Skip to main content
Download PDF

Isolation and functional characterization of JcFT, a FLOWERING LOCUS T (FT) homologous gene from the biofuel plant Jatropha curcas

BMC Plant Biology volume 14, Article number: 125 (2014) Cite this article

Abstract

Background

Physic nut (Jatropha curcas L.) is a potential feedstock for biofuel production because Jatropha oil is highly suitable for the production of the biodiesel and bio-jet fuels. However, Jatropha exhibits low seed yield as a result of unreliable and poor flowering. FLOWERING LOCUS T (FT) –like genes are important flowering regulators in higher plants. To date, the flowering genes in Jatropha have not yet been identified or characterized.

Results

To better understand the genetic control of flowering in Jatropha, an FT homolog was isolated from Jatropha and designated as JcFT. Sequence analysis and phylogenetic relationship of JcFT revealed a high sequence similarity with the FT genes of Litchi chinensis, Populus nigra and other perennial plants. JcFT was expressed in all tissues of adult plants except young leaves, with the highest expression level in female flowers. Overexpression of JcFT in Arabidopsis and Jatropha using the constitutive promoter cauliflower mosaic virus 35S or the phloem-specific promoter Arabidopsis SUCROSE TRANSPORTER 2 promoter resulted in an extremely early flowering phenotype. Furthermore, several flowering genes downstream of JcFT were up-regulated in the JcFT-overexpression transgenic plant lines.

Conclusions

JcFT may encode a florigen that acts as a key regulator in flowering pathway. This study is the first to functionally characterize a flowering gene, namely, JcFT, in the biofuel plant Jatropha.

Background

Physic nut (Jatropha curcas L.) is a perennial plant that belongs to the Euphorbiaceae family, and is monoecious with male and female flowers borne on the same plant within the same inflorescence [1]. The potential benefit of growing Jatropha as a cash crop for biofuel in tropical and sub-tropical countries is now widely recognized [2–4]. Jatropha has been propagated as a unique and potential biodiesel plant owing to its multipurpose value, high oil content, adaptability to marginal lands in a variety of agro-climatic conditions, non-competitiveness with food production, and high biomass productivity [2, 5]. The oil content of Jatropha seeds and the kernels ranges from 30% to 50% and 45% to 60% by weight, respectively. Oil from Jatropha contains high levels of polyunsaturated fatty acids, and it is therefore suitable as a fuel oil [6, 7]. However, the potential of Jatropha as a biofuel plant is limited by its low seed production. Despite the clear evidence of the abundant biomass generated by Jatropha, it is not indicative of high seed productivity [8]. There are too many vegetative shoots in Jatropha, which could develop into reproductive shoots under suitable conditions. It is therefore imperative to reduce undesired vegetative growth. In addition to these considerations, unreliable and poor flowering are important factors that contribute to low seed productivity in Jatropha [9]. The FLOWERING LOCUS T (FT) gene plays a crucial role in the transition from vegetative growth to flowering, which is a potent factor integrating the flowering signals. In this context, the function of JcFT, an FT homolog in Jatropha, was analyzed to improve the understanding of the flowering mechanism in Jatropha, which will be critical for the genetic improvement of this species.

The transition from vegetative to reproductive growth in plants is regulated by both environmental and endogenous cues [10]. The genetic network of flowering has been investigated primarily in the model plant Arabidopsis, and five major genetically pathways control flowering initiation: the photoperiod, vernalization, gibberellin, autonomous and age pathways [11]. Recent advances in transgenic plants and traditional grafting studies have revealed that FT protein acts as a mobile flowering signal, whose ability to induce flowering involves long-distance transport [12, 13]. The findings of many studies have helped establish the role of FT as a floral pathway integrator that respond to both environmental and endogenous flowering signals [14].

In Arabidopsis, FT is expressed in leaf phloem, and the FT protein subsequently moves to the shoot apex, where it forms a complex with the basic domain/leucine zipper protein FD. This FT/FD heterodimer activates the downstream floral meristem identity gene APETALA1 (AP1) [12, 15, 16]. FT-like genes have been isolated from many plants, including tomato [17], pumpkin [18], rice [19], barley [20], grape [21], apple [22], and potato [23], and the function of most FT genes is conserved [24].

In this study, we cloned and characterized the Jatropha FT homolog, JcFT. We also analyzed the function of JcFT in floral induction using transgenic Arabidopsis and Jatropha.

Results

Cloning and sequence analysis of JcFT

A combined reverse transcriptase-polymerase chain reaction (RT-PCR) and rapid-amplification of cDNA ends (RACE) strategy was used to isolate an FT-like cDNA from Jatropha. JcFT cDNA (GenBank accession no. KF113881) encoded a 176-amino acid protein with 89%, 83%, 80%, and 78% sequences identity with Litchi chinensis LcFT [25], Citrus unshiu CiFT [26], rice Hd3a [27], and Arabidopsis FT [28], respectively. The molecular weight and isoelectric point of the deduced protein were 20.03 kDa and 6.82, respectively.

The genomic sequence of JcFT consisted of four exons, which resembles the genomic structure of other FT genes (Figure 1A). A multiple alignment was performed using the JcFT sequence and the sequences of FT homologs from other species (Figure 1B). The conserved key amino acid residue Tyr (Y) found in FT homologs was identified at position 85 of the JcFT protein (Figure 1B). JcFT also contained two highly similar sequences to Arabidopsis FT in the 14-AA stretch known as “segment B” and in the LYN triad in “segment C” [29] (Figure 1B).

Figure 1
figure1

Comparison of JcFT and other FT -like genes. (A) Gene structures of JcFT, Hd3a, and AtFT. Boxes indicate exons and thin lines indicate introns. Exon sizes are indicated above each box. (B) Sequence alignment of amino acid sequences. Identical amino acid residues are shaded in black, and similar residues are shaded in gray. Dots denote gaps. Boxes indicating the 14-amino-acid stretch (segment B) and the LYN triad (segment C), and "Y" indicating the highly conserved amino acid Tyr (Y).

Full size image

A phylogenetic tree was constructed to analyze the phylogenetic relationship between JcFT and the FTs from other angiosperms (Figure 2). The analysis revealed that the JcFT protein (indicated with a red-boxed) was more closely related to the FTs of perennial woody plants such as Litchi chinensis, instead of annual herbaceous plants such as Arabidopsis.

Figure 2
figure2

Phylogenetic analysis of the FT homologs from different plant species. Species abbreviations: At, Arabidopsis thaliana; Ci, Citrus unshiu; Cp, Carica papaya; Cs, Cucumis sativus; Fc, Ficus carica; Gh, Gossypium hirsutum; Gt, Gentiana triflora; Jc, Jatropha curcus; Lc, Litchi chinensis; Lt, Lolium temulentum; Md, Malus domestica; Os, Oryza sativa; Phm, Phyllostachys meyeri; Pm, Prunus mume; Pn, Populus nigra; Pp, Prunus persica; Rc, Rosa chinensis; Sl, Solanum lycopersicum; Ta, Triticum aestivum.

Full size image

Expression pattern of JcFT in Jatropha

To assess the expression pattern of JcFT in Jatropha, we performed a quantitative RT-PCR (qRT-PCR) analysis using the specific primers listed in Table S1. JcFT was expressed in all adult plants tissues except young leaves (Figure 3). Interestingly, JcFT was primarily expressed in the reproductive organs rather than the leaves, where expression of a florigen-encoding gene is expressed (Figure 3).

Figure 3
figure3

Expression of JcFT in various organs of three-year-old adult Jatropha . The qRT-PCR results were obtained from two independent biological replicates and three technical replicates for each sample. The levels of detected amplicons were normalized using the amplified products of the JcActin1. The mRNA level in the root tissue was set as the standard with a value of 1.

Full size image

Constitutive overexpression and phloem-specific expression of JcFT in Arabidopsis induces early flowering and complements the ft-10mutant phenotype

To determine whether JcFT is involved in the regulation of flowering time, JcFT cDNA driven by the constitutive cauliflower mosaic virus 35S (CaMV 35S) promoter or the phloem-specific Arabidopsis SUCROSE TRANSPORTER 2 (SUC2) promoter was transformed into wild-type Arabidopsis Columbia (WT) and ft-10 mutant plants. An empty vector was transformed into WT as a control. Transgenic plants were confirmed by RT-PCR analysis of JcFT expression (Additional file 1: Figure S1A). Twenty-four and seven independent T0 transgenic lines were generated with the 35S::JcFT construct in WT and ft-10 mutant, respectively. For most of these lines, bolting occurred significantly earlier than in WT and ft-10 plants under inductive long-day (LD) conditions (Figures 4A and 5A).

Figure 4
figure4

Ectopic expression of JcFT causes early flowering in transgenic Arabidopsis. Growth under LD conditions (A) and SD conditions (B) at 28 days and 45 days after germination, respectively. Left to right: WT, ft-10, 35S::JcFT in Col, SUC2::JcFT in Col, 35S::JcFT in ft-10, and SUC2::JcFT in ft-10. (C and D) Inflorescences of WT and 35S::JcFT transgenic plants.

Full size image
Figure 5
figure5

Ectopic expression of JcFT affects flowering in Arabidopsis . (A) Days and leaves to bolting for several JcFT overexpression (CaMV 35S) and phloem- specific expression (SUC2) transgenic Arabidopsis lines, empty vector-transformed plants, WT and mutant ft-10 plants grown under LD conditions. (B) Days and leaves to bolting for transgenic lines in the Col and ft-10 background grown under SD conditions. Values are means ± SD of the results from ten plants of each transgenic line. Arrows at the top of bars for WT, empty vector-transformed Col and ft-10 indicate that plants have not flowered.

Full size image

We selected four independent homozygous lines in the T2 generation to examine the phenotypes. The L1 and L9 lines were created by transforming WT with the 35S::JcFT construct, and the C1 and C7 lines harbored the construct in the ft-10 mutant background. Lines L1 and L9 bolted 8–14 days earlier and produced 6–11 fewer rosette leaves than the WT control under LD conditions, whereas no differences in bolting time were observed when comparing WT and the transgenic lines transformed with the empty vector (Figure 5A). Under non-inductive short-day (SD) conditions, all transgenic plants flowered much earlier than WT and the ft-10 mutant, both of which did not flower until 60 days after sowing in soil (Figures 4B and 5B). JcFT overexpression in Arabidopsis did not cause any defects in flower development (Figure 4C and 4D), but it did significantly reduce vegetative growth time. Further analysis indicated that the promotion of flowering in 35S::JcFT transgenic Arabidopsis was correlated with a significant up-regulation of the flower meristem identity genes AP1 and LEAFY (LFY) (Additional file 2: Figure S1).

To determine whether FT-like genes are functionally conserved and active in vascular tissue, the phloem-specific promoter SUC2 has been used to drive the expression of FT-like genes in Arabidopsis and other species [12, 30–32]. We obtained ten WT and eight ft-10 independent T0 transgenic lines harboring the SUC2::JcFT construct. The S1 and S3 lines were created by transforming WT with the SUC2::JcFT construct, and the CS1 and CS4 lines harbored the construct in the ft-10 mutant background. Similar to the observations for the 35S::JcFT transgenic lines, lines S1 and CS1 flowered much earlier than WT and ft-10, respectively. Lines S3 and CS4 flowered at approximately the same time and produced as many leaves as WT (24 days, 12 leaves) or flowered slightly earlier (Figure 5A) under LD conditions. Similar to the 35S::JcFT transgenic lines, all the SUC2::JcFT transgenic lines flowered earlier than WT and ft-10 under SD conditions (Figure 5B).

Taken together, these findings demonstrated that ectopic expression of JcFT in Arabidopsis resulted in an early flowering phenotype.

Overexpression of JcFT in Jatropha causes early flowering in vitro

The transgenic analysis in Arabidopsis suggested that JcFT could be a floral activator in Jatropha. To test whether JcFT similarly resulted in an early-flowering phenotype in Jatropha, we generated transgenic Jatropha with the 35S::JcFT construct used for Arabidopsis transformation. Mature Jatropha cotyledons were used as explants for transformation, as previously described [33]. To our surprise, flower buds initiated directly from the Agrobacterium-transformed calli after in vitro culture for seven weeks (Figure 6A and 6B), whereas the control explants never produced flower buds under the same conditions. The in vitro cultured transgenic Jatropha also produced intact inflorescences, but the inflorescences did not produce as many small flowers as wild Jatropha in the field (Figure 6C and 6D). Nevertheless, these findings demonstrate that JcFT is a powerful inducer of flowering in Jatropha.

Figure 6
figure6

Early flowering of 35S:: JcFT transgenic Jatropha cultured in vitro. (A and B) Flower buds of transgenic Jatropha cultured in vitro for seven weeks. (C) Inflorescence of transgenic Jatropha cultured in vitro. (D) Inflorescence of wild Jatropha in the field. Red arrows indicate flower buds.

Full size image

Although flower buds were produced in vitro, most were abortive and wilted several weeks later. A few flower buds developed into flowers (Figure 7A and 7C), but these flowers also wilted. Furthermore, these in vitro flowers were abnormal; for example, the petals of the female flower could not spread (Figure 7A). By removing the sepals and petals of female flower, the pistil was made visible (Figure 7B). Compared with the wild-type female flower (Figure 7F), the stigma of transgenic female flower was shorter (Figure 7B). An abnormal in vitro hermaphrodite flower of transgenic Jatropha (Figure 7C) had six stamens with very short filaments (Figure 7D) in contrast to the normal male flower (Figure 7E, G), which has ten stamens (Figure 7H). Consequently, no regenerated transgenic plants harboring 35S::JcFT were obtained.

Figure 7
figure7

Abnormal flowers of transgenic Jatropha harboring 35S:: JcFT . (A) A female flower of transgenic Jatropha cultured in vitro. (B) Pistil of a transgenic female flower. (C) An abnormal hermaphrodite flower of transgenic Jatropha cultured in vitro. (D) Abnormal stamens from an abnormal hermaphrodite flower of transgenic Jatropha shown in (C). (E) Normal female and male flowers of wild Jatropha grown in the field. (F) Pistil of a wild-type female flower. (G and H) Stamens of a wild-type male flower. Bars in (A)-(D) and (F)-(H) represent 1 mm, and bar in (E) represents 5 mm. Red arrows indicate pistils, and blue arrows indicate stamens.

Full size image

To determine whether JcFT overexpression in the transgenic in vitro flowering lines altered the expression of downstream flowering genes, such as SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1), LFY, and AP1 homologs in Jatropha [11], qRT-PCR analysis was performed with RNA extracted from apex of the 35S::JcFT transgenic and wild-type shoots cultured in vitro. As expected, the transcript levels of JcLFY, JcAP1, and JcAP3 were significantly up-regulated (Figure 8). JcSOC1 was also strongly up-regulated in the transgenic in vitro flowering lines (Figure 8), indicating that it is a target of JcFT, which is consistent with the findings that SOC1 and AP1 are activated by the FT–FD complex in Arabidopsis [15, 16, 34].

Figure 8
figure8

Quantitative RT-PCR analysis of flowering genes downstream of JcFT in WT and 35S:: JcFT transgenic Jatropha . The qRT-PCR results were obtained using two independent biological replicates and three technical replicates for each RNA sample extracted from apex of the 35S::JcFT transgenic and wild-type (WT) shoots cultured in vitro. Transcript levels were normalized using JcActin1 gene as a reference. The mRNA level in WT was set as the standard with a value of 1.

Full size image

Discussion

Chailakhyan [35] coined the term “florigen” to refer to the floral stimulus, but exactly what contributes florigen remains unclear. Evidence indicating that Arabidopsis FT protein acts as a long-distance signal to induce flowering was published half a decade ago [12]. Subsequent findings have led to the now widely accepted view that FT protein is the mobile flowering signal (florigen), or at the very least, a component of it [14]. In the present study, we found that JcFT encoded an FT homolog in Jatropha, and thus represented a potential flowering activator.

FT-like genes have been isolated from many plants. There are two members of the FT-like subclade in Arabidopsis [36], five in Lombardy poplar [37], ten in soybean [38], three in chrysanthemum [39], thirteen in rice, and fifteen in maize [40]. In Jatropha, we cloned only one member of the FT-like subclade, and only one FT-like gene was identified in the whole genome sequence data of Jatropha [41, 42]. Many transgenic plants overexpressing FT homologs exhibit an early flowering phenotype [22, 38, 39, 43, 44], suggesting a conserved function of FT homologs in flowering induction in different plant species.

Although the leaf is generally expected to be the site where a florigen gene is translated into protein [13], many FT-like genes are abundantly expressed in reproductive organs, such as flowers and immature siliques in Arabidopsis [28], flowers and pods in soybean [38], capsules in poplar [37], inflorescence axes in Curcuma kwangsiensis [32], and flowers and berries in grapevine [45]. In the present study, JcFT was mainly expressed in flowers, fruits, and seeds, with the highest expression level in female flowers, suggesting that JcFT may be involved in the development of reproductive organs. In fact, FT-like genes in various species play multifaceted roles in plant development in addition to the crucial role of FT homologs in flowering induction [10].

Transgenic Arabidopsis ectopically expressing the JcFT exhibited an early flowering phenotype compared with the control plants (Figures 4 and 5). Similarly, transgenic Jatropha overexpressing JcFT flowered in vitro during regeneration (Figure 6), which may have resulted from the up-regulation of flowering gens downstream of JcFT (Figure 8). Unexpectedly, the transgenic Jatropha flower buds that were produced in vitro failed to develop normally into mature flowers. Many flower buds were abortive, and only a few developed into abnormal flowers. We supposed that the floral abnormalities and the failure of regeneration of the 35S::JcFT transgenic Jatropha plants could resulted from the ectopic overexpression of JcFT driven by the strong constitutive 35S promoter. Consistent with this hypothesis, by using a phloem-specific promoter SUC2, we successfully obtained SUC2::JcFT transgenic Jatropha shoots, which were grafted onto rootstocks of wild-type Jatropha seedlings. The grafted SUC2::JcFT transgenic Jatropha plants flowered earlier than did wild-type plants, and produced normal flowers (Additional file 2: Figure S2). Therefore, the production of normal transgenic Jatropha overexpressing JcFT for use in molecular breeding programs of Jatropha will likely require the use of weaker constitutive promoters [43], tissue-specific promoters [46], or inducible promoters [47] to confine the expression of the transgene JcFT to shoot meristems at an appropriate level. In addition, a loss of function analysis with a RNA interference construct targeted at JcFT will be necessary to determine the exact function of JcFT in Jatropha flowering.

Conclusions

The FT homolog of the biofuel plant Jatropha was isolated and characterized in the present study. JcFT is mainly expressed in the reproductive organs, including female flowers, fruits, and seeds. JcFT also induced early flowering in transgenic Arabidopsis and Jatropha, indicating that JcFT acts as a flowering promoter in Jatropha.

Materials and methods

Plant materials and growth conditions

The roots, stems, young leaves, mature leaves, flower buds, flowers, and fruits of Jatropha curcas L. were collected during the summer from the Xishuangbanna Tropical Botanical Garden of the Chinese Academy of Sciences, Mengla County, Yunnan Province in southwestern, China. Mature seeds were collected in autumn. All tissues prepared for qRT-PCR were immediately frozen in liquid N2 and stored at -80°C until use.

WT Arabidopsis thaliana ecotype Columbia (Col-0), the ft-10 mutant (a gift from Dr. Tao Huang, Xiamen University), and the transgenic lines were grown in peat soil in plant growth chambers at 22 ± 2°C under a 16/8 h (light/dark) or 8/16 h (light/dark) photoperiod, with cool-white fluorescent lamps used for lighting. Transgenic plants in the T2 homozygous generation were selected to examine flowering time and other phenotypes. For each genotype, ten plants were used to for characterization: the number of leaves was counted along with the number of days between sowing and when the first flower bud was visible.

Cloning of JcFTcDNA

Total RNA was extracted from the leaves of flowering Jatropha using the protocol described by Ding et al. [48] First-strand cDNA was synthesized using M-MLV-reverse transcriptase from TAKARA (Dalian, China) according to the manufacturer’s instructions. To clone the conserved region of JcFT cDNA, a pair of primers, ZF632 and ZF633, was designed according to the conserved regions of FT homologs from other plant species using the Primer Premier 5 software. The PCR products were isolated, cloned into the pMD19-T simple vector (TAKARA, Dalian, China), and sequenced. The cloned sequence was used to design gene-specific primers (GSPs) to amplify the cDNA 5′ and 3′ end. The primers were listed in Table S1. First round PCR and nested amplification were performed according to the instructions provided in the SMART™ RACE cDNA Amplification Kit User Manual (Clontech). The PCR products were subsequently cloned into pMD19-T and sequenced.

The full length JcFT cDNA was obtained by PCR using the primers JcFT-F and JcFT-R, which introduced KpnI and SalI recognition sites, respectively, to facilitate the transformation of JcFT into Arabidopsis and Jatropha. The PCR products were subsequently cloned into the pMD19-T and sequenced.

Sequence and phylogenetic analyses

Sequence chromatograms were examined and edited using Chromas Version 2.23. Related sequences were identified using BLAST (http://www.ncbi.nlm.nih.gov/BLAST/). To determine the amino acid identities, sequences from the alignment were pairwise compared using DNAMAN 6.0. A phylogenetic tree based on the protein sequences was constructed using MEGA5.0 (http://www.megasoftware.net). The amino acid sequences of the PEBP family were assembled using ClustalX. A Neighbor–Joining phylogenetic tree was generated with MEGA 5.0 using the Poisson model with gamma-distributed rates and 10000 bootstrap replicates. The molecular weight and isoelectric point of the protein were analyzed on-line using ExPASy (http://web.expasy.org/compute_pi/).

Plant expression vector construction and Arabidopsis and Jatrophatransformation

To construct the plant overexpression vector 35S::JcFT, the JcFT sequence was excised from the pMD19-T simple vector using the restriction enzymes KpnI and SalI and then cloned into the pOCA30 vector containing the CaMV 35S promoter and the 35S enhancer. The SUC2 promoter was obtained by PCR from Arabidopsis genomic DNA using primers SUC2-F and SUC2-R, which introduced HindIII and KpnI recognition sites, respectively. The PCR products were cloned into pMD19-T and sequenced. To construct the SUC2::JcFT plasmid, the 35S promoter of the vector containing 35S::JcFT was placed with the SUC2 promoter using the restriction enzymes HindIII and KpnI. The fidelity of the construct was confirmed by PCR and restriction digestion.

Transformation of WT Col-0 and ft-10 mutant plants with Agrobacterium strain EHA105 carrying the recombinant constructs was performed using the floral dip method [49]. Transgenic seedlings were selected for kanamycin resistance and confirmed by genomic PCR and RT-PCR.

Transformation of Jatropha with Agrobacterium strain LBA4404 carrying the overexpression construct was performed according to the protocol described by Pan et al. [33].

Expression analysis by qRT-PCR

Jatropha total RNA was extracted from frozen tissue as described by Ding et al. [48] Arabidopsis total RNA was extracted from frozen tissue using TRIzol reagent (Transgene, China). First-strand cDNA was synthesized using the PrimeScript® RT Reagent Kit with gDNA Eraser (TAKARA, Dalian, China) according to the manufacturer’s instructions. qRT-PCR was performed using SYBR® Premix Ex Taq™ II (TAKARA) on a Roche 480 Real-Time PCR Detection System (Roche Diagnostics).

The primes used for qRT-PCR are listed in Table S1. qRT-PCR was performed using two independent biological replicates and three technical replicates for each sample. Data were analyzed using the 2–ΔΔCT method as described by Livak and Schmittgen [50]. The transcript levels of specific genes were normalized using Jatropha Actin1 or Arabidopsis Actin2.

Availability of supporting data

All the supporting data of this article are included as additional files (Additional file 1: Figure S1; Additional file 2: Figure S2; Additional file 3: Table S1).

Authors’ information

CL and LN are PhD students, LL was a master student at the time of study, and QF is an associate professor, and ZFX is a professor and head of the laboratory.

Abbreviations

AP1:

APETALA1

FT:

FLOWERING LOCUS T

LFY:

LEAFY

LD:

long day

SD:

short day

SOC1:

SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1

SUC2:

sucrose transporter 2

qRT-PCR:

quantitative reverse transcriptase-polymerase chain reaction.

References

  1. 1.

    Divakara B, Upadhyaya H, Wani S, Gowda C: Biology and genetic improvement of Jatropha curcas L.: A review. Appl Energy. 2010, 87: 732-742. 10.1016/j.apenergy.2009.07.013.

    Article  CAS  Google Scholar 

  2. 2.

    Akashi K: Jatropha research: A new frontier for biofuel development. Plant Biotechnol. 2012, 29: 121-10.5511/plantbiotechnology.12.0003p.

    Article  Google Scholar 

  3. 3.

    Pua F-l, Fang Z, Zakaria S, Guo F, Chia C-h: Direct production of biodiesel from high-acid value Jatropha oil with solid acid catalyst derived from lignin. Biotechnol Biofuels. 2011, 4: 1-8. 10.1186/1754-6834-4-1.

    Article  Google Scholar 

  4. 4.

    Khalil H, Aprilia N, Bhat A, Jawaid M, Paridah M, Rudi D: A Jatropha biomass as renewable materials for biocomposites and its applications. Renew Sust Energ Rev. 2013, 22: 667-685.

    Article  Google Scholar 

  5. 5.

    Pandey VC, Singh K, Singh JS, Kumar A, Singh B, Singh RP: Jatropha curcas: A potential biofuel plant for sustainable environmental development. Renew Sust Energy Rev. 2012, 16: 2870-2883. 10.1016/j.rser.2012.02.004.

    Article  CAS  Google Scholar 

  6. 6.

    Ong H, Mahlia T, Masjuki H, Norhasyima R: Comparison of palm oil, Jatropha curcas and Calophyllum inophyllum for biodiesel: a review. Renew Sust Energy Rev. 2011, 15: 3501-3515. 10.1016/j.rser.2011.05.005.

    Article  CAS  Google Scholar 

  7. 7.

    Pramanik K: Properties and use of Jatropha curcas oil and diesel fuel blends in compression ignition engine. Renew Energ. 2003, 28: 239-248. 10.1016/S0960-1481(02)00027-7.

    Article  CAS  Google Scholar 

  8. 8.

    Ghosh A, Chaudhary D, Reddy M, Rao S, Chikara J, Pandya J, Patolia J, Gandhi M, Adimurthy S, Vaghela N, Mishra S, Rathod MR, Prakash AR, Shethia BD, Upadhyay SC, Balakrishna V, Prakash CR, Ghosh PK: Prospects for Jatropha methyl ester (biodiesel) in India. Int J Enviro Stud. 2007, 64: 659-674. 10.1080/00207230701766499.

    Article  CAS  Google Scholar 

  9. 9.

    Ghosh A, Chikara J, Chaudhary D, Prakash AR, Boricha G, Zala A: Paclobutrazol arrests vegetative growth and unveils unexpressed yield potential of Jatropha curcas. J Plant Growth Regul. 2010, 29: 307-315. 10.1007/s00344-010-9137-0.

    Article  CAS  Google Scholar 

  10. 10.

    Pin P, Nilsson O: The multifaceted roles of FLOWERING LOCUS T in plant development. Plant Cell Environ. 2012, 35: 1742-1755. 10.1111/j.1365-3040.2012.02558.x.

    Article  CAS  PubMed  Google Scholar 

  11. 11.

    Srikanth A, Schmid M: Regulation of flowering time: all roads lead to Rome. Cell Mol Life Sci. 2011, 68: 2013-2037. 10.1007/s00018-011-0673-y.

    Article  CAS  PubMed  Google Scholar 

  12. 12.

    Corbesier L, Vincent C, Jang S, Fornara F, Fan Q, Searle I, Giakountis A, Farrona S, Gissot L, Turnbull C, Coupland G: FT protein movement contributes to long-distance signaling in floral induction of Arabidopsis. Science. 2007, 316: 1030-1033. 10.1126/science.1141752.

    Article  CAS  PubMed  Google Scholar 

  13. 13.

    Turck F, Fornara F, Coupland G: Regulation and identity of florigen: FLOWERING LOCUS T moves center stage. Annu Rev Plant Biol. 2008, 59: 573-594. 10.1146/annurev.arplant.59.032607.092755.

    Article  CAS  PubMed  Google Scholar 

  14. 14.

    Wigge PA: FT, a mobile developmental signal in plants. Curr Biol. 2011, 21: R374-R378. 10.1016/j.cub.2011.03.038.

    Article  CAS  PubMed  Google Scholar 

  15. 15.

    Abe M, Kobayashi Y, Yamamoto S, Daimon Y, Yamaguchi A, Ikeda Y, Ichinoki H, Notaguchi M, Goto K, Araki T: FD, a bZIP protein mediating signals from the floral pathway integrator FT at the shoot apex. Science. 2005, 309: 1052-10.1126/science.1115983.

    Article  CAS  PubMed  Google Scholar 

  16. 16.

    Wigge PA, Kim MC, Jaeger KE, Busch W, Schmid M, Lohmann JU, Weigel D: Integration of spatial and temporal information during floral induction in Arabidopsis. Science. 2005, 309: 1056-10.1126/science.1114358.

    Article  CAS  PubMed  Google Scholar 

  17. 17.

    Lifschitz E, Eviatar T, Rozman A, Shalit A, Goldshmidt A, Amsellem Z, Alvarez JP, Eshed Y: The tomato FT ortholog triggers systemic signals that regulate growth and flowering and substitute for diverse environmental stimuli. Proc Natl Acad Sci. 2006, 103: 6398-6403. 10.1073/pnas.0601620103.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  18. 18.

    Lin M-K, Belanger H, Lee Y-J, Varkonyi-Gasic E, Taoka K-I, Miura E, Xoconostle-Cázares B, Gendler K, Jorgensen RA, Phinney B, Lough TJ, Lucas WJ: FLOWERING LOCUS T protein may act as the long-distance florigenic signal in the cucurbits. Plant Cell. 2007, 19: 1488-1506. 10.1105/tpc.107.051920.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  19. 19.

    Tamaki S, Matsuo S, Wong HL, Yokoi S, Shimamoto K: Hd3a protein is a mobile flowering signal in rice. Science. 2007, 316: 1033-10.1126/science.1141753.

    Article  CAS  PubMed  Google Scholar 

  20. 20.

    Faure S, Higgins J, Turner A, Laurie DA: The FLOWERING LOCUS T-like gene family in barley (Hordeum vulgare). Genetics. 2007, 176: 599-609. 10.1534/genetics.106.069500.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  21. 21.

    Carmona MJ, Calonje M, Martínez-Zapater JM: The FT/TFL1 gene family in grapevine. Plant Mol Biol. 2007, 63: 637-650. 10.1007/s11103-006-9113-z.

    Article  CAS  PubMed  Google Scholar 

  22. 22.

    Kotoda N, Hayashi H, Suzuki M, Igarashi M, Hatsuyama Y, Kidou S-i, Igasaki T, Nishiguchi M, Yano K, Shimizu T, Takahashi S, Iwanami H, Moriya S, Abe K: Molecular characterization of FLOWERING LOCUS T-like genes of apple (Malus× domestica Borkh.). Plant Cell Physiol. 2010, 51: 561-575. 10.1093/pcp/pcq021.

    Article  CAS  PubMed  Google Scholar 

  23. 23.

    Navarro C, Abelenda JA, Cruz-Oró E, Cuéllar CA, Tamaki S, Silva J, Shimamoto K, Prat S: Control of flowering and storage organ formation in potato by FLOWERING LOCUS T. Nature. 2011, 478: 119-122. 10.1038/nature10431.

    Article  CAS  PubMed  Google Scholar 

  24. 24.

    Xu F, Rong X, Huang X, Cheng S: Recent advances of FLOWERING LOCUS T gene in higher plants. Int J Mol Sci. 2012, 13: 3773-3781. 10.3390/ijms13033773.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  25. 25.

    Ding F, Peng H, He X, Li D, Zhu J, Qin X, Li H, Luo C, Cao H: Cloning and expression analysis of the FLOWERING LOCUS T (FT) homologous gene cDNA from Litchi chinensis. J Fruit Sci. 2012, 29: 75-80,160.

    CAS  Google Scholar 

  26. 26.

    Hisada S, Akihama T, Endo T, Moriguchi T, Omura M: Expressed sequence tags of Citrus fruit during rapid cell development phase. J Am Society Hortic Sci. 1997, 122: 808-812.

    CAS  Google Scholar 

  27. 27.

    Yamamoto T, Kuboki Y, Lin S, Sasaki T, Yano M: Fine mapping of quantitative trait loci Hd-1, Hd-2 and Hd-3, controlling heading date of rice, as single Mendelian factors. Theor Appl Genet. 1998, 97: 37-44. 10.1007/s001220050864.

    Article  CAS  Google Scholar 

  28. 28.

    Kobayashi Y, Kaya H, Goto K, Iwabuchi M, Araki T: A pair of related genes with antagonistic roles in mediating flowering signals. Science. 1999, 286: 1960-10.1126/science.286.5446.1960.

    Article  CAS  PubMed  Google Scholar 

  29. 29.

    Ahn JH, Miller D, Winter VJ, Banfield MJ, Lee JH, Yoo SY, Henz SR, Brady RL, Weigel D: A divergent external loop confers antagonistic activity on floral regulators FT and TFL1. EMBO J. 2006, 25: 605-614. 10.1038/sj.emboj.7600950.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  30. 30.

    Lazakis CM, Coneva V, Colasanti J: ZCN8 encodes a potential orthologue of Arabidopsis FT florigen that integrates both endogenous and photoperiod flowering signals in maize. J Exp Bot. 2011, 62: 4833-4842. 10.1093/jxb/err129.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  31. 31.

    Flachowsky H, Peil A, Hanke M-V, Tränkner C, Szankowski I, Lehmann S: Functional characterization of two antagonistic acting flowering genes in apple Malus× domestica Borkh. XXVIII International Horticultural Congress on Science and Horticulture for People (IHC2010): International Symposium on 929. 2010, 351-356.

    Google Scholar 

  32. 32.

    Varkonyi-Gasic E, Moss S, Voogd C, Wang T, Putterill J, Hellens RP: Homologs of FT, CEN and FD respond to developmental and environmental signals affecting growth and flowering in the perennial vine kiwifruit. New Phytol. 2013, 198: 732-746. 10.1111/nph.12162.

    Article  CAS  PubMed  Google Scholar 

  33. 33.

    Pan J, Fu Q, Xu Z-F: Agrobacterium tumefaciens-mediated transformation of biofuel plant Jatropha curcas using kanamycin selection. Afr J Biotechnol. 2010, 9: 6477-6481.

    CAS  Google Scholar 

  34. 34.

    Michaels SD: Flowering time regulation produces much fruit. Curr Opin Plant Biol. 2009, 12: 75-80. 10.1016/j.pbi.2008.09.005.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  35. 35.

    Chailakhyan MK: New facts in support of the hormonal theory of plant development. CR Acad Sci URSS. 1936, 13: 79-83.

    Google Scholar 

  36. 36.

    Yamaguchi A, Kobayashi Y, Goto K, Abe M, Araki T: TWIN SISTER OF FT (TSF) acts as a floral pathway integrator redundantly with FT. Plant Cell Physiol. 2005, 46: 1175-1189. 10.1093/pcp/pci151.

    Article  CAS  PubMed  Google Scholar 

  37. 37.

    Igasaki T, Watanabe Y, Nishiguchi M, Kotoda N: The FLOWERING LOCUS T/TERMINAL FLOWER 1 family in Lombardy poplar. Plant Cell Physiol. 2008, 49: 291-300. 10.1093/pcp/pcn010.

    Article  CAS  PubMed  Google Scholar 

  38. 38.

    Sun H, Jia Z, Cao D, Jiang B, Wu C, Hou W, Liu Y, Fei Z, Zhao D, Han T: GmFT2a, a soybean homolog of FLOWERING LOCUS T, is involved in flowering transition and maintenance. PLoS One. 2011, 6: e29238-10.1371/journal.pone.0029238.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  39. 39.

    Oda A, Narumi T, Li T, Kando T, Higuchi Y, Sumitomo K, Fukai S, Hisamatsu T: CsFTL3, a chrysanthemum FLOWERING LOCUS T-like gene, is a key regulator of photoperiodic flowering in chrysanthemums. J Exp Bot. 2012, 63: 1461-1477. 10.1093/jxb/err387.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  40. 40.

    Danilevskaya ON, Meng X, Hou Z, Ananiev EV, Simmons CR: A genomic and expression compendium of the expanded PEBP gene family from maize. Plant Physiol. 2008, 146: 250-264.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  41. 41.

    Sato S, Hirakawa H, Isobe S, Fukai E, Watanabe A, Kato M, Kawashima K, Minami C, Muraki A, Nakazaki N, Takahashi C, Nakayama S, Kishida Y, Kohara M, Yamada M, Tsuruoka H, Sasamoto S, Tabata S, Aizu T, Toyoda A, Shin-i T, Minakuchi Y, Kohara Y, Fujiyama A, Tsuchimoto S, Kajiyama S, Makigano E, Ohmido N, Shibagaki N, Cartagena JA, et al: Sequence analysis of the genome of an oil-bearing tree, Jatropha curcas L. DNA Res. 2011, 18: 65-76. 10.1093/dnares/dsq030.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  42. 42.

    Hirakawa H, Tsuchimoto S, Sakai H, Nakayama S, Fujishiro T, Kishida Y, Kohara M, Watanabe A, Yamada M, Aizu T, Toyoda A, Fujiyama A, Tabata S, Fukui K, Sato S: Upgraded genomic information of Jatropha curcas L. Plant Biotechnol. 2012, 29: 123-130. 10.5511/plantbiotechnology.12.0515a.

    Article  CAS  Google Scholar 

  43. 43.

    Hsu C-Y, Liu Y, Luthe DS, Yuceer C: Poplar FT2 shortens the juvenile phase and promotes seasonal flowering. Plant Cell. 2006, 18: 1846-1861. 10.1105/tpc.106.041038.

    PubMed Central  Article  CAS  PubMed  Google Scholar 

  44. 44.

    Imamura T, Nakatsuka T, Higuchi A, Nishihara M, Takahashi H: The gentian orthologs of the FT/TFL1 gene family control floral initiation in Gentiana. Plant Cell Physiol. 2011, 52: 1031-1041. 10.1093/pcp/pcr055.

    Article  CAS  PubMed  Google Scholar 

  45. 45.

    Sreekantan L, Thomas MR: VvFT and VvMADS8, the grapevine homologues of the floral integrators FT and SOC1, have unique expression patterns in grapevine and hasten flowering in Arabidopsis. Funct Plant Biol. 2006, 33: 1129-1139. 10.1071/FP06144.

    Article  CAS  Google Scholar 

  46. 46.

    Tränkner C, Lehmann S, Hoenicka H, Hanke M-V, Fladung M, Lenhardt D, Dunemann F, Gau A, Schlangen K, Malnoy M, Flachowsky H: Over-expression of an FT-homologous gene of apple induces early flowering in annual and perennial plants. Planta. 2010, 232: 1309-1324. 10.1007/s00425-010-1254-2.

    Article  PubMed  Google Scholar 

  47. 47.

    Wenzel S, Flachowsky H, Hanke M-V: The Fast-track breeding approach can be improved by heat-induced expression of the FLOWERING LOCUS T genes from poplar (Populus trichocarpa) in apple (Malus × domestica Borkh.). Plant Cell Tissue Organ Cult. 2013, 115: 127-137. 10.1007/s11240-013-0346-7.

    Article  CAS  Google Scholar 

  48. 48.

    Ding L-W, Sun Q-Y, Wang Z-Y, Sun Y-B, Xu Z-F: Using silica particles to isolate total RNA from plant tissues recalcitrant to extraction in guanidine thiocyanate. Anal Biochem. 2008, 374: 426-428. 10.1016/j.ab.2007.11.030.

    Article  CAS  PubMed  Google Scholar 

  49. 49.

    Clough SJ, Bent AF: Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 1998, 16: 735-743. 10.1046/j.1365-313x.1998.00343.x.

    Article  CAS  PubMed  Google Scholar 

  50. 50.

    Livak KJ, Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2- ΔΔCT method. Methods. 2001, 25: 402-408. 10.1006/meth.2001.1262.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We acknowledge Dr. Tao Huang for the Arabidopsis mutant ft-10. This work was supported by funding from the Top Science and Technology Talents Scheme of Yunnan Province (2009CI123), the Natural Science Foundation of Yunnan Province (2011FA034) and the CAS 135 Program (XTBG-T02) awarded to Z.-F. Xu. The authors gratefully acknowledge the Central Laboratory of the Xishuangbanna Tropical Botanical Garden for providing the research facilities.

Author information

Affiliations

  1. Key Laboratory of Tropical Plant Resources and Sustainable Use, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Menglun, Yunnan, 666303, China

    Chaoqiong Li, Qiantang Fu, Longjian Niu & Zeng-Fu Xu

  2. University of Chinese Academy of Sciences, Beijing, 100049, China

    Chaoqiong Li

  3. Key Laboratory of Gene Engineering of the Ministry of Education, and State Key Laboratory for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, Guangdong, 510275, China

    Li Luo

  4. School of Life Sciences, University of Science and Technology of China, Hefei, Anhui, 230027, China

    Longjian Niu

Authors
  1. Chaoqiong Li
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Li Luo
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Qiantang Fu
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Longjian Niu
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Zeng-Fu Xu
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Zeng-Fu Xu.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

CL and ZFX conceived the experiment and drafted the manuscript. LL cloned JcFT cDNA. CL constructed the vector and performed JcFT expression pattern analysis, Arabidopsis and Jatropha transformation, the transgenic plants bioassays. QF contributed to the data processing. LN collected the various Jatropha tissue samples. All authors read and approved the final manuscript.

Electronic supplementary material

Additional file 1: Figure S1: Semi-quantitative (A) and quantitative (B) RT-PCR analysis of flowering genes downstream of FT in WT and transgenic Arabidopsis. Arabidopsis seedlings were collected 20 days after germination. For semi-quantitative RT-PCR, 25 cycles were used for the reference gene AtActin2, and 30 cycles were used for the target genes. The qRT-PCR results were obtained from three technical replicates for each sample. Values were normalized using AtActin2 gene as a reference. The mRNA level in WT was set as the standard with a value of 1. (TIFF 398 KB)

Additional file 2: Figure S2: Early flowering of SUC2::JcFT transgenic Jatropha. Transgenic shoot grafted onto a non-transgenic rootstock showing the precocious flowers (red oval) forty days after grafting. Red arrows indicate the graft sites. (TIFF 4 MB)

Additional file 3: Table S1: Primers used in this study. (DOCX 20 KB)

Authors’ original submitted files for images

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Li, C., Luo, L., Fu, Q. et al. Isolation and functional characterization of JcFT, a FLOWERING LOCUS T (FT) homologous gene from the biofuel plant Jatropha curcas. BMC Plant Biol 14, 125 (2014). https://doi.org/10.1186/1471-2229-14-125

Download citation

Keywords

  • Biofuel
  • Early flowering
  • Florigen
  • FLOWERING LOCUS T
  • Physic nut

BMC Plant Biology

ISSN: 1471-2229

Contact us