opposed to a unique numerical identifier. The fourth gene, N.sylPIP1;8, has been retained in both N. sylvestris and tobacco as a functional gene (purple star, Fig. 5). A single gene duplication event was recognized in N. tomentosiformis, giving rise to PIP2;2 and PIP2;3 orthologs which were both inherited and subsequently retained as functional genes in tobacco (orange star, Fig. 5).
Tobacco AQP gene expression
The NtAQP transcriptome dataset
To provide insight into possible physiological roles of the various NtAQP isoforms, publicly available whole transcriptome RNA-seq datasets [42, 43] were processed and analysed to compare organ-specific expression patterns of the 76 tobacco AQPs. Although, all datasets had great read depth (100–200 million paired reads per tissue), the Sierro et al. (2014) transcriptome of the TN90 cultivar was chosen for analysis, as it provided the most extensive sampling of different tissues at various developmental stages (young leaf, mature leaf, senescent leaf, stem, root, young flower, mature flower, senescent flower and dry capsules).
Although the NtAQP sister genes are highly homologous in their nucleotide coding sequences (~ 96.5%), the SNPs that are present occur at a frequency and distribution enabling unique mapping of reads to differentiate between sister genes. In the TN90 dataset, we detected expression from 75 out of 76 NtAQPs, with only NtXIP1;4 t having no mapped mRNA reads. However, NtXIP1;4 t is an expressed gene, albeit at very low levels, as indicated by the low transcript abundance detected in the K326 cultivar (data not shown). To validate the accuracy of the NtAQP expression profiles, we compared it to RNA-seq data from N. sylvestris and N. tomentosiformis; with the assumption that the majority of AQP orthologs will have retained similar expression profiles between these closely related species. The parental datasets are independently derived from those of the tobacco dataset, and sampled root, leaf and floral tissues at substantial read depths (~ 265 million paired reads per tissue) . Correlations of relative transcript abundances was compared in two-dimensions; (i) between AQPs within a given tissue and (ii) a given AQP across tissues (Additional file 2: Figure S6). Within equivalent tissues, the relative transcript abundance of N.sylAQP vs. NtAQPs and N.tomAQP vs. NtAQPt genes, correlated well (R2 root, leaf, flower: 0.91, 0.74, 0.98 and 0.65, 0.74, 0.80, respectively). Across tissues, the majority (> 80%) of NtAQPs and NtAQPt genes showed matching expression profile to their respective parental orthologs (Additional file 2: Figure S6). As expected, the relative transcript abundance between AQP sister genes within tobacco (i.e. NtAQPs vs. NtAQPt), correlated better than orthologs between parental lines (i.e. N.sylAQP vs. N.tomAQP) (Additional file 2: Figure S6). Overall, the largely conserved patterns indicate that the tobacco transcriptome data provides a suitably accurate representation of the NtAQP transcriptome.
Profiling the NtAQP transcriptome
Among the NtAQP subfamilies, gene expression of PIPs and TIPs was generally greater than for SIPs, XIPs and NIPs (Fig. 6a). Among the most highly expressed NtAQPs, PIP1;5 s, PIP1;5 t, PIP1;3 s and PIP1;3 t stood out as being constitutively expressed in all major plant organs, while TIP1;1 s and TIP1;1 t, were present in all tissues except for the dry capsule (Fig. 6a). Some highly expressed genes also showed a level of tissue specificity, with NIP4;1 s and NIP4;1 t expressed only in flowers, and TIP3;1 s, TIP3;1 t and TIP3;2 t predominantly in the flower capsule (Fig. 6a).
To examine differential expression between plant organs, the expression levels of a given AQP were standardised relative to its highest expressing tissue (Fig. 6b). AQPs with a broad expression distribution throughout the plant could be readily identified (e.g. SIP1;2 and PIP1;5 sister pairs, Fig. 6b). Other AQPs show tissue specific expression: young flowers (PIP2;11 s & PIP2;11 t; NIP2;1 s), leaves (PIP2;5 s and PIP2;5 t; XIP1;6 s; PIP2;1x) or roots (TIP1;2, TIP1;3, TIP2;2, and TIP2;3 genes). At the sub-family scale, NtNIPs and NtTIPs are found to be preferentially expressed in roots, stems and flowers, with a low tendency for expression in leaves (Fig. 6b). NtPIPs and NtSIPs are more broadly expressed, while there is no expression of NtXIPs in either the stem or dry capsule (Fig. 6b). Within subfamilies we see gene members with specialised or preferential tissue expression. For example, some NtPIPs preferentially expressed in the roots (PIP1;1 s & PIP1;1 t; PIP2;4 s & PIP2;4 t), others express preferentially in leaves (e.g. PIP2;5 t & PIP2;1x), while PIP2;11 s & PIP2;11 t have become specialised in young flowers (Fig. 6b). Discrete tissue-specific specialisation was also observed for members of the other families, for instance, TIP3;1 and TIP3;2 genes express only in dry capsule (seeds), and expression of NIP4;1 and NIP4;2 was only detected in flowers (Fig. 6b).
Next we compared differences in expression between sister genes to explore possible functional divergence. In general, sister gene pairs showed matching patterns of tissue-specific expression (Fig. 6b). However, of the 31 proposed sister gene pairs, 18 showed notable differential expression levels in at least one tissue (Fig. 6c). In the majority of these instances a single sister gene of the pair was more highly expressed in several plant organs. Examples include, NIP5;1 s, SIP2;1 t, SIP1;2 t, PIP2;6 t, PIP2;4 s, PIP1;3 t and PIP1;1 s. There were also several instances of contrasting expression where sister genes show distinctions in preferential expression between plant organs. For example, TIP3;1 s with 4-fold higher expression in the capsule compared to its sister pair TIP3;1 t, which is expressed > 10-fold higher in roots (Fig. 6c). Further examples of contrasting expression include, NtPIP2;5 t (leaves) against NtPIP2;5 s (roots) and NtNIP6;1 s (leaves and dry capsule) against NtNIP6;1 t (roots) (Fig. 6c).
Conservation with other Solanaceae species
As a means of exploring conservation in biological activities and physiological functions between AQP orthologous of different species, we compared tissue-specific expression levels of NtAQPs with their orthologs from the closely related tomato and potato species. This was done by comparing the relative gene expression across root, leaf and floral tissues of AQP genes we have identified as being orthologs between the Solanaceae species (e.g. NtPIP1;1 s & NtPIP1;1 t in tobacco, SlPIP1;1 in tomato and StPIP1;2 in potato; listed Additional file 1: Table S2). We were able to perform this analysis on the PIPs, TIPs, NIPs and SIPs but not the XIPs given the previously mentioned difficulty of assigning orthology between the species. Even randomised pairwise comparisons of expression patterns between NtXIPs with those of tomato and potato, could not find consensus patterns, hinting further towards the unique intra-species diversification of XIPs within the Solanaceae (Additional file 2: Figure S7).
In the majority of instances (25 of 36 Solanaceae AQP ortholog sets), the tobacco sister genes had similar patterns of relative expression levels between the three organs to their orthologs from both tomato and potato, implying conserved physiological roles for the orthologs across the Solanaceae family (e.g. NIP1;1, NIP3;1, NIP4;2, PIP2;6, PIP2;9, PIP2;11, TIP5;1, and SIP1;1; Fig. 7). Some deviations in tissue-specific expression patterns were observed between orthologs, suggesting possible species-specific functional diversification. The predominant observed deviations were instances where either the tobacco, tomato or potato AQP differed in their tissue-specific expression pattern compared to the orthologs from the other Solanaceae. Examples include; the tobacco NtNIP5;1, NtPIP1;2, TIP1;1; the tomato SlPIP2;8, SlTIP2;1, SlTIP3;1, and SlTIP3;2 genes; and the potato StPIP1;2 (NtPIP1;1 ortholog), StTIP1;2, StTIP1;1 (NtTIP1;3 ortholog) and StTIP2;4 (NtTIP2;3 ortholog) genes (Fig. 7). Additionally, we observed one case where a NtAQP sister gene (NtPIP2;5 s), differed in expression from the tomato, potato and its NtAQP “t” sister gene; suggesting a potential diversification in gene function within tobacco. More complex deviations were also observed involving tobacco sister genes having contrasting expression to each other, that matched a similar contrast in expression between the tomato and potato orthologs (e.g. NtPIP2;1 and NtNIP6;1 sister genes; Fig. 7).
The growing amount of research into AQPs is greatly advancing our understanding of their diversity and functional roles, towards manipulating them to potentially enhance plant performance and resilience to environmental stresses [5, 29, 31, 65, 66]. The establishment of the tobacco AQP gene family allowed us to efficiently contribute to the current knowledge of AQP biology by, comparing regions of homology within and across closely related species, analysing pore-lining residues, identifying key structural characteristics, and providing necessary information and candidates for future functional screens. Furthermore, elucidating orthology between the already characterised tomato  and potato  AQPs, enables comparisons between isoforms across these Solanaceae species, which will facilitate the translation of knowledge from tobacco into its closely related and horticulturally important crop species.
NtAQP protein sequence analysis and associations with AQP function
We found that the tobacco AQP family comprises of 76 members, making it one of the largest AQP families characterised to date; second only to the polyploid canola (Brassica napus) with 121 members [14, 15]. The 76 NtAPQs include members of each of the five major AQP subfamilies common to angiosperms (i.e. NIPs, PIP, TIPs, SIPs, and XIPs). Correctly defining and analysing the NtAQP protein structures, sequence homology, and comparison of functionally relevant residues, helps towards predicting potential permeating substrates, post-translational regulation, and subcellular localisations. AQP monomers have a highly conserved structure, with transmembrane (TM) segments providing a structural scaffold and defining the channel environment, with the connecting loops also having significant roles in channel function . We found a high conservation in length and sequence identity of the NtAQP TM domains; their variability likely constrained to maintain structural integrity of the AQP monomer . Additionally, conservation of critical residues in TM domains is essential for tetramer formation, with modifications leading to aberrant AQP oligomerisation . NtAQP loops and termini had notable differences in lengths and lower sequence conservation across subfamilies; such variation has implications for AQP monomer interactions, pore accessibility and cellular membrane destinations [54, 69].
AQP solute selectivity are conferred through specific structural features of the AQP monomer’s pore, and substrate interactions with pore-lining residues. We surveyed known specificity-determining residues across the NtAQPs, including the aromatic arginine (ar/R) filter, NPA domains, and Froger’s positions [7, 8, 11, 70]. We observed an increased sub-family conservation in the loops harbouring these specificity-determining residues, in particular Loops B and E which have a direct role in forming the transmembrane pore. Each subfamily had their unique characteristic combination of amino acids at these locations concordant with known subfamily substrate specificities. For example, NtPIPs have more polar residues in their ar/R filter which is consistent with PIPs in general having the propensity to permeate water, whereas the NtNIPs have more hydrophobic amino acids in their ar/R filter, consistent with their poorer water permeability and preference for substrates such as ammonia, urea and metalloids instead [7, 11].
Additional to the specificity-determining pore lining residues, post-translational modification of specific residues (e.g. through protonation or phosphorylation), also directly or indirectly determine the transport mechanics of the AQP monomer . Plants rely on these secondary mechanisms to ensure tight regulation of AQPs, especially in response to stresses. Gating of the monomeric pore in response to external stimuli is a key control over AQP function. Among currently characterised residues involved in gating (listed in Table 2), we found subfamily-specific conservation across the NtAQPs. For example, all NtPIPs had the Loop D Histidine (His193) which is highly conserved across all plant PIPs, and can be protonated in response to changes in cytosolic pH (e.g. flooding induce hypoxia), and leading to the closure of the PIP pores . pH regulated responses are important for AQP as is the C-terminal tail of the PIP proteins . These facts drew our attention to the identified Lysine/Arginine > Histidine substitution in the C-terminal tails of NtPIP1;5 and NtPIP2;11 (Addition file 2: Figure S5). The normally positively charged Lysine/Arginine residue present in all other NtPIPs, and highly conserved across plant PIPs in general, directly precedes a functionally important phosphorylated serine. Together this suggests a likely functional relevance of a positively charged residue at this position in PIP regulation. The Histidine present at the equivalent position in NtPIP1;5 and NtPIP2;11 can still obtain the conserved positive charge upon protonation, implying a possible novel pH control over the regulatory influences normally imposed by the PIP C-terminal tail.
Some sharing of gating mechanisms between NtAQPs from different subfamilies can be inferred from our analysis. For example, the Loop B serine (Ser155) which in PIPs is involved in phosphorylation dependent disruption of N-terminal tail gating [45, 46], is conserved in some members of the other NtAQP subfamilies. NtPIPs and NtNIPs both seem to be regulated by phosphorylation in their C-terminal tails given the abundance of serine residues. The phosphorylation state of the C-terminal tail is known to regulate channel activity and also control trafficking to the plasma membrane [46, 72]. Interestingly, the NtTIPs had a dearth of serine residues in the C-terminal tail, suggesting a lack of a C-terminal phosphorylation-dependent regulation mechanism. This perhaps is due to differences in functional requirements being integrated into the vacuole membrane versus the plasma membrane integration of PIPs and NIPs. Consistent with differing regulatory requirements, we found that NtTIP2 and NtTIP5 proteins possessed a conserved histidine (His131) in loop C that is involved in a similar pH regulated gating of the pore to that of His193 in Loop D of PIPs and NIPs [52, 53] (erroneously reported as located in loop D of VvTnTIP2;1 in Leitão et al., 2012). However, unlike the cytosolic PIP/NIP Loop D His193, the TIP Loop C His131 is likely orientated into the vacuole and thus responding to the vacuole contents and environment.
Other structural features NtAQP of note include: the longer Loop D of PIPs compared to the other subfamilies which aids in its ability to cap the pore entrance ; the substantially longer Loop A of PIPs compared to the other NtAQPs, known to play a role in tetramer formation by mediating disulphide bonds between PIP1 and PIP2 isoforms ; the long N- and C-terminal tails of NtNIPs, important for protein regulation, trafficking, and protein-protein interactions ; the distinctly short N-terminal of SIPs associated with their intracellular destination into the ER ; the long Loop C of NtXIPs, characteristically enriched with flexible glycine residues allowing it to tuck into the channel opening and interact with selectivity filter residues and permeating solutes [54, 75].
NtAQP subcellular localisation
Determining AQP subcellular localisations can help elucidate physiological roles within the plant. For instance, integration into plasma membrane indicates solute transport in and out of the cell; localisation to the tonoplast implies a role in vacuole storage; or retained in the ER membranes to coordinate shuttling of substrates and nutrients between plant membranes [28, 56, 74, 76, 77]. We utilised sub-cellular localisation prediction software commonly used for fast in silico predictions of AQP isoform membrane integration. These software incorporate known sorting signals, amino acid composition and functional domains to generate results . Using three software prediction tools (Plant-mPLoc, WolfPsort and YLoc) generally concluded that PIP, NIPs and XIPs are predominantly localise to the PM; all of the Plant-mPloc and some of the WolfPsort outputs predicted tonoplast localisation for the TIPs; and the SIP localisations were quite varied. Although these predictions are a useful beginning, it should be noted that we only found a 46% consensus in the predicted AQP subcellular localisations between the three software tools. The discrepancies highlight the complexity of AQP membrane integration processes and our current limited understanding of AQP trafficking motifs .
GFP:NtAQP fusions and crucially a set of established subcellular GFP marker lines, allowed us to directly visualise and confidently determine in planta sub-cellular localisation of representative NtAQPs. The representative PIP (NtPIP2;5 t), NIP (NtNIP2;1 s) and TIP (NtTIP1;1 s) NtAQPs had distinct sub-cellular localisations, consistent with what is known about these AQP subfamilies in other plants . Concordant with studies of these subfamilies in other species [22, 78], we found that the NtPIP and NtTIP localised to the plasma membrane and tonoplast, respectively. The NtNIP2;1 co-localised to the PM and ER, which was not captured with the prediction software, which instead reported only PM integration. This sub-optimal PM targeting could limit the functional capacity of NtNIP2;1 and its subsequent physiological role (see discussion).
Nicotiana AQP gene evolution
Tobacco recently descended from a allotetraploid hybridisation event between N. sylvestris and N. tomentosiformis, which are distantly related within the Nicotiana genus . Genome downsizing is a widespread biological response to polyploidization, eventually leading to diploidization . However, due to the short evolutionary time frame since its inception (0.2 M years), tobacco has undergone a limited amount of genome downsizing. As a result, the NtAQP family is characteristically comprised of sister gene pairs, which we could assign to their given parental origins. Tobacco has lost only around 10% of it duplicated genes with no observed preferential gene loss from either parent . Concordant with this estimation, 7 gene loss events (~ 8.6% of total inherited parental AQPs) were identified in tobacco, with 3 and 4 of these being redundant ortholog losses from the N. sylvestris and N. tomentosiformis genomes, respectively. According to our expression analysis, the NtAQP gene copies inherited from both N. sylvestris and N. tomentosiformis (‘s’ and ‘t’ genes, respectively), were overall equally expressed, which agrees with broader genomic studies on tobacco . The redundancy of the homeologs presumably would allow for one of the sister genes to accumulate mutations without an immediate effect on fitness, most often leading to non-functionalisation (gene-loss), or in some instances sub-functionalisation or even neo-functionalisation. To this end, we observed instances where one AQP gene of a sister pair was consistently preferentially expressed throughout several plant organs (e.g. PIP1;1 s, PIP1;3 t, SIP2;1 t and NIP5;1 s); suggesting that the redundant lower-expressing sister gene could become non-functional over time. Alternatively, some sister genes showed distinct tissue-specific diversification, such as the NtPIP2;5 gene pair, where the s- and t-genes were more highly expressed in the roots and leaves, respectively, and which maybe candidates for sub- or even neo-functionalisation.
We were able to identify several AQP gene gain and loss events between the parents since their divergence within the Nicotiana genus, ~ 15 Ma ago . Both the N. sylvestris and N.tomentosiformis have a genome rich of repeat expansion (accumulation of transposable elements), making them nearly 3 times the size of that of tomato and potato (2.6 Gb vs. 0.9 Gb) [64, 81, 82]. Regardless of the discrepancy in genome size, there was close conservation of AQP ortholog numbers within these diploid Solanaceae species; with the PIPs and TIPs consistently the larger subfamilies. We saw a significant diversity in XIPs occurring in the Solanum (tomato and potato) and the Nicotiana species. This diversity manifested as discrepancies in isoform numbers between the species and as lower sequence identity; depicted in the phylogeny as a separation of tomato, potato and Nicotiana isoforms into distinct groups. XIPs are a more recently characterised AQP subfamily, with isoforms lacking in monocots and in Brassicaceae, and having a lower overall sequence identity compared to other AQP subfamilies . The tomato and potato XIP are predominantly found clustered on a single chromosome, indicating that recent segmental gene duplications within tomato and potato likely explain the lack of direct gene orthology to tobacco XIPs .
Gene expression analysis
The NtAQP transcriptome was found to be largely conserved with those of its parental species, consistent with it recent evolutionary emergence. We also noted that the expression profiles between AQP sister genes within tobacco, correlated better than the expression patterns of the orthologous AQP between the parental lines. Such improved homogeneity in expression patterns is a common outcome of hybridisation events as both genomes (e.g. the ‘s’ and ‘t’ AQPs genes) are now subjected to the same regulatory network [84, 85].
Within tobacco, our NtAQP gene expression analysis revealed a wide range of patterns across tissue types, consistent with the known diversity of AQP functions . It revealed that some AQPs had high levels across numerous tissues throughout the plant (e.g. PIP1;3 t and PIP1;5, TIP1;1 sister pairs), implicating involvement in broad spanning processes (e.g. substrate transport from roots to shoots to flowers), while others had highly organ specific expression (e.g. TIP1;3, NIP4;1, and TIP3;1 sister genes, in roots, flowers and seed capsules, respectively). In general, the XIPs and majority of NIPs had lower overall expression levels, although there is the possibility that their expression might change in response to a specific stimulus, or that they are expressed at similar levels, but in very specific cell types making up a small population of the total tissue sampled for RNA-seq.
Tissue specific expression patterns can help towards assigning physiological roles for the NtAQPs. We observed general trends between the AQP subfamilies. The NtXIPs were observed to have low but ubiquitous expression throughout the plant and previously reported to permeate bulky solutes such as urea and boric acid, but not water. Little is known about XIP physiological roles, but their unique transport capacity and rapid evolutionary diversification, even just within the Solanaceae, implies a role in environmental adaptive responses.
The tobacco PIPs appeared to have more isoforms with leaf-specific expression compared to the other subfamilies. These are likely to be involved in roles typically reported for PIPs across plants species, including; leaf cell expansion, leaf movement, mediating water exiting the xylem, control of stomatal aperture and gas transport (e.g. CO2) for photosynthesis [86,87,88]. Several PIPs have targeted expression in flowers (PIP1;7 t, PIP1;8 s, PIP2;2 t, PIP2;3 t, and PIP2;8, PIP2;9, PIP2;11, PIP2;13 sister pairs), some of which would be involved in mediating water supply during stigma, anther and petal development [89, 90].
Much like the PIPs, several isoforms within the NIPs (NIP4;3 s and NIP4;1 and NIP4;2 sister genes) and TIPs (TIP5;1 sister genes) had targeted expression to the flower. The tissue-specificity of these NtNIPs and NtTIPs is consistent with the floral tissue localisation of Arabidopsis NIP4;1, NIP4;2 and TIP5;1, which have known roles in pollen development and pollen germination [53, 91]. Additionally, we identified NtTIP3;1 and NtTIP3;2 as being exclusively expressed in the seed capsule. This is consistent with the seed-specific expression of their orthologs in other species [92,93,94] where they accumulate in mature embryos and later function in water uptake during seed imbibition and germination [94,95,96]. The consistent expression pattern between species implies functional conservation, meaning that NtNIP4;1, NtNIP4;2 and NtTIP5;1 likely fulfil roles in different aspects of tobacco pollen biology, and NtTIP3;1 and NtTIP3;2 are expected to aid tobacco seed germination.
Several PIP and TIP isoforms were found with exclusive or preferential expression in the roots (e.g. PIP1;1, PIP2;4, PIP2;5 s, PIP2;6, TIP1;2, TIP1;3, TIP2;5 and TIP2;2 s), where they could be functioning in lateral root emergence [97, 98], regulation of cell water uptake and homeostasis , or nutrient absorption through ammonium loading in vacuoles [99, 100]. The latter possible role of ammonium loading is especially pertinent to the two NtTIP2 proteins listed, which have a histidine residue in the ar/R LC position characteristic of ammonia transporting TIPs  .
The putative roles put forward for the various NtAQPs above, could equally apply to many of the tomato and potato AQPs and vice versa, given the general family-wide conservation in tissue-specific expression patterns between these three Solanaceae species. The generally high conservation in expression patterns between Solanaceae AQP orthologs supports the accuracy of our NtAQP orthology; assigned based on protein sequence homology. The similarity at both the protein and transcript levels strongly implies functional conservation for many of the AQP orthologs across these Solanaceae species. Knowledge of the extent of such conservation is valuable as it can help facilitate translation of findings across Solanaceae species for traits of agronomic importance and help direct engineering efforts. Deviations are also interesting (of which we observed several), as they hint at potential novel species-specific functions, or help explain physiological differences between species. For example, NIP2;1 is an unique NIP with a distinct GSGR ar/R filter motif and a precise loop C spacing between NPA motifs allowing it to permeate and aid silicon transport from root to shoot in a number of high silicon accumulating species [101, 102]. But, Solanaceae species are considered poor silicon accumulators [101, 102], which matches an apparent deterioration of the NIP2;1 lineage in Solanaceae as seen in our cross-species comparisons with; NIP2;1 being lost in N. tomentosiformis prior to tobacco hybridisation; a subsequent absence of a NtNIP2;1 t gene; both N.sylNIP2;1 and NtNIP2;1 s have a unfavourable loop C length for silicon transport, as does SlNIP2;1; potato does not possess a NIP2;1; the different expression patterns of NtNIP2;1 and SlNIP2;1 hint at diverging roles; NtNIP2;1:GFP is poorly localised to the PM likely limiting function capacity; and no other NtNIP has a GSGR ar/R filter configuration for redundancy.
We determined that the tobacco AQP family consists of 76 members divided into five subfamilies each with subtle characteristic variations in protein structures, pore lining residues, and post-translational regulatory mechanisms. Characterisations of key residues and regions broaden our knowledge of AQP biology by guiding future functional studies to help identify substrate specificity residue combinations. The annotation of putative post-translational regulatory sites supports current knowledge of AQP regulation not only within the more widely studied PIP subfamily, but also across the TIP, NIP, SIP and XIP sub-groups. Members of the different NtAQP subfamilies were found to localise to specific sub-cellular membranes, which contribute collectively to a dynamic and extensive transport system. These subcellular profiles help towards elucidating physiological roles with, for example, PM-localising NtAQPs likely facilitating diffusion of solutes in and out of cells, and tonoplast-localising isoforms helping with intracellular distribution of solutes. Tobacco is a recent allotetraploid, which accounts for its large AQP family size and characteristic phylogenetic pairing of sister genes inherited and retained from its parents; Nicotiana sylvestris and Nicotiana tomentosiformis. By establishing heritage of NtAQP sister genes we were able to reconstruct the recent evolutionary history of the NtAQP family, which contributes to establishing potential functional homology of candidate genes. Expression analysis of the NtAQPs revealed diverse tissue-specificities, consistent with the broad spanning physiological functions of AQP. Some NtAQPs were expressed widely, while other showed specialised or strong preferential expression within a single tissue. We found that the expression specificity for a number of NtAQPs resembled that of orthologous AQPs with established physiological roles in other species, allowing us to assign putative homologous functions in tobacco. The conservation in AQP protein structure and gene expression patterns were high with other Solanaceae species, which will facilitate the translation of knowledge from tobacco into closely related and horticulturally important crops.
Identification of tobacco, N.sylvestris and N.tomentosiformis AQPs
The tobacco genome and the protein sequences for TN90  and K326-Nitab4.5v  cultivars were obtained from the Solanaceae Genomics Network  and imported into the Geneious (V9.1.5) software . To comprehensively identify putative aquaporin genes in tobacco, multiple BLASTP searches were performed against the TN90 tobacco predicted proteome, using each of the potato (Solanum tuberosum) and tomato (Solanum lycopersicum) aquaporin proteins sequences as queries. From each individual homology search, the top 3–5 matches were compiled as putative NtAQPs; with the list being consolidated at the end of the search routine. A similar process was used to identify AQPs in N. sylvestris and N. tomentosiformis (tobacco parental genomes), however tobacco aquaporin coding sequences were used in BLASTN queries. Sequence alignments were conducted using MUSCLE . Whole family and sub-family sequence alignments were used to flag aberrant AQP protein sequences for closer inspection.
Phylogenetic analysis and classification of tobacco, N. sylvestris and N. tomentosiformis AQPs
MUSCLE aligned nucleotide or protein sequences were used to construct phylogenetic trees using neighbour-joining (NJ) method (pair-wise deletion; bootstrap = 1000) in MEGA7 software . Tobacco AQP naming convention was based on homology to that of the tomato AQPs. N. sylvestris and N.tomentosiformis AQP gene names were assigned based on homology to tobacco AQPs.
Structural features of tobacco AQPs
The tobacco aquaporin intron/exon structures were identified by aligning CDS and genomic sequences. Comparisons of gene sequences (computed and our curations) and RNA-seq data were visualised through JBrowse. The topologies of the curated NtAQPs were defined using TOPCONS . The complement of known functionally relevant residues were collected from MUSCLE aligned NtAQP protein sequences. Alignment statistics (e.g. % sequence identity and similarity using BLSM62 matrix) were collected from MUSCLE aligned sequences of individual subfamilies. Prediction of phosphorylation sites were performed using NetPhos 3.1 prediction score ≥ 0.8 .
Subcellular localisation in planta (Arabidopsis)
Tobacco AQP GFP fusion constructs were generated via Gateway cloning of a TIP (NtTIP1,1 s), PIP (NtPIP2;5 t) and NIP (NtNIP5;1 t) coding sequences from pZeo entry vectors into the pMDC43 destination vector ; which produced N-terminal GFP:NtAQP fusion proteins driven by the constitutive 2x35S CaMV promoter. Arabidopsis transgenic lines were generated via agrobacterium (GV3101) floral dipping plant transformation method (Clough and Bent 1998). The GFP marker line (MG0100.15) used as a cytosolic localisation marker was generated in our lab via the Gateway cloning of the mGFP6 variant of GFP contained as a pZeo entry clone into the pMDC32 destination vector ; which drives constitutive expression of the mGFP6 transgene via the 2x35S CaMV promoter. The PM:GFP line was also generated in our lab, built in the pMDC83 Gateway destination vector and consisting of the Arabidopsis PIP2;1 (an already established PM marker ) with a mGFP6 C-terminal fusion, all driven by the 2x35S CaMV promoter.
Arabidopsis seeds were liquid sterilised using hypochlorite, washed several times and sown on Gamorg’s B5 medium containing 0.8% Agar and the antibiotic hygromycin for selection of transformants. After 8 days of growth, arabidopsis seedlings were gently removed from the agar, mounted in Phosphate Buffer (100 mM NaPO4 buffer, pH 7.2) on a standard slide and covered with coverslip, and visualised with a Zeiss LSM 780 Confocal microscope using a 40x water immersion objective (1.2 NA). Light micrographs of cortical cells in the root elongation zone were visualised using Differential Interference Contrast (DIC), with GFP fluorescence captured using excitation at 488 nm and emission detection across the 490–526 nm range. Autofluorescence was detected in the 570–674 nm range and excluded from GFP detection channel. Images were processed using Fiji (ImageJ) program .
AQP gene expression analysis
Transcript expression of the identified aquaporins was extracted from published, publicly available datasets, via two avenues ; mining of processed transcript expression matrices and  analyses of raw RNA-Seq reads uploaded to GenBank Sequence Read Archive (SRA). Processed transcript expression of N. tabacum K326  was extracted from The Sol Genomics Network . Data was extracted as transcripts per million (TPM) and so was mined without further processing. This data set contained tissue specific expression of the leaf and root. Raw RNA-Seq reads from both N. tabacum K326 and TN90  were downloaded from the GenBank SRA (TN90: SRP029183; K326: SRP029184) via command line into paired end fastq files. Read libraries were tissue specific from either the leaf, root, young leaf, young flower, mature leaf, mature flower, senescent leaf, senescent flower or dry capsule. On average each tissue was represented by a RNA-seq library of ~ 110 million paired reads. The raw reads were processed using Trimmomatic  to remove adapter sequences. Processed reads were aligned to the N. tabacum genome, either the K326  or TN90 , using the Quasi align mode within Salmon  invoking a k-mer length of 31, with relative abundance reported as transcripts per million (TPM). Mapping rates of the K326 and TN90 transcriptomes were between 73 and 78%, and 89–94%, respectively. Raw RNA-seq reads for the parental genomes of N. sylvestris and N. tomentosiformis were obtained from . RNA-seq libraries were libraries were derived from root, leaf, and flower tissues, with an average of 265 million paired reads for each tissue type. Reads were processed as above and mapped to the N. sylvestris and N. tomentosiformis genomes obtained from .
Availability of data and materials
We declare that the dataset(s) supporting the conclusions of this article are included within the article and its additional file(s). All of our curated aquaporin CDS nucleotide and protein sequence data reported for Nicotiana tabacum, N. sylvestris and N. tomentosiformis is available in the Third-Party Annotation Section of the DDBJ/ENA/GenBank databases under the accession numbers TPA: BK011376-BK011532; BankIt2254789.
Coding DNA sequence
Major intrinsic protein
Nodulin26-like Intrinsic protein
- N. syl:
- N. tom:
Plasma membrane intrinsic PROTEIN
Tonoplast intrinsic protein
X Intrinsic Protein
Marschner H. Marschner's mineral nutrition of higher plants: academic press; 2011.
Hedrich R, Marten I. 30-year progress of membrane transport in plants. Planta. 2006;224(4):725–39.
Chrispeels MJ, Crawford NM, Schroeder JI. Proteins for transport of water and mineral nutrients across the membranes of plant cells. Plant Cell. 1999;11(4):661–75.
Hachez C, Zelazny E, Chaumont F. Modulating the expression of aquaporin genes in planta: a key to understand their physiological functions? Biochim Biophys Acta (BBA)-Biomembranes. 2006;1758(8):1142–56.
Groszmann M, Osborn HL, Evans JR. Carbon dioxide and water transport through plant aquaporins. Plant Cell Environ. 2017;40(6):938–61.
Frick A, Järvå M, Ekvall M, Uzdavinys P, Nyblom M, Törnroth-Horsefield S. Mercury increases water permeability of a plant aquaporin through a non-cysteine-related mechanism. Biochem J. 2013;454(3):491–9.
Hove RM, Bhave M. Plant aquaporins with non-aqua functions: deciphering the signature sequences. Plant Mol Biol. 2011;75(4):413–30.
Froger A, Thomas D, Delamarche C, Tallur B. Prediction of functional residues in water channels and related proteins. Protein Sci. 1998;7(6):1458–68.
Mitani-Ueno N, Yamaji N, Zhao F-J, Ma JF. The aromatic/arginine selectivity filter of NIP aquaporins plays a critical role in substrate selectivity for silicon, boron, and arsenic. J Exp Bot. 2011;62(12):4391–8.
Murata K, Mitsuoka K, Hirai T, Walz T, Agre P, Heymann JB, et al. Structural determinants of water permeation through aquaporin-1. Nature. 2000;407(6804):599.
Wu B, Beitz E. Aquaporins with selectivity for unconventional permeants. Cell Mol Life Sci. 2007;64(18):2413–21.
Abascal F, Irisarri I, Zardoya R. Diversity and evolution of membrane intrinsic proteins. Biochim Biophys Acta (BBA)-Gen Subj. 2014;1840(5):1468–81.
Laloux T, Junqueira B, Maistriaux LC, Ahmed J, Jurkiewicz A, Chaumont F. Plant and mammal aquaporins: same but different. Int J Mol Sci. 2018;19(2):521.
Sonah H, Deshmukh RK, Labbé C, Bélanger RR. Analysis of aquaporins in Brassicaceae species reveals high-level of conservation and dynamic role against biotic and abiotic stress in canola. Sci Rep. 2017;7(1):2771.
Yuan D, Li W, Hua Y, King GJ, Xu F, Shi L. Genome-wide identification and characterization of the aquaporin gene family and transcriptional responses to boron deficiency in Brassica napus. Front Plant Sci. 2017;8:1336.
Chaumont F, Tyerman S. Plant Aquaporins: From Transport to Signalling. Cham:Springer. 2017.
Danielson JÅ, Johanson U. Unexpected complexity of the aquaporin gene family in the moss Physcomitrella patens. BMC Plant Biol. 2008;8(1):45.
Johanson U, Gustavsson S. A new subfamily of major intrinsic proteins in plants. Mol Biol Evol. 2002;19(4):456–61.
Kaldenhoff R, Fischer M. Aquaporins in plants. Acta Physiol. 2006;187(1–2):169–76.
Gomes D, Agasse A, Thiébaud P, Delrot S, Gerós H, Chaumont F. Aquaporins are multifunctional water and solute transporters highly divergent in living organisms. Biochim Biophys Acta (BBA)-Biomembranes. 2009;1788(6):1213–28.
Pommerrenig B, Diehn TA, Bienert GP. Metalloido-porins: essentiality of Nodulin 26-like intrinsic proteins in metalloid transport. Plant Sci. 2015;238:212–27.
Choi W-G, Roberts DM. Arabidopsis NIP2; 1, a major intrinsic protein transporter of lactic acid induced by anoxic stress. J Biol Chem. 2007;282(33):24209–18.
Zwiazek JJ, Xu H, Tan X, Navarro-Ródenas A, Morte A. Significance of oxygen transport through aquaporins. Sci Rep. 2017;7:40411.
Byrt CS, Zhao M, Kourghi M, Bose J, Henderson SW, Qiu J, et al. Non-selective cation channel activity of aquaporin AtPIP2; 1 regulated by Ca2+ and pH. Plant Cell Environ. 2017;40(6):802–15.
Bienert GP, Desguin B, Chaumont F, Hols P. Channel-mediated lactic acid transport: a novel function for aquaglyceroporins in bacteria. Biochem J. 2013;454(3):559–70.
Reichel M, Liao Y, Rettel M, Ragan C, Evers M, Alleaume A-M, et al. In planta determination of the mRNA-binding proteome of Arabidopsis etiolated seedlings. Plant Cell. 2016;28(10):2435–52.
Santoni V. Plant aquaporin posttranslational regulation. Plant Aquaporins: From Transport to Signalling. Cham:Springer; 2017:83–105.
Luu DT, Maurel C. Aquaporin trafficking in plant cells: an emerging membrane-protein model. Traffic. 2013;14(6):629–35.
Li G, Santoni V, Maurel C. Plant aquaporins: roles in plant physiology. Biochim Biophys Acta (BBA)-Gen Subj. 2014;1840(5):1574–82.
Flexas J, Ribas-Carbó M, Hanson DT, Bota J, Otto B, Cifre J, et al. Tobacco aquaporin NtAQP1 is involved in mesophyll conductance to CO2in vivo. Plant J. 2006;48(3):427–39.
Xu F, Wang K, Yuan W, Xu W, Shuang L, Kronzucker HJ, et al. Overexpression of rice aquaporin OsPIP1; 2 improves yield by enhancing mesophyll CO2 conductance and phloem sucrose transport. J Exp Bot. 2018;70(2):671–81.
Zargar SM, Nagar P, Deshmukh R, Nazir M, Wani AA, Masoodi KZ, et al. Aquaporins as potential drought tolerance inducing proteins: towards instigating stress tolerance. J Proteome. 2017;169:233–8.
Gambetta GA, Knipfer T, Fricke W, McElrone AJ. Aquaporins and root water uptake. Plant Aquaporins: From Transport to Signalling. Cham:Springer; 2017:133–53.
Schnurbusch T, Hayes J, Hrmova M, Baumann U, Ramesh SA, Tyerman SD, et al. Boron toxicity tolerance in barley through reduced expression of the multifunctional aquaporin HvNIP2; 1. Plant Physiol. 2010;153(4):1706–15.
Bienert MD, Bienert GP. Plant aquaporins and metalloids. Plant Aquaporins: From Transport to Signalling. Cham:Springer, 2017:297–332.
Gebhardt C. The historical role of species from the Solanaceae plant family in genetic research. Theor Appl Genet. 2016;129(12):2281–94.
Vanhercke T, El Tahchy A, Liu Q, Zhou XR, Shrestha P, Divi UK, et al. Metabolic engineering of biomass for high energy density: oilseed-like triacylglycerol yields from plant leaves. Plant Biotechnol J. 2014;12(2):231–9.
Tusé D, Tu T, McDonald KA. Manufacturing economics of plant-made biologics: case studies in therapeutic and industrial enzymes. Biomed Res Int. 2014;1-16.
Ma JKC, Drossard J, Lewis D, Altmann F, Boyle J, Christou P, et al. Regulatory approval and a first-in-human phase I clinical trial of a monoclonal antibody produced in transgenic tobacco plants. Plant Biotechnol J. 2015;13(8):1106–20.
Reuscher S, Akiyama M, Mori C, Aoki K, Shibata D, Shiratake K. Genome-wide identification and expression analysis of aquaporins in tomato. PLoS One. 2013;8(11):e79052.
Venkatesh J, Yu J-W, Park SW. Genome-wide analysis and expression profiling of the Solanum tuberosum aquaporins. Plant Physiol Biochem. 2013;73:392–404.
Sierro N, Battey JN, Ouadi S, Bakaher N, Bovet L, Willig A, et al. The tobacco genome sequence and its comparison with those of tomato and potato. Nat Commun. 2014;5:3833.
Edwards K, Fernandez-Pozo N, Drake-Stowe K, Humphry M, Evans A, Bombarely A, et al. A reference genome for Nicotiana tabacum enables map-based cloning of homeologous loci implicated in nitrogen utilization efficiency. BMC Genomics. 2017;18(1):448.
Biela A, Grote K, Otto B, Hoth S, Hedrich R, Kaldenhoff R. The Nicotiana tabacum plasma membrane aquaporin NtAQP1 is mercury-insensitive and permeable for glycerol. Plant J. 1999;18(5):565–70.
Törnroth-Horsefield S, Wang Y, Hedfalk K, Johanson U, Karlsson M, Tajkhorshid E, et al. Structural mechanism of plant aquaporin gating. Nature. 2006;439(7077):688.
Nyblom M, Frick A, Wang Y, Ekvall M, Hallgren K, Hedfalk K, et al. Structural and functional analysis of SoPIP2; 1 mutants adds insight into plant aquaporin gating. J Mol Biol. 2009;387(3):653–68.
Tournaire-Roux C, Sutka M, Javot H, Gout E, Gerbeau P, Luu D-T, et al. Cytosolic pH regulates root water transport during anoxic stress through gating of aquaporins. Nature. 2003;425(6956):393.
Roche JV, Törnroth-Horsefield S. Aquaporin protein-protein interactions. Int J Mol Sci. 2017;18(11):2255.
Bienert GP, Cavez D, Besserer A, Berny MC, Gilis D, Rooman M, et al. A conserved cysteine residue is involved in disulfide bond formation between plant plasma membrane aquaporin monomers. Biochem J. 2012;445(1):101–11.
Chevalier AS, Chaumont F. Trafficking of plant plasma membrane aquaporins: multiple regulation levels and complex sorting signals. Plant Cell Physiol. 2014;56(5):819–29.
Kirscht A, Kaptan SS, Bienert GP, Chaumont F, Nissen P, de Groot BL, et al. Crystal structure of an ammonia-permeable aquaporin. PLoS Biol. 2016;14(3):e1002411.
Leitão L, Prista C, Moura TF, Loureiro-Dias MC, Soveral G. Grapevine aquaporins: gating of a tonoplast intrinsic protein (TIP2; 1) by cytosolic pH. PLoS One. 2012;7(3):e33219.
Soto G, Fox R, Ayub N, Alleva K, Guaimas F, Erijman EJ, et al. TIP5; 1 is an aquaporin specifically targeted to pollen mitochondria and is probably involved in nitrogen remobilization in Arabidopsis thaliana. Plant J. 2010;64(6):1038–47.
Gupta AB, Sankararamakrishnan R. Genome-wide analysis of major intrinsic proteins in the tree plant Populus trichocarpa: characterization of XIP subfamily of aquaporins from evolutionary perspective. BMC Plant Biol. 2009;9(1):134.
Briesemeister S, Rahnenf¿½hrer J, Kohlbacher O. YLoc—an interpretable web server for predicting subcellular localization. Nucleic Acids Res. 2010;38(suppl_2):W497–502.
Bienert GP, Bienert MD, Jahn TP, Boutry M, Chaumont F. Solanaceae XIPs are plasma membrane aquaporins that facilitate the transport of many uncharged substrates. Plant J. 2011;66(2):306–17.
Wu W-Z, Peng X-L, Di W. Isolation of a plasmalemma aquaporin encoding gene StPIP1 from Solanum tuberosum L. and its expression in transgenic tobacco. Agric Sci China. 2009;8(10):1174–86.
Li R, Wang J, Li S, Zhang L, Qi C, Weeda S, et al. Plasma membrane intrinsic proteins SlPIP2;1, SlPIP2;7 and SlPIP2;5 conferring enhanced drought stress tolerance in tomato. Sci Rep. 2016;6:31814.
Hu W, Yuan Q, Wang Y, Cai R, Deng X, Wang J, et al. Overexpression of a wheat aquaporin gene, TaAQP8, enhances salt stress tolerance in transgenic tobacco. Plant Cell Physiol. 2012;53(12):2127–41.
Zhu Y-X, Yang L, Liu N, Yang J, Zhou X-K, Xia Y-C, et al. Genome-wide identification, structure characterization, and expression pattern profiling of aquaporin gene family in cucumber. BMC Plant Biol. 2019;19(1):345.
Pang Y, Li L, Ren F, Lu P, Wei P, Cai J, et al. Overexpression of the tonoplast aquaporin AtTIP5; 1 conferred tolerance to boron toxicity in Arabidopsis. J Gen Genomics. 2010;37(6):389–97.
Wang Y, Li R, Li D, Jia X, Zhou D, Li J, et al. NIP1; 2 is a plasma membrane-localized transporter mediating aluminum uptake, translocation, and tolerance in Arabidopsis. Proc Natl Acad Sci. 2017;114(19):5047–52.
Nelson BK, Cai X, Nebenführ A. A multicolored set of in vivo organelle markers for co-localization studies in Arabidopsis and other plants. Plant J. 2007;51(6):1126–36.
Sierro N, Battey JN, Ouadi S, Bovet L, Goepfert S, Bakaher N, et al. Reference genomes and transcriptomes of Nicotiana sylvestris and Nicotiana tomentosiformis. Genome Biol. 2013;14(6):R60.
Uehlein N, Lovisolo C, Siefritz F, Kaldenhoff R. The tobacco aquaporin NtAQP1 is a membrane CO2 pore with physiological functions. Nature. 2003;425(6959):734–7.
Maurel C, Verdoucq L, Luu D-T, Santoni V. Plant aquaporins: membrane channels with multiple integrated functions. Annu Rev Plant Biol. 2008;59:595–624.
Berny MC, Gilis D, Rooman M, Chaumont F. Single mutations in the transmembrane domains of maize plasma membrane aquaporins affect the activity of monomers within a heterotetramer. Mol Plant. 2016;9(7):986–1003.
Yoo Y-J, Lee HK, Han W, Kim DH, Lee MH, Jeon J, et al. Interactions between transmembrane helices within monomers of the aquaporin AtPIP2; 1 play a crucial role in tetramer formation. Mol Plant. 2016;9(7):1004–17.
Takano J, Yoshinari A, Luu D-T. Plant aquaporin trafficking. Plant Aquaporins: From Transport to Signalling. Cham:Springer; 2017:47–81.
Sui H, Han B-G, Lee JK, Walian P, Jap BK. Structural basis of water-specific transport through the AQP1 water channel. Nature. 2001;414(6866):872.
Luang S, Hrmova M. Structural basis of the permeation function of plant aquaporins. Plant Aquaporins: From Transport to Signalling. Cham:Springer; 2017:1–28.
Prak S, Hem S, Boudet J, Viennois G, Sommerer N, Rossignol M, et al. Multiple phosphorylations in the C-terminal tail of plant plasma membrane aquaporins: role in subcellular trafficking of AtPIP2; 1 in response to salt stress. Mol Cell Proteomics. 2008;7(6):1019–30.
Diehn TA, Pommerrenig B, Bernhardt N, Hartmann A, Bienert GP. Genome-wide identification of aquaporin encoding genes in Brassica oleracea and their phylogenetic sequence comparison to Brassica crops and Arabidopsis. Front Plant Sci. 2015;6:166.
Maeshima M, Ishikawa F. ER membrane aquaporins in plants. Pflügers Arch. 2008;456(4):709–16.
Newby ZE, O'Connell Iii J, Robles-Colmenares Y, Khademi S, Miercke LJ, Stroud RM. Crystal structure of the aquaglyceroporin PfAQP from the malarial parasite plasmodium falciparum. Nat Struct Mol Biol. 2008;15(6):619.
Mizutani M, Watanabe S, Nakagawa T, Maeshima M. Aquaporin NIP2; 1 is mainly localized to the ER membrane and shows root-specific accumulation in Arabidopsis thaliana. Plant Cell Physiol. 2006;47(10):1420–6.
Ishikawa F, Suga S, Uemura T, Sato MH, Maeshima M. Novel type aquaporin SIPs are mainly localized to the ER membrane and show cell-specific expression in Arabidopsis thaliana. FEBS Lett. 2005;579(25):5814–20.
Takano J, Wada M, Ludewig U, Schaaf G, Von Wirén N, Fujiwara T. The Arabidopsis major intrinsic protein NIP5; 1 is essential for efficient boron uptake and plant development under boron limitation. Plant Cell. 2006;18(6):1498–509.
Leitch I, Hanson L, Lim K, Kovarik A, Chase M, Clarkson J, et al. The ups and downs of genome size evolution in polyploid species of Nicotiana (Solanaceae). Ann Bot. 2008;101(6):805–14.
Leitch I, Bennett M. Genome downsizing in polyploid plants. Biol J Linn Soc. 2004;82(4):651–63.
Sato S, Tabata S, Hirakawa H, Asamizu E, Shirasawa K, Isobe S, et al. The tomato genome sequence provides insights into fleshy fruit evolution. Nature. 2012;485(7400):635.
Xu X, Pan S, Cheng S, Zhang B, Mu D, Ni P, et al. Genome sequence and analysis of the tuber crop potato. Nature. 2011;475(7355):189.
Venkatesh J, Yu J-W, Gaston D, Park SW. Molecular evolution and functional divergence of X-intrinsic protein genes in plants. Mol Gen Genomics. 2015;290(2):443–60.
Groszmann M, Greaves IK, Fujimoto R, Peacock WJ, Dennis ES. The role of epigenetics in hybrid vigour. Trends Genet. 2013;29(12):684–90.
Groszmann M, Greaves IK, Albert N, Fujimoto R, Helliwell CA, Dennis ES, et al. Epigenetics in plants—vernalisation and hybrid vigour. Biochim Biophys Acta (BBA)-Gene Regul Mech. 2011;1809(8):427–37.
Wei W, Alexandersson E, Golldack D, Miller AJ, Kjellbom PO, Fricke W. HvPIP1; 6, a barley (Hordeum vulgare L.) plasma membrane water channel particularly expressed in growing compared with non-growing leaf tissues. Plant Cell Physiol. 2007;48(8):1132–47.
Hachez C, Heinen RB, Draye X, Chaumont F. The expression pattern of plasma membrane aquaporins in maize leaf highlights their role in hydraulic regulation. Plant Mol Biol. 2008;68(4–5):337.
Heinen RB, Ye Q, Chaumont F. Role of aquaporins in leaf physiology. J Exp Bot. 2009;60(11):2971–85.
Bots M, Feron R, Uehlein N, Weterings K, Kaldenhoff R, Mariani T. PIP1 and PIP2 aquaporins are differentially expressed during tobacco anther and stigma development. J Exp Bot. 2005;56(409):113–21.
Ma N, Xue J, Li Y, Liu X, Dai F, Jia W, et al. Rh-PIP2; 1, a rose aquaporin gene, is involved in ethylene-regulated petal expansion. Plant Physiol. 2008;148(2):894–907.
Di Giorgio JP, Bienert GP, Ayub N, Yaneff A, Barberini ML, Mecchia MA, et al. Pollen-specific aquaporins NIP4; 1 and NIP4; 2 are required for pollen development and pollination in Arabidopsis thaliana. Plant Cell. 2016;28:1053–77.
Utsugi S, Shibasaka M, Maekawa M, Katsuhara M. Control of the water transport activity of barley HvTIP3; 1 specifically expressed in seeds. Plant Cell Physiol. 2015;56(9):1831–40.
Li G-W, Peng Y-H, Yu X, Zhang M-H, Cai W-M, Sun W-N, et al. Transport functions and expression analysis of vacuolar membrane aquaporins in response to various stresses in rice. J Plant Physiol. 2008;165(18):1879–88.
Footitt S, Clewes R, Feeney M, Finch-Savage WE, Frigerio L. Aquaporins influence seed dormancy and germination in response to stress. Plant Cell Environ. 2019;42:2325–39.
Mao Z, Sun W. Arabidopsis seed-specific vacuolar aquaporins are involved in maintaining seed longevity under the control of ABSCISIC ACID INSENSITIVE 3. J Exp Bot. 2015;66(15):4781–94.
Hoai PTT, Tyerman SD, Schnell N, Tucker M, McGaughey SA, Qiu J, et al. Deciphering aquaporin regulation and roles in seed biology. J Exp Bot. 2020. https://0-doi-org.brum.beds.ac.uk/10.1093/jxb/erz555.
Péret B, Li G, Zhao J, Band LR, Voß U, Postaire O, et al. Auxin regulates aquaporin function to facilitate lateral root emergence. Nat Cell Biol. 2012;14(10):991.
Reinhardt H, Hachez C, Bienert MD, Beebo A, Swarup K, Voß U, et al. Tonoplast aquaporins facilitate lateral root emergence. Plant Physiol. 2016;170(3):1640–54.
Lopez F, Bousser A, Sissoëff I, Hoarau J, Mahé A. Characterization in maize of ZmTIP2-3, a root-specific tonoplast intrinsic protein exhibiting aquaporin activity. J Exp Bot. 2004;55(396):539–41.
Loqué D, Ludewig U, Yuan L, von Wirén N. Tonoplast intrinsic proteins AtTIP2; 1 and AtTIP2; 3 facilitate NH3 transport into the vacuole. Plant Physiol. 2005;137(2):671–80.
Deshmukh RK, Vivancos J, Ramakrishnan G, Guérin V, Carpentier G, Sonah H, et al. A precise spacing between the NPA domains of aquaporins is essential for silicon permeability in plants. Plant J. 2015;83(3):489–500.
Coskun D, Deshmukh R, Sonah H, Shivaraj SM, Frenette-Cotton R, Tremblay L, et al. Si permeability of a deficient Lsi1 aquaporin in tobacco can be enhanced through a conserved residue substitution. Plant Direct. 2019;3(8):e00163.
Fernandez-Pozo N, Menda N, Edwards JD, Saha S, Tecle IY, Strickler SR, et al. The sol genomics network (SGN)—from genotype to phenotype to breeding. Nucleic Acids Res. 2014;43(D1):D1036–D41.
Drummond A, Ashton B, Buxton S, Cheung M, Cooper A, Duran C, et al. Geneious. Biomatters Ltd. 2011.
Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004;32(5):1792–7.
Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016;33(7):1870–4.
Tsirigos KD, Peters C, Shu N, Käll L, Elofsson A. The TOPCONS web server for consensus prediction of membrane protein topology and signal peptides. Nucleic Acids Res. 2015;43(W1):W401–7.
Blom N, Gammeltoft S, Brunak S. Sequence and structure-based prediction of eukaryotic protein phosphorylation sites. J Mol Biol. 1999;294(5):1351–62.
Horton P, Park K-J, Obayashi T, Fujita N, Harada H, Adams-Collier C, et al. WoLF PSORT: protein localization predictor. Nucleic Acids Res. 2007;35(suppl_2):W585–W7.
Chou K-C, Shen H-B. Plant-mPLoc: a top-down strategy to augment the power for predicting plant protein subcellular localization. PLoS One. 2010;5(6):e11335.
Curtis MD, Grossniklaus U. A gateway cloning vector set for high-throughput functional analysis of genes in planta. Plant Physiol. 2003;133(2):462–9.
Schindelin J, Arganda-Carreras I, Frise E, Kaynig V, Longair M, Pietzsch T, et al. Fiji: an open-source platform for biological-image analysis. Nat Methods. 2012;9(7):676.
Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30(15):2114–20.
Patro R, Duggal G, Love MI, Irizarry RA, Kingsford C. Salmon provides fast and bias-aware quantification of transcript expression. Nat Methods. 2017;14(4):417.
Chattopadhyay D, Tyagi AK, Sato S, Zamir D, Giuliano G, Consortium TG. The tomato genome sequence provides insights into fleshy fruit evolution. 2012.
Consortium PGS. Genome sequence and analysis of the tuber crop potato. Nature. 2011;475(7355):189.
We thank Rosemary White from CSIRO for providing seeds of the Tonoplast:GFP and ER:GFP marker lines . The authors acknowledge the facilities and the scientific and technical assistance (Darryl Webb) of Microscopy Australia at the Advanced Imaging Precinct at the Australian National University; a facility funded by the ANU, and State and Federal Governments of Australia. We acknowledge that National Collaborative Research Infrastructure Strategy (NCRIS) of the Australian Government, providing The Australian National University with the growth facilities utilised as part of the Australian Plant Phenomics Facility.
ADR, AWL, JRE, and MG, were supported by the Australian Research Council Centre of Excellence for Translational Photosynthesis (CE140100015). The funding agency had no role in the design of the study and collection, analysis and interpretation of data or in writing the manuscript.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Tobacco AQP pseudo genes. Table of sequences that encode for incomplete AQPs within the tobacco TN90 genome sequence (Sierro et al. 2014), that we have subsequently assigned as pseudo genes. Notes on trans-membrane domains were sourced from analysis using TOPCONs protein topology prediction software. Table S2. Extended information on the 76 tobacco aquaporins identified in this study. Provided are protein lengths, gene identifiers, gene structures, chromosome and/or scaffold locations in the TN90  (Sierro et al. 2014) and K326  (Edwards et al. 2017) cultivar genomes, comparison of whether the computed gene models derived from each study matched gene structures curated in this study (Y-yes or N-no) and NCBI accessions. NtTIP2;5 s, NtNIP4;2 s and NtNIP4;3 t genes were not identified in the K326  cultivar’s genome. Also listed are the corresponding tomato and potato orthologs and their respective gene (inton/exon) structures. Table S3. Amended annotations of previously reported tomato, potato and tobacco AQPs. In analysing the NtAQP family, we identified misannotations in previously reported AQPs from tomato (Solanum lycopersicum), potato (Solanum tuberosum) and tobacco (Nicotiana tabacum). Provided is a brief description of the error. Corrected sequences can be found in Additional file 3.
AQP subfamily alignments for genes with incorrect protein sequences reported in Edwards et al. (2017). In red is the Edwards et al. (2017) predicted protein sequence and in black is the curated protein sequence from this study. Figure S2. Alignment of regions surrounding Histidine 207 in NtAQP1 (NtPIP1;5 s). Partial regions of a protein sequence alignment surrounding Histidine 207 of the NtAQP1 (NtPIP1;5) identified in this study, against the seemingly erroneous NtAQP1 sequence reported in (Biela et al., 1999; NCBI AF024511 and AJ001416) and closest BlastP matches from various other Solanaceae species. Figure S3. Phylogeny of Arabidopsis, tomato, rubber tree, rice, soybean and tobacco AQPs. Figure too large for this PDF; See Additional file 4. Figure S4. Phylogeny of Arabidopsis and currently identified Solanaceae AQPs. Phylogenetic trees for each AQP sub-family were generated using the neighbour-joining method from MUSCLE aligned protein sequences. Confidence levels (%) of branch points generated through bootstrapping analysis (n = 1000). Solanaceae species included in this phylogeny include; N.sylvestris (orange), N.tomentosiformis (blue), tomato (green), potato (brown) and tobacco (black). Arabidopsis genes are coloured red. Black stars indicate NtAQPs which did not have an obvious tomato ortholog. Figure S5. Sequence alignment of C-terminal tails of NtPIP and NtNIP proteins. Serine residues in red are those predicted to be phosphorylated by NetPhos 3.1 (prediction score ≥ 0.8). Underlined red serine residues in GmNOD26, SoPIP2;1 and AtPIP2;1 have been experimentally confirmed as being phosphorylated in plants. Bold residues indicate the substitution of strongly conserved positively charged Lys(K)/Arg(R) residues to a His(H) residue (blue) occurring in NtPIP1;5 and NtPIP2;1 proteins. Figure S6. Comparisons of expression profile between AQPs from tobacco (NtAQPs and NtAQPt, genes), Nicotiana sylvestris (N.syl) and Nicotiana tomentosiformis (N.tom). Correlations of relative transcript abundances was compared in two-dimensions; (i) between AQPs within a given tissue (vertically) and (ii) a given AQP across tissues (horizontally). Figure S7. Tissue-specific expression patterns of tomato XIP isoforms (SlPXIP1;1-SlXIP1;6) and the tobacco NtXIP1;7 sister genes. Comparison of relative gene expression in roots, leaves and flowers of tobacco NtXIP1;7 sister genes (blue) against all the tomato XIP isoforms (red, SlXIP1;1-SlXIP6), with potato orthologs (brown), in an attempt to find matches between the various XIPs which were difficult to assign orthology based on protein sequence alone.
Repository of sequences examined in this study. Genomic (gff3 format), CDS, and protein sequences for all 76 NtAQPs. CDS and protein sequences for all N.sylvestris and N.tomentosiformis AQPs. Amended sequences for potato StXIP3;1, StXIP4;1, and tomato SlXIP1;6, SlPIP2;1, SlTIP2;2 proteins (see also Additional file 1: Table S3)
Phylogeny of Arabidopsis, tomato, rubber tree, rice, soybean and tobacco AQPs. Phylogenetic analysis of tobacco AQPs with those from species belonging to a diverse set of plant species from across the angiosperm lineage: Arabidopsis (Brassicales), tomato (Solanales), rubber tree (Malpighiales), rice (Poales) and soy bean (Fabales). Tree was generated using the neighbour-joining method from MUSCLE-aligned protein sequences. Confidence levels (%) of branch points generated through bootstrapping analysis (n = 1000). AQP subfamilies annotated are TIP (blue), NIP (purple), XIP (yellow), PIP (orange), SIP (green).
About this article
Cite this article
De Rosa, A., Watson-Lazowski, A., Evans, J.R. et al. Genome-wide identification and characterisation of Aquaporins in Nicotiana tabacum and their relationships with other Solanaceae species. BMC Plant Biol 20, 266 (2020). https://0-doi-org.brum.beds.ac.uk/10.1186/s12870-020-02412-5
- Major intrinsic protein
- Gene structure and evolution
- Gene expression profile
- Nicotiana sylvestris
- Nicotiana tomentosiformis
- Solanum lycopersicum
- Solanum tuberosum