Genetic studies aimed at onion improvement have been limited because of high heterozygosity, a very large genome size with a high level of repetitive DNA and a biennial life cycle. Onion bulb initiation is daylength-dependent, which places a significant barrier to adapting new varieties for growth at different latitudes. Compared to the photoperiodic regulation of flowering, relatively little is known about genetic regulation of the bulbing process. This study aims to identify the role of gene sequences involved in daylength-regulated bulb formation and tissue specific expression of onion. A comprehensive set of developmental and spatial quantitative mRNA expression experiments were carried out to investigate expression of onion FLOWERING LOCUS T (AcFT), LEAFY (AcLFY) and GIBBERELLIN-3 OXIDASE (GA3ox1) during the bulbing response. Bulbing ratios were used to measure the response of onion plants under long day (LD) and short day (SD) conditions. AcFT1 was expressed in LD, which induces bulb formation, while AcFT4 was expressed in SD, which inhibits bulb formation. AcFT5 and AcFT6 were expressed in LD and might also be involved in bulb formation itself. All AcFT, AcLFY and GA3ox1 genes showed distinctive patterns of tissue specific expression in onion, with AcFT genes found primarily in the sites of perception in the leaf and LFY in the basal tissues, the site of response. The results are consistent with AcFT1 expression being the signal for LD-induced bulb initiation and AcFT4, being involved in suppressing bulbing in SD.
Onion (Allium cepa L.) is an edible monocotyledonous bulbous perennial (often biennial) vegetable crop, belonging to the family Alliaceae and is cultivated in temperate, tropical and sub-tropical regions1,2,3. It is included in the order Asparagales, the second most economically important monocotyledons, next to Poales, which include the cereal crops2,4. Global production of onions in 2016 was 82.85 million tonnes from 4.2 million hectares of land. The Food and Agriculture Organization of the United Nations5 reported that in terms of total annual world production, onion ranks second among horticultural crops, next to tomato. Onion is consumed at both the green and mature stage for salad and spice. In addition to its economic importance, it has nutritional and health benefits because of its high content of valuable phytochemicals, antioxidants, and sulphur compounds, which contribute to its flavour.
The onion life cycle can be divided into three main stages, namely seedling, bulb and flowering6,7. In temperate onion, during the first growth phase onion seed will start to germinate after sowing1. After a few days of germination, the seedlings/sets are planted in the spring and the plants undergo a juvenile phase of growth during which plants will not bulb regardless of being exposed to inductive conditions. Following that, onion leaves require continuous exposure to a suitable photoperiod in order to initiate and complete bulbing2. Onion leaves are composed of a photosynthetic leaf blade and a fleshy leaf sheath/storage leaf base or scale8. After receiving the photoperiodic stimulus, bladed green leaves formation near the apical meristem ceases and they are transformed into only bladeless leaves. Bulb sheath cells expand in response to a photoperiod signal from the leaf blade and act as a sink for the leaf carbohydrates such as glucose, fructose, sucrose and fructans. With the maturity of the bulb, the outer (oldest) one to four leaf scales dry out and become protective skin1. The onion plant then overwinters as a bulb and during this time, if the environment is favourable, flowering is induced after vernalisation in response to prolonged cold temperature. The onion plant then flowers and sets seed during the spring/summer of its second year of growth and thus its life cycle is completed1,9.
Bulb formation in temperate onion is daylength-dependent and the leaves of the plant are the photoperiodic stimulus receptor10. Bulb initiation can be defined as the point at which the ‘bulbing ratio’, the ratio of the maximum bulb diameter at the base to the minimum at the neck/sheath, increases to greater than two (>2)11. Long-day (LD) onions are grown in temperate regions and require at least 14 or more hours of light to stimulate bulb initiation, while, short-day (SD) onions are grown in more tropical regions and require a daylength of only 10 h or more for bulbing2. The matter is further complicated as some onion varieties are intermediate where they need 12 h or more of daylight before they will start producing the onion bulb. This daylength-dependent bulb initiation is similar to the photoperiodic regulation of flowering in other plants12,13. Therefore, it is hypothesised that the genes involved in the daylength regulation of flowering in Arabidopsis are also responsible for the daylength regulation of bulb formation in onion. Both processes are induced by LD, signal perception is in the leaf blade, response at the meristem and both are promoted by far-red light, through phytochrome A (PHYA)14,15. Bulbing is a reversible process and plants grown under inductive conditions promote bulb formation but if transferred to non-inductive condition, they rapidly revert to vegetative growth11,16.
The flowering locus T gene (FT), first identified in A. thaliana17,18, has been shown to be the major component of the floral signal molecule, florigen19. This FT plays a major role in the photoperiodic pathway for the initiation of flowering in the apical meristem with the help of other floral homeotic genes like LFY20. Furthermore, FT is a target of constans (CO) and acts upstream of suppressor of constans overexpression (SOC1) and can act as a mobile flowering signal to induce flowering by long-distance transportation21,22. For bulbing, as with flowering, daylength perception occurs in the leaves, while the response is in the meristem2. These suggest that a mobile signal with properties similar to FT might be involved.
In addition to the regulation of flowering, FT genes have been found to be involved in a range of physiological processes, suggesting more general function as a plant hormone9. For example, an FT promotes vegetative growth and inhibition of bud set in poplar in response to warm temperatures and LD photoperiods23,24,25, in tomato and maize, FT genes have been found to function as general growth regulator26,27. Other than vegetative growth and flowering, FT is also involved in the SD induction of tuberisation in potato28.
Characterising genes involved in the daylength requirement of bulb formation will help in understanding the basis of the difference between different daylength types, which is important for adapting new varieties for growth and development at different latitudes. Six FT genes (AcFT1-6) have been identified in double haploid onion line CUDH2150 and the authors proposed that AcFT1 and AcFT4 genes promote and inhibit bulb formation, respectively, while AcFT2 acts to promote flowering15. In addition, FKF1 and GI, which are involved in the photoperiodic regulation of flowering in Arabidopsis are also conserved in onion12.
This study characterises the developmental and spatial expression of putative photoperiodism-related genes by quantitative gene expression analysis in different response types of onion under a range of bulbing and non-bulbing conditions in order to further understand their potential roles in the daylength regulation of bulbing.
Materials and Methods
The long day (LD) onion (Allium cepa L.) variety ‘Renate F1’ (also called Renate) (Elsoms Seeds Ltd., Spalding, UK) and the short day (SD) onion variety ‘Hojem’ were used for these experiments. Varieties with different daylength responses were originally sourced from the Warwick Genetic Resources Unit and the seeds provided by Dr. Andrew Taylor, Warwick Crop Centre. Seeds of Hojem were collected from the Vegetable Genetic Improvement Network (VeGIN, UK) project Diversity Set.
Time-course experiment to study gene expression for Renate F1 during development
This experiment was conducted to characterise the response of bulb initiation in relation to daylength as a prelude to more detailed later experiments. Onion plants were grown in natural conditions within a glasshouse at the Crop Centre in Wellesbourne during the period from 6th March to 7th May 2013 when daylight was 11 h 15 min to 15 h 37 min, respectively. Initially, Renate F1 seeds were sown in modular trays and after 4 weeks plants were potted up into 9 cm pots containing Levington M2 compost (Supplementary Fig. S1). At 48 d when plants had initiated bulbing, half of them were transferred to constant LD (16 h photoperiod including 8 h fluorescent followed by 8 h incandescent light) and the other half to constant SD (8 h fluorescent light) in SANYO 2279 controlled environment cabinets at the Phytobiology Facility for another 2 weeks (Supplementary Fig. S2). Both SANYO cabinets were set at 22 °C day and 18 °C night temperatures with 60% relative humidity and ambient CO2 concentration, and provided with a Photosynthetic Photon Flux Density (PPFD) of 100 Wm−2. Sampling was carried at 62 d at Zeitgeber time 10 (ZT10) and involved removing the middle part of the first newly expanded leaf and the middle to the basal portion of bulb, chopped into small pieces, and freezing in liquid nitrogen before storing at −80 °C. The harvested materials were used for molecular analyses.
Experiment 2: Generating materials for molecular analyses
Onion plants were grown in natural conditions in a glasshouse at the University of Warwick Phytobiology Facility but otherwise as described for experiment 1. They were grown during the period from 19th June to 6th August 2013 when daylight was 16 h 38 min to 15 h 7 min, respectively. At 48 days from sowing (DFS), the rest of the plants were divided into 3 groups, one group was transferred to constant LD, one to constant SD, using similar controlled condition as described in Experiment 1, and one group kept in NC. From 30 d, measurements of bulb and neck diameter were taken using slide callipers at weekly interval for 2 weeks and then twice a week for the rest of the growth period. Onion leaf and bulb material was harvested at ZT10 and at sampling, 3 plants were pooled together for replication using a Completely Randomised Design (CRD). Sampling removing the middle part of the first newly expanded leaf and the middle of the white basal portion of the leaf chopped into small pieces, and freezing in liquid nitrogen before storing at −80 °C. Plants were selected for harvesting using a random number generator29. The harvested materials were used for molecular analyses. ‘Bulbing ratio’ was calculated by dividing the maximum bulb diameter by the minimum neck diameter and bulb initiation was considered to have been initiated when the bulbing ratio reached a value greater than 230. Means, standard deviations and standard errors were calculated for all data points using Microsoft Excel and the significance of the differences in bulbing ratio between treatments were assessed by using factorial analysis of variance (ANOVA) with repeated measures. ANOVA was carried out using statistical software package SPSS.
Time-course experiment to study gene expression for Hojem during development
The plants were grown during the period from 17th March to 8th August 2014 in a photoperiod-controlled glasshouse compartment of the Phytobiology Facility to give 12 h daylight and provide other environmental conditions as for Renate. From 35 d, measurements of bulb and neck diameter were taken from both varieties at weekly interval throughout the growth period using slide callipers. Harvesting and sampling was carried out and stored at −80 °C. Plants were selected for harvesting using a random number generator29. The harvested materials were used for molecular analyses. ‘Bulbing ratio’ was calculated and statistical analysis was conducted.
Spatial patterns of gene expression in leaves of Renate F1
Onion plants were grown under NC in the glasshouse at the University of Warwick Phytobiology Facility during the period from 26th July to 27th September 2013 when daylight was 15 h 42 min to 11 h 52 min, respectively. Supplementary illumination with HPS lamps was provided to maintain a minimum 16 h daylength. At 61 d when plants had initiated bulbing, half of them were transferred to constant LD (16 h photoperiod including 8 h fluorescent followed by 8 h incandescent light) and the other half to constant SD (8 h fluorescent light) in SANYO 2279 controlled environment cabinets at the Phytobiology Facility for another 2 weeks. On the last day, plants were harvested at ZT10 and leaves were separated. The 5th number leaf was taken and cut into 12 pieces of 1 cm starting from the base and 6 plants were pooled together for both LD and SD conditions (Supplementary Fig. S3). The samples were immediately frozen in liquid nitrogen before storing at −80 °C. The harvested materials were used for molecular analyses.
Gene identification and isolation
Key genes, which have known functions in Arabidopsis flowering and regulate other important pathways such as sucrose and gibberellins pathways, were selected. The sequences of each gene in Arabidopsis were obtained from NCBI database (www.ncbi.nlm.nih.gov). An onion EST sequence was obtained by blasting the sequence of each gene in Arabidopsis homologs against onion database (www.ncbi.nlm.nih.gov/nucest/?term=onion). After obtaining the EST sequences, they were aligned with Arabidopsis sequences using MegAlignTM. ESTs were then used to design primers (Supplementary Table S1). From alignment information, the positions of sequence identity were obtained and primers (Forward and Reverse) for each gene amplification designed using Primer3Plus (http://www.bioinformatics.nl/cgi-bin/primer3plus/primer3plus.cgi.
RNA extraction, DNase treatment, cDNA synthesis and sequencing of PCR products
Total RNA was extracted from leaf and bulb material from onion grown under LD and SD using the Z6 buffer method, following the manufacturer’s (Roche manufacturing Ltd., Republic of Ireland) guidelines. Samples were ground using pestle and mortar and then approximately 100 mg of frozen plant tissue was homogenised using a Dremel drill. In this step, Z6 buffer reagent and b-Mercaptoethanol were added which act to remove RNase. Two extra reagents, 3 M Sodium acetate (NaOAC) and 7.5 M Lithium chloride, which remove carbohydrates and polysaccharides, respectively, were included in this method to obtain high quality RNA. After isolation, the quality and quantity of total RNA was measured with the Thermo Scientific NanoDropTM 1000 Spectrophotometer (NanoDrop Technologies, Inc., USA).
The TURBO DNA-free treatment kit (Ambion, USA) was used to eliminate the genomic DNA contamination following the manufacturer’s guidelines. A PCR was set up to check for genomic DNA contamination using primers for ALLINASE (ALL) gene and visualized on RNA gel electrophoresis. Sequencing of PCR products from genomic DNA confirmed that the primers contained no mismatches. cDNA was synthesised using 2 μg total RNA using ThermoScriptTM Reverse transcription polymerase chain reaction (RT-PCR) System (Invitrogen by Life Technologies, Cat. No. 11146-016) for RT-PCR using oligo(dT) following the manufacturer’s guidelines and subsequently treated with RNase H. PCR products were purified following PCR and agarose gel electrophoresis using QIAquick PCR Purification Kit (QIAGEN) and QIAquick Gel Extraction Kit (QIAGEN), respectively, following the manufacturer’s guidelines and samples were eluted in 30–50 µl of SDW. For gel purification, bands were cut out under UV light with a wavelength of 302 nm (Bio-Rad UV Transilluminator 2000) using a scalpel blade. A volume of 1 µl purified DNA was quantified using a NanoDrop™ ND-1000 spectrophotometer (Thermo Scientific). A total amount of 10 μl (Premix 5 μl template of 20–80 ng/μl conc. + 5 μl Primer of 5 pmol/μl conc.) purified PCR products were sent to GATC Biotech for sequencing. Sequence files were viewed and edited using the EditSeq package of DNAStar Lasergene (DNAStar Inc.). Chromatograms where analysed and interpreted using 4Peaks Chromatogram and edited using SeqManTM, SeqBuilderTM and MegAlignTM of DNAStar Lasergene (DNAStar Inc.).
Analysis of gene expression using qRT-PCR
Total RNA was extracted from 100 mg of leaf material harvested at each time point using Trizol® reagent (Invitrogen) following the manufacturer’s guidelines. Samples were DNase treated using TURBO DNA-freeTM (Ambion) and first-strand cDNA synthesized from 2 μg of total RNA using SuperscriptTM II Reverse Transcriptase (Invitrogen) following the manufacturer’s guidelines12. The expression of reference genes and genes of interest was analysed by qRT-PCR using the CFX384 TouchTM Real-time PCR machine from BioRad (Bio-Rad Laboratories Ltd. UK). For all other qRT–PCR analyses, a MESA GREEN qPCR MasterMix for SYBR® green with fluorescein (Eurogentec) was used, following the manufacturer’s guidelines. Reactions were carried out in 15 μl volumes, containing 0.5 μl of cDNA. Three replications (triplicate) were carried out for each sample and the average CT value calculated. The protocol and primer details are provided in Supplementary Tables S2–S5. The qRT-PCR data were normalised against the house keeping genes PP2AA3, PP2A1, TIP41 and UBL for each sample (Supplementary Table S3) using Biogazelle qBase+ software (www.biogazelle.com). The same housekeeping genes namely PP2A1, UBL and TIP41 were used in all the developmental time course experiments and the housekeeping genes viz. PP2AA3, UBL and TIP41 were used in all the spatial time course experiments. The significance of the differences in gene expression between treatments were assessed by using two-way analysis of variance (ANOVA). ANOVA was carried out using statistical software package Prism 7.
Daylength regulation of bulbing in onion
Plants were initially grown under natural conditions, transferred to LD or SD in controlled environment (CE) at 48 d or kept under natural LD conditions (NC). A clear visible difference was observed in bulb development between plants grown at different daylengths (Fig. 1a). At 21 days after transfer (DAT), the LD (NC) and LD (CE) plants showed increased bulb diameter, which consequently increased bulbing ratio (Fig. 1b), whereas, the plants in SD showed only a small increase in bulb diameter, and continued producing new leaves, which resulted in an increase in neck diameter. Samples from this experiment were used for gene expression analysis. From ANOVA results, it was found that LD and SD treatments were significantly different from each other and the number of days from sowing had a significant effect on bulbing ratio (Supplementary Table S6). Moreover, the interaction between days from sowing (DFS) and daylength was shown to be significant showing that the pattern of bulbing ratio during the period of development of onion is affected by daylength. Therefore, it was confirmed that bulb initiation in Renate was controlled by daylength with LD conditions stimulating the bulbing process16.
To compare the responses of the LD variety Renate with the SD variety Hojem, plants were grown in a photoperiod-controlled glasshouse compartment of PBF at 12 h daylight. A clear difference was observed in bulb development between Hojem and Renate plants (Fig. 1c). Statistical analysis also showed that bulbing ratios were significantly different between Hojem and Renate F1 varieties in response to the daylength (Supplementary Table S7). Taking a bulbing ratio of 2 as representing bulb formation, bulbing was observed in Hojem at around 104 DFS, but was not seen in Renate even at 132 DFS (Fig. 1d). This reflects the critical daylength requirement, where SD onions start making bulbs at 10 to 12 h of daylight, while temperate (LD) onion requires at least 14 h of daylight to stimulate bulbing process13. Even though 12 h daylength would be long enough for bulbing in SD varieties of onion, there was a long period (104 DFS) to bulb initiation in Hojem, compared to the time to bulbing in Renate plants grown initially in NC. This could be due to the low light integral during the early stage of plant growth in the 12 h daylength chamber compared to NC31. Samples from this experiment were used for gene expression analysis.
Gene identification and isolation
In preliminary RT-PCR experiments, the expression of the genes under study was determined in pooled samples of Renate F1 using qRT-PCR primers (Table 1). PCR products were run on a gel and showed a clear band at the right product size (Supplementary Fig. S4). All were shown to represent the expected gene through sequencing of PCR products. FT3 shared 83% identity with FT5, and these two genes were not distinguished in the qRT-PCR analysis. In the initial PCR, AcFT1 and AcFT4 mRNA bands of Renate F1 pooled sample were not clearly visible on the gel (Supplementary Fig. S4a), suggesting they were expressed at a relatively low level. However, re-amplified PCR showed clearly visible bands on the gel (Supplementary Fig. S4b). In addition, clear cDNA bands for Hojem and Renate F1 grown under 12 h daylength were also found on gel (Supplementary Fig. S4c–f).
Temporal gene expression in onion in response to LD and SD
Expression of FT genes in different daylengths
In Renate, AcFT1 was expressed in LD (NC) and LD (CE), i.e. the conditions that promoted bulbing, but not expressed in SD, where foliage leaves continued to be produced (Fig. 2a). It was observed that the level of expression of AcFT1 was significantly higher in LD (NC) than to LD (CE). Two-way ANOVA confirmed that the difference in AcFT1 expression between LD (NC), LD (CE) and SD conditions was significant (Supplementary Table S7). This result is consistent with the earlier study conducted by Lee et al. (2013), where the authors found that AcFT1 was only expressed in LD-grown plants but was not expressed in SD-grown plants. AcFT4, in contrast, was expressed in SD but was not expressed in LD (NC) or LD (CE) conditions (Fig. 2b). This result is also consistent with the previous study conducted by Lee et al. (2013), where they proposed that AcFT4 prevents AcFT1 upregulation and inhibits bulbing in transgenic onions9. Therefore, it could be confirmed that the expression of AcFT4 is negatively correlated with AcFT1.
It was also seen that AcFT4 expression was not detected during the early stages of seedling growth, even though the natural daylength was less than the critical daylength of 14 h for LD varieties. Two-way ANOVA confirmed that the difference in AcFT4 expression between LD (NC), LD (CE) and SD conditions was significant (Supplementary Table S8). It was also confirmed that the number of days from sowing had a significant effect on AcFT4 expression (Supplementary Table S9). This suggests that AcFT4 is under developmental as well as daylength regulation.
AcFT5 was strongly expressed throughout the development in LD (NC), but showed very limited expression in LD (CE) and it was not expressed in SD (Fig. 2c). The level of expression was significantly higher in LD (NC) than to LD (CE). Comparing different daylengths, the expression of AcFT5 is consistent with AcFT1, however, AcFT5 showed an interesting pattern of expression, which is different to that of AcFT1. It was observed that AcFT5 showed higher expression during early stage of growth and the expression was sharply decreased at the time of bulb formation and then sharply increaed during the rest of the bulb development period. However, this result is inconsistent with the previous study conducted by Lee et al. (2013), where the authors proposed that AcFT5 expression did not appeared to be strongly affected by daylengths9. ANOVA confirmed that the difference in AcFT5 expression between LD (NC), LD (CE) and SD conditions was significant. It was also confirmed that the number of days from sowing had a significant effect on AcFT5 expression (Supplementary Table S10).
AcFT6 was only expressed in LD (NC) but not in LD (CE) or SD conditions (Fig. 2d). In addition, the expression level of AcFT6 in LD (NC) was very low during the early stage of plant growth and was only higher immediately after bulb initiation. A limited expression of AcFT6 was found in both LD (CE) and SD conditions at the later stage of bulb development in Renate. The difference in AcFT6 expression between LD (NC), LD (CE) and SD conditions was statistically significant. It was also confirmed that the number of days from sowing had a significant effect on AcFT6 expression (Supplementary Table S11).
Expression of FT in 12 h days
In Hojem at 12 h, bulbing took place at about 104 DFS and became detectable at 118 DFS (Fig. 1c). AcFT1 showed higher levels of expression during the later stage of bulb development and maturity (Fig. 2e). The data suggest that AcFT1 induces bulb formation and development in Hojem. On the other hand, bulbing was not observed in Renate at 12 h daylength even at 132 DFS and AcFT1 showed very limited expression throughout the development period. This result is consistent with the results in the previous experiment, where AcFT1 was not expressed in Renate at 8 h daylength. Thus, AcFT1 is only expressed when the daylength is greater than 12 h in Renate, which is consistent with it having a role in the daylength dependence of bulbing. Two-way ANOVA confirmed that the difference in AcFT1 expression between Hojem and Renate F1 under 12 h daylength was significant. It was also confirmed that the number of days from sowing had a significant affect on AcFT1 expression (Supplementary Table S12).
In Hojem at 12 h, AcFT4 showed higher expression at the early stage of plant growth and was down-regulated at about the time of bulb formation (Fig. 2f). Lee et al. (2013), found that AcFT4 was expressed at relatively high levels in leaves of young seedlings under both SD and LD contions9. However, in Renate at 12 h, AcFT4 overall expression was low compared to experiment 1. AcFT4 was expressed during the later part of development and expression was up-regulated at the time when plants would generally bullb if in LD. The difference in AcFT4 expression between Hojem and Renate F1 under 12 h daylength was statistically significant (Supplementary Table S14).
AcFT5 was expressed throughout the growth and development period in both Hojem and Renate at 12 h daylight (Fig. 2g) with no significant difference found between two varieties. (Supplementary Table S15). In contrast, AcFT6 was expressed at the early stage of plant growth in Hojem, while it was expressed at the middle stage of development in Renate. (Fig. 2h). AcFT6 was down-regulated before bulb formation in Hojem and was not expressed during the rest of the bulb development. The interaction between days from sowing and variety was also shown to be statistically significant (Supplementary Table S16), showing that the expression of the AcFT6 over time is affected by daylength.
The expression of AcFT2 was also assessed in the 12 h experiment. Lee et al. (2013) proposed that FT2 was responsible for flowering but not bulbing. We were unable to detct AcFT2 in Renate but it was expressed in Hojem during the later stage of bulb development and maturity (Supplementary Fig. S5). The expression of AcFT2 is quite similar to the expression of AcFT1 in Hojem at 12 h but the functional significance of AcFT2 expression is not known. Two-way ANOVA confirmed that the variety and days from sowing had no significant effects on AcFT2 expression (Supplementary Table S13).
Expression of AcLFY and GA3Ox1
The expression of AcLFY in basal scale tissues (bulb) of Renate was assayed by qRT-PCR during development under different daylengths. AcLFY was strongly expressed in basal tissue at the early stage of plant growth and at the later stage of bulb development but was not expressed in either LD (CE) or SD conditions (Fig. 3a). Early stage expression suggest that AcLFY might be maintaining vegetative growth in the early stage under LD (NC) but it is inhibited when bulbing starts. No expression was found in any of the three conditions after bulbing had been intiated in NC. The difference in AcLFY expression between LD (NC), LD (CE) and SD conditions was significant (Supplementary Table S17).
At 12 h, AcLFY showed significantly higher expression in Hojem than Renate throughout the early growth and development, while showing very limited expression in Renate at 62 and 69 DFS (Fig. 3b). As with AcFT4, expression of AcLFY in Renate was lower in the 12 h experiment than in Experiment 1. The level of expression of this gene was lower at the early stage of development in Hojem, increased during the period of bulb initiation before reducing with the bulb development and maturity. The difference in AcLFY expression between Hojem and Renate F1 under 12 h daylength was significant (Supplementary Table S18).
In Renate, GA3ox1 was expressed in all three conditions of LD (NC), LD (CE) and SD throughout the bulb initiation and development (Fig. 3c). Data suggest that GA3ox1 was not directly involved in onion bulb initiation and development. At 12 h, GA3ox1 was expressed throughout the growth and development in both Hojem and Renate F1 (Fig. 3d). However, it was observed that the expression level was similar hroughout the growth and development in both varieties of onion.
Spatial gene expression
An experiment was performed to determine spatial expression of the genes of interest in onion. In particular, we were interested in the expression of these genes in the site of perception (green leaf) or response (basal tissues) under bulbing and non-bulbing daylegths.
Expression of FT genes
AcFT1 showed differential expression in Renate F1 leaf under LD and SD (Fig. 4a). In LD, it was expressed all throughout the green part of the leaf, although the expression was slowly increased from the transition zone to the mature green leaf tissue. In SD, the expression of AcFT1 was limited to the transitional part of the leaf and then sharply decreased in the older green tissues at the site of perception. it was observed that in both LD and SD conditions, AcFT1 was not expressed in the basal tissue i.e. the site of response in either LD or SD. The difference in AcFT1 expression between LD and SD conditions was significant as was the position of the leaf segment (Supplementary Table S19).
AcFT4 was expressed in the green part of the leaf but was not expressed in the basal tissue or transitional part of the leaf under either LD and SD conditions (Fig. 4b). However, the expression was significantly different between two daylengths, being high in SD and low in LD. This tissue-specific expression pattern of AcFT4 in SD indicates that this gene might inhibit bulb formation in Renate F1 at SD which is consistent with the previous experimental results. The difference in AcFT4 expression between LD and SD and the position of the leaf segments was significant (Supplementary Table S20).
AcFT5 was expressed throughout the leaf from the bulb through tho the oldest green tissues in both LD and SD, (Fig. 4c). However, AcFT5 showed higher level of expression in basal tissue to the transitional part than to green leaf tissue under LD, while, it showed lower level of expresssion in the basal tissue than to the green part under SD. The difference in AcFT5 expression between LD and SD conditions was not significant although the leaf segments had significant effect on AcFT5 expression and the interaction between leaf segment and daylength was also shown to be significant (Supplementary Table S21). Thus, the pattern of expression of AcFT5 the leaf segments is affected by daylength.
AcFT6 was expressed throughout the leaf from the site of perception (green part) to the site of response (basal tissue) in both LD and SD (Fig. 4d). However, AcFT6 showed higher level of expression in basal tissue then sharply decreased in the rest part of the leaf under LD In SD it showed lower levels of expresssion in the basal tissue and then showed similar level of expression to the rest of the leaf. ANOVA confirmed that the leaf segment position had a significant effect on AcFT6 expression and the interaction between leaf segment and daylength was also shown to be significant (Supplementary Table S22).
Expression of AcLFY and GA3Ox1
AcLFY was mostly expressed in basal part of the leaf (site of response) under both LD and SD conditions (Fig. 5a). This result is consistent with results in the previous experiment, where AcLFY mRNA band was only found in basal tissue under LD and SD conditions through RT-PCR. Therefore, it could be confirmed that AcLFY is a bulb tissue specific gene. However, the qRT-PCR expression of AcLFY in Renate F1 was significantly higher in bulb tissue under LD than to SD. Two-way ANOVA confirmed that both the difference in AcLFY expression between LD and SD conditions and the position of the leaf segments was significant (Supplementary Table S23). GA3ox1 was expressed throughout the leaf under both LD and SD conditions, although the level of expression was very low in the basal tissue (site of response) and slowly increased to top of the leaf (Fig. 5b). There was no significant difference found for GA3ox1 expression in either leaf or bulb tissue under LD and SD. This result suggests that the tissue specificity of expression of this gene is not dependent on daylength.
Being a biennial species, it takes more time to improve onion crops by conventional breeding methods such as hybridization, recombination and selection. Also the presence of severe inbreeding depression makes it difficult to produce and maintain a large number of near homozygous inbred lines ideal for genetic linkage and analysis2,32,33. Daylength sensitivity places a significant barrier to onion breeding programmes as a trait in a particular daylength group cannot be transferred to another daylength group by cross breeding because the specific daylength response of the progeny will be unknown. In addition, crossing onions with different daylength requirements is difficult, as the progeny will be compromised. In comparison to the knowledge gained regarding photoperiodic regulation of flowering, relatively little is known about genetic regulation of bulbing process and only a small number of quantitative genes with easily visible effects have been described in onion2,9,12,34.
The main aim of this work was to gain a better understanding of the molecular regulation of bulbing in response to daylength and specifically to test whether the molecular regulation involved genes controlling flowering by daylength in Arabidopsis. To test this hypothesis, a series of physiological and molecular experiments were carried out throughout the project. The results obtained suggest that a few genes identified and isolated in onion such as AcFT1, AcFT4, AcFT5, AcFT6, AcLFY and AcGA3ox1 were potentially involved in daylength control of bulb formation and support the concept that bulb formation in response to daylength is similar to the daylength regulation of flowering in Arabidopsis.
Daylength regulation of bulbing in onion
Bulb formation in temperate onions is daylength-dependent and LD of at least 14 h of light are required to stimulate bulb initiation8,10,13. Therefore, the objectives of this study were to optimise the experimental conditions for daylength-dependent bulb initiation in onion by a comprehensive set of developmental time-course experiments and to generate materials for molecular analyses. In an initial time-course experiment, it was observed that onions form bulbs (measured by bulbing ratio) around 48 DFS when daylength extends beyond 14 h. The leaf and bulb materials obtained from this experiment were used for molecular analyses. Based on the timing of the bulb response, in the later experiment in Renate F1 shown that the bulbing ratio increased in plants kept in LD (NC) or transferred to LD (CE) at the time that bulbing was just beginning, but not in those transferred to SD at that time. Statistical analysis also supports this result. This confirmed that bulb initiation was controlled by daylength and LD conditions with fourteen to sixteen hours of light stimulating the bulbing process in Renate F116. The onion plants grown under LD (NC) produced larger sized bulbs than those grown in LD (CE) which is probably due to the higher light levels and longer days in the glasshouse in mid summer, both of which have been shown to accelerate bulb formation35. The light quantities used under each daylength conditions in this experiment are shown in Supplementary Fig. S6. Light quality also has a major effect on bulb initiation36 with high far-red or far-red to red ratios being promotive and thought to be mediated by Phytochrome A. Blue light, to a lesser extent, also controls bulb initiation37. It seems that light quality has a more pronounced effect on bulb initiation in onion. Under natural conditions, light will contain both far-red and blue light and thus daylength will be the limiting factor controlling bulb initiation in LD onions16. This allows for a seasonal response, bulbing being initiated when the days get longer in the spring in the UK and allows for rapid bulb development under favourable environmental conditions e.g. warm temperatures and high irradiance during early to mid summer. The reason behind the delay in measurable bulb formation could be because bulb scales form quite quickly but the scales expand slowly38.
In ID (12 h daylength) conditions, it was observed that the SD variety Hojem forms bulbs at around 104 DFS, while Renate F1 did not form any bulbs even at 132 DFS. Statistical analysis also supports this result. The daylength requirement for onion bulb formation varies with the type of cultivar, ranging from 10 to 16 hours39. The adaptation to a certain production area depends largely on adaptation to daylength through the daylength requirement of the specific cultivar40. Therefore, the daylength at a specific production area or latitude at the time of bulb initiation will influence on the selection of onion cultivars. Even though a 12 h daylength would be long enough to promote bulbing in SD varieties of onion, there was a long period of time (104 DFS) to bulb initiation in Hojem, compared to the time to bulbing in Renate F1 plants grown initially in NC. This delay could be due to the reduced light integral during the early stage of plant growth in the 12 h daylength chamber compared to NC31. In addition, the slow increase of bulbing ratio in Renate F1 under SD or delay in bulb initiation in Hojem at 12 h could be due the accumulation of an inhibitor of bulb formation in SD conditions or at constant 12 h, so that plants would then take a longer time to initiate bulbs, as the inhibitor would have to be degraded. It is not surprising that sometimes, onions sown in springtime fail to complete bulb formation and they revert to leaf blade production, resulting in thick-necked plants. It was also clearly observed that following bulb initiation in Hojem, bulbs grew more rapidly in plants that had bulbed later than earlier bulbing ones. This might be due to the age of plants, which has been shown to affect the rate of bulb formation41. Statistical analysis also showed that bulbing ratios were significantly different between Hojem and Renate varieties in response to the daylength and the age of the plants (Supplementary Table S7).
Temporal gene expression in onion in response to daylength
Onion is a biennial plant, where bulb formation, being an overwintering stage2 occurs in the first year and flowering occurs following a period of vernalisation11 in the second year. Therefore, a question arises of which genes are involved in the photoperiodic flowering pathway and which are involved in onion bulbing16. It was clearly observed that onions initiate bulbing under inductive daylengths in the first year, when flowering is inhibited, suggesting that bulb formation and not floral initiation is the daylength response2,8,12. Previous reports also revealed that FT is a target of CO42 and has been shown to be the major component of the floral signal molecule, florigen and thus can induce flowering by long-distance transportation to the apical meristem with the help of other floral homeotic genes like LFY19,20,21,22. At the physiological level, bulb initiation in onion is very similar to the floral initiation in Arabidopsis20. Thus, FT, which is the mobile signal controlling flowering in Arabidopsis21,43. could control bulb initiation in onion16. The experimental hypothesis is that, if FT genes regulate bulbing, their expression should be correlated with bulb formation under a range of conditions and in different response types. For genes involved in daylength sensing, they should be related to the bulbing response e.g. present in the sites of daylength perception, but independent of the bulbing process. To test this hypothesis, this study focused on the quantitative gene expression analysis in different response types of onion under a range of bulbing and non-bulbing conditions.
FT genes have been shown to act as long distance signals mediating resposnses to daylength in a range of species. In Renate F1, we were able to confirm the presence of six sequences as published by Lee et al.9. They proposed that FT1 promoted bulb formation, whereas FT4 inhibited it. We tested this hypothesis by looking at FT gene expression in a range of conditions. If FT1 was correlated bulbing in response to daylength, we would expect that it would be expressed at higher levels in LD than SD in the site of perception. The data we obtained by quantitative PCR was consistent with this prediction.
During development, FT1 was expressed in LD at all stages in Renate, including the early stages, prior to the onset of bulbing but not expressed in SD. In addition, AcFT1 showed significantly higher expression in LD (NC) than in LD (CE). This could be due to the much higher light level in LD (NC) during the summer compared to the LD (CE) chamber31. However, transfer of plants to SD when bulbing initiated resulted in expression being repressed. Some expression of FT1 was detected in the transition zone in SD. FT1 is proposed to travel from the leaf to the apex as part of the supply of assimilates from photosynthesising, i.e. exporting tissues. It is likely that the transition tissue acts as a sink and does not supply assimilates to the apex. FT1 expressed in these tissues may thus be inactive for bulbing. AcFT1 showed very high expression in Hojem during the later stage of bulb development and maturity, but showed very limited, or no, expression in Renate F1 at 12 h throughout development. This result could also be suppported by a previous study in A. cepa, where the authors proposed that AcFT1 was down-regulated in the early maturity line under both SD and LD conditions (Manoharan et al., 2016). Overall, the expression characteristics are consistent with FT1 promoting bulbing in onions9. In contrast, when Renate F1 plants were transferred from LD to SD during development, AcFT4 was only expressed in SD which might inhibit bulb formation but was not expressed in either LD (NC) or LD (CE) and AcFT4 expression was upregulated at the same time that bulbing was inhibited. These results are also supported by the previous studies, where the authors proposed that AcFT1 promotes bulb formation, while, AcFT4 down-regulates the expression of AcFT1, hence inhibits bulb formation in onion9,44. It could be confirmed that the expression of AcFT1 is negatively correlated with AcFT4.
The expression pattern in Hojem differed from that in Renate F1 in that AcFT4 was expressed during early development in ID, and decreased during bulbing, which may indicate that the function of this gene has diverged in different daylength types. The data suggest that AcFT4 might inhibit bulb formation in Hojem at the early stage of growth or during the juvenile phase by suppressing AcFT1. In certain tree species, it was reported that the juvenile phase has been shortened by the overexpression of the FLOWERING LOCUS T (FT) gene25. Down-regulation of AcFT4 in Hojem during bulb initiation and development could be due to the suppression by, or strong expression of, AcFT1. On the other hand, up-regulation of AcFT4 might down-regulate the expression of AcFT1 in Renate F1 under ID conditions. Therefore, the temporal expression patterns of FT1 and FT4 genes in two different onion cultivars in response to daylengths suggest that these genes might be negatively co-ordinated with each other. Lee et al. (2013) proposed that two antagonistic FT-like genes regulate bulb initiation, where AcFT1 promotes bulb formation, while AcFT4 prevents upregulation of AcFT1 and inhibits bulbing in transgenic onions9. These results could also be supported by the previous studies in sugar beet, where a similar regulatory pathway has evolved and was found that two FT genes with opposite expression profiles functions antagonistically for control of flowering45,46. The negative co-ordination of FT with DORMANCY ASSOCIATED MADS-BOX (DAM) was observed in leafy spurge (Euphorbia esula L.), where it was found that DAM proteins potentially controls dormancy transition and maintenance by negatively regulating the expression of FT47. FT also shows further inhibitory role in plants, where it controls seed dormancy through the inhibition of proanthocyanidin synthesis in fruits and thus altered the seed coat tannin content48.
The expression of AcFT2 was similar to that of AcFT1 in ID conditions. It might be speculated that both AcFT1 and AcFT2 induce bulb formation and development in Hojem although previous studies produced no evidence that AcFT2 has a role in bulb formation but found it was a flower promoting gene9.
AcFT5 showed an interesting pattern of expression in Renate F1 under different daylengths. Like AcFT1, AcFT5 showed a significantly higher level of expression in LD (NC) than in LD (CE). This could also be due to the sufficient light level in LD (NC) during the summer compared to the LD (CE) chamber31. AcFT6 expression was different from that of the other FTs and only appeared in LD (NC). It has been demonstrated that FT is rapidly upregulated in Arabidopsis and other plants, when plants are shifted from non-inductive conditions to an inductive photoperiod21,49. AcFT5 might not be involved in the bulb induction process itself in either Hojem or Renate F1 under ID conditions. AcFT6 was expressed at the early stage of plant growth in Hojem, while it was expressed at the middle stage of development in Renate F1 at 12 h. However, these results are incosistent with the previous study of Lee et al. (2013), where the authors suggest that the expression of AcFT5 and AcFT6 were similar at the three stages (young, mature and bulb) of development and did not appear to be affected by daylength9. Further work is required to understand the roles of these genes.
LFY and GA3ox1
In this study, our hypothesis was that if LFY or GA3ox1 were involved in bulb formation in response to daylength it would be reflected in their patterns of expression. In Renate F1, AcLFY was strongly expressed in bulb tissue under LD (NC) at the early stage of plant growth and at the later stage of bulb development but was not expressed in either LD (CE) or SD conditions suggested that this gene causes the plant to be less sensitive to environmental signals at this time50. Therefore, AcLFY might need AcFT1 to correlate onion bulbing process in LD. This could be supported by the role of LFY in Arabidopsis, which triggers the expression of the floral homeotic genes at the floral apical meristem and causes flowering51, whereas, in onion, the apex is present at the base of plant (bulb). Disappearance of its expression after bulb formation in all three conditions could be due to suppression by other genes like FLOWERING LOCUS C (FLC), which is a negative repressor for autonomous pathways in Arabidopsis20. As there is a small increase in bulbing ratio, even in the SD treatment, it may suggest AcLFY may be involved in maintaining vegetative development. Re-emergence of AcLFY in LD (NC) at bulb maturity suggests that this gene might also play an important role in maintaining the apical meristem after bulb development and prior to flowering. In addition, the strong expression of AcLFY in Hojem leaf tissue under ID throughout development suggests that it might play a significant role in bulb development irrespective of onion varieties. This is supported by previous studies that reported LFY is expressed widely in both vegetative and reproductive tissues in a range of higher plants, and plays an important role in promoting flower formation by mutual interaction and coordination in a complex network with other genes such as TFL, AP1, AP2, FT, AP3, CO, and GA152,53.
GA3ox1, on the other hand was expressed in Renate F1 under all three daylengths as well as all throughout the development in both Hojem and Renate F1 at 12 h, suggesting that this is daylength insensitive irrespective of onion cultivars and might not directly be involved in onion bulb formation. Gibberellin was successful to promote flowering in Arabidopsis (A. thaliana) through the activation of the promoter of the floral integrator gene LFY54 and is also involved in onion flowering55. Previous studies showed that an inhibitor of gibberellin biosynthesis promotes bulbing in non-inductive photoperiods which suggests an inhibitory role in bulb initiation55,56. Therefore, it can be speculated that there is a crossover between the genetic control of flowering and bulbing in onion. Although the role of GA has not been fully characterised in onion, it was clearly shown that GA3ox1 was strongly expressed in the green part of the leaf, which is the site of perception. It may be that there are other members of the gene family in onion, one or more of which might be related to the bulb response. This could be supported by previous studies, where four GA3ox genes were identified in Arabidopsis, each of which exhibits a unique organ-specific expression pattern; suggesting individual AtGA3ox member played a distinct developmental roles57,58.
Spatial gene expression in onion in response to daylength
As monocotyledon leaves develop from a basal meristem, during leaf growth, cells move through the basal region into a transition zone and then into the green, photosynthesising part of the leaf. The photosynthetic and basal parts of the leaf can be considered as the sites of perception and response, respectively. By looking at the expression of genes at different points along the length of the leaf, it is possible to determine the extent to which their expression correlates with the different functional regions and also give a picture of how expression changes in cells of increasing age. Both AcFT1 and AcFT4 genes showed tissue specific expression pattern under either LD or SD conditions. However, the results suggest that the both AcFT1 and AcFT4 genes were expressed differently under LD and SD but produced in the same leaf tissue.
It was also observed that AcFT4 expression pattern in Renate F1 leaf was opposite to that of AcFT1 in both LD and SD conditions., supporting the idea that AcFT4 is negatively correlated with AcFT1. AcFT5 and AcFT6 were expressed throughout the leaf from the site of perception (green tissue) to the site of response (basal tissue) in both LD and SD. Statistical analysis revealed that the interaction of AcFT5 and AcFT6 expression in leaf tissue was significantly different when grown under LD compared to that of the SD conditions, indicating that their spatial expression pattern is affected by daylength. These results could support a role for these genes in onion bulb formation but this would need to be confirmed by functional analysis of their roles.
AcLFY showed mostly bulb-specific expression pattern in both LD and SD conditions. Statistical analysis also supports these results. This is because LFY causes a group of undifferentiated cells named meristems to develop into flowers instead of leaves associated with shoots59,60,61,62,63,64,65,66,67. GA3ox1 expression was present everywhere in the leaf tissue from the site of perception (green tissue) to the site of response (basal tissue) under both LD and SD conditions, suggesting no tissue specific expression pattern of this gene.
Brewster, J. L. Onions and Other Vegetable Alliums (1st ed.). Wallingford, UK: CAB International. 16. 2 (1994).
Brewster, J. L. Onions and Other Vegetable Alliums. In Crop Production Science in Horticulture Series, 2nd, ed. (CABI) (2008).
McCallum, J., Leite, D., Pither-Joyce, M. & Havey, M. J. Expressed sequence markers for genetic analysis of bulb onion (Allium cepa L.). Theoretical and Applied Genetics. 103, 979 (2001).
Mathew, B. A Review of Allium section Allium (Royal Botanic Gardens, Kew, UK) (1996).
FAO. Crop production data. FAOSTATFood and Agriculture Organization of the United Nations, Rome, available online at, http://faostat3.fao.org/faostat-gateway/go/to/download/Q/*/E (2018).
Bosch Serra, A. D. & Casanova, D. Estimation of onion (Allium cepa L.) biomass and light interception from reflectance measurements at field level. Acta Horticulturae. 519 (1979).
Brewster, J. L. Physiology of Crop Growth and Bulbing. In Onions and Allied Crops, Volume I: Botany, Physiology, and Genetics, Rabinowitch, H. D. & Brewster, J. L. eds (Boca Raton: CRC Press), 53–88 (1990).
Lancaster, J. E., De Ruiter, J. M., Triggs, C. M. & Gandar, P. W. Bulbing in onions: Photoperiod and temperature requirements and prediction of bulb size and maturity. Annals of Botany. 78, 423 (1996).
Lee, R., Baldwin, S., Kenel, F., McCallum, J. & Macknight, R. FLOWERING LOCUS T genes control onion bulb formation and flowering. Nature communications. 4, 2884 (2013).
Okporie, E. O. & Ekpe, I. I. Effect of photoperiod on the growth and bulbing of two tropical onion (Allium cepa L.) varieties. Journal of Agricultural Science. 4, 36–39 (2008).
Brewster, J. L. Environmental physiology of the onion: towards quantitative models for the effects of photoperiod, temperature and irradiance on bulbing, flowering and growth. Acta Horticulturae. 433, 347–373 (1997).
Taylor, A., Massiah, A. J. & Thomas, B. Conservation of Arabidopsis thaliana photoperiodic flowering time genes in onion (Allium cepa L.). Plant and Cell Physiology. 51, 1638–1647 (2010).
Mettananda, K. A. & Fordham, R. The effects of 12 and 16 hour daylength treatments on the onset of bulbing in 21 onion cultivars (Allium cepa L) and its application to screening germplasm for use in the tropics. Journal of Horticultural Science and Biotechnology. 72, 981 (1997).
Lercari, B. Role Of Phytochrome In Photoperiodic Regulation Of Bulbing And Growth In The Long Day Plant Allium cepa. Physiologia Plantarum. 60, 433–436 (1984).
Sobeih, W. Y. & Wright, C. J. The Photoperiodic Regulation Of Bulbing In Onions (Allium cepa L) Response To Red-Far-Red Ratio And Cyclic Lighting. Journal of Horticultural Science. 62, 379–389 (1987).
Taylor, A. Functional Genomics of Photoperiodic Bulb Initiation in Onion (Allium cepa) (Warwick HRI: the University of Warwick), 255 (2009).
Kardailsky, I. et al. Activation tagging of the floral inducer FT. Science. 286, 1962–1965 (1999).
Kobayashi, Y., Kaya, H., Goto, K., Iwabuchi, M. & Araki, T. A pair of related genes with antagonistic roles in mediating flowering signals. Science. 286, 1960–1962 (1999).
Andres, F. & Coupland, G. The genetic basis of flowering responses to seasonal cues. Nature Reviews Genetics. 13, 627–639 (2012).
Thomas, B., Carre, I. & Jackson, S. Photoperidism and flowering. In Jordan, B. R. [ed.], The Molecular Biology and Biotechnology of Flowering, CAB International (2006).
Corbesier, L. et al. FT protein movement contributes to long-distance signaling in floral induction of Arabidopsis. Science. 316, 1030–1033 (2007).
Purwestri, Y. A., Ogaki, Y., Tamaki, S., Tsuji, H. & Shimamoto, K. The 14-3-3 protein GF14c acts as a negative regulator of flowering in rice by interacting with the florigen Hd3a. Plant and Cell Physiology. 50, 429–438 (2009).
Bohlenius, H. et al. CO/FT regulatory module controls timing of flowering and seasonal growth cessation in trees. Science 312, 1040–1043 (2006).
Hsu, C. Y. et al. FLOWERING LOCUS T duplication coordinates reproductive and vegetative growth in perennial poplar. Proceedings of the National Academy of Sciences of the United States of America. 108, 10756–10761 (2011).
Hsu, C. Y., Liu, Y., Luthe, D. S. & Yuceer, C. Poplar FT2 shortens the juvenile phase and promotes seasonal flowering. The Plant Cell. 18, 1846–1861 (2006).
Danilevskaya, O. N., Meng, X., McGonigle, B. & Muszynski, M. G. Beyond flowering time: pleiotropic function of the maize flowering hormone florigen. Plant Signal Behaviour. 6, 1267–1270 (2011).
Lifschitz, E. et al. The tomato FT ortholog triggers systemic signals that regulate growth and flowering and substitute for diverse environmental stimuli. Proceedings of the National Academy of Sciences of the United States of America. 103, 6398–6403 (2006).
Navarro, C. et al. Control of flowering and storage organ formation in potato by FLOWERING LOCUS T. Nature. 478, 119–122 (2011).
Haahr, M. Random Integrator Generator. [online]. Available at, http://www.random.org/integers/ (2006)
Clark, J. E. & Heath, O. V. S. Studies in the Physiology of the Onion Plant: V. An investigation into the growth substance content of bulbing onions. Journal of Experimental Botany. 13, 227–249 (1962).
Thomas, B. & Vince-Prue, D. Photoperiodism in Plants, Second edn (Academic Press Limited, 24–28 Oval Road, London NW1 7DX, UK) (1997).
Lawande, K. E. et al. Onion and garlic research in India. The Journal of Horticultural Science. 4, 91–119 (2009).
McCallum, J. et al. AlliumMap-A comparative genomics resource for cultivated Allium vegetables. BMC Genomics. 13, 168 (2012).
Osterlund, M. T. & Paterson, A. H. Applied plant genomics: the secret is integration. Current Opinion in Plant Biology. 5, 141–145 (2002).
Wright, C. J. & Sobeih, W. Y. The Photoperiodic Regulation Of Bulbing In Onions (Allium cepa L.). 1. Effects Of Irradiance. Journal of Horticultural Science. 61, 331–335 (1986).
Austin, R. B. Bulb formation in onions as affected by photoperiod and spectral quality of light. Journal of Horticultural Science. 47, 493–504 (1972).
Terabun, M. Studies on the bulb formation in onion plants. I. Effects of light quality on the bulb formation and growth. Journal of the Japanese Society for Horticultural Science. 34, 52–60 (1965).
Heath, O. V. S. & Hollies, M. A. Studies in the Physiology of the Onion Plant: VI. A sensitive morphological test for bulbing and its use in detecting bulb development in sterile culture. Journal of Experimental Botany. 16, 128–144 (1965).
van den Berg, A.A., de Wet, H. & Coertze, A. F. Onion cultivars. Onions C.1. (Agricultural Research Council, Vegetable and Ornamental Plant Institute, Pretoria, South Africa) (1997).
Wiles, G. C. The feect of light and temperature on bulb initiation in tropical cultivars of onion (Allium cepa L.) (1989).
Sobeih, W. Y. & Wright, C. J. The Photoperiodic Regulation Of Bulbing In Onions (Allium cepa L). 2. Effects Of Plant-Age And Size. Journal of Horticultural Science. 61, 337–341 (1986).
Suarez-Lopez, P. et al. CONSTANS mediates between the circadian clock and the control of flowering in Arabidopsis. Nature. 410, 1116–1120 (2001).
Jaeger, K. E. & Wigge, P. A. FT Protein Acts as a Long-Range Signal in Arabidopsis. Current Biology. 17, 1050–1054 (2007).
Manoharan, R. K. et al. Molecular and Functional Characterization of FLOWERING LOCUS T Homologs in Allium cepa. Molecules 21, 217 (2016).
Pin, P. A. & Nilsson, O. The multifaceted roles of FLOWERING LOCUS T in plant development. Plant, Cell and Environment. 35, 1742–1755 (2012).
Pin, P. A. et al. An antagonistic pair of FT homologs mediates the control of flowering time in sugar beet. Science. 330, 1397–1400 (2010).
Hao, X., Chao, W., Yang, Y. & Horvath, D. Coordinated Expression of FLOWERING LOCUS T and DORMANCY ASSOCIATED MADS-BOX-Like Genes in Leafy Spurge. PloS one 10, e0126030 (2015).
Chen, M. et al. Maternal temperature history activates FlLOWERING LOCUS T in fruits to control progeny dormancy according to time of year. Proceedings of the National Academy of Sciences of the United States of America. 111, 18787–18792 (2014).
Laurie, R. E. et al. The Medicago FLOWERING LOCUS T homolog, MtFTa1, is a key regulator of flowering time. Plant physiology 156, 2207–2224 (2011).
Weigel, D. & Nilsson, O. A developmental switch sufficient for flower initiation in diverse plants. Nature. 377, 495–500 (1995).
Yoo, S. K. et al. CONSTANS activates SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 through FLOWERING LOCUS T to promote flowering in Arabidopsis. Plant Physiology. 139, 770–778 (2005).
Siriwardana, N. S. & Lamb, R. S. The poetry of reproduction: the role of LEAFY in Arabidopsis thaliana flower formation. The International journal of developmental biology. 56, 207–221 (2012).
Wang, L. L., Liang, H. M., Pang, J. L. & Zhu, M. Y. Regulation network and biological roles of LEAFY in Arabidopsis thaliana in floral development. Yi chuan = Hereditas/Zhongguo yi chuan xue hui bian ji. 26, 137–142 (2004).
Blazquez, M. A., Green, R., Nilsson, O., Sussman, M. R. & Weigel, D. Gibberellins promote flowering of Arabidopsis by activating the LEAFY promoter. Plant Cell. 10, 791–800 (1998).
Rabinowitch, H. D. Physiology of Flowering. In Onions and Allied Crops, Volume I: Botany, Physiology, and Genetics, Rabinowitch, H. D. & Brewster, J. L., eds (Boca Raton: CRC Press), 151–160 (1990).
Mita, T. & Shibaoka, H. Effects of S-3307, an Inhibitor of Gibberellin Biosynthesis, on Swelling of Leaf Sheath Cells and on the Arrangement of Cortical Microtubules in Onion Seedlings. Plant and Cell Physiology. 25, 1531–1539 (1984).
Williams, J., Phillips, A. L., Gaskin, P. & Hedden, P. Function and substrate specificity of the GIBBERELLIN 3BETA-HYDROXYLASE encoded by the Arabidopsis GA4 gene. Plant Physiology. 117, 559–563 (1998).
Yamaguchi, S., Smith, M. W., Brown, R. G., Kamiya, Y. & Sun, T. Phytochrome regulation and differential expression of GIBBERELLIN 3BETA-HYDROXYLASE genes in germinating Arabidopsis seeds. The Plant Cell. 10, 2115–2126 (1998).
Weigel, D., Alvarez, J., Smyth, D. R., Yanofsky, M. F. & Meyerowitz, E. M. LEAFY controls floral meristem identity in Arabidopsis. Cell. 69, 843–859 (1992).
Friesen, N., Fritsch, R. & Nlattner, F. R. Phylogeny and new intrageneric classification of Allium (Alliaceae) based on nuclear ribosomal DNA ITS sequences. Paper presented at: Proceedings of the Third International Conference on the Comparative Biology of the Monocotyledons (Rancho Santa Ana Botanic Garden, Claremont, California) (2006).
Fritsch, R. M. & Friesen, N. Evolution, Domestication & Taxonomy. In Allium Crop Science: Recent Advances, Rabinowitch, H. D. & Currah, L. eds (Oxon: CABI Publishing), 5–30 (2002).
Eady, C. C. Towards the transformation of onion (Allium cepa L.). New Zealand Journal of Crop and Horticultural Science. 23, 239–250 (1995).
Mettananda, K. A. & Fordham, R. The effects of plant size and leaf number on the bulbing of tropical short-day onion cultivars (Allium cepa L.) under controlled environments in the United Kingdom and tropical field conditions in Sri Lanka. Journal of Horticultural Science and Biotechnology. 74, 622–631 (1999).
Mondal, M. F., Brewster, J. L., Morris, G. E. L. & Butler, H. A. Bulb Development in Onion (Allium cepa L.) II. The Influence of Red: Far-red Spectral Ratio and of Photon Flux Density. Annals of Botany. 58, 197–206 (1986).
Garner, W. W. & Allard, H. A. Effect on the relative length of day and night and other factors of the environment on growth and reproduction in plants. Journal of Agricultural Research. 18, 553–606 (1920).
Heath, O. V. S. & Holdsworth, M. Morphogenic factors as exemplified by the onion plant. Symposium Society Experimental Biology. 2, 326–350 (1948).
Jackson, S. D. Plant responses to photoperiod. The New Phytologist. 181, 517–531 (2009).
The authors are pleased to thank the Chancellors’ International Scholarship/Midland Integrative Biosciences Training Partnership (MIBTP) Programme, The University of Warwick, Coventry, CV4 7AL, UK, and Medical and Life Sciences (MLS) Research Fund, University of Warwick Sciences Park, Sir William Lyons Road, Coventry, CV4 7EZ, UK for funding this research. The nucleotide sequences reported in this paper have been submitted to NCBI database (NCBI, 2016) with Accession Numbers (KY072880, KY072874, KY072882, KY072881, JX275963, AB303422).
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Rashid, M.H.A., Cheng, W. & Thomas, B. Temporal and Spatial Expression of Arabidopsis Gene Homologs Control Daylength Adaptation and Bulb Formation in Onion (Allium cepa L.). Sci Rep 9, 14629 (2019). https://doi.org/10.1038/s41598-019-51262-1