- Research article
- Open Access
Gibberellin mediates daylength-controlled differentiation of vegetative meristems in strawberry (Fragaria × ananassaDuch)
BMC Plant Biology volume 9, Article number: 18 (2009)
Differentiation of long and short shoots is an important developmental trait in several species of the Rosaceae family. However, the physiological mechanisms controlling this differentiation are largely unknown. We have studied the role of gibberellin (GA) in regulation of shoot differentiation in strawberry (Fragaria × ananassa Duch.) cv. Korona. In strawberry, differentiation of axillary buds to runners (long shoot) or to crown branches (short shoot) is promoted by long-day and short-day conditions, respectively. Formation of crown branches is a prerequisite for satisfactory flowering because inflorescences are formed from the apical meristems of the crown.
We found that both prohexadione-calcium and short photoperiod inhibited runner initiation and consequently led to induction of crown branching. In both cases, this correlated with a similar decline in GA1 level. Exogenous GA3 completely reversed the effect of prohexadione-calcium in a long photoperiod, but was only marginally effective in short-day grown plants. However, transfer of GA3-treated plants from short days to long days restored the normal runner formation. This did not occur in plants that were not treated with GA3. We also studied GA signalling homeostasis and found that the expression levels of several GA biosynthetic, signalling and target genes were similarly affected by prohexadione-calcium and short photoperiod in runner tips and axillary buds, respectively.
GA is needed for runner initiation in strawberry, and the inhibition of GA biosynthesis leads to the formation of crown branches. Our findings of similar changes in GA levels and in GA signalling homeostasis after prohexadione-calcium and short-day treatments, and photoperiod-dependent responsiveness of the axillary buds to GA indicate that GA plays a role also in the photoperiod-regulated differentiation of axillary buds. We propose that tightly regulated GA activity may control induction of cell division in subapical tissues of axillary buds, being one of the signals determining bud fate.
Formation of long and short shoots (also called spurs) is a common developmental trait in several economically important species of the Rosaceae family, including apple (Malus × domestica Borkh.), pear (Pyrus communis L.), apricot (Prunus armeniaca L.) and sour and sweet cherry (Prunus ceracus L., Prunus avium L.). Long shoots have long internodes, whereas short shoots are lateral organs with very short internodes and leaf rosette-like appearance. In these species, diverse flowering habits can be found and even the cultivars can differ from each other in this respect. Typically, flowers are borne either on terminal (apple, pear) or lateral (cherry, apricot) buds of short shoots [1–3].
Both shoot types can be found in strawberry (Fragaria sp.; e.g. F. × ananassa Duch., F. vesca L.). Strawberry is a perennial rosette plant with short internodes in its crown. Strawberry axillary buds may form both short and long shoots; branch crowns and runners, respectively. Runners are composed of successive units of two long internodes, followed by a leaf rosette (daughter plant). When the terminal bud of the runner forms a daughter plant, the axillary bud in the second node of the runner produces the next sympodial unit. Inflorescences are formed terminally in the short shoots, while the uppermost axillary bud(s) continue vegetative growth of the crown [4, 5].
Junebearing strawberry cultivars are facultative short-day (SD) plants; short daylength is the primary factor for induction of flowering, but a strong interaction exists between photoperiod and temperature [6–8]. Daylength also controls vegetative differentiation of axillary buds in strawberry. In long-day (LD) conditions, runners are formed, and in SD crown branching occurs [4, 9, 10]. Crown branching is a prerequisite for satisfactory flowering, and consequently, for berry crop production because the inflorescences are formed from the apical meristems of the crown and axillary buds containing at least two leaf initials [10, 11].
In the late 1950s, Guttridge  proposed that a transmissible hormone produced in LD enhances petiole elongation and runnering and inhibits flowering in strawberry, the effects mimicked by gibberellin (GA) application [13–16]. Inhibitors of GA biosynthesis have the opposite effect on vegetative growth [17–20], but their effect on flowering time is unknown. Prohexadione-calcium (Pro-Ca), the inhibitor of GA 3-oxidase enzyme , has recently been shown to effectively inhibit runner formation and enhance crown branching in strawberry under field conditions , with a concomitant increase in berry yield .
In strawberry, the early 13-hydroxylation pathway appears to be a predominant GA biosynthesis pathway [24–26]. In this pathway, GA12 is 13-hydroxylated to GA53, which is further converted to other GAs in cytosol by three enzymes, encoded by small gene families . GA 20-oxidases are multifunctional enzymes responsible for conversion of GA53 to GA20 through GA44 and GA19. GA 3-oxidases produce bioactive GA1 from GA20, and GA 2-oxidases catalyse the inactivation steps GA20 to GA29 and GA1 to GA8, respectively. Many of the GA oxidase genes are subjected to tight developmental [28, 29] and/or light (light quality, photoperiod) regulation [30–32].
GA receptors have recently been cloned, one from rice and three, GID1a, GID1b and GID1c, from Arabidopsis [33, 34]. Binding of GA to GID1 leads to a physical interaction between GID1 and DELLA transcriptional repressors , the central components of the GA signalling pathway that suppress GA-mediated growth responses . SLY1 F-box protein, a component of E3 ubiquitin ligase SCF complex (SKP/Cullin/F-box), recruits the receptor-bound DELLA proteins and targets them to degradation in 26S proteasome, leading to the release of plant growth from DELLA-mediated restraint .
The GA pathway is tightly regulated by GA itself at multiple levels, a phenomenon called GA signalling homeostasis . Some of the GA biosynthetic (GA20ox and GA3ox) genes and positive regulators of GA signalling (GID1, SLY1) are feedback-regulated, and catabolic genes (GA2ox) and negative signalling components (DELLA genes) are feed-forward regulated by GA. In addition, a reduced level of one DELLA protein can be compensated by accumulation of another DELLA .
Despite the importance of short and long shoot differentiation in many cultivated species of the Rosaceae family, the physiological and genetic mechanisms of this differentiation remain largely unknown. In this paper, we studied the role of GA in regulating short/long shoot differentiation in strawberry, which is one of the best-developed model species for Rosaceae . We report the effects of daylength and GA biosynthesis inhibitor Pro-Ca on axillary bud differentiation, GA levels and GA signalling homeostasis. The results indicate that GA is one of the key signals affecting axillary bud differentiation.
Photoperiod, prohexadione-calcium and GA3affect the differentiation of strawberry axillary buds
As shown in Table 1, 10-, and 14-h photoperiods (SD) promoted crown branching equally, whereas no branch crowns were found in plants grown under an 18-h photoperiod (LD). Pro-Ca treatment of 50 mg l-1 reduced the elongation of runners and petioles rapidly in all photoperiods (Figure 1A, B). This treatment also strongly enhanced crown branching and reduced the number of runners compared with control plants (Figure 1C). The effect of Pro-Ca was completely reversed by 25 μg of GA3 (p < 0,001) applied twice to the youngest fully open leaf, suggesting that the reduced level of active GA was responsible for the altered bud fate. Our data show that both SD and Pro-Ca treatment similarly promoted branch crown formation, whereas GA3 or LD enhanced runner formation from axillary buds of the strawberry crown.
Short photoperiod promotes crown bud differentiation on strawberry runners
Based on our observations on axillary bud differentiation in crowns, we wanted to test whether the developmental fate of axillary buds on runners is similarly regulated by photoperiod. These buds are more accessible and easier to collect than buds of the crown and could provide a good model system for analytical and molecular studies. Strawberry runners consist of sympodial units of two long internodes, followed by a daughter plant with short internodes (Figure 2D). We tested photoperiodic responses of the axillary bud on the second node of the runner (axillary bud #2). In an 18-h photoperiod, axillary bud #2 formed a new sympodial unit after the production of a daughter plant by the apical meristem of the previous unit. This was continuously repeated until the end of the experiment, when the longest runners consisted of about four sympodial units, i.e. eight internodes (Table 1). In contrast, both 10- and 14-h photoperiods (SD) stopped runner growth after the formation of the first or second daughter plant. In this case, axillary bud #2 differentiated into a crown bud instead of continuing runner growth.
To further study the photoperiodic control of bud differentiation, newly emerged 2- to 3-cm-long (~2-day-old) runners were marked 4, 8, 12 and 16 days after transfer to SD. Axillary bud #2 differentiated into a normal branch crown in all runners (n = 10) marked 8 days or later after transfer to SD. In runners marked after four days in SD, the differentiation of axillary bud #2 into crown buds was incomplete; four out of nine buds formed one elongated internode (> 3 mm) before producing a normal leaf rosette. Thus, axillary bud #2 differentiated into a crown bud in runners, which started to form 2 – 6 days after transfer to SD. In conclusion, the differentiation of runner axillary bud #2 can be strictly controlled, and therefore, it provides a good model to study bud differentiation in strawberry.
Timing of differentiation of axillary buds in runners
Anatomical studies of developing axillary buds on 6- and 10-day-old runners show that differentiation to either crown or runner bud takes place between these time points. On day six, SD- and LD-grown axillary buds were morphologically almost indistinguishable (Figure 2A), except that the number of cells in the first (oldest) internode was slightly higher in LD than in SD. In 10-day-old runners the buds developed in SD and LD were clearly different (Figure 2B, C). In SD buds, probably already determined as crown buds, the cell length had not increased, and the number of cells in the longitudinal axis of the first internode of the bud was almost the same as four days earlier; 26 and 30 cells (n = 5) in 6- and 10-day-old runners, respectively. By contrast, in LD, the cell number had increased, and the length of LD buds was double that of SD buds in 10-day-old runners (Figure 2C). In addition, clear longitudinal cell files were found in late LD buds compared with less regular organization of cells in SD (Figure 2B, C).
We wanted to confirm the results for timing of differentiation with Pro-Ca treatments. Nineteen 4- to 8-day-old runners were treated with 200 mg l-1 Pro-Ca under LD conditions, and the developmental fate of axillary bud #2 was determined. Axillary buds of all 4- to 6-day-old runners (8 runners) treated with Pro-Ca differentiated into branch crowns, whereas the buds in older runners (11 runners) were only partially affected; the branch crowns with an elongated first internode (5 – 10 mm) or short runners were formed. In runners older than eight days, axillary bud #2 was already committed to developing into a runner and Pro-Ca treatment could not alter or restore its fate. Thus, under the LD conditions applied, the identity of axillary bud #2 is determined in 'Korona', when the age of the runner is between 6 and 8 days.
Pro-Ca treatment and short photoperiod lead to reduced GA levels
Pro-Ca treatment of whole plants resulted in rapid changes in the levels of several 13-hydroxylated GAs in runner tips (Figure 3). The level of active GA1 was nearly halved already one day after the Pro-Ca treatment and three days later only one quarter was left compared with non-treated control plants. In contrast, after four days of treatment, the levels of GA20 and GA19, the immediate precursors of GA1, were increased five- and twofold, respectively. Changes in GA20 and GA1 levels were reflected in the levels of their 2β-hydroxylation products, GA29 and GA8, respectively.
The analysed samples consisted of both bud meristems and internode tissues. To obtain more precise information about GAs in the buds themselves, we collected axillary bud samples from runners of SD- and LD-grown strawberry plants and analysed the levels of bioactive GA and the expression levels of several candidate genes. The first samples consisted of buds just prior to the determination of bud identity (axillary bud #2 from a 6-day-old runner, Figure 2A), and the next sampling was done four days later, when bud differentiation was clearly visible (Figure 2B, C). We observed that GA1 level was slightly higher in SD-grown axillary buds than in LD buds prior to determination of bud identity (Figure 4B). However, four days later, an over 50% reduction in GA1 level occurred in SD buds, whereas in LD-grown buds the GA1 level remained constant.
Short photoperiod reduces GA sensitivity of axillary buds
If reduced level of active GA found in SD is responsible for changes in bud fate, GA treatment should restore runner initiation from axillary buds under SD. Therefore, we applied 25 μg of GA3 to the SD-grown 2- to 4-day-old runner tips and observed the final length of the treated runners (two internodes preceding axillary bud #2) and the fate of axillary bud #2. This GA treatment did not significantly increase the length of the runners in SD, and the fate of axillary bud #2 was affected only in a few plants (Table 2). Three out of nine buds initiated runner after GA treatment in SD, and all newly formed runners remained short (1 – 4 cm). However, moving of plants to LD after GA treatment had a strong effect on the length of treated runner and fully restored the runner growth from axillary bud #2. LD without GA treatment, in contrast, neither increased the final length of the runners nor affected the fate of axillary bud #2. These findings suggest that, in addition to bud GA1 levels, photoperiod affects the sensitivity of buds and elongating runners to GA. Similarly, the growth of strawberry petioles in SD was reduced before the GA1 levels were reduced .
Identification of putative GA biosynthesis, signalling and target genes
For gene expression studies, we isolated full-length cDNAs encoding putative strawberry GA 20-oxidase (FaGA20ox) [GenBank: DQ195504] and GA 3-oxidase (FaGA3ox) [GenBank DQ195505]. The EST clone for a putative GA 2-oxidase was sequenced earlier . A search on public databases revealed no additional GA oxidase sequences in strawberry. In addition to GA biosynthetic genes, we cloned a 816-bp fragment of putative GA signalling repressor, FaRGA [GenBank: DQ195503], and identified homologues of putative GA signalling genes SLY1 and GAI as well as two putative GA receptors, GID1b and GID1c, from public databases. In addition, a 558-bp fragment of a putative SPY homologue was found from our own Fragaria vesca EST collection (Mouhu K et al., unpublished data). As putative target genes for GA regulation we searched strawberry sequences homologous to Arabidopsis GA regulated genes and identified XERICO  and FaGAST . XERICO is a RING-H2 zinc finger protein, and FaGAST is homologous to the GA-induced GASA family of Arabidopsis and the GAST family of tomato . For the sake of clarity, common names of Arabidopsis genes are used for corresponding strawberry EST sequences.
Effect of Pro-Ca on gene expression in runner tips
Several genes, involved in GA biosynthesis and signalling, are regulated by GA in Arabidopsis [35, 41]. We compared the expression levels of ten putative GA biosynthesis, signalling and target genes in Pro-Ca-treated and non-treated strawberry runner samples two and four days after treatment. At these time points, bioactive GA1 levels were reduced by 68% and 74%, respectively (Figure 3). The reduced GA1 levels were associated with upregulation of GA-biosynthetic gene FaGA3ox and severalfold downregulation of FaGA2ox (Table 3). Based on RNA-blot analysis, Pro-Ca did not affect GA20ox expression levels (data not shown).
Positive regulators of GA signalling, SLY and GID1b, were upregulated in Pro-Ca-treated plants, as was the XERICO homologue (Table 3). Among the negative regulators of GA signalling, both DELLA genes (GAI and RGA) were slightly downregulated by Pro-Ca. In contrast to earlier studies , GAST was upregulated in samples with reduced GA1 levels four days after Pro-Ca treatment.
Effect of photoperiod on gene expression in axillary buds
In addition to runner tips, we analysed gene expression in axillary bud #2. GA oxidase genes GA3ox and GA2ox were twofold and sevenfold reduced, respectively, in differentiated SD grown buds compared with LD buds (Table 3). In contrast, no clear differences between SD and LD were found in non-differentiated buds. Reduced GA3ox mRNA abundance in SD buds was contrary to our results for Pro-Ca-treated runners, indicating that photoperiod rather than feedback mechanism controls transcription of this gene in buds. Therefore, we analysed GA3ox expression levels also in runner tips grown in SD and LD conditions for 8 or 12 days, but no significant differences were found in these samples. However, GA2ox was 7.4-fold downregulated in SD-grown axillary buds compared with runner tips, indicating more active GA signalling in runners. In conclusion, GA3ox and GA2ox expression levels were unaffected by photoperiod in elongating runner tissues, but were downregulated in SD-grown axillary buds with crown bud identity.
Based on similar reductions in GA1 levels in SD-grown buds and Pro-Ca-treated runners, we expected to observe upregulation of GID1b, SLY, XERICO and GAST and downregulation of both DELLA genes in SD-grown differentiated axillary buds. This was in fact true for all of these genes (Table 3). However, the transcription of XERICO, GID1b, SLY and GAST was clearly upregulated also in non-differentiated SD-grown buds, although the GA1 level was not reduced (Table 3), possibly indicating some early reduced GA signalling event.
Our results confirm earlier studies on photoperiodic control of vegetative growth in strawberry and provide further evidence for involvement of GA in regulation of axillary bud differentiation into branch crowns or runners in strawberry cv. Korona. Differentiation of axillary buds in the strawberry crown is strictly regulated by photoperiod [9, 10]. We have shown that this also applies to axillary buds of runners (axillary bud #2), which can be used as models to study the regulation of bud fate. The critical photoperiod to induce runner formation in 'Korona' was between 14 and 18 h in axillary buds of both crowns and runners. Moreover, these buds responded similarly to Pro-Ca and GA3 applications, indicating a similar regulation of bud fate in crown and runners.
Different GA biosynthesis inhibitors have been shown to affect strawberry vegetative development, including runner formation and crown branching [17, 18, 22]. We found that Pro-Ca rapidly reduced elongation growth of petioles and runners and inhibited runner initiation from axillary buds after 1 – 2 days. The inhibition correlated with a moderate (41 – 68%) reduction in the level of GA1, which has been shown to be the predominant bioactive GA in strawberry [this study, [24–26]]. Interestingly, a similar reduction in GA1 level was found in SD-grown differentiated axillary bud #2 compared with differentiated LD buds, while GA1 levels were not clearly affected by photoperiod in four days younger non-differentiated buds. Olsen et al.  reported a similar drop in GA1 level in subapical tissues of Salix pentandra before the cessation of elongation growth.
GA3 application completely reversed the effect of Pro-Ca on axillary buds, but was only marginally effective on SD-grown axillary bud #2. However, the movement of plants to LD after GA3 treatment fully restored runner formation from this bud, whereas the movement of non-treated plants to LD did not affect bud fate. According to these data, a moderate drop in GA1 level in SD-grown axillary buds and in Pro-Ca-treated plants may alter bud fate, but it is also possible that photoperiod alters GA responsiveness of the buds. A similar effect has been observed in Salix pentandra .
The first anatomical sign of runner identity in LD-grown axillary buds is rapid longitudinal cell division occurring in the first internode. In contrast to LD-grown buds, cell division in internodes of SD buds is more disorganized and ceases soon after determination of branch crown identity. GA has been shown to affect elongation growth both by controlling alignment of cortical microtubules [45, 46] and by controlling cell division [47–49]. Accordingly, higher GA level/action in LD-grown strawberry axillary buds, compared with SD buds, may induce the transverse orientation of microtubules in the longitudinal axis of the cells, thereby determining the direction of cell division. Furthermore, GA may be a major inductive signal starting cell division in strawberry LD buds.
Gene expression analysis revealed that the expression of GA2ox, involved in GA inactivation, was sevenfold downregulated after both Pro-Ca and SD treatment and correlated with reduced GA1 levels. This suggests a strong feed-forward regulation, which is a common feature for several GA biosynthetic genes [35, 38, 41]. GA3ox expression was upregulated in Pro-Ca-treated plants, also indicating feedback regulation. However, we did not observe similar feedback control in SD-grown axillary buds. Instead, GA3ox expression was reduced in relation to changed GA1 level, suggesting that photoperiod may regulate its activity. Photoperiodic regulation of GA3ox was further tested in SD- and LD-grown runner tips, but no changes were found after 8 or 12 SD cycles compared with LD. We therefore postulate that GA3ox in strawberry is not necessarily regulated by photoperiod or that its regulation in buds and in runner tips is different. A local, bud-specific decrease in GA activity is supported by the finding that GA2ox was sevenfold downregulated in SD-grown axillary bud #2 compared with runner tips, while under LD it had a similar expression level in both tissues. These data are consistent with earlier findings that the biosynthesis of active GA occurs at the site of GA action [43, 50–52]. In strawberry axillary buds, subapical tissue is a potential site of GA biosynthesis and action. Thus, some unknown photoperiod-regulated factor may activate or repress runner initiation by affecting the biosynthesis of GA1 in the subapical tissues of the bud, consequently determining bud fate.
In addition to GA biosynthetic genes, we also identified six putative GA signalling and two putative target genes in strawberry. Most of these transcripts showed similar GA regulation in strawberry as the corresponding genes in Arabidopsis [35, 41]. The expression of putative positive regulators of GA signalling, GID1b and SLY, was upregulated, while that of negative regulators, RGA and GAI, was downregulated by Pro-Ca and SD, following changes at the level of GA1. Moreover, GA-responsive XERICO and GAST were upregulated after both Pro-Ca and SD treatments. The GA and SD regulation of these genes, in addition to GA2ox, indicates strictly regulated GA signalling homeostasis and reflects more active GA signalling in LD, providing molecular evidence for GA regulation of strawberry axillary bud differentiation.
XERICO, GID1b, SLY and GAST were upregulated also in non-differentiated SD-grown buds, although the GA1 level was unchanged. This may be explained by GA-independent regulation of these genes or by an early event of altered responsiveness of buds to GA in SD. This is supported by the finding that the response of strawberry axillary buds and runners to exogenous GA3 was indeed reduced in SD. In Arabidopsis, the overexpression of XERICO, a GA-downregulated RING-H2 zinc finger protein, increases ABA accumulation, being a possible link between antagonistic ABA and GA pathways . Moreover, ABA, induced by flooding, has been shown to regulate responsiveness to GA in deepwater rice intercalary meristems . Thus, threefold upregulation of XERICO in non-differentiated axillary buds in SD compared with LD could indicate that XERICO and ABA are regulators of axillary bud fate upstream of GA.
One interesting feature of strawberry is an obvious antagonism between runner formation and flowering induction. These processes have opposite responses to both exogenous GA and photoperiod, thereby raising the question about common regulation [5, 9, 13]. However, in Fragaria vesca L., seasonal flowering (SD genotype) vs. perpentual flowering as well as runnering vs. non-runnering phenotypes are determined by different single genes, "seasonal flowering locus" and "runnering locus", seasonal flowering and runnering being dominant characters [54, 55]. Emerging data from different plant species indicate that CONSTANS (CO) and FLOWERING LOCUS T (FT) are central regulators of daylength-dependent flowering induction and that FT protein acts as a long-distance signal [56–58]. Interestingly, the CO/FT module may have a more general role in daylength responses, including growth cessation and tuberization [59–61]. Hybrid poplar CENTRORADIALIS-LIKE 1 (CENL1), a gene belonging to same gene family as FT, also coincides with growth cessation . This gene is expressed mainly in the rib meristem area, and is downregulated in the shoot apex by SD. A gene homologous to CENL1 is also found in strawberry, and our gene expression data show that it is upregulated threefold in differentiated LD-grown axillary buds compared with SD buds. Moreover, anti-sense expression of apple TFL1 homologue in apple reduces the juvenile phase and produces dwarf plants, supporting the role of TFL1 in the regulation of stem elongation . The role of the CO/FT module and TFL1 in photoperiodic responses in strawberry warrants further study. In contrast to other plants, studies in Lolium temulentum indicate that photoperiodic flowering is mediated by GA5 . However, the link between photoperiodic effects and GA biosynthesis/action also remains an open question .
Our results indicate that GA functions as one of the key signals regulating the developmental fate of vegetative buds in strawberry. Some photoperiod-dependent factor(s) regulates GA biosynthesis and/or signalling in the subapical tissues of strawberry axillary buds, thereby determining bud fate. In light of these data, identification and functional characterization of the Fragaria "runnering locus" gene is of great interest. Strawberry is a potential model plant for molecular studies of short shoot/long shoot differentiation, and these studies may uncover new possibilities for controlling yield formation in various small fruit and fruit species.
Plant material and growing conditions
Cultivated strawberry (Fragaria × ananassa, Duch.) cv. Korona plants were used for the experiments carried out in greenhouse conditions at the University of Helsinki. Plants were propagated from runner cuttings, which were rooted on sphagnum peat. Plants were irrigated when needed with a complete fertilizer solution containing Ca(NO3)2 (Kemira GrowHow, Finland) and a strawberry fertilizer mixture (Mansikan täyslannos, Kemira GrowHow, Finland) in a ratio of 1:3. Air temperature in the greenhouse was maintained at 18/15°C (day/night), and daylight was supplemented with high pressure sodium (HPS) lamps (Osram NAV-T 400W, 90 ± 10 μmol m-2 s-1) for 18 h daily.
All short-day (SD) treatments (photoperiod 10, 12 or 14 h) were carried out at the greenhouse using darkening curtains, while long-day (LD) control treatments (photoperiod 18 h) were conducted in a similar greenhouse compartment without curtains. The main light period (the shortest photoperiod in each experiment) was given during natural day, which was 7 – 12 h during the experiments (October – March). During the main light period plants were illuminated by HPS lamps (90 ± 10 μmol m-2 s-1 at plant height plus natural light), and incandescent lamps were used for low-intensity daylength extension (5 ± 1 μmol m-2 s-1 at plant height), yielding nearly equal total irradiance in all photoperiods. Air temperature was 18°C during the main light period, otherwise 15°C.
Pro-Ca and GA3treatments
Pro-Ca 10% w/w a.i. (BAS 125 growth regulator, BASF, Ludwigshafen, Germany) was dissolved in water and diluted to indicated concentrations. Two to three drops of Tween 20 was added to facilitate uptake of Pro-Ca. Water containing Tween 20 was applied to control plants. Pro-Ca sprays were applied to drip-point, using a hand sprayer. To examine whether Pro-Ca-induced growth changes were caused by decreased GA levels, 25 μg of GA3 (Duchefa, Haarlem, The Netherlands) in 5 μl of 70% ethanol was applied to the tip of the youngest fully open leaf twice, one and two weeks after Pro-Ca treatments. Control plants were treated similarly with ethanol containing no GA3. Runner GA treatments were carried out by applying 25 μg of GA3 in 5 μl of 70% ethanol to the runner tip once, and control plants were similarly treated with 70% ethanol.
Gibberellin extraction, purification and detection
All samples for GA analysis were collected 5 – 7 h after the beginning of the subjective day to avoid possible diurnal changes. Runner tip samples 3 cm in length were collected from Pro-Ca-treated (50 mg l-1 a.i.) plants 1, 2 and 4 days after treatment and from water-treated control plants (day 0). Samples were collected during the linear growth stage of the runners, freeze-dried and stored at -80°C until GA extraction. Runner tip samples of 1 – 2 g (FW) were homogenized, and GAs were extracted with 85% aqueous methanol at 4°C in a shaker with added internal standards, 10 ng (runner tips) each of [2H2] GA 1, 4, 8, 9, 19, 20, 29, 53 and [2H1] GA 44 (all deuterated GAs were obtained from Prof. L. Mander, Australian National University, Canberra). Purification of GAs was done according to Junttila et al. , with the following modifications: Volumes were scaled down and purification was performed in 2 ml Eppendorf tubes. After partitioning of samples against ethylacetate, borax/hydrochloric acid pH 8 buffer (Einecs, Fluka) was applied to the samples to facilitate pH adjustment. Bead volume of Sephadex columns was 0.5 ml. In addition, smaller (100 mg) C18- and aminopropylsilyl solid-phase extraction columns (Sep-Pak, Waters, Milford, MA, USA) were used. HPLC purification and fractionation of samples and GA analysis by GC-MS were done at the University of Tromsø, as described earlier . The instrumentation consisted of a PAL autoinjector (CTC Analytics AG, Zwingen, Switzerland) and a Factor Four capillary column (VF-5 ms, 30 m × 0.25 mm ID; 0.10 μm film thickness, Varian, Middelburg, The Netherlands) installed in a Trace GC connected to a Trace DSQ single quadropole mass selective detector (ThermoFinnigan, Austin, TX, USA). XCalibur 1.3 software (ThermoFinnigan) was used to control the system and to review the data. For each GA and its 2H analogue, at least two characteristic ions were recorded. Two biological duplicates were performed for each sample.
Axillary bud samples of 5 – 15 mg (FW) were collected from LD (18 h) and SD (12 h) grown 6- and 10-day-old runner tips under a dissecting microscope, frozen in liquid nitrogen and stored at -80°C. Homogenized bud samples were extracted with added internal standards (100 pg each) and GAs were purified according to King et al. . GA analyses by GC-MS were done at the Umeå Plant Science Centre, as described earlier .
RNA extraction, cDNA synthesis and gene cloning
Strawberry total RNA was isolated using the pine tree method . mRNA was extracted with a NucleoTrap mRNA purification kit (BD Biosciences, Palo Alto, NC, USA). cDNA synthesis was performed using the 1st strand cDNA synthesis kit (Roche Diagnostics, Indianapolis, IN, US). cDNA fragments of FaGA20ox, FaGA3ox and FaRGA genes were amplified from runner tip cDNA samples by a standard RT-PCR protocol using Taq Polymerase (Roche Diagnostics). The following degenerate primers were used: FaGA20ox; 5'-TGG CCI GAY SAB GAR AAR CC-3' (sense) and 5'-CCR TTY GAW AGI GCC ATR AA-3' (anti-sense), FaGA3ox; 5'-AAR CKY ATG TGG TIY GAR GGI TT-3' (sense) and 5'-TCB GTR TGI GCD SCI AGM CCC AT-3' (anti-sense), FaRGA; 5'-GCW CAR AAR CTY GAR CAG CTT GA-3' (sense) and 5'-AAV GCT TCV AGR ATV GCT TGA TT-3' (anti-sense). The BD Smart RACE cDNA amplification kit (BD Biosciences) was used to amplify the 5' and 3' ends of FaGA20ox and FaGA3ox genes. All PCR products were cloned into a pGEM T Easy vector (Promega, Madison, WI, USA) and sequenced by ABI Prism 3100 16-capillary sequencer (Applied Biosystems, Foster City, CA, USA). Strawberry GA 2-oxidase gene has been cloned earlier . Full-length cDNA of FaGA2ox was obtained from Dr. Asaph Aharoni (Plant Research International, Wageningen, The Netherlands).
Identification of putative GA signalling and target sequences
Fragaria sequences homologous to Arabidopsis GA biosynthetic, signalling and target genes were searched for in the Genbank nucleotide and EST databases by using the tBLASTn algorithm. Homologous strawberry sequences were further analysed by the BLASTx algorithm, and only sequences showing the highest sequence homology with the corresponding Arabidopsis genes were included in real-time RT-PCR analysis.
cDNAs for real-time reverse transcription PCR were synthesized from total RNA using a Superscript III RT kit (Invitrogen, Carlsbad, USA) and dT18VN anchor primers. LightCycler 480 SYBR Green I Master kit (Roche Diagnostics) was used to perform 15 μl real-time RT-PCR reactions in 384-well plates according to the manufacturer's instructions (Light Cycler 480 real-time PCR system, Roche Diagnostics). PCR primers with Tm value of 60°C were used (Table 4), and the presence of single PCR product was verified by dissociation analysis. Relative quantification was performed by using UBI14 or UBI14 + Rubisco small subunit 1a as control genes for axillary bud or runner samples, respectively.
Growth measurement data were subjected to one-way ANOVA when applicable. Comparisons of the means were done by Tukey's test. Statistical analyses were conducted using NCSS 2000 software.
Tukey HB: Dwarfed fruit trees. New York: The Macmillan company; 1964.
Westwood MN: Temperate-zone pomology: physiology and culture. Singapore: Timber Press; 1993.
Dennis F: Flowering, pollination and fruit set and development. Apples: botany, production and uses. Edited by: Ferree DC, Warrington IJ. Cambridge: CABI Publishing; 2003:153-166.
Darrow GM: The strawberry. History, breeding and physiology. New York: Holt, Rinehart and Winston;1966.
Guttridge CG: Fragaria × ananassa. CRC Handbook of Flowering. Edited by: Halevy A. Boca Raton: CRC Press, 1985, III: 16-33.
Heide O: Photoperiod and temperature interactions in growth and flowering of strawberry. Physiol Plant. 1977, 40: 21-26. 10.1111/j.1399-3054.1977.tb01486.x.
Durner EF, Poling EB: Strawberry developmental responses to photoperiod and temperature: a review. Advances Strawb Prod. 1988, 7: 6-15.
Sønsteby A, Nes A: Short days and temperature effects on growth and flowering in strawberry (Fragaria × ananassa Duch.). J Hort Sci Biotech. 1998, 73: 730-736.
Konsin M, Voipio I, Palonen P: Influence of photoperiod and duration of short-day treatment on vegetative growth and flowering of strawberry (Fragaria × ananassa Duch.). J Hort Sci Biotech. 2001, 76: 77-82.
Hytönen T, Palonen P, Mouhu K, Junttila O: Crown branching and cropping potential in strawberry (Fragaria × ananassa, Duch.) can be enhanced by daylength treatments. J Hort Sci Biotech. 2004, 79: 466-471.
Arney SE: Studies of the growth and development of the genus Fragaria. II. The initiation, growth and emergence of leaf primordia in Fragaria. Annals Bot. 1953, 17: 477-492.
Guttridge CG: Further evidence for a growth-promoting and flower-inhibiting hormone in strawberry. Annals Bot. 1959, 23: 612-621.
Thompson PA, Guttridge CG: Effect of gibberellic acid on the initiation of flowers and runners in the strawberry. Nature. 1959, 184: 72-73.
Guttridge CG, Thompson PA: The effects of gibberellins on growth and flowering of Fragaria and Duchesnea. J Exp Bot. 1963, 15: 631-646. 10.1093/jxb/15.3.631.
Tafazoli E, Vince-Prue D: A comparison of the effects of long days and exogenous growth regulators on growth and flowering in strawberry, Fragaria × ananassa, Duch. J Hort Sci. 1978, 53: 255-259.
Paroussi G, Voyiatzis DG, Paroussis PD, Drogoudi PD: Growth, flowering and yield responses to GA3 of strawberry grown under different environmental conditions. Sci Hort. 2002, 96: 103-113. 10.1016/S0304-4238(02)00058-4.
Avigdori-Avidov H, Goldschmidt EE, Kedar N: Involvement of endogenous gibberellins in the chilling requirements of strawberry (Fragaria × ananassa, Duch.). Annals Bot. 1977, 41: 927-936.
Nishizawa T: The effect of paclobutrazol on growth and yield during first year greenhouse strawberry production. Sci Hort. 1993, 54: 267-274. 10.1016/0304-4238(93)90105-Y.
Wiseman NJ, Turnbull CGN: Effects of photoperiod and paclobutrazol on growth dynamics of petioles in strawberry (Fragaria × ananassa). Australian J Plant Physiol. 1999, 26: 353-358.
Reekie JYC, Hickleton PR: Strawberry growth response to prohexadione-calcium. Proc North Amer Strawb Conf. 2002, 5: 147-152.
Rademacher W: Growth retardants: Effects on gibberellin biosynthesis and other metabolic pathways. Annu Rev Plant Physiol Mol Biol. 2000, 51: 501-531. 10.1146/annurev.arplant.51.1.501.
Black BL: Prohexadione-calcium decreases fall runners and advances branch crowns of 'Chandler' strawberry in a cold-climate annual production system. J Amer Soc Hort Sci. 2004, 129: 479-485.
Hytönen T, Mouhu K, Koivu I, Elomaa P, Junttila O: Prohexadione-calcium increases the cropping potential and yield in strawberry. Eur J Hort Sci. 73: 210-215.
Taylor DR, Blake PS, Browning G: Identification of gibberellins in leaf tissues of strawberry (Fragaria × ananassa, Duch.) grown under different photoperiods. Plant Growth Regul. 1994, 15: 235-240. 10.1007/BF00029896.
Wiseman NJ, Turnbull CGN: Endogenous gibberellin content does not correlate with photoperiod-induced growth changes in strawberry petioles. Australian J Plant Physiol. 1999, 26: 359-366.
Taylor DR, Blake PS, Crisp CM: Identification of gibberellins in leaf exudates of strawberry (Fragaria × ananassa, Duch.). Plant Growth Regul. 2000, 30: 221-223. 10.1023/A:1006385617161.
Hedden P, Phillips AL: Gibberellin metabolism: new insights revealed by the genes. Trends Plant Sci. 2000, 5: 523-530. 10.1016/S1360-1385(00)01790-8.
Ross JJ, Davidson SE, Wolbang CM, Bayly-Stark E, Smith JJ, Reid JB: Developmental regulation of the gibberellin pathway in pea shoots. Functional Plant Biol. 2003, 30: 83-89. 10.1071/FP02108.
Mitchum MG, Yamaguchi S, Hanada A, Kuwahara A, Yoshioka Y, Kato T, Tabata S, Kamiya Y, Sun T: Distinct and overlapping roles of two gibberellin 3-oxidases in Arabidopsis development. Plant J. 2006, 45: 804-818. 10.1111/j.1365-313X.2005.02642.x.
Xu Y-L, Gage DA, Zeevaart JA: Gibberellins and stem growth in Arabidopsis thaliana. Effects of photoperiod on expression of the GA4 an GA5 loci. Plant Physiol. 1997, 114: 1471-1476. 10.1104/pp.114.4.1471.
García-Martinez JL, Gil J: Light regulation of gibberellins biosynthesis and mode of action. J Plant Growth Regul. 2002, 20: 354-368. 10.1007/s003440010033.
Zhao X-Y, Yu X-H, Liu X-M, Lin C-T: Light regulation of gibberellins metabolism in seedling development. J Integr Plant Biol. 2007, 49: 21-27. 10.1111/j.1744-7909.2006.00407.x.
Uecuchi-Tanaka M, Ashikari M, Nakajima M, Itoh H, Katoh E, Kobayashi M, Chow T, Hsing Y-C, Kitano H, Yamacuchi I, Matsuoka M: GIBBERELLIN INSENSITIVE DWARF1 encodes a soluble receptor for gibberellins. Nature. 2005, 437: 693-698. 10.1038/nature04028.
Nakajima M, Shimada A, Takashi Y, Kim Y-C, Park S-H, Uecuchi-Tanaka M, Suzuki H, Katoh E, Iuchi S, Kobayashi M, Maeda T, Matsuoka M, Yamaguchi I: Identification and characterization of Arabidopsis gibberellins receptors. Plant J. 2006, 46: 880-889. 10.1111/j.1365-313X.2006.02748.x.
Willige BC, Ghosh S, Nill C, Zourelidou M, Dohmann EM, Maier A, Schwechheimer C: The DELLA domain of GA INSENSITIVE mediates the interaction with the GA INSENSITIVE DWARF1A gibberellin receptor of Arabidopsis. Plant Cell. 2007, 19: 1209-1220. 10.1105/tpc.107.051441.
Jiang C, Fu X: GA action: turning on de-DELLA repressing signalling. Curr Opin Plant Biol. 2007, 10: 461-465. 10.1016/j.pbi.2007.08.011.
Dill A, Thomas SG, Hu J, Steber CM, Sun T: The Arabidopsis F-box protein SLEEPY1 targets gibberellin signalling repressors for gibberellins-induced degradation. Plant Cell. 2004, 16: 1392-1405. 10.1105/tpc.020958.
Schwechheimer C: Understanding gibberellic acid signalling -are we there yet?. Curr Opin Plant Biol. 2008, 11: 9-15. 10.1016/j.pbi.2007.10.011.
Shulaev V, Korban SS, Sosinski B, Abbott AG, Aldwinkle HS, Folta KM, Iezzoni A, Main D, Arus P, Dandekar AM, Lewers K, Brown SK, Davis TM, Gardiner SE, Potter D, Veilleux RE: Multiple models for Rosaceae genomics. Plant Physiol. 2008, 147: 985-1003. 10.1104/pp.107.115618.
Aharoni A, O'Connell AP: Gene expression analysis of strawberry achene and receptacle maturation using DNA microarrays. J Exp Bot. 2002, 53: 2073-2087. 10.1093/jxb/erf026.
Zentella R, Zhang Z-L, Park M, Thomas SG, Endo A, Murase K, Fleet CM, Jikumaru Y, Nambara E, Kamiya Y, Sun T-P: Global analysis of DELLA direct targets in early gibberellins signalling in Arabiodopsis. Plant Cell. 2007, 19: 3037-3057. 10.1105/tpc.107.054999.
de la Fuente JI, Amaya I, Castillejo C, Sanches-Sevilla JF, Quesada MA, Botella MA, Valpuesta V: The strawberry gene FaGAST affects plant growth through inhibition of cell elongation. J Exp Bot. 2006, 57: 2401-2411. 10.1093/jxb/erj213.
Olsen JE, Junttila O, Moritz T: A localized decrease of GA1 in shoot tips of Salix pentandra seedlings precedes cessation of shoot elongation under short photoperiod. Physiol Plant. 1995, 95: 627-632. 10.1111/j.1399-3054.1995.tb05532.x.
Junttila O, Jensen E: Gibberellins and photoperiodic control of shoot elongation in Salix. Physiol Plant. 1988, 74: 371-376. 10.1111/j.1399-3054.1988.tb00645.x.
Shibaoka H: Regulation by gibberellins of the orientation of cortical microtubules in plant cells. Australian J Plant Physiol. 1993, 20: 461-470.
Rodríguez-Falcón M, Bou J, Prat S: Seasonal control of tuberization in potato: Conserved elements with the flowering response. Annu Rev Plant Biol. 2006, 57: 151-180. 10.1146/annurev.arplant.57.032905.105224.
Sauter M: Differential expression of CAK (cdc2-activating kinase)-like protein kinase, cyclins and cdc2 genes from rice during the cell cycle and in response to gibberellins. Plant J. 1997, 11: 181-190. 10.1046/j.1365-313X.1997.11020181.x.
Hansen E, Olsen JE, Junttila O: Gibberellins and subapical cell divisions in relation to bud set and bud break in Salix pentandra. J Plant Growth Regul. 18: 167-170. 10.1007/PL00007065.
Fagoaga C, Tadeo FR, Iglesias DJ, Huerta L, Liiso I, Vidal AM, Talon M, Navarro L, Garcia-Martinez JL, Pena L: Engineering of gibberellin levels in citrus by sense and antisense overexpression of a GA 20-oxidase gene modifies plant architecture. J Exp Bot. 2007, 58: 1407-1420. 10.1093/jxb/erm004.
Itoh H, Tanaka-Uecuchi M, Kawaide H, Chen X, Kamiya Y, Matsuoka M: The gene encoding tobacco gibberellin 3β-hydroxylase is expressed at the site of GA action during stem elongation and flower organ development. Plant J. 1999, 20: 15-24. 10.1046/j.1365-313X.1999.00568.x.
Kaneko M, Itoh H, Inukai Y, Sakamoto T, Ueguchi-Tanaka M, Ashikari M, Matsuoka M: Where do gibberellin biosynthesis and gibberellin signaling occur in rice plants?. Plant J. 2003, 35: 104-115. 10.1046/j.1365-313X.2003.01780.x.
Israelsson M, Sundberg B, Moritz T: Tissue-specific localization of gibberellins and expression of gibberellin biosynthetic and signalling genes in wood-forming tissues in aspen. Plant J. 2005, 44: 494-504. 10.1111/j.1365-313X.2005.02547.x.
Kende H, Knaap van der E, Cho H-T: A deepwater rice: a model to study stem elongation. Plant Physiol. 1998, 118: 1105-1110. 10.1104/pp.118.4.1105.
Brown T, Wareign PF: The genetic control of the everbearing habit and three other characters in varieties of Fragaria vesca. Euphytica. 1965, 14: 97-112.
Battey N, Miere P, Tehranifar A, Cekic C, Taylor S, Shrives K, Hadley P, Greenland A, Darby J, Wilkinson M: Genetic and environmental control of flowering in strawberry. Genetic and Environmental Manipulation of Horticultural Crops. Edited by: Cockshull KE, Gray D, Seymour GB, Thomas B. Wallingford, UK, Cab International,1998, 111-131.
Lifschitz E, Eviatar T, Rozman A, Shalit A, Goldschmidt 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. PNAS. 2006, 103: 6398-6403. 10.1073/pnas.0601620103.
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 signalling in floral induction of Arabidopsis. Science. 2007, 316: 1030-1033. 10.1126/science.1141752.
Lin M-K, Belanger H, Lee Y-J, Varkonyi-Gasic E, Taoka KI, 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.
Martínez-García JF, Virgós-Soler A, Prat S: Control of photoperiod-regulated tuberization in potato by the Arabidopsis flowering-time gene CONSTANS. PNAS. 2002, 99: 15211-15216. 10.1073/pnas.222390599.
Böhlenius H, Huang T, Charbonnel-Cambaa L, Brunner AM, Jansson S, Strauss SH, Nilsson O: CO/FT regulatory module controls timing of flowering and seasonal growth cessation in trees. Science. 2006, 312: 1040-1043. 10.1126/science.1126038.
Gyllenstrand N, Clapham D, Källman T, Lagercrantz U: A Norway spruce FLOWERING LOCUS T homolog is implicated in control of growth rhythm in conifers. Plant Physiol. 2007, 144: 248-257. 10.1104/pp.107.095802.
Ruonala R, Rinne PLH, Kangasjärvi J, Schoot van der C: CENL1 expression in the rib meristem affects stem elongation and the transition to dormancy in Populus. Plant Cell. 2008, 20: 59-74. 10.1105/tpc.107.056721.
Kotoda N, Iwanami H, Takahashi S, Abe K: Antisense expression of MdTFL1, a TFL1-like gene, reduces the juvenile phase in apple. J Amer Soc Hort Sci. 2006, 131: 74-81.
King RW, Moritz T, Evans LT, Junttila O, Herlt AJ: Long-day induction of flowering in Lolium temulentum involves sequential increases in specific gibberellins at the shoot apex. Plant Physiol. 2001, 127: 624-632. 10.1104/pp.010378.
Nemhauser JL: Dawning of a new era: photomorphogenesis as an integrated molecular network. Curr Opin Plant Biol. 2008, 11: 4-8. 10.1016/j.pbi.2007.10.005.
Junttila O, Heide OM, Lindgård B, Ernstsen A: Gibberellins and the photoperiodic control of leaf growth in Poa pratensis. Physiol Plant. 1997, 101: 599-605. 10.1111/j.1399-3054.1997.tb01043.x.
Monte D, Somerville S: Pine tree method for isolation of plant RNA. DNA microarrays: a molecular cloning manual. Edited by: Bowtell D, Sambrook J. New York: Cold Spring Harbour Laboratory Press; 2002:124-126.
We thank Bente Lindgård and Dr. Arild Ernstsen (University of Tromsø, Norway) for their help in GA analysis. Dr. Asaph Aharoni (Plant Research International, Wageningen, The Netherlands) is acknowledged for providing the FaGA2ox EST clone and Dr. Wilhelm Rademacher (BASF, Germany) for providing the BAS 125 growth regulator.
TH participated in the design of the study, carried out most of the experimental work and drafted the manuscript. TM analysed GA levels in the axillary buds. PE and OJ participated in the design and coordination of the study and helped to draft the manuscript. All authors read and approved the final manuscript.
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Hytönen, T., Elomaa, P., Moritz, T. et al. Gibberellin mediates daylength-controlled differentiation of vegetative meristems in strawberry (Fragaria × ananassaDuch). BMC Plant Biol 9, 18 (2009). https://doi.org/10.1186/1471-2229-9-18
- Branch Crown
- Daughter Plant
- Runner Formation
- Strawberry Runner
- GA3ox Expression