Figures
Abstract
Background
Phospholipase C (PLC) is one of the major lipid hydrolysing enzymes, implicated in lipid mediated signaling. PLCs have been found to play a significant role in abiotic stress triggered signaling and developmental processes in various plant species. Genome wide identification and expression analysis have been carried out for this gene family in Arabidopsis, yet not much has been accomplished in crop plant rice.
Methodology/Principal Findings
An exhaustive in-silico exploration of rice genome using various online databases and tools resulted in the identification of nine PLC encoding genes. Based on sequence, motif and phylogenetic analysis rice PLC gene family could be divided into phosphatidylinositol-specific PLCs (PI-PLCs) and phosphatidylcholine- PLCs (PC-PLC or NPC) classes with four and five members, respectively. A comparative analysis revealed that PLCs are conserved in Arabidopsis (dicots) and rice (monocot) at gene structure and protein level but they might have evolved through a separate evolutionary path. Transcript profiling using gene chip microarray and quantitative RT-PCR showed that most of the PLC members expressed significantly and differentially under abiotic stresses (salt, cold and drought) and during various developmental stages with condition/stage specific and overlapping expression. This finding suggested an important role of different rice PLC members in abiotic stress triggered signaling and plant development, which was also supported by the presence of relevant cis-regulatory elements in their promoters. Sub-cellular localization of few selected PLC members in Nicotiana benthamiana and onion epidermal cells has provided a clue about their site of action and functional behaviour.
Citation: Singh A, Kanwar P, Pandey A, Tyagi AK, Sopory SK, Kapoor S, et al. (2013) Comprehensive Genomic Analysis and Expression Profiling of Phospholipase C Gene Family during Abiotic Stresses and Development in Rice. PLoS ONE 8(4): e62494. https://doi.org/10.1371/journal.pone.0062494
Editor: Miguel A. Andrade-Navarro, Max Delbrück Center for Molecular Medicine, Germany
Received: November 5, 2012; Accepted: March 22, 2013; Published: April 30, 2013
Copyright: © 2013 Singh et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors acknowledge Department of Biotechnology (DBT), Department of Science and Technology (DST) and Council for Scientific and Industrial Research (CSIR), INDIA for funding the research in GKP's lab. AS and PK acknowledge senior research fellowship from CSIR, India. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Lipid signaling is one of the major signaling networks triggered in plants as an adaptive response upon exposure to various environmental cues and stress stimuli. Initial impact of a stress stimulus usually happens on the cell membrane and it leads to the hydrolysis of membrane lipids. This process is mediated by phospholipases as various stress stimuli activate phospholipase enzymes, which then catalyse the initial step of phospholipid breakdown and leads to generation of multiple lipid-derived second messengers [1]–[3]. Phospholipase C (PLC) constitutes an important group of lipid hydrolysing enzymes in animals and plants. Two major categories of PLCs have been identified in the plants based on their affinities to different substrates. A well-studied group of phosphatidylinositol-specific PLCs (PI-PLCs), which specifically act upon phosphatidylinositides (PIP2) at the membrane and results in the generation of second messengers such as diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3). In animals, DAG remains attached to the membrane and it activates protein kinase C (PKC) and IP3 is released into the cytoplasm where it bind to the ligand gated Ca2+ channel (IP3 receptors) in the intracellular membranes and leads to the release of Ca2+ from the intracellular reservoirs [4]. However, plant cell lack the equivalents of animal PKC and IP3 receptors, therefore the exact function of PLC reaction products DAG and IP3 remains enigmatic in plants. Rather, it has been postulated that the phosphorylated products of DAG i.e. phosphatidic acid (PA) and diacylglycerol pyrophosphate (DGPP), and hexakisphosphate (IP6), which is the phosphorylated product of IP3 may function as second messengers in plants [5]–[10]. Another recently identified class of PLCs in plants is phosphatidylcholine-PLC (PC-PLC), which preferentially hydrolyse phosphatidylcholine (PC) but can also act upon other lipids such as phosphatidylethanolamine (PE) and therefore also referred as non-specific phospholipase C (NPC) [11]–[12]. Both plant and animal PLCs constitute a multigene family and are represented by different isoforms. Mammalian PI-PLC family has been comprised of 13 members, which have been divided into six isoforms β, γ, δ, ε, η and ζ on the basis of their domain structures and organization [13]–[15]. Arabidopsis comprised of nine PI-PLCs (AtPLC1-AtPLC9) [16]–[18] and six NPC (NPC1-NPC6) members in its genome [11]. Recently, six PI-PLC members have been characterised in the solanaceae plant tomato [4] and also in other plant species such as potato [19], pea [20], Physcomitrella [21], soybean [22] and Vigna radiata (Mung bean) [23]. Structurally, a plant PI-PLC is composed of a minimal set of domains including catalytic X domain and Y domain, essential for phosphoesterase activity, followed by Ca2+/phospholipid binding C2 domain at the C-terminus and an EF-hand motif like “EF Loop” is present at the N-terminus, however it is poorly conserved across the plant species [15], [18], [19], [24]. Plant PI-PLCs are structurally close to the mammalian PLCζ because both lack a typical Pleckstrin Homology (PH) domain, which is present in other mammalian PLC isoforms [13], [15], [18]. Although structures of several PI-PLCs have been deciphered in plants but knowledge about the structure of NPCs is miniscule. All the six Arabidopsis NPCs range 514–538 amino acid in size and comprised of three conserved domains, which are uncharacterised so far [11], [25]. Sequence analysis showed that Arabidopsis NPCs bear a high homology with bacterial PC-PLCs [11].
Different PLC members have been implicated in abiotic stress triggered signal transduction in various plant species. All Arabidopsis PI-PLC members (except AtPLC2) were found to be highly up-regulated under different abiotic stresses such as salinity, drought and cold [18]. Similarly, mung bean PI-PLC member Vr-PLC3 was readily induced by salinity and drought stresses [23]. Recently, Arabidopsis NPC4 was found to be involved in salt stress response in the roots [26]. In addition, some PLC members have also been found to be involved in plant development. The significant role has been suggested for the PI-PLCs in regulating cytosolic calcium level in response to auxin and ABA [10], [15], [27]. Suppression of PI-PLC leads to irregular pollen tube growth and improper plant development [10], [28]. Arabidopsis NPC3 and NPC4 have been implicated in the root development [25]. These reports suggest the involvement of PLCs in abiotic stress signaling and development in plant such as Arabidopsis and others but the knowledge related to the functions of PLCs is limited in monocot crop plants such as rice. It is expected that PLCs may perform similar function in crop plant rice. Moreover, a comprehensive genome wide account and expression profile of rice PLCs have not been presented till date. The possibility of direct connection between the expression profile and the functional role during abiotic stresses and development, enticed us to perform a genome wide identification and expression analysis of rice phospholipase C gene family.
In this study, we are reporting the entire set of phospholipase C encoding genes in the rice genome for the first time. The rice PLCs have been divided into phosphatidylinositol-PLC (PI-PLC) and phosphatidylcholine-PLC (PC-PLC) or nonspecific PLCs (NPCs, and will be named as NPCs in this manuscript here onwards) based on the domain structure, conserved motif and phylogeny. Detailed expression analysis has been carried out for all the PLCs employing microarray and real time PCR under three abiotic stresses i.e. salt, cold and drought and during various stages of vegetative and reproductive development. In addition, GFP based sub-cellular localization analysis has been performed for a few PLCs to yield a clue regarding their site of action in the cell.
Results
Identification and Genomic Distribution of Rice PLCs
Rice genome exploration by various strategies resulted in the identification of a total of nine non-redundant phospholipase C encoding genes. Demarcation of distinct and characteristic domains and sequence motifs by analysis tools such as simple modular architecture research tool (SMART) (http://smart.embl-heidelberg.de/), InterPro (http://www.ebi.ac.uk/Tools/InterProScan) and Pfam (http://www.pfam.sanger.ac.uk/) differentiated entire rice PLC gene family into two major classes, namely phosphatidylinositol specific-PLC (PI-PLCs) and nonspecific phospholipase C (NPC). PI-PLC subfamily is represented by four members, which are named as OsPLC1 to OsPLC4 and NPC subfamily is comprised of five members; OsNPC1 to OsNPC5. Gene structure analysis showed that all the PI-PLC genes are made up of multiple intron-exons and intron number varied from six to eight, whereas OsNPCs are simpler in gene structure and members such as OsNPC4 and OsNPC5 are intronless while other members have one to three introns (Figure 1A). All the rice PI-PLC genes were found to contain the catalytic PI-PLC-X (PF00388), PI-PLC-Y (PF00387) domain and Ca2+/phospholipid binding C2 domain (PF00168), whereas an EF hand like motif (PF09279) was found only in two members OsPLC1 and OsPLC4 (Figure 1B). All the OsNPC members harboured a characteristic catalytic phosphoesterase (PF04185) domain with highly conserved motifs I, II and III (Figure 1B, S1). The protein size of all the PLC members is comparable, with PI-PLCs ranging from 591–599 aa (OsPLC2 is the only exception with 491 aa) and all the NPCs falling in the narrow range of 521–548 aa (Table 1). Expression evidence could be obtained for entire PLC gene family in terms of full length cDNA, total ESTs and microarray profiles (Table 1).
(A) Exon-intron organization is shown for both PI-PLC and NPC groups of rice PLCs and the gene names are mentioned at left. Genes are shown according to their phylogenetic clustering and not in the order of their numbers. Purple bars represent the exon, lines represent the intron while grey colour bars indicate the un-translated region (UTR) both at 5′ and 3′ position. (B) Protein structure of rice PLC gene family is showing the presence of highly conserved characteristic domains PI-PLC-X (Pfam identity- PF00388), PI-PLC-Y (PF00387) and C2 (PF00168) in all the PI-PLC members while EF hand like motif (PF09279) was marked only in two of the members. Phosphoesterase (PF04185) domain is present in all the NPC members. Numbers on each domain depict amino acid residue at the start and end of a particular domain and direction of a protein is depicted by N and C terminal.
Phylogenetic Analysis
Phylogenetic analysis was performed by taking protein sequences of rice and Arabidopsis PLCs to understand the evolutionary relatedness of this gene family in monocot and dicot plant species. Based on the statistical analysis and high bootstrap support value OsPLC1, OsPLC2 and OsPLC3 have very high sequence homology and they make a separate small clade while OsPLC4 falls apart. Moreover, rice PI-PLCs made a phylogenetic clade with Arabidopsis PI-PLCs with very low bootstrap support value, suggested their diversification during the course of evolution even after being originated from common ancestor (Figure 2). On the other hand, rice NPCs fall in the same clade with Arabidopsis NPCs with very high bootstrap value, indicating a high sequence homology, common ancestory and similar evolutionary path for this group of genes in both the diverse plant species. The phylogenetic analysis helped in the nomenclature and classification of rice PLC genes.
An un-rooted neighbour joining phylogenetic tree was constructed from the protein sequences of rice and Arabidopsis PLCs, including both PI-PLCs and NPCs. Multiple sequence alignment was carried out using clustalX2.0 and the tree was generated using MEGA5. Rice and Arabidopsis PI-PLCs and NPCs are clustered together based on significant bootstrap value (>50%). Scale bar indicates 0.1 amino acid substitution per site.
Expression Analysis under Abiotic Stresses
Expression profile of entire rice PLC gene family was generated using Affymetrix rice genome arrays for the 7 days old rice seedling, treated with three abiotic stress conditions (salt, cold and drought). Most of the members from both PI-PLC and NPC classes were found to be expressed differentially under one or multiple abiotic stresses (Figure S2; Table S1). From the PI-PLC, two members OsPLC1 and OsPLC3 were up-regulated while OsPLC4 was significantly down-regulated under all the three abiotic stresses. OsPLC2 did not show any significant change in expression under abiotic stresses in comparison to untreated control. Up-regulated PI-PLCs were induced more under salt and drought stresses than under cold stress. Similarly, out of the five rice NPC members four exhibited differential expression pattern while one member OsNPC3 did not show any significant change in the expression under abiotic stresses. OsNPC1, OsNPC2 and OsNPC4 were found to be up-regulated while OsNPC5 exhibited down-regulation. OsNPC2 and OsNPC4 were up-regulated in salt and drought stresses together. OsNPC1 exhibited up-regulation in salt stress and down-regulation under cold stress. OsNPC5 did not have any significant change under salt stress while commonly down-regulated under cold and drought stresses. None of the PLC gene was expressed commonly under salt and cold or drought and cold stresses together. Under cold stress conditions, none of the PLC genes was found to be up-regulated.
Expression Analysis during Development
Affymetrix rice whole genome arrays data was used to generate the expression profile of entire set of rice PLC genes during plant development, covering 11 stages of reproductive development, which includes six stages of panicle (P1–P6) and five stages of seed (S1–S5) development and three vegetative developmental stages (leaf, root and seedling). Most of the PLC genes were found to be expressed in reproductive as well as in vegetative stages of development. A careful in-depth analysis revealed that eight out of nine PLC genes expressed differentially during reproductive developmental stages in comparison to the vegetative developmental stages (Figure 3, S2; Table S2). One of the NPC members, OsNPC3 did not show any significant variation in expression during developmental stages. From the set of genes, which expressed differentially during reproductive development, five and three genes were up-regulated and down-regulated, respectively. Among the up-regulated genes, two members belonged to PI-PLC (OsPLC2 and OsPLC3) and three genes belonged to NPC (OsNPC2, OsNPC4 and OsNPC5). Two genes each were up-regulated and down-regulated commonly during panicle and seed developmental stages. Both the commonly up-regulated genes belonged to NPC group (OsNPC2 and OsNPC5) while both commonly down-regulated genes belonged to PI-PLC group (OsPLC1 and OsPLC4). A typical observation for the unique expression pattern revealed that OsPLC2 and OsPLC3 were exclusively up-regulated during panicle developmental stages whereas, OsNPC4 exhibited exclusive up-regulation during later seed developmental stages. Interestingly, OsPLC3 which was up-regulated in panicle developmental stages exhibited down-regulation in seed stages while OsNPC1 showed exclusive down-regulation during panicle developmental stages.
Average signal intensity (GCRMA) value of three replicates from microarray for all the developmental stages (three vegetative; L-mature leaf, R-root, SDL-seven day old seedling, six panicle stages; P1–P6 and five seed stages; S1–S5) has been plotted to show the differential expression. Standard error bars have been shown. Y-axis represents signal values from microarray and X-axis shows different developmental stages.
Overlapping Expression under Abiotic Stresses and Development
Analysis was done for overlapping expression of PLC genes under abiotic stresses and reproductive development, keeping the fact in mind that abiotic stress and reproductive development triggered signaling is mediated by many common factors and at some critical stages these are interconnected phenomenon of plant life cycle [29]–[31]. Remarkably, all the PLC genes which expressed significantly and differentially under abiotic stresses were found to have significant expression pattern during two phases of reproductive development (panicle and seed development) in rice (Table S1, S2). A single NPC member (OsNPC2) was found to be up-regulated commonly under abiotic stresses and both panicle and seed development while OsPLC4 was commonly down-regulated. OsPLC3 was found to be commonly induced during panicle development and abiotic stresses and OsNPC4 during seed development and abiotic stresses together whereas, none of the PLCs was down-regulated under these conditions or stages. Observation for overlap between two developmental stages (panicle and seed) revealed that only OsNPC5 was commonly up-regulated and OsPLC1 was commonly down-regulated. Interestingly, OsPLC3, which was commonly up-regulated in abiotic stress and panicle stages together, was down-regulated in seed developmental stages and similarly, OsNPC5 was commonly up-regulated in both the developmental phases but was found to be down-regulated under abiotic stresses.
Microarray Expression Validation under Abiotic Stresses by Q-PCR
Quantitative expression analysis was performed by real time RT-PCR for all the rice PLC genes (including both PI-PLC and NPCs) under three abiotic stress conditions (salt, cold and drought) to verify the microarray expression data. Out of a total of nine PLC gene family members, expression pattern for six members was found to be in accordance with microarray expression, however, the magnitude of expression varied slightly in few samples for some genes (Figure 4). For three PLC genes; OsPLC2, OsPLC3 and OsNPC3 the expression pattern deviated from microarray as shown by the real time PCR analysis. There was no significant differential change observed in the expression of OsPLC2 and OsNPC3 by microarray under the treatment of abiotic stresses w.r.t. control whereas, real time PCR revealed up-regulation of OsPLC2 under cold and drought conditions and OsNPC3 up-regulated under salt and drought stresses. Since actual transcript level of these two genes is very low in all the conditions as suggested by both the techniques, even minute differences in the sensitivity to detect transcripts might account for the deviation in the relative expression profile. Similarly, OsPLC3 was shown to be down-regulated under cold stress condition in contrary to the slight up-regulation revealed by microarray. This kind of discrepancy in the expression pattern by these two techniques has been reported in several previous studies also [30]–[32].
Microarray expression profile was generated using three biological replicate and two biological replicates were used for Q-PCR expression analysis. Standard error bars have been shown for the data from both the techniques. Y-axis represents the normalized expression values and X-axis represents different experimental conditions. Green and grey columns denote the expression values from microarray and real time PCR, respectively.
Cis-regulatory Elements in the Promoter of rice PLC Genes
In-silico analysis of 1 kb upstream region (from translation start site) of all the rice PLC members revealed the presence of various regulatory elements, which included ABRE (abscisic acid responsive element), MBS (myb binding site), Skn-1, RY-element, GCN4, TC-rich repeat and C-repeat/DRE (Figure 5). These motifs have been previously known to regulate various stress responses and plant development [33]–[37]. The motifs were variably present in the promoter of all the PLC genes. Most regulatory elements were present on the 1 kb upstream region of OsNPC4 containing eight elements including three MBS and two ABRE motifs, which might account for the responsive nature of this gene under abiotic stresses and seed developmental stages. Surprisingly, the promoter of OsPLC4, which has been down-regulated under all the abiotic stresses and developmental stages, contain seven cis-regulatory elements. All the rice PLC genes contained at least two regulatory elements in their promoter region.
Cis-regulatory elements in the 1 kb upstream region (from translation start site) of the promoter of all the rice PLC genes were analysed using PlantCARE database. Various elements such as ABRE, MBS, TC-rich repeat, C-repeat/DRE, RY-elements, Skn-1 and GCN4 are present in the forward and reverse strands and are indicated by the arrowhead mark above and below the line, respectively. Scale over the promoters indicates the specific location of the elements. Differential regulation (up- or down-regulation) of the genes under different abiotic stresses; S-salt, C-cold, D-drought and during reproductive developmental phases; P- panicle and Sd- seed, is indicated on the right side of each gene.
Sub-cellular Localization of PLC Proteins
To assess the functionality of rice PLC genes, two representative members from both PLC classes; PI-PLC (OsPLC1 and OsPLC4) and NPC (OsNPC1 and OsNPC3) were selected for subcellular localization analysis. All four genes were fused to C terminus of GFP as the reporter molecule, which were transiently expressed in both Nicotiana benthamiana and onion epidermal cells. OsPLC1 and OsPLC4 were found to be distributed throughout the cytoplasm as well as in the nucleus of Nicotiana cells (Figure 6) and similar localization pattern was observed in onion epidermal cells (Figure S3). Whereas, in the case of OsNPC1 and OsNPC3 dotted structure patterns were observed, which were found to be overlapping with the red chlorophyll auto-fluorescence as seen in the overlay with the green fluorescence (Figure 7). This suggested that OsNPC3 protein might be localized in the chloroplast/plastids. OsNPC1 appears to be localized mainly in the cytoplasm; however, the closer look in the magnified image of the cell suggested that this protein is concentrated around the chloroplast as it was surrounding by a patch of chloroplasts, which were clearly visible with chlorophyll auto-fluorescence (Figure S4).
Agrobacterium-infiltrated tobacco leaves expressing the GFP-PLC fusion protein driven by the 2XCaMV 35S promoter. Confocal images of fluorescence (green) for cell expressing OsPLC1 and OsPLC4 are showing their distribution throughout the cytoplasm and nucleus (first and second row). Expressed GFP-OsNPC1 fusion protein, mainly localized to cytoplasm and small spots like structures in the cell (third row), and GFP-OsNPC3 fusion protein showed preferential localization to small punctate structures in the cell (fourth row). Cells transformed with vector only (CaMV35S-GFP) are shown in the lowermost row. All the images were taken in 5 different sections in z direction and merges together. Scale bar = 40 µm.
Confocal images of Nicotiana benthamiana cell expressing GFP-OsNPC1 (upper panel) and GFP-OsNPC3 (lower panel). Green GFP signal merges with red auto-fluorescence of chloroplast, as seen in the merged regions (yellowish orange) in the overlay. All the images were taken in 5 different sections in z direction and merges together. Scale bar = 40 µm.
Discussion
Phospholipase C Gene Family in Rice
Exhaustive genome wide exploration through various databases and tools revealed the existence of a total of nine phospholipase C encoding genes in rice genome. Entire rice PLC gene family could be differentiated into two major classes namely; PI-PLC and NPC with four and five members, respectively, based on in-depth sequence, structure and phylogenetic analysis. PI-PLC represent a major class of PLC in plants as suggested by the genomic survey of some of the model plants such as Arabidopsis, which has nine PI-PLC member in its genome [16]–[18], and tomato (Lycopersicon esculentum) genome encodes six PI-PLC genes [4]. Surprisingly, rice genome found to have fewer PI-PLC encoding genes in comparison to Arabidopsis, which has much smaller genome size. In rice genome, we could identify five members of NPC (OsNPC1-5) class, which is recently discovered class of plant PLCs and till date it has been reported in the genome of Arabidopsis only with six members [11]. Domain and motif analysis revealed the presence of characteristic PI-PLC-X and PI-PLC-Y catalytic domains and phospholipid binding C2 domain at the C-terminal in all the PI-PLC members. Notably, an EF-hand like motif was found only in two PI-PLC members (OsPLC1 and OsPLC4). Previously, it has been suggested that EF-hand motifs in plant PI-PLCs may interact with the C2 domain and facilitate the membrane targeting and catalytic activity [15], [16]. Similarly, all the NPC members were identified by the presence of highly conserved signature motif I, II and III (Figure 1B, S1), which confirmed the integrity of all the identified rice PLC genes. Structural analysis of rice PLC genes in terms of intron-exon architecture showed that all the PI-PLC members contain 6–8 introns and this intron-exon pattern is conserved among Arabidopsis PI-PLC members also. However, NPC members of rice contain 0–3 introns while Arabidopsis genes belonging to this group of PLC are comprised of 2–4 introns. Moreover, Arabidopsis NPC members are divided into two groups (I and II) based on the number of introns they contain. Gene members of Arabidopsis group I of NPC found to contain 2 introns while all the members of group II contain 4 introns [25]. This gene structure pattern could not be observed in rice NPC genes; therefore, they could not be divided into groups like Arabidopsis. Analysis of protein size of rice PLCs showed that all the PI-PLC proteins are ∼66 kDa while NPCs are ∼60 kDa and approximately similar protein size was noted for their Arabidopsis orthologs. This indicated towards the structural conservation of PLC proteins across different plant species.
PLCs are Evolutionarily Diverse in Rice and Arabidopsis
Evolutionary study of rice PLCs members indicated that three members of PI-PLCs (OsPLC1, OsPLC2 and OsPLC3) group together with highly significant bootstrap support value in a phylogenetic tree and OsPLC4 is placed separately (Figure 2). Notably, these three members have similar expression profile under abiotic stresses and development with up-regulation in these conditions/stages while OsPLC4 showed completely opposite behaviour i.e. down-regulation in all the conditions and stages. This observation indicates towards the functional significance of phylogenetic closeness of the rice PI-PLC members. In-depth analysis of the phylogeny showed that most of the rice PI-PLCs are separated from their Arabidopsis orthologs and seems to have gone through a diverse evolutionary path even after being originated from a common ancestor. Interestingly, NPC members from both the plant species seem to be evolutionarily more closed and conserved at sequence level. Moreover, gene duplication analysis showed that rice PLC genes did not participate in significant duplication event. In contrary, their Arabidopsis counterparts have gone through substantial gene duplication process and members from PI-PLC and NPC classes have been found in the clusters of tandem duplicates on respective chromosomes (Table S3). This pattern of duplication suggested that PLC gene family in Arabidopsis have evolved through gene duplication process while rice PLC gene family has followed a diverse path rather than gene duplication event.
PLCs are Vital Players in Abiotic Stress Triggered Signaling and Plant Development
To get a clue about the functional role of various members of rice PLC gene family, genome wide expression profile was generated for entire PLC members using gene chip microarray data. The analysis showed that most of the members from PI-PLC and NPC groups were differentially expressed under three abiotic stresses (salt, cold and drought) in the 7 days old rice seedlings. From this microarray analysis, a higher number of genes were found to be up-regulated than down-regulated under one or more stress conditions. This expression pattern was also validated by real time RT-PCR, which corroborated the expression pattern for most of the genes and conditions. This critical information about the expression status of rice PLC genes suggested that members from this group of phospholipases might play a significant role in abiotic stress triggered signaling and stress tolerance in crop plants. This assumption has been supported by the previous studies in different plant species where this group of genes has been implicated in abiotic stress mediated signaling and tolerance. In Arabidopsis, RT-PCR based expression analysis showed that almost all the PI-PLC members (except AtPLC2) were induced several fold under similar abiotic stresses and ABA treatment [17]–[18]. Similarly, expression was rapidly induced for one of the mung bean (Vigna radiata L.) PI-PLC members, Vr-PLC3 under drought and high salinity conditions [23]. Wang and co-workers showed that overexpression of a maize PLC1 (ZmPLC1) could lead to better drought tolerance [38]. Recently, one of the tobacco PLC genes has been characterized where its transcript levels were escalated under salt and drought stresses and the transgenic plants overexpressing this gene could tolerate these abiotic stresses [39]. Recently identified group of plant PLCs, NPC has been mainly implicated in phosphate starvation; however, some recent reports have shown their significant role in abiotic stress signaling. Arabidopsis plants deficient in NPC4 were found to have reduced tolerance to salt and dehydration stresses while overexpression plants exhibited improved tolerance to these stresses [12]. Similar results were also found for the NPC4 in Arabidopsis roots in another recent study [26]. Moreover, the promoters for entire set of rice PLCs were found to contain one or more important cis-regulatory elements such as ABRE, MBS, TC-rich repeat, C-repeat/DRE (Figure 5), which might also be involved in regulation of expression of rice PLCs under these stress conditions, since these elements have been known to regulate abiotic stress mediated responses of various genes. Apart from PLCs, other important classes of rice phospholipases (PLA and PLD) have also been found to be expressed differentially under similar abiotic stress treatments [40]–[42], which signify the role of different classes of phospholipases and lipid mediated signaling in abiotic stress physiology and responses in crop plants.
Apart from understanding the effect of different stresses on the transcript levels of various rice PLC genes, it is also important to conceive about the expression level of this group of genes at various stages of development and also relate the effect on abiotic stresses and plant development. Moreover, genes involved in regulation of panicle and seed development are major determinants of yield and productivity of rice crop. Therefore, it is of great significance to understand their regulation, which will be an important step towards developing high yielding rice varieties. Relevant to this, we found that eight out of a total of nine rice PLC genes were differentially expressed during the critical stages of rice development including six panicle (P1–P6) and five seed stages (S1–S5). These critical stages represent the floral organ development (P1), meiosis (P2–P3) to mature pollen (P6) and early globular embryo (S1), embryo morphogenesis and maturation (S3–S4) to dormancy and dehydration tolerance (S5) phase of reproductive development. Different members from both PI-PLC and NPC have been found to be significantly up-regulated and down-regulated during these stages either specifically or commonly (Figure 3, S2). Spatial and temporal fluctuations in the expression of these genes might affect specific developmental stages either positively or negatively and ultimately might affect overall development and yield of rice grains. Abiotic stresses are among the major factors, which significantly influence the growth, development and productivity of the plants in the environment and at the molecular level abiotic stresses (especially drought) and plant development has been found to be interconnected in previous studies [29]–[31]. Keeping this view in mind, we have investigated the PLC genes with overlapping expression in abiotic stresses and developmental stages. Surprisingly, all the genes, which expressed differentially under abiotic stresses, were also involved in one or both the developmental phases (panicle and seed development stages). The information pertaining to the expression of such genes (OsPLC3, OsPLC4, OsNPC2 and OsNPC4) might explain for a connection or interaction of signaling pathways triggered by abiotic stresses and during development resulting in the “cross talk” of these signaling cascades. This cross talk could possibly be the result of involvement of some common signaling components such as “calcium” or “ABA” which have been implicated at the conjuncture of abiotic stress and developmental triggered responses [43]–[47]. This speculation might be justified by the presence of ABRE element in the promoter of gene such as OsNPC4, which is commonly induced during abiotic stresses and seed development. Furthermore, overexpression of Brassica napus PI-PLC2 resulted in alteration in expression level of genes, which included stress related genes, hormone regulated and regulatory genes, and a number of calcium regulated genes and transcription factors. Moreover, Brassica napus PI-PLC2 overexpressing transgenic plants exhibited improved drought tolerance and early flowering [48]. NPC class of plant PLCs has not been investigated for its functional role sufficiently, but recently significant role has been established for Arabidopsis NPC3 in root development [25].
Subcellular Localization of OsPLCs Revealed Possible Site of Action
Knowledge obtained about a gene from genomic analysis and its expression status at transcript level require functional validation at protein level for further in-depth analysis and characterization. Therefore, we successfully assessed the subcellular localization of four rice PLCs in Nicotiana benthamiana as well as in onion epidermal cells. Both the members of PI-PLC class; OsPLC1 and OsPLC4 were clearly found to be localized to cytosol and nucleus. In higher plants, PI-PLCs have been divided into two groups as one group found to be present predominantly in cytosol and other group at plasma membrane [16], [22]–[23], [49]–[50]. However, a recent study revealed that Arabidopsis and rice PLCs might be localized in the cytoplasm, nucleus and the mitochondria, and lack a transmembrane domain, myristoylation and GPI-anchor protein modifications [51]. Sub-cellular localization analysis of two members of rice non-specific PLCs; OsNPC1 and OsNPC3 suggested the possible localization of OsNPC3 to the chloroplast in Nicotiana benthamiana, as the GFP-OsNPC3 fluorescence could be co-localized with the chlorophyll auto-fluorescence (Figure 7). On the other hand, OsNPC1 seems to be a cytosolic protein localized in close proximity to chloroplast (Figure S4). Non-specific PLC is the recently identified class of plant PLCs, therefore, not much has been known about their sub-cellular localization and functional aspects, however, in Arabidopsis one of the NPC member NPC5 is cytosolic and found to be translocated to chloroplast under phosphate starvation condition, and the DAG produced from the activity of NPC5 is used in galactolipid biosynthesis [11], [52]. Therefore, rice NPC members might also be participating in similar cellular processes. The diverse localization pattern for rice PLC proteins indicates their significant role in important cellular processes regulated by lipid mediated signaling.
Conclusions
In conclusion, in this study, for the first time we are presenting a comprehensive account of the entire set of PLC encoding genes in the rice genome by elaborating their genomic organization, sequence and phylogenetic analysis. Detailed expression analysis proposed a vital role for PLC enzymes in abiotic stress and development triggered lipid signaling in rice. Successful sub-cellular localization of selected PLC members provide a clue about their possible site of action and involvement in concerned processes in the plant cell. This study opens up the avenues for the detail functional characterization of candidate PLC genes to establish their certain role in lipid mediated signaling in crop plant rice.
Materials and Methods
Identification of PLCs in the Rice Genome
Rice genome databases in RGAP version 6.1 and NCBI were explored to identify the putative PLC members, using different keywords such as “phospholipase C”, “phosphatidylinositol-phospholipase C”, “phosphatidylcholine - phospholipase C” and “phosphoesterase” and by phospholipase C domain annotation in SUPERFAMILY database (http://supfam.cs.bris.ac.uk/SUPERFAMILY). Hidden Markov Model (HMM) profiles generated by the seed alignment at default parameters (E value –1.0) were obtained for different PLC classes from Pfam database and used to search protein database at RGAP. Arabidopsis PLC sequences were searched and obtained from TAIR 10.0 (The Arabidopsis Information Resource). Homology search was performed using Arabidopsis sequences as query, employing BLASTP and BLASTN tools both in RGAP and NCBI. The putative rice PLC sequences having very high homology with Arabidopsis PLCs were retained for further analysis. After the merger of results from all these strategies, unique entries (with unique locus ID) were identified to remove the redundancy. All the sequences were further scanned through SMART, InterPro and Pfam tools for the presence of characteristic and functionally important domains and motifs.
Multiple Sequence Alignment and Phylogenetic Analysis
To mark the conserved and characteristic catalytic domains and motifs, the amino acid sequences of all the rice PI-PLCs and NPCs were aligned using ClustalW method in MegAlign software of DNASTAR. For phylogenetic analysis, the protein sequences of all the non-redundant PLC candidates from rice and Arabidopsis were used for multiple sequence alignment employing clustalX (version 2.0). The multiple sequence alignment was used to construct a maximum likelihood, un-rooted phylogenetic tree to infer the evolutionary history for all the PLC genes. The tree was generated by neighbour-joining (NJ) algorithm with p-distance method and pairwise deletion of gaps, employing MEGA version 5 [53], using default parameters. A bootstrap statistical analysis was performed with 1000 replicates to test the phylogeny.
Gene Nomenclature and Properties
Rice PLC genes (PI-PLC and NPCs) have been named according to their Arabidopsis orthologs as suggested by phylogenetic analysis and by their sequence and domain structure analysis. Various properties and attributes of PLC genes such as locus ID, protein size (AA), introns and expression evidence in terms of total number of ESTs were extracted from RGAP 6.1 and full length cDNA accession from knowledge based oryza molecular biological encyclopedia (KOME) (http://cdna01.dna.affrc.go.jp/cDNA) and NCBI.
Plant Growth and Abiotic Stress Treatment
The tissues were collected for different stages of panicle (P1–P6) and seed (S1–S5) development from field grown rice plants (Oryza sativa ssp. Indica var. IR64) and instantly frozen in liquid nitrogen to avoid any wounding or damage during handling. As per the requirement of this journal, we declare that no specific permits were required, the location is not privately owned and IR64 is not endangered or protected species of rice.
For stress treatment, dehusked rice seeds were sterilized with 70% ethanol and 0.1% HgCl2 and grown in culture room at 28±1°C with a daily photoperiodic cycle of 14 h light/10 h dark. After 7 days growth, salt, cold and drought stress treatments were given to the seedlings parallel to untreated control according to Ray et al., 2007 [54]. Treated seedlings were immediately frozen in liquid nitrogen.
Gene Chip Microarray Experiments
Microarray experiments were performed taking 11 reproductive stages (P1–P6 and S1–S5; representing panicle and seed developmental stages, respectively) of rice along-with three vegetative stages (mature leaf, 7 days old seedling and their roots) and three abiotic stress conditions, i.e. cold, salt, and drought. For each stage/treatment, total RNA was isolated from three biological replicates and microarray experiments were carried out using 51 Affymetrix Gene Chip Rice Genome Arrays (Gene Expression Omnibus, GEO, platform accession number GPL2025). For further detailed analysis of the data, the raw data (*.cel) files, generated from all the chips were imported to Array Assist 5.5.1 software (Stratagene, USA). Microarray analysis was performed according to Ray et al., 2007 [54]. The microarray data generated from this study has been deposited in the gene expression omnibus (GEO) database at NCBI, under the series accession numbers GSE6893 and GSE6901.
Expression Analysis by Real Time RT-PCR
Real time RT-PCR was performed to validate the microarray data for all the rice PLC genes under abiotic stresses. The primers were design for all the genes preferentially from 3′ end, using PRIMER EXPRESS (PE Applied Biosystems, USA), with default parameters. Primers were checked for their specificity using BLAST tool of NCBI and dissociation curve analysis after the PCR reaction (Table S4). First strand cDNA was prepared from 4 µg of DNase treated total RNA, in 100 µl of reaction volume using high-capacity cDNA Archive kit (Applied Biosystems, USA). KAPA SYBR FAST Master Mix (KAPABIOSYSTEMS, USA) was used to detect the expression for the genes in ABI Prism 7000 sequence detection system (Applied Biosystems, USA). Biological duplicates of each sample were taken for the analysis. The average Ct values were calculated by taking the average of three technical replicates for each sample. The cDNA variance among samples was normalized using ACTIN, as the endogenous control. Relative expression values were calculated by ΔΔCt method and normalized the data against the maximum average expression value from microarray.
Promoter Analysis
One kb upstream region from the translation start site was extracted from RGAP version 6.1 for all the rice PLC genes to identify various cis-acting regulatory elements in their promoter. One kb upstream region was subsequently analysed in plantCARE [55] database and various cis-regulatory elements and motifs involved in abiotic stress responses and development were identified.
GFP-PLC Constructs Preparation for Sub-cellular Localization
Protein coding region (without stop codon) of respective PLCs were amplified from stress treated cDNA of rice (IR64) with gene specific primers (Table S5), using iProof high-fidelity DNA polymerase (Bio-Rad). All the GFP-PLC constructs were prepared by cloning the amplified PLC CDS in Gateway® entry vector pENTR-D/TOPO (Invitrogen) and subsequent mobilization to gateway compatible binary vector pSITE2CA [56] by Gateway cloning protocol (Invitrogen). In pSITE2CA vector, the 2XCaMV 35S promoter regulates the expression of cloned gene. Successful preparation of all the constructs was confirmed by sequencing.
Nicotiana Benthamiana Infiltration, Particle Bombardment in Onion Peel and Confocal Microscopy
Agrobacterium tumefaciens (GV3101::pMP90) was transformed with GFP-PLC construct plasmid, which was then used to transfect the leaves of 4–6 weeks glass-house grown Nicotiana benthamiana plants. After infiltration, plants were kept for incubation (3–5 days) under 12 h light/12 h dark photoperiodic cycle at 20°C with 60% atmospheric humidity [57]–[58]. Biolistic or particle bombardment in onion epidermal peels was carried out according to Singh et al., 2012 [41]. Transiently transformed epidermal peel cells were analyzed in TCS SP5 laser scanning confocal microscope (Leica, Germany) to detect the fluorescence. GFP fluorescence signals were detected at 500–535 nm after excitation at 488 nm. Auto-fluorescence of plastids was detected at 650 to 720 nm. For the co-localization experiments, sequential scanning was done for both the channels and then merged together to shows overlapping signals. All the images were further processed using Leica LAS AF Lite software.
Supporting Information
Figure S1.
Multiple sequence alignment of rice PI-PLC and NPC showing the consensus and conserved domains and motifs. Protein sequences were aligned for both the PLC classes separately employing clustalW tool of MegAlign-DNA STAR. The conserved and characteristic domains and sequences of PI-PLCs and NPCs have been marked with red underline.
https://doi.org/10.1371/journal.pone.0062494.s001
(TIF)
Figure S2.
Microarray expression profile of rice PLC gene family. Separate heatmaps are depicting the expression profiles of PI-PLC and NPC groups of rice PLC under abiotic stresses and development. Three abiotic stress conditions are denoted by C: cold, D: drought, S: salt and SL: seven day old untreated seedling as control. Developmental stages include three vegetative stages L: mature leaf, R: root, SL: seven day old seedling and eleven reproductive stages comprising six panicle developmental stages [P1 (0–3 cm), P2 (3–5 cm), P3 (5–10 cm), P4 (10–15 cm), P5 (15–22 cm), and P6(22–30 cm)] and five stages of seed [S1 (0–2 DAP), S2 (3–4 DAP), S3 (4–10 DAP), S4 (11–20 DAP) and S5 (21–29 DAP)]. The colour scale at the bottom of each heat map is given in log2 intensity value.
https://doi.org/10.1371/journal.pone.0062494.s002
(TIF)
Figure S3.
Subcellular localization of rice PLC proteins in onion epidermal cells. Onion epidermal cells expressing the GFP-PLC fusion protein driven by the 2X CaMV35S promoter. Confocal images of fluorescence (green) are shown for onion cell expressing GFP-OsPLC1 and GFP-OsPLC4 fusion protein showing its distribution throughout the cytoplasm and nucleus (upper two rows); expressed GFP-OsNPC1 and GFP-OsNPC3 fusion protein showing their preferential dotted localization (third and fourth rows). Cells transformed with vector only (CaMV35S-GFP) are shown in the lowermost row. All the images were taken in 5 different sections in z direction and merges together. Scale bar = 40 µm.
https://doi.org/10.1371/journal.pone.0062494.s003
(TIF)
Figure S4.
Preferential localization of OsNPC1 proteins in close proximity of chloroplast in Nicotiana cells. Expressed GFP-OsNPC1 fusion protein in Nicotiana cells, the upper panel showing cytoplasmic localization with small spots in the cell, which surround the chloroplasts in the overlay (Scale bar = 40 µm), which can be seen clearly in the magnified view of the spot in the lower panel. (Scale bar = 10 µm). All the images were taken in 5 different sections in z direction and merges together.
https://doi.org/10.1371/journal.pone.0062494.s004
(TIF)
Table S1.
Microarray expression data for OsPLCs under three abiotic stresses.
https://doi.org/10.1371/journal.pone.0062494.s005
(XLSX)
Table S2.
Microarray expression data for OsPLCs during development.
https://doi.org/10.1371/journal.pone.0062494.s006
(XLSX)
Table S3.
Gene duplication exhibited by Arabidopsis PLC gene family.
https://doi.org/10.1371/journal.pone.0062494.s007
(XLSX)
Table S4.
List of primers used for real time RT-PCR expression analysis of OsPLCs.
https://doi.org/10.1371/journal.pone.0062494.s008
(XLSX)
Table S5.
List of primers used for cloning of OsPLCs for sub-cellular localization.
https://doi.org/10.1371/journal.pone.0062494.s009
(XLSX)
Acknowledgments
We kindly acknowledge Dr. Michael Goodin (Department of Plant Pathology, University of Kentucky, USA) for pSITE 2CA vectors for subcellular localization.
Author Contributions
Conceived and designed the experiments: GKP. Performed the experiments: AS PK AP. Analyzed the data: AS PK AP AKT SKS SK GKP. Contributed reagents/materials/analysis tools: AKT SK. Wrote the paper: AS GKP.
References
- 1. Bargmann BO, Munnik T (2006) The role of phospholipase D in plant stress responses. Curr Opin Plant Biol 9: 515–522.
- 2. Boss W, Lynch D, Wang X (2008) Lipid-mediated signaling. Annual Plant Reviews. 33: 202–43.
- 3. Tuteja N, Sopory SK (2008) Plant signaling in stress: G-protein coupled receptors, heterotrimeric G-proteins and signal coupling via phospholipases. Plant Signal Behav 3: 79–86.
- 4. Vossen JH, Abd-El-Haliem A, Fradin EF, van den Berg GC, Ekengren SK, et al. (2010) Identification of tomato phosphatidylinositol-specific phospholipase-C (PI-PLC) family members and the role of PLC4 and PLC6 in HR and disease resistance. Plant J 62: 224–239.
- 5. Laxalt AM, Munnik T (2002) Phospholipid signalling in plant defence. Curr Opin Plant Biol 5: 332–338.
- 6. Xia HJ, Brearley C, Elge S, Kaplan B, Fromm H, et al. (2003) Arabidopsis inositol polyphosphate 6−/3-kinase is a nuclear protein that complements a yeast mutant lacking a functional ArgR-Mcm1 transcription complex. Plant Cell 15: 449–463.
- 7. van Schooten B, Testerink C, Munnik T (2006) Signalling diacylglycerol pyrophosphate, a new phosphatidic acid metabolite. Biochim Biophys Acta 1761: 151–159.
- 8. Zonia L, Munnik T (2006) Cracking the green paradigm: functional coding of phosphoinositide signals in plant stress responses. Subcell Biochem 39: 207–237.
- 9. van Leeuwen W, Vermeer JE, Gadella TW Jr, Munnik T (2007) Visualization of phosphatidylinositol 4,5-bisphosphate in the plasma membrane of suspension-cultured tobacco BY-2 cells and whole Arabidopsis seedlings. Plant J 52: 1014–1026.
- 10. Xue H, Chen X, Li G (2007) Involvement of phospholipid signaling in plant growth and hormone effects. Curr Opin Plant Biol 10: 483–489.
- 11. Nakamura Y, Awai K, Masuda T, Yoshioka Y, Takamiya K, et al. (2005) A novel phosphatidylcholine-hydrolyzing phospholipase C induced by phosphate starvation in Arabidopsis. J Biol Chem 280: 7469–7476.
- 12. Peters C, Li M, Narasimhan R, Roth M, Welti R, et al. (2010) Nonspecific phospholipase C NPC4 promotes responses to abscisic acid and tolerance to hyperosmotic stress in Arabidopsis. Plant Cell 22: 2642–2659.
- 13. Munnik T, Testerink C (2009) Plant phospholipid signaling: “in a nutshell”. J Lipid Res 50 Suppl: S260–265
- 14. Bunney TD, Katan M (2011) PLC regulation: emerging pictures for molecular mechanisms. Trends Biochem Sci 36: 88–96.
- 15. Chen G, Snyder CL, Greer MS, Weselake RJ (2011) Biology and biochemistry of plant phospholipases. Critical Reviews in Plant Sciences 30: 239–258.
- 16. Mueller-Roeber B, Pical C (2002) Inositol phospholipid metabolism in Arabidopsis. Characterized and putative isoforms of inositol phospholipid kinase and phosphoinositide-specific phospholipase C. Plant Physiol 130: 22–46.
- 17. Hunt L, Otterhag L, Leel JC, Lasheen T, Hunt J, Seki M, et al. (2004) Gene-specific expression and calcium activation of Arabidopsis thaliana phospholipase C isoforms. New Phytologist 162: 643–654.
- 18. Tasma IM, Brendel V, Whitham SA, Bhattacharyya MK (2008) Expression and evolution of the phosphoinositide-specific phospholipase C gene family in Arabidopsis thaliana. Plant Physiol Biochem 46: 627–637.
- 19. Kopka J, Pical C, Gray JE, Muller-Rober B (1998) Molecular and enzymatic characterization of three phosphoinositide-specific phospholipase C isoforms from potato. Plant Physiol 116: 239–250.
- 20. Venkataraman G, Goswami M, Tuteja N, Reddy MK, Sopory SK (2003) Isolation and characterization of a phospholipase C delta isoform from pea that is regulated by light in a tissue specific manner. Mol Genet Genomics 270: 378–386.
- 21. Mikami K, Repp A, Graebe-Abts E, Hartmann E (2004) Isolation of cDNAs encoding typical and novel types of phosphoinositide-specific phospholipase C from the moss Physcomitrella patens. J Exp Bot 55: 1437–1439.
- 22. Shi J, Gonzales RA, Bhattacharyya MK (1995) Characterization of a plasma membrane-associated phosphoinositide-specific phospholipase C from soybean. Plant J 8: 381–390.
- 23. Kim YJ, Kim JE, Lee JH, Lee MH, Jung HW, et al. (2004) The Vr-PLC3 gene encodes a putative plasma membrane-localized phosphoinositide-specific phospholipase C whose expression is induced by abiotic stress in mung bean (Vigna radiata L.). FEBS Lett 556: 127–136.
- 24. Wang X (2001) Plant Phospholipases. Annu Rev Plant Physiol Plant Mol Biol 52: 211–231.
- 25. Wimalasekera R, Pejchar P, Holk A, Martinec J, Scherer GF Plant phosphatidylcholine-hydrolyzing phospholipases C NPC3 and NPC4 with roles in root development and brassinolide signaling in Arabidopsis thaliana. Mol Plant 3: 610–625.
- 26. Kocourkova D, Krckova Z, Pejchar P, Veselkova S, Valentova O, et al. (2011) The phosphatidylcholine-hydrolysing phospholipase C NPC4 plays a role in response of Arabidopsis roots to salt stress. J Exp Bot 62: 3753–3763.
- 27. Sanchez JP, Chua NH (2001) Arabidopsis PLC1 is required for secondary responses to abscisic acid signals. Plant Cell 13: 1143–1154.
- 28. Perera IY, Heilmann I, Chang SC, Boss WF, Kaufman PB (2001) A role for inositol 1,4,5-trisphosphate in gravitropic signaling and the retention of cold-perceived gravistimulation of oat shoot pulvini. Plant Physiol 125: 1499–1507.
- 29. Schroeder JI, Kwak JM, Allen GJ (2001) Guard cell abscisic acid signalling and engineering drought hardiness in plants. Nature 410: 327–330.
- 30. Vij S, Giri J, Dansana PK, Kapoor S, Tyagi AK (2008) The receptor-like cytoplasmic kinase (OsRLCK) gene family in rice: organization, phylogenetic relationship, and expression during development and stress. Mol Plant 1: 732–750.
- 31. Singh A, Giri J, Kapoor S, Tyagi AK, Pandey GK (2010) Protein phosphatase complement in rice: genome-wide identification and transcriptional analysis under abiotic stress conditions and reproductive development. BMC Genomics 11: 435.
- 32. Dallas PB, Gottardo NG, Firth MJ, Beesley AH, Hoffmann K, et al. (2005) Gene expression levels assessed by oligonucleotide microarray analysis and quantitative real-time RT-PCR: how well do they correlate? BMC Genomics 6: 59.
- 33. Narusaka Y, Nakashima K, Shinwari ZK, Sakuma Y, Furihata T, et al. (2003) Interaction between two cis-acting elements, ABRE and DRE, in ABA-dependent expression of Arabidopsis rd29A gene in response to dehydration and high-salinity stresses. Plant J 34: 137–148.
- 34. Jiang C, Iu B, Singh J (1996) Requirement of a CCGAC cis-acting element for cold induction of the BN115 gene from winter Brassica napus. Plant Mol Biol 30: 679–684.
- 35. Takaiwa F, Oono K, Kato A (1991) Analysis of the 5′ flanking region responsible for the endosperm-specific expression of a rice glutelin chimeric gene in transgenic tobacco. Plant Mol Biol 16: 49–58.
- 36. Kim SY, Wu R (1990) Multiple protein factors bind to a rice glutelin promoter region. Nucleic Acids Res 18: 6845–6852.
- 37. Abe H, Urao T, Ito T, Seki M, Shinozaki K, et al. (2003) Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) function as transcriptional activators in abscisic acid signaling. Plant Cell 15: 63–78.
- 38. Wang CR, Yang AF, Yue GD, Gao Q, Yin HY, et al. (2008) Enhanced expression of phospholipase C 1 (ZmPLC1) improves drought tolerance in transgenic maize. Planta 227: 1127–1140.
- 39. Tripathy MK, Tyagi W, Goswami M, Kaul T, Singla-Pareek SL, Deswal R, Reddy MK, Sudhir Sopory SK (2012) Characterization and functional validation of tobacco PLC delta for abiotic stress tolerance. Plant Mol Biol Rep. 30(2): 488–497.
- 40. Li G, Lin F, Xue HW (2007) Genome-wide analysis of the phospholipase D family in Oryza sativa and functional characterization of PLD beta 1 in seed germination. Cell Res 17: 881–894.
- 41. Singh A, Baranwal V, Shankar A, Kanwar P, Ranjan R, et al. (2012) Rice phospholipase A superfamily: organization, phylogenetic and expression analysis during abiotic stresses and development. PLoS One 7: e30947.
- 42. Singh A, Pandey A, Baranwal V, Kapoor S, Pandey GK (2012) Comprehensive expression analysis of rice phospholipase D gene family during abiotic stresses and development. Plant Signal Behav 7: 847–855.
- 43. Knight H, Knight MR (2001) Abiotic stress signalling pathways: specificity and cross-talk. Trends Plant Sci 6: 262–267.
- 44. Luan S, Kudla J, Rodriguez-Concepcion M, Yalovsky S, Gruissem W (2002) Calmodulins and calcineurin B-like proteins: calcium sensors for specific signal response coupling in plants. Plant Cell 14 Suppl: S389–400
- 45. Pandey GK (2008) Emergence of a novel calcium signaling pathway in plants: CBL-CIPK signaling network. Physiol. Mol. Biol. Plants. 14(1): 51–68.
- 46. Weinl S, Kudla J (2009) The CBL-CIPK Ca2+-decoding signaling network: function and perspectives. New Phytol 184: 517–528.
- 47. Das R, Pandey GK (2010) Expressional analysis and role of calcium regulated kinases in abiotic stress signaling. Curr Genomics 11: 2–13.
- 48. Georges F, Das S, Ray H, Bock C, Nokhrina K, et al. (2009) Over-expression of Brassica napus phosphatidylinositol-phospholipase C2 in canola induces significant changes in gene expression and phytohormone distribution patterns, enhances drought tolerance and promotes early flowering and maturation. Plant Cell Environ 32: 1664–1681.
- 49. Yotsushima K, Mitsui T, Takaoka T, Hayakawa T, Igaue I (1993) Purification and characterization of membrane-bound inositol phospholipid-specific phospholipase C from suspension cultured rice (Oryza sativa L.) cells (identification of a regulatory factor). Plant Physiol 102: 165–172.
- 50. Huang CH, Tate BF, Crain RC, Coté GG (1995) Multiple phosphoinositide-specific phospholipases C in oat roots. Characterization and partial purification. Plant J 8: 257–268.
- 51. Rupwate SD, Rajasekharan R (2012) C2 domain is responsible for targeting rice phosphoinositide specific phospholipase C. Plant Mol Biol. 78: 247–258.
- 52. Gaude N, Nakamura Y, Scheible WR, Ohta H, Dormann P (2008) Phospholipase C5 (NPC5) is involved in galactolipid accumulation during phosphate limitation in leaves of Arabidopsis. Plant J 56: 28–39.
- 53. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, et al. (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28: 2731–2739.
- 54. Ray S, Agarwal P, Arora R, Kapoor S, Tyagi AK (2007) Expression analysis of calcium-dependent protein kinase gene family during reproductive development and abiotic stress conditions in rice (Oryza sativa L. ssp. indica). Mol Genet Genomics 278: 493–505.
- 55. Lescot M, Dehais P, Thijs G, Marchal K, Moreau Y, et al. (2002) PlantCARE, a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences. Nucleic Acids Res 30: 325–327.
- 56. Chakrabarty R, Banerjee R, Chung SM, Farman M, Citovsky V, et al. (2007) PSITE vectors for stable integration or transient expression of autofluorescent protein fusions in plants: probing Nicotiana benthamiana-virus interactions. Mol Plant Microbe Interact 20: 740–750.
- 57. Walter M, Chaban C, Schutze K, Batistic O, Weckermann K, et al. (2004) Visualization of protein interactions in living plant cells using bimolecular fluorescence complementation. Plant J 40: 428–438.
- 58.
Waadt R, Kudla J (2008) In planta visualization of protein interactions using bimolecular fluorescence complementation (BiFC). CSH Protoc 2008: pdb prot4995.