- Open Access
A systems biology approach toward understanding seed composition in soybean
BMC Genomics volume 16, Article number: S9 (2015)
The molecular, biochemical, and genetic mechanisms that regulate the complex metabolic network of soybean seed development determine the ultimate balance of protein, lipid, and carbohydrate stored in the mature seed. Many of the genes and metabolites that participate in seed metabolism are unknown or poorly defined; even more remains to be understood about the regulation of their metabolic networks. A global omics analysis can provide insights into the regulation of seed metabolism, even without a priori assumptions about the structure of these networks.
With the future goal of predictive biology in mind, we have combined metabolomics, transcriptomics, and metabolic flux technologies to reveal the global developmental and metabolic networks that determine the structure and composition of the mature soybean seed. We have coupled this global approach with interactive bioinformatics and statistical analyses to gain insights into the biochemical programs that determine soybean seed composition. For this purpose, we used Plant/Eukaryotic and Microbial Metabolomics Systems Resource (PMR, http://www.metnetdb.org/pmr, a platform that incorporates metabolomics data to develop hypotheses concerning the organization and regulation of metabolic networks, and MetNet systems biology tools http://www.metnetdb.org for plant omics data, a framework to enable interactive visualization of metabolic and regulatory networks.
This combination of high-throughput experimental data and bioinformatics analyses has revealed sets of specific genes, genetic perturbations and mechanisms, and metabolic changes that are associated with the developmental variation in soybean seed composition. Researchers can explore these metabolomics and transcriptomics data interactively at PMR.
As the propagule that ensures the dissemination of plants, seeds also support human activity as one of the major products of agriculture. Both of these functions are contingent on biochemical storage reserves that are deposited within the seed during its development. Despite the vast taxonomic variation in the organ and tissue structures that are used to store these reserves, chemically they fall into three general categories: proteins, oils and carbohydrates . In addition to being a major source of food, animal feed, and industrial feedstocks, these seed reserves are the primary source of carbon, nitrogen, sulfur, and energy required for seed germination and establishment of the growing seedling. During germination prior to the seedling becoming photoautotrophic, seed reserves are mobilized and their catabolism provides the emerging seedling with energy and biochemical precursors needed for growth [2, 3].
There is considerable taxonomic variation in the relative ratios of seed reserves. The genetic basis for these taxonomic differences in seed composition is unclear. In each species, however, oil, carbohydrate and protein reserves are biosynthesized by the programmed expression of a metabolic network during seed development. This metabolic network converts imported photosynthetically-derived carbon (usually in the form of sucrose) and imported nitrogen (usually as amino acids) into the final proportion of protein, oil and carbohydrate [3–5].
On average, most commercial lines of soybean grown in the Midwestern states of the US are composed of 40% protein, 20% oil, 15% soluble carbohydrate, and 15% fiber . Soybean seeds provide about 27% of the world's supply of oils and about 44% of the world's supply of proteins . As with other plant species, soybean seeds undergo a developmentally-programmed switch in metabolism to a "seed fill" mode, such that by maturity the embryo within the seed has accumulated the three major classes of reserves. There is considerable knowledge concerning the basic biochemical processes by which imported carbon and nitrogen are converted to the final products, protein, oil and carbohydrate. A great deal remains to be learned, however, concerning the molecular, biochemical and genetic mechanisms that regulate these complex metabolic networks.
Recent developments in omics have started to provide the catalogue of genes/metabolites that are required for seed development. Analyses of mRNA abundance during seed development, maturation, and beyond are providing clues as to the global gene expression that determines final seed structure and composition in Arabidopsis [8–12], Medicago truncatula [13–15], Brassica napus [16, 17], rice [18, 19], barley , and soybean . The final chemical composition of a seed is a consequence of gene expression during its development. However, this provides only a partial picture. Most genetically, developmentally, or environmentally induced alterations in biology are ultimately manifested as changes in the concentration of metabolites. Metabolomics thus can provide snapshots of the chemical composition of biological tissues over time that indicate how changes in mRNA accumulation might impact metabolism, and reveal alterations of metabolism that might result from genetic or environmental perturbations. Technological advances in metabolomics have greatly enhanced sensitivity and resolution, making it an important tool for functional genomics [22–25]. Metabolite profiling, extensively used in the design of pharmaceuticals (e.g., [26–30]), is thus providing a powerful approach to addressing plant biology [31–39]. Recently, transcriptomics and metabolomics data have been obtained to identify major developmental and metabolic transitions during soybean var. Williams 82 embryo development . Metabolic flux mapping enables identification of the critical metabolic pathways in quasi-steady-state conditions such as seed fill [40–47], and has been applied to understand the metabolism of soybean filling , the effect of temperature on soybean composition , and the impact of light in seed fill .
Here, we have coupled developmental profiles of mRNA abundance with metabolomics analysis and metabolic flux within the embryo to gain insights into these integration and expression of the biochemical program that controls soybean seed development and its regulatory networks. To explore the data, and to enable others to do the same, we have deposited the transcriptomics and metabolomics data for developing soybean seeds in the public platform, PMR (Plant/Eukaryotic and Microbial Metabolomics Systems Resource, http://www.metnetdb.org/pmr. These platforms, integrated the MetNet computational tool suite http://metnetdb.org/[38, 49, 50], were combined with targeted statistical analyses. The software empowers researchers to use metabolomics data and transcriptomics data of developing soybean seeds to develop hypotheses concerning the organization and regulation of metabolic networks. The combined use of these tools provides novel insights into the structure and regulation of the network that supports soybean seed development.
Results and discussion
Systems biology approach
Many current models of biological networks are based solely on transcript accumulation data , which cannot give a complete picture of cellular metabolism . Thus, combined analysis of omics datasets is essential [37, 53], and software is being developed to address these "big data" analyses . In this study, we integrated metabolomics, transcriptomics and metabolic flux analyses to better understand the metabolic and regulatory programs that control soybean seed composition. Targeted statistical methods in R , combined with the MetNet systems biology platform http://www.metnetdb.org[38, 49, 50], were used for data analyses.
Specifically, to empower the use of soybean metabolomics and transcriptomics data in the development of hypotheses concerning the organization and regulation of metabolic networks, we modified Plant/Eukaryotic and Microbial Metabolomics Systems Resource (PMR: http://www.metnetdb.org/pmr by incorporating soybean gene annotations from SoyBase http://www.soybase.org/. Additional functional annotations of the 37,593 Glycine max probes were deduced via sequence homology with Arabidopsis genome annotations (TAIR10).
PMR, an interactive public database with associated analysis tools, is designed for data exploration and hypothesis formulation by researchers. In order to achieve the high power computations required for analyses of omics data, we utilize the emerging database system, NoSQL , which accelerates retrieval of large data from databases. Because PMR is based on a NoSQL environment , co-analysis of correlations with associated false discovery rate (FDR) values is quick and efficient even in big datasets such as transcriptomics data. These co-analyses can be visualized and used to postulate the genes/metabolites that may be involved in particular metabolic processes and these postulates can then be experimentally tested.
Pathways consist of a large number of entities (e.g., genes, proteins, protein complexes, enzymes, transcripts, and metabolites) and interactions among these entities. The pathways in MetNetDB are classified into different categories and visualized online http://metnetonline.org/browse_class.php. To identify over-represented pathways associated with the entities-list (e.g., differentially expressed genes in a sample), MetNet/PMR provides an "Over-representation Search" function, which ranks known metabolic pathways by the statistical significance (using Fisher's exact test) .
Evans seed development
The development of embryos into seeds is marked by large metabolic conversions as imported photosynthate and amino acid precursors are converted to protein, oil and polysaccharide seed reserves. The timing of this developmental program is genetically predetermined and influenced substantially by environmental effects. In soybeans, this program is completed within 60 days after pollination. We used line Evans (PI 548.560), a high-yielding commercial variety previously grown in the Northern US market, to investigate the expression and accumulation profiles during this developmental timeline. Pods of a similar length containing three homogenous seeds were harvested from field-grown plants at five time points from 25 to 50 days after flowering (DAF), and seeds were placed directly into liquid N2. Figure 1A shows the typical morphology of the harvested pods and two of the enclosed seeds at the times of harvest. By 20 DAF, pods had reached their mature lengths and the seeds were undergoing filling (Figures 1A and 1B).
Seed filling involves increasing accumulation of protein and oil reserves, whereas starch levels decline (Figure 1C); concomitantly, these seeds gradually desiccate through this process (Figure 1B). Proportionately, oil content (% per dry weight) increases at the expense of starch content, but protein content (% per dry weight) stays relatively constant throughout this developmental program (Figure 1D). This general profile has also been reported in the oilseed Arabidopsis, which has little starch in the mature seed. However, analysis of the Arabidopsis starch-in-mature-seed sse1 mutant indicated that starch may be converted to oil in Arabidopsis seeds . Interestingly, starch biosynthetic mutations did not increase the oil content in the sse1 background . This suggested the decreased oil was not the result of increased carbon to starch in the sse1 mutant. Whether oil is generated directly from metabolism of starch in soybeans is not known, but the fact that the oil accumulation precedes the decline in starch content by >15 days (Figure 1D, 20-35 DAF) implies a more complex conversion process.
Metabolomic determinations during seed development
To identify metabolic changes associated with seed development and storage product accumulation, metabolomic analysis was conducted on developing seeds harvested at 25, 30, 35, 45 and 50 DAF. A combination of targeted (free amino acids, esterified fatty acids, and sterols) and non-targeted profiling platforms resulted in about 400 analyte peaks, each representing one (or more) metabolic entities. Of these, 273 were above the detection limit of the analytical platforms for all replicates of at least one time point: 148 of these analytes were chemically defined (amino acids and amines (31), aromatics (7), esterified fatty acids (12), free fatty acids (12), organic acids (15), and sugars and derivatives (alcohols and acids: 41, sterols and tocopherols: 30)), and the remaining 125 are as yet unidentified.
Each metabolite's abundance data (natural log transformed and median centered) was used to identify which metabolites were differentially accumulated during seed development and q-values were calculated . Interestingly, all metabolites had a q-value (FDR) < 0.17, and 173 of the metabolites had a q-value < 0.05 (Additional file 1: Table S1a). These analyses indicate that the relative abundances of the majority of the 273 metabolites varied significantly during seed development.
Metabolites were grouped together with similar patterns over seed development into five clusters (designated as Clusters M1-5, where M indicates it is a cluster of metabolites) (Figures 2A, B and Additional file 1: Table S1a). Each cluster showed distinguishing characteristics relative to the timing of the changes in abundance levels. In Cluster M1, metabolites steadily increased throughout seed development. Metabolites in Cluster M2 stayed at a steady basal level during early stages of seed fill, but increased around 40 to 50 DAF. Metabolite abundances in Cluster M3 peaked at 40 DAF. Metabolites in Cluster M4 reached a basal level by 45 DAF; metabolites in Cluster M5 decreased throughout seed fill.
The metabolites from the eight chemical classes of metabolites are not distributed in each cluster in proportion to their distribution in the whole group (all p-values < 0.05, Table 1 right column). Further, the metabolites in amino acids and amines, esterified fatty acids, free fatty acids, and sterols are not evenly distributed in each cluster (p-value < 0.05, Table 1 bottom row). As indicated in Figure 2B and Table 1 free fatty acids, esterified fatty acids, aromatics, and sterols are mostly grouped in Clusters M1, M2 and M3, whereas free amino acids and the organic acids are predominantly in Clusters M4 and M5. Sugars and derivatives show a mixed pattern, some increasing and other decreasing over time. We interpret these data to reflect the differential roles of different classes of metabolites during seed development, revealing the differential timing of the complex metabolic network in the seed that supports establishment of mechanisms that will enable the ensuing seedling to thrive.
Total free amino acids decreased during seed development, and their relative ratio also changed (Figure 2C and Additional file 1: Table S1b). Of the 20 free amino acids identified by the targeted platform that had a decreasing pattern during seed development (Figure 2C), at the early stages of seed fill asparagine was the most abundant, followed by histidine, glutamine, glutamate, lysine, aspartate and serine. As seeds developed, the relative proportions of asparagine, histidine, and glutamine decreased, while the relative proportions of glutamate, lysine, and aspartate increased so that by 50 DAF glutamate, lysine, and aspartate were the most abundant free amino acids. The accumulation of some amino acids (including asparagine, glutamate, serine, isoleucine, tyrosine, methionine, proline, valine, and particularly alanine) peaked at 30 DAF, while lysine, aspartate, phenylalanine, leucine, isoleucine, and methionine had a small peak at 45 DAF. Tryptophan accumulation increased throughout seed development. The concentration of free asparagine was reported to be positively correlated with protein content in maturing soybean seeds ; the relative high abundance of asparagine may play an important role in protein accumulation in Evans seeds.
The twelve most abundant esterified fatty acids all increased during seed development (i.e., they were in Clusters M1-3; Figure 2D and Additional file 1: Table S1c). Linoleate (18:2) was the most abundant fatty acid, followed by oleate (18:1), palmitate (16:0), stearate (18:0), and linolenate (18:3); while tricosanoic acid (23:0) was the least abundant. There was little change in the relative abundances of the individual fatty acids (Additional file 1: Table S1c).
Free fatty acid accumulation generally increased across seed development. Of the 17 free fatty acids identified by the non-targeted platform, linoleate (18:2) was the most abundant, followed by oleate (18:1), linolenic acid (18:3), and octadecanoate (22:0) (Figure 2E and Additional file 1: Table S1d). The rank of relative percent of most fatty acids compared to total fatty acids was similar; however, the rank of linolenic acid (18:3) and heptadecanoic acid (17:0) decreased when seeds were maturing.
Twenty-two of the 30 sterols, including sitosterol, campesterol, stigmasterol, phytol, and isofucosterol, increased in abundance during seed development (Figure 2F and Additional file 1: Table S1e). The relative abundance of them to total sterols was almost unchanged during seed development.
Transcriptomic changes during seed development
In parallel to the metabolomics experiments, aliquots of the seeds were subjected to transcriptomics profiling. RNA was isolated from seeds harvested at 25, 30, 35, 45 and 50 DAF, with two biological replicates at each time point. The levels of 37,593 transcripts represented by probes on the Glycine max Affymetrix chip were determined. The natural logarithm of the MAS 5.0 signal was median-centered and used as the measure of expression. The analysis focused on identifying those genes that are differentially expressed during seed development. Levels of transcripts represented by 6,389 of the 37,593 probes varied among the different time points (p-value < 0.01); 2,869 of these were differentially expressed over seed development when significance was defined as q-value < 0.01.
These 2,869 probes that were significantly differentially expressed were grouped into eight clusters according to their expression patterns during seed development (designated as Clusters T1-8, where T indicates it is a cluster of transcripts) (Figure 3 and Additional file 2: Table S2a).
The 2,869 differentially expressed soybean transcripts were mapped to 2,451 Arabidopsis locus IDs and had 2,430 orthologous unique Arabidopsis locus IDs that provide functional annotation data (Additional file 2: Table S2a); Gene Ontology (GO) functional categorization of cellular component, biological process and molecular function http://www.arabidopsis.org/tools/bulk/go/index.jsp provides a very rough indication of the constitution of each cluster according to the GO of the matched Arabidopsis locus IDs (Additional file 2: Table S2b). Metabolic processes rank high in each cluster, followed by stress responses and developmental processes.
MetNet AtGeneSearch http://www.metnetdb.org/MetNet_atGeneSearch.htm indicated that among the 2,451 differentially expressed genes, several pathways were represented and fell into one of four categories: biosynthesis, respiration and related energetics, signaling transduction and degradation or assimilation. Particularly, represented pathways were: 1) biosynthesis of carbohydrates (sucrose and starch), lipids (fatty acid biosynthesis and elongation, linoleate and sterol synthesis), and amino acids; 2) respiration, specifically, glycolysis and the TCA cycle; 3) regulatory and signaling pathways including the AGRIS regulatory network, jasmonate (JA) biosynthesis, IAA/ethylene/gibberellin acid signaling, and regulation of gibberellin metabolism/ethylene signaling; 4) catabolism of sucrose and some amino acids (e.g., phenylalanine, glutamate, and valine) (Additional file 2: Table S2c1).
MetNet's "Over-representation Search" http://metnetonline.org/searchpathway.php identifies over-represented pathways using Fisher's exact test given a user-supplied list of genes. The linoleate biosynthesis, chlorophyllide a biosynthesis, fatty acid β-oxidation, gibberellic acid biosynthesis, and 4-aminobutyrate degradation pathways are each over-represented from among all the 2,451 differentially expressed genes (Fisher's exact test p-value < 0.05) (Figure 4A and Additional file 2: Table S2c2).
Analysis of the genes from each cluster (Figure 3) shows that the pathways that most genes were involved in also belonged to one of the four groups mentioned above (Additional file 2: Table S2d); these pathways were predominantly related to the biosynthesis of carbohydrates, lipids, and amino acids. The "Over-representation Search" provided information about which pathways were over-represented in each cluster (Additional file 2: Table S2e). In particular, processes that are more enriched in particular clusters are: fatty acid beta-oxidation, jasmonic acid biosynthesis and valine and methionine degradation (Cluster T1); flavonoid synthesis, IAA signaling and lysine degradation (Cluster T2), linoleate synthesis and sorbitol degradation (Cluster T3), ricinoleate biosynthesis (Cluster T4), arginine biosynthesis, photosynthesis, glycolysis, ethylene signaling and sucrose degradation (Cluster T5), homoserine, threonine biosynthesis, glycolysis, pentose phosphate pathway, and the TCA cycle, GA and JA signaling, ammonia assimilation and glutamate degradation (Cluster T6), flavonoid biosynthesis, GA and ethylene signaling, and stress regulation (Cluster T7), and chlorophyll a biosynthesis (Cluster T8).
Statistical analyses of the transcriptomics and metabolomics data
After an initial examination of the transcriptomics data, we focused on the 2,451 transcripts with matched Arabidopsis genes (with better annotations and pathway information than the soybean locus IDs) that showed significant changes during seed development. Using these 2,451 genes as an initial gene list, we have queried MetNetDB to identify pathways that were over-represented in the overall list, and in each gene Cluster (T1-8) as above. Here we used two statistical calculations: a) multiresponse permutation procedure (MRPP) ; and b) Fisher's exact test . The MRPP method has the power to find pathways/categories that display significantly non-constant patterns of accumulation over time and/or categories in which the correlation structure among genes/metabolites changes over time. The MRPP method tests if a group of genes/metabolites changed expression/accumulation significantly over the seed development time series. Pathway information in MetNetDB was used to identify those over-represented pathways that contained at least two members. In contrast to the MRPP analysis , the Fisher's exact test is used to find groups of transcripts/metabolites over-represented within significantly changed transcripts/metabolites.
Pathways analysis of transcriptomics data by MRPP identified 273 pathways whose joint expression distribution changed significantly during development at the level of q-value < 0.05 (Additional file 3: Table S3a1). The significantly changed pathways of amino acid biosynthesis are visualized by MetNet Plug-ins for Cytoscape http://www.metnetdb.org/MetNet_fcmodeler.htm (Figure 4B). The MetNet Plug-ins for Cytoscape http://www.cytoscape.org/ are a set of Java open-source programs for visualizing and analyzing biological networks . Analyses of the complex data can be linked to an interactive metabolic network display as specified by the user. This software allows for the display of a metabolic network that can be closely coupled with the other data displays and analyses; e.g., clustering, visualization, literature text processing, and data from high-throughput experiments (transcriptomics, proteomics and metabolomics) can be displayed and modeled in the context of the network graphs.
The Fisher's exact tests require at least two Affymetrix probe sets be affiliated with a pathway or category. The Fisher's exact tests identified 23 pathways/categories that are significantly over-represented among the 2,869 transcripts (Additional file 3: Table S3a2). Both MRPP tests and Fisher's exact tests identified starch and flavonoid biosynthesis (Additional file 3: Tables S3a1 and S3a2).
Gene categories defined using GO terms provided a rough idea of the results; i.e., all genes sharing any particular term were considered a category. However, not all GO terms yielded a gene category because we required that at least 2 Affymetrix probe sets be affiliated with a term before establishing a category. Both MRPP tests and Fisher's exact tests identified steroid and amino acid biosynthesis (Additional file 3: Tables S3b1-S3b6) in GO biological process.
Pathways analysis of metabolomics data by MRPP tests (Additional file 3: Table S3c1) identified 45 pathways including amino acid biosynthesis (Figure 4C), sterol and hormone synthesis. Fisher's exact tests (Additional file 3: Table S3c2) analysis identified seven pathways enriched among metabolites with differential accumulation, including arginine and sterol biosynthesis.
Pathways analysis of transcriptomics and metabolomics data by MRPP tests (Additional file 3: Table S3d) identified sterol and starch pathways as significant, as well as phospholipid, glutamate, histidine, proline biosynthesis, sucrose and starch metabolism in photosynthetic tissue, and IAA biosynthesis. These analyses indicate that genes/metabolites involved in these pathways change significantly over the time.
Exploration of transcription factor genes that may regulate expression of the transcripts
To identify transcription factors that were candidates as regulators of expression of genes in clusters T1-8, we conducted a promoter motif analysis on the promoter regions taken as 1000 bp upstream of the "ATG" translational start-codon of each soybean transcript, using the annotation from SoyBase . Within each of the promoter-regions, we identified potential motifs that regulate transcription, and compared their distribution among the promoters of the genes of each of the eight transcriptomics clusters with the promoters of all soybean genes. Fisher's exact test was used to evaluate this comparison; motifs with p-value < 0.05 are detailed in Additional file 4: Table S4. These motifs predict transcription-factor binding motifs that may control the expression of each cluster. For example, promoters from Cluster T6 genes are enriched in JA signaling and response motifs (Additional file 2: Table S2d). Particularly, 111 genes within Cluster T6 (out of 400 total), contained the promoter motif "T/GBOXATPIN2" (Additional file 4: Table S4). This "T/G-box" motif was identified in the tomato proteinase inhibitor II (pin2) and leucine aminopeptidase (LAP) gene promoters, and was thought to be involved in the JA induction of these genes; moreover, bHLH-Leu zipper transcription factors, JAMYC2 and JAMYC10 specifically recognized this motif . The jasmonate biosynthesis pathway was also over-represented in this cluster. Thus, a hypothesis that we could derive from this analysis is that member(s) of the bHLH-Leu class of transcription factors in soybean, analogous to JAMYC2 and JAMYC10 in tomato and Arabidopsis, have a significant role in regulating the expression of many genes found in Cluster T6.
Metabolic flux changes during early seed development
Carbon regulation can be evaluated by analyzing the fluxes and the flux ratios of various branch points in the reaction network . Comparing flux through metabolic pathways with metabolomic and transcriptomic data can provide a novel perspective into metabolic expression resulting from genetic programing. Metabolic flux has been evaluated in soybean seeds under a number of conditions, and in several genotypes [45, 46, 48]. Here we used Evans seeds to provide a parallel determination of flux, and compared with the metabolomics and transcriptomics data.
The flux of metabolites was determined in isolated cotyledons in medium containing 13C [45, 46] (Additional file 5: Tables S5a and S5b). The flux represents the pathway dynamics in the cotyledons at the quasi-steady-state developmental stage of early seed fill (21-26 DAF). The metabolic flux map representing central carbon metabolism is visualized in Figure 5A. The metabolic reaction network in early seed-fill soybean cotyledons consists of parallel pathways of glycolysis and oxidative pentose phosphate pathway (oxPPP) in the cytosol and the plastid. Flux through the γ-aminobutyric acid (GABA) shunt was quite high, as was the flux through glycolysis, the TCA cycle, and oxPPP. The high flux through the GABA shunt may reflect the need to shuttle glutamine and α-ketoglutarate between mitochondria (where the TCA cycle is located), and the plastids (the site of glutamine assimilation). Our analyses of the transcriptomics and metabolomics data identified pathways that were significantly changed during seed development (Additional file 3: Table S3) among those pathways identified as having a high flux. For example, in the transcriptomics data the TCA cycle and glycolysis were over-represented by Fisher's Exact test, with representative genes of these pathways decreasing during seed development (Clusters T5 and T6), and the MRPP test indicated these processes were significantly changed. Similarly, levels of metabolites in the TCA cycle and that of glutamate were altered. The flux through non-oxidative reactions of the oxPPP catalyzed by the transketolase (tkt) and transaldolase (tal) enzymes was much greater in the plastid as compared to the comparable cytosolic reactions. F16BPase, a key reaction of gluconeogenesis, was also higher in the plastid than the cytosol. The relative flux rate through a number of amino acid biosynthetic pathways (e.g., serine, glycine and cysteine) was comparatively low at this stage of seed development; this may indicate that these amino acids are formed predominantly via interconversion from other intermediates.
In most cases, the conclusions from the metabolic flux data were supported by the transcriptomics data (shown as green-color arrows in Figure 5B). For enzymes that are present in multiple subcellular compartments (e.g., cytosol, plastid, and mitochondrion), conclusions were supported by the transcriptomics data with the appropriate subcellular located isozyme-coding transcripts matching the flux analyses. The transcript levels of many genes of the GABA shunt, TCA cycle and glycolysis accumulated at far above median level; these transcript levels often reflect their metabolomic flux rate levels. For example, the flux through glutamate synthase (GOGAT) was about 21-fold greater than the flux through xylulose-5-P/P translocator (p5pT). Following the same trend, the level of the transcript encoding GOGAT was about 30-fold higher than the level of the transcript encoding p5pT.
Integration of metabolomics and transcriptomics data in metabolic networking
We integrated these complex datasets to interpret metabolic changes associated with seed composition, highlighting as examples, the metabolism of asparagine, starch, and fatty acids. The amino acid asparagine is the major form of nitrogen imported from the vegetative soybean plant by the developing embryo and interconverted to other amino acids to support protein synthesis; it is therefore considered to be important to protein content in mature seeds . We evaluated this aspect of metabolism using PMR. Volcano plots comparing the metabolomics of seeds at 25 and 50 DAF indicate that free amino acids are more abundant in 25 DAF seeds (also reported for several amino acids in Collakova et al ), while sterols are greatly increased in 50 DAF seeds (Figure 6A). As indicated by Figure 2C, Asn was the most abundant free amino acid in the developing Evans seeds but decreased quickly after 30 DAF. Co-analysis of the metabolomics and transcriptomic data indicated that Asn concentration varied during seed development and that this pattern strongly correlated with one of the six transcripts computationally predicted to encode an asparaginase-like gene (soybean locus ID: Glyma05g07420; Figure 6B). These data lead us to predict that the Glyma05g07420 gene encodes the particular asparaginase enzyme that is associated with amino acid interconversion during seed fill.
Further scrutiny of the over-represented pathways of the gene list identified by co-analysis of Asn to all transcripts (Pearson correlation 0.9-1.0; p-value < 0.05) (Figure 6C) revealed pathways involved in biosynthesis, respiration, regulatory and signaling pathways, and catabolism, particularly asparagine biosynthesis, were also over-represented. Figure 6D showed a pathway-graph for asparagine degradation from the over-represented pathways list in PMR. Co-analysis of Asn to all metabolites (Pearson correlation 0.88-1.0; p-value < 0.05) revealed amino acids, as well as lipid (such as trans-butenedioic Acid), and oligosaccharide etc.
Figure 7 illustrates a MetaOmGraph visualization http://www.metnetdb.org/MetNet_MetaOmGraph.htm of the levels of the transcripts known or postulated to be in starch and fatty acid metabolism during soybean seed development. Consistent with measured starch accumulation, which decreased rapidly after 45 DAF (Figure 1C and 1D), the levels of transcripts involved in starch synthesis and of those related transporters decreased after 45 DAF, while those involved in starch degradation had a rapid increase after 45 DAF. Expression of many postulated and known fatty acid metabolism genes was correlated with oil accumulation (Figure 1C and 1D). Oil increased steadily till 40 DAF, at which point oil content declined somewhat. A decrease in oil content at late seed maturation has also been reported previously in seeds of Arabidopsis and soybean [12, 21]. The genes putatively involved in fatty acid synthesis and elongation decreased expression after 40 DAF, whereas genes involved in β-oxidation increased expression after 45 DAF. This may reflect, as has been shown for Arabidopsis , that during the later part of development, seeds prepare for the coming germination process when β-oxidation will be required to mobilize the stored oil reserves.
The global profiling of genome expression during seed development provides the basis to formulate testable hypotheses regarding the function of genes and ultimately to identify the genetic regulatory networks that determine the structure and composition of the mature seed. Here, we detail the metabolomic and transcriptomic profiles of developing seeds of Glycine max, var. Evans, from early seed fill to maturation and desiccation. Furthermore, we illustrate the utility of Plant/Eukaryotic and Microbial Metabolomics Systems Resource (PMR). In part because it is an NoSQL environment, PMR provides rapid co-analysis of correlations with associated statistical determinations even for big data. PMR thus enables life scientists to explore metabolomics, transcriptomics datasets and to develop and extract biologically informed hypotheses from the data.
Soybean seed filling follows a developmental program in which protein and oil reserves increase, while starch levels decrease during seed development. Overall, the data substantiate the dynamic nature of seed development. During early seed fill, metabolic flux was greatest through the GABA shunt, glycolysis, the TCA cycle, and oxPPP. This is reflected in the transcriptomic and metabolomic data collected during seed development, with changes in metabolites and transcript levels being consistent with the changes in flux through these pathways. Interactive analysis of the transcriptomics data led to the identification of a transcription factor class, bHLH-Leu, that we postulate may participate in regulating the expression pattern of a co-expressed cluster of genes enriched in JA signaling and response motifs during soybean seed fill.
Our analyses indicate that during seed development modulations in end-products of metabolism are affected by a small proportion of the soybean genome, and that the majority of gene transcripts showed a relatively constant level of expression. In contrast, although the metabolite profiling is not as comprehensive as the transcriptomic profiling, the levels of almost every detectable metabolite are modulated during seed development. These metabolites are primarily the intermediates of the final storage reserves (i.e., intermediates of starch metabolism, and phospholipid and amino acid biosynthesis), but also includes metabolites that are unrelated to the seed reserves (e.g., sterol metabolism). These findings suggest that the metabolome is more sensitive to the developmental program than is the transcriptome. This is probably indicative of the fact that as genetic information is expressed through the processes of transcription and translation, coupled with the catalytic properties of the proteome, subtle changes at the transcriptome level are amplified at the level of the metabolome.
The combination of genetic resources, high-throughput experimental data and integrated bioinformatic analyses presented herein has enabled correlative-led depiction of complex programmed metabolic changes, which determine the composition of soybean seeds. The full transcriptomics and metabolomics data are freely available to researchers at PMR, http://www.metnetdb.org/pmr.
Plant growth and harvest
Glycine max variety Evans was grown in the field at the Bruner Research Farm near Ames, IA. Flowers at mid-plant nodes were tagged as they opened. Pods were harvested at 20, 25, 30, 35, 40, 45, and 50 DAF. Two replicate samples of three-seed pods were collected for each stage; 20 pods from five or six different plants were pooled for each replicate.
Oil, protein, and starch determination
Oil was extracted from 100 mg freeze-dried tissue with 1 ml hexanes at 45°C for 60 min. The residue was pelleted by centrifugation at 5500 g for 10 min, and the extraction procedure was repeated four times. The pellet was retained for protein and starch analysis. The combined hexane-supernatants were pooled, dried at 60°C for 48 h. Soluble protein in the defatted pellet was precipitated 3 times in 1 ml of 240 g kg-1 trichloroacetic acid and quantified by a Micro-Kjeldahl procedure . Starch content was determined from 25 mg of the dried defatted pellet. Soluble sugars were removed by extracting the pellet with 4 treatments of 1 mL of 800 mL L-1 ethanol heated at 60°C for 20 min, then centrifuged at 5500 g for 10 min. Starch in the final pellet was solubilized in water at 100°C and digested with amyloglucosidase according to Adams et al . The liberated glucose was determined using a glucose oxidase technique  employing a microsample plate reader. Starch content was calculated as (mg glucose × 0.9).
Plant material for transcriptomics and metabolomics
Pods were frozen immediately in dry ice and stored at -80°C until analysis. Frozen seeds were removed from the pods and selected visually for uniformity in size within each sample. The number of seeds extracted varied with seed development (7, 5, 4, 3, and 4 seeds were pooled at 25, 30, 40, 45, and 50 DAF, respectively).
RNA and microarray analysis
RNA was extracted using the TRIzol RNA isolation protocol (Invitrogen Life Technologies, CA), and purified by Qiagen RNeasy Mini Kit (Qiagen, CA). Synthesis of labeled cRNAs, hybridization with Soybean Genome Arrays (Affymetrix, Santa Clara, CA), and scanning of the probe array were performed at the Iowa State University GeneChip Facility (Ames, IA). For data analysis, relative expression intensities were generated and normalized with Microarray Suite (MAS) 5.0 software (Affymetrix, CA) in the form of signal values. Global scaling (Affymetrix, CA) was used to normalize the data by adjusting the mean expression level of each chip to a value of 500.
The consensus sequences on the GeneChip® Soybean Genome Array downloaded from Affymetrix http://www.affymetrix.com/support were used to identify the Arabidopsis orthologs. The annotation is available in SoyBase http://soybase.org/AffyChip/AffychipAnnotation_Glyma1.1.txt?Submit=Submit.
Four different analytical procedures were used to evaluate the relative abundance of metabolites in developing soybean seeds. Frozen seeds were initially pulverized into a powder while frozen in liquid N2 using a Freezer/Mill (SPEX SamplePrep, NJ). The powder was stored at -70°C until extraction.
Three of the four analytical procedures were targeted to specific class of metabolites (free amino acids, free fatty acids and phytosterols), the fourth was a non-targeted metabolite profiling procedure. A known weight of between 10 and 50 mg of pulverized soybean seeds were used in each analytical procedure. Details of each procedure are available at PMR http://www.metnetdb.org/pmr, as are the experimental data and metadata. We have previously used these methods to profile such metabolites in soybean , Arabidopsis [69–71], and Hypericum spp . Combining the data from all these analytical platforms provided relative abundances of 338 analytes. Of these, 171 could be classified into seven chemically defined classes: free amino acids and amines (36 entities), aromatics (9 entities), esterified fatty acids (12 entities), free fatty acids (17 entities), organic acids (19 entities), sterols (30 entities), and sugars and derivatives (48 entities); an additional 167 analytes are chemically undefined (the eighth class of metabolites).
Seed growth, harvest, and culture for metabolic flux analysis
The plants were gown, seeds were harvested, and cotyledons were cultured and analyzed as previously described . Plants were grown in growth chambers under controlled conditions 27°C/20°C day/night, and 14-hour light. Pods were harvested 21 DAF. Four cotyledons (one from each seed) were isolated and cultured for six days. The medium was replaced after three days to ensure sucrose, the primary source of carbon to the cotyledons in planta, did not limit cotyledon growth in vitro. The flasks were shaken at 100 rpm, 26°C. Cotyledons were harvested after 6 days in culture for flux analyses. The absolute and relative metabolic fluxes were analyzed as described previously [45, 46].
Metabolic and transcriptomic data analysis
Metabolite accumulation levels were natural log transformed and median centered; similar data transformation was applied to Affymetrix signal values within each chip. These normalized log signals were analyzed separately for each metabolite/probe set using a linear model. Each linear model included fixed effects for replications and time points. As part of each linear model analysis, an overall F-test was conducted to scan for any change in mean accumulation/expression across the time points examined. The p-values from these F-tests were converted to q-values  to control FDR at specified levels.
Cluster and over-representation analysis
K-medoids cluster analysis  was used to organize and visualize the accumulation patterns of the 273 metabolites that were above detection limits for at least one of the five time points during seed development. A similar analysis was also conducted for the 2,869 transcripts with q-values less than 0.01 in the overall F-test for change of expression over time. Euclidean distance between standardized accumulation/expression profiles was used to determine the dissimilarity between metabolites/genes when clustering. The number clusters were selected using the criterion described by Krzanowski and Lai , five for metabolites and eight for transcripts. The method of Nettleton et al.  and Fisher's exact test  were used to identify categories of genes/metabolites whose joint expression/accumulation distribution underwent changes during development. To determine over-representation of the transcripts and metabolites in the 351 pathways in MetNet and the transcripts in Gene Ontology categories, separate analyses for genes/metabolites were conducted for the pathways and for each of the three ontologies molecular function (1,053 categories), biological process (1,787 categories), and cellular component (381 categories).
Systems bioinformatics analysis and data storage
MetNet systems biology tool suite http://www.metnetdb.org, http://metnetonline.org/index.php[49, 50] for plant omics, and Plant/Eukaryotic and Microbial Metabolomics Systems Resource (PMR: http://www.metnetdb.org/pmr, were used for data deposition and statistical and interactive analyses of transcriptomics and metabolomics data. PMR currently contains multiple experiments from 26 species of plants and other organisms. Metabolomics or metabolomics/transcriptomics data can be submitted as private by any researcher for analysis; it is made public upon publication. PMR is platform-independent and species-independent. Because tens of thousands of data points are in each metabolomics/transcriptomics dataset, different researchers can explore diverse areas of metabolism and signal transduction within the same dataset. PMR stores metabolomics (and associated transcriptomics) data, evaluates data quality, compares metabolomes across biological samples, manages metadata, and co-analyzes metabolomics and transcriptomics data. Within PMR, metabolomics data can be compared across different biological samples by statistical analysis including t-test and principal components analysis. Computed values are stored graphically and presented using "volcano plots" . PMR supports co-analysis of metabolomics and transcriptomics data from the same samples, allowing discovery of genes whose expression is associated with accumulation of specific metabolites; for co-analysis, correlation values is computed among metabolomics data, and between metabolomics and transcriptomics data.
TAIR 10  identified 33,602 genes in Arabidopsis thaliana, with 41,671 gene models. The AraCyc-annotated database  consists of 521 pathways, with 3,325 enzymatic reactions, 8,846 individual proteins, 8,884 enzymes, and 2,614 metabolites. The original MetNetDB pathway database  was based on a traditional relational database management system (RDBMS). However, in order to traverse along a path in multiple pathways using a relational database, an RDBMS would suffer from the inefficiencies associated with multiple 'joining tables' which each may have >10,000 entities. To overcome this limitation of RDBMS, we employed the graph database, Neo4j [78, 79], based on NoSQL to model the pathway database. Since the metabolic pathways and the chemical interactions can be represented into a directed graph, we established a graph-based MetNetDB, a web-based, computational frame-work that enables interactive visualization of metabolic and regulatory networks (Lee, Hur and Wurtele, unpublished). Networks can be retrieved as lists of such entities as genes, proteins, metabolites, and transcripts from the graph-based MetNetDB, and relationships among the entities can be represented as graphs. New features such as paths between two different entities (e.g., paths between a gene and a metabolite) can be obtained by applying graph theory. If a list of entities is too large to visualize, interpretable graph filters can be implemented to reduce the complexity and focus the list on the most likely pathways.
The cis-acting motifs in the gene promoters (1000 bp upstream of ATG) of the 2,869 transcripts in eight transcriptomics clusters, were evaluated using PLACE: A Database of Plant Cis-acting Regulatory DNA Elements http://www.dna.affrc.go.jp/PLACE/signalup.html.
Availability of supporting data
The data sets supporting the results of this article are included within the article and its additional files. The metabolomics and transcriptomics dataset supporting the results of this article is available from PMR http://www.metnetdb.org/pmr; transcriptomics data are available online from the NCBI Gene Expression Omnibus http://www.ncbi.nlm.nih.gov/geo/ submission number GSE61350.
days after flowering
amino acids and amines, AR, aromatics, eFA, esterified fatty acid, fFA, free fatty acid, OA, organic acid, SGD, sugars and derivatives (alcohols and acids), ST, sterols and tocopherols, UK, unclassified or unknown
Plant/Eukaryotic and Microbial Metabolomics Systems Resource
multiresponse permutation procedure
false discovery rate
relational database management system
oxidative pentose phosphate pathway.
Levin DA: The oil content of seeds: An ecological perspective. The American Naturalist. 1974, 108: 193-206. 10.1086/282899.
Eastmond PJ, Rawsthorne S: Coordinate changes in carbon partitioning and plastidial metabolism during the development of oilseed rape embryos. Plant Physiol. 2000, 122 (3): 767-774. 10.1104/pp.122.3.767.
Eastmond PJ: SUGAR-DEPENDENT1 encodes a patatin domain triacylglycerol lipase that initiates storage oil breakdown in germinating Arabidopsis seeds. Plant Cell. 2006, 18 (3): 665-675. 10.1105/tpc.105.040543.
Schiltz S, Gallardo K, Huart M, Negroni L, Sommerer N, Burstin J: Proteome reference maps of vegetative tissues in pea. An investigation of nitrogen mobilization from leaves during seed filling. Plant Physiol. 2004, 135 (4): 2241-2260. 10.1104/pp.104.041947.
Eastmond PJ, Dennis DT, Rawsthorne S: Evidence that a malate/inorganic phosphate exchange translocator imports carbon across the leucoplast envelope for fatty acid synthesis in developing castor seed endosperm. Plant Physiol. 1997, 114 (3): 851-856.
Wilson RF: Seed metabolism. Soybeans: Improvement, Production and Uses. Edited by: Wilcox JR. 1987, Madison, WI: American Society of Agronomy, 643-686. Second
Agralytica: CONNECTIONS 2012: Soybean market scan; A Report for United Soybean Board. Alexandria, VA. 2012
Ruuska SA, Girke T, Benning C, Ohlrogge JB: Contrapuntal networks of gene expression during Arabidopsis seed filling. Plant Cell. 2002, 14 (6): 1191-1206. 10.1105/tpc.000877.
Endo A, Tatematsu K, Hanada K, Duermeyer L, Okamoto M, Yonekura-Sakakibara K, Saito K, Toyoda T, Kawakami N, Kamiya Y, et al: Tissue-specific transcriptome analysis reveals cell wall metabolism, flavonol biosynthesis and defense responses are activated in the endosperm of germinating Arabidopsis thaliana seeds. Plant & cell physiology. 2012, 53 (1): 16-27. 10.1093/pcp/pcr171.
Palovaara J, Saiga S, Weijers D: Transcriptomics approaches in the early Arabidopsis embryo. Trends in Plant Science. 2013, 18 (9): 514-521. 10.1016/j.tplants.2013.04.011.
Angelovici R, Galili G, Fernie AR, Fait A: Seed desiccation: a bridge between maturation and germination. Trends Plant Sci. 2010, 15 (4): 211-218. 10.1016/j.tplants.2010.01.003.
Fait A, Angelovici R, Less H, Ohad I, Urbanczyk-Wochniak E, Fernie AR, Galili G: Arabidopsis seed development and germination is associated with temporally distinct metabolic switches. Plant physiology. 2006, 142 (3): 839-854. 10.1104/pp.106.086694.
Aziz N, Paiva NL, May GD, Dixon RA: Transcriptome analysis of alfalfa glandular trichomes. Planta. 2005, 221 (1): 28-38. 10.1007/s00425-004-1424-1.
Fedorova M, van de Mortel J, Matsumoto PA, Cho J, Town CD, VandenBosch KA, Gantt JS, Vance CP: Genome-wide identification of nodule-specific transcripts in the model legume Medicago truncatula. Plant Physiol. 2002, 130 (2): 519-537. 10.1104/pp.006833.
Gallardo K, Firnhaber C, Zuber H, Hericher D, Belghazi M, Henry C, Kuster H, Thompson R: A combined proteome and transcriptome analysis of developing Medicago truncatula seeds: evidence for metabolic specialization of maternal and filial tissues. Molecular & cellular proteomics: MCP. 2007, 6 (12): 2165-2179. 10.1074/mcp.M700171-MCP200.
Li F, Wu X, Tsang E, Cutler AJ: Transcriptional profiling of imbibed Brassica napus seed. Genomics. 2005, 86 (6): 718-730. 10.1016/j.ygeno.2005.07.006.
Yin H, Li S, Zhao X, Du Y, Ma X: cDNA microarray analysis of gene expression in Brassica napus treated with oligochitosan elicitor. Plant Physiol Biochem. 2006, 44 (11-12): 910-916. 10.1016/j.plaphy.2006.10.002.
Lan L, Chen W, Lai Y, Suo J, Kong Z, Li C, Lu Y, Zhang Y, Zhao X, Zhang X, et al: Monitoring of gene expression profiles and isolation of candidate genes involved in pollination and fertilization in rice (Oryza sativa L.) with a 10K cDNA microarray. Plant Mol Biol. 2004, 54 (4): 471-487.
Furutani I, Sukegawa S, Kyozuka J: Genome-wide analysis of spatial and temporal gene expression in rice panicle development. Plant J. 2006, 46 (3): 503-511. 10.1111/j.1365-313X.2006.02703.x.
Watson L, Henry RJ: Microarray analysis of gene expression in germinating barley embryos (Hordeum vulgare L.). Funct Integr Genomics. 2005, 5 (3): 155-162. 10.1007/s10142-005-0133-6.
Collakova E, Aghamirzaie D, Fang Y, Klumas C, Tabataba F, Kakumanu A, Myers E, Heath LS, Grene R: Metabolic and Transcriptional Reprogramming in Developing Soybean (Glycine max) Embryos. Metabolites. 2013, 3 (2): 347-372. 10.3390/metabo3020347.
Baran R, Ivanova NN, Jose N, Garcia-Pichel F, Kyrpides NC, Gugger M, Northen TR: Functional genomics of novel secondary metabolites from diverse cyanobacteria using untargeted metabolomics. Marine drugs. 2013, 11 (10): 3617-3631. 10.3390/md11103617.
Lin H, Rao J, Shi J, Hu C, Cheng F, Wilson ZA, Zhang D, Quan S: Seed metabolomic study reveals significant metabolite variations and correlations among different soybean cultivars. Journal of integrative plant biology. 2014
Lu Y, Lam H, Pi E, Zhan Q, Tsai S, Wang C, Kwan Y, Ngai S: Comparative metabolomics in Glycine max and Glycine soja under salt stress to reveal the phenotypes of their offspring. Journal of agricultural and food chemistry. 2013, 61 (36): 8711-8721. 10.1021/jf402043m.
Saito K, Matsuda F: Metabolomics for functional genomics, systems biology, and biotechnology. Annual review of plant biology. 2010, 61: 463-489. 10.1146/annurev.arplant.043008.092035.
Pool WF, Woolf TF, Reily MD, Caprathe BW, Emmerling MR, Jaen JC: Identification of a 3-hydroxylated tacrine metabolite in rat and man: metabolic profiling implications and pharmacology. Journal of medicinal chemistry. 1996, 39 (15): 3014-3018. 10.1021/jm9602266.
Flurer CL: Analysis of antibiotics by capillary electrophoresis. Electrophoresis. 1999, 20 (15-16): 3269-3279. 10.1002/(SICI)1522-2683(19991001)20:15/16<3269::AID-ELPS3269>3.0.CO;2-3.
Beaudry F, Yves Le Blanc JC, Coutu M, Ramier I, Moreau JP, Brown NK: Metabolite profiling study of propranolol in rat using LC/MS/MS analysis. Biomedical chromatography: BMC. 1999, 13 (5): 363-369. 10.1002/(SICI)1099-0801(199908)13:5<363::AID-BMC894>3.0.CO;2-G.
Hempel R, Schupke H, McNeilly PJ, Heinecke K, Kronbach C, Grunwald C, Zimmermann G, Griesinger C, Engel J, Kronbach T: Metabolism of retigabine (D-23129), a novel anticonvulsant. Drug metabolism and disposition: the biological fate of chemicals. 1999, 27 (5): 613-622.
Lim HK, Stellingweif S, Sisenwine S, Chan KW: Rapid drug metabolite profiling using fast liquid chromatography, automated multiple-stage mass spectrometry and receptor-binding. Journal of chromatography A. 1999, 831 (2): 227-241. 10.1016/S0021-9673(98)00956-X.
Fiehn O, Kopka J, Dormann P, Altmann T, Trethewey RN, Willmitzer L: Metabolite profiling for plant functional genomics. Nature biotechnology. 2000, 18 (11): 1157-1161. 10.1038/81137.
Fiehn O, Kopka J, Trethewey RN, Willmitzer L: Identification of uncommon plant metabolites based on calculation of elemental compositions using gas chromatography and quadrupole mass spectrometry. Analytical chemistry. 2000, 72 (15): 3573-3580. 10.1021/ac991142i.
Roessner U, Luedemann A, Brust D, Fiehn O, Linke T, Willmitzer L, Fernie A: Metabolic profiling allows comprehensive phenotyping of genetically or environmentally modified plant systems. The Plant cell. 2001, 13 (1): 11-29. 10.1105/tpc.13.1.11.
Roessner U, Willmitzer L, Fernie AR: High-resolution metabolic phenotyping of genetically and environmentally diverse potato tuber systems. Identification of phenocopies. Plant physiology. 2001, 127 (3): 749-764. 10.1104/pp.010316.
Qi X, Zhang D: Plant metabolomics and metabolic biology. Journal of integrative plant biology. 2014
Schwahn K, de Souza LP, Fernie AR, Tohge T: Metabolomics-assisted refinement of the pathways of steroidal glycoalkaloid biosynthesis in the tomato clade. Journal of integrative plant biology. 2014
Hur M, Campbell AA, Almeida-de-Macedo M, Li L, Ransom N, Jose A, Crispin M, Nikolau BJ, Wurtele ES: A global approach to analysis and interpretation of metabolic data for plant natural product discovery. Nat Prod Rep. 2013
Wurtele ES, Li L, Berleant D, Cook D, Dickerson JA, Ding J, Hofmann H, Lawrence M, Lee E-K, Li J, et al: Metnet: Systems biology tools for arabidopsis. Concepts in Plant Metabolomics. 2007, 145-157.
Bais P, Moon SM, He K, Leitao R, Dreher K, Walk T, Sucaet Y, Barkan L, Wohlgemuth G, Roth MR, et al: PlantMetabolomics.org: a web portal for plant metabolomics experiments. Plant physiology. 2010, 152 (4): 1807-1816. 10.1104/pp.109.151027.
Fernie AR, Geigenberger P, Stitt M: Flux an important, but neglected, component of functional genomics. Current Opinion in Plant Biology. 2005, 8 (2): 174-182. 10.1016/j.pbi.2005.01.008.
Morgan JA, Rhodes D: Mathematical modeling of plant metabolic pathways. Metabolic Engineering. 2002, 4: 80-89. 10.1006/mben.2001.0211.
Ratcliffe R, Shachar-Hill Y: Measuring multiple fluxes through plant metabolic networks. The Plant Journal. 2006, 45 (4): 490-511. 10.1111/j.1365-313X.2005.02649.x.
Schwender J, Ohlrogge J, Shachar-Hill Y: Understanding flux in plant metabolic networks. Current Opinion in Plant Biology. 2004, 7 (3): 309-317. 10.1016/j.pbi.2004.03.016.
Libourel IGL, Shachar-Hill Y: Metabolic Flux Analysis in Plants: From Intelligent Design to Rational Engineering. Annual Review of Plant Biology. 2008, 59 (1): 625-650. 10.1146/annurev.arplant.58.032806.103822.
Iyer VV, Sriram G, Fulton DB, Zhou R, Westgate ME, Shanks JV: Metabolic flux maps comparing the effect of temperature on protein and oil biosynthesis in developing soybean cotyledons. Plant, cell & environment. 2008, 31 (4): 506-517. 10.1111/j.1365-3040.2008.01781.x.
Sriram G, Fulton DB, Iyer VV, Peterson JM, Zhou R, Westgate ME, Spalding MH, Shanks JV: Quantification of compartmented metabolic fluxes in developing soybean embryos by employing biosynthetically directed fractional (13)C labeling, two-dimensional [(13)C, (1)H] nuclear magnetic resonance, and comprehensive isotopomer balancing. Plant physiology. 2004, 136 (2): 3043-3057. 10.1104/pp.104.050625.
Truong Q, Koch K, Yoon JM, Everard JD, Shanks JV: Influence of carbon to nitrogen ratios on soybean somatic embryo (cv. Jack) growth and composition. Journal of experimental botany. 2013, 64 (10): 2985-2995. 10.1093/jxb/ert138.
Allen DK, Ohlrogge JB, Shachar-Hill Y: The role of light in soybean seed filling metabolism. The Plant journal: for cell and molecular biology. 2009, 58 (2): 220-234. 10.1111/j.1365-313X.2008.03771.x.
Wurtele ES, Li J, Diao L, Zhang H, Foster CM, Fatland B, Dickerson J, Brown A, Cox Z, Cook D, et al: MetNet: Software to Build and Model the Biogenetic Lattice of Arabidopsis. Comparative and functional genomics. 2003, 4 (2): 239-245. 10.1002/cfg.285.
Sucaet Y, Wang Y, Li J, Wurtele ES: MetNet Online: a novel integrated resource for plant systems biology. BMC bioinformatics. 2012, 13: 267-10.1186/1471-2105-13-267.
Gurwitz D: From transcriptomics to biological networks. Drug development research. 2014, 75 (5): 267-270. 10.1002/ddr.21221.
Hatzimanikatis V, Lee KH: Dynamical analysis of gene networks requires both mRNA and protein expression information. Metabolic engineering. 1999, 1 (4): 275-281. 10.1006/mben.1999.0115.
Buescher JM, Liebermeister W, Jules M, Uhr M, Muntel J, Botella E, Hessling B, Kleijn RJ, Le Chat L, Lecointe F, et al: Global network reorganization during dynamic adaptations of Bacillus subtilis metabolism. Science. 2012, 335 (6072): 1099-1103. 10.1126/science.1206871.
R Core Team: R: A language and environment for statistical computing. 2013, R Foundation for Statistical Computing, Vienna, Austria
Grant D, Nelson RT, Cannon SB, Shoemaker RC: SoyBase, the USDA-ARS soybean genetics and genomics database. Nucleic Acids Res. 2010, D843-846. 38 Database
Fisher RA: On the Interpretation of χ2 from Contingency Tables, and the Calculation of P. Journal of the Royal Statistical Society. 1922, 85 (1): 87-94. 10.2307/2340521.
Lin Y, Sun L, Nguyen LV, Rachubinski RA, Goodman HM: The Pex16p homolog SSE1 and storage organelle formation in Arabidopsis seeds. Science. 1999, 284 (5412): 328-330. 10.1126/science.284.5412.328.
Lin Y, Cluette-Brown JE, Goodman HM: The peroxisome deficient Arabidopsis mutant sse1 exhibits impaired fatty acid synthesis. Plant physiology. 2004, 135 (2): 814-827. 10.1104/pp.103.036772.
Storey JD, Tibshirani R: Statistical significance for genomewide studies. Proc Natl Acad Sci USA. 2003, 100 (16): 9440-9445. 10.1073/pnas.1530509100.
Pandurangan S, Pajak A, Molnar SJ, Cober ER, Dhaubhadel S, Hernandez-Sebastia C, Kaiser WM, Nelson RL, Huber SC, Marsolais F: Relationship between asparagine metabolism and protein concentration in soybean seed. Journal of experimental botany. 2012, 63 (8): 3173-3184. 10.1093/jxb/ers039.
Nettleton D, Recknor J, Reecy JM: Identification of differentially expressed gene categories in microarray studies using nonparametric multivariate analysis. Bioinformatics. 2008, 24 (2): 192-201. 10.1093/bioinformatics/btm583.
Jia M, Li L, Boggess E, Wurtele ES, Dickerson JA: Visualizing Multivariate Hierarchic Data Using Enhanced Radial Space-Filling Layout. Advances in Visual Computing, Pt I. 2010, 6453: 350-360. 10.1007/978-3-642-17289-2_34.
Boter M, Ruiz-Rivero O, Abdeen A, Prat S: Conserved MYC transcription factors play a key role in jasmonate signaling both in tomato and Arabidopsis. Genes & development. 2004, 18 (13): 1577-1591. 10.1101/gad.297704.
Stephanopoulos G, Vallino JJ: Network rigidity and metabolic engineering in metabolite overproduction. Science. 1991, 252 (5013): 1675-1681. 10.1126/science.1904627.
Miller L, Houghton JA: The micro-kjeldahl determination of the nitrogen content of amino acids and proteins. Journal of Biological Chemistry. 1945, 159 (2): 373-383.
Adams CA, Rinne RW, Fjerstad MC: Starch Deposition and Carbohydrase Activities in Developing and Germinating Soya Bean Seeds. Annals of Botany. 1980, 45 (5): 577-582.
Fox JD, Robyt JF: Miniaturization of three carbohydrate analyses using a microsample plate reader. Analytical biochemistry. 1991, 195 (1): 93-96. 10.1016/0003-2697(91)90300-I.
Schmidt MA, Barbazuk WB, Sandford M, May G, Song Z, Zhou W, Nikolau BJ, Herman EM: Silencing of soybean seed storage proteins results in a rebalanced protein composition preserving seed protein content without major collateral changes in the metabolome and transcriptome. Plant physiol. 2011, 156 (1): 330-345. 10.1104/pp.111.173807.
Quanbeck SMM, Brachova L, Campbell AA, Guan X, Perera A, He K, Rhee SY, Bais P, Dickerson J, Dixon P, et al: Metabolomics as a hypothesis-generating functional genomics tool for the annotation of Arabidopsis thaliana genes of "unknown function". Frontiers in Plant Science. 2012, 3:
Jin H, Song Z, Nikolau BJ: Reverse genetic characterization of two paralogous acetoacetyl CoA thiolase genes in Arabidopsis reveals their importance in plant growth and development. Plant J. 2012, 70 (6): 1015-1032. 10.1111/j.1365-313X.2012.04942.x.
Ding G, Che P, Ilarslan H, Wurtele ES, Nikolau BJ: Genetic dissection of methylcrotonyl CoA carboxylase indicates a complex role for mitochondrial leucine catabolism during seed development and germination. Plant J. 2012, 70 (4): 562-577. 10.1111/j.1365-313X.2011.04893.x.
Crispin MC, Hur M, Park T, Kim YH, Wurtele ES: Identification and biosynthesis of acylphloroglucinols in Hypericum gentianoides. Physiologia plantarum. 2013, 148 (3): 354-370. 10.1111/ppl.12063.
Kaufman L, Rousseeuw PJ: Partitioning Around Medoids (Program PAM). Finding Groups in Data: An Introduction to Cluster Analysis. 1990, John Wiley & Sons, Inc, 68-125.
Krzanowski WJ, Lai YT: A Criterion for Determining the Number of Groups in a Data Set Using Sum-of-Squares Clustering. Biometrics. 1988, 44: 23-34. 10.2307/2531893.
Cui X, Churchill G: Statistical tests for differential expression in cDNA microarray experiments. Genome Biology. 2003, 4 (4): 210-10.1186/gb-2003-4-4-210.
Lamesch P, Berardini TZ, Li D, Swarbreck D, Wilks C, Sasidharan R, Muller R, Dreher K, Alexander DL, Garcia-Hernandez M, et al: The Arabidopsis Information Resource (TAIR): improved gene annotation and new tools. Nucleic Acids Research. 2012, 40 (D1): D1202-D1210. 10.1093/nar/gkr1090.
Chae L, Lee I, Shin J, Rhee SY: Towards understanding how molecular networks evolve in plants. Current opinion in plant biology. 2012, 15 (2): 177-184. 10.1016/j.pbi.2012.01.006.
Partner J, Vukotic A, Watt N: Neo4j in Action. 2014
Robinson I, Webber J, Eifrem E: Graph Databases. 2013, O'Reilly Media, 1
We gratefully acknowledge funding and support from National Science Foundation MCB-0951170 (to ESW and LL) and IOS-1139489 (to BJN), the United Soybean Board award 2287 (to LL), the Center for Metabolic Biology, Iowa State University, and the state of Iowa. Metabolomics analyses were conducted at the Iowa State University WM Keck Metabolomics Research Laboratory, and we thank Dr. Ann Perera for her expert advice. Funding for publication of the article has come from the National Science Foundation under award numbers: MCB-0951170 (to ESW and LL) and IOS-1139489 (to BJN).
This article has been published as part of BMC Genomics Volume 16 Supplement 3, 2015: Selected articles from the 10th International Symposium on Bioinformatics Research and Applications (ISBRA-14): Genomics. The full contents of the supplement are available online at http://www.biomedcentral.com/bmcgenomics/supplements/16/S3.
The authors declare that they have no competing interests.
Conceived and designed the experiments: BJN, LL and ESW. Performed the experiments: LL, WZ, VI, MW, and CYD. Analyzed the data: ZS, DN, VI, JS, BJN, ESW and LL. Bioinformatics development: LL, ESW, MH, JL, ZA and NR. Contributed materials/analysis tools: MW. Wrote the paper: LL, BJN, and ESW. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 2: Table S2. Transcripts, shown in Figure 3, which exhibited significant variation and were grouped into eight clusters based on co-accumulation patterns across the five time points of soybean seed development. (XLS 2 MB)
Additional file 3: Table S3. Statistical analyses of the transcripts and metabolites in the co-expression clusters based on pathway membership and Gene Ontology terms. (XLS 1 MB)
Additional file 4: Table S4. Statistical analyses of the transcripts in the eight co-expression clusters, based on promoter motifs. (XLS 478 KB)
About this article
Cite this article
Li, L., Hur, M., Lee, JY. et al. A systems biology approach toward understanding seed composition in soybean. BMC Genomics 16, S9 (2015). https://doi.org/10.1186/1471-2164-16-S3-S9
- Glycine max
- seed development
- seed composition
- metabolic flux