- Research article
- Open Access
Identification of the family of aquaporin genes and their expression in upland cotton (Gossypium hirsutumL.)
BMC Plant Biology volume 10, Article number: 142 (2010)
Cotton (Gossypium spp.) is produced in over 30 countries and represents the most important natural fiber in the world. One of the primary factors affecting both the quantity and quality of cotton production is water. A major facilitator of water movement through cell membranes of cotton and other plants are the aquaporin proteins. Aquaporin proteins are present as diverse forms in plants, where they function as transport systems for water and other small molecules. The plant aquaporins belong to the large major intrinsic protein (MIP) family. In higher plants, they consist of five subfamilies including plasma membrane intrinsic proteins (PIP), tonoplast intrinsic proteins (TIP), NOD26-like intrinsic proteins (NIP), small basic intrinsic proteins (SIP), and the recently discovered X intrinsic proteins (XIP). Although a great deal is known about aquaporins in plants, very little is known in cotton.
From a molecular cloning effort, together with a bioinformatic homology search, 71 upland cotton (G. hirsutum) aquaporin genes were identified. The cotton aquaporins consist of 28 PIP and 23 TIP members with high sequence similarity. We also identified 12 NIP and 7 SIP members that showed more divergence. In addition, one XIP member was identified that formed a distinct 5th subfamily. To explore the physiological roles of these aquaporin genes in cotton, expression analyses were performed for a select set of aquaporin genes from each subfamily using semi-quantitative reverse transcription (RT)-PCR. Our results suggest that many cotton aquaporin genes have high sequence similarity and diverse roles as evidenced by analysis of sequences and their expression.
This study presents a comprehensive identification of 71 cotton aquaporin genes. Phylogenetic analysis of amino acid sequences divided the large and highly similar multi-gene family into the known 5 aquaporin subfamilies. Together with expression and bioinformatic analyses, our results support the idea that the genes identified in this study represent an important genetic resource providing potential targets to modify the water use properties of cotton.
Cotton is the most important naturally produced fiber in the world and represents a significant global agricultural commodity. Not taking into account additional economic value captured through cotton processing and associated byproducts, from 2005-2007, the average farm gate value of cotton equaled US $28 billion (World Bank, http://web.worldbank.org). Although the majority of cotton's value resides in the lint fiber used by textile manufacturers, additional benefits are obtained from cottonseed products that include animal feeds and various oil-derived products.
Similar to many other economically important crops, one of the major factors affecting both the quantity and quality of cotton production is water. Waddle  estimated that a successful cotton production system generally requires a minimum of 50 cm of water during the growing season. Hence, in planta efforts to decrease the quantity of water used and to improve cotton water use efficiency are highly desirable. At the molecular level, a potential target for manipulating water use efficiency is represented by the aquaporin proteins.
Aquaporin proteins represent a large family of the major intrinsic protein (MIP) superfamily and are known to facilitate transport of diverse small molecules including water and other small nutrients through biological membranes. Plant growth and development require water and nutrient uptake by transport mechanisms including a process mediated by aquaporins. Although the first plant aquaporin gene was cloned in soybean root nodules , it is now well known that plant aquaporins are ubiquitously distributed across plant tissue types. In higher plants, aquaporins consist of five subfamilies that include; 1) plasma membrane intrinsic proteins (PIP), 2) tonoplast intrinsic proteins (TIP), 3) NOD26-like intrinsic proteins (NIP), 4) small basic intrinsic proteins (SIP), and 5) the recently identified X (or unrecognized) intrinsic proteins (XIP) .
Aquaporin gene identification studies in plants have primarily relied on in silico methods. By using whole genome sequences, 35 aquaporin genes were identified in Arabidopsis , 33 from Oryza sativa L. , 28 from Vitis vinifera L.  and 23 from a moss, Physcomitrella patens . Recently, 55 full-length aquaporins have been analyzed from Populus trichocarpa genome sequence data . Expression sequence tag (EST) data analysis also identified the presence of at least 33 aquaporin genes from Zea mays L. . In addition, many aquaporin isoforms have also been isolated from various plants including Triticum aestivum L. , Nicotiana tabacum L. , and Pisum sativum L. .
Although PIP, TIP, NIP and SIP subfamilies are conserved in plants, homology comparisons demonstrate that plant aquaporins have divergent sequence and function. For example, as a result of sequence divergence, the PIP subfamily has been classified further into two subgroups, PIP1 and PIP2. Aquaporins from each PIP subgroup can act individually in a different manner  or may interact together as a heterodimer to facilitate subcellular trafficking toward the plasma membrane [13, 14]. In cotton, to date four PIP members have been characterized [15, 16]. TIPs are divided phylogenetically into 5 different subgroups  and δ-TIP represented the first identified aquaporin gene in cotton . The NIP proteins were initially thought to only be present in the nodules of nitrogen fixing legumes such as soybean [2, 18]. However, NIP proteins have also been isolated from many non-leguminous plants including Arabidopsis , rice , and maize  and are known to represent a less conserved plant-specific aquaporin subfamily. Compared to PIP and TIP aquaporin subfamilies, the SIP aquaporin subfamily is not as well characterized. In Arabidopsis, SIP members appear to localize to the endoplasmic reticulum (ER) . The XIP is a newly discovered, phylogenetically distinct subfamily and has been found widely in moss, fungi, and dicot plants . To date, extensive functional characterization of the XIP subfamily has not been reported .
The role of aquaporins in plant water relations has been demonstrated structurally and physiologically [22, 23]. As established earlier in human erythrocytes and bovine lens cells, the functional role of plant aquaporins is quite similar to that of animal aquaporins [24, 25]. As a characteristic transmembrane channel protein, aquaporins have 6 membrane-spanning domains with two cytoplasmic termini. An additional important structural feature is the Asn-Pro-Ala (NPA) motif that is conserved in loops B (LB) and E (LE), in which two NPA motifs are placed in two short, fold-back alpha helices following second and fifth transmembrane helices, respectively. Along with aromatic/Arginine (ar/R) selective filters, this conserved NPA motif is known to provide substrate selectivity for molecular transport . The expression of each aquaporin gene member is regulated differentially. Some aquaporins are constitutively expressed while many others are controlled in a tissue specific and environmentally sensitive manner [27, 28]. In addition, proper subcellular localization represents another layer of mechanistic regulation of aquaporin activity that probably relies on its ability to form multimers between members of different subgroups .
While a great deal is known about aquaporin proteins and the genes that encode them in a wide variety of plant genera and species, very little is known about the aquaporins in cotton. Although the allotetraploid chromosome structure of upland cotton makes it an excellent model system to study polyploidization and genome duplication by mechanisms many crops have used to evolve from diploid ancestors [29, 30], the complicated genetic structure of upland cotton challenges efforts aimed to discover gene families such as the aquaporins. Derived from two diploid species (AA and DD), the allopolyploid composition of the cotton genome affects gene expression primarily due to different contributions of alloalleles combined with allele-specific gene silencing [17, 31]. In fact, several alloalleles of aquaporin genes have been described in cotton  and maize [32, 33], although no allele-specific gene expression analysis has been described for aquaporins. Thus, it is interesting to reveal how the evolutionally conserved, multigene aquaporin family behaves in polyploid species such as cotton. To our knowledge there have only been seven aquaporin genes reported from allotetraploid cotton in the literature [15–17]. Therefore, a first step in investigating the role of aquaporins in cotton water relations is to identify the aquaporin gene family. With that in mind, our objective in this study was to identify cotton aquaporin genes and investigate both their structural properties and expression patterns.
Isolation of the aquaporin gene family from upland cotton
Using PCR cloning and EST data, we identified 71 candidate cotton aquaporin genes. Information including gene names, accession numbers, identification methods, the length of deduced polypeptides, and gene homology is summarized in Table 1. Twenty-five genes were identified by both PCR and EST homology searches. Twenty genes were detected by PCR cloning alone (See Additional file 1 for the sequence information of primers used in PCR cloning) and 26 genes were identified using only bioinformatic database search methods. Eighteen out of 45 PCR-generated clones were isolated repeatedly up to ten times while 27 PCR clones were identified once. Among these 27 PCR clones, 11 were also found using bioinformatic database search methods. RACE PCR was also used to clone the full-length sequence of PIP1;11, TIP1;7, TIP2;3, and XIP1;1.
By comparing amino acid sequences of cotton aquaporins with previously identified plant aquaporins, cotton aquaporin candidates were successfully classified as 28 PIPs (15 PIP1s and 13 PIP2s), 23 TIPs (14 TIP1s and 9 other TIPs), 12 NIPs, 7 SIPs and 1 XIP (Figure 1). Eight of the deduced amino acid sequences (PIP1;13, PIP1;14, PIP2;11, PIP2;12, PIP2;7, TIP1;3, TIP4;2 and NIP6;6) encoded 100% identical sequences to other members (Additional file 2), and 63 cotton aquaporin protein sequences (encoded from 71 genes) were phylogenetically analyzed with members from other plants (Figure 1). As a rule, in naming the identified cotton aquaporin genes, we followed previous nomenclature of other plants guided by sequence homology and phylogenetic analysis. To systematically classify cotton aquaporin genes and determine phylogenetic relationships with aquaporin genes from other plants, full-length aquaporin members from Arabidopsis, rice, grape and Populus were included in phylogenetic analysis and the result is presented in Figure 1. For XIP aquaporin comparisons, several XIPs were also added from moss (P. patens), tomato, tobacco, and common bean .
Overall, cotton aquaporin genes followed the phylogenetic clustering pattern as previously reported in other plants [4, 7]. PIP subfamily members were further divided into PIP1 and PIP2 subgroups and TIPs were partitioned into TIP1 and two other TIP subgroups (TIP2 and TIP4). Similar to Populus aquaporins, many cotton PIP and TIP members had a tendency to cluster with other members in the same subfamily. Four and one subgroups appeared for NIP (NIP1, NIP2, NIP5, and NIP6) and SIP (SIP1), respectively. We did not identify cotton members of several subgroups identified in other plants; these subgroups included TIP3, NIP3, and NIP4. In Table 2, sequence information is summarized to show conserved amino acid residues, the prediction of transmembrane domains, and subcellular localization.
By analyzing 197 total aquaporin genes from cotton and several different plant species, many aquaporin members from allotetraploid cotton appeared phylogenetically more close to members from Populus and grape for PIP and TIP subfamilies. The close relationship between cotton and Populus aquaporins was less apparent for NIP, SIP, and XIP subfamilies.
Cotton aquaporin gene family
PIP1 open reading frames (ORFs) of full-length clones were predicted to encode polypeptides of 257 - 289 amino acids in length with 82 - 100% sequence identity in cotton. It has been shown that in many crops including cotton, there are duplicated copies of genes resulting from genome merger and/or genome doubling [34, 35]. In the present study, we identified several aquaporin genes with very high sequence similarity sharing 99 -100% identity in predicted amino acid sequences. These candidates include 'PIP1;1, PIP1;11, and PIP1;14', and 'PIP1;3, PIP1;4, PIP1;13 and PIP1;15' (Additional file 2). More detailed information for these genes including expression analysis is summarized in Table 3. The length of the PIP2 ORF ranged from 261 to 286 amino acids with 71 - 100% identity. PIP2;2, PIP2;4, and PIP2;5 are 100% identical to PIP2;12, PIP2;11, and PIP2;7, respectively. In addition, PIP2;3 and PIP2;13 shared 99% amino acid sequence identity. PIP1 and PIP2 groups showed 63 - 81% identity with each other. Structurally, PIP1 had a longer extension at the N-terminus, while PIP2 had a longer C-terminal end (Additional file 3). However, as shown in Table 1, the overall lengths of estimated ORFs were quite similar between PIP1 and PIP2. All of the PIP members contained conserved dual NPA motifs in loops B and E, respectively; whereas the aromatic/Arg (ar/R) selectivity filter harbored identical residues, Phe (F), His (H), Thr (T), and Arg (R) in all of the PIP members except PIP2;8 where Phe (F) was replaced by Val (V). In addition, four out of five (P1 to P5) Froger's positions, recognized as differentially conserved residues between aquaporins and aquaglyceroporins and thereby providing functional specificities, were conserved in all of the full-length PIP sequences. Only the P1 site was less conserved, as one of three amino acids Glu (E), Met (M), and Gln (Q) appeared in this position (Table 2). In addition to dual NPA motifs, the ar/R selectivity filter, and five Froger's positions, it was reported that Val (V) for PIP2 and Ile (I) for PIP1 residues near the second NPA motif have been identified as key residues for water channel activity in radish . The Val (V) and Ile (I) residues were also conserved in cotton PIP1 and PIP2 members, respectively.
The predicted polypeptides of TIP1 subfamily members ranged from 249 - 284 amino acids in length and showed 77 - 100% identity. However, 'TIP1;1, TIP1;3, and TIP1;8' and 'TIP1;5 and TIP1;14' shared 99 - 100% amino acid sequence identity (Table 1). Nine other TIP members belonged to TIP2 and TIP4 with ORF lengths ranging from 245 to 250 amino acids and 75 - 100% identity in each subgroup. Within 'TIP2;1, TIP2;2, TIP2;3 and TIP2;5', 'TIP2;6 and TIP2;7', and 'TIP4;1 and TIP4;2' we also observed very high sequence similarity (Additional file 2). The ar/R selectivity filter in TIP1 was His (H), Ile (I), Ala (A), and Val (V) with no exception; whereas the five Froger's positions were also very well conserved in all predictable sites as Thr (T), Ala (A), Ser (S), Tyr (Y), and Trp (W). Conservation in the ar/R selectivity filter and five Froger's positions provides evidence that TIP1 aquaporins likely perform similar biological functions. In other TIPs, these predicted functional sites were perfectly conserved within each subgroup and P1 - P5 were Thr (T), Ser (S), Ala (A), Tyr (Y), and Trp (W) in all TIPs (Table 2). Two conserved NPA motifs were also observed in this subfamily. Most of the full-length TIP protein sequences were predicted to be localized to the tonoplast or plasma membrane (Table 2).
The current study represents the first description of NIP aquaporins from allotetraploid cotton. Lengths of predicted NIP polypeptide sequences were 259 - 288 amino acids. Twelve NIP gene members were present in four subgroups with a minimum of approximately 40% identity while showing sequence identities ranging from 96 to 100% within each subgroup. Characteristic residues were less conserved in the NIP subfamily in which low sequence identity was evident across whole sequences. The NPA motifs for NIP members also showed divergence inconsistent with PIP and TIP subfamilies, with amino acid conversions from Ala (A) to Ser (S), Thr (T) or Val (V). In two NIP5 members, Ala (A) residues from both NPA motifs were converted to Ser (S) and Val (V) in the first and second NPA motifs, respectively. In the case of NIP2;1, ar/R selectivity filters were very well conserved with Populus NIP2. Four amino acid residues, which include Gly (G), Ser (S), Gly (G), and Arg (R), show characteristics of the NIP2;1 group that have been identified as silicon transporters . Apart from cotton NIP2;1 and homologues in other plants (Populus and rice), AtNIP2;1 was phylogenetically not closely related to the NIP2;1 as shown in Figure 1. Based on EST sequence data and PCR sequences from cDNAs and genomic DNA, two of the NIP6 subgroup members, NIP6;1 and NIP6;2 showed very high sequence similarity to NIP6;6 (Table 1 and Table 3).
The current study represents the first description of SIP aquaporins from allotetraploid cotton. Predicted SIP polypeptides had relatively short ORFs ranging from 240 to 247 amino acids (Table 1). These proteins also shared low sequence identity with a minimum 45% and all of the identified cotton SIPs were classified phylogenetically in a single SIP1 subgroup. Sites of characteristic residues were quite divergent compared to other subfamilies, which provides evidence of different solute permeability. An Ala (A) residue present in the first NPA motif was converted to Thr (T) in four SIPs (Table 2). In addition, the Asn (N) residue present in the first NPA motif of SIP1;1 was converted to Asp (D) acid. This amino acid change (Asn (N) to other amino acids) is the only case of the conversion of Asn (N) in the NPA motif among all of the cotton aquaporins.
Overall, XIP aquaporins represent a recently discovered subfamily and the current study represents the first characterization of the specific XIP member from upland cotton. We identified a single, full-length cotton XIP gene coding for a 302 amino acid polypeptide. This polypeptide contains a distinct ar/R selectivity filter, Ile (I), Thr (T), Val (V), and Arg (R) (Table 2). In this gene, the first NPA motif was converted to NPV. By conducting a homology search using a D-genome G. ramondii GrXIP EST CO092422 that has 88% similarity to GhXIP1;1 at the deduced amino acid level, two additional cotton XIP EST sequences (GaXIP1;1 BG443509 and GaXIP1;2 BQ411475) were identified. These ESTs were derived from an A-genome species G. arboreum with identity of 96% and 61% to GhXIP1;1, respectively. The identification of an additional G. arboreum aquaporin provides evidence that at least one additional XIP copy may be present in the tetraploid G. hirsutum genome.
By comparing exon-intron tandem arrays predicted from several genomic and cDNA clones of cotton aquaporin genes, several structural features of interest were observed. PIP1;1 and PIP1;11 showed very high sequence homology (99%) with identical exon-intron structures and lengths (Figure 2). This structural identity was also conserved between PIP2;4 and PIP2;9, which were 98% identical. Moreover, these two sets of pairs from different subgroups, although having lower sequence homology, appeared structurally very similar. The gene structure exhibited three introns at similar locations, and lengths of exons and introns were almost identical as reported earlier [9, 16]. Consistent with the observation of Liu et. al. , two NPA motifs were found in the beginning of the second exon and in the middle of the third exon, respectively.
Exons were well conserved within each aquaporin subfamily (98 - 99% on average) compared to introns (94 - 95% on average). Meanwhile, in spite of highly similar exon-intron structure, the average identity between PIP1;11 and PIP2;4 was only 70% in four exons and 48% in three introns (Figure 2A). This structural and sequence similarity was also found in the TIP subfamily. Genomic sequences of two closely related genes, TIP1;1 and TIP1;3, showed these genes had at least one intron separating two exons. One TIP2 genomic clone identified in this study (TIP2;3) also had a similar exon-intron structure to TIP1 genes; however, their nucleotide sequences shared less than 65% identity (Figure 2A). This finding provides evidence that aquaporin genes have diverged at the nucleotide sequence level, while preserving structural characteristics such as the exon-intron splicing junction. Because of the location of primers used for genomic DNA amplification in our study, only one intron sequence was predicted in TIP1 and TIP2. Previously, Ferguson et al.  and Liu et al.  reported that GhγTIP1 (GhTIP1;2) and Ghδ-TIP (GhTIP2;1) contained two introns in their genomic sequences. Figure 2B also showed three additional genomic clones with complex gene structure. Particularly, NIP1;1 and NIP 6;1 genes had long introns with 3 and 4 exons, respectively. NIP6;1 and NIP6;2 also shared very high identity between partial intron sequences (data not shown).
Previous reports have suggested that aquaporins are present in all plant tissues and are regulated temporally and spatially depending on developmental stage and environmental conditions [38, 39]. Because the level of mRNA transcript is an important factor of gene regulation, we initially examined the expression of a set of aquaporin genes by semi-quantitative RT-PCR.
Six genes from PIP (PIP1;1, PIP1;14, PIP1;3, PIP1;6, PIP2;1, and PIP2;9), 5 genes from TIP (TIP1;8, TIP1;11, TIP2;3, TIP2;6, and TIP2;7), 3 each from NIP (NIP1;1, NIP2;1, and NIP6;2) and SIP (SIP1;1, SIP1;3, and SIP1;4), and XIP1;1 were analyzed to compare the abundance of mRNA transcripts in various tissues. The plant tissues represented were harvested from two developmental stages of roots and leaves, young stems, and fibers (Figure 3). Most of the PIP members were expressed in all of the tissues tested, except PIP1;6, which was not expressed in the mature root. PIP1;1, PIP1;14 and PIP2;9 were abundant in all tissues and constitutively expressed compared to other PIP members (Figure 3A). PIP1;6 and PIP2;1 showed higher expression levels in young root and mature leaf. For the TIP aquaporins, the levels of mRNA transcripts were variable across tissues and some were expressed tissue specifically. TIP1;8 was detected only in stem and fiber while TIP2;3 and TIP2;6 (TIP2;7) were most abundant in young root (Figure 3B). In general, NIP aquaporin genes were less abundantly expressed. Among the NIPs, NIP1;1 had relatively higher expression in young root and fiber, NIP2;1 in mature leaf, and NIP6;2 in young root and mature leaf. SIP1;1 and SIP1;4 aquaporin genes were constitutively and highly expressed in all tissues; whereas SIP1;3 was abundant in young root and fiber. Interestingly, although XIP1;1 was highly expressed in mature leaf tissues, no transcript was detected in roots (Figure 3C).
Analysis of cotton PUT contig sequences
Assembled EST data provides a useful resource for the identification and analyses of nucleotide sequence information. This is especially true for many polyploid crops such as cotton and wheat , when whole genomic sequences are not available. It is also important to use this information with care - especially when dealing with multigene families. Because sequences with high similarity are often assembled together into a single contig, it can result in inadvertent assembly-induced sequence recombination . After we initially identified aquaporin candidate genes, each of those genes were blasted against PlantGDB-assembled unique transcripts (PUT) sequences in PlantGDB http://www.plantgdb.org/. PlantGDB is a database of plant EST sequences that are assembled into contigs representing tentative unique genes .
Initially, PUT contigs corresponding to each aquaporin gene were identified. Then, to minimize potential errors in contig assemblies, sequence alignments of each PUT contig were visually inspected. This was accomplished, as suggested by Dong et. al. , by examining and reconstituting all sets of EST populations. Two interesting phenomena were uncovered from this analysis as follows. First, 10 PUT sequence contigs were identified as mixtures of two or three sub-contigs that could be separated and matched to an individual aquaporin gene (Table 3). Second, in seven out of ten PUTs analyzed, a subset of ESTs was differentiated from one another according to their tissue origin. Accordingly, we separated those PUT sequences into two or three individual aquaporin genes. For example, PUT41616 consisted of 18 ESTs which were divided into two aquaporins, PIP1;1 and PIP1;14. Ten of the 16 ESTs for PIP1;1 originated from fiber ESTs. The remaining two ESTs belonged to PIP1;14 and originated from stem ESTs (Additional file 4). A similar pattern was found for TIP2;1 and TIP2;3. In fact, both genes were isolated independently by PCR cloning and were matched to different ESTs. However, by comparing PUT contig data, the EST sequences representing TIP2;1 and TIP2;3 were shown to be a part of the same PUT contig, PUT3730. As a result of visual analysis of PUT3730, it appeared that 16 ESTs represented TIP2;1 while TIP2;3 was reconstituted by 12 other ESTs isolated from stem (5 ESTs) and root (2 ESTs). RT-PCR analysis also showed that TIP2;3 was highly abundant in young root, stem and leaf tissues, which supported the result of TIP2;3 abundance from the PUT analysis. From this analysis, it was possible to annotate cotton aquaporin genes more precisely. Furthermore, comparable expression data were obtained (Table 3) that supported RT-PCR data (Figure 3).
Highly similar and divergent cotton aquaporin genes
The significance of the multigene family of aquaporin transmembrane proteins is emerging from studies aimed at optimizing water and nutrient use efficiency. This large gene family has been shown to be highly diversified in plants and thus likely harbors functionally multifaceted behaviors in plants under various growth circumstances. Since the global importance of cotton as a primary natural fiber source in production agriculture is well established, our goal in this study was to identify all the members of the aquaporin family in the cotton genome. Toward this end, combined efforts were required from bioinformatic homology search and the cloning of cDNA and genomic DNA gene fragments. Bioinformatic sequence data of cotton are limited in both EST databases and an available genomic sequence; the majority of cotton EST databases consist of sequences known to be expressed in fiber tissues  and thus are not sufficient in expressed sequences from other plant tissues.
Our combined approach enabled us to identify a total of 71 aquaporin genes in cotton. The number of aquaporin genes described in this study almost doubles previously reported numbers within most single species and is greater than the largest number (55 members) recently identified Populus aquaporin genes . This increase is likely the result from highly similar aquaporin members within each aquaporin subfamily, primarily in PIP (28 in cotton vs. 15 in Populus) and TIP subfamilies (23 in cotton vs. 17 in Populus) (Figure 1 and Table 1). Meanwhile, the number of NIP and SIP aquaporin genes identified here are similar to the number identified in other plant species; hence, it is possible that more genes belonging to these subfamilies are yet to be isolated in cotton. It is also plausible that the large number of aquaporin genes identified in this study is somewhat inflated due to gene duplication, which has been reported in tetraploid cotton . Accordingly, determining the genome assignment (A or D) of each identified candidate aquaporin gene will be important to investigate the evolutionary history of cotton aquaporin genes during allotetraploid formation. In the case of XIP aquaporins, thus far only one member has been cloned in tetraploid cotton, while 6 have been cloned in Populus. From the comparison mentioned above between cotton and Populus aquaporins, it is plausible that genome merger/doubling during cotton domestication affected the expansion of PIP and TIP subfamilies while NIP, SIP, and XIP subfamilies were not affected or subsequently deleted after genome duplication. From the presence of three additional XIP EST sequences in A or D genome cotton species, it is also possible that tetraploid cotton may have evolved to contain more copies of aquaporin genes belonging to XIP subfamily. Also, as shown in Table 3, when we analyzed our sequence data along with PUT assembly contig sequences, a set of aquaporin gene pairs existed with several nucleotide substitutions while conserving their amino acid sequence. In these cases, most of the amino acid sites remained unchanged in spite of nucleotide substitution. Because we cloned PCR fragments from allotetraploid cotton, each cloned pair of genes with high sequence homology might represent duplicated copies present in the A and D genomes .
From the preliminary analysis, it appeared that several PCR clones identified as individual sequences belonged to the same PUT assembly contig. Those PCR sequences were pairs of TIP1;1 and TIP 1;3 (for PUT295101081), TIP2;1 and TIP2;3 (for PUT3730), and NIP6;1 and NIP6;2 (for PUT83990). Interestingly, we compared the partial aquaporin fragment previously isolated by Smart et al. from cotton fiber , and found the fragment differed from TIP2;4 and TIP2;5 by a single amino acid. Considering the polyploid nature of upland cotton, we decided to compare all candidate aquaporin genes with PUT contig sequences and subsequently inspected the assembled data visually in each PUT. This analysis allowed us to separate genes with high sequence similarity from a unique PUT transcript into individual aquaporin genes. In the case of the PIP1;1 contig from PlantGDB, PUT-165a-Gossypium_hirsutum-41616 consisted of 18 ESTs. Two of the 18 ESTs [GI84144149 and GI84144380] represented a different sequence which had 4 nucleotide differences. Therefore, we were able to differentiate PIP1;1 and PIP1;14 from the original contig, PUT41616 (Additional file 4). Moreover, these two ESTs [GI84144149 and GI84144380] were derived from the same tissue (stem). This finding prompted us to differentiate EST sequences from one another in a PUT contig assembly sequence. Because of the highly conserved sequence similarity, this type of combined assembling event has been previously reported when analyzing ESTs derived from allotetraploid cotton . Likewise, a PUT contig (PUT-165a-Gossypium_hirsutum-368101081) assembled from 13 ESTs was separated into two individual aquaporin genes. One of the two genes was PIP2;3, originally cloned as a PCR fragment, and the other was PIP2;13 which differs at 9 nucleotide positions from PIP2;3 (Table 3). When predicted proteins were aligned together, six of nine predicted amino acid positions remained unchanged. One of the conserved positions was a P2 Froger's position known as a residue of functional importance (data not shown) . It is also interesting that all of the EST sequences for PIP2;3 are derived from samples containing stems while PIP2;13 ESTs are from a mixture of tissues.
Although we detected an XIP gene in cotton, to date, XIP genes have not been identified in monocots or Arabidopsis. Hence, it is plausible that functional characteristics of XIP aquaporins have not been evolutionarily conserved to the extent of other aquaporin subfamilies such as PIP and TIP. Our data indicates that GhXIP1;1 does not accumulate in root tissue. However, it is highly expressed in mature leaf tissue, and moderately in other aerial tissues (Figure 3C). This expression data, along with the presence of a specialized ar/R filter in XIP, implies that XIP may have different substrate specificity or affect solute transport in different manners from other aquaporin subfamilies.
Sequence-function relationship in cotton aquaporins
An obvious question drawn from the existence of at least 71 cotton aquaporin genes is why are so many aquaporins necessary? Subcellular localization of all PIP members is predicted to reside in the plasma membrane (Table 2). Therefore, an abundant number of channel proteins, PIP1 and PIP2 would be important for movement of water and other non-polar small molecules. These PIP isoforms are known to form multimeric tetramers in vivo and in vitro. For example, PIP1 isoforms in maize and rice are not functionally expressed alone in oocytes. This defect is alleviated by the co-expression of PIP2 isoforms causing the correct localization toward the plasma membrane and/or formation of a heterotetramer [13, 46, 47]. Thus, the multigenic nature of aquaporins in plants might facilitate their ability to regulate transport activities for water and other small molecules by redundantly modulating the abundance or multiple pairing of aquaporin water channels as demonstrated earlier . In addition, it was demonstrated that functionally distinct vacuoles were labeled with different combinations of TIP antibodies in plant cells, supporting the diversification of the TIP subfamily in relation to vacuolar differentiation . It is important to note that questions have been raised against the possible roles that TIPs play as different vacuole markers . Recently, using confocal microscopy, distinct subcellular localization has been detected for ten Arabidopsis TIPs that showed cell-type or tissue-specific expression .
Highly conserved residues have been shown to be functionally important for substrate filtering and gating of aquaporin channel proteins . Considering the NIP subfamily of aquaporins, it is noteworthy that the predicted Si transporters in the aquaporin channel protein family belong to NIP2 aquaporin genes . As demonstrated in Table 2, four amino acids (G, S, G, R) in NIP2;1 are very well conserved at the ar/R selectivity filter across plants including cotton . However, Arabidopsis NIP2;1 is an exception, as it is impermeable to Si and structurally less conserved compared to other NIP2;1 members . Hence, it appears that AtNIP2;1 is phylogenetically not closely related to cotton NIP2;1, PtNIP2;1, and OsNIP2;1. Further investigations on the role of NIP2;1/silicon transporters in cotton and other dicot plants are needed since the Si transporter activity of NIP2;1 has been studied predominantly in monocots.
In addition, by comparing 153 MIPs among plants and animals, it has been demonstrated that five amino acid residues were distinguishable between aquaporin and glycerol channel proteins . The importance of these residues was partially confirmed by modifying two residues in P4 and P5 sites of an insect aquaporin . Therefore, the ar/R selectivity filter and Froger's position mentioned in Table 2 will provide a basis to understand a broad spectrum of aquaporin activities in cotton.
In this study, we demonstrated that the cotton aquaporins consist of a large and highly similar multi-gene family phylogenetically divided into 5 subfamilies. The members of this gene family represent potential targets to modify the water use properties of cotton and may provide a target to manipulate water/nutrient uptake and photosynthesis efficiency [57, 58]. Despite recent progress on the functional identification of aquaporins [59–61], the contribution of each aquaporin protein on substrate uptake and plant physiology remains to be elucidated. This will be achieved through sophisticated approaches such as global expression studies, knock-out experiments, and promoter analyses as well as substrate specificities under various physiological conditions in relation to water balance and nutrient uptake in cotton and other plant systems.
Plant Materials and Growth Conditions
Young leaf, stem, and root tissues were harvested from 1 month old plants (G. hirsutum, cv. TM-1) grown in a growth chamber (16 h light/8 h dark, 35°C/26°C). TM-1 was selected as it is considered the G. hirsutum genetic standard and has been maintained by repeated self-pollination since its release in 1970 . Mature leaf and root tissues of TM-1 were harvested from field-grown cotton plants at the flowering stage. Fiber tissues were obtained 15-days post anthesis (DPA) from field grown plants. Leaf, stem and root tissues were frozen with liquid nitrogen and preserved at - 80°C before grinding. Fibers were submerged in RNA-later solution (Ambion) and stored at 4°C until RNA isolation.
RNA and DNA Isolation
All tissues were ground extensively in liquid nitrogen using a mortar and pestle. Following the general procedure of Wan and Wilkins, RNA was isolated using the XT buffer system with the addition of chloroform/iso-amyl alcohol extractions and LiCl precipitation steps . For RT-PCR, 1 μg of total RNA was treated with Turbo DNase (Ambion) followed by phenol extraction and alcohol precipitation. For 5'- and 3'-RACE (Rapid Amplification of cDNA Ends) PCR, mRNAs were purified using the OligoTex mRNA purification kit (Qiagen) from each of 20 μg of total RNAs of mixed tissues (young and mature roots and leaves, young stem). Purified mRNA was treated with Turbo DNase followed by phenol extraction and alcohol precipitation.
Genomic DNA was also isolated from mature leaf tissue following a modification of the RNA isolation procedure. Briefly, 0.6 volume of isopropyl alcohol was mixed with the supernatant obtained from the LiCl RNA precipitation step as above. After incubation at - 20°C for 1 hour, the precipitated pellet was dissolved in 0.9 ml of water and then 1/3 volume of 5 M potassium acetate solution was added followed by 30 min incubation at -20°C. After centrifugation, DNA was precipitated by adding 2/3 volume of isopropyl alcohol to the supernatant and incubating for 1 hour at - 20°C. After washing with 70% alcohol, the dried pellet was resuspended in 1 ml TE buffer and DNA concentration was measured with a UV-spectrophotometer (DU 730, Beckman Coulter).
PCR amplification, cloning and sequencing
Using sequence alignment analysis of known aquaporin genes from cotton and several other plants, conserved sequence regions were selected for use in designing degenerate primers in the forward and reverse direction (Additional file 1). A suitable reaction condition for each primer set was determined using genomic DNA prior to the actual reaction. Amplification of aquaporin genes was performed by RT-PCR and genomic DNA PCR using a DNA thermocycler (DNA Engine Dyad, Bio-Rad). RT- PCR reactions were performed with M-MuLV Reverse Transcriptase and oligo d(T) primer. High fidelity Pfusion hot start DNA polymerase was used to amplify desired fragments with degenerate primers following the manufacturer's instruction (NEB). For each primer set, a touch-down PCR condition was employed with various annealing temperatures. Twenty ng of genomic DNA or 1/20 volume of 1st-strand cDNA product was added as a template in a 20 μl PCR reaction volume. PCR products were electrophoresed and size separated in EtBr-containing agarose gels (0.8% - 1.2%) and desired bands were recovered under UV light using an Alpha Imager 3400 (Alpha Innotech).
Gene-cleaned PCR fragments were ligated to pCR4 Blunt-TOPO vectors followed by subsequent transformation into TOP10 E. coli competent cells. After colony PCR and the selection of positive clones, plasmids were isolated from bacterial clones grown in 96-well plates and bi-directional sequencing was performed using M13 forward and M13 reverse primers. For the 5' and 3' RACE PCR, an RNA adaptor was ligated to the 5' end of purified and decapped full-length messenger RNA (200 ng). Following, the ligation product was used for first strand cDNA synthesis. After initial and nested PCR amplification reactions (GeneRacer Kit, Invitrogen), amplified RACE PCR products were cloned and sequenced as above for the identification of cDNA ends.
Three to eleven recombinant plasmids per PCR fragment were subjected to bi-directional sequencing allowing for repeated isolation of identical clones from different sources of PCR fragments corresponding to about 660 sequencing reactions (Table 1). For the expression study, RT-PCR was performed similarly as mentioned above using a set of gene-specific primers. Primers used for the expression study and RACE-PCR are available upon request.
Homology search and sequence analysis
Sequence information from NCBI (National Center for Biotechnology Information, http://www.ncbi.nlm.nih.gov/) was used for various BLAST searches, including BLASTN, BLASTX, BLASTP, and TBLASTN. Using combinations of these blast homology searches, several known cotton aquaporin genes were queried against the cotton EST database to identify expressed cotton (G. hursutum) aquaporin sequences. Sequences obtained were analyzed by 6-frame translation to distinguish full-length, intact ORFs from partial or pseudogene-like incomplete sequences. To identify additional cotton aquaporin genes, several Arabidopsis aquaporin genes including members belonging to NIP and SIP subfamilies were also blasted by repeating homology searches. The top three to five intact EST sequences were chosen as candidate aquaporin genes from each homology comparison (E value below e-50 for the BLASTN). Genomic DNA and cDNA sequences obtained from sequencing of amplified clones were subjected to BLAST analyses and only clones identified as aquaporins with intact coding sequences were considered further. Genomic DNA clones were compared with ESTs, known aquaporin genes, and cDNA clones obtained in this study to determine intron-exon linearity by positioning.
We also used PlantGDB-assembled unique transcripts (PUT) data which provided sequence contigs assembled by multiple alignment using EST sequences from NCBI. All predicted amino acid sequences from cotton aquaporin genes (ESTs, cloned cDNAs and exon contigs from cloned genomic DNA) were used for phylogenetic analysis along with other plant aquaporin genes using CLUSTAL W2 http://www.ebi.ac.uk/Tools/clustalw2/index.html and TreeView program. The reliability of branches in resulting trees was supported with 1,000 bootstrap resamplings.
polymerase chain reaction.
Waddle BA: Crop growing practices. Cotton. Edited by: Kohel RJ, Lewis CF. 1984, Madison, WI: ASA-CSSA-SSSA, 233-263. 1984
Fortin MG, Morrison NA, Verma DP: Nodulin-26, a peribacteroid membrane nodulin is expressed independently of the development of the peribacteroid compartment. Nucleic Acids Res. 1987, 15 (2): 813-824. 10.1093/nar/15.2.813.
Danielson JA, Johanson U: Unexpected complexity of the aquaporin gene family in the moss Physcomitrella patens. BMC Plant Biol. 2008, 8: 45-10.1186/1471-2229-8-45.
Johanson U, Karlsson M, Johansson I, Gustavsson S, Sjovall S, Fraysse L, Weig AR, Kjellbom P: The complete set of genes encoding major intrinsic proteins in Arabidopsis provides a framework for a new nomenclature for major intrinsic proteins in plants. Plant Physiol. 2001, 126 (4): 1358-1369. 10.1104/pp.126.4.1358.
Sakurai J, Ishikawa F, Yamaguchi T, Uemura M, Maeshima M: Identification of 33 rice aquaporin genes and analysis of their expression and function. Plant Cell Physiol. 2005, 46 (9): 1568-1577. 10.1093/pcp/pci172.
Fouquet R, Leon C, Ollat N, Barrieu F: Identification of grapevine aquaporins and expression analysis in developing berries. Plant Cell Rep. 2008, 27 (9): 1541-1550. 10.1007/s00299-008-0566-1.
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: 134-10.1186/1471-2229-9-134.
Chaumont F, Barrieu F, Wojcik E, Chrispeels MJ, Jung R: Aquaporins constitute a large and highly divergent protein family in maize. Plant Physiol. 2001, 125 (3): 1206-1215. 10.1104/pp.125.3.1206.
Forrest KL, Bhave M: Major intrinsic proteins (MIPs) in plants: a complex gene family with major impacts on plant phenotype. Funct Integr Genomics. 2007, 7 (4): 263-289. 10.1007/s10142-007-0049-4.
Siefritz F, Biela A, Eckert M, Otto B, Uehlein N, Kaldenhoff R: The tobacco plasma membrane aquaporin NtAQP1. J Exp Bot. 2001, 52 (363): 1953-1957. 10.1093/jexbot/52.363.1953.
Schuurmans JA, van Dongen JT, Rutjens BP, Boonman A, Pieterse CM, Borstlap AC: Members of the aquaporin family in the developing pea seed coat include representatives of the PIP, TIP, and NIP subfamilies. Plant Mol Biol. 2003, 53 (5): 633-645. 10.1023/B:PLAN.0000019070.60954.77.
Zelazny E, Miecielica U, Borst JW, Hemminga MA, Chaumont F: An N-terminal diacidic motif is required for the trafficking of maize aquaporins ZmPIP2;4 and ZmPIP2;5 to the plasma membrane. Plant J. 2009, 57 (2): 346-355. 10.1111/j.1365-313X.2008.03691.x.
Fetter K, Van Wilder V, Moshelion M, Chaumont F: Interactions between plasma membrane aquaporins modulate their water channel activity. Plant Cell. 2004, 16 (1): 215-228. 10.1105/tpc.017194.
Zelazny E, Borst JW, Muylaert M, Batoko H, Hemminga MA, Chaumont F: FRET imaging in living maize cells reveals that plasma membrane aquaporins interact to regulate their subcellular localization. Proc Natl Acad Sci USA. 2007, 104 (30): 12359-12364. 10.1073/pnas.0701180104.
Li DD, Wu YJ, Ruan XM, Li B, Zhu L, Wang H, Li XB: Expression of three cotton genes encoding the PIP proteins are regulated in root development and in response to stresses. Plant Cell Rep. 2009, 28 (2): 291-300. 10.1007/s00299-008-0626-6.
Liu D, Tu L, Wang L, Li Y, Zhu L, Zhang X: Characterization and expression of plasma and tonoplast membrane aquaporins in elongating cotton fibers. Plant Cell Rep. 2008, 27 (8): 1385-1394. 10.1007/s00299-008-0545-6.
Ferguson DL, Turley RB, Kloth RH: Identification of a delta-TIP cDNA clone and determination of related A and D genome subfamilies in Gossypium species. Plant Mol Biol. 1997, 34 (1): 111-118. 10.1023/A:1005844016688.
Sandal NN, Marcker KA: Soybean nodulin 26 is homologous to the major intrinsic protein of the bovine lens fiber membrane. Nucleic Acids Res. 1988, 16 (19): 9347-10.1093/nar/16.19.9347.
Weig A, Deswarte C, Chrispeels MJ: The major intrinsic protein family of Arabidopsis has 23 members that form three distinct groups with functional aquaporins in each group. Plant Physiol. 1997, 114 (4): 1347-1357. 10.1104/pp.114.4.1347.
Mitani N, Yamaji N, Ma JF: Identification of maize silicon influx transporters. Plant and Cell Physiology. 2009, 50 (1): 5-12. 10.1093/pcp/pcn110.
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): 5814-5820.
Kaldenhoff R, Ribas-Carbo M, Sans JF, Lovisolo C, Heckwolf M, Uehlein N: Aquaporins and plant water balance. Plant Cell Environ. 2008, 31 (5): 658-666. 10.1111/j.1365-3040.2008.01792.x.
Maurel C: Plant aquaporins: novel functions and regulation properties. FEBS Lett. 2007, 581 (12): 2227-2236. 10.1016/j.febslet.2007.03.021.
Preston GM, Carroll TP, Guggino WB, Agre P: Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein. Science. 1992, 256 (5055): 385-387. 10.1126/science.256.5055.385.
Mulders SM, Preston GM, Deen PM, Guggino WB, van Os CH, Agre P: Water channel properties of major intrinsic protein of lens. J Biol Chem. 1995, 270 (15): 9010-9016. 10.1074/jbc.270.15.9010.
Tajkhorshid E, Nollert P, Jensen MO, Miercke LJ, O'Connell J, Stroud RM, Schulten K: Control of the selectivity of the aquaporin water channel family by global orientational tuning. Science. 2002, 296 (5567): 525-530. 10.1126/science.1067778.
Alexandersson E, Fraysse L, Sjovall-Larsen S, Gustavsson S, Fellert M, Karlsson M, Johanson U, Kjellbom P: Whole gene family expression and drought stress regulation of aquaporins. Plant Mol Biol. 2005, 59 (3): 469-484. 10.1007/s11103-005-0352-1.
Boursiac Y, Chen S, Luu DT, Sorieul M, van den Dries N, Maurel C: Early effects of salinity on water transport in Arabidopsis roots. Molecular and cellular features of aquaporin expression. Plant Physiol. 2005, 139 (2): 790-805. 10.1104/pp.105.065029.
Zhang HB, Li Y, Wang B, Chee PW: Recent advances in cotton genomics. Int J Plant Genomics. 2008, 2008: 742304-
Chen ZJ: Genetic and epigenetic mechanisms for gene expression and phenotypic variation in plant polyploids. Annu Rev Plant Biol. 2007, 58: 377-406. 10.1146/annurev.arplant.58.032806.103835.
Adams KL, Cronn R, Percifield R, Wendel JF: Genes duplicated by polyploidy show unequal contributions to the transcriptome and organ-specific reciprocal silencing. Proc Natl Acad Sci USA. 2003, 100 (8): 4649-4654. 10.1073/pnas.0630618100.
Gaspar M, Bousser A, Sissoëff I, Roche O, Hoarau J, Mahé A: Cloning and characterization of ZmPIP1-5b, an aquaporin transporting water and urea. Plant Science. 2003, 165 (1): 21-31. 10.1016/S0168-9452(03)00117-1.
Lopez F, Bousser A, Sissoeff I, Hoarau J, Mahe A: Characterization in maize of ZmTIP2-3, a root-specific tonoplast intrinsic protein exhibiting aquaporin activity. J Exp Bot. 2004, 55 (396): 539-541. 10.1093/jxb/052.
Cronn RC, Small RL, Wendel JF: Duplicated genes evolve independently after polyploid formation in cotton. Proc Natl Acad Sci USA. 1999, 96 (25): 14406-14411. 10.1073/pnas.96.25.14406.
Doyle JJ, Flagel LE, Paterson AH, Rapp RA, Soltis DE, Soltis PS, Wendel JF: Evolutionary genetics of genome merger and doubling in plants. Annu Rev Genet. 2008, 42: 443-461. 10.1146/annurev.genet.42.110807.091524.
Suga S, Maeshima M: Water channel activity of radish plasma membrane aquaporins heterologously expressed in yeast and their modification by site-directed mutagenesis. Plant Cell Physiol. 2004, 45 (7): 823-830. 10.1093/pcp/pch120.
Liu Q, Wang H, Zhang Z, Wu J, Feng Y, Zhu Z: Divergence in function and expression of the NOD26-like intrinsic proteins in plants. BMC Genomics. 2009, 10: 313-10.1186/1471-2164-10-313.
Wudick MM, Luu DT, Maurel C: A look inside: localization patterns and functions of intracellular plant aquaporins. New Phytol. 2009, 184: 289-302. 10.1111/j.1469-8137.2009.02985.x.
Heinen RB, Ye Q, Chaumont F: Role of aquaporins in leaf physiology. J Exp Bot. 2009, 60 (11): 2971-2985. 10.1093/jxb/erp171.
Forrest KL, Bhave M: The PIP and TIP aquaporins in wheat form a large and diverse family with unique gene structures and functionally important features. Funct Integr Genomics. 2008, 8 (2): 115-133. 10.1007/s10142-007-0065-4.
Udall JA, Swanson JM, Haller K, Rapp RA, Sparks ME, Hatfield J, Yu Y, Wu Y, Dowd C, Arpat AB, et al: A global assembly of cotton ESTs. Genome Res. 2006, 16 (3): 441-450. 10.1101/gr.4602906.
Dong Q, Lawrence CJ, Schlueter SD, Wilkerson MD, Kurtz S, Lushbough C, Brendel V: Comparative plant genomics resources at PlantGDB. Plant Physiol. 2005, 139 (2): 610-618. 10.1104/pp.104.059212.
Udall JA, Swanson JM, Nettleton D, Percifield RJ, Wendel JF: A novel approach for characterizing expression levels of genes duplicated by polyploidy. Genetics. 2006, 173 (3): 1823-1827. 10.1534/genetics.106.058271.
Smart LB, Vojdani F, Maeshima M, Wilkins TA: Genes involved in osmoregulation during turgor-driven cell expansion of developing cotton fibers are differentially regulated. Plant Physiol. 1998, 116 (4): 1539-1549. 10.1104/pp.116.4.1539.
Froger A, Rolland JP, Bron P, Lagree V, Le Caherec F, Deschamps S, Hubert JF, Pellerin I, Thomas D, Delamarche C: Functional characterization of a microbial aquaglyceroporin. Microbiology. 2001, 147 (Pt 5): 1129-1135.
Dean RM, Rivers RL, Zeidel ML, Roberts DM: Purification and functional reconstitution of soybean nodulin 26. An aquaporin with water and glycerol transport properties. Biochemistry. 1999, 38 (1): 347-353. 10.1021/bi982110c.
Matsumoto T, Lian HL, Su WA, Tanaka D, Liu C, Iwasaki I, Kitagawa Y: Role of the aquaporin PIP1 subfamily in the chilling tolerance of rice. Plant Cell Physiol. 2009, 50 (2): 216-229. 10.1093/pcp/pcn190.
Jauh GY, Phillips TE, Rogers JC: Tonoplast intrinsic protein isoforms as markers for vacuolar functions. Plant Cell. 1999, 11 (10): 1867-1882. 10.1105/tpc.11.10.1867.
Hunter PR, Craddock CP, Di Benedetto S, Roberts LM, Frigerio L: Fluorescent reporter proteins for the tonoplast and the vacuolar lumen identify a single vacuolar compartment in Arabidopsis cells. Plant Physiol. 2007, 145 (4): 1371-1382. 10.1104/pp.107.103945.
Gattolin S, Sorieul M, Hunter PR, Khonsari RH, Frigerio L: In vivo imaging of the tonoplast intrinsic protein family in Arabidopsis roots. BMC Plant Biol. 2009, 9: 133-10.1186/1471-2229-9-133.
Maurel C, Verdoucq L, Luu DT, Santoni V: Plant aquaporins: membrane channels with multiple integrated functions. Annu Rev Plant Biol. 2008, 59: 595-624. 10.1146/annurev.arplant.59.032607.092734.
Chiba Y, Mitani N, Yamaji N, Ma JF: HvLsi1 is a silicon influx transporter in barley. The Plant Journal. 2009, 57 (5): 810-818. 10.1111/j.1365-313X.2008.03728.x.
Bansal A, Sankararamakrishnan R: Homology modeling of major intrinsic proteins in rice, maize and Arabidopsis: comparative analysis of transmembrane helix association and aromatic/arginine selectivity filters. BMC Struct Biol. 2007, 7: 27-10.1186/1472-6807-7-27.
Bienert GP, Thorsen M, Schussler MD, Nilsson HR, Wagner A, Tamas MJ, Jahn TP: A subgroup of plant aquaporins facilitate the bi-directional diffusion of As(OH)3 and Sb(OH)3 across membranes. BMC Biol. 2008, 6: 26-10.1186/1741-7007-6-26.
Froger A, Tallur B, Thomas D, Delamarche C: Prediction of functional residues in water channels and related proteins. Protein Sci. 1998, 7 (6): 1458-1468. 10.1002/pro.5560070623.
Lagree V, Froger A, Deschamps S, Hubert JF, Delamarche C, Bonnec G, Thomas D, Gouranton J, Pellerin I: Switch from an aquaporin to a glycerol channel by two amino acids substitution. J Biol Chem. 1999, 274 (11): 6817-6819. 10.1074/jbc.274.11.6817.
Ma JF, Tamai K, Yamaji N, Mitani N, Konishi S, Katsuhara M, Ishiguro M, Murata Y, Yano M: A silicon transporter in rice. Nature. 2006, 440 (7084): 688-691. 10.1038/nature04590.
Uehlein N, Lovisolo C, Siefritz F, Kaldenhoff R: The tobacco aquaporin NtAQP1 is a membrane CO2 pore with physiological functions. Nature. 2003, 425 (6959): 734-737. 10.1038/nature02027.
Javot H, Lauvergeat V, Santoni V, Martin-Laurent F, Guclu J, Vinh J, Heyes J, Franck KI, Schaffner AR, Bouchez D, et al: Role of a single aquaporin isoform in root water uptake. Plant Cell. 2003, 15 (2): 509-522. 10.1105/tpc.008888.
Schussler MD, Alexandersson E, Bienert GP, Kichey T, Laursen KH, Johanson U, Kjellbom P, Schjoerring JK, Jahn TP: The effects of the loss of TIP1;1 and TIP1;2 aquaporins in Arabidopsis thaliana. Plant J. 2008, 56 (5): 756-767. 10.1111/j.1365-313X.2008.03632.x.
Uehlein N, Otto B, Hanson DT, Fischer M, McDowell N, Kaldenhoff R: Function of Nicotiana tabacum aquaporins as chloroplast gas pores challenges the concept of membrane CO2 permeability. Plant Cell. 2008, 20 (3): 648-657. 10.1105/tpc.107.054023.
Kohel R, Richmond TR, Lewis CF: Texas Marker-1. Description of a genetic standard for Gossypium hirsutum L. Crop Science. 1970, 10: 670-671. 10.2135/cropsci1970.0011183X001000060019x.
Wan CY, Wilkins TA: A modified hot borate method significantly enhances the yield of high-quality RNA from cotton (Gossypium hirsutum L.). Anal Biochem. 1994, 223 (1): 7-12. 10.1006/abio.1994.1538.
Krogh A, Larsson B, von Heijne G, Sonnhammer EL: Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J Mol Biol. 2001, 305 (3): 567-580. 10.1006/jmbi.2000.4315.
Horton P, Park KJ, Obayashi T, Fujita N, Harada H, Adams-Collier CJ, Nakai K: WoLF PSORT: protein localization predictor. Nucleic Acids Res. 2007, W585-587. 10.1093/nar/gkm259. 35 Web Server
Emanuelsson O, Nielsen H, von Heijne G: ChloroP, a neural network-based method for predicting chloroplast transit peptides and their cleavage sites. Protein Sci. 1999, 8 (5): 978-984. 10.1110/ps.8.5.978.
We appreciate Dr. Paxton Payton for providing the RNA isolation protocol. We also appreciate the technical assistance provided by Antoine Barr, Fanny Liu, and Bobby Fisher. The authors would also like to thank Drs. Jonathan Wendel and Martin Wubben for providing excellent comments and suggestions that strengthened this manuscript. This project was supported by funding from CRIS No. 6657-21000-005-00D of the U.S. Department of Agriculture. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture.
W.P. participated in the experimental design, performed experiments, analyzed data, and wrote the manuscript. B.E.S. performed DNA sequencing and participated in writing the manuscript. P.J.B. participated in the experimental design and writing the manuscript. B.T.C participated in the experimental design, supervised all procedures, analyzed data and wrote the manuscript. All authors have read and contributed to the writing of the manuscript.
Electronic supplementary material
Additional file 1: Degenerate primers used in this study. Sequences, positions, and degeneracy of primers are indicated. (PDF 18 KB)
Additional file 2: Similarity within each aquaporin subgroup in cotton. The identity of deduced amino acid sequences was compared for all aquaporin subfamilies except XIP. (PDF 77 KB)
Additional file 3: Multiple sequence alignment of cotton aquaporins. Deduced amino acid sequences were aligned using the CLUSTALW 2.01 program. NPA motifs, bold black (italic in NPA denotes non-conserved residues); ar/R filters (H2, H5, LE1, and LE2) are highlighted in yellow; Froger's 5 positions (P1 - P5) are also marked bold above alignment. Gene names with bold letters represent partial sequences. (PDF 219 KB)
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Park, W., Scheffler, B.E., Bauer, P.J. et al. Identification of the family of aquaporin genes and their expression in upland cotton (Gossypium hirsutumL.). BMC Plant Biol 10, 142 (2010). https://doi.org/10.1186/1471-2229-10-142
- Upland Cotton
- Selectivity Filter
- Aquaporin Gene
- Plasma Membrane Intrinsic Protein
- Tonoplast Intrinsic Protein