- Research article
- Open Access
Distinct expression and function of carotenoid metabolic genes and homoeologs in developing wheat grains
© The Author(s). 2016
Received: 23 April 2016
Accepted: 7 July 2016
Published: 12 July 2016
β-carotene, the most active provitamin A molecule produced by plants, plays important roles in human nutrition and health. β-carotene does not usually accumulate in the endosperm (i.e. flour) of mature wheat grains, which is a major food source of calories for humans. Therefore, enriching β-carotene accumulation in wheat grain endosperm will enable a sustainable dietary supplementation of provitamin A. Several metabolic genes affecting β-carotene accumulation have already been isolated from wheat, including phytoene synthase 1 (PSY1), lycopene ε-cyclase (LCYe) and carotenoid β-ring hydroxylase1/2 (HYD1/2).
In this work, we cloned and biochemically characterized two carotenoid cleavage dioxygenases (CCDs), CCD1 and CCD4, from wheat. While CCD1 homoeologs cleaved β-apo-8′-carotenal, β-carotene, lutein and zeaxanthin into apocarotenoid products, CCD4 homoeologs were inactive towards these substrates in in vitro assays. When analyzed by real-time qPCR, PSY1, LCYe, HYD1/2 and CCD1/4 homoeologs showed distinct expression patterns in vegetative tissues and sections of developing tetraploid and hexaploid wheat grains, suggesting that carotenoid metabolic genes and homoeologs are differentially regulated at the transcriptional level in wheat.
The CCD1/4 enzyme activity and the spatial-temporal gene expression data provide critical insights into the specific carotenoid metabolic gene homoeologs that control β-carotene accumulation in wheat grain endosperm, thus establishing the knowledge base for generation of wheat varieties with enhanced β-carotene in the endosperm through breeding and genome editing approaches.
Wheat (Triticum spp.), rice and maize constitute the three most widely consumed cereal grains worldwide. The color of wheat grain endosperm (i.e. flour) is determined largely by carotenoid pigments and has been selected according to consumer’s preference during the history of wheat breeding. Tetraploid durum wheat (T. turgidum) is used for making pasta and couscous and has been selected for increased concentrations of yellow pigments. Lutein, a non-provitamin A carotenoid exhibiting yellow color, is the major carotenoid molecule present in the endosperm of the mature tetraploid wheat grains. By contrast, hexaploid bread wheat (T. aestivum) has been selected for white flour, resulting in low concentrations of total carotenoids in the endosperm of the mature hexaploid wheat grains [1–3]. Therefore, wheat grain endosperm generally lacks provitamin A carotenoids for conversion into vitamin A in mammals.
Several metabolic genes controlling β-carotene accumulation have been isolated from wheat, including phytoene synthase 1 (PSY1) that channels carbon fluxes to carotenoid biosynthesis, lycopene ε-cyclase (LCYe) that diverts the common biosynthetic precursor lycopene to a competing pathway of lutein biosynthesis, and β-carotene hydroxylase1/2 (HYD1/2) that enable turnover of β-carotene to downstream hydroxylated products [8–10] (Fig. 1).
Besides hydroxylation, β-carotene and its derivatives can also be modified via conversion into smaller molecules (aka. apocarotenoids) by carotenoid cleavage dioxygenases (CCDs) (Fig. 1). Of the four plant CCDs (including CCD1, CCD4, CCD7 and CCD8), coupled actions of CCD7 and CCD8 are required for biosynthesis of strigolactones from 9-cis-β-carotene in root tissues . CCD1s identified from different plant species localize to the cytosol and have demonstrated cleavage activities towards all-trans-β-carotene (β-carotene hereafter) and additional linear or cyclic (apo)carotenoid substrates at different double bond positions (e.g. C9-C10/C9′-C10′, C7-C8/C7′-C8′ and C5-C6/C5′-C6′) in in vitro enzyme assays [12–32]. Among the CCD1s identified from monocots, rice and maize CCD1s (OsCCD1 and ZmCCD1) have been functionally characterized [15, 16, 30, 33]. Both enzymes cleave linear (e.g. lycopene) and cyclic (e.g. β-carotene and zeaxanthin) carotenoids symmetrically at C9-C10/C9′-C10′ or C7-C8/C7′-C8′ positions [15, 16, 30]. However, overexpression of OsCCD1 in Golden Rice endosperm (engineered for high β-carotene accumulation) did not change its β-carotene content significantly, arguing against a role of OsCCD1 in carotenoid cleavage in rice endosperm . It remains to be determined whether CCD1 enzymes can transform carotenoids into apocarotenoid products in other cereal grains, such as wheat.
In contrast to the cytosolic localization of CCD1s, CCD4 proteins contain transit peptides for targeting to the plastids [24, 35, 36]. Correlations between reduced CCD4 gene expression/activity and increased carotenoid accumulation or reduced apocarotenoid volatile emission in floral, fruit or storage tissues have been observed in Arabidopsis, chrysanthemum, grape, peach, potato and saffron, suggesting a role of CCD4s in carotenoid cleavage in these plants [19, 21, 24, 37–40]. However, increased violaxanthin accumulation was detected in RNAi knockdown lines of StCCD4 (potato CCD4), even though StCCD4 was unable to cleave violaxanthin in enzyme assays, suggesting that a reduction in CCD4 activity may not lead to the accumulation of its immediate substrates in planta . When assayed in vitro, the apple and chrysanthemum CCD4s showed substantial cleavage of β-carotene at C9-C10/C9′-C10′, while the Arabidopsis, rose and osmanthus CCD4s had little conversion of β-carotene into the apocarotenoid products [18, 42]. Although CsCCD4a/b/c of saffron (Crocus sativus) all cut β-carotene at C9-C10/C9′-C10′, minor cleavage activities of β-carotene at C7-C8/C7′-C8′ were only observed for CsCCD4c [24, 43]. Lutein, neoxanthin and violaxanthin may also serve as substrates for CsCCD4c as suggested by the carotenoid profiles of Nicotiana benthamiana plants transiently overexpressing CsCCD4c .
Since polyploid wheat has several subgenomes (AA, BB and DD genomes), multiple homoeologs are present for the carotenoid metabolic genes in wheat. While tetraploid wheat (genomes AABB) was formed from the hybridization of T. urartu (AA) and an unknown species from the Sitopsis group (BB) about 500,000 years ago, hexaploid wheat (genomes AABBDD) originated from the hybridization of tetraploid wheat (AABB) and diploid wheat (Aegilops tauschii) (DD) approximately 8000 to 10,000 years ago [42, 44]. It was proposed that genome duplication and evolution in tetraploid and hexaploid wheat may lead to subfunctionalization or neofunctionalization of gene homoeologs as has been reported for other polyploid plant species [45–47]. However, neofunctionalization occurs less often in polyploid wheat species due to their relatively short evolutionary time spans . Moreover, differences among wheat subgenomes are often manifested as differential expression of homoeologous genes (i.e. different homoeologs of the same gene). Consistent with this notion, we recently observed distinct expression patterns of HYD1/2 and LCYe genes and homoeologs in developing tetraploid and hexaploid wheat grains (whole grains were analyzed in this study) . Particularly, HYD-B1 homoeolog expression strongly resembles those of embryo-specific genes . These data raised the possibility that carotenoid metabolic gene homoeologs could be differentially regulated and may have specific functions in different sections of wheat grains.
The overall objective of this work is to obtain a comprehensive understanding of metabolic genes and homoeologs controlling carotenoid, particularly β-carotene, accumulation in wheat. Since CCD1/4 had not been isolated and functionally characterized in wheat, we first cloned CCD1 and CCD4 homoeologs from wheat and determined the in vitro enzyme activities of their encoded proteins. We then analyzed and compared carotenoid content as well as expression of carotenoid metabolic gene homoeologs (including PSY1, LCYe, HYD1/2 and CCD1/4) in vegetative tissues and three sections of developing tetraploid and hexaploid wheat grains.
Plant growth and tissue collection
Seeds of tetraploid wheat var. Kronos and hexaploid wheat breeding line UC1041 were germinated on pre-wetted filter paper and transferred, at 7 d post-germination, to either vermiculite followed by growing in a temperature-controlled growth chamber (for collection of vegetative tissues), or soil followed by growing in a temperature-controlled greenhouse (for collection of grains). Leaf, stem and root tissues of wheat seedlings were harvested after growing in the chamber for three weeks; the collected tissues were immediately frozen in liquid nitrogen. The greenhouse-grown wheat plants were tagged when first anthers became visible from the middle florets of an ear. Developing grains were harvested according to the six defined developmental stages, including watery/1, early milk/2, late milk/3, soft dough/4, hard dough/5 and ripening/6, as previously described . Grains of developmental stages 3–5 were dissected, using forceps and scalpels, into pericarp, endosperm and embryo sections. Grains at stages 1, 2 and 6 are not suitable for dissection as stages 1 and 2 grains are quite small and watery while stage 6 grains are very dry. The dissected grain tissues were immediately frozen in liquid nitrogen. Three biological replicates, each containing pooled sections from multiple grains harvested from several plants, were used for gene expression and metabolite analyses. The frozen vegetative tissues and grain sections were ground into fine powder in liquid nitrogen using mortar and pestle and stored at −80 °C until further analysis.
RNA extraction and cloning of wheat CCD1 and CCD4 homoeologs
Total RNA was extracted from wheat tissues using TRI reagent (Invitrogen, Carlsbad, CA). Quantity and quality of the RNA samples were determined using a Nanodrop® spectrophotometer, according to absorption at 260 nm (RNA quantity) as well as the ratios of A260/A280 and A260/A230 (RNA quality). RNA integrity was also evaluated by agarose gel electrophoresis. First strand cDNA synthesis was performed using the BioRad iScript cDNA synthesis kit with mixed random hexamers and oligo(dT)20 primers (Hercules, CA).
The coding sequences of wheat CCD1 or CCD4 homoeologs are highly similar at the 5′ and 3′ ends. Therefore, the same set of primers, except for CCD-B1, was used for amplification of wheat CCD1 or CCD4 homoeologs and cloning into the pENTR/D-TOPO vector (Invitrogen). Plasmids extracted from multiple colonies were sequenced in each cloning experiment to identify different homoeologs of CCD1 or CCD4. Upon sequence confirmation, the CCD1/4 gene homoeologs in pENTR/D-TOPO were then recombined into pDEST17 (Invitrogen) for expression as His-tagged proteins in E. coli. Arabidopsis thaliana CCD1 (AtCCD1) and β-glucuronidase (GUS) were also cloned into pDEST17 and used as positive and negative controls for carotenoid cleavage activities, respectively. To improve the solubility of the recombinant CCD4 proteins, His-tagged wheat CCD4 homoeologs were also subcloned into the pMAL-c2x vector (New England BioLabs, Ipswich, MA) for tagging of the maltose binding protein (MBP). The His-tagged wheat CCD-A1 was cloned into pMAL-c2x in parallel and used as a control for comparing the cleavage activities between His-tagged and MBP-His-tagged CCD proteins.
When analyzed by TargetP , wheat CCD4 homoeologs were predicted to contain N-terminal plastid transit peptides of various lengths (50 aa for CCD-A4, 65 aa for CCD-B4, and 49 aa for CCD-D4). Since it was suggested that removal of subcellular targeting sequences may improve recombinant protein expression in E. coli [49, 50], truncated CCD4 homoeologs (i.e. without the transit peptide-encoding DNA sequences) were also cloned into pENTR/D-TOPO and then pDEST17 for protein expression in E. coli. Primers used for cloning wheat CCD1 and CCD4 homoeologs are listed in Additional file 1: Table S1.
Purification of recombinant proteins and CCD enzyme assays
Recombinant plasmids carrying AtCCD1, GUS, wheat CCD1 or CCD4 (full length or truncated) homoeologs were transformed into chemically competent cells of E. coli strain Rosetta (DE3)pLysS. The E. coli cells were grown at 37 °C until OD600 reached 0.6-0.8. Isopropyl β-D-1-thiogalactopyranoside (IPTG) was added to the bacterial cell culture to a final concentration of 0.4 mM. The cells continued to grow at 16 °C for 20 h and were collected by centrifugation at 3000 x g for 20 min. Purification of His-tagged proteins was carried out using Ni-NTA agarose beads (Qiagen, Valencia, CA). MBP-His-tagged proteins were purified using amylose resins (New England BioLabs). Induction and purification of the recombinant proteins were examined by SDS-PAGE.
β-apo-8′-carotenal (Sigma Aldrich, St. Louis, MO), lutein (Chromadex, Irvine, CA) and zeaxanthin (purified from E. coli cells expressing pAC-ZEAX) were dissolved in ethanol containing 1.5 % n-octyl-β-D-glucopyranoside (Sigma Aldrich). β-carotene (Sigma Aldrich) was solubilized as previously described with slight modifications . Briefly, β-carotene was dissolved in 20 μl of chloroform with 2 % Tween-80. The mixture was dried under vacuum, resuspended in 20 μl of ethanol, and then added to the reaction mixture. For in vitro CCD enzyme assays, the 200 μl reaction mixture included 20 μg purified recombinant proteins, 100 mM Tris-HCl (pH 7.0), 0.5 mM FeSO4, 5 mM ascorbic acid, and the (apo)carotenoid substrate (120 μM β-apo-8′-carotenal, 40 μM β-carotene, 20 μM zeaxanthin or 100 μM lutein). The reaction was allowed to proceed at 30 °C for 2 h and stopped by extraction with ethyl acetate; 20 μl of the ethyl acetate extract was injected on a reverse phase HPLC. The enzyme assays were carried out in triplicate.
Recombinant plasmids carrying wheat CCD1 or CCD4 (full length) homoeologs as well as the GUS control were also transformed into E. coli JM109 (DE3) cells that express pAC-BETA (containing genes for β-carotene production). An overnight culture initiated from a single colony was used to inoculate 25-ml Luria Bertani (LB) with 1 % glucose and appropriate antibiotics. The bacterial culture was grown at room temperature with shaking until OD600 reached 0.6. IPTG was added to a final concentration of 0.02 mM and the cells continued to grow at room temperature for an additional 12 h. The growth media were then extracted with ether, dried under N2, and resuspended in ethyl acetate; 20 μl of the ethyl acetate resuspension was separated on HPLC. The medium extractions were repeated at least three times from independently transformed and grown bacterial cell cultures.
HPLC and MS analyses
The HPLC program for analysis of CCD enzyme assay products consisted of three solvents: (A) 20 % acetonitrile, (B) acetonitrile:H2O:triethylamine (900:99:1, v/v/v), and (C) ethyl acetate. The gradient elution included: 0–2 min, 100 % A; 2–5 min, 100-50 % A and 0–50 % B; 5–10 min, 50-0 % A and 50–100 % B; 10–13 min, 100-75 % B and 0–25 % C; 13–16 min, 75-30 % B and 25–70 % C; 16–19 min, 30-0 % B and 70–100 % C; 19–21 min, 100 % C; 21–22 min, 0–100 % A and 100-0 % C. Carotenoid extraction from wheat grain tissues as well as HPLC separation and quantification were carried out as previously described . The HPLC program for analysis of bacterial growth media included (A) 50 % acetonitrile, (B) acetonitrile:H2O:triethylamine (900:99:1, v/v/v), and (C) ethyl acetate, with the following gradient: 0–10 min, 100-0 % A and 0–100 % B; 10–13 min, 100-75 % B and 0–25 % C; 13–16 min, 75-30 % B and 25–70 % C; 16–19 min, 30-0 % B and 70–100 % C; 19–21 min, 100 % C; 21–22 min, 0–100 % B and 100-0 % C. The flow rate was maintained at 1 ml min−1 for all of the HPLC analysis.
Mass spectrometry (MS) analysis was performed on a Thermo Electron LTQ-Orbitrap Hybrid mass spectrometer (Thermo Scientific, Waltham, MA). Product peaks from the CCD enzyme assays were collected from the HPLC runs and used for injection onto the mass spectrometer. An isocratic flow of 50 % (A) H2O and 50 % (B) acetonitrile was maintained at 0.2 ml min−1 for MS analysis. The mass spectra were acquired by electrospray ionization (ESI) in the positive mode with a mass range of m/z 50–1000 Da.
Representative CCD and nine-cis-epoxycarotenoid dioxygenase (NCED) proteins from different plant species were selected for multiple sequence alignment using Multiple Sequence Comparison by Log-Expectation (MUSCLE) . The aligned sequences were then used for construction of a neighbor-joining (NJ) tree by MEGA5 with the pairwise deletion method . Robustness of the NJ tree was tested with 1000 rounds of bootstrapping. The rice (Os), sorghum (Sb) and maize (Zm) CCD and NCED sequences were obtained from . The GenBank (non-A. thaliana sequences) and AGI (A. thaliana sequences) accession numbers are: AtCCD1, At3g63520; AtCCD4, At4g19170; AtCCD7, At2g44990; AtCCD8, At4g32810; AtNCED2, At4g18350; AtNCED3, At3g14440; AtNCED5, At1g30100; AtNCED6, At3g24220; AtNCED9, At1g78390; CaCCD1, DQ157170; CcCCD1, DQ157166; CisCCD1, AB219165; ClCCD1, AB219168; CmCCD1, DQ269467; CsCCD1a, AJ132927; CsCCD1b, EU523661; CuCCD1, AB219164; DcCCD1, DQ192203; FaCCD1, ACA13522; OfCCD1, BAJ05401; PhCCD1, AY576003; RdCCD1, ABY47994; SlCCD1A, AY576001; SlCCD1B, AY576002; TaCCD-A1, KU975445; TaCCD-B1, KU975446; TaCCD-D1, KU975447; VvCCD1, AY856353; CsCCD4a, EU523662; CsCCD4b, EU523663; CsCCD4c, JN131499; CuCCD4, BAO18774; CxmCCD4a, ABY60885; CxmCCD4b, BAF36656; MdCCD4, ABY47995; OfCCD4, ABY60887; PpCCD4, JX309999; RdCCD4, ABY60886; StCCD4, XP_006359966; TaCCD-A4, KU975448; TaCCD-B4, KU975449; TaCCD-D4, KU975450; BoLCD, AJ489277; CsZCD, AJ489276. At, Arabidopsis thaliana; Bo, Bixa orellana; Ca, Coffea arabica; Cc, Coffea canephora; Cis, Citrus sinensis; Cl, Citrus limon; Cm, Cucumis melo; Cs, Crocus sativus; Cu, Citrus unshiu; Cxm, Chrysanthemum x morifolium; Dc, Daucas carota; Fa, Fragaria ananassa; Md, Malus x domestica; Of, Osmanthus fragans; Os, Oryza sativa; Ph, Petunia hybrida; Pp, Prunus persica; Rd, Rosa x damascene; Sb, Sorghum bicolor; Sl, Solanum lycopersicum; St, Solanum tuberosum; Ta, Triticum aestivum; Vv, Vitis vinifera; Zm, Zea mays. LCD, Lycopene Cleavage Dioxygenase; ZCD, Zeaxanthin Cleavage Dioxygenase.
Real-time qPCR analysis
Total RNA was treated with RNase-free DNase I (Fermentas, Glen Burnie, MD). cDNA synthesis was carried out using 5 μg total RNA, random hexamers, and the iScript cDNA synthesis kit (BioRad). Primers specific for wheat HYD1 and HYD2 homoeologs as well as the reference genes were reported previously . Primers specific for PSY1, LCYe, CCD1 and CCD4 homoeologs were designed and verified using nullisomic-tetrasomic and ditelosomic lines of hexaploid wheat var. Chinese Spring (Additional file 2: Table S2; Additional file 3: Figure S1). The qPCR products were cloned and sequenced to verify amplification of the target gene homoeologs.
Real-time qPCR analysis was carried out as previously described using the iTaq SYBR® Green Supermix . qPCR amplification efficiency for the target gene homoeologs was in the range of 90 % to 121 %. The relative standard curve method was used for quantification of the transcripts . cDNAs synthesized from whole grains were used for construction of the standard curves in order to allow comparison of homoeologs expressed in different grain sections. Normalization of gene expression was carried out using the geometric mean of two reference genes, Ta2291 and Ta54227, which are stably expressed in different wheat tissues .
One way Analysis of Variation (ANOVA) followed by unpaired, two-tailed t-test (carotenoid content as well as gene expression in tetraploid wheat) or Tukey’s test (gene expression in hexaploid wheat) were performed. All statistical analysis was carried out using JMP (SAS Institute, Cary, NC).
Cloning and biochemical characterization of wheat CCD1 and CCD4 homoeologs
Unlike the His-tagged CCD1 proteins that partially partitioned to the soluble protein fraction, His-tagged CCD4 proteins were largely insoluble (Additional file 4: Figure S2). CCD4 homoeologs were then expressed as MBP-His-tagged proteins and showed improved protein solubility (Additional file 4: Figure S2). Overall, the purified MBP-His-CCD4 proteins did not exhibit any cleavage activity towards β-apo-8′-carotenal, β-carotene, zeaxanthin and lutein in enzyme assays (Fig. 3; Additional files 5: Figure S3 and Additional file 6: Figure S4). In addition, β-ionone was not detected in growth media of β-carotene producing E. coli cells co-expressing wheat CCD4 homoeologs (Fig. 4; Additional file 7: Figure S5). To demine whether the MBP tag may affect protein activities, MBP-His-CCD-A1 was also expressed in E. coli and showed improved protein solubility as compared to His-CCD-A1 (Additional file 4: Figure S2). Comparable cleavage activities of the (apo)carotenoid substrates were demonstrated by MBP-His-CCD-A1 and His-CCD-A1, indicating that the MBP tag does not affect the activity of CCD proteins (Figs. 3 and 4). Upon removal of N-terminal plastid transit peptides, solubility of His-truncated CCD-4A/B/D proteins was moderately improved (Additional file 4: Figure S2). However, His-truncated CCD-4A/B/D proteins were not active towards β-apo-8′-carotenal, β-carotene, zeaxanthin and lutein (Additional file 8: Figure S6).
Carotenoid metabolite profiles in different sections of developing wheat grains
Carotenoid composition and content in developing tetraploid wheat (var. Kronos) grain sections
μg carotenoid pigment/g fresh weight of tissue
3.75 ± 0.15a
0.36 ± 0.05a
0.28 ± 0.04a
0.42 ± 0.04a
3.06 ± 0.14a
2.05 ± 0.17a
9.93 ± 0.2a
0.61 ± 0.04a
3.52 ± 0.12a
0.39 ± 0.06a
0.23 ± 0.05a
0.38 ± 0.08a
2.87 ± 0.22ab
1.85 ± 0.08a
9.24 ± 0.56a
0.62 ± 0.04a
2.46 ± 0.33b
0.39 ± 0.02a
0.34 ± 0.02a
2.55 ± 0.27b
1.83 ± 0.02a
7.33 ± 0.97b
0.51 ± 0.03b
4.65 ± 0.38c
1.51 ± 0.08c
6.16 ± 0.4c
3.09 ± 0.29c
4.99 ± 0.64c
1.28 ± 0.24c
6.27 ± 0.88bc
3.92 ± 0.21c
3.75 ± 0.3a
0.48 ± 0.07d
4.23 ± 0.25d
8.02 ± 1.57d
18.92 ± 2.62d
8.98 ± 1.44b
3.72 ± 0.64b
7.65 ± 1.02e
39.27 ± 5.69e
0.93 ± 0.01e
15.55 ± 1.43de
7.78 ± 0.5b
2.94 ± 0.3b
6.24 ± 0.66ef
32.5 ± 2.43e
0.92 ± 0.04e
12.09 ± 1.73e
5.01 ± 0.42c
2.02 ± 0.15c
4.81 ± 0.63f
23.93 ± 2.93f
1.02 ± 0.04f
Carotenoid composition and content in developing hexaploid wheat (breeding line 1041) grain sections
μg carotenoid pigment/g fresh weight of tissue
2.4 ± 0.33a
0.46 ± 0.05a
1.03 ± 0.06a
0.39 ± 0.02a
2.53 ± 0.23a
2.32 ± 0.03a
9.13 ± 0.69a
0.36 ± 0.03a
2.07 ± 0.23a
0.37 ± 0.04a
1.35 ± 0.05a
0.34 ± 0.04a
2.42 ± 0.44a
3.01 ± 0.04b
9.55 ± 0.74a
0.28 ± 0.01b
1.83 ± 0.54a
0.37 ± 0.05a
0.12 ± 0.03b
1.84 ± 0.39a
2.03 ± 0.27a
6.19 ± 1.16b
0.41 ± 0.06a
0.92 ± 0.1b
0.9 ± 0.13b
1.81 ± 0.23c
1.03 ± 0.04c
0.68 ± 0.02c
0.45 ± 0.01c
1.13 ± 0.01d
1.49 ± 0.07d
0.5 ± 0.06d
0.17 ± 0.01d
0.67 ± 0.07e
2.96 ± 0.3e
22.55 ± 3.22e
14.34 ± 2.06b
4.97 ± 0.84b
11.27 ± 1.62e
53.13 ± 7.74f
0.74 ± 0.01f
18.07 ± 1.81e
10.18 ± 1.01c
3.69 ± 0.35b
8.84 ± 0.82f
40.79 ± 3.99g
0.8 ± 0.01g
8.94 ± 1.67f
4.24 ± 0.58d
1.15 ± 0.43c
3.95 ± 0.4g
18.28 ± 3.07h
0.95 ± 0.03c
The pericarp of wheat grains contain β-carotene, neoxanthin, violaxanthin and lutein, resembling the carotenoid composition of photosynthetic tissues (Tables 1 and 2) . In the pericarp tissue, similar individual and total carotenoid levels were observed between stages 3 and 4 of tetraploid and hexaploid wheat; however, there was a consistent drop in carotenoid content at stage 5, which was significant for β-carotene, neoxanthin and total carotenoids (Tables 1 and 2). On the other hand, an increasing trend in the ratio of β,ε-/β,β-carotene branch (β,ε/β,β) carotenoids was evident for stages 3–5 of grain pericarp (Tables 1 and 2), indicating a shift in carotenoid accumulation favoring the α-carotene/lutein branch relative to the β-carotene/zeaxanthin branch (Fig. 1).
In contrast to pericarp, lutein and violaxanthin were the only detectable carotenoids in the endosperm of tetraploid and hexaploid wheat grains (Tables 1 and 2). The endosperm of tetraploid wheat consistently accumulated higher concentrations of lutein and violaxanthin than that of hexaploid wheat at each grain developmental stage. As grain endosperm matures, violaxanthin decreased more rapidly than lutein and led to a one-fold increase in the β,ε/β,β ratio at stage 5 of tetraploid and hexaploid wheat grains (Tables 1 and 2).
In addition to the carotenoids present in pericarp and endosperm tissues, antheraxanthin and zeaxanthin were also found in embryo (Tables 1 and 2). Particularly, antheraxanthin accounted for about 20 % of total carotenoids in the embryo tissue. As with pericarp and endosperm, total carotenoids in embryo decreased towards the late stage of grain development, contributed mainly by reduced lutein. While the β,ε/β,β ratios in maturing embryo decreased in tetraploid wheat, they remained mostly constant in hexaploid wheat (Tables 1 and 2).
Expression of carotenoid metabolic gene homoeologs in different sections of developing wheat grains
In the pericarp tissue, PSY-A1 and PSY-B1 showed comparable and similarly decreased expression during tetraploid wheat grain development, except in stage 5 where the PSY-B1 transcript level was significantly higher than that of PSY-A1 (Fig. 5). The preponderance of the B-genome PSY1 homoeolog was more evident in hexaploid wheat; PSY-B1 was the major PSY1 homoeolog expressed in stage 3 and the only PSY1 transcript detected in stages 4 and 5 (Figs. 5 and 6). While LCYe, HYD1 and HYD2 homoeologs exhibited similar transcript accumulation through grain development in tetraploid wheat, HYD1 homoeologs showed increased expression at stage 5 of grain development in hexaploid wheat. In addition, LCYe-A was the only LCYe homoeolog expressed in the pericarp of hexaploid wheat. Of the CCD1/4 homoeologs, CCD-B4 expression in pericarp increased gradually towards stage 5 of tetraploid and hexaploid wheat grains. The other CCD1/4 homoeologs showed similar or slightly decreased expression (CCD-A1) during tetraploid and hexaploid wheat grain development (Figs. 5 and 6).
In the endosperm tissue, transcripts of all three PSY1 homoeologs were under the detection limit of real-time qPCR in hexaploid wheat grains, contrasting to the high PSY1 homoeolog expression found in tetraploid wheat where decreased PSY-A1 and PSY-B1 transcript levels were observed in stages 3–5 (Figs. 5 and 6). Interestingly, LCYe-A was the only LCYe homoeolog expressed in the endosperm of both tetraploid and hexaploid wheat grains. Of the HYD1/2 genes, HYD1 homoeolog expression was not detectable, while the HYD2 homoeologs showed decreased expression in tetraploid and hexaploid wheat (Figs. 5 and 6). Only CCD-A1 and CCD-B4 expression was observed in tetraploid wheat grain endosperm. In contrast, all three CCD1 homoeologs were expressed in the hexaploid wheat grain endosperm, with CCD-A1 and CCD-D1 showing increased expression during grain development; on the other hand, none of the CCD4 homoeologs had detectable transcript accumulation in hexaploid wheat grain endosperm (Figs. 5 and 6).
In the embryo tissue, PSY-B1 and PSY-D1 were the most abundant PSY1 homoeolog in tetraploid and hexaploid wheat, respectively (Figs. 5 and 6). LCYe-B in tetraploid wheat as well as LCYe-A and LCYe-B in hexaploid wheat showed increased expression during grain maturation, particularly at stage 5. While HYD2 homoeologs had mostly consistent expression in the three grain developmental stages analyzed, enhanced HYD1 homoeolog expression was observed at the late stage of tetraploid and hexaploid wheat grain development (Figs. 5 and 6). Interestingly, transcripts of CCD1, but not CCD4, homoeologs were detectable in the embryo tissue of tetraploid and hexaploid wheat grains (Figs. 5 and 6).
Expression of carotenoid metabolic gene homoeologs in vegetative tissues
In leaves, HYD1/2 and CCD1/4 homoeologs showed similar expression in both tetraploid and hexaploid wheat. On the other hand, PSY-A1 and LCYe-A transcripts were relatively more abundant than their corresponding homoeologs in tetraploid wheat, whereas PSY-D1 and LCYe-B transcripts were relatively more abundant than their corresponding homoeologs in hexaploid wheat (Figs. 7 and 8).
In stems of tetraploid and hexaploid wheat, the relative expression patterns among PSY1, LCYe, HYD1 and CCD1/4 homoeologs generally resembled those in leaves. However, expression levels of PSY1 and CCD1/4 homoeologs were much reduced in stems as compared to leaves (Figs. 7 and 8). Unlike the comparable transcript accumulation of HYD2 homoeologs in leaves, HYD-A2 appeared to be the major HYD2 homoeolog expressed in stems of tetraploid and hexaploid wheat (Figs. 7 and 8).
In roots of tetraploid and hexaploid wheat, PSY1 and CCD4 homoeologs were under the limit of detection, and LCYe homoeologs were absent or very lowly expressed (Figs. 7 and 8). In tetraploid wheat roots, HYD-A1 and HYD-A2 were clearly the major HYD1 and HYD2 homoeologs, respectively. In contrast, comparable expression was observed for the three homoeologs of HYD2, while HYD-D1 had only baseline expression in hexaploid wheat roots (Figs. 7 and 8). CCD-A1 and CCD-B1 homoeolog expression did not differ significantly for both tetraploid and hexaploid wheat roots, whereas CCD-D1 showed two-fold higher expression than the other two CCD1 homoeologs in roots of hexaploid wheat seedlings (Figs. 7 and 8).
Lutein, but not β-carotene, accumulates in the endosperm (flour) of tetraploid and hexaploid wheat grains at varied levels (Tables 1 and 2). While re-directing the carbon flux from lutein to β-carotene formation may be accomplished in wheat grains by blocking the LCYe catalyzed reaction as demonstrated in maize grains and potato tubers [56, 57], it is crucial to understand whether the β-carotene produced could accumulate or will be turned over via hydroxylation by HYDs or cleavage by CCDs (Fig. 1). Our in vitro enzyme assay results showed that wheat CCD1 homoeologs could cleave β-carotene symmetrically, suggesting that CCD1 homoeologs can potentially contribute to the degradation of this provitamin A molecule in grains modified with increased β-carotene production (Figs. 3 and 4; Additional files 5: Figure S3 and Additional file 6: Figure S4). Since lutein can also serve as substrate to CCD1 homoeologs in vitro and it naturally accumulates in wheat grain endosperm, it is possible that the rate of lutein biosynthesis is higher than that of potential degradation by CCD1 homoeologs in this tissue. Alternatively, there could be unknown mechanisms that protect lutein from degradation by CCD1 homoeologs in wheat grain endosperm.
In contrast to CCD1 homoeologs, wheat CCD4 homoeologs did not act on β-carotene, lutein and zeaxanthin (Figs. 3 and 4; Additional files 5: Figure S3, Additional file 6: Figure S4, Additional file 7: Figure S5 and Additional file 8: Figures S6). It remains to be determined whether they could function towards other carotenoid molecules, such as violaxanthin, that were not used for in vitro testing. AtCCD4 (Arabidopsis CCD4) was previously found in the plastid-localized plastoglobules; in particular, it interacts with a zinc finger protein VAR3 in a protein complex required for normal chloroplast and palisade cell development [35, 58]. It will be interesting to determine whether wheat CCD4 homoeologs are also bound to plastoglobules and cooperates with VAR3-like proteins. Further reverse genetic analysis of wheat CCD4 homoeologs will help elucidate their enzymatic functions in planta and the role of their cleavage products in plastid, cell and tissue development.
It was previously shown that maize genotypes with low levels of CHY (i.e. HYD) and LCYe transcripts correlate with high levels of β-carotene accumulation in grains [57, 59], which suggests that carotenoid metabolic gene expression may be indicative of their functions in plants. We therefore examined the expression profiles of carotenoid metabolic gene homoeologs to determine the specific gene homoeologs that control β-carotene accumulation in different sections of developing wheat grains. Overall, the gene expression data indicated that homoeologous carotenoid metabolic genes are regulated at the transcriptional level in sections of wheat grains (Figs. 5, 6, 7 and 8). Additionally, tissue specific expression was more prominent than genome specific expression for the carotenoid metabolic gene homoeologs in wheat (Figs. 5, 6, 7 and 8). Recently, a genome-wide study examined homoeolog expression and genome interplay among three cell types (including endosperm, aleurone layer and transfer cells) of hexaploid wheat grains at 10-, 20- and 30-day after anthesis . Similar to that observed in our gene expression analysis, this study also reported differential expression of homoeologous genes without an overall dominance of a particular subgenome . However, embryo and pericarp tissues were not examined and expression of carotenoid metabolic gene homoeologs were not analyzed in this report .
In developing embryo of tetraploid and hexaploid wheat grains, LCYe-A and LCYe-B homoeologs showed increased expression contrasting to decreased lutein accumulation , suggesting that mechanisms other than transcriptional control could also be involved in the regulation of lutein metabolism in wheat grains. Accompanying largely reduced individual and total carotenoids in pericarp at the late stage of wheat grain development, CCD-B4 expression increased sharply, raising the possibility that it may be responsible for carotenoid degradation in pericarp during grain dehydration. This observation is consistent with a recent study in Arabidopsis where AtCCD4 expression rose during seed drying (comparable to wheat grain stages 4–5) and was shown genetically as a major contributor of β-carotene degradation during Arabidopsis seed desiccation . However, since whole Arabidopsis seeds were used in this study, the spatial location of AtCCD4 expression and β-carotene accumulation within Arabidopsis seeds were not determined.
Our gene expression results also provided important insights for future attempts to increase β-carotene content in wheat grain endosperm. In the endosperm of tetraploid and hexaploid wheat grains, HYD1 homoeologs were not expressed; CCD1 and CCD4 homoeologs were either non-detectable or had low level expression, thus may not impact carotenoid accumulation in this tissue. On the other hand, there were significant transcript accumulation of LCYe-A (but not LCYe-B or LCYe-D) and HYD2 homoeologs, suggesting that downregulation or loss-of-function of these homoeologs may be sufficient to result in more β-carotene in the endosperm of tetraploid and hexaploid wheat grains. Since the total carotenoid content in hexaploid wheat grain endosperm is low, more carbons will also need to the directed to the carotenoid biosynthetic pathway, such as introducing PSY1 genes with higher expression or activity, to increase β-carotene levels in hexaploid wheat grain endosperm.
Considering the critical roles that carotenoids play in light harvesting and photoprotection, it is important to ensure that downregulation of specific carotenoid metabolic gene homoeologs in grain endosperm will not compromise carotenoid biosynthesis and function in the photosynthetic tissue. LCYe, HYD1/2 and CCD1/4 homoeologs showed comparable expression in leaves (Figs. 7 and 8), suggesting that loss/reduction of activities of specific carotenoid metabolic gene homoeologs in the photosynthetic tissue could be compensated for by the overlapping activities of homologous (e.g. HYD1 and HYD2) and/or homoeologous (e.g. different homoeologs of HYD2) genes.
Taken together, the CCD1/4 enzyme activity and the spatial gene expression analyses suggested that reduced expression of LCYe-A and one or more of the loci, including HYD-A2, HYD-B2, and CCD1 homoeologs (only for hexaploid wheat), could lead to β-carotene enrichment in the endosperm of wheat grains without compromising carotenoid metabolism in leaves. Identification of the specific carotenoid metabolic gene homoeologs controlling β-carotene accumulation will facilitate efficient and effective provitamin A biofortification of wheat grains through plant breeding and genome editing technologies.
ANOVA, analysis of variation; CCD, carotenoid cleavage dioxygenase; ESI, electrospray ionization; GUS, β-glucuronidase; HYD, carotenoid β-ring hydroxylase; IPTG, isopropyl β-D-1-thiogalactopyranoside; LCD, lycopene cleavage dioxygenase; LCYe, lycopene ε-cyclase; MBP, maltose binding protein; MS, mass spectrometry; MUSCLE, multiple sequence comparison by log-expectation; NCED, nine-cis-epoxycarotenoid dioxygenase; NJ, neighbor-joining; PSY, phytoene synthase; ZCD, zeaxanthin cleavage dioxygenase
We thank Saarah Kuzay, Quoc Thiem and Hana Leist for assistance with wheat grain collection and dissection, and Dr. Francis Cunningham (University of Maryland) for providing the pAC-BETA and pAC-ZEAX plasmids. This work was supported by the startup fund from University of California, Davis to LT. SY was supported by Chinese Scholarship Council Fellowship and UC Davis, Department of Plant Sciences Graduate Research Fellowship. JD acknowledges support from the Howard Hughes Medical Institute and the Gordon and Betty Moore Foundation.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional files.
LT and XQ designed the experiment. XQ and KF collected and dissected wheat grains; XQ performed real-time qPCR analysis; XQ and SY conducted CCD enzyme assays; JD provided expertise in wheat genetics and sequence analysis and contributed to the revision of the manuscript; XQ, SY and LT analyzed the data; LT wrote the paper. All authors have read and approved the final version of the manuscript.
The authors declare that they have no competing interests.
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