Open Access

Evolutionary conservation of plant gibberellin signalling pathway components

  • Filip Vandenbussche1,
  • Ana C Fierro2,
  • Gertrud Wiedemann3,
  • Ralf Reski3 and
  • Dominique Van Der Straeten1Email author
BMC Plant Biology20077:65

DOI: 10.1186/1471-2229-7-65

Received: 03 August 2007

Accepted: 29 November 2007

Published: 29 November 2007



Gibberellins (GA) are plant hormones that can regulate germination, elongation growth, and sex determination. They ubiquitously occur in seed plants. The discovery of gibberellin receptors, together with advances in understanding the function of key components of GA signalling in Arabidopsis and rice, reveal a fairly short GA signal transduction route. The pathway essentially consists of GID1 gibberellin receptors that interact with F-box proteins, which in turn regulate degradation of downstream DELLA proteins, suppressors of GA-controlled responses.


Arabidopsis sequences of the gibberellin signalling compounds were used to screen databases from a variety of plants, including protists, for homologues, providing indications for the degree of conservation of the pathway. The pathway as such appears completely absent in protists, the moss Physcomitrella patens shares only a limited homology with the Arabidopsis proteins, thus lacking essential characteristics of the classical GA signalling pathway, while the lycophyte Selaginella moellendorffii contains a possible ortholog for each component. The occurrence of classical GA responses can as yet not be linked with the presence of homologues of the signalling pathway. Alignments and display in neighbour joining trees of the GA signalling components confirm the close relationship of gymnosperms, monocotyledonous and dicotyledonous plants, as suggested from previous studies.


Homologues of the GA-signalling pathway were mainly found in vascular plants. The GA signalling system may have its evolutionary molecular onset in Physcomitrella patens, where GAs at higher concentrations affect gravitropism and elongation growth.


Gibberellins (GAs) are a large family of hormones that are important for a vast array of responses throughout the life cycle of plants. They mainly stimulate germination, cause cell expansion, and regulate flowering time. Due to their high economical relevance, the effects of GAs on cell elongation are subject to intense scientific studies. The green revolution was based on selection for dwarfism in rice and wheat cultivars. Recently it was shown that these dwarfing genes interfere with either the production or the action of GAs [1]. Chemical interference with GA biosynthesis is often used to limit the growth of plants, including trees [2]. GAs were first isolated from Gibberella (Fusarium) fujikuroi [3]. This fungus causes extreme extension growth in rice, named bakanae or "foolish" rice, which hence is far more susceptible to lodging.

Apart from Gibberella, other fungi (Phaeospheria, Aphaceloma sp.) and various bacteria [4] are able to synthesize GAs. GAs were consequently found in many plant species and are widespread over photosynthesizing organisms. GA-like substances were detected in unicellular and multicellular algae [57], in lichens and mosses [8], and in ferns [4] But most of all, they are widely accepted as general growth controlling hormones in seed plants [4].

Presence of GAs in an organism does not necessarily mean that it is responsive to these compounds. For instance, Gibberella itself does not react to exogenous GA [3]. Depending on the species of unicellular algae, GA can slightly increase the biomass [9]. The effects of GAs on elongation growth of unicellular algae are either very small or absent in most species [10]. However, growth increases were reported for the multicellular alga Porphyra in the diploid, filamentous sporophyte conchocelis phase and, in combination with auxin, in stolons of Ulva lactuca [10, 11].

While ABA, auxin, and cytokinin induce specific developmental alterations in mosses like Physcomitrella patens, no such effects have been reported for GA-application [12, 13]. However, some older reports do exist, that GA-application on specific moss species may slightly enhance growth rates [14, 15]. In addition GA-application may interfere with gravitropism in the mosses Ceratodon purpureus [16] and Pottia intermedia [17]. In fact, to date gibberellins have not been identified in mosses, and it was proposed that the hormonal signalling pathway developed later in land plant evolution [13]. However, as such pathways do not appear completely de novo, precursors from which GA may have been evolved should be present in mosses. Ent-kaurene is the key intermediate in the biosynthesis of gibberellins. Recently, it was shown, that P. patens produces as a secondary metabolite such a tetracyclic diterpene as a volatile compound in huge amounts [18], and possesses a bifunctional ent-kaurene synthase [19].

To our knowledge, no reports are available for GA regulated growth in ferns. In contrast, their stimulatory effect on elongation and germination has been extensively documented for seed plants, such as conifers [20, 21] and angiosperms, both mono- and dicotyledonous plants.

Sex determination is another known GA effect. In species as Chara, GA promote antheridia (male sex organ) formation [22]. Likewise, they serve as promoters for antheridia formation in some ferns [23, 24]. Interestingly, in many eudicotyledonous plants as well, GAs promote male flower development [25]. By contrast, in the monocot maize, they promote female flower formation [26].

It is speculated that the GA signalling pathway, which ultimately leads to germination and elongation growth in seed plants, consists of a limited number of factors (figure 1A). Recently, GA receptors of rice (GID1) and Arabidopsis have been discovered [27, 28]. The receptors are able to interact, in a GA dependent way, with the DELLA proteins [27, 28]; the interactions solely depends on the presence of the DELLA-domain in the DELLA protein [29]. DELLA proteins (such as RGA in Arabidopsis) are inhibitors of GA responses, which are broken down in the presence of GAs, hence promoting germination and elongation growth [30]. This degradation is mediated by an E3 ligase, that is specified by an F-box protein (such as SLY1 in Arabidopsis or GID2 in rice) [3133]. Thus the GA signalling pathway essentially consists of three interacting players.
Figure 1

A) Current model for GA signalling. GA is bound to the GID1 GA receptor and which stimulates the interaction with the DELLA transcription factor. The F-box protein SLY1/GID2 connects the DELLA transcription factors to an SCF-E3 ubiquitin ligase. Ubiquitin is transferred from an E2 onto the DELLA target protein. The ensemble of these events causes subsequent rapid degradation by the 26S proteasome. B) Simplified overview of plant evolution based on the hyperbolic tree presented at [62]. Clades that are discussed in the text are retained in the graph. In parenthesis, genera and species mentioned in the text are indicated.

Over the last few years, three plant genomes have been entirely sequenced [3436] and a lot of effort is made to unravel the gene pool of "genomically more complex" plants by expressed sequenced tag (EST) sequencing and assembly. With the variety of open access EST and genome sequence databases, it becomes possible to perform comparative genomics and molecular phylogenetic analysis on a large number of species at a time (plantGDB, [37]). Based on the aforementioned tools, we investigated the conservation of the GA pathway formed by GID1, SLY1 and DELLA proteins from algae and plants throughout the plant kingdom, using reference species for different major plant groups (Figure 1B). Existing orthologues were retrieved from various higher plants, but are missing from Physcomitrella patens (Pp). The presence of the GA signalling pathway could thus be linked exclusively with vascular plants.


The gibberellin receptors

The GA receptors (GID1) belong to the large family of hormone sensitive lipases and have homologues throughout the plant kingdom, since they are related in sequence to various carboxylesterases [38]. Moreover, the predicted 3D structure of these proteins is similar. However, the GA receptors contain various regions, which distinguish them from their carboxylesterase relatives [28, 38]. Amino acid Arg265 is typically present, while the His340 residue from the catalytic site of the esterases is missing in GID1 proteins.

When performing TBLASTN searches, no homologues (E < e-10) were found in Cyanidioschyzon merolae (belonging to the phylum Rhodophyta, red algae), nor in Chlamydomonas reinhardtii (belonging to the phylum Chlorophyta, amongst the green algae). In the moss Physcomitrella patens (Pp), the closest homologue to the Arabidopsis GA receptors misses the Arg265, it has a Leu instead (Figure 2). This Arg is especially important for gibberellin binding, as proteins carrying the gid1-2 mutation, where this residue is changed into a Thr, are unable to bind gibberellins in vitro [27]. Furthermore, the N and C-terminal end of the Physcomitrella protein diverge from the GID1 proteins. The protein encoded by AT5G23530 also lacks Arg265, which is unique in the GA receptors, but retains the His340 from the catalytic site of the esterases, which is replaced by an Ile or Leu in the GA receptors and a Trp in the Pp homologue. These data support the idea that the closest homologue in Pp is part of the large carboxylesterase-like gene family, but lacks features essential for full gibberellin signalling and features conserved in esterases.
Figure 2

Alignment of GA receptor homologues. The arrow indicates Arg265 which is necessary for GA binding. Ath: Arabidopsis thaliana, Sm: Selaginella moellendorffii, Pp: Physcomitrella patens.

The seedless vascular plant Selaginella moellendorffii (belonging to the phylum of Lycopodiophyta) has a protein that appears a genuine GA receptor orthologue. It has an overall good aligment (47% similarity) and in contrast to the protein from Pp, it contains the Arg265 residue. It also has a conserved Ile in position 340 instead of a His, typical for known GA receptors.

From the analysis of a limited EST set (~8000) of the fern Adianthum capillus veneris (phylum Pteridophyta, order Polypodiales), we concluded that it has related carboxylesterases, all with the conserved His340 necessary for esterase activity. Yet the EST collection is too small to firmly exclude the existence of genuine GA receptor orthologues.

In seed plants, including gymnosperms and angiosperms, GID1 orthologues are widely present. A clear separation between monocots and eudicots is visible in a Neighbour-Joining (N-J) tree (Figure 3). Interestingly, the pine homologue falls within the various sequences from dicots, suggesting a high conservation for this protein among higher plants. On the whole, the ClustalW alignment based N-J tree of the GA receptors shows a relation that is highly reminiscent of the evolutionary schemes generally accepted today [39], with the overall most related plants clustering together.
Figure 3

Neighbour-Joining tree of DNA sequences homologous to that encoding the Arabidopsis GID1b GA receptor.

The SLEEPY homologues

No (E < 1e-4) homologues to the F-box protein SLY1 were found in Chlamydomonas reinhardtii, nor Cyanidioschyzon merolae using TBlastX.

A reciprocal blast yielding three other Arabidopsis proteins (At3g44326, At2g27310, At2g36090 with BLASTP scores of 71, 56, and 55 respectively) closer related to the Pp homologue of SLY1 (997094760 in Figure 4) than SLY1 itself (BLASTP score 54), indicates that SLY1 orthologues are not present in Pp. In fact, the highest homology with SLY1, within the Pp protein, occurs in the F-box region. This region is necessary for interactions with the Skp1 partner within the SCF-complex, and does not confer substrate specificity. The latter is usually achieved by the C-terminal part [40]. The C-terminal part of the Pp homologue is highly divergent from the rice and Arabidopsis F-Box proteins GID2 and SLY1 (Figure 4). The GGF (AA positions 120–160 in Figure 4) and LSL motives, conserved in the GID2 and SLY1 [31, 41], in the Pp homologue, have lower and almost no homology with the GA related F-box proteins. It is therefore questionable and rather unlikely that the Pp protein could recognize a DELLA protein as a substrate.
Figure 4

Alignment of the SLY1 homologues. Ath: Arabidopsis thaliana, Sm: Selaginella moellendorffii, Pp: Physcomitrella patens.

From Selaginella, a protein could be retrieved with homology to the SLY1 over its whole length, including a leucine rich box at the C-terminal end (Figure 4). A reciprocal blast indicates that the protein can be considered as an orthologue of those of higher plants (similarity 51%).

The EST database from the fern Ceratopteris only yielded an F-box protein with a divergent C-terminal end (data not shown). F-box proteins are thus present in ferns, but SLY1 orthologues remain to be discovered.

Similarly to the GA receptors, in gymnosperms and angiosperms, SLY1 orthologues are widely present. However, F-box proteins are a very divergent family of polypeptides. The eudicot SLY1 orthologues form a cluster in a N-J tree (Figure 5), while the monocots are grouped with the gymnosperms. There is a distinct group containing Sorghum, sugarcane and many conifer sequences. In this group of sequences, the evolutionary distance to SLY1 is larger than that to the Pp homologue. A second monocot-gymnosperm cluster groups with the closest SLY1 homologue in Arabidopsis, SNEEZY (SNE), and its homologues (Figure 5; [42]). Overexpression of SNE in Arabidopsis can take over GA signalling events, but a clear involvement in GA signalling in natural conditions has not been found.
Figure 5

Neighbour-Joining tree of DNA sequences homologous to that encoding the Arabidopsis F-box protein SLY1.

DELLA related transcription factors

DELLA proteins belong to the GRAS (GAI, RGA, SCARECROW) protein family, specific to plants [43]. The cDNA sequence of RGA1 of Arabidopsis was used in a TBLASTX screen for homologues in other species.

No DELLA homologues (yield is 0 with E = 1e-4) were detected in Cyanidioschyzon merolae or Chlamydomonas reinhardtii.

The N-terminal part of Arabidopsis RGA1 did not yield a counterpart using tBLASTx against the genome traces nor the ESTs of Pp. Reconstruction of the genomic region of the closest RGA1 homologue confirmed the absence of substantial homology in the N-terminal DELLA domain (Figure 6). Instead of the DELLA motif, the Pp protein has the amino acids DQGFR. Furthermore, the Pp protein lacks two of the four conserved Tyr residues that are structurally important in the Arabidopsis DELLA protein RGL2 and that render RGL2 susceptible to GA mediated degradation (Figure 6; [44]).
Figure 6

Alignment of the DELLA homologues. The DELLA region appears in the black frame. Ath: Arabidopsis thaliana, Sm: Selaginella moellendorffii, Pp: Physcomitrella patens, Pt: Pinus taeda. Arrows indicate structurally important tyrosine residues.

In contrast, Selaginella contains a clear RGA1 orthologue. The protein (Figure 6) was reconstructed from the genomic sequence, since the matching ESTs do not cover the N-terminal part, possibly due to absence of that part in the EST library. Parts of the sequence from the genomic reconstruction, may represent introns, although the EST that covers the C-terminal part (from position 340 onward in Figure 6) has the same sequence as the genomic.

From a limited EST set (~6000) of the fern Ceratopteris richardii, we only found a scarecrow-like gene (AY974159) as closest homologue to RGA1. However, as for SLY1, considering the small size of the EST collection we cannot exclude the existence of DELLA orthologues in ferns.

Although no complete DELLA protein sequence could be retrieved from the available contigs and ESTs of pine, overlapping homologous fragments from two different proteins suggest the existence of genuine orthologues (e.g. similarity of Pt TC59241-59240 with Ath RGA1 is 46%). In gymnosperms as well as angiosperms, DELLA orthologues are present in various species (Figure 7). Similarly to the situation of the GA receptors and the F-box proteins, the monocots are more closely related with the gymnosperms and/or Selaginella, than the eudicots.
Figure 7

Neighbour-Joining tree of DNA sequences homologous to that encoding the Arabidopsis RGA1 DELLA protein.

It is noteworthy that there are more ESTs with homology to DELLA coding sequences; however, these lack the N-terminal part spanning the DELLA domain (see Additional file 1). This may be either due to a lack of the 5'end of the coding sequence within the available EST collections or simply because some proteins contain only homology to the C-terminal part [45].

Effect of exogenous GA treatment on Physcomitrella growth

Since GAs are potent growth stimulating hormones in vascular plants, and Physcomitrella has at least a protein that is closely related to gibberellin receptors, the question is prompted whether or not Physcomitrella can respond to gibberellins. Treatment with 10, 100, 500 and 1000 μM of GA3 did not influence general growth of protonemata (comprised of chloronemata and caulonemata; [46]) under normal light conditions. However, when grown in the dark in upright position, the controls as well as plants treated with 10 μM GA developed elongated caulonemata growing positively gravitropic. At relatively high GA3 concentrations of 100 μM and more caulonema formation was strongly retarded and growth orientation was changed (Figure 8). While untreated protonemata grow vertically, GA3 treated ones grew in various direction showing angles divergent from the vertical, suggesting a defect in gravitropism (Figure 8K). This response is reminiscent of the effect of high concentrations of gibberellin (500 μM) that affect gravitropism in protonemata of another moss, Ceratodon purpureus [16].
Figure 8

Effect of various concentrations of GA3 on caulonema formation and growth direction of Physcomitrella protonemata after transfer to darkness and reorientation of Petri dishes into an upright position. A-E) Photographs of mock treated plants as controls for panels F-J respectively. F-J) Photographs of plants treated with 0 μM (F), 10 μM (G), 100 μM (H), 500 μM (I), 1000 μM (J) of GA3 (K) Quantification of direction of growth at a treatment of 100 μM GA3.


Where on an evolutionary scale did the GA signalling pathway arise?

A central node in evolutionary plant research may be the investigation of mosses for which Pp stands model [47, 48]. GAs are present in various moss species [8]. At present no data on GA content of Physcomitrella are available, but homologues to key enzymes (genes GA1-GA5 of Arabidopsis) of the GA biosynthetic pathway were found (data not shown). Although Physcomitrella has homologues to all three GA signalling components, it is questionable whether they are true orthologues. It is therefore likely that gibberellin signalling does not function in mosses as in vascular plants. Divergence from SLY1 of the F-box protein sequence outside of the F-box, and absence of homology to the "DELLA" region in the closest relative of RGA1, may indicate the existence of other recognition motives between the DELLA-like transcription factor and the SLY1/GID2-like F-box protein. In addition, the DELLA-like protein of Physcomitrella may not be functioning as a GA-regulated repressor of GA response as it is stable upon GA treatment when expressed in Arabidopsis [13]. It could rather play a regulatory role in plant development, being stable upon GA treatment, similarly to the SLR-like GRAS proteins of rice [45]. Furthermore, since "genuine" GA responses in Physcomitrella, e.g. stimulation of growth, are missing, this class of hormones might be less effective in mosses. However, exogenous gibberellins are effective in stimulating growth of seta from the liverwort Pellia epiphylla, suggesting the existence of gibberellin signalling earlier in evolution [49].

In conclusion, mosses may have lost the capacity of effective GA signalling or use an alternative system to that of vascular plants to pass on the signal. Whether this involves the homologues to the vascular plant pathway is not known. In the future, it may be interesting to study Chara, an even more primitive embryophyte than Physcomitrella, which was reported to be GA-responsive [22].

The lycophyte Selaginella moellendorffii has clear orthologues for all components of the GA pathway and is to our present knowledge the most primitive species to possess a full-potentially functional – GA signalling pathway; however, phenotypic responses still need to be discovered [13]. Hence, as suggested in earlier studies by its apical growth that is restricted to the sporophyte, the presence of vascular tissue, the formation of roots and leaves, and even by its genome sequences [50, 51], Selaginella is closely related to seed plants. This is confirmed at the level of the molecular components of GA signalling.

GA signalling in non vascular plants?

In recent years, no convincing effect of GA on elongation growth in non vascular plants has been reported. Early publications on GA effects on plants should be read with care, as purity of the compounds used in the treatments was often not that obvious [52], due to lack of modern analytical techniques. Moreover, some of the analyses were done in the presence of high concentrations of other hormones such as auxins or cytokinins [11]. Since in the last two decades, no true hormonal (at concentrations lower than 10 μM GA) effect in other organisms than vascular plants has been reported, it is tempting to speculate that GA signalling has arisen with the occurrence of vascular plants (hypothesis 1 in Figure 9).
Figure 9

Occurrence of the GA signalling pathway in the plant kingdom. Hypothesis 1: The GA signalling pathway of vascular plants arose after the separation of the Bryophytes. Hypothesis 2: The GA signalling pathway originated earlier than the branching of mosses from the ancestral line, but was lost in unicellular algae and evolved differently in mosses. Dots indicate possible point of appearance of GA signalling. X-marks indicate points of loss of GA signalling.

If the effects shown in those early studies are indeed true GA effects, then it may be that mosses and other clades lost their capacity to respond to GAs (hypothesis 2 in Figure 9). It is however also possible that non-vascular plants have adopted other mechanisms than those operating in vascular plants to pass on the GA signal, eventually serving for other, yet to be discovered, responses. Assuming that GA signalling as we know it is typical for vascular plants, and that non-vascular species have other compounds and an other mechanism to trigger GA-like responses, a parallel with the evolution of GA biosynthesis may exist. The fungus Gibberella has a totally different enzyme set to synthesize GAs than plants [3]. It has therefore been proposed that the synthesis of GAs is a case of convergent evolution in fungi and plants, involving paralogues rather than orthologues.

In ferns, we found homologues to members of the carboxylesterase and scarecrow-like gene families, to which respectively the GA receptors and the DELLA transcription factors belong. Considering the presence of GA responses in ferns [4] and the limited number of EST sequences available, it can be reasonably assumed that in the future, orthologues to GA signalling components will be found.

Gibberellin as sex determinant

Apart from a possible role in elongation, it is interesting that in non-seed plants as ferns and even Chara, and in some eudicotyledonous plants, male organs are promoted by GAs [23, 25]. At this moment it is not known whether the same receptor, F-box, and DELLA components are involved both in elongation growth and in sex determination. The first function of GAs may have been the stimulation of male gametophyte function. It is therefore possible that GA signalling arose as a sex determinant in the first place. The GA receptors were first implemented as part of the carboxylesterase family, showing homology to PrMC3. Intriguingly, PrMC3 was originally isolated from and shown to be expressed specifically in male cones of Pinus radiata [53]. Future molecular physiological research is necessary to unravel the importance of this family of carboxylesterases in plants and the reason why some of their members are present especially in (male) reproductive organs.


The gibberellin signalling pathway as it is known for Arabidopsis and rice is well conserved in lycophytes, gymnosperms and angiosperms, which reflects a wide spreading among land plants known to date. However, except perhaps for the receptor, the pathway components seem to be missing in the moss Physcomitrella, which indicates that bryophytes may have the evolutionary onset to respond efficiently to gibberellins, which yields other responses (e.g. gravitropism) than in vascular plants. No nuclear EST or genome sequences are available from other non vascular plants and protists such as Charales, nor from multicellular algae, and only limited in ferns. But, a large amount of EST collections and BAC clones of a variety of organisms is awaiting sequencing (CUGI, Clemson, SC). As more genomes will have been sequenced, a more complete picture of the phylogeny of GA signalling will be drawn.


Sequence retrieval

Arabidopsis cDNA sequences from the GID1b, SLY1, and RGA genes were taken from the TAIR website. These sequences were used to search for homologues by tBlastx with default parameters against the unigene collection of Tigr, the citrus HarvEST database (Wanamaker and Close, University of California), the Cosmoss transcriptome and genome (with an eight times sequencing coverage) databases (Stefan Rensing, University Freiburg, Germany), the PHYSCOBASE database [54], the Selaginella databases at Purdue University [55], the Cyanidioschyzon merolae database of Tokyo University [56], the loblolly pine ESTs from the CCGB of the University of Minnesota, the Cycas EST collection from the New York Botanical Garden and the sequenced EST collection of Adiantum capillis veneris, Marchantia polymorpha, Welwitschia mirabilis, Ceratopteris richardii, Mesostigma viridae gathered at plantGDB. Tables with reference numbers can be found in supplemental data (see Additional files 1, 2, 3).

Reconstruction of protein sequences

Retrieved ESTs from Selaginella moellendorffii were used to scan the Sellaginella genome for homologous sequences. 5' and 3' ends were taken to virtually walk over the chromosomes and isolate clones covering about 10 kbp around the original EST (which is homologous to the Arabidopsis sequence). For the Physcomitrella patens F-box protein, the same approach was used. For the the DELLA homologue, the Arabidopsis protein sequences were directly used to scan the genome traces of the Cosmoss dbase (Stefan Rensing, University Freiburg). The retrieved clones (see Additional files 4, 5, 6) were submitted to a PHRAP process to yield contigs. From these contigs, proteins were derived by doing an in silico translation [57]. The Pp F-box protein homologue and DELLA homologue translated as a single exon from the Cosmoss database. A Pp receptor homologue had a predicted intron between R157 and R158 (Figure 2). The predicted intron was left out in the reconstructed protein and was 2 bp out of frame at the 3'end. For the aligment in Figure 2, the sequence of Physcobase contig 12981 was used. In silico translation was also applied to the ESTs from pine. Open reading frames were detected and checked for homology with the original Arabidopsis proteins in a BlastP.


Protein alignments were performed using ClustalW algorithms included in the VectorNTI package (Invitrogen). Multiple alignments of coding sequences and ESTs were done on line, using ClustalW at [58] (Kyoto University Bioinformatics Center) using default parameters and choosing the PHYLIP output. Neigbour-Joining trees were generated at [58]. Various control runs were done using IUB (at [58]), Dialign in the Panta rhei package [59]; University of Bielefeld, Germany) and MAVID [60] alignment protocols. All controls yielded similar results. Similarity values were calculated with VectorNTI software (Invitrogen).

Gibberellin treatments of Physcomitrella

Physcomitrella patens (Hedw.) B.S.G. was cultured in liquid and solid Knop medium as described earlier [61]. GA3 was purchased by Duchefa (Haarlem, The Netherlands) and a 0.25 M stock solution was prepared in EtOH. For the treatments 5 μl of freshly subcultured moss protonema in liquid culture with a dry weight of 100 mg/l were placed on Knop plates containing 0, 10, 100, 500 and 1000 μM GA3 or control plates containing the corresponding amount of EtOH. After one week of growth at normal conditions (25°C, 16 h light with 55 μmol/sm2, 8 h darkness) the plates were covered with aluminium foil and put upright for 7 days. For documentation the plants were photographed.





Physcomitrella patens


Selaginella moellendorffii


gibberellin insensitive dwarf, a GA receptor


SLEEPY, an F-box protein involved in the GA signalling pathway


Repressor of ga1

one of the DELLA proteins: 

acting as a repressor of GA response



Filip Vandenbussche is a post-doctoral fellow of the Research Foundation Flanders (FWO). DVDS and RR acknowledge the Research Foundation Flanders (FWO G.0313.05) and DFG (RE837/7) respectively, for financial support. The authors thank Dr. J. Banks (Purdue University) for access to the Selaginella database.

Authors’ Affiliations

Unit Plant Hormone Signaling & Bio-imaging, Department of Molecular Genetics, Ghent University
Department Microbial and Molecular Systems
Plant Biotechnology, Faculty of Biology, University of Freiburg


  1. Hedden P: The genes of the Green Revolution. Trends Genet. 2003, 19 (1): 5-9. 10.1016/S0168-9525(02)00009-4.PubMedView ArticleGoogle Scholar
  2. Bai S, Chaney WR, Qi Y: Response of cambial and shoot growth in trees treated with paclobutrazol. Journal of Arboriculture. 2004, 30: 137-145.Google Scholar
  3. Hedden P, Phillips AL, Rojas MC, Carrera E, Tudzynski B: Gibberellin Biosynthesis in Plants and Fungi: A Case of Convergent Evolution?. J Plant Growth Regul. 2001, 20 (4): 319-331. 10.1007/s003440010037.PubMedView ArticleGoogle Scholar
  4. MacMillan J: Occurrence of Gibberellins in Vascular Plants, Fungi, and Bacteria. J Plant Growth Regul. 2001, 20 (4): 387-442. 10.1007/s003440010038.PubMedView ArticleGoogle Scholar
  5. Radley M: Gibberellic acid-like substances in plants. Nature. 1961, 191: 684-685. 10.1038/191684a0.PubMedView ArticleGoogle Scholar
  6. Kato J, Purves WK, Phinney BO: Gibberellin-like substances in plants. Nature. 1962, 196: 687-688. 10.1038/196687a0.PubMedView ArticleGoogle Scholar
  7. Mowat JA: A survey of results on the occurrence of auxins and gibberellins in algae. Botanica Marina. 1965, 8: 149-155.View ArticleGoogle Scholar
  8. Ergün N, Topcuoglu SF, Yildiz A: Auxin (Indole-3-Acetic Acid), Gibberellic Acid (GA3), Abscisic Acid (ABA) and Cytokinin (Zeatin) Production by Some Species of Mosses and Lichens. Turkish Journal of Botany. 2002, 26: 13-18.Google Scholar
  9. Erokhin VE: Preliminary studies of Algae Gibberellins. Ekologia Morja. 1999, 49: 39-43.Google Scholar
  10. Provasoli L, Carlucci AF: Vitamins and growth regulators. Algal physiology and biochemistry. 1974, Oxford , Blackwell Scientific Publications, 741-787.Google Scholar
  11. Provasoli L: Effect of plant hormones on Ulva. Biological Bulletin. 1958, 114: 375-384. 10.2307/1538992.View ArticleGoogle Scholar
  12. Decker EL, Frank W, Sarnighausen E, Reski R: Moss systems biology en route: phytohormones in Physcomitrella development. Plant Biol (Stuttg). 2006, 8 (3): 397-405. 10.1055/s-2006-923952.View ArticleGoogle Scholar
  13. Yasumura Y, Crumpton-Taylor M, Fuentes S, Harberd NP: Step-by-step acquisition of the gibberellin-DELLA growth-regulatory mechanism during land-plant evolution. Curr Biol. 2007, 17 (14): 1225-1230. 10.1016/j.cub.2007.06.037.PubMedView ArticleGoogle Scholar
  14. Chopra R, Mehta P: Effect of some chemical factors on protonemal growth and bud induction in three mosses grown in vitro. Phytomorphology. 1992, 42: 43-55.Google Scholar
  15. Chopra RN, Dhingra-Babbar S: Studies on bud induction in the moss Trematodon brevicalyx Dixon. New Phytologist. 1984, 97: 613-620. 10.1111/j.1469-8137.1984.tb03625.x.View ArticleGoogle Scholar
  16. Chaban CI, Kordyum EL, Demkiv OT, Khorkavtsiv OY, Khorkavtsiv Ya D: The gravireaction of Ceratodon protonemata treated with gibberellic acid. Adv Space Res. 1999, 24 (6): 717-721. 10.1016/S0273-1177(99)00404-4.PubMedView ArticleGoogle Scholar
  17. Chaban CI, Kern VD, Ripetskyj RT, Demkiv OT, Sack FD: Gravitropism in caulonemata of the moss Pottia intermedia. J Bryol. 1998, 20 (2): 287-299.PubMedView ArticleGoogle Scholar
  18. Von Schwartzenberg K, Schultze W, Kassner H: The moss Physcomitrella patens releases a tetracyclic diterpene. Plant Cell Rep. 2004, 22 (10): 780-786. 10.1007/s00299-004-0754-6.PubMedView ArticleGoogle Scholar
  19. Hayashi K, Kawaide H, Notomi M, Sakigi Y, Matsuo A, Nozaki H: Identification and functional analysis of bifunctional ent-kaurene synthase from the moss Physcomitrella patens. FEBS Lett. 2006, 580 (26): 6175-6181. 10.1016/j.febslet.2006.10.018.PubMedView ArticleGoogle Scholar
  20. Waghorn JJ, del Pozo T, Acevedo EA, Cardemil LA: The role of two isoenzymes of alpha-amylase of Araucaria araucana (Araucariaceae) on the digestion of starch granules during germination. J Exp Bot. 2003, 54 (384): 901-911. 10.1093/jxb/erg093.PubMedView ArticleGoogle Scholar
  21. Little CH, MacDonald JE: Effects of exogenous gibberellin and auxin on shoot elongation and vegetative bud development in seedlings of Pinus sylvestris and Picea glauca. Tree Physiol. 2003, 23 (2): 73-83.PubMedView ArticleGoogle Scholar
  22. Kwiatkowska M, Wojtczak A, Poptoriska K: Effect of GA3 Treatment on the Number of Spermatozoids and Endopolyploidy Levels of Non-Generative Cells in Antheridia of Chara vulgaris L. Plant and Cell Physiology. 1998, 39 (12): 1388-1390.View ArticleGoogle Scholar
  23. Kazmierczak A: Induction of cell division and cell expansion at the beginning of gibberellin A3-induced precocious antheridia formation in Anemia phyllitidis gametophytes. Plant Science. 2003, 165: 933-939. 10.1016/S0168-9452(03)00217-6.View ArticleGoogle Scholar
  24. Menendez V, Revilla MA, Bernard P, Gotor V, Fernandez H: Gibberellins and antheridiogen on sex in Blechnum spicant L. Plant Cell Rep. 2006, 25 (10): 1104-1110. 10.1007/s00299-006-0149-y.PubMedView ArticleGoogle Scholar
  25. Chalakhyan MK, Khryanin VN: Hormonal Regulation of Sex Expression in Plants. Plant Growth Substances. Edited by: Skoog F. 1979, 331-344.Google Scholar
  26. Dellaporta SL, Calderon-Urrea A: The sex determination process in maize. Science. 1994, 266 (5190): 1501-1505. 10.1126/science.7985019.PubMedView ArticleGoogle Scholar
  27. Ueguchi-Tanaka M, Ashikari M, Nakajima M, Itoh H, Katoh E, Kobayashi M, Chow TY, Hsing YI, Kitano H, Yamaguchi I, Matsuoka M: GIBBERELLIN INSENSITIVE DWARF1 encodes a soluble receptor for gibberellin. Nature. 2005, 437 (7059): 693-698. 10.1038/nature04028.PubMedView ArticleGoogle Scholar
  28. Nakajima M, Shimada A, Takashi Y, Kim YC, Park SH, Ueguchi-Tanaka M, Suzuki H, Katoh E, Iuchi S, Kobayashi M, Maeda T, Matsuoka M, Yamaguchi I: Identification and characterization of Arabidopsis gibberellin receptors. Plant J. 2006, 46 (5): 880-889. 10.1111/j.1365-313X.2006.02748.x.PubMedView ArticleGoogle Scholar
  29. 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 (4): 1209-1220. 10.1105/tpc.107.051441.PubMedPubMed CentralView ArticleGoogle Scholar
  30. Silverstone AL, Jung HS, Dill A, Kawaide H, Kamiya Y, Sun TP: Repressing a repressor: gibberellin-induced rapid reduction of the RGA protein in Arabidopsis. Plant Cell. 2001, 13 (7): 1555-1566. 10.1105/tpc.13.7.1555.PubMedPubMed CentralView ArticleGoogle Scholar
  31. McGinnis KM, Thomas SG, Soule JD, Strader LC, Zale JM, Sun TP, Steber CM: The Arabidopsis SLEEPY1 gene encodes a putative F-box subunit of an SCF E3 ubiquitin ligase. Plant Cell. 2003, 15 (5): 1120-1130. 10.1105/tpc.010827.PubMedPubMed CentralView ArticleGoogle Scholar
  32. Sasaki A, Itoh H, Gomi K, Ueguchi-Tanaka M, Ishiyama K, Kobayashi M, Jeong DH, An G, Kitano H, Ashikari M, Matsuoka M: Accumulation of phosphorylated repressor for gibberellin signaling in an F-box mutant. Science. 2003, 299 (5614): 1896-1898. 10.1126/science.1081077.PubMedView ArticleGoogle Scholar
  33. Dill A, Thomas SG, Hu J, Steber CM, Sun TP: The Arabidopsis F-box protein SLEEPY1 targets gibberellin signaling repressors for gibberellin-induced degradation. Plant Cell. 2004, 16 (6): 1392-1405. 10.1105/tpc.020958.PubMedPubMed CentralView ArticleGoogle Scholar
  34. AGI: Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature. 2000, 408: 796-815. 10.1038/35048692.View ArticleGoogle Scholar
  35. Goff SA, Ricke D, Lan TH, Presting G, Wang R, Dunn M, Glazebrook J, Sessions A, Oeller P, Varma H, Hadley D, Hutchison D, Martin C, Katagiri F, Lange BM, Moughamer T, Xia Y, Budworth P, Zhong J, Miguel T, Paszkowski U, Zhang S, Colbert M, Sun WL, Chen L, Cooper B, Park S, Wood TC, Mao L, Quail P, Wing R, Dean R, Yu Y, Zharkikh A, Shen R, Sahasrabudhe S, Thomas A, Cannings R, Gutin A, Pruss D, Reid J, Tavtigian S, Mitchell J, Eldredge G, Scholl T, Miller RM, Bhatnagar S, Adey N, Rubano T, Tusneem N, Robinson R, Feldhaus J, Macalma T, Oliphant A, Briggs S: A draft sequence of the rice genome (Oryza sativa L. ssp. japonica). Science. 2002, 296 (5565): 92-100. 10.1126/science.1068275.PubMedView ArticleGoogle Scholar
  36. Tuskan GA, Difazio S, Jansson S, Bohlmann J, Grigoriev I, Hellsten U, Putnam N, Ralph S, Rombauts S, Salamov A, Schein J, Sterck L, Aerts A, Bhalerao RR, Bhalerao RP, Blaudez D, Boerjan W, Brun A, Brunner A, Busov V, Campbell M, Carlson J, Chalot M, Chapman J, Chen GL, Cooper D, Coutinho PM, Couturier J, Covert S, Cronk Q, Cunningham R, Davis J, Degroeve S, Dejardin A, Depamphilis C, Detter J, Dirks B, Dubchak I, Duplessis S, Ehlting J, Ellis B, Gendler K, Goodstein D, Gribskov M, Grimwood J, Groover A, Gunter L, Hamberger B, Heinze B, Helariutta Y, Henrissat B, Holligan D, Holt R, Huang W, Islam-Faridi N, Jones S, Jones-Rhoades M, Jorgensen R, Joshi C, Kangasjarvi J, Karlsson J, Kelleher C, Kirkpatrick R, Kirst M, Kohler A, Kalluri U, Larimer F, Leebens-Mack J, Leple JC, Locascio P, Lou Y, Lucas S, Martin F, Montanini B, Napoli C, Nelson DR, Nelson C, Nieminen K, Nilsson O, Pereda V, Peter G, Philippe R, Pilate G, Poliakov A, Razumovskaya J, Richardson P, Rinaldi C, Ritland K, Rouze P, Ryaboy D, Schmutz J, Schrader J, Segerman B, Shin H, Siddiqui A, Sterky F, Terry A, Tsai CJ, Uberbacher E, Unneberg P, Vahala J, Wall K, Wessler S, Yang G, Yin T, Douglas C, Marra M, Sandberg G, Van de Peer Y, Rokhsar D: The genome of black cottonwood, Populus trichocarpa (Torr. & Gray). Science. 2006, 313 (5793): 1596-1604. 10.1126/science.1128691.PubMedView ArticleGoogle Scholar
  37. de la Torre JE, Egan MG, Katari MS, Brenner ED, Stevenson DW, Coruzzi GM, DeSalle R: ESTimating plant phylogeny: lessons from partitioning. BMC Evol Biol. 2006, 6: 48-10.1186/1471-2148-6-48.PubMedPubMed CentralView ArticleGoogle Scholar
  38. Marshall SD, Putterill JJ, Plummer KM, Newcomb RD: The carboxylesterase gene family from Arabidopsis thaliana. J Mol Evol. 2003, 57 (5): 487-500. 10.1007/s00239-003-2492-8.PubMedView ArticleGoogle Scholar
  39. Raven PH, Evert RF, Eichhorn SE: Biology of Plants : 7th edition. New York , WH Freeman and Company Publishers 2005.Google Scholar
  40. Kipreos ET, Pagano M: The F-box protein family. Genome Biol. 2000, 1 (5): REVIEWS3002-10.1186/gb-2000-1-5-reviews3002.PubMedPubMed CentralView ArticleGoogle Scholar
  41. Gomi K, Sasaki A, Itoh H, Ueguchi-Tanaka M, Ashikari M, Kitano H, Matsuoka M: GID2, an F-box subunit of the SCF E3 complex, specifically interacts with phosphorylated SLR1 protein and regulates the gibberellin-dependent degradation of SLR1 in rice. Plant J. 2004, 37 (4): 626-634. 10.1111/j.1365-313X.2003.01990.x.PubMedView ArticleGoogle Scholar
  42. Strader LC, Ritchie S, Soule JD, McGinnis KM, Steber CM: Recessive-interfering mutations in the gibberellin signaling gene SLEEPY1 are rescued by overexpression of its homologue, SNEEZY. Proc Natl Acad Sci U S A. 2004, 101 (34): 12771-12776. 10.1073/pnas.0404287101.PubMedPubMed CentralView ArticleGoogle Scholar
  43. Richards DE, Peng J, Harberd NP: Plant GRAS and metazoan STATs: one family?. Bioessays. 2000, 22 (6): 573-577. 10.1002/(SICI)1521-1878(200006)22:6<573::AID-BIES10>3.0.CO;2-H.PubMedView ArticleGoogle Scholar
  44. Hussain A, Cao D, Peng J: Identification of conserved tyrosine residues important for gibberellin sensitivity of Arabidopsis RGL2 protein. Planta. 2007, 226 (2): 475-483. 10.1007/s00425-007-0497-z.PubMedView ArticleGoogle Scholar
  45. Itoh H, Shimada A, Ueguchi-Tanaka M, Kamiya N, Hasegawa Y, Ashikari M, Matsuoka M: Overexpression of a GRAS protein lacking the DELLA domain confers altered gibberellin responses in rice. Plant J. 2005, 44 (4): 669-679. 10.1111/j.1365-313X.2005.02562.x.PubMedView ArticleGoogle Scholar
  46. Reski R: Development, genetics and molecular biology of mosses. Botanica Acta. 1998, 111: 1-15.View ArticleGoogle Scholar
  47. Rensing SA, Rombauts S, Van de Peer Y, Reski R: Moss transcriptome and beyond. Trends Plant Sci. 2002, 7 (12): 535-538. 10.1016/S1360-1385(02)02363-4.PubMedView ArticleGoogle Scholar
  48. Quatrano RS, McDaniel SF, Khandelwal A, Perroud PF, Cove DJ: Physcomitrella patens: mosses enter the genomic age. Curr Opin Plant Biol. 2007, 10 (2): 182-189. 10.1016/j.pbi.2007.01.005.PubMedView ArticleGoogle Scholar
  49. Asprey GF, Benson-Evans K, Lyon AG: Effect of Gibberellin and Indoleacetic Acid on Seta Elongation in Pellia epiphylla. Nature. 1958, 181: 1351-10.1038/1811351a0.View ArticleGoogle Scholar
  50. Weng JK, Tanurdzic M, Chapple C: Functional analysis and comparative genomics of expressed sequence tags from the lycophyte Selaginella moellendorffii. BMC Genomics. 2005, 6: 85-10.1186/1471-2164-6-85.PubMedPubMed CentralView ArticleGoogle Scholar
  51. Friedman WE, Moore RC, Purugganan MD: The evolution of plant development. American Journal of Botany. 2004, 91: 1726-1741.PubMedView ArticleGoogle Scholar
  52. Johnston R: Effects of Gibberellins on Marine Algae in Mixed Cultures. Limnology and Oceanography. 1963, 8: 270-275.View ArticleGoogle Scholar
  53. Walden AR, Walter C, Gardner RC: Genes expressed in Pinus radiata male cones include homologs to anther-specific and pathogenesis response genes. Plant Physiol. 1999, 121 (4): 1103-1116. 10.1104/pp.121.4.1103.PubMedPubMed CentralView ArticleGoogle Scholar
  54. []
  55. Wang W, Tanurdzic M, Luo M, Sisneros N, Kim HR, Weng JK, Kudrna D, Mueller C, Arumuganathan K, Carlson J, Chapple C, de Pamphilis C, Mandoli D, Tomkins J, Wing RA, Banks JA: Construction of a bacterial artificial chromosome library from the spikemoss Selaginella moellendorffii: a new resource for plant comparative genomics. BMC Plant Biol. 2005, 5: 10-10.1186/1471-2229-5-10.PubMedPubMed CentralView ArticleGoogle Scholar
  56. Matsuzaki M, Misumi O, Shin IT, Maruyama S, Takahara M, Miyagishima SY, Mori T, Nishida K, Yagisawa F, Nishida K, Yoshida Y, Nishimura Y, Nakao S, Kobayashi T, Momoyama Y, Higashiyama T, Minoda A, Sano M, Nomoto H, Oishi K, Hayashi H, Ohta F, Nishizaka S, Haga S, Miura S, Morishita T, Kabeya Y, Terasawa K, Suzuki Y, Ishii Y, Asakawa S, Takano H, Ohta N, Kuroiwa H, Tanaka K, Shimizu N, Sugano S, Sato N, Nozaki H, Ogasawara N, Kohara Y, Kuroiwa T: Genome sequence of the ultrasmall unicellular red alga Cyanidioschyzon merolae 10D. Nature. 2004, 428 (6983): 653-657. 10.1038/nature02398.PubMedView ArticleGoogle Scholar
  57. Bikandi J, San Millan R, Rementeria A, Garaizar J: In silico analysis of complete bacterial genomes: PCR, AFLP-PCR and endonuclease restriction. Bioinformatics. 2004, 20 (5): 798-799. 10.1093/bioinformatics/btg491.PubMedView ArticleGoogle Scholar
  58. []
  59. Sammeth M, Griebel T, Tille F, Stoye J: Panta rhei (QAlign2): an open graphical environment for sequence analysis. Bioinformatics. 2006, 22 (7): 889-890. 10.1093/bioinformatics/btl007.PubMedView ArticleGoogle Scholar
  60. Bray N, Pachter L: MAVID: constrained ancestral alignment of multiple sequences. Genome Res. 2004, 14 (4): 693-699. 10.1101/gr.1960404.PubMedPubMed CentralView ArticleGoogle Scholar
  61. Reski R, Abel WO: Induction of budding on chloronemata and caulonemata of the moss, Physcomitrella patens, using isopentenyladenine. Planta. 1985, 165: 354-358. 10.1007/BF00392232.PubMedView ArticleGoogle Scholar
  62. []


© Vandenbussche et al; licensee BioMed Central Ltd. 2007

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.