JXB Advance Access originally published online on July 24, 2008
Journal of Experimental Botany 2008 59(12):3383-3393; doi:10.1093/jxb/ern192
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© 2008 The Author(s).
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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RESEARCH PAPER |
Germination of photoblastic lettuce seeds is regulated via the control of endogenous physiologically active gibberellin content, rather than of gibberellin responsiveness
1Course of the Science of Bioresource, The United Graduate School of Agricultural Science, Iwate University, Morioka, Iwate 020-8550, Japan
2Department of Bioresource Engineering, Yamagata University, Tsuruoka, Yamagata 997-8555, Japan
3Institute of Symbiotic Science and Technology, Tokyo University of Agriculture and Technology, Fuchu, Tokyo, 183-8509, Japan
4Department of Applied Biological Chemistry, University of Tokyo, Bunkyo-ku, Tokyo, 113-8657, Japan
5Faculty of Science and Technology, Tokyo University of Sciece, Noda, Chiba 278-8510, Japan
6Department of Agriculture, Yamagata University, Tsuruoka, 997-8555, Japan
To whom correspondence should be addressed. E-mail: toyomasu{at}tds1.tr.yamagata-u.ac.jp
Received 30 March 2008; Revised 4 June 2008 Accepted 24 June 2008
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Abstract |
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Phytochrome regulates lettuce (Lactuca sativa L. cv. Grand Rapids) seed germination via the control of the endogenous level of bioactive gibberellin (GA). In addition to the previously identified LsGA20ox1, LsGA20ox2, LsGA3ox1, LsGA3ox2, LsGA2ox1, and LsGA2ox2, five cDNAs were isolated from lettuce seeds: LsCPS, LsKS, LsKO1, LsKO2, and LsKAO. Using an Escherichia coli expression system and functional assays, it is shown that LsCPS and LsKS encode ent-copalyl diphosphate synthase and ent-kaurene synthase, respectively. Using a Pichia pastoris system, it was found that LsKO1 and LsKO2 encode ent-kaurene oxidases and LsKAO encodes ent-kaurenoic acid oxidase. A comprehensive expression analysis of GA metabolism genes using the quantitative reverse transcription polymerase chain reaction suggested that transcripts of LsGA3ox1 and LsGA3ox2, both of which encode GA 3-oxidase for GA activation, were primarily expressed in the hypocotyl end of lettuce seeds, were expressed at much lower levels than the other genes tested, and were potently up-regulated by phytochrome. Furthermore, LsDELLA1 and LsDELLA2 cDNAs that encode DELLA proteins, which act as negative regulators in the GA signalling pathway, were isolated from lettuce seeds. The transcript levels of these two genes were little affected by light. Lettuce seeds in which de novo GA biosynthesis was suppressed responded almost identically to exogenously applied GA, irrespective of the light conditions, suggesting that GA responsiveness is not significantly affected by light in lettuce seeds. It is proposed that lettuce seed germination is regulated mainly via the control of the endogenous content of bioactive GA, rather than the control of GA responsiveness.
Key words: Germination, gibberellin metabolism, gibberellin signalling, lettuce
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Introduction |
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Light-inducible seed germination, termed photoblastism, occurs in some higher plants and allows buried seeds to remain dormant until exhumed. This phenomenon was discovered in lettuce (Lactuca sativa L. cv. Grand Rapids) seeds using a germination assay (Borthwick et al., 1952). The germination of photoblastic lettuce seeds is regulated by phytochrome, which is a red (R) and far-red (FR) light receptor in plants (Butler et al., 1959). Red light irradiation induces the germination of lettuce seeds, and FR irradiation given after R cancels the effect of R; hence, phytochrome-induced changes in seeds are reversibly modulated by different light frequencies. The regulation of lettuce seed germination by phytochrome is thought to be mediated by gibberellin (GA).
Gibberellins are tetracyclic diterpenoid phytohormones that regulate various aspects of plant growth and development such as seed germination, leaf expansion, stem elongation, flowering, and seed development (Thomas and Hedden, 2006). Bioactive GAs are biosynthesized from geranylgeranyl diphosphate (GGDP), a common diterpenoid precursor, through several steps (Fig. 1), as reviewed by Thomas and Hedden (2006). Geranylgeranyl diphosphate is converted to the tetracyclic hydrocarbon ent-kaurene through ent-copalyl diphosphate (ent-CDP) by two distinct diterpene cyclases in plastids: ent-CDP synthase (CPS) and ent-kaurene synthase (KS). Furthermore, ent-kaurene is converted into GA12 via ent-kaurenoic acid by separate cytochrome P450 mono-oxygenases contained in the ER membrane: ent-kaurene oxidase (KO) and ent-kaurenoic acid oxidase (KAO). Gibberellin A12 and GA53 (13-hydroxylated GA12) are converted to GA4 and GA1 by cytosolic 2-oxoglutarate-dependent dioxygenases (2ODDs): GA 20-oxidase (GA20ox) and GA 3-oxidase (GA3ox). Gibberellin A4 and GA1 are the major bioactive GAs in higher plants and are deactivated by GA 2-oxidase (GA2ox)-catalysed 2-hydroxylation.
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In lettuce seeds, the application of exogenous bioactive GAs (GA1 or GA3, 1,2-dehydro-GA1) mimics the effect of R light (Kahn and Goss, 1957; Ikuma and Thimann, 1960; Toyomasu et al., 1993). Gibberellin A1, GA20, and GA19 are endogenous in lettuce seeds, and phytochrome specifically regulates endogenous levels of GA1, but not GA19 and GA20 (Toyomasu et al., 1993). Furthermore, the analysis and expression of six genes encoding 2ODDs (LsGA20ox1, LsGA20ox2, LsGA3ox1, LsGA3ox2, LsGA2ox1, and LsGA2ox2) showed that increases in GA1 are caused by the phytochrome-induced up-regulation of LsGA3ox1 (Toyomasu et al., 1998) and the slight down-regulation of LsGA2ox2 (Nakaminami et al., 2003). The expression of these two genes is limited in the hypocotyl end of lettuce seeds (Sawada et al., 2008), which contains the R-perception site (Inoue and Nagashima, 1991).
Over the past decade, genetic and biochemical approaches have revealed that Arabidopsis seeds, for which phytochrome also regulates germination, control GA metabolism in a light-responsive manner (Yamaguchi et al., 1998, 2001; Seo et al., 2006; Yamauchi et al., 2007). The down-regulation of two DELLA genes, i.e. GA-INSENSITIVE (GAI) and REPRESSOR OF GA1-3 (RGA), by phytochrome results in the up-regulation of GA responsiveness in Arabidopsis seeds (Oh et al., 2007). DELLA proteins are well-characterized negative regulators of GA signalling (Fig. 1) and are rapidly degraded when plants are exposed to bioactive GA (Ueguchi-Tanaka et al., 2007). Nevertheless, the mechanism(s) that modulate GA responsiveness in lettuce seeds remain unclear.
cDNAs encoding CPS, KS, KO, and KAO were isolated and characterized from lettuce seeds and the transcript levels of GA metabolism genes quantified using the quantitative real-time polymerase chain reaction (QRT-PCR) in imbibed whole lettuce seeds or in the hypocotyl and cotyledon ends of seeds after different light treatments. The transcript levels of GA metabolism genes in the seeds were measured under conditions in which germination was suppressed by treatment with abscisic acid (ABA) (Kahn, 1968; Sankhla and Sankhla, 1968), a phytohormone that regulates seed maturation and dormancy (Marion-Poll and Leung, 2006). To gain a better understanding of how DELLA genes regulate GA responsiveness in lettuce seeds, cDNAs encoding DELLA proteins were isolated and characterized, and germination assays were carried out in the presence of various concentrations of GA3.
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Materials and methods |
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Light sources and plant materials
Red (6.5 W m–2) and FR (5 W m–2) light were used as described previously (Toyomasu et al., 1993). Lettuce seeds (Lactuca sativa L. cv. Grand Rapids) similar to those used in previous studies (Sawada et al., 2008) were stored at 4 °C with silica gel until needed. For each treatment, 50 mg of seeds (approximately 50 seeds) were incubated according to the method of Nakaminami et al. (2003). Seeds were exposed to one of three light treatments 3 h after the start of imbibition: irradiation with FR (FR treatment); FR followed by R (FR/R treatment); and FR followed by R and FR (FR/R/FR treatment). Each light irradiation lasted 5 min. Seeds imbibed in the dark for 3 h were also harvested immediately prior to light treatment (0 h). After light treatment, the seeds were incubated in the dark at 25 °C for 2, 4, and 6 h. The seeds were then frozen in liquid nitrogen. The application of 0.1 mM ABA to the seeds was performed by buffer exchange before light treatment. For dark incubations, seeds were handled under a dim green safety light.
Molecular cloning
The design of the degenerate primers used to clone CPS, KS, KO, KAO, and DELLA was based on the respective conserved amino acid regions among sequences from other plant species (see Supplementary Table S1 at JXB online). Template cDNA derived from lettuce seeds (Toyomasu et al., 1998) was used for PCR. The 50 µl reaction mixture contained 0.2 mM dNTPs, 1.5 mM MgCl2, 1 µM of each primer, and 2.5 units of Expand HF (Roche Diagnostics, Indianapolis, IN, USA). The samples were heated to 94 °C for 2 min, then subjected to 40 cycles at 94 °C for 1 min, 40 °C (CPS) or 45 °C (KS, KO, KAO, and DELLA) for 1 min, and 72 °C for 1 min, followed by a final extension for 7 min. Fragments obtained by PCR were subcloned using a pGEM-T Easy vector (Promega, Madison, WI, USA). DNA sequencing was performed using a Big Dye terminator cycle sequencing kit (Applied Biosystems, Foster City, CA, USA) and an ABI PRISM 310 Genetic Analyser (Applied Biosystems). Rapid amplification of cDNA ends (RACE) was performed using the methods of Toyomasu et al. (1998). Homology database searches were performed by BLAST analysis (http://www.ncbi.nlm.nih.gov/).
Functional analysis of LsCPS and LsKS (diterpene cyclases)
The coding regions of LsCPS and LsKS cDNAs were amplified by RT-PCR using primers (see Supplementary Table S2 at JXB online) with the proper restriction enzyme sites for subcloning into pGEX-4T-3 vector (GE Healthcare, Piscataway, NJ, USA). The preparation of plasmids, heterologous expression in Escherichia coli, extraction and purification of recombinant enzymes, and enzyme assays were performed using the method described by Otomo et al. (2004b) for LsCPS and by Otomo et al. (2004a) for LsKS. The reaction products were detected and analysed by gas chromatography–mass spectrometry (GC–MS) using an Agilent 6890N GC-5973N MSD mass selective detector system (ionization voltage 70 eV) fitted with a fused silica chemically bonded capillary column DB-WAX (0.25 mm diameter, 60 m length, and 0.25 µm film thickness; J&W Scientific, Folson, CA). Samples were injected into the column at 250 °C in the splitless mode. After isothermal hold at 80 °C for 2 min, the column temperature was increased by 5 °C min–1 to 250 °C, with an isothermal hold at 250 °C for 15 min. The flow rate of the helium carrier gas was 1 ml min–1.
Functional analysis of LsKO and LsKAO (P450 mono-oxygenases)
The coding regions of LsKO1, LsKO2, and LsKAO were amplified using specific primer sequences (see Supplementary Table S2 at JXB online). Each fragment was ligated into a yeast expression vector (pPICZ) using the appropriate restriction enzyme sites. Recombinant enzymes were co-expressed by the addition of methanol in each yeast (Pichia pastoris X-33) transformant harbouring both the NADPH-P450 reductase gene and the targeted P450 gene. The microsome fraction was prepared by ultracentrifugation (100 000 g, 4 °C, 1 h) and was then incubated with the proper substrate in the presence of 5 mM NADPH. The sample was analysed by GC-MS (JEOL JMS-Bu25) equipped with a DB-5 capillary column (0.25 mm diameter, 15 m length, and 0.25 µm film thickness; J&W Scientific). For the analysis of KO products, samples were derivatized with diazomethane and injected into the GC–MS instrument. After an isothermal hold at 80 °C for 1 min, the column temperature was increased by 30 °C min–1 to 200 °C and then by 5 °C min–1 to 280 °C. For the analysis of KAO products, derivatized samples were analysed by GC-MS as described by Kawaide et al. (1995).
Functional analysis of lettuce DELLA
The coding regions of LsDELLA1 and LsDELLA2 cDNA were amplified by RT–PCR with specific primers (see Supplementary Table S2 at JXB online) that had suitable restriction enzyme sites at the 5' end of each primer. The products obtained by PCR were subcloned into pGEX-4T-3 vector. The preparation of plasmids, heterologous expression in E. coli, and extraction and purification of recombinant proteins were performed using the methods of Otomo et al. (2004b). Experiments to probe the interactions of AtGID1c-GA with LsDELLA were performed using the methods described previously (Ueguchi-Tanaka et al., 2005; Nakajima et al., 2006). The [1, 2, 16, 17-3H4]-16, 17-dihydro–GA4 was used as labelled GA, and unlabelled GA4 was used as competitor to test for non-specific binding. For the glutathione S-transferase (GST) pull-down assay, GST-LsDELLA or GST (negative control) bound to glutathione-Sepharose 4B beads (GE Healthcare) was mixed with crude Trx-AtGID1c or Trx (negative control) in 270 µl of binding buffer (PBS, pH 7.0) with or without 0.1 mM GA4 and incubated at 25 °C for 30 min. The beads were then sedimented by centrifugation and washed with binding buffer. The beads were resuspended in 15 µl of elution buffer (50 mM TRIS-HCl, pH 8.0, containing 10 mM glutathione) and centrifuged. Proteins in the supernatant were separated by 10% sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and stained with Coomassie Brilliant Blue (CBB).
Quantitative real-time PCR
Total RNA was extracted from frozen samples using an RNAqueous column with the Plant RNA Isolation Aid (Ambion, Austion, TX, USA). For the expression analysis of half-cut seeds, frozen seeds were divided into two parts on dry ice using a razor. Complementary DNA was prepared from 1 µg of total RNA using the QuantiTect Reverse Transcription Kit (Qiagen, Hilden, Germany). Quantitative RT-PCR using SYBR Green I was carried out on a Thermal Cycler Dice Real Time System (TP800, Takara bio, Otsu, Japan) as described previously (Bustin, 2000; Sawada et al., 2008) using specific primers (see Supplementary Table S3 at JXB online). The means of two or three replicates were normalized using 18S rRNA internal controls.
Germination assay
Twenty decoated lettuce seeds were incubated in the dark at 25 °C with 50 µM uniconazol-P and various concentrations of GA3. The decoated lettuce seeds did not contain seed coats. At 2 h after the start of imbibition, seeds were exposed to R light (3.3 W m–2) for 3 min. The seeds were then incubated in the dark for 24 h, and the germination frequency was recorded. Germination of decoated seeds was determined by the protrusion of root tip from remained endosperm layer. Five independent experiments were performed.
Accession numbers
Sequence data were deposited with the GenBank/EMBL data libraries under accession numbers AB031204
[GenBank]
(LsCPS), AB031205
[GenBank]
(LsKS), AB370235 (LsKO1), AB370236 (LsKO2), AB370237 (LsKAO), AB370238 (LsDELLA1), and AB370240 (LsDELLA2).
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Results |
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Cloning of cDNAs encoding CPS and KS in lettuce
To clone CPS and KS, degenerate primers were designed based on the conserved amino acid sequences of other plant CPSs and KSs, respectively. Complementary DNA fragments of the expected size of approximately 810 bp (CPS) and 510 bp (KS) were amplified from the templates derived from R light-treated seeds by RT–PCR using the degenerate primers. Subcloned fragments were analysed according to their sequence similarity with other plant cyclases, indicating that one CPS-like fragment and one KS-like fragment were present. RACE was performed to determine each full-length cDNA sequence using gene-specific primers. End-to-end PCR was then performed using 5'- and 3'-end primers. The clones were named LsCPS and LsKS. The predicted coding regions of LsCPS and LsKS were 2400 and 2367 bp, encoding 799 and 788 amino acid residues, respectively. The predicted amino acid sequence of LsCPS showed 74% homology with Stevia rebaudiana CPS (AF034545 [GenBank] ), and that of LsKS showed 70% homology with Stevia KS (AF097310 [GenBank] ).
The enzymatic functions of LsCPS and LsKS were characterized in in vitro assays using recombinant proteins expressed in bacteria. The coding regions of LsCPS and LsKS cDNA were subcloned into bacterial expression vectors, and the recombinant enzymes were fused with GST at the N terminus. The GST fusion proteins were purified by affinity chromatography. GST-LsCPS was then incubated with GGDP. After dephosphorylation using bacterial alkaline phosphatase, the reaction product was identified by full-scan GC-MS as the alcohol derivative. The retention time and mass spectrum of the dephosphorylated product were identical to those of authentic ent-copalol (see Supplementary Table S4 at JXB online). Recombinant GST-LsKS was incubated with GGDP and GST-LsCPS, and the product was analysed by GC-MS. A peak with a retention time and mass spectrum identical to authentic ent-kaurene was observed (see Supplementary Table S4 at JXB online). Collectively, these analyses showed that the GST-LsCPS product ent-CDP was converted into ent-kaurene by GST-LsKS and suggested that LsCPS and LsKS encode CPS and KS, respectively.
Cloning of cDNAs encoding KO and KAO in lettuce
To clone KO and KAO homologues from lettuce, RT-PCR was performed with specific degenerate primers, which were designed based on the conserved amino acid sequences of other plant KOs and KAOs, respectively. Bands were amplified at approximately 420 bp (KO) and 440 bp (KAO). Nucleotide sequencing of each subcloned fragment indicated that two KO-like fragments (LsKO1 and LsKO2) and one KAO-like fragment (LsKAO) were obtained. Each full-length sequence was determined by RACE. The predicted coding regions of LsKO1, LsKO2, and LsKAO were 1536, 1539, and 1482 bp, encoding 511, 512, and 493 amino acid residues, respectively. These three clones were named LsKO1, LsKO2, and LsKAO. The predicted coding regions of these cDNAs were highly homologous to those from other plant species and were 71% (LsKO1/Stevia KO: AY364317
[GenBank]
), 78% (LsKO2/Stevia KO), and 65% (LsKAO/Arabidopsis KAO1: NM100394) similar in amino acid sequence.
Assays to elucidate the functions of the translated gene products were carried out in vitro using a yeast expression system based on Pichia pastoris. Each cDNA was expressed in yeast harbouring an Arabidopsis P450 reductase to yield the recombinant protein. ent-Kaurene and ent-kaurenoic acid were used as substrates in enzyme assays for KO and KAO, respectively, using yeast microsomal fractions. The reaction products were identified by GC–MS as methyl ester derivatives. ent-Kaurenoic acid and GA12 were identified as major products converted from ent-kaurene by LsKO1 and LsKO2 and from ent-kaurenoic acid by LsKAO, respectively (see Supplementary Table S5 at JXB online). These results suggest that LsKO1 and LsKO2 encode KO and that LsKAO encodes KAO.
Gene expression during germination
Three types of pulsed light treatment were used in the germination studies. The FR light treatment was used to suppress germination in the dark and thus served as a negative control for germination. The FR/R light treatment was used to induce germination. The FR/R/FR light treatment was performed to confirm the regulation of germination by phytochrome. In the FR/R treatment group, the radicle appeared 8 h after the light treatment (Fig. 2A). To determine the expression levels of GA metabolism genes in the lettuce seeds, QRT-PCR analyses were performed (Fig. 2B). LsGA2ox1 transcripts were the most abundant of the GA metabolic genes in the imbibed seeds; the expression levels of two LsGA3ox genes were much lower than those of other GA metabolic genes. The transcript level of LsKAO in FR/R-treated seeds increased slightly compared with that in FR- and FR/R/FR-treated seeds until 6 h. The transcript levels of LsCPS, LsKS, LsKO1, and LsKO2 were not affected by light treatment. Consistent with previous results (Toyomasu et al., 1998), the transcript level of LsGA20ox2 decreased and that of LsGA3ox1 increased robustly after FR/R treatment. The expression of LsGA20ox1 increased very slightly after FR/R treatment. Similar to LsGA3ox1, the transcript level of LsGA3ox2 increased considerably after FR/R treatment. The effects of R light on the expression of LsGA20ox2, LsGA3ox1, and LsGA3ox2 were abolished by successive FR irradiation (FR/R/FR). The expression of LsGA2ox1 was not affected by light treatment, and the transcript level of LsGA2ox2 in FR/R seeds was lower than that in FR seeds, similar to previous results (Nakaminami et al., 2003). Nevertheless, the transcript level of LsGA2ox2 in FR-treated seeds was different from that in FR/R/FR-treated seeds 6 h after light treatment. Nakaminami et al. (2003) showed that the regulation of LsGA2ox2 expression is photoreversible using one-point expression analysis. Non-photoreversible regulation of LsGA2ox2 was observed using time-course expression analysis. These results suggest that the regulatory mechanism of LsGA2ox2 expression is somewhat different from that of LsGA20ox2, LsGA3ox1, and LsGA3ox2. Hence, the comprehensive expression analysis of GA metabolic genes strongly suggests that the robust up-regulation of LsGA3ox1 and LsGA3ox2 and down-regulation of LsGA2ox2 is primarily responsible for GA1 augmentation after FR/R treatment in imbibed lettuce seeds (Toyomasu et al., 1993), although we could not completely remove the possibility that unidentified paralogues of GA3ox and GA2ox in lettuce are involved.
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Sawada et al. (2008) detected LsGA3ox1 and LsGA2ox2 transcripts mainly on the hypocotyl end of the seed during germination. To examine the expression of other GA metabolic genes on both ends of lettuce seeds, the transcripts of GA metabolic genes on the cotyledon and hypocotyl ends of lettuce seeds were studied using QRT-PCR (Fig. 3B) following the methods of Sawada et al. (2008). The cotyledon end of the seed is composed of the cotyledons, fruit wall, seed coat, and endosperm; the hypocotyl end of the seed includes the hypocotyl, root apical meristem, shoot apical meristem, and part of the cotyledons, fruit wall, seed coat, and endosperm (Fig. 3A). The transcript levels of LsCPS, LsKO1, and LsGA20ox1 in the hypocotyl end were higher than those in the cotyledon end, whereas the transcript levels of LsKS, LsKO2, LsGA20ox2, and LsGA2ox1 were similar in the hypocotyl end to those in the cotyledon end. The expression of LsGA20ox1 was slightly up-regulated by FR/R treatment in the cotyledon end, but not in the hypocotyl end, whereas the expression of LsGA20ox2 was down-regulated in both ends. The very slight increase in LsGA20ox1 expression in whole seeds (Fig. 2B) may have been caused by increases in the cotyledon end. Transcripts of LsKAO and LsGA3ox2 were also detected mainly on the hypocotyl end, rather than the cotyledon end. The expression of LsGA3ox1 and LsGA3ox2 was dramatically up-regulated and that of LsGA2ox2 was down-regulated, whereas the expression of LsKAO was slightly up-regulated in the hypocotyl end after FR/R treatment compared to FR treatment. These patterns of gene expression in the hypocotyl end of the seed agreed with those in whole seeds. It is noteworthy that transcripts that are regarded as involved in the up-regulation of GA1 content after FR/R treatment, such as LsGA3ox1, LsGA3ox2, and LsGA2ox2, are mainly localized in the hypocotyl end of the seed.
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Effects of ABA treatment on the expression of GA metabolism genes during seed germination
Lettuce seed germination induced by R light or by GA treatment is inhibited by the application of ABA (Kahn, 1968; Sankhla and Sankhla, 1968). Under our experimental conditions, lettuce seed germination in FR/R-treated seeds was completely suppressed by the application of 0.1 mM ABA (Fig. 2A). To examine whether GA metabolism genes are affected by exogenously applied ABA, QRT-PCR was performed on 11 GA metabolism genes using ABA-treated seeds. Among the genes of which the expression is regulated mainly by light, ABA treatment slightly down-regulated the expression of LsGA3ox1 and slightly up-regulated that of LsGA2ox2, whereas the expression of LsGA20ox2 and LsGA3ox2 was not affected (see FR/R and FR/R+ABA seeds in Fig. 4A). The expression of the other seven genes that were examined was not markedly affected by ABA (data not shown). These results were confirmed by QRT-PCR using half-cut seeds. The up-regulation of LsGA3ox1 and the down-regulation of LsGA2ox2 by FR/R treatment in the hypocotyl end of the seed were partly abolished by ABA treatment, whereas the up-regulation of LsGA3ox2 by FR/R treatment was unaffected (Fig. 4B).
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Cloning of cDNA encoding DELLA proteins in lettuce
To examine the expression levels of DELLA genes in lettuce seeds, cDNA that encodes DELLA proteins was isolated. One set of degenerate primers was designed based on the conserved amino acid sequences of DELLA proteins in Arabidopsis and rice (Oryza sativa L.). A band of the expected size (
590 bp) was amplified from the cDNA template derived from R-treated seeds by RT-PCR using the degenerate primers. Nucleotide sequence analyses indicated the presence of two different DELLA-like fragments. The two fragments were named LsDELLA1 and LsDELLA2. The RACE and end-to-end PCR analyses indicated that the predicted coding regions of LsDELLA1 and LsDELLA2 were 1710 bp and 1773 bp, encoding 569 and 590 amino acid residues, respectively. The amino acid sequences of LsDELLA1 and LsDELLA2 showed 62% and 61% similarity with that of Arabidopsis GAI (NM101361), respectively. Gibberellin insensitive dwarf 1 (GID1) encodes a soluble GA receptor in rice (Ueguchi-Tanaka et al., 2005); three orthologues (AtGID1a, AtGID1b, and AtGID1c) were identified in Arabidopsis (Nakajima et al., 2006). It has been shown that GID1 binds directly to DELLA in the presence of bioactive GA. To determine whether LsDELLA1 and LsDELLA2 also bind GID1, pull-down assays were performed using recombinant LsDELLA and AtGID1c. Each coding region of LsDELLA1 and LsDELLA2 cDNA was subcloned into a bacterial expression vector; recombinant proteins that were fused with GST at the N terminus were purified. Crude recombinant AtGID1c fused with thioredoxin (TRX) at the N terminus was also obtained. The affinity-purified GST-LsDELLA proteins or GST alone (negative control) were incubated with crude TRX-AtGID1c or TRX alone (negative control) in the presence or absence of GA4. TRX-AtGID1c interacted with GST-LsDELLAs, which were precipitated by glutathione resin, in the presence of GA4 (Fig. 5A). To examine whether LsDELLAs increase the GA-binding activity of AtGID1c, an in vitro binding assay was performed using labelled GA in accordance with protocols used in rice and Arabidopsis (Ueguchi-Tanaka et al., 2005; Nakajima et al., 2006). After mixing labelled 16,17-dihydro-GA4 and AtGID1c, each affinity-purified LsDELLA was added to the mixture, and its GA-binding activity was measured. The activity of AtGID1c increased after the addition of not only Arabidopsis GAI (positive control) but also LsDELLAs (Fig. 5B). These results suggest that LsDELLA1 and LsDELLA2 encode DELLA proteins.
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GA responsiveness in imbibed lettuce seeds
Red light treatment up-regulates the GA responsiveness of Arabidopsis seeds through PHYTOCHROME-INTERACTING FACTOR3-LIKE5 (PIL5), a helix-loop-helix protein. In Arabidopsis seeds, the expression of two DELLA genes, i.e. RGA and GAI, is down-regulated by phytochrome (Oh et al., 2007). To determine if similar phenomena occur in lettuce seeds, LsDELLA genes were examined by QRT-PCR after different light treatments (Fig. 6A). The transcript level of LsDELLA1 was much higher than that of LsDELLA2 and was unaffected by light treatment. The transcript level of LsDELLA2 was slightly increased after FR/R treatment. Furthermore, expression analysis using half-cut seeds showed that the two LsDELLA transcripts accumulated almost equally on both the cotyledon and the hypocotyl ends of the seed (Fig. 6B). Slight increases in LsDELLA2 transcripts were observed on both ends of the seed after FR/R treatment (Fig. 6B). These results suggest that the expression of LsDELLA genes is not markedly affected by light treatment and that their expression patterns in lettuce seeds differ from those of RGA and GAI in Arabidopsis (Oh et al., 2007).
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These collective observations led us to posit that GA responsiveness is not altered by light treatment in lettuce seeds. Therefore, the germination of decoated lettuce seeds was examined in which de novo GA biosynthesis was suppressed by uniconazole-P (GA biosynthesis inhibitor) in the presence of various concentrations of GA3. Notably, GA3 is not metabolized by GA2ox (Nakayama et al., 1990; Oh et al., 2007). Uniconazole-P treatment suppressed radicle emergence in seeds treated with R light and in non-irradiated seeds (Fig. 6C). The germination frequency of decoated lettuce seeds after R treatment increased in a manner similar to that of the GA dose response in non-irradiated seeds (Fig. 6C). These results suggest that GA responsiveness is not markedly altered by R light in lettuce seeds.
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Discussion |
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Since the 1950s, many studies have explored the regulatory mechanisms of photoblastic lettuce seed germination, including biochemical, physical, and physiological studies (see many references that have been published). Of the regulatory mechanisms, the role of GAs and ABA in the regulation of lettuce seed germination is critical. Using biochemical and expression analyses, the control of endogenous GA levels has been shown to be critical for the germination of lettuce seeds after R irradiation (Toyomasu et al., 1993, 1998; Nakaminami et al., 2003; Sawada et al., 2008). This view has also been reported for Arabidopsis seeds (Yamaguchi et al., 1998, 2001; Ogawa et al., 2003; Seo et al., 2006; Yamauchi et al., 2007). Three classes of GA metabolism enzymes have been identified in several higher plant species, including Arabidopsis and rice (Thomas and Hedden, 2006). These include diterpene cyclases (CPS and KS), P450 mono-oxygenases (KO and KAO), and 2ODDs (GA20ox and GA3ox for GA biosynthesis and GA2ox for GA deactivation). In addition to LsGA20ox1, LsGA20ox2, LsGA3ox1, LsGA3ox2, LsGA2ox1, and LsGA2ox2 (Toyomasu et al., 1998; Nakaminami et al., 2003), cDNAs that encode CPS, KS, KO, and KAO were isolated and comprehensive expression analyses were performed to clarify the regulation of GA metabolism in lettuce seeds. To our knowledge, no detailed quantification by QRT-PCR of the transcripts of overall GA metabolism genes in imbibed seeds has yet been reported.
Our comprehensive expression analysis using QRT-PCR showed that the transcript levels of LsGA3ox1 and LsGA3ox2 were much lower than those of the other genes tested and were dramatically up-regulated by R irradiation (Fig. 2B). In imbibed lettuce seeds, endogenous levels of GA1 were much lower than those of GA19 (approximately 1/10th) and GA20 (approximately 1/100th), both of which are GA1 precursors (Toyomasu et al., 1993). These data suggest that GA1 levels are strictly regulated by GA3ox in lettuce seeds and that higher levels of GA19 and GA20 could be a result of the greater expression of other GA biosynthetic genes. The expression of LsKAO, LsGA20ox1, LsGA3ox1, and LsGA3ox2 was suggested to be primarily responsible for GA1 biosynthesis after FR/R treatment, whereas the physiological role of the down-regulation of LsGA20ox2 expression by R light remains unclear (Fig. 2B). Transcripts of LsKAO, LsGA3ox1, and LsGA3ox2 were mainly detected in the hypocotyl end of the seed (Fig. 3B). The ent-kaurenoic acid oxidase converts the ent-kaurene skeleton into the ent-gibberellane skeleton, resulting in the production of GA12, which is the first step in the formation of GA. Generally, the step catalysed by CPS (conversion of GGDP into ent-CDP) is regarded as the first committed step in GA biosynthesis. However, ent-CDP is converted into ent-pimaradiene-related phytoalexins in rice (Cho et al., 2004; Otomo et al., 2004a), and ent-kaurenoic acid is converted into stevioside in Stevia (Tanina et al., 2006). Little is known about the detailed metabolic pathways of diterpenoids in imbibed lettuce seeds; regardless, KAO most probably catalyses the first step of GA biosynthesis. This strongly suggests that GA is mainly synthesized de novo in the hypocotyl end of germinating lettuce seeds, although the localization of accumulated GAs in lettuce seeds remains unclear.
The transcript of LsGA2ox1, a GA deactivation gene that was not regulated by light, was detected in both ends of lettuce seeds (Figs 2B, 3B). Another GA deactivation gene that was detected mainly in the hypocotyl end, LsGA2ox2, was down-regulated by R light treatment (Figs 2B, 3B). Nakaminami et al. (2003) found that recombinant LsGA2ox1 hydroxylated C2 of GA20, as well as that of GA1, and recombinant LsGA2ox2 hydoxylated C2 of GA20 in vitro, although the substrate specificity of both enzymes was not confirmed in vivo. LsGA2ox1 may be responsible for the constitutive metabolism of GA1 and GA20 in imbibed seeds; the down-regulation of LsGA2ox2 in the hypocotyl end of seeds as a result of R irradiation could contribute to GA1 increment.
The patterns of regulation by light of the two GA3ox genes in lettuce are similar to those in Arabidopsis (Yamaguchi et al., 1998). In Arabidopsis seeds, the regulation of AtGA3ox1/GA4 and AtGA3ox2/GA4H gene expression differs; AtGA3ox2/GA4H expression is regulated by PHYB and is not subject to feedback regulation by the GA signal, whereas AtGA3ox1/GA4 expression is regulated by other phytochromes and is subject to feedback regulation (Yamaguchi et al., 1998). Transcripts of both of the genes were detected in the cortex of R-treated seeds (Yamaguchi et al., 2001). The regulation of LsGA3ox1 and LsGA3ox2, both of which were detected in the hypocotyl end of lettuce seeds (Fig. 3B), differed in terms of the involvement of ABA. ABA treatment down-regulated the expression of LsGA3ox1; however, LsGA3ox2 expression was not down-regulated, even in ABA-treated seeds that did not germinate (Fig. 4). In Arabidopsis, both AtGA3ox genes were down-regulated in the ABA-overaccumulating mutant cyp707a2-1 seeds (Seo et al., 2006). Furthermore, ABA deficiency (nced6-1, aba2-2, aao3-4) enhances the germination frequency, increases levels of endogenous physiologically active GA (GA4), and augments the transcript levels of AtGA3ox1 and AtGA3ox2 in FR-treated seeds (Seo et al., 2006). Thus, Seo et al. (2006) suggested that ABA affects GA biosynthesis during Arabidopsis seed germination. Conversely, GA affects ABA levels by controlling the expression of ABA metabolism genes in Arabidopsis (Oh et al., 2007). Sawada et al. (2008) reported that endogenous levels of ABA decrease after the induction of germination by GA treatment via the down-regulation of LsNCED4. It appears that GA and ABA diametrically oppose each other in both Arabidopsis and lettuce seeds, although detailed regulation patterns of the targeted genes differ. In future studies, the measurement of endogenous GA levels after ABA treatment could provide more information on the interaction between GA and ABA in lettuce seeds.
Light alters both GA responsiveness and GA metabolism in Arabidopsis seeds. Specifically, PIL5 regulates GA responsiveness by directly binding to the promoters of GAI and RGA in Arabidopsis seeds (Oh et al., 2007). The Arabidopsis genome contains five DELLA genes (GAI, RGA, RGL1, RGL2, and RGL3) and the rice genome contains one (SLR1) (Ueguchi-Tanaka et al., 2007). Two DELLA genes were isolated from lettuce seeds (Fig. 5). Because knowledge of the lettuce genome and expressed sequence tag sequences is limited, it is not known how many DELLA genes are present in lettuce; however, most of the genes that are expressed in imbibed lettuce seeds are thought to have already been isolated. In contrast to Arabidopsis seeds, the expression of the two DELLA genes was not down-regulated after FR/R treatment (Fig. 6A, B). These results were consistent with those in lettuce seeds that showed that GA responsiveness was unaffected by R light treatment (Fig. 6C). The major limitation of our study was that the DELLA protein expression levels were not examined. DELLA proteins are also regulated by changes in protein stability and turnover, and DELLA proteins are rapidly degraded by the ubiquitin-proteasome system when plants are treated with GA (Ueguchi-Tanaka et al., 2007). Hence, future studies should examine both the transcript levels and translated products of LsDELLA genes.
Regardless, of all of the GA metabolism genes, the expression of LsGA3ox1 and LsGA3ox2 is most potently regulated by phytochrome in the hypocotyl end of imbibed lettuce seeds. This supports the view that lettuce seed germination is regulated mainly via the control of endogenous levels of physiologically active GA, rather than the control of GA responsiveness. Therefore, it is suggested that GA signalling is regulated by the control of the endogenous GA content and/or the control of GA responsiveness, which may vary with the plant species or cultivar.
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Supplementary data |
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TopAbstractIntroductionMaterials and methodsResultsDiscussionSupplementary dataReferences |
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Supplementary data are available at JXB online.
Table S1. Degenerate primer sets used in cDNA cloning.
Table S2. Specific primer sets used in construction of plasmids for functional analysis.
Table S3. Specific primer sets used in the QRT-PCR.
Table S4. GC-MS analysis of the products converted by GST-LsCPS and GST-LsKS.
Table S5. GC-MS analysis of the methyl ester derivatives of products by recombinant LsKO1 and 2 and LsKAO expressed in yeast.
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Acknowledgements |
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This work was supported in part by Grants-in-Aid for the Encouragement of Young Scientists (B) nos 09760111, 11760085, and 15780081 to TT from the Japan Society for the Promotion of Science (JSPS) and by a Grant-in-Aid for the 21st Century Centers of Excellence Program to YS from the JSPS. We thank Mr Mitsuaki Akutsu, Ms Yuko Takeya, and Ms Miyoko Kondo (Yamagata University) for technical support and are grateful to Drs Shinjiro Yamaguchi and Eiji Nambara (RIKEN Plant Science Center) for critical discussions.
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Footnotes |
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* Present address: Division of Plant and Soil Sciences, Davis College of Agriculture, West Virginia University, Morgantown, WV 26506–6108, USA.
Present address: National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA.
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References |
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TopAbstractIntroductionMaterials and methodsResultsDiscussionSupplementary dataReferences |
|---|
Borthwick HA, Hendricks SB, Parker MW, Toole EH, Toole VK. A reversible photoreaction controlling seed germination. Proceedings of the National Academy of Sciences, USA (1952) 38:662–666.
Bustin SA. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. Journal of Molecular Endocrinology (2000) 25:169–193.[Abstract]
Butler WL, Norris KH, Siegelman HW, Hendricks SB. Detection, assay, and preliminary purification of the pigment controlling photoresponsive development of plants. Proceedings of the National Academy of Sciences, USA (1959) 45:1703–1708.
Cho EM, Okada A, Kenmoku H, et al. Molecular cloning and characterization of a cDNA encoding ent-cassa-12, 15-diene synthase, from suspension-cultured rice cells treated with a chitin elicitor. The Plant Journal (2004) 37:1–8.[CrossRef][ISI][Medline]
Inoue Y, Nagashima H. Photoperceptive site in phytochrome-mediated lettuce (Lactuca sativa L. cv. Grand Rapids) seed germination. Journal of Plant Physiology (1991) 137:669–673.[ISI]
Ikuma H, Thimann KV. Action of gibberellic acid on lettuce seed germination. Plant Physiology (1960) 35:557–566.
Kahn AA. Inhibition of gibberellic acid-induced germination by abscisic acid and reversal by cytokinins. Science (1968) 125:645–646.[CrossRef]
Kahn A, Goss JA. Effect of gibberellin on germination of lettuce seed. Science (1957) 125:645–646.
Kawaide H, Sassa T, Kamiya Y. Plantlike biosynthesis of gibberellin A1 in the fungus Phaeosphaeria sp. L487. Phytochemistry (1995) 39:305–310.[CrossRef][ISI]
Marion-Poll A, Leung J. Abscisic acid synthesis, metabolism and signal transduction. In: Plant hormone signalling—Hedden P, Thomas SG, eds. (2006) Oxford, UK: Blackwell Publishing. 1–36.
Nakajima M, Shimada A, Takashi Y, et al. Identification and characterization of Arabidopsis gibberellin receptors. The Plant Journal (2006) 46:880–889.[CrossRef][ISI][Medline]
Nakaminami K, Sawada Y, Suzuki M, Kenmoku H, Kawaide H, Mitsuhashi W, Sassa T, Inoue Y, Kamiya Y, Toyomasu T. Deactivation of gibberellin by 2-oxidation during germination of photoblastic lettuce seeds. Bioscience, Biotechnology, and Biochemistry (2003) 67:1551–1558.[CrossRef][Medline]
Nakayama I, Miyazawa T, Kobayashi M, Kamiya Y, Abe H, Sakurai A. Effects of a new plant growth regulator prohexadione calcium (BX-112) on shoot elongation caused by exogenously applied gibberellins in rice (Oryza sativa L.) seedlings. The Plant Cell (1990) 15:195–200.
Ogawa M, Hanada A, Yamauchi Y, Kuwahara A, Kamiya Y, Yamaguchi S. Gibberellin biosynthesis and response during Arabidopsis seed germination. The Plant Cell (2003) 15:1591–1604.
Oh E, Yamaguchi S, Hu J, Jikumaru Y, Jung B, Paik I, Lee HS, Sun TP, Kamiya Y, Choi G. PIL5, a phytochrome-interacting bHLH protein, regulates gibberellin responsiveness by binding directly to the GAI and RGA promoters in Arabidopsis seeds. The Plant Cell (2007) 19:1192–1208.
Otomo K, Kanno Y, Motegi A, et al. Diterpene cyclases responsible for the biosynthesis of phytoalexins, momilactones A, B, and oryzalexins A–F in rice. Bioscience, Biotechnology, and Biochemistry (2004a) 68:2001–2006.[CrossRef][Medline]
Otomo K, Kenmoku H, Oikawa H, König WA, Toshima H, Mitsuhashi W, Yamane H, Sassa T, Toyomasu T. Biological functions of ent- and syn-copalyl diphosphate synthases in rice: key enzymes for the branch point of gibberellin and phytoalexin biosynthesis. The Plant Journal (2004b) 39:886–893.[CrossRef][ISI][Medline]
Sankhla N, Sankhla D. Reversal of (±)-abscisin II-induced inhibition of lettuce seed germination. Physiologia Plantarum (1968) 21:190–195.[CrossRef]
Sawada Y, Aoki M, Nakaminami K, et al. Phytochrome- and gibberellin-mediated regulation of abscisic acid metabolism during germination of photoblastic lettuce seeds. Plant Physiology (2008) 146:1386–1396.
Seo M, Hanada A, Kuwahara A, Endo A, et al. Regulation of hormone metabolism in Arabidopsis seeds: phytochrome regulation of abscisic acid metabolism and abscisic acid regulation of gibberellin metabolism. The Plant Journal (2006) 48:354–366.[CrossRef][ISI][Medline]
Tanina VH, Alex AR, Rima M, Jim EB. Spatial organization of four enzymes from Stevia rebaudiana that are involved in steviol glycoside synthesis. Plant Molecular Biology (2006) 61:47–62.[CrossRef][ISI][Medline]
Thomas SG, Hedden P. Gibberellin metabolism and signal transduction. In: Plant hormone signalling—Hedden P, Thomas SG, eds. (2006) Oxford, UK: Blackwell Publishing. 147–184.
Toyomasu T, Tsuji H, Yamane H, Nakayama M, Yamaguchi I, Murofushi N, Takahashi N, Inoue Y. Light effects on endogenous levels of gibberellins in photoblastic lettuce seeds. Journal of Plant Growth Regulation (1993) 12:85–90.
Toyomasu T, Kawaide H, Mitsuhashi W, Inoue Y, Kamiya Y. Phytochrome regulation gibberellin biosynthesis during germination of photoblastic lettuce seeds. Plant Physiology (1998) 118:1517–1523.
Ueguchi-Tanaka M, Ashikari M, Nakajima M, et al. GIBBERELLIN INSENSITIVE DWARF1 encodes a soluble receptor for gibberellin. Nature (2005) 437:693–698.[CrossRef][ISI][Medline]
Ueguchi-Tanaka M, Nakajima M, Ashikari M, Matsuoka M. Gibberellin receptor and its role in gibberellin signaling in plants. Annual Review of Plant Biology (2007) 58:183–189.[CrossRef][Medline]
Yamaguchi S, Smith MW, Brown RG, Kamiya Y, Sun TP. Phytochrome regulation and differential expression of gibberellin 3β-hydoroxylase genes in germinating Arabidopsis seeds. The Plant Cell (1998) 10:2115–2126.
Yamaguchi S, Kamiya Y, Sun TP. Distinct cell-specific expression patterns of early and late gibberellin biosynthetic genes during Arabidopsis seed germination. The Plant Journal (2001) 28:443–453.[CrossRef][ISI][Medline]
Yamauchi Y, Takeda-Kamiya N, Hanada A, Ogawa M, Kuwahara A, Seo M, Kamiya Y, Yamaguchi S. Contribution of gibberellin deactivation by AtGA2ox2 to the suppression of germination of dark-imbibed Arabidopsis thaliana seeds. Plant and Cell Physiology (2007) 48:555–561.
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