Abstract
Two cDNA sequences, named OepHPT and OepMPBQ MT, encoding homogentisate phytyltransferase (HPT) and methylphytylbenzoquinol methyltransferase (MPBQ MT), respectively, have been cloned from olive (Olea europaea cv. Picual). Sequence analysis displayed the distinguishing characteristics typical of the HPT and MPBQ MT families and along with phylogenetic analysis indicated that they code for homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase enzymes, respectively. Transcriptional analysis in distinct olive tissues indicated that expression levels of HPT and MPBQ MT genes are spatially and temporally regulated in a cultivar-dependent manner and together with tocopherol analysis pointed out that both genes participate in the biosynthesis of the tocopherols present in olive mesocarp. These data also suggest that in olive mesocarp, HPT but not MPBQ MT could be implicated in the transcriptional regulation of the tocopherol biosynthetic pathway. In addition, HPT and MPBQ MT transcript levels are regulated by water status, temperature, light, and wounding in the olive fruit mesocarp, suggesting that both genes could be implicated in the abiotic stress response. Overall, this research constitutes a significant advance to elucidate the factors that regulate the tocopherol biosynthesis in olive fruit to obtain virgin olive oils with enhanced α-tocopherol content.
Introduction
In nature, four tocopherols and four tocotrienols have been described, constituting a group of lipid-soluble antioxidants named tocochromanols that belong to the group of vitamin E compounds (). The basic structure of tocochromanols is simple, comprising a polar chromanol ring and a lipophilic polyprenil side chain, which is saturated in tocopherols and 3-fold unsaturated in tocotrienols (). The number of methyl groups in the chromanol ring determines the four α- (three-methyl groups), β- and γ- (two-methyl groups), and δ- (one-methyl group) tocopherol and tocotrienol subforms (). Tocopherols are found in all photosynthetic organisms, whereas tocotrienols are only present in certain plant groups ().
In higher plants, the content and composition of tocopherols differ considerably in distinct tissues, being generally present in the green parts (). Commonly, seeds of many plant species accumulate γ-tocopherol, while leaves are rich in α-tocopherol (), with some important exceptions such as sunflower where the main tocopherol form in the seed is α-tocopherol (). α-Tocopherol is localized in the chloroplasts, specifically in the inner envelope and thylakoid membranes, and in some cases in plastoglobuli ().
Tocopherol biosynthesis takes place in the plastids of photosynthetic organisms. The first reaction of the pathway consists in the condensation of the polar aromatic head group homogentisic acid (HGA) with the polyprenyl side chain phytyl diphosphate (PDP), which is catalyzed by the enzyme homogentisate phytyltransferase (HPT), producing 2-methyl-6-phytyl-1,4-benzoquinol (MPBQ) (; ). Regarding the origin of both substrates, the formation of HGA is derived from the shikimate pathway and is catalyzed by the p-hydroxyphenylpyruvate dioxygenase, whereas PDP is originated from the methylerytrithol phosphate pathway and synthesized by the geranylgeranyl reductase from geranylgeranyl diphosphate, as well as from the recycling of free phytol derived from chlorophyll degradation catalyzed sequentially by two phytol kinases (; ). The reaction product MPBQ can be methylated via MPBQ methyltransferase (MPBQ MT) to 2,3-dimethyl-6-phytyl-1,4-benzoquinol (DMPBQ). MPBQ and DMPBQ are then further cyclized by the tocopherol cyclase (TC) to produce δ- and γ-tocopherols, respectively. Finally, the enzyme γ-tocopherol methyltransferase (γ-TMT) catalyzes the methylation of δ- and γ-tocopherols into β- and α-tocopherols, respectively ().
HPT catalyzes the first committed step of tocopherol biosynthesis. Arabidopsis plants lacking HPT are completely deficient in all tocopherols and pathway intermediates in both, seeds and leaves, indicating that this is a limiting step in tocopherol biosynthesis (). The genes encoding HPT, also named VTE2, were initially cloned from Arabidopsis and Synechocystis (; ). Overexpression of AtHPT in Arabidopsis plants resulted in a 2-fold increment in total tocopherol level in seeds (; ). In the same way, overexpression of AtHPT in rapeseed plants increased the total tocopherol content in the transgenic seeds (). In contrast, overexpression of HPT genes in soybean did not significantly enhance the tocopherol content in the seeds (). These data suggest that HPT activity is at least partially limiting in seeds. Interestingly, only a minor increment was observed when the seed-specific expression of the Synechocystis HPT gene was carried out in rapeseed, indicating species-specific differences in the regulation of tocopherol biosynthesis (). In leaves, the constitutive overexpression of the HPT gene brought about a considerable increase in the total tocopherol content in Arabidopsis (; ), tomato (; ), and lettuce (). Overall, these results indicate that HPT clearly limits leaf tocopherol synthesis, whereas it is not a major bottleneck in tocopherol metabolism in seeds ().
The MPBQ MT enzyme catalyzes the step of the tocopherol biosynthetic pathway that controls the ratio between α- and γ-tocopherols with respect to β- and δ-tocopherols, competing for the same MPBQ substrate with the TC enzyme. Additionally, the MPBQ MT enzyme is also involved in the methylation of 2-methyl-6-solanyl-1,4-benzoquinone (MSBQ) to produce plastoquinol-9 in the synthesis of plastoquinones (). The first MPBQ MT gene, also called VTE3, was isolated from Synechocystis because of its homology to γ-TMT (). Arabidopsis vte3-2 mutant lines, which have a complete gene disruption, were deficient in α- and γ-tocopherols, as well as plastoquinones, but accumulating β- and δ-tocopherols (; ). Overexpression of AtMPBQ MT in Arabidopsis and soybean seeds did not have a substantial increase in total tocopherol amounts, but highly altered tocopherol composition decreasing β- and δ-tocopherols, with a corresponding increment in α- and γ-tocopherols (; ).
In photosynthetic organisms, the main physiological role of tocopherols has been associated with their non-enzymatic antioxidant activity that protects lipids from oxidation by scavenging lipid peroxy radicals and quenching singlet molecular oxygen during stress conditions (). More recently, several studies suggest that tocopherols are essential for plant development and are involved in several functions such as the plant response to environmental stresses, the maintenance of membrane stability, transcript regulation, and intracellular signaling (; ; ; ; ).
In mammalian systems, the role of vitamin E has been widely studied since its discovery in 1922. In addition to its essential role in animal reproduction, vitamin E has beneficial functions in human health (). A sufficient uptake of vitamin E can help to prevent chronic diseases and neurological disorders, mainly those with an oxidative stress component such as cancer or atherosclerosis (; ). Among tocochromanols, the most biologically active form of vitamin E is α-tocopherol because it exhibits the highest affinity to the α-tocopherol transfer protein, a cytoplasmic protein that transports tocochromanols from the endosomal fraction of hepatocytes into the bloodstream of animals (). Because humans cannot synthesize vitamin E, it is an essential part of our diet. It is commonly found in nuts, seeds, grains, and vegetable oils, but also in fruits and leafy vegetables (). Wheat germ and sunflower oils are the best sources of α-tocopherol, while γ-tocopherol can be found in high concentrations in rapeseed, corn, and soybean oils (). Therefore, the enrichment in vitamin E content and the increase of α-tocopherol in vegetable oils are of particular interest in crop breeding ().
Virgin olive oil (VOO) is mainly constituted of triacylglycerols esterified by fatty acids, which are the major components (≥98%), and a highly diverse mixture of chemical compounds called “minor compounds” (≤2%) (). Among the minor components present in the VOO are the tocopherols. Their total content ranges between 90 and 1400 mg/kg, with α-tocopherol representing more than 95% (). β- and γ-tocopherols are also present but only in minor amounts. Almost all the tocopherols present in VOO derive from the mesocarp of the olive fruit, with a minor contribution from the seed (). In olive mesocarp, total tocopherols varied from 135 to 579 mg/kg (). Tocopherol content and composition in VOO and olive fruit are affected by genetic and agronomic factors such as cultivar, fruit ripeness, and agroclimatic conditions (; ). Unlike the phenolic compounds with secoiridoid structures, tocopherols do not suffer any relevant chemical or enzymatic transformation during the oil extraction process, being directly transferred from the olive fruit to the VOO. However, a certain loss of tocopherols is produced in the added water during the centrifugation step due to their amphipathic nature ().
In recent years, the generation of novel olive cultivars producing VOO with improved functional quality, including the increase in vitamin E content, has been considered an important target of olive breeding programs (). To achieve that, the identification of molecular markers associated with high vitamin E content in VOO is needed. However, unlike oilseeds and leaves, molecular studies about tocopherol biosynthesis in oil fruits are very limited. In olive, no genes specific to the tocopherol biosynthetic pathway have been cloned and characterized to date, although their expression levels have been measured in the mesocarp of several Greek olive cultivars (; ; ). In the present work, we report the isolation and characterization of HPT and MPBQ MT genes in olive. Tocopherol and expression analysis during the development and ripening of olive fruit from different cultivars were performed to investigate their specific roles in tocopherol biosynthesis and their possible implication in the response to several environmental stresses in the olive mesocarp.
Materials and methods
Plant material and stress treatments
Olive (Olea europaea L.) trees (cv. Picual and Arbequina) were cultivated in the experimental orchard of Instituto de la Grasa, Seville (Spain), using drip irrigation and fertirrigation (irrigation with suitable fertilizers in the solution) from the time of full bloom to fruit ripening. Young drupes, developing seeds, and mesocarp tissue were collected from at least three different olive trees at different weeks after flowering (WAF) corresponding to distinct developmental stages of the olive fruit: green (9, 12, 16, and 19 WAF); yellowish (23 WAF); turning or veraison (28 and 31 WAF); and mature or fully ripen (35 WAF). Young leaves were harvested as well.
Olive trees (cv. Klon-14, Abou Kanani, Dokkar, and Piñonera) from the Worldwide Olive Germplasm Bank of Córdoba located at IFAPA (Alameda del Obispo, Córdoba, Spain) were grown by using standard culture practices. Mesocarp tissue from these cultivars was collected at distinct developmental stages of the olive fruit: green (20 WAF); yellowish (24 WAF); turning or veraison (27 WAF) and mature or fully ripen (31 WAF).
To study the effect of water deficit, mesocarp tissue at different WAF was collected at the Sanabria orchard, a commercial super high-density olive (cv. Arbequina) orchard near Seville, as previously described (). Full irrigation (FI) and two regulated deficit irrigation (RDI) treatments (60RDI and 30RDI) were applied.
Stress treatments were conducted as described by using olive branches collected from different olive trees (cv. Picual and Arbequina) with around 100 olive fruit at the turning stage (28 WAF) and incubated in a growth chamber with a 12 h light/12 h dark cycle (light intensity of 300 µmol m-2 s-1.) at 25°C. These incubation parameters were considered the standard conditions since they mimic the physiological conditions of the tree. For stress treatments, standard conditions were changed according to the effect studied. To assess the influence of low and high temperatures, the branches were incubated at 15 or 35°C, respectively. To study the impact of the darkness, the light was turned off. For wounding experiments, the entire surface of the olive fruit was mechanically damaged affecting mesocarp tissue, with pressure at zero time using forceps with serrated tips. The zero time of each treatment was chosen 2 h after the beginning of the light period to preserve the natural photoperiod day/night of the olive fruit. The duration of stress exposure was 24 h. This short-term exposition was selected because longer times can cause tissue damage in the olive fruits, since they are not in the olive tree but in branches incubated in chambers.
In all cases, olive tissues were frozen in liquid nitrogen immediately after harvest and stored at -80°C.
Isolation of homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase full-length cDNA clones
Candidate olive HPT and MPBQ MT sequences were identified in the olive transcriptome () and the wild olive (var. sylvestris) genome () using the tblastn algorithm together with the amino acid sequences of Arabidopsis HPT and MPBQ MT genes (At2g18950 and At3g63410, respectively). Based on these two new sequences, specific pairs of primers for each gene were designed and used for PCR amplification with VELOCITY DNA polymerase (Bioline, Spain), which has proofreading activity. An aliquot of an olive Uni-ZAP XR cDNA library constructed with mRNA isolated from 13 WAF olive (cv. Picual) fruit () was utilized as a DNA template. One fragment with the expected size was obtained in each reaction, subcloned into the vector pSpark® I (Canvax, Spain), and sequenced in both directions. DNA sequencing was carried out by GATC Biotech (Germany).
The DNA sequence data were compiled and analyzed with the LASERGENE software package (DNAStar, Madison, WI). The multiple sequence alignments of olive HPT and MPBQ MT amino acid sequences were calculated using the ClustalX program and displayed with GeneDoc. Phylogenetic tree analysis was performed using the neighbor-joining method implemented in the Phylip package using Kimura’s correction for multiple substitutions and a 1000 bootstrap data set. TreeView was used to display the tree. The conserved domains in the deduced amino acid sequences were analyzed using the NCBI Conserved Domain Search (http://www.ncbi.nlm.nih.gov/structure/cdd/wrpsb.cgi) and Pfam software (https://pfam.xfam.org/). TMHMM analysis was carried out (http://www.cbs.dtu.dk/services/TMHMM/) and subcellular localization was predicted using three different programs: ProtComp 9.0 (http://www.softberry.com), WoLF PSORT (https://wolfpsort.hgc.jp/) and TargetP-2.0 (http://www.cbs.dtu.dk/services/TargetP/). Prediction of N-terminal chloroplast targeting peptides was performed using ChloroP 1.1 software (http://www.cbs.dtu.dk/services/ChloroP/).
Total RNA isolation and cDNA synthesis
Total RNA isolation was carried out according to using 1.5 g of frozen olive tissue. RNA quality verification, removal of contaminating DNA, and cDNA synthesis were performed as described by .
Expression analysis of homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase genes
Gene expression levels of the olive HPT and MPBQ MT were analyzed by quantitative real-time PCR (qRT-PCR) using a CFX Connect real-time PCR System and iTaq Universal SYBR Green Supermix (BioRad, California, USA) as described by . Primers for gene-specific amplification of OeHPT and OeMPBQ MT were designed using the Primer3 program (http://bioinfo.ut.ee/primer3/) and the Gene Runner program (Supplementary Table 1). The housekeeping olive ubiquitin2 gene (OeUBQ2, AF429430) was used as an endogenous reference to normalize (). The qRT-PCR data were calibrated relative to the corresponding gene expression level at 12 WAF ‘Picual’ mesocarp for developmental studies, at 13 WAF ‘Arbequina’ mesocarp of FI treatment for water deficit study, and zero time for each stress treatment and cultivar, respectively, as calibrator. The relative expression level of each gene was calculated following the 2-ΔΔCt method for relative quantification (). The data are presented as means ± SD of three biological replicates, each having two technical replicates per 96 well plate.
Tocopherol analysis
Lyophilized mesocarp tissue (500 mg DW) was processed in a glass tube with 3 mL of hexane and the mixture was shaken for 15 min including 1 min vortexing. After centrifugation at 2000 rpm for 10 min at RT, the hexane phase was recovered, and the tissue was extracted twice. The hexane phases were mixed, and hexane was added to complete an exact volume of 10 mL in a graduated flask. An aliquot of the extracts was filtered and injected into an HPLC. The tocopherols were determined according to , using a Supersphere Si60 Lichrocart 250-4 HPLC cartridge (Merck), and eluted with hexane:2-propanol (99:1) at a flow rate of 1 mL/min. A fluorescence detector (Shimadzu RF535) was used, setting the excitation and emission wavelengths at 290 and 330 nm, respectively. The injection volume of the sample was 20 µL. Peaks of α-, β-, γ- and δ-tocopherol were identified using a mix standard solution of all the four compounds. The quantitative evaluation was performed by external standardization using an α-tocopherol calibration curve. The data are presented as means ± SD of three biological replicates, each having three technical replicates.
Results and discussion
cDNA cloning and sequence analysis of olive homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase genes
Two sequences were identified from the olive transcriptome () and the olive (var. sylvestris) genome (), which displayed an elevated degree of similarity to the Arabidopsis HPT and MPBQ MT genes (; ). Based on these sequences, specific primer pairs were designed and utilized for PCR amplification, along with an aliquot of an olive fruit (13 WAF) cDNA library (cv. Picual). Two full-length cDNA clones were isolated and named OepHPT and OepMPBQ MT, with sizes of 1296 and 1264 bp, respectively. They exhibited ORFs encoding predicted proteins of 408 and 346 amino acid residues, which correspond to calculated molecular masses of 45.7 and 38.8 kDa, respectively, and pI values of 9.6 for OepHPT and 9.1 for OepMPBQ MT. Alignment of the olive HPT deduced amino acid sequences with Arabidopsis HPT indicated that they displayed 60% identity (Figure 1A), while olive MPBQ MT shared 75% identity with Arabidopsis MPBQ MT (Figure 1B).
Figure 1
The Conserved Domain search revealed that the olive HPT protein belongs to the PLNO2878 superfamily, with homogentisate phytyltransferase activity, whereas olive MPBQ MT belongs to the PLNO2490 superfamily, with MPBQ methyltransferase activity. In addition, Pfam analysis indicated the presence of an UbiA prenyltransferase domain between amino acids 137-396 for OepHPT, and a methyltransferase and an UbiE methyltransferase domain between amino acids 123-215 and 232-262, respectively, in the case of OepMPBQ MT.
Various distinctive conserved motifs were identified in the alignment of the HPT deduced amino acid sequences (Figure 1A). Among them, OepHPT contains prenyl-DP and divalent cation binding motifs typical for polyprenyltransferases (; ). In addition, an Asp-rich motif is also present in the olive HPT sequence, which is involved in substrate binding (). Regarding olive MPBQ MT (Figure 1B), three conserved domains (SAM I, II, and III) were detected in the alignment, which are characteristic of S-adenosylmethionine-dependent methyltransferases (; ). SAM I and II correspond to the binding sites for substrate S-adenosylmethionine, while SAM III corresponds to the binding site of catalytic products.
Regarding the subcellular localization, analysis of the deduced olive HPT and MPBQ MT protein sequences with subcellular localization prediction software such as ProtComp, WoLF PSORT, or TargetP suggests that both proteins could be located in the chloroplast. In addition, an N-terminal transit peptide with the characteristic features of chloroplast targeting peptides was detected by ChloroP software in both sequences (Figure 1), with a predicted cleavage site after Cys at residue 39 and Ser at residue 65 for OepHPT and OepMPBQ MT, respectively. In line with these observations, experimental evidence of chloroplast localization for HPT and MPBQ MT from sweet potato in tobacco leaves has been reported ().
As shown in Supplementary Figure 1, both olive HPT and MPBQ MT proteins are highly hydrophobic based on hydropathy plotting (), indicating that they are membrane proteins. Concerning the membrane topology, transmembrane predictions based on a hidden Markov model (TMHMM) analysis of the olive HPT and MPBQ MT proteins were generated (Supplementary Figure 2). OepHPT showed nine putative transmembrane domains as reported for other plant HPT proteins (), whereas, in the OepMPBQ MT sequence, only one transmembrane domain was found in the C-terminal region at positions 316-335. This transmembrane domain was previously identified in the Arabidopsis MPBQ MT and it has been suggested that the protein is anchored to the inner chloroplast envelope membrane at this position ().
Two unrooted phylogenetic trees based on deduced amino acid sequences of known and characterized plant HPT (Figure 2A) and MPBQ MT (Figure 2B) were generated to investigate the phylogenetic relationship of olive HPT and MPBQ MT, respectively. In agreement with previous findings (; ), plant HPT and MPBQ MT could be classified into two separate monocot and dicot-specific clades, with OepHPT and OepMPBQ MT being positioned, respectively, in the branch accompanied by other HPT and MPBQ MT from dicots plants. It seems that HPT and MPBQ MT evolved differently between dicots and monocots species.
Figure 2
Altogether, sequence analysis of the olive HPT and MPBQ MT displayed the distinguishing characteristics typical of the HPT and MPBQ MT families and along with phylogenetic analysis indicated that they code for homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase enzymes, respectively.
Tissue specificity of olive homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase genes
Olive HPT and MPBQ MT transcript levels were determined in distinct olive organs and tissues from ‘Picual’ and ‘Arbequina’, the two main cultivars for oil production, using qRT-PCR (Figure 3) to investigate their physiological function. Both genes exhibit higher expression levels in green tissues from both cultivars such as young drupes, green mesocarp, and leaves compared to mature mesocarp or young seeds. Analogous observations have been reported in the case of oil palm HPT () and tomato MPBQ MT (). The high transcript levels detected for both genes in green tissues are consistent with the elevated tocopherol content characteristic of photosynthetic organs, given the protective role of tocopherols against photooxidation and photoinactivation (). In addition, all these data indicate a spatial regulation of HPT and MPBQ MT genes in olive considering that they were differentially expressed in all organs and tissues studied.
Figure 3
Developmental expression of homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase genes in the olive fruit in relation to the tocopherol content
Afterward, the expression levels of olive HPT and MPBQ MT genes in the olive fruit were studied in more detail. Specifically, seeds and mesocarp tissue during the development and ripening of olive fruit from the cultivars Picual and Arbequina were analyzed.
Concerning developing seeds (Supplementary Figure 3), gene expression analysis revealed that HPT and MPBQ MT genes exhibited an increase in their transcript levels during the whole period of olive fruit development and ripening in both cultivars, showing maximum values for both genes at 35 and 31 WAF for ‘Picual’ and ‘Arbequina’, respectively. The detected increase of HPT and MPBQ MT transcripts during seed development has been previously observed in other plants, as in the case of the rice and blackberry HPT (; ), and the HPT and MPBQ MT from oat (). However, in the case of olive, this increase in HPT and MPBQ MT expression levels detected in the seed is not in accordance with the slight continuous decrease of tocopherol content observed in oils from Picual and Arbequina cultivars obtained at different stages of development and ripening (), likely because the contribution of the seed to the final composition of the VOO is very minor ().
A similar investigation was performed in the olive mesocarp of Picual and Arbequina cultivars (Figure 4). The observed pattern in HPT and MPBQ MT expression levels during olive mesocarp development and ripening (Figure 4B) is in line with that of the total tocopherol content and the (α+γ)-tocopherol/(β+δ)-tocopherol ratio (Figure 4A), respectively, with a peak at 28 WAF in the case of ‘Picual’, coinciding with the beginning of the ripening period. In the case of the cultivar Koroneiki, a decrease in their expression levels has been described for both genes (). All these data point out that in olive fruit the expression of HPT and MPBQ MT genes seems to be temporally regulated.
Figure 4
Concerning other fruits, a reduction of HPT expression levels has been reported during fruit ripening in apple and the pulp of Citrus species (; ), whereas a significant up-regulation was observed for oil palm HPT at late stages of mesocarp ripening (). On the contrary, MPBQ MT from tomato fruit and the pulp of Citrus species exhibited comparable transcript levels along development and ripening (; ).
Our study was expanded to other olive cultivars characterized by a low (190 and 285 mg/kg oil for ‘Klon-14’ and ‘Abou Kanani’, respectively) or high (820 and 1610 mg/kg oil for ‘Piñonera’ and ‘Dokkar’, respectively) tocopherol content in their oils (), using mesocarp tissue corresponding to four different representative stages of fruit development and ripening (Figure 5). Unlike OeMPBQ MT which shows similar expression levels for each stage of these four cultivars (Figure 5B), the transcript levels of OeHPT were higher in those cultivars with a higher tocopherol content such as ‘Piñonera’ and ‘Dokkar’ (Figure 5A). In contrast, in ‘Klon-14’ and ‘Abou Kanani’, characterized by a low content of tocopherols, their expression levels were lower. These data suggest that HPT, but not MPBQ MT, could be involved in the regulation of the tocopherol biosynthetic pathway in olive mesocarp at the transcriptional level, which is consistent with its role in catalyzing the first committed step of this route. However, the variation in the OeHPT and OeMPBQ MT transcript levels during olive mesocarp development and ripening (Figure 5B) was not parallel to that of the total tocopherol content and the (α+γ)-tocopherol/(β+δ)-tocopherol ratio (Figure 5A), respectively. This fact indicates that not only HPT but also other factors such as the availability of HGA and PDP as precursors regulate the flux of the tocopherol biosynthetic pathway ().
Figure 5
Collectively, these results point out that olive HPT and MPBQ MT participate in the biosynthesis of the tocopherols present in VOO and their gene expression levels are cultivar-dependent, as reported from five Greek cultivars ().
Effect of regulated deficit irrigation on homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase gene expression in the olive fruit mesocarp
It is well described that drought stress increases tocopherol content in the leaves of several plant species, including olive juvenile trees (). The effect of three distinct RDI treatments on the oil accumulation, fatty acid profile, and fatty acid desaturase gene expression levels in ‘Arbequina’ fruit mesocarp has been previously studied by our group (). However, data related to the effect of water stress on the expression levels of olive genes belonging to the tocopherol biosynthetic pathway are lacking. In the present work, higher expression levels of HPT and MPBQ MT genes were found along all the fruit developmental and ripening processes in ‘Arbequina’ mesocarp from olives subjected to 30RDI and 60RDI treatments, which produced substantial levels of water stress, in comparison to FI treatment (Figure 6). This result is in agreement with the increase of tocopherol content reported by in oils obtained from the same olive fruit samples when comparing FI and RDI treatments (255, 327, and 321 mg/kg oil; for FI, 60RDI and 30RDI treatments, respectively). Therefore, the tocopherol biosynthetic pathway appears to be transcriptionally up-regulated in water-stressed olive mesocarp, with OeHPT and OeMPBQ MT genes increasing their expression levels and causing an increment in the tocopherol content in ‘Arbequina’ mesocarp and, consequently, in the corresponding oils. In line with these data, the transcription of genes involved in tocopherol biosynthesis in olives from the Koroneiki cultivar was up-regulated in response to lower rainfall during consecutive seasons ().
Figure 6
An increase in the HPT expression levels has also been detected in leaves from other plants under drought stress, such as Cistus cetricus (), lettuce (), sweet potato (), or barley (). Furthermore, it has been reported that drought-induced expression of HPT from Solanum chilense in tobacco plants results in the accumulation of α-tocopherol and increases tolerance to drought stress by delaying foliar tissue damage (), demonstrating the role of HPT in drought stress resistance. On the contrary, no significant effect on MPBQ MT transcript levels has been described in plants under drought stress to date.
Transcriptional regulation of homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase genes in the olive fruit mesocarp under different environmental stresses
To investigate the effect of several abiotic stresses on the expression levels of the olive HPT and MPBQ MT genes in mesocarp tissue from ‘Picual’ and ‘Arbequina’, olive tree branches holding olive fruit at the turning stage (28 WAF) were incubated for 24 h modifying the standard conditions (25°C with 12 h light/12 h dark cycle) dependent on the effect to be examined. No significant changes in the olive HPT and MPBQ MT transcript levels were observed in the mesocarp tissue when olive fruit were incubated under the above-mentioned standard conditions (Supplementary Figure 4).
It has been shown that tocopherols play a key role in the low-temperature adaptation of plants such as maize () or Arabidopsis (). When olive fruit was incubated at a low temperature (15°C) a significant increment in the expression levels of HPT and MPBQ MT genes in the mesocarp from both cultivars was noticed (Figure 7A). In ‘Picual’, a strong transient increase was observed for the transcript levels of both genes with maximum values after 0.5-1 h and 3-6 h of treatment for HPT and MPBQ MT, respectively. In contrast, in ‘Arbequina’ mesocarp a continuous increase was detected along all the incubation time, being higher in the case of the OeMPBQ MT gene. A similar up-regulation of HPT and MPBQ MT transcript levels has been described in mandarin fruit and grapefruit during long-term cold storage (; ). In the same way, when Chlamydomonas reinhardtii cells were incubated at low temperature, an increase in HPT expression levels was observed (). In addition, HPT has been demonstrated to be essential for cold tolerance and low-temperature adaptation, since Arabidopsis and rice vte2 mutants were hypersensitive to cold stress (; ; ).
Figure 7
Regarding high temperature, when olive fruit from both cultivars were incubated at 35°C the transcript levels of HPT and MPBQ MT showed a severe reduction until undetectable values were reached (Figure 7B). Both genes started to decrease their transcript levels after 6 h of incubation in the case of ‘Picual’, while in ‘Arbequina’ the diminution began sharp and rapidly from the start of the treatment. Interestingly, it has been reported that total tocopherol concentrations in olive fruit at the end of the oil accumulation period were generally higher when the air temperature was increased by 4°C in young trees from Arbequina and Coratina cultivars (). However, these authors suggest that the observed increase in total tocopherols appeared to be related to a reduction in fruit oil concentration with heating. In line with our results, C. reinhardtii cells incubated at high temperature exhibited a slight decrease in HPT expression levels (), and leaves of Cinnamomum camphora under high temperature showed a down-regulation of the MPBQ MT transcript levels ().
Previous studies in plant tissues demonstrated that the tocopherol content is light regulated (). To examine whether darkness affects HPT and MPBQ MT expression levels in olive mesocarp from Picual and Arbequina cultivars, olive branches were incubated at 25°C for 24 h in the darkness. Expression analysis showed a substantial decline of OeHPT and OeMPBQ MT transcript levels in both cultivars mostly during the first 3-6 h of treatment, remaining with small values the rest of the experiment (Figure 8A). In agreement with these results, a down-regulation of the HPT expression levels has also been observed in dark-grown tomato fruit and grapefruit (; ). In addition, reported a fast and strong reduction of HPT transcripts in C. reinhardtii cells transferred to darkness. In the case of MPBQ MT, very low transcript levels were found in the leaves of Arabidopsis plants grown in the dark (). These data indicate that HPT and MPBQ MT are regulated by light.
Figure 8
Finally, the impact of wounding on the HPT and MPBQ MT gene expression levels was investigated for the first time. In particular, this effect was studied in the mesocarp of olive fruit from Picual and Arbequina cultivars subjected to mechanical damage from branches incubated at standard conditions. In both cultivars, OeHPT and OeMPBQ MT transcript levels exhibited a slight transient induction, showing peak values after 1 h of treatment and followed by a decrease, especially marked in the case of MPBQ MT (Figure 8B). Notably, a role for tocopherol biosynthesis in Arabidopsis basal immunity to bacterial infection has been recently proposed (). Specifically, a substantial increase of HPT gene expression levels was detected in Arabidopsis leaf in response to inoculation with Pseudomonas syringae, and an enhanced susceptibility toward P. syringae was observed in Arabidopsis vte2 mutant plants. In contrast, no significant differences in HPT and MPBQ MT transcript levels were found in sweet potato leaves infected with the bacterial pathogen Pectobacterium chrysanthemi compared to the control ().
Conclusion
The isolation and characterization of olive HPT and MPBQ MT genes have been performed. Sequence analysis of both genes shows that they code for HPT and MPBQ MT enzymes, respectively. Tocopherol and expression analysis reveals not only a spatial and temporal regulation of olive HPT and MPBQ MT transcript levels in olive fruit in the course of development and ripening but also indicates that both genes are involved in the biosynthesis of the tocopherols present in VOO. These data also point out that olive HPT and MPBQ MT gene expression is cultivar-dependent and suggest that in olive mesocarp HPT, but not MPBQ MT, could be involved in the regulation of the tocopherol biosynthetic pathway at the transcriptional level. Our results have also shown that the expression of HPT and MPBQ MT genes in olive fruit is regulated by water status, temperature, light, and wounding, suggesting that HPT and MPBQ MT participate in the response to abiotic stresses. This study represents substantial progress in the knowledge of the regulation of tocopherol biosynthesis in olive fruit. In addition, it will help to establish optimum conditions for olive tree cultivation and olive fruit harvesting to obtain VOO with enhanced α-tocopherol content. Furthermore, this information will allow the generation of molecular markers for the marker-assisted selection of new olive cultivars with increased tocopherol content in the VOO.
Statements
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.ncbi.nlm.nih.gov/genbank/, PQ479102 https://www.ncbi.nlm.nih.gov/genbank/, PQ479103.
Author contributions
IN: Formal analysis, Writing – review & editing, Data curation, Investigation, Methodology, Software. LH: Data curation, Formal analysis, Investigation, Methodology, Software, Writing – review & editing, Supervision. MS: Data curation, Formal analysis, Investigation, Methodology, Writing – review & editing. DV-P: Data curation, Writing – review & editing, Supervision. WM: Supervision, Writing – review & editing, Methodology. JM-R: Supervision, Writing – review & editing, Conceptualization, Formal analysis, Funding acquisition, Project administration, Resources, Writing – original draft.
Funding
The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was funded by Consejería de Universidad, Investigación e Innovación, Junta de Andalucía (ProyExcel_00710; Call 2021).
Acknowledgments
The authors thank Dr. Angjelina Belaj from IFAPA Centro Alameda del Obispo (Córdoba, Spain) for the availability of the Worldwide Olive Germplasm Bank to harvest olive fruit samples from different cultivars and Drs. José Enrique Fernández and Antonio Díaz-Espejo from IRNAS-CSIC (Sevilla, Spain) for the availability of the Sanabria olive orchard to harvest olive fruit samples with different irrigation treatments.
Conflict of interest
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.
The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision
Generative AI statement
The author(s) declare that no Generative AI was used in the creation of this manuscript.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2025.1526815/full#supplementary-material
References
1
AbdallahI. B.TliliN.Martinez-ForceE.RubioA. G. P.Perez-CaminoM. C.AlbouchiA.et al. (2015). Content of carotenoids, tocopherols, sterols, triterpenic and aliphatic alcohols, and volatile compounds in six walnuts (Juglans regia L.) varieties. Food Chem.173, 972–978. doi: 10.1016/j.foodchem.2014.10.095
2
AparicioR.HarwoodJ. L. (2013). Handbook of olive oil: analysis and properties (New York, USA: Springer).
3
BaccariS.ElloumiO.Chaari-RkhisA.FenollosaE.MoralesM.DriraN.et al. (2020). Linking leaf water potential, photosynthesis and chlorophyll loss with mechanisms of photo- and antioxidant protection in juvenile olive trees subjected to severe drought. Front. Plant Sci.11. doi: 10.3389/fpls.2020.614144
4
BeltránG.JiménezA.Del RíoC.SánchezS.MartínezL.UcedaM.et al. (2010). Variability of vitamin E in virgin olive oil by agronomical and genetic factors. J. Food Comp. Anal.23, 633–639. doi: 10.1016/j.jfca.2010.03.003
5
Brigelius-FloheR.TraberM. G. (1999). Vitamin E: function and metabolism. FASEB J.13, 1145–1155. doi: 10.1096/fasebj.13.10.1145
6
ChaudharyN.KhuranaP. (2009). Vitamin E biosynthesis genes in rice: Molecular characterization, expression profiling and comparative phylogenetic analysis. Plant Sci.177, 479–491. doi: 10.1016/j.plantsci.2009.07.014
7
ChengZ.SattlerS.MaedaH.SakuragiY.BryantD. A.DellaPennaD. (2003). Highly divergent methyltransferases catalyze a conserved reaction in tocopherol and plastoquinone synthesis in cyanobacteria and photosynthetic eukaryotes. Plant Cell15, 2343–2356. doi: 10.1105/tpc.013656
8
CollakovaE.DellaPennaD. (2001). Isolation and functional analysis of homogentisate phytyltransferase from Synechocystis sp. PCC 6803 and Arabidopsis. Plant Physiol.127, 1113–1124. doi: 10.1104/pp.010421
9
CollakovaE.DellaPennaD. (2003a). Homogentisate phytyltransferase activity is limiting for tocopherol biosynthesis in Arabidopsis. Plant Physiol.131, 632–642. doi: 10.1104/pp.015222
10
CollakovaE.DellaPennaD. (2003b). The role of homogentisate phytyltransferase and other tocopherol pathway enzymes in the regulation of tocopherol synthesis during abiotic stress. Plant Physiol.133, 930–940. doi: 10.1104/pp.103.026138
11
DellaPennaD.LastR. L. (2006). Progress in the dissection and manipulation of plant vitamin E biosynthesis. Physiol. Plant126, 356–368. doi: 10.1111/j.1399-3054.2005.00611.x
12
EspinozaA.San MartinA.Lopez-ClimentM.Ruiz-LaraS.Gomez-CadenasA.CasarettoJ. A. (2013). Engineered drought-induced biosynthesis of α-tocopherol alleviates stress-induced leaf damage in tobacco. J. Plant Physiol.170, 1285–1294. doi: 10.1016/j.jplph.2013.04.004
13
FalkJ.Munné-BoschS. (2010). Tocochromanol functions in plants: antioxidation and beyond. J. Exp. Bot.61, 1549–1566. doi: 10.1093/jxb/erq030
14
FritscheS.WangX.JungC. (2017). Recent advances in our understanding of tocopherol biosynthesis in plants: an overview of key genes, functions, and breeding of vitamin E improved crops. Antioxidants6, 99. doi: 10.3390/antiox6040099
15
GalliF.AzziA.BirringerM.Cook-MillsJ. M.EggersdorferM.FrankJ.et al. (2017). Vitamin E: Emerging aspects and new directions. Free Radic. Biol. Med.102, 16–36. doi: 10.1016/j.freeradbiomed.2016.09.017
16
Gálvez-ValdiviesoG.CardeñosaR.PinedaM.AguilarM. (2015). Homogentisate phytyltransferase from the unicellular green alga. Chlamydomonas reinhardtii. J. Plant Physiol.188, 80–88. doi: 10.1016/j.jplph.2015.09.010
17
GarcíaJ. M.Morales-SilleroA.Pérez-RubioA. G.Diaz-EspejoA.MonteroA.FernándezJ. E. (2017). Virgin olive oil quality of hedgerow ‘Arbequina’ olive trees under deficit irrigation. J. Sci. Food Agric.97, 1018–1026. doi: 10.1002/jsfa.7828
18
GeorgiadouE. C.GoulasV.NtourouT.ManganarisG. A.KalaitzisP.FotopoulosV. (2016). Regulation of on-tree vitamin E biosynthesis in olive fruit during successive growing years: The impact of fruit development and environmental cues. Front. Plant Sci.7. doi: 10.3389/fpls.2016.01656
19
GeorgiadouE. C.KoubourisG.GoulasV.SergentaniC.NikoloudakisN.ManganarisG. A.et al. (2019). Genotype-dependent regulation of vitamin E biosynthesis in olive fruits as revealed through metabolic and transcriptional profiles. Plant Biol.21, 604–614. doi: 10.1111/plb.12950
20
GeorgiadouE. C.NtourouT.GoulasV.ManganarisG. A.KalaitzisP.FotopoulosV. (2015). Temporal analysis reveals a key role for VTE5 in vitamin E biosynthesis in olive fruit during on-tree development. Front. Plant Sci.6. doi: 10.3389/fpls.2015.00871
21
GramegnaG.RosadoD.Sánchez CarranzaA. P.CruzA. B.Simon-MoyaM.LlorenteB.et al. (2019). PHYTOCHROME-INTERACTING FACTOR 3 mediates light-dependent induction of tocopherol biosynthesis during tomato fruit ripening. Plant Cell Environ.42, 1328–1339. doi: 10.1111/pce.13467
22
Gutierrez-GonzalezJ. J.GarvinD. F. (2016). Subgenome-specific assembly of vitamin E biosynthesis genes and expression patterns during seed development provide insight into the evolution of oat genome. Plant Biotechnol. J.14, 2147–2157. doi: 10.1111/pbi.12571
23
HamzeL.MiserereA.MolinaM. S.MaestriD.SearlesP. S.RousseauxM. C. (2022). Influence of environmental growth temperature on tocopherol and sterol oil concentrations in olive fruit. J. Sci. Food Agric.102, 2741–2749. doi: 10.1002/jsfa.11615
24
HaralampidisK.MilioniD.SánchezJ.BaltruschM.HeinzE.HatzopoulosP. (1998). Temporal and transient expression of stearoyl-ACP carrier protein desaturase gene during olive fruit development. J. Exp. Bot.49, 1661–1669. doi: 10.1093/jexbot/49.327.1661
25
HavauxM.EymeryF.PorfirovaS.ReyP.DörmannP. (2005). Vitamin E protects against photoinhibition and photooxidative stress in Arabidopsis thaliana. Plant Cell17, 3451–3469. doi: 10.1105/tpc.105.037036
26
HernándezM. L.ManchaM.Martínez-RivasJ. M. (2005). Molecular cloning and characterization of genes encoding two microsomal oleate desaturases (FAD2) from olive. Phytochemistry66, 1417–1426. doi: 10.1016/j.phytochem.2005.04.004
27
HernándezM. L.PadillaM. N.ManchaM.Martinez-RivasJ. M. (2009). Expression analysis identifies FAD2-2 as the olive oleate desaturase gene mainly responsible for the linoleic acid content in virgin olive oil. J. Agric. Food Chem.57, 6199–62206. doi: 10.1021/jf900678z
28
HernándezM. L.SicardoM. D.AlfonsoM.Martínez-RivasJ. M. (2019). Transcriptional regulation of stearoyl-acyl carrier protein desaturase genes in response to abiotic stresses leads to changes in the unsaturated fatty acids composition of olive mesocarp. Front. Plant Sci.10. doi: 10.3389/fpls.2019.00251
29
HernándezM. L.SicardoM. D.Martínez-RivasJ. M. (2016). Differential contribution of endoplasmic reticulum and chloroplast ω-3 fatty acid desaturase genes to the linolenic acid content of olive (Olea europaea) fruit. Plant Cell Physiol.57, 138–151. doi: 10.1093/pcp/pcv159
30
HernándezM. L.Velázquez-PalmeroD.SicardoM. D.FernándezJ. E.Diaz-EspejoA.Martínez-RivasJ. M. (2018). Effect of a regulated deficit irrigation strategy in a hedgerow ‘Arbequina’ olive orchard on the mesocarp fatty acid composition and desaturase gene expression with respect to olive oil quality. Agric. Water Manage.204, 100–106. doi: 10.1016/j.agwat.2018.04.002
31
HorvathG.WessjohannL.BigirimanaJ.MonicaH.JansenM.GuisezY.et al. (2006). Accumulation of tocopherols and tocotrienols during seed development of grape (Vitis vinifera L. cv. Albert Lavallée). Plant Physiol. Biochem.44, 724–731. doi: 10.1016/j.plaphy.2006.10.010
32
HosomiA.AritaM.SatoY.KiyoseC.UedaT.IgarashiO.et al. (1997). Affinity of α-tocopherol transfer protein as a determinant of the biological activities of vitamin E analogs. FEBS Lett.409, 105–108. doi: 10.1016/s0014-5793(97)00499-7
33
HuangH.LevinE. J.LiuS.BaiY.LocklessS. W.ZhouM. (2014). Structure of a membrane-embedded prenyltransferase homologous to UBIAD1. PloS Biol.12, e1001911. doi: 10.1371/journal.pbio.1001911
34
HussainN.IrshadF.JabeenZ.ShamsiI. H.LiZ.JiangL. (2013). Biosynthesis, structural, and functional attributes of tocopherols in planta; past, present, and future perspectives. J. Agric. Food Chem.61, 6137–6149. doi: 10.1021/jf4010302
35
JiC. Y.KimY.-H.KimH. S.KeQ.KimG.-W.ParkS.-C.et al. (2016). Molecular characterization of tocopherol biosynthetic genes in sweetpotato that respond to stress and activate the tocopherol production in tobacco. Plant Physiol. Biochem.106, 118–128. doi: 10.1016/j.plaphy.2016.04.037
36
JoshiC.ChiangV. (1998). Conserved sequence motifs in plant S-adenosyl-L-methionine-dependent methyltransferases. Plant Mol. Biol.37, 663–674. doi: 10.1023/a:1006035210889
37
KaganR. M.ClarkeS. (1994). Widespread occurrence of three sequence motifs in diverse S adenosylmethionine-dependent methyltransferases suggests a common structure for these enzymes. Arch. Biochem. Biophys.310, 417–427. doi: 10.1006/abbi.1994.1187
38
KarunanandaaB.QiQ.HaoM.BaszisS. R.JensenP. K.WongY. H. H.et al. (2005). Metabolically engineered oilseed crops with enhanced seed tocopherol. Metab. Eng.7, 384–400. doi: 10.1016/j.ymben.2005.05.005
39
KyteJ.DoolittleR. F. (1982). A simple method for displaying the hydropathic character of a protein. J. Mol. Biol.157, 105–132. doi: 10.1016/0022-2836(82)90515-0
40
LassnerM. W.SavidgeB.WeissJ. D.MitskyT. A.Post-BeittenmillerM. A.ValentinH. E. (2001). Nucleic acid sequences to proteins involved in tocopherol synthesis. WO02/33060.
41
LavelliV.BondesanL. (2005). Secoiridoids, tocopherols, and antioxidant activity of monovarietal extra virgin olive oils extracted from destoned fruits. J. Agric. Food Chem.53, 1102–1107. doi: 10.1021/jf048848k
42
LeeK.LeeS. M.ParkS.-R.JungJ.MoonJ.-K.CheongJ.-J.et al. (2007). Overexpression of Arabidopsis homogentisate phytyltransferase or tocopherol cyclase elevates vitamin E content by increasing γ-tocopherol level in lettuce (Lactuca sativa L.). Mol. Cells24, 301–306. doi: 10.1016/S1016-8478(23)07343-0
43
LeipnerJ.FracheboudY.StampP. (1999). Effect of growing season on the photosynthetic apparatus and leaf antioxidative defenses in two maize genotypes of different chilling tolerance. Environ. Exp. Bot.42, 129–139. doi: 10.1016/s0098-8472(99)00026-x
44
LiG. X.LeeM. J.LiuA. B.YangZ.LinY.ShihW. J.et al. (2011). δ-tocopherol is more active than α-or γ-tocopherol in inhibiting lung tumorigenesis in vivo. Cancer Prev. Res.4, 404–413. doi: 10.1158/1940-6207.CAPR-10-0130
45
LiY.ZhouY.WangZ.SunX.TangK. (2010). Engineering tocopherol biosynthetic pathway in Arabidopsis leaves and its effect on antioxidant metabolism. Plant Sci.178, 312–320. doi: 10.1016/j.plantsci.2010.01.004
46
LichtenthalerH. K. (2007). Biosynthesis, accumulation and emission of carotenoids, α-tocopherol, plastoquinone, and isoprene in leaves under high photosynthetic irradiance. Photosynth. Res.92, 163–179. doi: 10.1007/s11120-007-9204-y
47
LingK. S.AbdullahS. N. A.LingH. C.AmiruddinM. D. (2016). Molecular cloning, gene expression profiling and in silico sequence analysis of vitamin E biosynthetic genes from the oil palm. Plant Gene5, 100–108. doi: 10.1016/j.plgene.2016.01.003
48
LivakK. J.SchmittgenT. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods25, 402–408. doi: 10.1006/meth.2001.1262
49
LopezJ. C.RyanS.BlankenshipR. E. (1996). Sequence of the bchG gene from Chloroflexus aurantiacus: relationship between chlorophyll synthase and other polyprenyltransferases. J. Bacteriol.178, 3369–3373. doi: 10.1128/jb.178.11.3369-3373.1996
50
LuY.RijzaaniH.KarcherD.RufS.BockR. (2013). Efficient metabolic pathway engineering in transgenic tobacco and tomato plastids with synthetic multigene operons. Proc. Natl. Acad. Sci. U.S.A.110, E623–E632. doi: 10.1073/pnas.1216898110
51
LushchakV. I.SemchukN. M. (2012). Tocopherol biosynthesis: chemistry, regulation and effects of environmental factors. Acta Physiol. Plant34, 1607–1628. doi: 10.1007/s11738-012-0988-9
52
MaJ.QiuD.PangY.GaoH.WangX.QinY. (2020). Diverse roles of tocopherols in response to abiotic and biotic stresses and strategies for genetic biofortification in plants. Mol. Breed.40, 18. doi: 10.1007/s11032-019-1097-x
53
MaedaH.SageT. L.IsaacG.WeltiR.DellaPennaD. (2008). Tocopherols modulate extraplastidic polyunsaturated fatty acid metabolism in Arabidopsis at low temperature. Plant Cell20, 452–470. doi: 10.1105/tpc.107.054718
54
MaedaH.SongW.SageT. L.DellaPennaD. (2006). Tocopherols play a crucial role in low-temperature adaptation and phloem loading in Arabidopsis. Plant Cell18, 2710–2732. doi: 10.1105/tpc.105.039404
55
Mène-SaffranéL. (2018). Vitamin E biosynthesis and its regulation in plants. Antioxidants7, 2. doi: 10.3390/antiox7010002
56
Mène-SaffranéL.PellaudS. (2017). Current strategies for vitamin E biofortification of crops. Curr. Opin. Biotechnol.44, 189–197. doi: 10.1016/j.copbio.2017.01.007
57
MesaT.Munné-BoschS. (2023). α-Tocopherol in chloroplasts: Nothing more than an antioxidant? Curr. Opin. Plant Biol.74, 102400. doi: 10.1016/j.pbi.2023.102400
58
MotohashiR.ItoT.KobayashiM.TajiT.NagataN.AsamiT.et al. (2003). Functional analysis of the 37 kDa inner envelope membrane polypeptide in chloroplast biogenesis using a Ds-tagged Arabidopsis pale-green mutant. Plant J.34, 719–731. doi: 10.1046/j.1365-313x.2003.01763.x
59
MousaviS.StanzioneV.MariottiR.MastioV.AzariadisA.PasseriV.et al. (2022). Bioactive compound profiling of olive fruit: The contribution of genotype. Antioxidants11, 672. doi: 10.3390/antiox11040672
60
Munné-BoschS.AlegreL. (2002). The function of tocopherols and tocotrienols in plants. Crit. Rev. Plant Sci.21, 31–57. doi: 10.1080/0735-260291044179
61
Munné-BoschS.FalaraV.PaterakiI.Lopez-CarbonellM.CelaJ.KanellisA. K. (2009). Physiological and molecular responses of the isoprenoid biosynthetic pathway in a drought-resistant Mediterranean shrub, Cistus creticus exposed to water deficit. J. Plant Physiol.166, 136–145. doi: 10.1016/j.jplph.2008.02.011
62
MuñozP.Munné-BoschS. (2019). Vitamin E in plants: Biosynthesis, transport, and function. Trends Plant Sci.24, 1040–1051. doi: 10.1016/j.tplants.2019.08.006
63
Muñoz-MéridaA.González-PlazaJ. J.CañadaA.BlancoA. M.García-LópezM. C.RodríguezJ. M.et al. (2013). De novo assembly and functional annotation of the olive (Olea europaea) transcriptome. DNA Res.20, 93–108. doi: 10.1093/dnares/dss036
64
NiuY.ZhangQ.WangJ.LiY.WangX.BaoY. (2022). Vitamin E synthesis and response in plants. Front. Plant Sci.13. doi: 10.3389/fpls.2022.994058
65
Oliveras-LópezM. J.Quesada GranadosJ. J.Martín BermudoF.López-García-de-la-SerranaH.López MartínezM. C. (2008). Influence of milling conditions on the α-tocopherol content of Picual olive oil. Eur. J. Lipid Sci. Technol.110, 530–553. doi: 10.1002/ejlt.200700192
66
PellaudS.Mène-SaffranéL. (2017). Metabolic origins and transport of vitamin E biosynthetic precursors. Front. Plant Sci.8. doi: 10.3389/fpls.2017.01959
67
PérezA. G.LeónL.PascualM.de la RosaR.BelajA.SanzC. (2019). Analysis of olive (Olea europaea L.) genetic resources in relation to the content of vitamin E in virgin olive oil. Antioxidants8, 242. doi: 10.3390/antiox8080242
68
QuadranaL.AlmeidaJ.AsisR.DuffyT.DominguezP. G.BermudezL.et al. (2014). Natural occurring epialleles determine vitamin E accumulation in tomato fruits. Nat. Commun.5, 3027. doi: 10.1038/ncomms5027
69
QureshiA. A.SamiS. A.SalserW. A.KhanF. A. (2002). Dose-dependent suppression of serum cholesterol by tocotrienol-rich fraction (TRF25) of rice bran in hypercholesterolemic humans. Atherosclerosis161, 199–207. doi: 10.1016/s0021-9150(01)00619-0
70
RenW.ZhaoL.ZhangL.WangY.CuiL.TangY.et al. (2011). Molecular analysis of a homogentisate phytyltransferase gene from Lactuca sativa L. Mol. Biol. Rep.38, 1813–1819. doi: 10.1007/s11033-010-0297-6
71
ReyF.RodrigoM. J.DirettoG.ZacaríasL. (2021c). Effect of fruit shading and cold storage on tocopherol biosynthesis and its involvement in the susceptibility of Star Ruby grapefruit to chilling injury. Food Chem.: Mol. Sci.3, 100037. doi: 10.1016/j.fochms.2021.100037
72
ReyF.RodrigoM. J.ZacaríasL. (2021a). Accumulation of tocopherols and transcriptional regulation of their biosynthesis during cold storage of mandarin fruit. Postharvest Biol. Technol.180, 111594. doi: 10.1016/j.postharvbio.2021.111594
73
ReyF.ZacaríasL.RodrigoM. J. (2021b). Regulation of tocopherol biosynthesis during fruit maturation of different Citrus species. Front. Plant Sci.12, 743993, doi: 10.3389/fpls.2021.743993
74
SattlerS. E.GillilandL. U.Magallanes-LundbackM.PollardM.DellaPennaD. (2004). Vitamin E is essential for seed longevity and for preventing lipid peroxidation during germination. Plant Cell16, 1419–1432. doi: 10.1105/tpc.021360
75
SavidgeB.WeissJ. D.WongY.-H. H.LassnerM. W.MitkyT. A.ShewmakerC. K.et al. (2002). Isolation and characterization of homogentisate phytyltransferase genes from Synechocystis sp. PCC 6803 and Arabidopsis. Plant Physiol.129, 321–332. doi: 10.1104/pp.010747
76
SchledzM.SeidlerA.BeyerP.NeuhausG. (2001). A novel phytyltransferase from Synechocystis sp. PCC 6803 involved in tocopherol biosynthesis. FEBS Lett.499, 15–20. doi: 10.1016/S0014-5793(01)02508-X
77
SchuyC.GrothJ.AmmonA.EydamJ.BaierS.SchweizerG.et al. (2019). Deciphering the genetic basis for vitamin E accumulation in leaves and grains of different barley accessions. Sci. Rep.9, 9470. doi: 10.1038/s41598-019-45572-7
78
SeoY. S.KimS. Y.HarnC. H.KimW. T. (2011). Ectopic expression of apple fruit homogentisate phytyltransferase gene (MdHPT1) increases tocopherol in transgenic tomato (Solanum lycopersicum cv. Micro-Tom) leaves and fruits. Phytochemistry72, 321–329. doi: 10.1016/j.phytochem.2010.12.013
79
ShintaniD. K.ChengZ.DellaPennaD. (2002). The role of 2-methyl-6-phytylbenzoquinone methyltransferase in determining tocopherol composition in Synechocystis sp. PCC6803. FEBS Lett.511, 1–5. doi: 10.1016/s0014-5793(01)03223-9
80
StahlE.HartmannM.ScholtenN.ZeierJ. (2019). A role for tocopherol biosynthesis in Arabidopsis basal immunity to bacterial infection. Plant Physiol.181, 1008–1028. doi: 10.1104/pp.19.00618
81
UnverT.WuZ.SterckL.TurktasM.LohausR.LiZ.et al. (2017). Genome of wild olive and the evolution of oil biosynthesis. Proc. Natl. Acad. Sci. U.S.A.114, 9413–9422. doi: 10.1073/pnas.1708621114
82
Van EenennaamA. L.LincolnK.DurrettT. P.ValentinH. E.ShewmakerC. K.ThorneG. M.et al. (2003). Engineering vitamin E content: From Arabidopsis mutant to soy oil. Plant Cell15, 3007–3019. doi: 10.1105/tpc.015875
83
VelascoL.Fernández-MartínezJ.Garcia-RuizR.DomínguezJ. (2002). Genetic and environmental variation for tocopherol content and composition in sunflower commercial hybrids. J. Agric. Sci.139, 425–429. doi: 10.1017/S0021859602002678
84
WangY.QianQ.XuH.ZuoZ. (2023). Dynamic physiological responses of Cinnamomum camphora with monoterpene protection under high temperature shock. Forests14, 2005. doi: 10.3390/f14102005
85
WangX.SongY.LiJ. (2013). High expression of tocochromanol biosynthesis genes increases the vitamin E level in a new line of giant embryo rice. J. Agric. Food Chem.61, 5860–5869. doi: 10.1021/jf401325e
86
WangD.WangY.LongW.NiuM.ZhaoZ.TengX.et al. (2017). SGD1, a key enzyme in tocopherol biosynthesis, is essential for plant development and cold tolerance in rice. Plant Sci.260, 90–100. doi: 10.1016/j.plantsci.2017.04.008
87
WunnakupT.VimolmangkangS.De-EknamkulW. (2018). Transient expression of the homogentisate phytyltransferase gene from Clitoria ternatea causes metabolic enhancement of α-tocopherol biosynthesis and chlorophyll degradation in tomato leaves. J. Plant Biochem. Biotechnol.27, 55–67. doi: 10.1007/s13562-017-0415-9
88
YangH. Y.DongS. S.ZhangC. H.WuW. L.LyuL. F.LiW. L. (2020). Investigation of tocopherol biosynthesis in blackberry seeds (Rubus spp.). Russ. J. Plant Physiol.67, 76–84. doi: 10.1134/S1021443720010252
89
ZhangY.LiuK.ZhuX.WuY.ZhangS.ChenH.et al. (2018). Rice tocopherol deficiency 1 encodes a homogentisate phytyltransferase essential for tocopherol biosynthesis and plant development in rice. Plant Cell Rep.37, 775–787. doi: 10.1007/s00299-018-2266-9
Summary
Keywords
Olea europaea, olive, vitamin E, HPT, MPBQ MT, gene expression, abiotic stresses
Citation
Narváez I, Hernández ML, Sicardo MD, Velázquez-Palmero D, Moreda W and Martínez-Rivas JM (2025) Molecular characterization of homogentisate phytyltransferase and methylphytylbenzoquinol methyltransferase genes from olive fruit with regard to the tocopherol content and the response to abiotic stresses. Front. Plant Sci. 16:1526815. doi: 10.3389/fpls.2025.1526815
Received
12 November 2024
Accepted
10 February 2025
Published
03 March 2025
Volume
16 - 2025
Edited by
Giampiero Cai, University of Siena, Italy
Reviewed by
Angela Rubio Moraga, University of Castilla-La Mancha, Spain
Chunsheng Hou, Chinese Academy of Agricultural Sciences, China
Maria Celeste Pereira Dias, University of Coimbra, Portugal
Updates
Copyright
© 2025 Narváez, Hernández, Sicardo, Velázquez-Palmero, Moreda and Martínez-Rivas.
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) and the copyright owner(s) 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: José M. Martínez-Rivas, mrivas@ig.csic.es
†Present addresses: Isabel Narváez, Instituto de Hortofruticultura Subtropical y Mediterránea, Universidad de Málaga (IHSM-UMA-CSIC), Málaga, Spain M. Luisa Hernández, Departamento de Bioquímica Vegetal y Biología Molecular/Instituto de Bioquímica Vegetal y Fotosíntesis, Universidad de Sevilla-Consejo Superior de Investigaciones Científicas (CSIC), Seville, Spain
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