Functional analysis of the omega-6 fatty acid desaturase (CaFAD2) gene family of the oil seed crop Crambe abyssinica
© Cheng et al.; licensee BioMed Central Ltd. 2013
Received: 8 May 2013
Accepted: 24 September 2013
Published: 1 October 2013
Crambe abyssinica produces high erucic acid (C22:1, 55-60%) in the seed oil, which can be further increased by reduction of polyunsaturated fatty acid (PUFA) levels. The omega-6 fatty acid desaturase enzyme (FAD2) is known to be involved in PUFA biosynthesis. In crambe, three CaFAD2 genes, CaFAD2-C1, CaFAD2-C2 and CaFAD2-C3 are expressed.
The individual effect of each CaFAD2 gene on oil composition was investigated through studying transgenic lines (CaFAD2-RNAi) for differential expression levels in relation to the composition of seed-oil. Six first generation transgenic plants (T1) showed C18:1 increase (by 6% to 10.5%) and PUFA reduction (by 8.6% to 10.2%). The silencing effect in these T1-plants ranged from the moderate silencing (40% to 50% reduction) of all three CaFAD2 genes to strong silencing (95% reduction) of CaFAD2-C3 alone. The progeny of two T1-plants (WG4-4 and WG19-6) was further analysed. Four or five transgene insertions are characterized in the progeny (T2) of WG19-6 in contrast to a single insertion in the T2 progeny of WG4-4. For the individual T2-plants of both families (WG19-6 and WG4-4), seed-specific silencing of CaFAD2-C1 and CaFAD2-C2 was observed in several individual T2-plants but, on average in both families, the level of silencing of these genes was not significant. A significant reduction in expression level (P < 0.01) in both families was only observed for CaFAD2-C3 together with significantly different C18:1 and PUFA levels in oil.
CaFAD2-C3 expression is highly correlated to levels of C18:1 (r = -0.78) and PUFA (r = 0.75), which suggests that CaFAD2-C3 is the most important one for changing the oil composition of crambe.
Crambe (Crambe abyssinica Hochst ex. R. E. Fr.) belongs to the Brassicaceae plant family. The seed oil of crambe contains a high content of erucic acid (C22:1, 55% to 60%) and this oil thus has applications as industrial oil . Erucic acid in form of erucamide, a major derivative from C22:1, can be used as slip agent in plastics, or lubricants, nylon and cosmetics . More recently, crambe oil is considered to be potential to produce biofuel . The cultivation of crambe yields up to 1 t ha-1 of oil, comparative to that of high erucic acid rapeseed (HEAR). Furthermore, the processing costs for crambe oil extraction are in the same range of that for rapeseed [1, 4, 5]. The high yield and the fact that crambe is not able to cross with food oil crops in nature make crambe an ideal platform to produce industrial oils [6, 7]. In addition to high erucic acid (C22:1), crambe oil contains also certain amounts of oleic acid (C18:1), linoleic acid (C18:2) and linolenic acid (C18:3).
The value of crambe oil can be further improved not only by increasing the C22:1 content but also by reducing the content of polyunsaturated fatty acids (PUFA, C18:2 + C18:3). Firstly, an increase in C22:1 can reduce the purification cost of C22:1 from C18-fatty acids. It was estimated that 10% increase of C22:1 in oil would reduce the processing costs by half . Secondly, reduction in PUFA is beneficial for storage and extending the shelf life of the oil because PUFA are highly prone to oxidation during storage. Thirdly, high PUFA content causes higher viscosity for the oil (a disadvantage to biodiesel) . Considerable efforts have been made to reduce PUFA in oil. A common chemical approach is to reduce the PUFA content or increase the C18:1 content through hydrogenation [9, 11]. However, this hydrogenating process is expensive and adds extra 2 to 3 cent per pound cost to the price of oil .
Molecular breeding approaches to change composition of seed oil are targeting important genes involved in the fatty acid biosynthesis pathways, which have been intensively studied and many genes involved have been characterized. In short, C18:1 is de novo synthesized in plastids and transported into the endoplasmic reticulum where the C18:1 is incorporated into phosphatidylcholine (PC) and may undergo desaturation to C18:2 and next to C18:3 by the actions of two microsomal enzymes; delta-12-fatty acid desaturase (FAD2) [omega-6 desaturase] and delta-15-fatty acid desaturase (FAD3) [omega-3 desaturase], respectively [9, 13]. Alternatively, C18:1 may undergo elongation to very long chain fatty acids (VLCFA, C22:1 for example) by the action of fatty acid elongation (FAE) complex [2, 14–17]. Mutant and genetic mapping studies showed that the enzyme FAD2 was found to be mainly responsible for C18:1 and PUFA content although FAD3 also contributes to a limited degree to these traits [9, 18]. In addition, the acyl flux between the two pathways, the prokaryotic (plastidial) and eukaryotic (mainly in the ER) pathway, is influencing the C18:1 pool [19–21].
Genetic modification (GM) aimed at regulating the FAD2 expression has been applied to produce oils with higher C18:1 in various oil crops [8, 22, 23]. For example, by anti-sense suppression of FAD2 in Brassica juncea, a transgenic line was obtained that produced oil with higher C18:1 (73%) and lower PUFA (8% of C18:2; 9% of C18:3) compared to the wild type (53% of C18:1; 24% of C18:2; 16% of C18:3) . Similarly, a significant change in C18:1 and PUFA and even a C22:1 increase in the seed oil was observed when silencing FAD2 with both co-suppression and anti-sense in Brassica carinata. Gene silencing by RNAi has been considered to be a particularly efficient way to obtain stable transgenic plants with the silenced target genes [24, 25]. RNAi-mediated silencing of GhFAD2 in cotton enabled over 60% increase in C18:1 . Simultaneous RNAi-mediated silencing of FAD2 and FAE1 in Brassica napus caused not only significant increase in C18:1 (from 62% to 85%), but also reduction in C22:1 and PUFA (from 26% to 10% and from 0.87% to 0% respectively) . Recently, several efficient protocols for crambe transformation are available [27, 28] and RNAi has shown to be an effective gene knockdown tool for crambe where CaFAD2 RNAi gene silencing resulted in increased C18:1 levels (from 14.5% to 24.9%) . Introduction of two heterologous genes, LdLPAAT and BnFAE1, in such CaFAD2-RNAi lines directed the oil biosynthesis towards the incorporation of C22:1 at the sn-2 position of triacylglycerol, thereby the C22:1 level increased from 60% in the wild type to 73% in the best transgenic crambe line .
An obstacle to adaptation of such genetic modified (GM) crops is the lack of broad acceptance by a part of the community in many countries . Furthermore, there are some cases where RNAi-mediated traits are not completely reliable on the long term in generating stable target gene suppression . Currently, breeding of the allo-hexaploid crambe mainly relies on traditional approaches, however, the possibilities are restricted by the lack of genetic variation for important agronomic traits [1, 31, 32]. In such situations and particularly when genes controlling a phenotype are known, mutation breeding of induced or natural mutations, identified via “TILLING” (Targeting Induced Local Lesions IN Genomes) , offers a reliable, stable, non-GM approach to obtain the desired oil quality in crambe. A drawback is that “TILLING” is still a challenging task in polyploid crops, where the multiple alleles are creating problems in identifying desirable genetic changes due to gene redundancy. Despite these problems successful cases of targeted mutagenesis have been reported in polyploid crops [34–38]. For instance, targeted mutation breeding of natural or induced variation in the FAD2 gene or mining natural variants has been used to develop crops with high C22:1 or less PUFA [38–40]. By combining mutations or natural variants of FAD2 and FAD3, it was possible to produce oils with higher C18:1 and lower C18:3 in soybean and Brassica napus[9, 11]. In the allo-hexaploid genome of Crambe abyssinica cv. 'Galactica’ seven FAD2 genes are present, of which only three are transcriptionally active throughout plant development (CaFAD2-C1, CaFAD2-C2 and CaFAD2-C3) . The possibility of functional redundancy among the active CaFAD2 family members may complicate the gain of crambe lines with desirable oil composition via mutation breeding.
The aim of the present study is to specify which of the FAD2 genes in crambe is the key gene for increasing the C18:1 level, but reducing the PUFA content. FAD2-RNAi lines of crambe cv. 'Galactica’ were studied for functional correlations between the individual CaFAD2 family members, CaFAD2-C1, CaFAD2-C2 and CaFAD2-C3 and seed-oil composition. Seed-oil composition and gene expression studies were performed in two independent families of the second generation transgenic lines (T2-plants). In addition, two other genes, CaFAD3 and CaFAE1 that are acting in close connection to CaFAD2, were also involved in the study.
We have previously shown that the major expressed CaFAD2 gene in developing crambe seeds is CaFAD2-C3, while the other two genes CaFAD2-C1 and CaFAD2-C2 are naturally expressed to much lower levels (4 and 100 times lower than CaFAD2-C3 respectively) . A DNA fragment of CaFAD2-C2, sharing 97% and 96% nucleotide identity with CaFAD2-C1 and CaFAD2-C3 respectively, was used to trigger RNAi-mediated silencing of the CaFAD2 genes in crambe. Two primary transgenic plants (T0 generation,WG4 and WG19) that showed significantly lower contents of C18:2 and C18:3, but higher level of C18:1 in the seed-oil were used in this study . For these two independent transgenic lines, the effect of RNAi-silencing on the expression of the individual CaFAD2 genes and the composition of the seed-oil were analysed for the seeds produced by the first generation (T1) and the second generation (T2). In the T2 generation the transgene copy number was determined and the relative gene-expression of the individual genes was correlated to differences in seed-oil composition to determine the effect of silencing of the individual CaFAD2 gene(s).
CaFAD2 gene-silencing and oil composition in T1-generation
Oil composition (%) in seeds of T 1 lines of C. abyssinica
No. of seed
Oleic acid (C18:1)
Linoleic acid (C18:2)
Linolenic acid (C18:3)
Erucic acid (C22:1 )
Mean ± SD a
20.1 ± 2.4**
2.7 ± 0.9**
3.0 ± 0.8**
65.5 ± 3.4**
Mean ± SD
20.0 ± 1.1**
2.3 ± 0.5**
3.0 ± 0.5**
67 ± 2.5**
Mean ± SD
21.9 ± 3.5**
2.1 ± 1.8**
2.3 ± 0.9**
63.5 ± 3.2
Mean ± SD
22.6 ± 2.3**
1.6 ± 0.2**
2.5 ± 0.3**
60.7 ± 5.2
Mean ± SD
21.4 ± 3.2**
2.7 ± 1.8**
3.3 ± 0.7*
60 ± 4.6
Mean ± SD
18.0 ± 0.9*
2.0 ± 0.4**
2.4 ± 0.3**
66.2 ± 1.0**
Mean ± SD
12.0 ± 0.5
8.2 ± 0.4
5.1 ± 0.2
63.1 ± 0.8
An explanation for the fact that the level of CaFAD2 silencing and the oil composition are not clearly correlated in T1 generation may reside in differences in zygosity level of the transgene copies among the T1-plants. As the expression profile was analysed on bulks of five to ten seeds, variation in transgene copy number and the presence of seeds that have segregated to the wild-type may mask the silencing effect. Indeed, among the fatty acid profiles of the individual seeds of WG4-5 and WG19-5 segregation to the wild-type oil composition was observed (Additional file 1).
CaFAD2 silencing and oil composition in T2-generation
Two T1-plants (WG4-4 and WG19-6) with stable and high C18:1 content were chosen to develop a second generation for an extensive study of the inheritance of the “high C18:1, low PUFA” oil-phenotype and to examine the correlation between silencing of the respective CaFAD2 genes, the oil composition and the expression of two other genes involved in the seed oil biosynthesis (CaFAD3 and CaFAE1).
Seventeen T2-plants (5 from WG4-4 and 12 from WG19-6, designated as family WG4-4 and WG19-6) were randomly selected and characterised for the number of transgene insertion by Southern analysis. Four or five transgene insertions were detected in the progeny of WG19-6 with a similar pattern. In contrast, a single insertion was detected in all five analysed progeny plants of WG4-4 (Additional file 2).
In contrast to the constant and strong silencing of CaFAD2-C3, more variation in silencing is found for CaFAD2-C2 and CaFAD2-C1 in both families. In the single copy transgenic T2-plants of the WG4-4 family, CaFAD2-C2 showed strong silencing in almost half (3 out of 7) of the WG4-4 family (WG4-4-1, WG4-4-2 and WG4-4-4) whereas in the other T2-plants of WG4-4 this gene was not silenced (Figure 2A). In the other family, WG19-6, 60% of the T2-plants (9 out of 15) showed strong silencing of CaFAD2-C2 whereas the rest showed zero- to moderate silencing of CaFAD2-C2. Also, CaFAD2-C1 showed various silencing levels in both T2 families with strong silencing in three WG4-4 T2 -plants (3 out of 7; 43%) and five WG19-6 T2-plants (5 out of 15; 33%) (Figure 2A).
The average expression levels of the respective genes were calculated for each T2 family in comparison with the control. In both families (WG4-4 and WG19-6), only the expression of CaFAD2-C3 is constantly and significantly different to the average control level (Figure 2B). For CaFAD2-C1 and CaFAD2-C2, the average expression levels in both families are not significantly different from the average expression level observed in the control (Figure 2B).
Inheritance of CaFAD2 silencing
As compared over two generations (T1 and T2), the level of silencing in WG19-6, the line which carries multiple transgene insertions, increased from zero silencing in the T1 to ~40%, 60% and 70% reduction for respectively CaFAD2-C1, -C2 and -C3 in the T2. Over two generations, T1 and T2, of the single copy transgene WG4-4 the expression patterns of the CaFAD2 genes were similar. In both generations, only CaFAD2-C3 was dominantly down-regulated in expression (Figure 1 and 2B).
Effect of CaFAD2 silencing on CaFAD3 and CaFAE1 expression
As a consequence of CaFAD2 gene silencing, and accompanying changes in the substrate flow in the oil biosynthesis pathway, the expression of other genes acting in the pathway may change. Therefore, the expression of two genes, FAD3, involved in the conversion of C18:2 to C18:3, and FAE1, acting in the production of very long chain fatty acids (i.e. C22:1) by chain-elongation of C18:1, were studied in the two T2 families (WG4-4 and WG19-6) and the control. Both genes showed differential expression among the individual plants within families, but on average no significant differences were observed between the two T2 families and the control (Figure 2B). Notably, CaFAD3 and CaFAE1 showed a similar regulation pattern because both of them were up- or down-regulated within the same plant with exception of two plants, WG19-6-11 and WG19-6-12 (Figure 2A).
Correlation between gene expression and oil composition
C. abyssinica, an under-utilized crop, has limited genetic variation and the improvement of crambe oil by traditional breeding has reached a bottleneck. Recently, using a genetic engineering approach, crambe lines with a desirable oil type have been obtained by silencing CaFAD2 genes . In C. abyssinica, three functional FAD2 genes are present (CaFAD2-C1 to -C3) . Even though the functional defect of one of the family members may be complemented by the other members of the gene family , one or few of these family members usually play a predominant role, so that a primary functional analysis of gene family members is normally required prior to mutation breeding . Our study was initiated to characterise the effect of the three functional CaFAD2 genes (CaFAD2-C1 to -C3) to determine the appropriate targets for a targeted mutation approach (TILLING) to develop non-GM crambe lines with novel oil types.
Here we used a construct containing a part of the CaFAD2-C2 sequence, which is 96% to 97% identical to the sequences of other expressed CaFAD2 genes, to obtain seed-specific silencing (Napin promoter) of the endogenous CaFAD2 gene family members in crambe. The results proved that one RNAi trigger is able to affect the expression of multiple members of the gene family but in different patterns (Figure 1). In T2-plants, the main FAD2 gene expressed in crambe seeds, CaFAD2-C3, is strongly silenced whereas the two lower expressed genes, CaFAD2-C2 and -C1 (respectively 4 and 100 times lower than CaFAD2-C3 at 20 DAP ), are silenced to different levels ranging from strong- to zero silencing. The reason why no reduction of CaFAD2 gene expression was detected in two T1-plants (WG19-5 and WG19-6), which nevertheless showed significant difference for seed-oil composition, is probably due to the heterozygous nature of the seed samples. This can cause that segregating wild-type seeds can be present in the seed bulks used for expression analysis, whereas the oil composition was measured on single seeds. Another possibility is that silencing in these lines took place in the developing seeds at other time points beyond the expression peak at 20 days after pollination (DAP). Indeed, the results of Southern analysis do suggest that the T1-plant WG19-6 is heterozygous, because a varying number of transgene insertions was detected in its offspring (T2), and also that WG4-4 (T1-plant) is most likely homozygous because a single transgene insertion was observed in all randomly tested progeny (T2) of WG4-4 (Additional file 2).
Over two generations (T1 and T2), the expression patterns of CaFAD2 in WG4-4, carrying a single transgene insertion, were similar whereas differences in silencing levels over generations were observed for WG19-6. The multiple transgene insertions in WG19-6 may cause different types of variation in the T2 population, which may influence the level of silencing. It is known that trace amount of dsRNA is sufficient to trigger gene silencing  and the degree of silencing has no association with insert copy number . Therefore, a plausible explanation to different silencing levels over T1 and T2 generations of WG19-6 is that a higher level of homozygosity in the seeds of the T2 generation leads to a lower number of segregating wild type seeds, which is of importance if the seeds are analysed for expression “in bulk”.
The T2 progenies of two FAD2-RNAi plants (WG4-4 and WG19-6) were tested in detail for the level of gene expression of the different CaFAD2 gene family members (Figure 2A and B) and for oil composition (Figure 3 and 4). The results showed that the silencing of gene expression is stably inherited to the subsequent generation. The stability of RNAi-silencing was also reflected at the seed-oil composition, for instance, in the T2-progeny of WG4-4, the C18:1 level was significantly higher and PUFA level was significantly lower than those of the control plants (Table 1 and Figure 3). The values of important individual oil compounds are close to the average of the parental T1-plants for both lines, WG4-4 and WG19-6, indicating that the high C18:1 and low PUFA traits were stably transmitted to the subsequent generation.
Correlation and expression regulation analysis
Compared to CaFAD2-C1 and CaFAD2-C2, CaFAD2-C3 was strong and stably silenced by the seed specific RNAi trigger. On average, silencing of CaFAD2-C3 is constantly significant in both T2 families (offspring of WG4-4 and WG19-6). Although some T2-plants show a clear silencing of CaFAD2-C1 and CaFAD2-C2, the overall family average of these genes are not significantly different from the control for both families. Consequently, the only significant difference in gene expression observed between the two T2 families is the difference in CaFAD2-C2 expression (Figure 2B).
Taken together with the fact that a change in oil composition was found in all T2-plants and that out of the three CaFAD2 genes CaFAD2-C3 is the highest expressor in developing crambe seeds , it is most likely that this gene plays a direct role in seed oil synthesis. This idea is supported by the study on the seed-oil of individual T2-plants (Figure 5). Based on the differential silencing of CaFAD2-C2 among T2 plants of both families and the silencing of CaFAD2-C1 observed in several individual T2 plants, there is no clear evidence showing that the expression of these two genes is correlated to changes in the seed oil composition (Figure 5). Furthermore, the changes in oil composition due to CaFAD2-C3-silencing were not complemented in individual T2-plants in which CaFAD2-C1 and CaFAD2-C2 were unaffected and expressed to wild-type levels.
The trait of high C18:1 is controlled by quantitative trait loci and thus needs coordinated regulation of multiple loci . Previous studies proved that the FAD2 gene plays an essential role for this trait [9, 38]. In addition, FAD3, FAE1 and other loci with minor effect are likely required to establish high C18:1 pool during oil biosynthesis [21, 45]. In this study, we also investigated the regulation of FAD3 and FAE1 while silencing the CaFAD2 genes. It is known that FAD3 and FAE1 are regulated by abscisic acid . Herein, we found that the expression of FAE1 is positively related to that of FAD3 and one of the FAD2 genes, CaFAD2-C2 (Figure 5). This finding is consistent to previous studies in which these functionally related genes (FAD3 and FAE1) showed coordinated regulation in Arabidopsis and Brassica napus[46, 47]. However, it is unknown why the other two CaFAD2 genes do not show a similar co-regulation with FAD3 and FAE1.
The CaFAD2-C3gene is a target gene for crambe oil improvement by mutation breeding
Here, we show that CaFAD2-C3 is the main CaFAD2-gene involved in determining the C18:1 and PUFA contents in crambe oil (Figure 5). Embryo tissue is the main compartment of oil storage in crambe seed, so the oil composition in the seeds is mainly determined by that in the embryo. Therefore, CaFAD2-C3 is most likely responsible for fatty acid synthesis in the embryo. The other two genes, CaFAD2-C1 and CaFAD2-C2, might be responsible to change fatty acid contents in other seed compartments (e.g. seed coat and endosperm). For instance in olive (Olea europaea), two FAD2 genes (OeFAD2-1 and OeFAD2-2) are expressed both in two seed compartments, seed coat and embryo. Of these two OeFAD2 genes, the expression of OeFAD2-2 was positively correlated to C18:2 content in the seed coat rather than in the embryo under cold condition .
The finding that the prominent role of CaFAD2-C3 is further substantiated by the observation that the effect on oil-composition caused by CaFAD2-C3 silencing is not restored in individual T2-plants with wild-type expression of CaFAD2-C2 and -C1 respectively. This finding suggests that CaFAD2-C3 may provide an important target gene for TILLING and mutation breeding aiming at pronounced changes of C18:1 and PUFA in crambe oil.
C. abyssinica cv. 'Galactica’ was previously transformed with an RNAi construct (pWatergate) . This construct contains an inverted repeat (IR) of the CaFAD2-C2 coding sequence (355 base pairs for each IR part, 97% identical to CaFAD2-C1 and 96% identical to CaFAD2-C3) following a seed specific promoter (Napin) (Additional file 4). The plant used as control was transformed with an empty construct (pRCNG) which contains no genes involved in fatty acids biosynthesis . Two T0 lines were used to develop six T1 plants/lines (WG4-3, WG4-4, WG4-5, WG19-4, WG19-5 and WG19-6), grown in the greenhouse with temperature of 22°C and photoperiod of 16 h. From these T1 plants, the developing seeds at 20 DAP (days after pollination) were collected for RNA isolation for gene expression analysis and ripe seeds were harvested for oil composition analysis. Seeds of two T1-lines, WG4-4 and WG19-6, were used to produce T2-plants. The young leaves of T2-plants were collected for Southern analysis. The developing seeds (20 DAP) and ripe seeds of the T2-plants were harvested for RNA isolation and oil composition analysis respectively.
Quantitative reverse transcription PCR (qRT-PCR) and data analysis
To examine the level of gene-silencing, the expression of the individual crambe FAD2 genes, CaFAD2-C1, CaFAD2-C2 and CaFAD2-C3, was measured in six T1 plants (WG4-3, WG4-4, WG4-5, WG19-4, WG19-5 and WG19-6) on bulks of five to ten developing seeds (20 DAP, days after pollination) and compared to their expression level in the control (plant transformed with an empty construct). The primers specific for the different crambe FAD2 genes were developed based on their sequences in C. abyssinica cv. 'Galactica’ (GenBank: JX964743, JX964744, JX964745), and the primers of FAD3 and FAE1 were developed on the sequences of AtFAD3 (GenBank: 42570333) and crambe FAE1 (GenBank: 60543786). The gene β-actin 2 (GenBank: 20465834) was used as a reference gene. All primers used in qRT-PCR are listed in Additional file 5. Total RNA was extracted from bulked seeds of T1-and T2 -plants respectively (5 to 10 seeds per T1-plant and per T2-plant, 20 DAP) with RNeasy Plant Mini Kits (Qiagen, Germany) according to the manufacturer’s instructions. The isolated RNA was treated with RNase-free TURBO DNase (Ambion, USA) to remove residual genomic DNA. First-strand cDNA was synthesized in 20 μl from 1 μg of total RNA with iScript™ cDNA Synthesis Kit (Bio-rad, USA), in parallel 1 μg of RNA of each sample was treated in the same way but without adding reverse transcriptase, as negative controls (RT-). The cDNA was 20 × diluted and used as templates for real-time PCR. The PCR reaction contains 2 μl templates, 5 μl SYBR Green Super Mix (Bio-rad, USA), and 1 μl of each of the forward and reverse primers (3 μM) in total 10 μl reaction. Cycling conditions were 1 cycle at 95°C for 3 min followed by 30 cycles at 95°C for 10 s, 60°C for 1 min, then a final melt step from 65°C to 95°C ramp with 0.5°C increments per cycle to monitor specificity. PCR reactions were performed in triplicate. The expression of each replicate was normalized by the reference gene, β-actin 2, which has shown to be stably expressed in both, crambe seedlings under arsenate stress and various Brassica napus cultivars [47, 50]. The relative expression level of each replicate was calculated according to the comparative CT method (User bulletin no. 2, ABI PRISM 7700 Sequence Detection System, December 1997; Perkin-Elmer, Applied Biosystems). The mean of three replicates represents the relative expression level of a line.
Oil composition and correlation analysis
The fatty acid (FA) fraction was extracted from single crambe seeds, and fatty acid methyl esters (FAMEs) were analysed using gas chromatograph (GC, column/DB-23, Agilent). For each T1-plant 20, and for each T2-plant 10 individual ripe seeds were collected respectively per plant for fatty acid extraction. The pods of single seeds were removed and then crushed in a plastic tube with screw cap and 300 μl of hexane and 40 μl of KOH (5 M)/methanol were added, followed by vortexing and heating samples at 60°C for 6 min. The samples were then allowed to cool down to room temperature before centrifugation at 3000 rpm for 5 min, the upper layer was used for GC. The extraction (1 μl) was injected into GC with split ratio 1:20 and the condition of oven was 180°C for 10 min, ramp to 240°C for 7 min with 7.5°C increments per min. The mean percentages of FA compounds of each line were calculated from the average of 20 or 10 single seed values. The data of gene expression and oil composition in the seeds of T2 generation were used for correlation analysis. These data were plotted and a Pearson correlation was run to determine correlation with R package .
Genomic DNA was isolated from young leaves of T2 plants with the method described by Aldrich and Cullis  but with 1% (w/v) polyvinylpyrrolidone-10 in the DNA extraction buffer. A probe (686 base pairs) was designed on the nptII gene in the WG construct and labelled with [32P]ATP. The primers for nptII probe preparation are listed in Additional file 5.
For copy number determination, a total of 40 μg of DNA extracted was digested overnight with Dra I, an enzyme that cuts the T-DNA in a site outside the probe sequence, fractionated on 0.8% agarose gel and transferred to Hybond N + membrane (Amersham Biosciences, UK) according to the manufacturer’s recommendations. The procedures of hybridization and visualization were performed as described by Cheng et al. .
This work was supported by the EU-project ICON (Industrial crops producing added value oils for novel chemicals) with co-funding of a Dutch R&D program Biobased Economy (Kennis Basis Biobased Economy).
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