ORIGINAL RESEARCH article
Transcriptional and biochemical responses of monoacylglycerol acyltransferase-mediated oil synthesis and associated senescence-like responses in Nicotiana benthamiana
- 1CSIRO Food Futures National Research Flagship, Canberra, ACT, Australia
- 2Bioinformatics, CSIRO Plant Industry, Canberra, ACT, Australia
Triacylglycerol (TAG) accumulates in plant seeds as a major renewable source of carbon for food, fuel and industrial feedstock. Approaches to enhance TAG content by altering lipid pathways and genes in vegetative parts have gained significant attention for biofuel and other applications. However, consequences of these modifications are not always studied in detail. In an attempt to increase TAG levels in leaves we previously demonstrated that a novel substrate, monoacylglycerol (MAG), can be used for the biosynthesis of diacylglycerol (DAG) and TAG. Transient expression of the Mus musculus monoacylglycerol acyltransferases MGAT1 and 2 in the model plant Nicotiana benthamiana increased TAG levels at 5 days post-infiltration (dpi). Here we show that increased TAG and DAG levels can be achieved as early as 2 dpi. In addition, the MGAT1 infiltrated areas showed senescence-like symptoms from 3 dpi onwards. To unravel underlying molecular mechanisms, Illumina deep sequencing was carried out (a) for de-novo assembling and annotation of N. benthamiana leaf transcripts and (b) to characterize MGAT1-responsive transcriptome. We found that MGAT1-responsive genes are involved in several processes including TAG biosynthesis, photosynthesis, cell-wall, cutin, suberin, wax and mucilage biosynthesis, lipid and hormone metabolism. Comparative analysis with transcript profiles from other senescence studies identified characteristic gene expression changes involved in senescence induction. We confirmed that increased TAG and observed senescence-symptoms are due to the MAG depletion caused by MGAT1 activity and suggest a mechanism for MGAT1 induced TAG increase and senescence-like symptoms. The data generated will serve as a valuable resource for oil and senescence related studies and for future N. benthamiana transcriptome studies.
Demand for production and use of biofuels is rapidly increasing and current agricultural practices are unable to produce sufficient amounts cost-effectively. Multiple approaches are being employed to develop plants with altered carbon and energy content to meet this demand. Accumulation of energy-dense lipids like triacylglycerols (TAG) in the vegetative parts of plants has attracted significant attention due to the potential to produce large amounts of energy rich biomass (Vanhercke et al., 2014a,b). Approaches to increase TAG levels in diverse plant tissues have targeted different steps of TAG biosynthesis and storage that can be generally divided into (a) “Push”- mobilizing carbon flux to increase fatty acid biosynthesis, (b) “Pull”—TAG assembly, and (c) “Protect”—increasing TAG storage/decreasing TAG breakdown (Vanhercke et al., 2013a,b). Examples of the “Push approach” include ectopic expression of transcription factors (LEC1, LEC2 and WRI1) that control seed development and maturation (Santos Mendoza et al., 2005; Andrianov et al., 2010; Liu et al., 2010) as well as diverting carbon flow from starch to lipid biosynthesis by silencing ADP-glucose-pyrophosphorylase (AGPase) in plant leaves (Sanjaya et al., 2011). “Pull approaches” consist of overexpression of acetyl-CoA carboxylase (Klaus et al., 2004) and overexpression of diacylglycerol acyltransferase (DGAT) and other enzymes involved in TAG assembly (Bouvier-Navé et al., 2000; Jako et al., 2001; Weselake et al., 2008; Petrie et al., 2012). Finally, retaining fatty acid (FA) content (“Protect approach”) by blocking FA movement to peroxisomes or via other mechanisms can also increase TAG levels in leaves (Xu et al., 2005; Slocombe et al., 2009). Many studies which combine several of these approaches (Andrianov et al., 2010; Sanjaya et al., 2011; Vanhercke et al., 2013a) have provided “proof of concept” results for oil increase, although the TAG levels achieved are not yet necessarily of industrial relevance. However, recently substantial progress had been made in this direction by metabolic engineering of plant leaves for high energy dense oil-seed like TAG (Vanhercke et al., 2014a).
In plants diacylglycerol (DAG), the immediate precursor of TAG, is synthesized mainly by: (1) Kennedy pathway for de novo DAG synthesis (Kennedy, 1961), and (2) transfer of phosphocholine head group from phosphatidylcholine (PC) to PC-derived DAG by phosphatidylcholine:diacylglycerol cholinephosphotransferase (PDCT) (Lu et al., 2009). Another pathway that involves the conversion of monoacylglycerol (MAG) to DAG by monoacylglycerol acyltransferase (MGAT) has been well characterized in animals (Yen et al., 2002; Cao et al., 2003). Although the presence of MAG in plant tissues has been reported (Perry and Harwood, 1993; Yang et al., 2002), it is only believed to serve as a precursor for cuticular wax biosynthesis (Li-Beisson et al., 2013). Recently, a plant MGAT gene and an OLEOSIN (OLEO3) isolated from peanut were shown to enhance TAG accumulation when over-expressed in Saccharomyces cerevisiae (Parthibane et al., 2012; Vijayaraj et al., 2012). In addition, the concept of oil increase in vegetative tissue via a MAG pathway was recently demonstrated by (Petrie et al., 2012). The authors showed that heterologous expression of mouse MGATs (MGAT1 and 2) in Nicotiana benthamiana leaves can lead to utilization of MAG for DAG synthesis, thereby significantly increasing TAG accumulation. TAG levels were increased 9.2-fold by MGAT1 and 7.3-fold by MGAT2 at 5 days post-infiltration (dpi) in the infiltrated leaves.
In addition to increased TAG, we found that MGAT1 infiltrated leaf areas of N. benthamiana turn yellow at 3 dpi and exhibit senescence-like symptoms by 5 dpi. These symptoms are specific to MGAT1 infiltration and can be reduced by MAG supplementation or inhibition of MGAT activity. In order to better understand the molecular mechanisms underlying the observed symptoms and TAG increase, we undertook a global gene expression study of MGAT1-mediated responses in the N. benthamiana transient leaf infiltration system. This system has been proven particularly useful for the metabolic engineering of lipid biosynthesis pathways (Wood et al., 2009; Petrie et al., 2010; Vanhercke et al., 2013b) and for functional confirmation of novel genes (Dussert et al., 2013). Availability of genetic resources will further broaden the scope for this model plant to understand the consequences of gene/pathway manipulation. Efforts in this direction have been initiated with the draft genome being recently published (Bombarely et al., 2012) and the transcriptome sequenced from a pooled library representing nine different tissues (Nakasugi et al., 2013). Here we describe the lipid pathway related transcripts of N. benthamiana leaf tissue and employed RNA-seq to identify genes differentially expressed in MGAT1 infiltrated leaves. This study provides a comprehensive overview of cellular metabolic processes caused by the utilization of MAG for TAG synthesis and associated senescence-like response resulting from transient expression of mouse MGAT1 in N. benthamiana.
Results and Discussion
Physiological and Biochemical Responses of MGAT1 Infiltration
Transient expression of M. musculus MGATs (MGAT1 or MGAT2) is known to increase TAG accumulation by 5 days post-infiltration (dpi) in N. benthamiana leaves (Petrie et al., 2012). However, the MGAT1-infiltrated areas showed cell-death by 5 dpi (Figure 1A), with senescence-like symptoms being visible from 3 dpi onwards (Figure 1A). Surprisingly, the MGAT2 infiltrated leaves show no senescence symptoms even at 5 dpi. Differences in expression patterns, functions and biochemical activities between mammalian MGATs have been reported (Cao et al., 2003, 2007). Further, we have shown previously that MGAT1 displays considerable DGAT side-activity with 58% of the labeled DAG converted to TAG by MGAT1 in contrast with only 6% conversion by MGAT2 (Petrie et al., 2012). Hence, we focused this study on understanding the relationship between transient MGAT1 expression and the observed senescence-like responses. As a first step, we measured the TAG levels in MGAT1 infiltrated leaves before the onset of senescence symptoms. Lipid analysis on MGAT1 infiltrated leaves at an early time point of 2 dpi showed a 4-fold increase in TAG levels (Figure 1B). In addition, DAG levels were also increased while a clear decrease in MAG levels was observed indicating its conversion to DAG. Since TAG accumulation occurs at 2 dpi and senescence symptoms do not start to appear, this early time point was deemed suitable for gene expression studies.
Figure 1. Physiological and biochemical responses of monoacylglycerol acyltransferase (MGAT1) transient expression in Nicotiana benthamiana leaves. (A) Senescence symptoms observed in leaf tissue infiltrated with MGAT1 at 3 days post-infiltration (dpi) and 5 dpi. Infiltrations were performed along with p19 viral suppressor protein as control (Petrie et al., 2012). (B) Lipid analysis showing monoacylglycerol (MAG), diacylglycerol (DAG) and triacylglycerol (TAG) levels in p19 and p19+MGAT1 infiltrated leaf spots, harvested at 2 dpi. Data shown are average of three replicates and error bars represent standard error.
De novo Transcriptome Assembly and Annotation
RNA was extracted from the leaves of 6-week old un-infiltrated plants for de novo transcriptome assembly. Illumina sequencing followed by processing of raw reads produced a total of 55 million clean reads (Table 1A). Assembling of the reads using Trinity (Grabherr et al., 2011) produced 92,857 non-redundant contigs out of which 77,679 were singletons and 15,178 were distinct clusters (Table 1A). The length distribution of contigs is shown in Supplementary Figure 1. The mean contig length was 503 bp with a N50 weightage of 706 for the assembly (Table 1A). The contig sequences can be downloaded from CSIRO data access portal (http://dx.doi.org/10.4225/08/524ABB9C42D91).
The 92,857 contigs were searched against various public databases using BLASTX (1e−5). The number of transcripts annotated by each database is summarized in Table 1B. The NCBI non-redundant (nr) database (ftp://ftp.ncbi.nlm.nih.gov/blast/db/) search retrieved annotations for 48,952 contigs. Function annotations for 31,572 contigs were obtained from Swiss-Prot (Magrane and Consortium, 2011) and “Clusters of Orthologous Groups of Proteins” (COG; http://www.ncbi.nlm.nih.gov/COG) database search annotated 13,972 contigs. Gene Ontology (GO) annotation terms were retrieved for 23,568 contigs using Blast2GO (Conesa et al., 2005). Thus, a total of 49,180 contigs were annotated from all the databases indicating that nearly 52% of the transcripts were annotated. The list of contigs and their annotations from each database are described in Supplementary data 1. The COG functional class distribution and categorization into the GO categories are illustrated in Supplementary Figure 2. For metabolic pathway annotations, the contigs were searched against Kyoto Encyclopedia of Genes and Genomes database (KEGG; http://www.genome.jp/kegg/). The enriched pathways and number of transcripts related to each pathway are illustrated in Supplementary Figure 3. About 34.5% (32,030) of transcripts were annotated to the KEGG pathways, the majority of which were under the broad category of metabolic pathway (21.28%). Biosynthesis of secondary metabolites (9.62%), plant hormone signal transduction (6.19%) and plant-pathogen interaction (5.68%) were the other major pathway categories (Supplementary Figure 3). From the pathway analysis, N. benthamiana contigs related to lipid pathways are identified and summarized in Table 2.
Table 2. Summary of N. benthamiana contigs related to different lipid pathways identified by KEGG pathway analysis.
The identified transcripts and their annotations were confirmed by randomly BLASTing a number of contig sequences against the N. benthamiana transcriptome database (http://sydney.edu.au/science/molecular_bioscience/sites/benthamiana/). No disagreement in annotation was observed between the matched sequences from both studies.
Identification of Leaf Acyl-Lipid Metabolism Genes of N. benthamiana
Acyl-lipids include a wide range of lipid classes with diverse functions in cell membranes and sub-cellular organelles (Li-Beisson et al., 2010). Identification of acyl-lipid genes of N. benthamiana is important in the context that this model plant can be used extensively for manipulating lipid pathways in leaf tissue. The N. benthamiana contig sequences were mapped against the Arabidopsis TAIR10 protein sequences (http://www.arabidopsis.org/) using BLASTX (1e−5) in CLC Genomics Workbench 5 (http://www.clcbio.com). Identified contigs with an Arabidopsis thaliana homolog were analyzed against acyl-lipid metabolism gene list obtained from “The Arabidopsis Acyl-Lipid Metabolism” website (ARALIP; http://aralip.plantbiology.msu.edu). A total of 1648 acyl-lipid contigs of N. benthamiana leaf were identified. The distribution of these transcripts into 23 different lipid-related function categories and transcript count for each category are shown in Figure 2. In plants, the majority of the seed oil is stored as TAG. The N. benthamiana transcripts that are involved in TAG biosynthesis were identified and are described in Supplementary Table 1. A list of all the contigs identified with a role in acyl-lipid metabolism is shown in Supplementary data 2.
Figure 2. Identification of leaf acyl-lipid metabolism transcripts of N. benthamiana. Contigs mapped to A. thaliana sequences were searched against “The Arabidopsis Acyl-Lipid Metabolism” website (ARALIP; http://aralip.plantbiology.msu.edu) to identify acyl-lipid related transcripts. Distribution of identified transcripts into different acyl-lipid metabolism categories and number of contigs in each category is illustrated.
Transcriptional Responses of MGAT1 Infiltration
In order to understand the molecular mechanisms underlying MGAT1-mediated TAG accumulation and senescence-like responses, RNA-seq analysis was performed on MGAT1 infiltrated vs. control infiltrated leaves. The early time point of 2 dpi showing TAG accumulation but not senescence symptoms along with an additional time point of 1 dpi was selected for identifying differentially expressed genes. RNA was extracted from the control (p19) and MGAT1-infiltrated leaf areas, pooled from at least 10 different leaves for each treatment at each time point, and Illumina sequencing reads were obtained. The expression levels were estimated as Reads Per Kilobase of Exon per Million mapped reads (RPKM) by mapping against the de novo assembled transcriptome (92,857 contigs) in CLC Genomics. Differentially expressed transcripts were identified according to the RNA-seq workflow in CLC Genomics and also by using a R package DESeq (Anders and Huber, 2010). No significant differences were observed in the fold changes derived from both tools. Gene lists derived from DESeq containing p-values (cut-off p < 0.05) adjusted for multiple testing by Benjamini-Hochberg procedure were used for further analysis. After applying a fold change (FC) cut-off of ≥2/≤−2 (p < 0.05), 178 genes were up-regulated and 134 genes were down-regulated at 1 dpi. At 2 dpi, 846 genes were up-regulated and 2434 genes down-regulated (Supplementary Figure 4A). A. thaliana homologs were identified for 152 (1 dpi) and 482 (2 dpi) up-regulated genes, and 103 (1 dpi) and 1890 (2 dpi) down-regulated genes. It is note-worthy that, similar to MGAT1 response at 2 dpi, several senescence studies noted a larger number of genes being down-regulated than up-regulated genes under senescing conditions (Troncoso-Ponce et al., 2013). A scatter plot using the log2 FC values of 4 genes estimated by RNA-seq and qRT-PCR is shown in Supplementary Figure 4B. Further, the expression of MGAT1 in infiltrated leaves was confirmed by RT-PCR (Supplementary Figure 4C).
Gene Ontology (GO) and Pathway (MapMan) Annotations of Differentially Expressed Genes
Further analysis was performed on contigs having an A. thaliana homolog by taking advantage of the available resources. Since major changes in gene expression were observed at 2 dpi only, this category of genes was selected for further analysis. After removing duplications in annotations, 1666 transcripts were found to be changed at 2 dpi, out of which 1333 were down-regulated and 333 were up-regulated. The up- and down-regulated genes of 2 dpi were analyzed for enriched GO terms (p < 0.05) using Classification SuperViewer tool at The Bio-Analytic Resource (BAR) for Plant Biology (http://bar.utoronto.ca), as illustrated in Figure 3. The up-regulated genes were highly enriched in stress response, abiotic or biotic stimulus and signal transduction biological responses (Figure 3A). This indicates that, in addition to accumulation of increased TAG, MGAT1 infiltrated areas were also experiencing and responding to stress. A significant number of down-regulated genes were located in plastid, chloroplast and cell-wall (Figure 3B), suggesting that cellular processes localized to these organelles could be negatively impacted by MGAT1. Indeed the electron transport and energy pathways were highly enriched in down-regulated genes indicating a suppressive effect on these processes by MGAT1.
Figure 3. Gene ontology (GO) annotations of differentially expressed genes (DEG). Classification SuperViewer tool at The Bio-Analytic Resource (BAR) for Plant Biology (http://bar.utoronto.ca) was used. (A,B) GO term annotation of up-regulated (A) and down-regulated genes (B). Significantly enriched terms are highlighted in bold.
To provide an overview of MGAT1 effect on individual metabolic pathways, significantly changed genes (≥2/≤−2-fold; p < 0.05) along with their fold changes were mapped on pathway bins of MapMan 3.5.1R2 (http://mapman.gabipd.org). Metabolism overview revealed that the majority of MGAT1 responsive genes map to cell-wall, lipids and PS bins (Figure 4A). Most of the cell-wall related genes including cellulose synthases (CESA 2–6), cellulose synthase like (CSL) genes, and arabinogalactan proteins (AGPs) such as salt overly sensitive 5 (SOS 5) involved in cell-wall biosynthesis (Xu et al., 2008) were down-regulated. Cell-wall modifying genes like expansins, xyloglucan endotransglycosylase (XETs) and pectin esterases were also down-regulated. Down-regulation of cell-wall synthesis and modification genes indicates a possible disruption in cell-wall integrity. Genes involved in carbohydrate (CHO) metabolism were also affected by MGAT1 (Figure 4A). While many major CHO genes related to sucrose and starch metabolism were down-regulated, a cell-wall invertase (AtcwINV2; At3g52600) and a vacuolar invertase (At1g62660) were up-regulated. Decline of photosynthesis (PS) initiates senescence and a role for invertases in this process has been demonstrated (Dickinson et al., 1991; Ding et al., 1993). Minor CHO related genes including trehalose-6-phosphate phosphatases (TPPs) and two trehalose-phosphate synthases (TPS 5 and 11) were also up-regulated by MGAT1 (Figure 4A). An overview of MGAT1 effect on PS is illustrated in Figure 4B and corresponding genes are summarized in Supplementary Table 2. In agreement with the GO analysis showing down-regulated terms of electron transport, energy and plastid, PS showed largest down-regulation effect by MGAT1, as compared to other pathways. The collapse of PS, cell-wall, major CHO metabolism and electron transport/ATP synthesis are major indicators of senescence induction that can cause the visible symptoms observed at 3 dpi.
Figure 4. MapMan pathway overview analysis of DEG. (A) Overview of MGAT1 effect on transcripts related to different pathways generated by “Metabolism overview” analysis in MapMan. Fold changes (Log2) are indicated by the colour scale. Distribution of transcripts into different pathways and their expression trend in each pathway is illustrated. (B) Effect of MGAT1 on photosynthesis (PS) related transcripts. All PS related genes were down-regulated. The number of transcripts, their distribution into sub-classes of PS and expression trend are illustrated. The 17 sub-classes and the genes in each sub-class are described in Supplementary Table 2.
Genes Involved in MGAT1 Induced Tag Biosynthesis
The N. benthamiana acyl-lipid transcripts identified in the study were analyzed for differentially regulated genes and lipid processes induced by MGAT1 infiltration. Expression of 94 transcripts mapped to ARALIP genes were altered by MGAT1 expression, of which only 12 were up-regulated (Supplementary Table 3). The only lipid process enriched with up-regulated genes was TAG biosynthesis, while genes involved in FA synthesis and modification, TAG degradation, FA elongation, wax biosynthesis, cutin and suberin synthesis and transport were all found to be down-regulated (Figure 5). These responses are indicative of the induction of TAG biosynthesis machinery by MGAT1 expression while trancripts involved in FA degradation, synthesis and transport of wax, suberin and cuticular structures appear to be suppressed. Two TAG biosynthesis related genes, diacylglycerol acyltransferase (DGAT1) and phosphatidylcholine:diacylglycerol cholinephosphotransferase (PDCT) were up-regulated. FA degradation genes down-regulated included two MAG lipases (MAGL) and a TAG lipase (TAGL). PDCT and the transiently expressed MGAT1 are involved in synthesizing DAG from PC and MAG, respectively. DAG is the only substrate of DGAT1 for conversion to TAG. Transient expression of MGAT1 and the subsequent up-regulation of PDCT and DGAT1 could explain the increased DAG and TAG levels detected in MGAT1 infiltrated areas in combination with depletion in MAG levels compared to the negative control (p19). Down-regulation of MAG and TAG lipases could result in reduced neutral lipid turnover thereby contributing to a net increase in TAG levels.
Figure 5. Identification of MGAT1 DEGs involved in acyl-lipid metabolism. Distribution of genes differentially expressed by MGAT1 into different categories of acyl-lipid metabolism is illustrated. Down-regulation (blue) of transcripts in majority of classes including FA elongation, cutin, suberin and wax biosynthesis can be seen, while TAG biosynthesis contains more up-regulated (green) genes.
Expression Profiles of MGAT1 Responsive Lipid-Related Genes During Senescence
Recently, Troncoso-Ponce et al. (2013) have developed a database by compiling and plotting the senescence responsive profiles of lipid-related genes from three independent studies (Schmid et al., 2005; Van Der Graaff et al., 2006; Breeze et al., 2011). We chose Breeze et al. (2011) and Van Der Graaff et al. (2006) studies only to compare the MGAT1 responsive profiles of the lipid-related genes as Schmid et al. study was not specifically directed at senescence. Breeze et al., analyzed expression pattern of A. thaliana genes from 19 days after sowing (DAS) to 39 DAS. Van der Graaff et al. studied expression profiles of developmental leaf senescence (NS), darkening-induced senescence in intact leaves (DIS) and senescence in dark-incubated detached leaves (DET) at different stages. Out of the 12 lipid-related genes identified to be up-regulated by MGAT1, 11 genes were also up-regulated during senescence in both studies (Figure 6A). A large number (69) of lipid-related genes were down-regulated by MGAT1. While no clear trend emerged, the majority of these genes were also down-regulated in both Breeze et al. (78%) and Van der Graaff et al. (52%) senescence studies (Supplementaty Figure 5). These results indicate that transcriptional changes caused by MGAT1 infiltration are similar to those induced by senescence as discussed below.
Figure 6. MGAT1 and senescence responsive transcripts. (A) Expression profiles of MGAT1 responsive lipid related genes during senescence. Senescence profiles from two earlier studies (Van Der Graaff et al., 2006; Breeze et al., 2011) were downloaded from Troncoso-Ponce et al. (2013) database and shown. Eleven out of twelve lipid-related genes up-regulated by MGAT1 were also up-regulated during progression of senescence shown as days after sowing (DAS). (B) Comparative analysis of MGAT1 and senescence responsive transcriptome. Venn diagram showing gene overlap between MGAT1, Breeze et al. and Vander Graff et al.
One of the characteristic responses of lipid-related genes during senescence is a co-ordinated decrease in the transcripts for FA synthesis and desaturation, while the glycerolipid assembly transcripts including DGAT1 increase in expression (Troncoso-Ponce et al., 2013). In line with this, transcripts involved in FA synthesis such as KASI, KASII, β-ketoacyl-CoA synthase (KCS) and long-chain acyl-CoA synthase (LACS2), as well as FAD3 and 5 involved in FA desaturation were down-regulated by MGAT1, while DGAT1 and PDCT involved in glycerolipid assembly were up-regulated. In contrast to the up-regulation of some glycerol-3-phosphate acyltransferases (GPAT9 and GPAT1) during senescence (Troncoso-Ponce et al., 2013), GPAT4 required for MAG accumulation was down-regulated by MGAT1. This finding indicates that in addition to utilizing MAG for conversion to DAG, MGAT1 also affects MAG synthesis by decreasing GPAT4 expression which can result in further reduction of MAG levels in MGAT1 infiltrated leaves. Up-regulation of genes encoding various lipases except for phospholipase D (PLD) and genes involved in β-oxidation pathway is a feature of lipid turnover during natural senescence (Thompson et al., 1998; Troncoso-Ponce et al., 2013). Somewhat unexpectedly, transcripts of two putative MAG lipases and a TAG lipase were down-regulated by MGAT1 expression, while no change was observed for β-oxidation genes. In addition, PLD-β and PLD-δ transcripts were up-regulated by MGAT1. Several putative ABC transporters involved in FA transport were also down-regulated by MGAT1. Blocking of FA transport to peroxisomes by mutating an ABC transporter resulted in increased TAG levels during senescence (Slocombe et al., 2009). Thus, while several MGAT1 induced lipid-responses are similar to senescence responses including increase in DGAT1 transcripts and higher TAG levels, it appears that MGAT1 also blocks FA turnover resulting in reduced TAG turnover.
Comparative Analysis of MGAT1 and Senescence Responsive Gene Expression
To understand the relation between MGAT1 expression and senescence, the entire set of MGAT1-responsive genes was compared with senescence response gene lists from both Breeze et al. (6323 genes) and Van der Graaff et al. (4109 genes) studies. The expression of 466 out of 1666 (27.9%) MGAT1-responsive genes were also changed in both studies. While 314 genes showed a specific overlap with Breeze et al., 191 MGAT1-responsive genes overlapped specifically with Van der Graaff et al. As expected, a larger proportion (2532) of genes was common between the two senescence studies. About 47.1% (695) of MGAT1-responsive genes were specific to MGAT1 and were unaffected in either study (Figure 6B). Interestingly, this subset includes transcription factors MYB5 and TRANSPARENT TESTA GLABRA (TTG2), found to be down-regulated by MGAT1. In A. thaliana, MYB5 and TTG2 are key components in regulation of mucilage biosynthesis (Western et al., 2004). While myb5-1 mutants exhibit loss of mucilage and enhanced oil accumulation (Shi et al., 2012), TTG2 is required for the expression of GLABRA2 (GL2), a negative regulator of seed oil accumulation (Shen et al., 2006; Shi et al., 2012). Taken together, it is apparent from these results that in addition to a good overlap with senescence related genes, MGAT1-specific changes were also abundant.
In order to perform comparisons based on expression pattern and associated functions, cluster analysis was performed on gene lists from all three studies using MapMan. Genes from each study were categorized into up- and down-regulated and given a value of “2” and “−2” respectively. Genes that did not change in a given condition or gene list were given a value of “1.” Using eucledian distance metric, 15 clusters were generated (Supplementary Figure 6). Interestingly, 216 genes were down-regulated in all studies and grouped to Cluster A1. Out of these 24% belong to PS. Genes related to cell-wall, lipid and protein metabolism, secondary metabolism and RNA regulation were also present in this cluster. Clusters A2–5 consists of genes down-regulated by MGAT1 and in one or more other studies. Clusters A3 (56 genes) and A4 (30 genes) together represent the second largest set of genes. This set includes many transcription factors and signaling kinases along with FA synthesis genes KASII and LACS (A3). These profiles point to the similarities of MGAT1 responses to natural senescence in affecting PS and lipid pathways. Cluster B1 genes were up-regulated in almost every condition. This subset includes SRG3, PR4 (PATHOGENESIS-RELATED 4), heat shock protein (HSP17.8-CI), HSP70, SIP4 (SOS3-INTERACTING PROTEIN 4) and CML37 (CALMODULIN LIKE 37) with known roles in biotic and abiotic stresses. The key gene for ethylene biosynthesis, ACS2 (At1g01480) is also present in this cluster. Up-regulation of these genes in all conditions is indicative of stress and senescence related responses and increased synthesis of the senescence hormone ethylene. Genes up-regulated by MGAT1 but either down-regulated or unchanged in one or more of the other conditions were grouped in clusters B2 to B5. This set includes a senescence marker gene YLS9 (YELLOW-LEAF-SPECIFIC GENE 9) that is responsive to late senescence, dark, ethylene and ABA (Yoshida et al., 2001), PLDBETA1 (PHOSPHOLIPASE D BETA 1) [cluster B3]; the ABA biosynthesis gene, NCED3 (NINE-CIS-EPOXYCAROTENOID DIOXYGENASE 3), two Ethylene signaling genes EBF2 (EIN3-BINDING F BOX PROTEIN 2) and RRTF1 (REDOX RESPONSIVE TRANSCRIPTION FACTOR 1), and the transcription factor STZ (salt tolerance to zinc finger) [Cluster B4]. STZ is a key factor controlling the expression of senescence related NAC transcription factors (Breeze et al., 2011). Cluster C1 consists of 5 genes specifically up-regulated by MGAT1 which include a cell-wall synthesis related gene MATERNAL EFFECT EMBRYO ARREST (MEE31) and a peroxidise (PER12). Genes down-regulated specifically by MGAT1 were grouped in clusters C2 (31 genes) and C3 (30 genes). Among the C3 genes, 7 were transcription factors which include two ethylene signaling genes ETHYLENE-RESPONSIVE ELEMENT BINDING PROTEIN (ATEB, At3g16770) and ETHYLENE-INSENSITIVE 3 (EIN3). Genes down-regulated by MGAT1 and in DET were grouped in cluster C4. Important in this cluster was an ABA biosynthesis gene, NCED4 that was down-regulated in NS as well. These results point to senescence-like gene expression changes in response to MGAT1 infiltration, the majority of which affect PS. Similarities in phytohormone-related gene expression patterns were also apparent.
MGAT1 and Leaf Senescence
To confirm the role of MGAT1 in the observed senescence, N. benthamiana leaves were infiltrated with four different concentrations of Agrobacterium tumefaciens (AGL1) containing MGAT1. A clear correlation between MGAT1 concentration and leaf yellowing was observed at 3 dpi (Figures 7Ac–f). No significant yellowing was visible at 0.03 OD concentration (Figure 7Ac), while yellowing appeared at 0.0625 OD (Figure 7Ad) and was much more pronounced at 0.125 (Figure 7Ae) and 0.25 OD (Figure 7Af). Infiltrations with A. tumefaciens cultures containing p19 at OD 0.125 and 0.375 did not result in a senescence phenotypic response (Figures 7Aa,b). Although the above results indicated a clear role of MGAT1 in the induction of senescence-like responses, we further confirmed this hypothesis by blocking the MGAT1 activity. The zwitterionic detergent, CHAPS has been used extensively to inhibit the MGAT and DGAT activities of MGAT enzymes (Cao et al., 2007; Vijayaraj et al., 2012). Co-infiltration of 1 mM CHAPS along with MGAT1 did not show senescence symptoms in the infiltrated area (Figures 7Bg) while symptoms were observed in the MGAT1 infiltrated areas of the same leaves (Figure 7Bd). These results clearly show that the activity of infiltrated MGAT1 is required for observed senescence-like symptoms.
Figure 7. Effect of MGAT1 expression and MAG depletion on observed senescence symptoms. (A) Leaf spots infiltrated with two different concentrations of p19 [OD 0.125 (Aa) and OD 0.375 (Ab)] and four different concentrations of p19 + MGAT1 [0.03 OD (Ac), 0.0625 OD (Ad), 0.125 OD (Ae) and 0.25 OD (Af)]. The severity of visible symptoms is correlated to MGAT1 concentration. (B) Co-infiltration of CHAPS or diacylglycerol acyltransferase (DGAT1) with MGAT1. No senescence symptoms are detected in the control treatments—p19 (a), p19 + 1 mM CHAPS (b) and p19 + DGAT1 (c). Senescence induced by MGAT1 (d) is abolished by including 1 mM CHAPS in infiltration mix containing MGAT1 (g). No effect was observed when DGAT1 was co-infiltrated [0.125 OD (e) and 0.25 OD (f)]. (C) MAG supplementation: 2-Oleoylglycerol was added to the infiltration buffer to obtain 10 μM (c), 20 μM (d), 40 μM (e), or 60 μM (f) final concentrations. Senescence was considerably reduced in the presence of 60 μM MAG (f) in comparison to MGAT1 alone (b). Increase in MAG concentration was accompanied by a decrease in visible senescence (c–f). (D) Co-infiltration of a glycerol-3-phosphate acyltransferase (AtGPAT4) with MGAT1 (d) considerably reduced visible senescence as compared to the MGAT1 control (b). Infiltration of AtGPAT4 by itself (c) did not induce senescence. (E) Ion-conductivity measurement of MGAT1 induced senescence. Ion conductivity of infiltrated leaf discs was measured by floating in water. Water with no leaf discs floated (H20) and un-infiltrated (WT) leaf discs served as controls. Data shown are average of three replicates and error bars represent standard error.
Role of MAG in MGAT1-Induced Senescence-Like Response
Although we confirmed the role of MGAT1 in the induction of senescence-like symptoms, the involvement of MAG depletion or DAG/TAG accumulation was still not clear. Since accumulation of DAG or TAG has not always been associated with senescence, we hypothesized that decrease in MAG levels by MGAT1 activity could be involved. However, since it is known that co-infiltration of DGAT1 together with MGAT2 leads to the efficient conversion of accumulated DAG to TAG by the co-expressed DGAT1 (Petrie et al., 2012), we first tested the effect of DGAT1 co-infiltration with MGAT1 on observed senescence. As shown in Figure 7B, no significant changes in visible senescence were observed between MGAT1 (Figure 7Bd) infiltration and co-infiltration with DGAT1 at two different concentrations of 0.125 and 0.25 OD (Figures 7Be–f). DGAT1 itself did not cause any senescence (Figure 7Bc). These results, although not conclusive, indicate that DGAT1 activity had no effect on senescence. The fact that the observed senescence was comparable between MGAT1 and MGAT1+DGAT1 pointed to a relation between reduced MAG levels and senescence. Indeed, supplementation with an 18:1 sn-2 MAG (2-Oleoylglycerol) at different concentrations (10–60 μM) during infiltration alongside MGAT1 rescued the observed senescence symptoms in a concentration dependent manner (Figures 7Cc–f) as compared to MGAT1 only (Figure 7Cb). To further confirm the role of MAG depletion in senescence, GPAT4 gene encoding a sn-2 specific acyltransferase involved in MAG synthesis was co-infiltrated with MGAT1. Similar to MAG supplementation, GPAT4 co-infiltration (Figure 7Dd) reduced the severity of senescence symptoms induced by MGAT1 (Figure 7Db). A tight correlation between observed senescence and supplementation by both exogenous and genetic modes are indicative of a role for MAG depletion in MGAT1 induced senescence. It is noteworthy that GPAT4 was also down-regulated by MGAT1.
Ion-Conductivity Measurement of MGAT1 Induced Senescence-Like Response
In order to quantify the cell damage, electrical conductivity of infiltrated leaf areas was measured as described in methods. Leaves were infiltrated with MGAT1, MGAT1 + 60 μM MAG, MGAT1 + GPAT4 and MGAT1 + 1 mM CHAPS alongside appropriate controls for each treatment. Leaf discs harvested from infiltrated leaves were floated overnight in sterile water for measuring conductivity. Similar to the visual observations, MGAT1 infiltrated leaves showed highest conductivity (30 μS). Both MAG (60 μM) supplementation and GPAT4 co-infiltration reduced the conductivity by 24.5% and 29.7% respectively, whereas a 34% reduction was observed in presence of 1 mM CHAPS (Figure 7E). All controls including p19 showed a mean conductivity of 15 μS. These results show that MAG depletion due to conversion to DAG by MGAT1 can induce senescence-like symptoms that can be rescued by providing additional MAG substrate. Measurement of TAG, DAG and MAG levels under different senescence rescue treatments should provide further biochemical evidence for the role of MAG in senescence.
We have shown that recruiting MAG for TAG synthesis via MGAT1 transient expression results in increased TAG accumulation as early as 2 dpi and also induces senescence-like response in N. benthamiana infiltrated leaves. A de novo transcriptome data set was generated from leaf tissue to study the underlying molecular changes. This data set allowed identification of genes involved in lipid pathways of the model plant N. benthamiana and can serve as a resource for future transcriptomic studies in this system. Using this transcriptome as reference we have identified genes differentially expressed by MGAT1 infiltration. Similarities in transcriptional responses to MGAT1 expression and development of senescence were identified by comparative analysis. These similarities include a majority of down-regulated genes, down-regulation of entire set of photosynthesis related genes, activation of senescence hormone responses, decrease in FA synthesis and desaturation related transcripts. On the other hand, genes involved in glycerolipid assembly such as PDCT and DGAT1 were found to be up-regulated. These results provide a mechanism for MGAT-mediated TAG synthesis in which transient expression of MGAT1 and subsequent up-regulation of PDCT results in enhanced DAG synthesis from MAG and PC, respectively. Subsequently, DAG is efficiently converted to TAG due to (a) the co-ordinated up-regulation of DGAT1 and (b) the DGAT side-activity of MGAT1 (Figure 8). In addition, interesting MGAT1 responses were identified including the down-regulation of transcription factors MYB5 and TTG2 involved in the regulation of mucilage biosynthesis. The senescence related responses of MGAT1 include dramatic decrease in PS-related genes, down-regulation of cutin, suberin and wax biosynthesis genes including GPAT4 (Figure 8). Further, we demonstrate that MGAT1 inhibition, addition of MAG or co-infiltration of GPAT4 can reduce the observed senescence as indicated by a decrease in ion-conductivity. Taken together, these findings suggest that MAG conversion to DAG by MGAT1 leads to MAG depletion affecting diverse biological processes via gene expression changes thereby initiating a senescence-like response. DAG has been suggested as a signaling molecule (Dong et al., 2012). While its role in MGAT1 mediated senescence-like response cannot be ruled out, the N. benthamiana system will allow further characterization of the role of different DAG molecular species under senescence-promoting and -rescue conditions. Finally, MGAT1 transient expression could provide a valuable tool for the study of surface lipids biosynthesis such as cutin, wax and suberin as well as plant-pathogen research due to the ability to induce controlled cell-death in the leaves of a model plant.
Figure 8. Schematic overview of MGAT1-induced TAG increase and senescence-like response. Up- (red) and down-regulated (bue) genes are highlighted. Transient expression of MGAT1 and subsequent up-regulation of PDCT possibly result in enhanced DAG synthesis from MAG and PC, respectively. DAG is subsequently converted to TAG due to the co-ordinated up-regulation of DGAT1 and DGAT side-activity of MGAT1. Down-regulation of TAG and MAG lipases (TAGL and MAGL) indicate decreased FA degradation and increased TAG retention. Down-regulation of cutin, wax and suberin biosynthesis transcripts including GPAT4 and diversion of MAG for TAG synthesis is likely to affect biosynthesis of surface lipids. In addition, down-regulation of photosynthesis genes and up-regulation of senescence hormone related genes indicate a co-ordinated mechanism that might initiate senescence-like response.
Materials and Methods
Transient Expression in N. benthamiana
All infiltrations of Agrobacterium tumefaciens (AGL1) for transient gene expression in N. benthamiana were performed on 6 week old leaves as described previously (Voinnet et al., 2003; Wood et al., 2009). RNA extracted from 6 weeks old un-infiltrated N. benthamiana leaves was used for de novo transcriptome assembly. For differential gene expression analysis, MGAT1 and p19 genes were transiently expressed. Infiltrated areas from at least 10 different leaves were pooled after 1 and 2 dpi separately and frozen for RNA extraction. 10 mM CHAPS (3-[(3-Cholamidopropyl)dimethylammonio]-1-propanesulfonate); (Sigma-Aldrich, USA) solution prepared in deionized water was included in the infiltration buffer to yield a final concentration of 1 mM. For MAG supplementation, 2-Oleoylglycerol (Sigma-Aldrich) dissolved in acetonitrile was added to the infiltration buffer to obtain 10, 20, 40, or 60 μM final concentrations. The mouse MGAT1 and A. thaliana DGAT1 and GPAT4 sequences used in this study were described previously (Yang et al., 2002; Petrie et al., 2012).
RNA (20 μg) extracted from frozen leaf tissues using RNeasy Plant Mini kit (Qiagen, Hilden, Germany) was used for cDNA library preparation and sequencing at Beijing Genome Institute (BGI, Shenzhen, China). Briefly, poly (A) mRNA was isolated with Oligo(dT) attached beads and subjected to fragmentation. First strand cDNA synthesis by random hexamers was followed by second-strand synthesis and purification (QiaQuick PCR purification kit, Qiagen), end repair and adapter ligation. Equimolar concentrations of single end, 100 bp libraries generated after size selection and PCR enrichment were sequenced in a single lane of Illumina HiSeq™ 2000 system.
De novo assembly and annotation
The RNA-Seq reads generated were initially processed to remove the adapter sequences, ambiguous reads (5%) and low quality sequences (Q20). Reads were de novo assembled to contigs using Trinity (Grabherr et al., 2011). Singletons and clusters with isoforms were identified by building de Brujin graphs using Chrysalis module in Trinity. The contigs were mapped against public databases including nr (ftp://ftp.ncbi.nlm.nih.gov/blast/db/), Swiss-prot (http://www.uniprot.org/), COG (http://www.ncbi.nlm.nih.gov/COG) and KEGG (http://www.genome.jp/kegg/) using BLASTX (E-value cutoff 1e−5) for functional annotation. Gene Ontology (GO) annotation terms were obtained by using Blast2GO (Conesa et al., 2005). The contigs were aligned against the A. thaliana protein database TAIR 10 (http://www.arabidopsis.org/) by downloading the sequences and BLASTing (cut-off 1e−5) in CLC Genomics Workbench 5 (http://www.clcbio.com). The A. thaliana acyl-lipid gene list was obtained from “The Arabidopsis Acyl-Lipid Metabolism” website (ARALIP; http://aralip.plantbiology.msu.edu). The GO term enrichment analysis was performed by Classification SuperViewer tool at BAR (http://bar.utoronto.ca).
Differential gene expression analysis
RNA-Seq reads from the MGAT1 and p19 (control) RNA samples were loaded on to CLCBio Genomics workbench 5 for expression analysis. The expression values of transcripts in each sample were measured as RPKM (Mortazavi et al., 2008) in the RNA-seq workflow of CLC Genomics. The parameters used include maximum number of 2 mismatches and minimum read count of 10. Fold change analyses was performed in CLC Genomics by setting up a two group comparison experiment. Differential expression analysis was also carried using DESeq package (1.14.0) in R (2.15.3). The nbinomTest function was used to estimate fold changes which employs Benjamini-Hochberg procedure for false discovery rate (FDR) control and outputs the fold changes and the p-values for statistical significance (Anders and Huber, 2010). Transcripts with 2-fold up- or down-regulation (p ≤ 0.05) and having assigned A. thaliana genes were further analyzed. The A. thaliana gene expression data during natural senescence (Troncoso-Ponce et al., 2013) was used for comparing the MGAT1 responsive expression profiles at day 2. The MGAT1 responsive gene list (1666 genes), Supplementary data set of Breeze et al. and Supplement Table 3 of Vander Graaff et al. were used for comparative analysis and for cluster analysis in MapMan 3.5.1R2 (http://mapman.gabipd.org).
Total RNA (1 μg) was converted to cDNA using First-Strand cDNA synthesis mix (OriGene Inc., Australia). Diluted cDNA (0.2X) was used for quantitative real-time PCR by Bio-Rad CFX Real-Time System (BIO-RAD, USA) using iQSYBR Green Supermix (BIO-RAD). Primer validation was performed for all target genes with five dilutions of template concentration along with the N. benthamiana ACTIN and GAPDH control genes. Reactions were carried out with initial denaturation at 95°C for 3 min, followed by 35 cycles of 95°C for 10 s, 58°C for 30 s and 68°C for 30 s. Relative fold differences were determined by ΔΔ CT method (Livak and Schmittgen, 2001). Primer sequences and description of the target and control sequences are provided in Supplementary Table 4.
Six week old N. benthamiana leaves were infiltrated as described above. Infiltrated leaf discs (0.5 cm diameter) were harvested after 2 days, rinsed twice (2–3 min) with deionized water and subsequently floated on 15 mL of deionized water with shaking (80 rpm) at room temperature. The electrolyte leakage in the solution was measured after 17 h of floating using a conductivity meter (CD-4301, Lutron). All measurements were done on three biological replicates by pooling samples from six plants (two plants per replicate). Values are the average of three replicates and error bars represent standard error.
Leaf discs (2 cm diameter) were cut from 6 different plants (two plants per replicate). Total lipids were extracted from freeze dried tissue as previously reported (Petrie et al., 2012), run on a TLC plate (20 cm2, Silica gel 60, Merck) and developed using a two-step solvent system. Samples were first run to 12 cm in chloroform:methanol:acetic acid:water (68:22:6:4, v:v:v:v), followed by a second separation in hexane:diethyl ether:acetic acid (70:30:1, v:v:v). TAG, DAG and MAG bands were visualized using iodine vapor and isolated from the silica gel. Fatty acid methyl esters were prepared from each isolated lipid fraction and analyzed by GC-FID (7890A GC, Agilent Technologies, Palo Alto, CA, USA) equipped with a 30 m BPX70 column (SGE, Austin, TX, USA) as described previously (Petrie et al., 2012). Peaks were integrated with Agilent Technologies ChemStation software (Revion B.04.03).
Uday K. Divi conceived of the study, carried out transcriptomic analysis, transient expression studies, conducted data analysis and interpretation and drafted the manuscript. Anna El Tahchy carried out lipid analysis and participated in drafting of the manuscript. Thomas Vanhercke and James R. Petrie participated in design and coordination of the study, data interpretation and critical review of the manuscript. Jose A. Robles-Martinez provided R scripts for differential expression analysis. Surinder P. Singh participated in conceptualization, design and coordination of the study and critical review of the manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This work was supported by post-doctoral fellowships of CSIRO's Office of the Chief Executive to Uday K. Divi and Food Futures Flagship to Anna El Tahchy. We thank Cheryl Blundell and Lijun Tian for excellent assistance with plant growth.
The Supplementary Material for this article can be found online at: http://www.frontiersin.org/Journal/10.3389/fpls.2014.00204/abstract
Andrianov, V., Borisjuk, N., Pogrebnyak, N., Brinker, A., Dixon, J., Spitsin, S., et al. (2010). Tobacco as a production platform for biofuel: overexpression of Arabidopsis DGAT and LEC2 genes increases accumulation and shifts the composition of lipids in green biomass. Plant Biotechnol. J. 8, 277–287. doi: 10.1111/j.1467-7652.2009.00458.x
Bombarely, A., Rosli, H. G., Vrebalov, J., Moffett, P., Mueller, L. A., and Martin, G. B. (2012). A draft genome sequence of Nicotiana benthamiana to enhance molecular plant-microbe biology research. Mol. Plant Microbe Interact. 25, 1523–1530. doi: 10.1094/MPMI-06-12-0148-TA
Bouvier-Navé, P., Benveniste, P., Oelkers, P., Sturley, S. L., and Schaller, H. (2000). Expression in yeast and tobacco of plant cDNAs encoding acyl CoA:diacylglycerol acyltransferase. Eur. J. Biochem. 267, 85–96. doi: 10.1046/j.1432-1327.2000.00961.x
Breeze, E., Harrison, E., McHattie, S., Hughes, L., Hickman, R., Hill, C., et al. (2011). High-resolution temporal profiling of transcripts during arabidopsis leaf senescence reveals a distinct chronology of processes and regulation. Plant Cell 23, 873–894. doi: 10.1105/tpc.111.083345
Cao, J., Lockwood, J., Burn, P., and Shi, Y. (2003). Cloning and functional characterization of a mouse intestinal acyl-CoA:monoacylglycerol acyltransferase, MGAT2. J. Biol. Chem. 278, 13860–13866. doi: 10.1074/jbc.M300139200
Conesa, A., Gotz, S., Garcia-Gomez, J. M., Terol, J., Talon, M., and Robles, M. (2005). Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics 21, 3674–3676. doi: 10.1093/bioinformatics/bti610
Ding, B., Haudenshield, J., Willmitzer, L., and Lucas, W. (1993). Correlation between arrested secondary plasmodesmal development and onset of accelerated leaf senescence in yeast acid invertase transgenic tobacco plants. Plant J. 4, 179–189. doi: 10.1046/j.1365-313X.1993.04010179.x
Dussert, S., Guerin, C., Andersson, M., Joët, T., Tranbarger, T., Pizot, M., et al. (2013). Comparative transcriptome analysis of three oil palm fruit and seed tissues that differ in oil content and Fatty Acid composition. Plant Physiol. 162, 1337–1358. doi: 10.1104/pp.113.220525
Grabherr, M. G., Haas, B. J., Yassour, M., Levin, J. Z., Thompson, D. A., Amit, I., et al. (2011). Full-length transcriptome assembly from RNA-Seq data without a reference genome. Nat. Biotechnol. 29, 644–652. doi: 10.1038/nbt.1883
Jako, C., Kumar, A., Wei, Y., Zou, J., Barton, D. L., Giblin, E. M., et al. (2001). Seed-specific over-expression of an arabidopsis cDNA encoding a diacylglycerol acyltransferase enhances seed oil content and seed weight. Plant Physiol. 126, 861–874. doi: 10.1104/pp.126.2.861
Klaus, D., Ohlrogge, J. B., Neuhaus, H. E., and Dörmann, P. (2004). Increased fatty acid production in potato by engineering of acetyl-CoA carboxylase. Planta 219, 389–396. doi: 10.1007/s00425-004-1236-3
Liu, J., Hua, W., Zhan, G., Wei, F., Wang, X., Liu, G., et al. (2010). Increasing seed mass and oil content in transgenic Arabidopsis by the overexpression of wri1-like gene from Brassica napus. Plant Physiol. Biochem. 48, 9–15. doi: 10.1016/j.plaphy.2009.09.007
Lu, C. F., Xin, Z. G., Ren, Z. H., Miquel, M., and Browse, J. (2009). An enzyme regulating triacylglycerol composition is encoded by the ROD1 gene of Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 106, 18837–18842. doi: 10.1073/pnas.0908848106
Nakasugi, K., Crowhurst, R. N., Bally, J., Wood, C. C., Hellens, R. P., and Waterhouse, P. M. (2013). De novo transcriptome sequence assembly and analysis of RNA silencing genes of Nicotiana benthamiana. PLoS ONE 8:e59534. doi: 10.1371/journal.pone.0059534
Parthibane, V., Rajakumari, S., Venkateshwari, V., Iyappan, R., and Rajasekharan, R. (2012). Oleosin is bifunctional enzyme that has both monoacylglycerol acyltransferase and phospholipase activities. J. Biol. Chem. 287, 1946–1954. doi: 10.1074/jbc.M111.309955
Perry, H. J., and Harwood, J. L. (1993). Radiolabelling studies of acyl lipids in developing seeds of Brassica napus: use of [1–14C]acetate precursor. Phytochemistry 33, 329–333. doi: 10.1016/0031-9422(93)85512-P
Petrie, J. R., Shrestha, P., Liu, Q., Mansour, M. P., Wood, C. C., Zhou, X. R., et al. (2010). Rapid expression of transgenes driven by seed-specific constructs in leaf tissue: DHA production. Plant Methods 6:8. doi: 10.1186/1746-4811-6-8
Petrie, J. R., Vanhercke, T., Shrestha, P., El Tahchy, A., White, A., Zhou, X.-R., et al. (2012). Recruiting a new substrate for triacylglycerol synthesis in plants: the monoacylglycerol acyltransferase pathway. PLoS ONE 7:e35214. doi: 10.1371/journal.pone.0035214
Sanjaya, Durrett, T. P., Weise, S. E., and Benning, C. (2011). Increasing the energy density of vegetative tissues by diverting carbon from starch to oil biosynthesis in transgenic Arabidopsis. Plant Biotechnol. J. 9, 874–883. doi: 10.1111/j.1467-7652.2011.00599.x
Santos Mendoza, M., Dubreucq, B., Miquel, M., Caboche, M., and Lepiniec, L. (2005). LEAFY COTYLEDON 2 activation is sufficient to trigger the accumulation of oil and seed specific mRNAs in Arabidopsis leaves. FEBS Lett. 579, 4666–4670. doi: 10.1016/j.febslet.2005.07.037
Shi, L., Katavic, V., Yu, Y., Kunst, L., and Haughn, G. (2012). Arabidopsis glabra2 mutant seeds deficient in mucilage biosynthesis produce more oil. Plant J. 69, 37–46. doi: 10.1111/j.1365-313X.2011.04768.x
Slocombe, S. P., Cornah, J., Pinfield-Wells, H., Soady, K., Zhang, Q., Gilday, A., et al. (2009). Oil accumulation in leaves directed by modification of fatty acid breakdown and lipid synthesis pathways. Plant Biotechnol. J. 7, 694–703. doi: 10.1111/j.1467-7652.2009.00435.x
Van Der Graaff, E., Schwacke, R., Schneider, A., Desimone, M., Flügge, U.-I., and Kunze, R. (2006). Transcription analysis of arabidopsis membrane transporters and hormone pathways during developmental and induced leaf senescence. Plant Physiol. 141, 776–792. doi: 10.1104/pp.106.079293
Vanhercke, T., El Tahchy, A., Liu, Q., Zhou, X.-R., Shrestha, P., Divi, U., et al. (2014a). Metabolic engineering of biomass for high energy density: oilseed-like triacylglycerol yields from plant leaves. Plant Biotechnol. J. 12, 231–239. doi: 10.1111/pbi.12131
Vanhercke, T., El Tahchy, A., Shrestha, P., Zhou, X.-R., Singh, S., and Petrie, J. (2013a). Synergistic effect of WRI1 and DGAT1 coexpression on triacylglycerol biosynthesis in plants. FEBS Lett. 587, 364–369. doi: 10.1016/j.febslet.2012.12.018
Vanhercke, T., Petrie, J. R., and Singh, S. P. (2014b). Energy densification in vegetative biomass through metabolic engineering. Biocatal. Agric. Biotechnol. 3, 75–80. doi: 10.1016/j.bcab.2013.11.010
Vanhercke, T., Wood, C. C., Stymne, S., Singh, S. P., and Green, A. G. (2013b). Metabolic engineering of plant oils and waxes for use as industrial feedstocks. Plant Biotechnol. J. 11, 197–210. doi: 10.1111/pbi.12023
Vijayaraj, P., Jashal, C. B., Vijayakumar, A., Rani, S. H., Venkata Rao, D. K., and Rajasekharan, R. (2012). A bifunctional enzyme that has both monoacylglycerol acyltransferase and acyl hydrolase activities. Plant Physiol. 160, 667–683. doi: 10.1104/pp.112.202135
Voinnet, O., Rivas, S., Mestre, P., and Baulcombe, D. (2003). An enhanced transient expression system in plants based on suppression of gene silencing by the p19 protein of tomato bushy stunt virus. Plant J. 33, 949–956. doi: 10.1046/j.1365-313X.2003.01676.x
Weselake, R. J., Shah, S., Tang, M., Quant, P. A., Snyder, C. L., Furukawa-Stoffer, T. L., et al. (2008). Metabolic control analysis is helpful for informed genetic manipulation of oilseed rape (Brassica napus) to increase seed oil content. J. Exp. Bot. 59, 3543–3549. doi: 10.1093/jxb/ern206
Western, T., Young, D., Dean, G., Tan, W., Samuels, A., and Haughn, G. (2004). MUCILAGE-MODIFIED4 encodes a putative pectin biosynthetic enzyme developmentally regulated by APETALA2, TRANSPARENT TESTA GLABRA1, and GLABRA2 in the Arabidopsis seed coat. Plant Physiol. 134, 296–306. doi: 10.1104/pp.103.035519
Wood, C., Petrie, J., Shrestha, P., Mansour, M., Nichols, P., Green, A., et al. (2009). A leaf-based assay using interchangeable design principles to rapidly assemble multistep recombinant pathways. Plant Biotechnol. J. 7, 914–924. doi: 10.1111/j.1467-7652.2009.00453.x
Xu, C., Fan, J., Froehlich, J. E., Awai, K., and Benning, C. (2005). Mutation of the TGD1 chloroplast envelope protein affects phosphatidate metabolism in Arabidopsis. Plant Cell 17, 3094–3110. doi: 10.1105/tpc.105.035592
Xu, S.-L., Rahman, A., Baskin, T. I., and Kieber, J. J. (2008). Two leucine-rich repeat receptor kinases mediate signaling, linking cell wall biosynthesis and ACC synthase in Arabidopsis. Plant Cell Online 20, 3065–3079. doi: 10.1105/tpc.108.063354
Yang, W., Pollard, M., Li-Beisson, Y., Beisson, F., Feig, M., and Ohlrogge, J., et al. (2002). Identification of a gene encoding MGAT1, a monoacylglycerol acyltransferase. Proc. Natl. Acad. Sci. 99, 8512–8517. doi: 10.1073/pnas.132274899
Yen, C. L., Stone, S. J., Cases, S., Zhou, P., and Farese, R. V. Jr. (2002). Identification of a gene encoding MGAT1, a monoacylglycerol acyltransferase. Proc. Natl. Acad. Sci. U.S.A. 99, 8512–8517. doi: 10.1073/pnas.132274899
Yoshida, S., Ito, M., Nishida, I., and Watanabe, A. (2001). Isolation and RNA gel blot analysis of genes that could serve as potential molecular markers for leaf senescence in Arabidopsis thaliana. Plant Cell Physiol. 42, 170–178. doi: 10.1093/pcp/pce021
Keywords: Nicotiana benthamiana, monoacylglycerol, diacylglycerol, triacylglycerol, acyltransferase, oil increase, senescence, differential gene expression
Citation: Divi UK, El Tahchy A, Vanhercke T, Petrie JR, Robles-Martinez JA and Singh SP (2014) Transcriptional and biochemical responses of monoacylglycerol acyltransferase-mediated oil synthesis and associated senescence-like responses in Nicotiana benthamiana. Front. Plant Sci. 5:204. doi: 10.3389/fpls.2014.00204
Received: 18 February 2014; Accepted: 27 April 2014;
Published online: 26 May 2014.
Edited by:Hanjo A. Hellmann, Washington State University, USA
Reviewed by:Aymeric Goyer, Oregon State University, USA
Roy Navarre, United States Department of Agriculture, USA
Copyright © 2014 Divi, El Tahchy, Vanhercke, Petrie, Robles-Martinez and Singh. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Uday K. Divi, CSIRO Plant Industry, PO Box 1600, Canberra, ACT 2601, Australia e-mail: firstname.lastname@example.org
†Present address: Jose A. Robles-Martinez, Australian Curriculum Assessment and Reporting Authority, Sydney, Australia