Long-Chain Polyisoprenoids Are Synthesized by AtCPT1 in Arabidopsis thaliana

Abstract

Arabidopsis roots accumulate a complex mixture of dolichols composed of three families, (i.e., short-, medium- and long-chain dolichols), but until now none of the cis-prenyltransferases (CPTs) predicted in the Arabidopsis genome has been considered responsible for their synthesis. In this report, using homo- and heterologous (yeast and tobacco) models, we have characterized the AtCPT1 gene (At2g23410) which encodes a CPT responsible for the formation of long-chain dolichols, Dol-18 to -23, with Dol-21 dominating, in Arabidopsis. The content of these dolichols was significantly reduced in AtCPT1 T-DNA insertion mutant lines and highly increased in AtCPT1-overexpressing plants. Similar to the majority of eukaryotic CPTs, AtCPT1 is localized to the endoplasmic reticulum (ER). Functional complementation tests using yeast rer2Δ or srt1Δ mutants devoid of medium- or long-chain dolichols, respectively, confirmed that this enzyme synthesizes long-chain dolichols, although the dolichol chains thus formed are somewhat shorter than those synthesized in planta. Moreover, AtCPT1 acts as a homomeric CPT and does not need LEW1 for its activity. AtCPT1 is the first plant CPT producing long-chain polyisoprenoids that does not form a complex with the NgBR/NUS1 homologue.

1. Introduction

Lipids, beside nucleic acids and proteins are vital constituents of all living cells. They have many biological functions in cells as integral components of biological membranes, regulators of metabolic processes or signaling molecules. Many of them are essential for plant survival. Hydrophilic isoprenoids and their derivatives play important role in photosynthesis (plastoquinone, chlorophylls), respiration (ubiquinone), hormonal regulation of metabolism and membrane stabilization (sterols), regulation of growth and development (giberellic acid, abscisic acid, brassinosteroids) and defense against oxidative stress (tocopherol, carotenoids, ubiquinol, plastoquinol). Among these are polyisoprenoids playing a crucial role in posttranslational protein modifications as indispensable saccharide carriers in the biosynthesis of glycosyl-phosphoinositol (GPI) anchor, and protein N-, O- and C-glycosylation [1,2,3] as well as donors of isoprenoid groups in protein prenylation [4]. Moreover, they are involved in cell adaptation to adverse environmental conditions [5], possibly via modulation of the properties of biological membranes—by increasing their permeability and fluidity [6]. Plant polyprenols accumulated in chloroplasts determine the fluidity of thylakoid membranes that affect photosynthetic efficiency [7]. Despite the fact that they were identified already in the 1960s, and regardless of extensive studies, relatively little is still known about the regulation of polyisoprenoid synthesis.

Polyisoprenoid alcohols have been found in the cells of all living organisms from bacteria to human. These linear polymers, built from five to more than 100 isoprene units, are divided into two subgroups of compounds with either a hydrogenated (dolichols) or an unsaturated (polyprenols) double bond in the α-unit (Figure 1). Dolichols are mainly present in animal cells, yeasts and plant roots whereas polyprenols in bacteria and plant photosynthetic tissues. In eukaryotic cells polyisoprenoids frequently occur as a mixture of homologues named ‘family’ with one dominant component. Several plant species accumulate more complex mixtures containing two or three ‘families’.

The biosynthesis of the polyisoprenoid skeleton in plants is a complex process and occurs in three steps. At first, the five carbon molecules of IPP (isopentenyl diphosphate) and DMAPP (its allylic isomer dimethylallyl diphosphate) are synthesized via the cytoplasmic mevalonic acid (MVA) and the plastidial 2-methyl-d-erythritol-4-phosphate (MEP) pathways. Next, cis-prenyltransferases (CPTs) catalyze the formation of a linear polymer, usually 70–130 carbons in length, by sequential condensations of IPP to short-chain oligoprenyl precursors, most often farnesyl diphosphate (FPP) or geranylgeranyl diphosphate (GGPP) [6]. Eukaryotic CPTs form a broad range of products of variable chain-length, both short and long-chain [8]. In all cells CPTs produce prenyl diphosphate that in some tissues finally is converted to dolichol due to the activity of polyprenol reductase [9,10].

The prenyl diphosphate biosynthetic pathway in eukaryotic cells requires the interaction of CPT with an accessory CPT-binding protein for determination of polyprenol chain length and examples of such complexes are human (hCIT/NgBR) [11], yeast (Rer2/Srt1/NUS1) [12] and some plants, including tomato (SlCPT3/SlCPTBP) [13], lettuce (CPT3/CPTL2) [14], Arabidopsis (CPT3/LEW1) [15], ginseng (CPT1/PgCPLT2) [16] and guayule (PaCPT1-3/PaCBP) [17].

Plant cells usually express a family of genes encoding potential CPTs while the capacity to synthesize polyisoprenoid chains is confirmed for only some of them. Thus seven genes encoding CPT are identified in tomato (SlCPT1–SlCPT7) [8], two in Hevea brasiliensis (HRT1 and HRT2) [18], three in Taraxacum koksaghyz (TkCPT1–TkCPT3) [19] and one (LAA66) in Lilium longiflorum [20]. The Arabidopsis genome contains nine putative cis-prenyltransferase encoding genes (AtCPT1 to AtCPT9) that are expressed in tissue-specific manner. Three of them, AtCPT1, -6 and -9 are exclusively expressed in roots [21]. Simultaneously several dolichols are identified in this tissue (hairy roots): a single dolichol Dol-7 and three families of dolichols, with Dol-13, Dol-16 and Dol-21/23 dominating [22]. So far, only one root CPT, AtCPT6 involved in Dol-7 biosynthesis has been characterized in planta [23,24]. The enzymes responsible for the biosynthesis of the remaining dolichols in Arabidopsis thaliana roots have not yet been described. AtCPT1 (At2g23410) has been identified [25,26] but its location and function in the plant cell remains unknown. In contrast to roots the profile of polyisoprenoids is much simpler in the leaves; only one family of polyprenols (Pren-10 dominating) together with the expression of AtCPT7 is detected [7].

In the present study, an activity of AtCPT1 (At2g23410) was analyzed in hetero- and homologous systems. Both, transient expression in Nicotiana benthamiana leaves and stable overexpression in Arabidopsis thaliana revealed that AtCPT1 is localized to the endoplasmic reticulum (ER) and catalyzes the synthesis of a family of long-chain dolichols ranging from 19 to 24 i.u., with Dol-21/23 dominating. Moreover, comparing to wild type plants the content of these dolichols was highly increased in the roots upon AtCPT1 overexpression and significantly lowered for AtCPT1 T-DNA insertion mutants. Furthermore, upon expression in yeast cells, this plant CPT was involved in the synthesis of a family of polyisoprenoids with chains somewhat shorter than those synthesized in planta (i.e., a mixture of dolichols composed of 16 to 20 i.u.), with Dol-17/18 dominating. Taken together, data presented here document that AtCPT1 catalyzes the formation of long-chain polyisoprenoid products in plant roots.

2. Results and Discussion

2.1. AtCPT1 Synthesizes the Family of Long-Chain Dolichols in Planta

To characterize the role of AtCPT1 in dolichol biosynthesis in Arabidopsis roots, we obtained three transferred DNA (T-DNA) inserted AtCPT1 mutants: cpt1-1 (SALK_038151+/−), cpt1-2 (SALK_032276+/−, previously described as a T-DNA insertion mutant of At1G11755 (LEW1) gene [27]) and cpt1-3 (SALK_100795−/−) and AtCPT1 overexpressing line CPT1-OE in the Columbia (Col-0) background. We confirmed that all of the above mutant lines contained the T-DNA insertion sites in At2G23410 gene by PCR with T-DNA-specific and flanking primers and by sequencing PCR products. cpt1-1 line carried a T-DNA insertion in the promoter, cpt1-2—in the second exon and cpt1-3—in the 3′UTR region (Figure 2A). It appeared impossible to obtain homozygous T-DNA insertion plants of cpt1-1 and cpt1-2 mutant lines which might suggest that complete disruption of AtCPT1 is lethal.

Quantitative Real Time PCR analysis of AtCPT1 expression in the roots of mutant lines indicated that AtCPT1 transcripts were significantly reduced, by approximately 80–95%, in all insertion lines and significantly (100-fold) elevated in the CPT1-OE line relative to wild type levels (Figure 2B). AtCPT1 deficiency or overexpression did not affect the expression of the remaining AtCPT genes expressed in roots (Figure S1A). Residual AtCPT1 expression was also noted in the leaves of the wild type (WT) plants while for the leaves of the transgenic CPT1-OE plants it was increased 800-fold relative to the WT control (Figure S2A).

Analysis of the content of total polyisoprenoids confirmed that roots of WT plants accumulated a three family mixture of dolichols: short-chain dolichols (Dol-13 dominant), medium-chain dolichols (Dol-16) and long-chain ones (Dol-21) accompanied by respective polyprenols (Figure 2C). The content of long-chain polyisoprenoid family with Pren/Dol-21 dominating was significantly decreased in all of the T-DNA mutant lines (cpt1-1, cpt1-2 and cpt1-3) to 30%, 42 and 52% of the WT level, respectively, while it was significantly increased (8-fold) in CPT1-OE plants (Figure 2C,D). AtCPT1 deficiency or overexpression did not affect the content of the remaining dolichols in Arabidopsis roots (Figure S1B). In line with an increased transcript level, a large amount of long-chain dolichols was also detected in leaves of AtCPT1-OE plants (Figure S2A) while those of wild type plants did not accumulate products of such length (Figure S2B). It is worth noting that the dominating homologue in this case was Dol-23.

Likewise, a qualitative analysis of polyisoprenoids extracted from Nicotiana benthamiana leaves transiently expressing AtCPT1 revealed the presence of an additional dolichol family ranging from 19 to 24 i.u., with Dol-23 dominating, in comparison to mock leaves (Figure S2C).

This discrepancy in dominating homologue between long-chain dolichols accumulated in roots and leaves upon AtCPT1 expression might result from divergent mechanisms responsible for regulation of AtCPT1 activity/specificity on these tissues, moreover it might be due to differences in the availability of a precursor. In line with this, we previously observed that in Arabidopsis hairy root cultures obtained from callus the profile of long-chain polyprenols and dolichols was variable and dependent on the sugar type and its concentration in the growth medium [22]. Also in S. cerevisiae cells upon starvation (glucose vs. ethanol) the shift of dominating long-chain dolichol from Dol-21 to Dol-23 was observed [28].

Taken together, these results clearly indicate that AtCPT1 is responsible for the synthesis of long-chain polyisoprenoids in plants similarly to Srt1 in yeast [29,30]. Alike Srt1 [28] polyprenol products of AtCPT1 are not efficiently reduced to dolichols.

2.2. Shortage of Long-Chain Dolichols Leads to the Growth Defects

The role of long-chain dolichols in plants is still unknown. In Arabidopsis hairy roots their profile is modulated by the sugar type and availability [22]. In Saccharomyces cerevisiae long-chain dolichols synthesized by Srt1 are involved in spore wall formation [31].

All three cpt1 mutants analyzed by us exhibited growth defects. Comparing to the wild type and CPT1-OE, the cpt1 mutants seedlings showed extremely stunted growth and shorter root length (Figure 3). In tomato the reduced expression of SlCPT3, responsible for medium-chain dolichol biosynthesis, led to a pleiotropic phenotype, which included mottled, wilted leaves and stunted growth [13]. In contrast, none of the so far characterized Arabidopsis CPT loss-of-function mutants, AtCPT6 [24] or AtCPT7 [7] (synthesizing Dol-7 or Pren-9 to -11, respectively) showed any phenotypic aberrations. Similarly, the yeast srt1∆ mutant has no clear morphological phenotype, although it lacks the outer spore wall layer due to a defect in chitin synthesis [31]. Observed disturbances in the growth of cpt1 mutants require explanation and will be addressed in future work.

2.3. AtCPT1 Is Localized to the ER

The eukaryotic cis-prenyltransferases implicated in dolichol biosynthesis are mainly located in the endoplasmic reticulum (ER) with the exception of yeast Srt1 producing long-chain dolichols that is localized to lipid bodies [30,31]. Membrane topology analysis (TMHMM server) predicted one transmembrane domain in the AtCPT1 amino acid sequence suggesting that this CPT can be an integral organellar membrane protein. Moreover, computational tools to predict subcellular location of proteins (e.g., BaCelLo, TargetP) indicated AtCPT1 localization in the ER/Golgi network. To determine the subcellular localization of AtCPT1, AtCPT1:G3GFP construct, encoding a C-terminal fusion with fluorescent protein was transiently co-expressed with plant organelle markers (mCherry or CFP fusions) in Nicotiana benthamiana leaves. Confocal laser microscopy clearly showed that GFP signal fully overlapped with that of CFP fluorescence of the ER marker (Figure 4A). The same fluorescence pattern was observed in the parallel experiment when the ER-mCherry marker was used (Figure 4B). On the contrary, no overlap of AtCPT1-GFP and Golgi-mCherry marker was noted (Figure 4C).

Despite the fact that AtCPT1 synthesizes dolichols of similar length to yeast Srt1, its subcellular location is different from the yeast CPT.

2.4. AtCPT1 Complements the Function of Yeast Rer2 cis-Prenyltransferase

To confirm whether AtCPT1 can fulfill its function in yeast, the full length AtCPT1 cDNA was introduced into the thermosensitive rer2Δ yeast strain devoid of one of the two yeast CPTs, Rer2 and its ability to suppress the growth and protein N-glycosylation defects was studied. Transformation with AtCPT1 suppressed the growth defects of the rer2Δ mutant at 37 °C while the empty vector did not restore growth at the non-permissive temperature. Wild type yeast exhibited normal growth in these unfavorable conditions (Figure 5A). This result is in agreement with observations described previously [25].

To verify that the rescue of rer2Δ growth by AtCPT1 was due to the complementation of the defect in CPT activity, the effect of AtCPT1 expression on the glycosylation status of lysosomal protein carboxypeptidase Y (CPY) was examined. WT yeast cells contain only a mature fully glycosylated form of CPY with four N-glycan chains in contrast to rer2Δ mutant where both the mature and hypoglycosylated CPY variants are present (Figure 5B). Expression of AtCPT1 fully restored normal N-glycosylation of CPY. In conclusion, experiments performed using rer2Δ mutant clearly show that AtCPT1 can functionally replace the yeast CPT Rer2.

Finally, to confirm the role of AtCPT1 in long-chain dolichol biosynthesis we analyzed the polyisoprenoid profile of yeast strains, rer2Δ and srt1Δ devoid of one of the two yeast CPTs, Rer2 or Srt1, respectively expressing AtCPT1. HPLC/UV analysis revealed that both rer2Δ/AtCPT1 and srt1Δ/AtCPT1 yeast transformants accumulated an additional family of dolichols composed of 15 up to 20 i.u., with Dol-17/18 dominating (Figure 5C). This result shows that upon expression in yeast cells, AtCPT1 is able to synthesize a family of polyisoprenoids although their chains are shorter than those synthesized in planta. This observation is consistent with the result observed previously upon in vitro assay where a membrane fraction prepared from yeast transformed with AtCPT1 (called DPS) was used as a source of enzyme. In these experimental conditions, a mixture of dolichols ranging in chain length from C75 to C95 was formed [25]. Moreover, similar lipid products were obtained in vitro when recombinant AtCPT1 (ACPT) protein purified from E. coli was used [26]. This interesting discrepancy requires explanation and suggests that long-chain dolichol biosynthetic machinery in Arabidopsis is complex and possibly other plant regulatory protein(s) is necessary to modulate elongation of polyisoprenoid chains. One such candidate is Arabidopsis LEW1, a homolog of human NgBR and yeast Nus1. Nus1 is compatible with heterologous CPT to form an enzymatically active complex (e.g., Rer2 of S. pombe and human CIT), but the dominant polyisoprenoid products synthesized by the hybrid enzymes are different than those produced by the wild type enzyme complex [12].

To explain whether AtCPT1 requires activity of CPT-binding protein for formation of long-chain dolichols we co-expressed the plant NgBR/NUS1 homologue: LEW1 and AtCPT1 in rer2Δ mutant cells. HPLC/UV analysis revealed that both yeast transformants expressing either LEW1/AtCPT1 or an individual AtCPT1 accumulated the same family of dolichols with dominating Dol-17/18 while no such products were observed upon expression of LEW1 or transformation with an empty vector (Figure 5C). This might suggest that LEW1 does not serve as a regulatory protein for AtCPT1 and is consistent with the concept that CPTs with an RXG motif do not need a NgBR/NUS1 homologue protein for their activity [32]. Experimental data and in silico analysis (Figure 6) revealed that AtCPT1, similarly to AtCPT6 and -7 [7,24], was classified into a group of homomeric CPT in contrast to heteromeric CPTs (e.g., AtCPT3) which require the interaction with LEW1 for polyisoprenoid chain biosynthesis [15]. Bacteria possess homomeric while animals and yeast possess heteromeric CPTs; interestingly both types of CPTs are found in plants.

In summary, the results of experiments presented above clearly identify AtCPT1 as an enzyme responsible for biosynthesis of long-chain dolichols in Arabidopsis. The mechanism of regulation of AtCPT1 activity in plant and yeast cells remains elusive and requires clarification. One might speculate that NgBR/NUS1-independent machinery might be needed to modulate the activity of AtCPT1 and affect the length of the synthesized polyprenol chain. This intriguing question will be a subject of future studies.

3. Materials and Methods

3.1. Chemicals

All polyprenol and dolichol standards were from the Collection of Polyprenols of the Institute of Biochemistry and Biophysics (Warsaw, Poland). Components of growth media were purchased from BioShop (Burlington, ON, Canada). Chromatographic materials and HPLC solvents were from Merck (Darmstadt, Germany). All other chemicals were of practical grade (p.a.) quality and were purchased from Sigma-Aldrich Chemie GmbH (Poznan, Poland).

3.2. Plant Materials and Growth Conditions

Arabidopsis thaliana ecotype Columbia 0 (Col-0) and At2g23410 insertion mutants cpt1-1 (SALK_038151), cpt1-2 (SALK_032276) and cpt1-3 (SALK_100795) were obtained from the Nottingham Arabidopsis Stock Center (Loughborough, UK).

Plants for genotyping were grown in potting soil in a greenhouse under a long-day (16 h light) photoperiod at 21/18 °C. Genotyping was performed with specific primers designed with the aid of T-primer design tool and LBb1.3 primer (Table S1).

Plants for RNA isolation, RT-PCR and polyisoprenoid extraction were grown hydroponically in long day photoperiod (16 h day, 8 h night; 21 or 18 °C, respectively). The culture medium (Gibeaut’s solution) was prepared according to the literature [33].

Plants for root elongation measurements were sown on ½ Murashige and Skoog (MS) basal salt mixture medium (pH 5.7) supplemented with vitamin and solidified with 0.8% agar (w/v). Before sowing seeds were surface-sterilized in 20% (w/v) chlorine bleach and then washed with 70% (w/v) ethanol and sterile distilled water. After sowing seeds were allowed to imbibe in the dark at 4 °C for 2 days and were then grown on vertically oriented plates at 21/18 °C with a 16 h/8 h light/dark photoperiod.

Nicotiana benthamiana were cultivated in potting soil in a greenhouse under a long-day photoperiod.

3.3. Yeast Materials

Saccharomyces cerevisiae strains used in this study:

• SS328 (wild type, MATα ade2-101 ura3-52his3Δ 200lys2-801) and
• YG932 (rer2Δ mutant, MATα rer2Δ::kanMX4 ade2-101 ura3-52his3Δ 200 lys-801) were kind gifts of Dr. C.J. Waechter (University of Kentucky College of Medicine, Lexington, KY, USA).
• YG938 (srt1Δ mutant, MATα Δ srt1::kanMX4 ade2-101 ura3-52 his3Δ200 lys2-801) was obtained from Dr. M. Aebi, (ETH, Zurich, Switzerland).

3.4. Preparation of AtCPT1 and LEW1 Expression Constructs

Total RNA was isolated from Arabidopsis Col-0 roots and purified using the RNeasy Plant Mini Kit (Qiagen, Hilden, Germany), transcribed to cDNA using SuperScript^® First-Strand Synthesis System (Invitrogen, Carlsbad, CA, USA), and AtCPT1 and LEW1 CDSs were amplified by PCR using specific primers (Table S1).

The purified PCR product of AtCPT1 was subcloned into the pENTR vector according to the manufacturer’s instructions (pENTR D-TOPO; Invitrogen). The AtCPT1 CDS was recombined from the pENTR vector into the destination vectors: yeast expression vector pYES-DEST52 or plant expression Gateway binary vectors [34] containing 35S promoters: ImpGWB402 (no tag) or ImpGWB451 (C-terminal G3GFP tag) using the Gateway LR Clonase enzyme mix (Invitrogen) according to the manufacturer’s protocol.

Coding regions of AtCPT1 and LEW1 were amplified by PCR using gene specific primers (Table S1) and subcloned into pESC-URA yeast dual expression vector (Agilent, Santa Clara, CA, USA) according to the manufacturer’s protocol. The PCR product for AtCPT1 was digested with restriction enzymes NotI and BcuI and inserted into the corresponding site behind the Gal-10 promoter in the correct orientation. The PCR product for LEW1 was digested with BamHI and SalI and inserted into the corresponding site behind the Gal-1 promoter in the correct orientation.

3.5. Generation of Arabidopsis Plants Overexpressing AtCPT1

The S35::AtCPT1 construct was introduced into Agrobacterium tumefaciens GV3101 strain and then used for transformation of A. thaliana (Col-0) wild type plants by the floral dip method [35]. F1 seeds were screened on ½ MS agar plates supplemented with 50 mg/L kanamycin (Sigma) and verified by PCR using specific primers for the S35 promoter and AtCPT1. F3 of two CPT1-OE lines (24 and 25) was used for the expression and lipid content analyses.

3.6. Transient Expression of AtCPT1 in Nicotiana benthamiana

The S35::AtCPT1-GFP or S35::AtCPT1 constructs, respectively, were introduced into Agrobacterium tumefaciens GV3101 strain. The Agrobacterium cultures were grown in liquid LB medium supplemented with 100 mg/L spectinomycin at 28 °C to an OD₆₀₀ of 1.5, diluted to an OD₆₀₀ of 0.4 in infiltration medium containing 10 mM MES (pH 5.6) 10 mM MgCl₂ and 100 µM acetosyringone and infiltrated into the abaxial side of the N. benthamiana leaves. Infiltrated leaves (2 or 4 days post infiltration, dpi) were observed using a confocal microscope or harvested for polyisoprenoid extraction, respectively.

3.7. Generation of Yeast Overexpressing AtCPT1

Preparation and transformation of competent S. cerevisiae cells was performed using S. c. EasyComp™ Transformation Kit (Invitrogen) according to manufacturer’s protocol. Transformant selection was performed on plates containing minimal medium without uracil (SC-U) with 2% glucose and G418 antibiotic for 3 days at 28 °C. To induce protein expression, the transformants were grown in SC-U medium with 2% galactose and G418. After 2–4 days of growth the yeast cells were collected for polyisoprenoid and CPY analyses. In vivo complementation assay of rer2Δ mutation with AtCPT1 was performed as described previously [24].

3.8. Polyisoprenoid Extraction and Purification

Plant polyisoprenoid: 1.5 g of Arabidopsis or Nicotiana leaves were homogenized in a mixture of chloroform/methanol (C/M, v/v) supplemented with internal standard of Pren-14 (10 μg) for 48 h at room temperature. Extracted lipids were dissolved in 5 mL of a mixture containing toluene/7.5% KOH/95% ethanol (20/17/3, v/v/v) and hydrolyzed for 1 h at 95 °C, then extracted with hexane, purified on silica gel columns, dissolved in propan-2-ol and analyzed as described earlier [7].

Yeast polyisoprenoid: Yeast cells were harvested by centrifugation of 100 mL of yeast culture at 3300× g (Allegra; Beckman, Indianapolis, IN, USA) for 10 min at room temperature, washed with water and hydrolyzed for 1 h at 95 °C in 10 mL of solution containing 25% KOH and 65% ethanol supplemented with internal standard Pren-28 (10 μg). Subsequently, lipids were extracted with hexane, purified on silica gel columns, dissolved in propan-2-ol and analyzed as described earlier [36].

3.9. HPLC/UV Analysis of Polyisoprenoids

Lipids extracted from Arabidopsis roots were analyzed using 4.6 × 75 mm ZORBAX XDB-C18 (3.5 μm) reversed-phase column (Agilent, Santa Clara, CA, USA) and Waters Photodiode Array Detector (210 nm, Milford, MA, USA).

Lipids extracted from yeast and Arabidopsis and tobacco leaves were analyzed using 4.6 × 50 mm Cortecs-C18 (2.7 μm) reversed-phase column (Waters) and UHPLC Waters Acquity Arc UV/Vis Detector (210 nm).

The external standards of a polyprenol mixture (Pren-9, 11–23, 25) and dolichol mixture (Dol-15 to Dol-24) were used to identify of chain length of polyisoprenoids. Pren-27 was used as internal standard for quantitative determination of polyisoprenoids.

3.10. Confocal Microscopy

For subcellular localization analysis of AtCPT1 cd3-959 (ER m-Cherry), cd3-954 (ER CFP) and cd-967 (Golgi m-Cherry) vectors were used as organelle markers [37]. Confocal Images were taken under an Nikon C1 confocal system built on TE2000E with 408, 488 and 543 nm laser excitations for CFP (450/35 nm emission filter), GFP (515/30 nm emission filter), and m-Cherry (605/75 emission filter), respectively.

3.11. Statistical Analysis

Statistical analysis was performed using the data analysis tool Student’s t test in the Graph Pad Prism program (Graphpad software, version 5, San Diego, CA, USA). All experiments were repeated at least three times with similar trends.

3.12. Accession Numbers

Arabidopsis Genome Initiative locus identifiers for the genes mentioned in this article are as follows: AtCPT1 (At2g23410), AtCPT3 (At2g17570), AtCPT6 (At5g58780), AtCPT7 (At5g58770) and AtCPT9 (At5g58784).