Lotus japonicus karrikin receptors display divergent ligand-binding specificities and organ-dependent redundancy

Abstract

Karrikins (KARs), smoke-derived butenolides, are perceived by the α/β-fold hydrolase KARRIKIN INSENSITIVE2 (KAI2) and thought to mimic endogenous, yet elusive plant hormones tentatively called KAI2-ligands (KLs). The sensitivity to different karrikin types as well as the number of KAI2 paralogs varies among plant species, suggesting diversification and co-evolution of ligand-receptor relationships. We found that the genomes of legumes, comprising a number of important crops with protein-rich, nutritious seed, contain two or more KAI2 copies. We uncover sub-functionalization of the two KAI2 versions in the model legume Lotus japonicus and demonstrate differences in their ability to bind the synthetic ligand GR24^ent-5DS in vitro and in genetic assays with Lotus japonicus and the heterologous Arabidopsis thaliana background. These differences can be explained by the exchange of a widely conserved phenylalanine in the binding pocket of KAI2a with a tryptophan in KAI2b, which arose independently in KAI2 proteins of several unrelated angiosperms. Furthermore, two polymorphic residues in the binding pocket are conserved across a number of legumes and may contribute to ligand binding preferences. The diversification of KAI2 binding pockets suggests the occurrence of several different KLs acting in non-fire following plants, or an escape from possible antagonistic exogenous molecules. Unexpectedly, L. japonicus responds to diverse synthetic KAI2-ligands in an organ-specific manner. Hypocotyl growth responds to KAR₁, KAR₂ and rac-GR24, while root system development responds only to KAR₁. This differential responsiveness cannot be explained by receptor-ligand preferences alone, because LjKAI2a is sufficient for karrikin responses in the hypocotyl, while LjKAI2a and LjKAI2b operate redundantly in roots. Instead, it likely reflects differences between plant organs in their ability to transport or metabolise the synthetic KLs. Our findings provide new insights into the evolution and diversity of butenolide ligand-receptor relationships, and open novel research avenues into their ecological significance and the mechanisms controlling developmental responses to divergent KLs.

Author summary

Plant hormone signaling is crucial for development and for adequate responses to biotic and abiotic environmental conditions. The most recently discovered plant hormone receptor KARRIKIN INSENSITVE 2 (KAI2), binds a small butenolide called karrikin that was discovered in smoke and induces germination of fire-following plants. Several lines of evidence suggest a yet elusive endogenous hormone, which acts as ligand for KAI2. Until its identification, synthetic karrikins or the strigolactone-like molecule GR24 are used to probe the karrikin signaling pathway. While the model plant Arabidopsis contains only one KAI2 gene, several copies are maintained in other species suggesting sub-functionalization. We report that genomes of species in the legume hologalegina clade encode two KAI2 versions. In Lotus japonicus, they diverge in their binding ability to synthetic ligands due to three amino acid changes in their binding pocket, of which two are conserved across legumes and one has independently occurred in several species across the angiosperm phylogeny. Surprisingly, L. japonicus hypocotyls react with developmental responses to two different karrikins (KAR₁, KAR₂) and a synthetic strigolactone rac-GR24, while root development responds only to KAR₁. This shows that there is not only diversity in ligand-receptor relationships but possibly also organ-specific uptake or metabolism of divergent butenolide molecules.

Introduction

Karrikins (KARs) are small butenolide compounds derived from smoke of burning vegetation that were identified as germination stimulants of fire-following plants [1]. They can also accelerate seed germination of species that do not grow in fire-prone environments such as Arabidopsis thaliana, which enabled the identification of genes encoding karrikin receptor components via forward and reverse genetics. The α/β-fold hydrolase KARRIKIN INSENSITIVE2 (KAI2) is thought to bind KARs, and interacts with the F-box protein MORE AXILLIARY GROWTH 2 (MAX2) that is required for ubiquitylation of repressor proteins via the Skp1-Cullin-F-box (SCF) complex [2–9]. There are six known KARs, of which KAR₁ is most abundant in smoke-water and most active on seed germination of fire-following plants [1,10,11], but Arabidopsis responds more strongly to KAR_2, which lacks the methyl group at the butenolide ring that is characteristic for KAR₁ [2,3,11]. Both KAR₁ and KAR₂ are commercially available and commonly used in research.

Arabidopsis KAI2 regulates several traits in addition to seed germination, including light-dependent hypocotyl growth inhibition, cotyledon and rosette leaf area, cuticle thickness, root hair length and density, root skewing and lateral root density [4,12–15]. Moreover, the rice orthologs of KAI2 (D14-LIKE) and MAX2 (D3) are essential for root colonization by arbuscular mycorrhiza (AM) fungi, and are involved in regulating mesocotyl elongation [7,16,17]. These roles of KAI2, unrelated to smoke and seed germination, suggest that karrikins mimic yet-unknown endogenous (and possibly AM fungus-derived) signaling molecules that bind to KAI2 to regulate plant development or AM symbiosis, and are provisionally called KAI2-ligands (KLs) [12,18].

Structurally, KARs resemble the apocarotenoid strigolactones (SLs), which were originally discovered in root exudates in the rhizosphere [19], where they act as germination cues for parasitic weeds [19] and as stimulants of AM fungi [20,21]. In addition to their function in the rhizosphere, SLs function endogenously as phytohormones and repress shoot branching [22,23]. SL signaling also affects secondary growth; and co-regulates lateral and adventitious root formation and rice mesocotyl elongation with the karrikin signaling pathway [7,15,24,25]. As with KARs, SLs are perceived by an α/β-fold hydrolase D14/DAD2 that, like KAI2, depends for function on a serine–histidine–aspartate catalytic triad within the ligand binding pocket [26,27]. As KAI2, D14 interacts with the SCF-complex via the same F-box protein MAX2 [9,26] to ubiquitylate repressors of the SMXL family and mark them for degradation by the 26S proteasome [28–31].

Phylogenetic analysis of the α/β-fold hydrolase receptors in extant land plants revealed that an ancestral KAI2 is already present in charophyte algae, while the so-called eu-KAI2 is ubiquitous among land plants. The strigolactone receptor gene, D14 evolved only in the seed plants likely through duplication of KAI2 and sub-functionalization [32]. An additional duplication in the seed plants gave rise to D14-LIKE2 (DLK2), an α/β-fold hydrolase of unknown function, which is transcriptionally induced in response to KAR treatment in a KAI2- and MAX2-dependent manner, and currently represents the best-characterized KAR marker gene in Arabidopsis [4,33]. Despite their similarity, KAI2 and D14 cannot replace each other in Arabidopsis, as shown by promoter swap experiments [34]. This indicates that their expression pattern does not determine their signaling specificity. Instead, this is reached by ligand-receptor preference, and most likely the tissue-specific presence of their ligands, as well as distinctive interaction with other proteins, such as repressors of the SMXL family to trigger downstream signaling [35].

In Arabidopsis and rice, in which KAR/KL signaling has so far been mostly studied, KAI2 is a single copy gene. However, KAI2 has multiplied and diversified in other species. For example, the Physcomitrella patens genome contains 11 genes encoding KAI2-like proteins [36]. Of these some preferentially bind KAR and others the SL 5-deoxystrigol in vitro and this preference is determined by polymorphic amino acids in a loop that determines the rigidity of the ligand-binding pocket [37]. The genomes of parasitic plants of the Orobanchaceae also contain several KAI2 copies. Some of these have evolved to perceive strigolactones, some can restore KAR-responses in Arabidopsis kai2 mutants, and others do not mediate responses to any of these molecules in Arabidopsis [12,38,39]. Thus, in plant species with an expanded KAI2-family there is scope for a diverse range of ligands and ligand-binding specificities, as well as for diverse protein interaction partners. Apart from discriminating KARs from SLs, it was very recently reported that KAI2 genes have diversified in the genome of the fire follower Brassica tournefortii to encode KAI2 receptors, with different ligand preferences towards KAR₁ and KAR₂ [40]_. Of these, BtKAI2a mediates stronger responses to KAR_2, while BtKAI2b mediates stronger responses to KAR₁, when expressed in the heterologous Arabidopsis background. This binding preference is determined by two valine (BtKAI2a) to leucine (BtKAI2b) substitutions at the ligand binding pocket [40]. Also, among plants with a single copy KAI2 gene, the responsiveness to karrikin molecules can differ significantly: Arabidopsis plants respond more strongly to KAR₂ than to KAR₁ [4,15]. In contrast, rice roots did not display any transcriptional response to KAR₂, not even for the marker gene DLK2 [16]. It is yet unclear what determines these differences in KAR₂ responsiveness among plant species.

Legumes comprise a number of agronomically important crops and they are special among plants as most species in the family can form nitrogen-fixing root nodule symbiosis with rhizobia in addition to arbuscular mycorrhiza. Given the possible diversity in KAI2-ligand specificities among plant species, we characterized the karrikin receptor machinery in a legume, using L. japonicus as a model. We found that KAI2 has duplicated prior to the diversification of legumes and that L. japonicus KAI2a and KAI2b differ in their binding preferences to synthetic ligands in vitro and in the heterologous Arabidopsis kai2 and kai2 d14 mutant backgrounds. We demonstrate that these ligand binding preferences can be explained by substitution of a highly conserved phenylalanine to a tryptophan in the binding pocket of LjKAI2b. This tryptophan occurs rarely also in other unrelated angiosperm species, and seems to have arisen several times independently. Two additional polymorphic residues that are conserved in the KAI2a and KAI2b clades across several legumes may also contribute to ligand binding preference. In addition, we found a surprising organ-specific responsiveness to synthetic KAI2-ligands, with L. japonicus hypocotyl development responding to KAR₁, KAR₂ and the strigolactone/karrikin analog rac-GR24, and root system development responding only to KAR₁. These responses depend only on LjKAI2a in hypocotyls, while LjKAI2a and LjKAI2b operate redundantly in roots. Together these findings suggest that a diversity of mechanisms may influence KAR/KL responses including receptor-ligand binding specificity or organ-specific interaction of KAI2 with other proteins.

Results

KAI2 underwent duplication prior to diversification of the legumes

To characterize the karrikin and the strigolactone perception machinery in L. japonicus, we retrieved KAI2, D14 and MAX2 by protein BLAST using Arabidopsis KAI2, D14 and MAX2 as templates. A phylogenetic tree revealed that LjD14 (Lj5g3v0310140.4) is a single copy gene whereas LjKAI2 has duplicated (Fig 1), resulting in two paralogs LjKAI2a (Lj2g3v1931930.1) and LjKAI2b (Lj0g3v0117039.1). The KAI2 duplication event must have occurred prior to the diversification of the legumes or at least before the separation of the Millettioids and the ‘Hologalegina’ clade [41] because a similar duplication pattern as in L. japonicus (Hologalegina) is also detected in pea, Medicago truncatula (both Hologalegina) and soybean (Millettioid). The Millettioid soybean genome additionally contains a third, more distantly related KAI2 copy (KAI2c).

Fig 1. The KAI2 gene underwent duplication prior to diversification of the legumes.

Phylogenetic tree of KAI2 and D14 rooted with bacterial RbsQ from indicated species (Lotus japonicus; Glycine max; Pisum sativum; Medicago truncatula; Arabidopsis thaliana; Populus trichocarpa; Oryza sativa; Zea mays; Sorghum bicolor; Marchantia polymorpha). MEGAX was used to align the protein sequences with MUSCLE and generate a tree inferred by Maximum Likelihood method [72]. The tree with the highest log likelihood (-7359.19) is shown. The percentage of trees in which the associated taxa clustered together is shown next to the branches. Values below 50 were ignored. KAI2 duplication in the legumes is highlighted by red and blue branches.

The F-box protein-encoding gene LjMAX2 also underwent duplication likely as a result of whole genome duplication, because the two LjMAX2 copies are in two syntenic regions of the genome (S1A Fig). However, only one LjMAX2 copy (Lj3g3v2851180.1) is functional. The other copy ΨMAX2-like (Lj0g3v0059909.1) appears to be a pseudogene, as it contains an early stop codon, thus encoding a putative truncated protein of 216 instead of 710 amino acids (S1B Fig). It appears that an insertion of one nucleotide into ΨMAX2-like created a frameshift, as manual deletion of thymine 453 restores a correct nucleotide and amino acid sequence (S1B Fig).

We hypothesized that L. japonicus (and other legumes) retained two intact KAI2 copies because they may have functionally diverged, perhaps through changes in their expression pattern and/or sequence, possibly resulting in a divergent spatial distribution, ligand affinity and/or ability to interact with other proteins. We examined transcript accumulation of LjKAI2a and LjKAI2b, as well as LjD14 and LjMAX2 in different organs of L. japonicus (S2 Fig). Overall, both LjKAI2a and LjKAI2b transcripts accumulated to higher levels than those of LjD14 and LjMAX2. LjKAI2a transcripts accumulated approximately 100-fold more in aerial organs than LjKAI2b, whereas LjKAI2b accumulated 10-fold more than LjKAI2a in roots of adult plants, which were grown in a sand-vermiculite mix in pots under long day conditions (16h light /8h dark). However, 1-week-old seedlings grown on water-agar in Petri dishes under short-day conditions (8h light/16h dark), displayed 10-fold higher transcript levels of LjKAI2a than LjKAI2b in both roots and hypocotyls (S2B Fig). Thus, LjKAI2a and LjKAI2b are regulated in an organ-specific, age- and/or environment-dependent manner, suggesting that their individual expression involves at least partially different transcriptional regulators.

Fusions of the four corresponding proteins with T-Sapphire or mOrange in transiently transformed Nicotiana benthamiana leaves showed similar subcellular localization as in Arabidopsis and rice [16,17,42,43]. T-Sapphire-MAX2 was detected exclusively in the nucleus, while the α/β-hydrolases (D14, KAI2a and KAI2b) fused to mOrange localized to the nucleus and cytoplasm (S3A Fig). Western blot analysis confirmed that the mOrange signal observed in the cytoplasm resulted from the full-length fusion protein and not from free mOrange (S3B Fig).

L. japonicus KAI2a, KAI2b and D14 can replace their orthologs in Arabidopsis

To examine whether both LjKAI2a and LjKAI2b function in a canonical manner, we employed a well-established hypocotyl elongation assay in Arabidopsis [12,34], after transgenically complementing the Arabidopsis thaliana kai2-2 mutant [4] with LjKAI2a and LjKAI2b driven by the AtKAI2 promoter. Both restored inhibition of hypocotyl elongation in the kai2-2 mutant (Fig 2A and 2B). LjD14 driven by the AtKAI2 promoter was unable to restore hypocotyl growth inhibition, but it restored repression of shoot branching of the Arabidopsis d14-1 mutant [4], when driven by the Arabidopsis D14 promoter. As expected, LjKAI2a and LjKAI2b could not do the same (Fig 2C and 2D). Together with the phylogenetic analysis (Fig 1), these results demonstrate that L. japonicus KAI2a and KAI2b are both functional orthologs of the Arabidopsis karrikin/KL receptor gene KAI2, whereas L. japonicus D14 is the functional orthologue of the Arabidopsis strigolactone receptor gene D14. Furthermore, the L. japonicus KAI2 genes are not interchangeable with D14 [34].

Fig 2. Lotus japonicus D14, KAI2a and KAI2b can replace D14 and KAI2 in Arabidopsis, respectively.

(A-B) Hypocotyl length of A. thaliana wild-type (Ler), kai2-2 and kai2-2 lines complemented by AtD14, AtKAI2, LjD14, LjKAI2a and LjKAI2b, driven by the AtKAI2 promoter at 6 days post germination (dpg). Seedlings were grown in 16h light/8h dark periods (n = 37–122). Scale bar = 5mm. (C) Shoots of A. thaliana Col-0 and d14-1, d14-1, with an empty vector (EV) or complemented with AtD14, AtKAI2, LjD14, LjKAI2a and LjKAI2b, driven by the AtD14 promoter at 26 dpg. Scale bar = 10 cm. (C) Rosette branch number at 26 dpg of A. thaliana wild-type (Col-0), d14-1 and d14-1 lines carrying an empty vector (EV) or plasmids containing AtD14, AtKAI2, LjD14, LjKAI2a and LjKAI2b, driven by the AtD14 promoter (n = 24). Letters indicate different statistical groups (ANOVA, post-hoc Tukey test).

Lotus japonicus KAI2a and KAI2b differ in their ligand binding specificity

To explore whether L. japonicus KAI2a and KAI2b can mediate hypocotyl responses to karrikins, we quantified hypocotyl length of the Atkai2-2 lines transgenically complemented with LjKAI2a or LjKAI2b after treatment with KAR₁ and KAR₂ (Fig 3A and 3B). Two independent lines complemented with LjKAI2a displayed a similar reduction in hypocotyl growth in response to both KAR₁ and KAR₂. However, the two lines expressing LjKAI2b responded more strongly to KAR₁ than to KAR₂, contrasting with the common observation, that Arabidopsis hypocotyl growth tends to be more responsive to KAR₂ [4,44]. We wondered if the preference towards a specific KAR compound is also observed with KAI2 from other species. To this end, we tested the karrikin response in a line resulting from a cross of the kai2 mutant htl-2 with an Arabidopsis line transgenic for the cDNA of the rice D14L/KAI2 [16]. In contrast to LjKAI2b, OsD14L/KAI2 mediated a stronger response to KAR₂ than to KAR₁ (Fig 3C). Thus, the differential responsiveness of transgenic Arabidopsis lines to KAR₁ and KAR₂ does not result from a general incompatibility of a heterologous KAI2 protein with the Arabidopsis background, but suggests different ligand affinities of the transgenic receptors to the karrikins or their possible metabolised products [34,40].

Fig 3. Lotus japonicus KAI2a, KAI2b and rice D14L confer divergent hypocotyl growth responses to KAR₁ and KAR₂ in Arabidopsis.

(A) Structures of KAR₁, KAR₂, GR24^5DS and GR24^ent-5DS. (B-C) Hypocotyl length of A. thaliana kai2 mutants complemented with KAI2 from A. thaliana, L. japonicus and rice, after treatment with solvent (Mock), 1 μM KAR₁ or KAR₂ at 6 dpg. (B) Ler wild-type, kai2-2 and kai2-2 lines complemented with AtKAI2, LjKAI2a and LjKAI2b, driven by the AtKAI2 promoter (n = 33–128). (C) Ler and Col-0 wild-type, htl-2 (Ler), K02821-line transgenic for p35S:OsD14L (Col-0), and two homozygous F₃ lines from the htl-2 x K02821 cross [16] (n = 80–138). (D) Hypocotyl length of A. thaliana Col-0 wild-type, d14-1 kai2-2 double mutants, and d14-1 kai2-2 lines complemented with LjKAI2a and LjKAI2b, driven by the AtKAI2 promoter after treatment with solvent (Mock), 1 μM GR24^5DS or GR24^ent-5DS (n = 59–134). (B-D) Seedlings were grown in 8h light/16h dark periods. Letters indicate different statistical groups (ANOVA, post-hoc Tukey test).

The two enantiomers of the synthetic strigolactone rac-GR24, namely GR24^5DS and GR24^ent-5DS, trigger developmental and transcriptional responses via D14 as well as KAI2, respectively, in Arabidopsis [15,45]. For some KAI2-mediated responses, GR24^ent-5DS was shown to be more active than karrikin [46] and it has been hypothesized that karrikin may need to be metabolized in planta, to yield a high affinity KAI2 ligand, while this may not be necessary for GR24^ent-5DS [34,46,47]. We examined whether LjKAI2a and LjKAI2b can mediate hypocotyl growth responses to GR24^5DS and GR24^ent-5DS in the Arabidopsis thaliana d14-1 kai2-2 double mutant background (Fig 3D). Lines expressing LjKAI2a responded to both enantiomers with reduced hypocotyl elongation, but displayed a much stronger response to the preferred KAI2 ligand GR24^ent-5DS. Unexpectedly, the lines expressing LjKAI2b did not significantly respond to either of the two enantiomers. This contrasting sensitivity to GR24 enantiomers together with the differences in response to KAR₁ and KAR₂ suggests that LjKAI2a and LjKAI2b differ in their binding pocket, resulting in divergent affinity to the synthetic ligands.

Replacement of a conserved phenylalanine by a tryptophan at the binding pocket of KAI2b explains rejection of GR24^ent-5DS

We used differential scanning fluorimetry (DSF) to examine whether purified recombinant LjKAI2a and LjKAI2b (S4A Fig) display a different ligand affinity in vitro, employing GR24^5DS and GR24^ent-5DS as model ligands (Figs 4 and S4). The DSF assay has been widely used for deducing GR24^5DS and GR24^ent-5DS binding to D14 and KAI2 proteins respectively, by means of thermal destabilization [26,34,40,48–50]. However, DSF is unfortunately not suitable for the characterization of karrikin binding [34,40]. Neither LjKAI2a nor LjKAI2b were destabilized in the presence of GR24^5DS (S4B Fig). GR24^ent-5DS induced a significant thermal destabilization of LjKAI2a at a concentration > 50 μM (Fig 4C). In contrast, it did not cause any significant thermal shift of LjKAI2b (Fig 4D), thus recapitulating the difference in hypocotyl growth response between Arabidopsis lines expressing LjKAI2a and LjKAI2b (Fig 3D).

Fig 4. Binding of GR24^ent-5DS to LjKAI2a is determined by three amino acids.

(A-B) The ligand-binding cavity regions of LjKAI2a and LjKAI2b proteins after structural homology modelling on the KAI2 crystal structure of A. thaliana [5]. Conserved residues in the cavity that differ between the KAI2a and KAI2b clades, and that are also different between LjKAI2b and AtKAI2, are shown in green. The phenylalanine residue in LjKAI2a, which is changed to tryptophan in LjKAI2b, is shown in violet. The catalytic triad is coloured in red. (C-J) DSF curves of purified SUMO fusion proteins of (C-D) wild-type LjKAI2a and LjKAI2b, and (E-J) versions with swapped amino acids (E-F) LjKAI2a^M160,L190, LjKAI2b^L161,S191, (G-H) LjKAI2a^{W157,M160,L190}, LjKAI2b^{F158,L161,S191}, (I-J) LjKAI2a^W157, LjKAI2b^F158 at the indicated concentrations of GR24^ent-5DS. The first derivative of the change of fluorescence was plotted against the temperature. Each curve is the arithmetic mean of three sets of reactions, each comprising four technical replicates. Peaks indicate the protein melting temperature. The shift of the peak in LjKAI2a indicates ligand-induced thermal destabilisation consistent with a protein-ligand interaction. Insets plot the minimum value of (-dF/dT) at the melting point of the protein as determined in the absence of ligand (means ± SE, n = 3). Asterisks indicate significant differences to the solvent control (ANOVA, post-hoc Dunnett test, N.S.>0.05, *≤0.05, **≤0.01, ***≤0.001, ****≤0.0001).

We found 16 conserved amino acid differences between the KAI2a and the KAI2b clade of the investigated legumes (S5 Fig), which may contribute to functional diversification of KAI2a and KAI2b. Modelling of LjKAI2a and LjKAI2b on the KAR₁-bound AtKAI2 crystal structure (4JYM) [5] revealed that only three of these were located at the binding pocket, namely L160/M161, S190/L191 and M218/L219 (for the KAI2a/KAI2b comparison, Fig 4A and 4B). Out of these three, L219 was conserved between LjKAI2b and the KAI2 proteins from Arabidopsis and rice, which displayed an opposite response pattern to KAR₁ and KAR₂ compared to LjKAI2b, when expressed in the Arabidopsis background (Fig 3). Therefore, we concluded that the M218/L219 polymorphism likely does not play a major role in determining the observed differential ligand-preference between LjKAI2a and LjKAI2b and discounted it as a candidate. However, we also found that in LjKAI2b exclusively, a highly conserved phenylalanine inside the pocket is replaced by tryptophan at position 158 (S5 Fig). Although this tryptophan is not conserved among other legume KAI2b versions used for the alignment (S5 Fig), we predicted that this bulky residue should have a strong impact on ligand binding.

To understand the impact of the three divergent candidate amino acids on ligand binding, we generated chimeric receptor proteins (S4A Fig). Exchanging only the two amino acids that are conserved across KAI2a and KAI2b clades comprising the investigated legumes (S5 Fig) was sufficient to influence the melting temperature of the two proteins in response to GR24^ent-5DS. LjKAI2a^M160,L190 became less responsive relative to LjKAI2a and displayed a slight shift in melting temperature only with 200 μM GR24^ent-5DS (Fig 4E), whereas LjKAI2b^L161,S191 gained a weak ability to respond to GR24^ent-5DS at 200 μM (Fig 4F). When all three amino acids were swapped, the melting response to GR24^ent-5DS was entirely switched between the two receptor proteins: LjKAI2a^{M160,L190,W157} did not display any thermal shift in presence of GR24^ent-5DS (Fig 4G), whereas LjKAI2b^{L161,S191,F158} gained a strong response to GR24^ent-5DS and displayed a thermal shift with ligand concentrations as low as 25 μM (Fig 4H). Thus, LjKAI2b^{L161,S191,F158} seemed to be slightly more prone to ligand-induced destabilisation than wild-type LjKAI2a. As W158 appeared to be a critical amino acid for restricting the response to GR24^ent-5DS, we also tested whether swapping F157 with W158 alone would suffice to exchange the ability of the receptors to respond to GR24^ent-5DS. In effect, LjKAI2b^F158 recapitulated the response of LjKAI2a to GR24^ent-5DS and likewise LjKAI2a^W157 resembled LjKAI2b (Fig 4I and 4J). Thus, changing this one amino acid in the binding pocket was sufficient to swap ligand specificity. We conclude that the F158/W159 polymorphism predominantly determines the ability of LjKAI2 proteins to bind GR24^ent-5DS, while there is a weaker contribution of L160/M161 and S190/L191.

As an alternative means to probe ligand-receptor interactions, intrinsic tryptophan fluorescence assays confirmed the response of wild-type LjKAI2a and LjKAI2b and all mutant versions to GR24^ent-5DS (S6 Fig). Unfortunately, because GR24^ent-5DS precipitated above 500 μM, this assay did not allow us to calculate K_d values because saturation of the response could not be achieved. Nevertheless, the qualitative results reiterate the strong impact of F158/W159 on the relative affinities of LjKAI2a and LjKAI2b for GR24^ent-5DS.

To examine whether the three amino acid residues determine ligand discrimination in planta, we transformed Arabidopsis d14 kai2 double mutants with the mutated LjKAI2a and LjKAI2b genes driven by the Arabidopsis KAI2 promoter and performed the hypocotyl growth assay in the presence of GR24^ent-5DS. Swapping only the two amino acids conserved in legumes (M160/L161 and S190/L191) was insufficient to exchange the GR24^ent-5DS response between lines expressing LjKAI2a vs. LjKAI2b. However, swapping all three amino acids, negatively affected the capacity of LjKAI2a^{M160,L190,W157} to mediate a hypocotyl response to GR24^ent-5DS, whereas it reconstituted a response via LjKAI2b^{L161,S191,F158} in three independent transgenic lines (Fig 5A and 5B). Although these results do not rule out a contribution of M160/L161 and S190/L191 towards ligand preference, they confirm that the phenylalanine to tryptophan substitution at position 157/158 is critical for determining the difference in GR24^ent-5DS binding preference between the two L. japonicus karrikin receptors KAI2a and KAI2b.

Fig 5. Amino acid swaps reverse sensitivity of LjKAI2a and LjKAI2b to GR24^ent-5DS in Arabidopsis hypocotyls.

Hypocotyl length of A. thaliana Col-0 wild-type, d14-1 kai2-2 double mutants, and d14-1 kai2-2 lines complemented with LjKAI2a and LjKAI2b variants driven by the AtKAI2 promoter and after treatment with solvent (Mock), 1 μM GR24^5DS or GR24^ent-5DS. (A) LjKAI2a^M160,L190 and LjKAI2a^{M160,L190,W157} (n = 46–84). (B) LjKAI2b^L161,S191 and LjKAI2b^{L161,S191,F158} (n = 49–102). (A-B) Seedlings were grown in 8h light/16h dark periods Asterisks indicate significant differences versus mock treatment (Welch t.test, *≤0.05, **≤0.01, ***≤0.001, ****≤0.0001).

The phenylalanine to tryptophan exchange occurred in other angiosperms independently

The phenylalanine-to-tryptophan transition requires two base changes at position two and three of the codon. We asked whether this change also occurred in other species and searched for KAI2 sequences across the plant phylogeny by BLAST-P against the EnsemblPlants, NCBI and 1KP databases [51], and retrieved KAI2 sequences of the parasitic plants Striga hermonthica, Orobanche fasciculata and Orobanche minor from Conn et al. 2015 [38]. This analysis showed that the KAI2c copy, we detected in the soybean genome (Fig 1) occurred in all analysed genomes of Milletioid legumes, the Genistoid legume Lupinus albus and the Mimosoid legume Prosopsis alba (S7 Fig). This suggests that the members of the Hologalegina clade, such as L. japonicus, have secondarily lost KAI2c. Importantly, among the 156 KAI2 sequences we analysed, ten in addition to LjKAI2b contain a tryptophan at the position corresponding to 157 in Arabidopsis KAI2 (S7 Fig). One of them was present in another legume (Prosopis alba). Five were present in other eudicots, of which three were in the Lamiales (Paulowniaceae: Paulownia fargesii; Phrymaceae: Erythranthe guttata, Orobanchaceae: Orobanche fasciculata) and two in the Ericales (Primulaceae: Ardisia evoluta and Ardisia humilis). Furthermore, we found four in monocots of the Bromeliacae (Ananas comosus), Dioscoreaceae (Dioscorea rotundata) and Iridaceae (Sisyrinchium angustifolium). In these species, W157 does not co-occur with M160 and L190 as in LjKAI2b, but mostly in combination with the more widely conserved residues L160 and A190 and also with L160 and L190 in Prosopis alba and Ananas comosus (S7 Fig). The genomes of all dicotyledon species encoding a KAI2 version with W157 contained at least one second copy encoding F157. In the monocot Dioscorea rotundata two KAI2 copies encoded the W157, whereas in Ananas comosus and Sisyrinchium angustifolium, we detected only one KAI2 copy. However, we cannot exclude the existence of additional copies as several transcriptomes in the 1KP database are likely incomplete.

In summary, we demonstrate that the F to W transition has occurred several times independently in the angiosperms without co-dependency on M160 and L190 of LjKAI2b, and in most cases it occurred in a duplicate KAI2 version. Thus, the binding pocket of KAI2 proteins appears to be subject to diversification, broadening the range of diverse KAI2-ligand variants that can be recognized, and at the same time extending the opportunities for binding- and signaling-specificity through KAI2 variants with a less (F157) and/or more (W157) restrictive binding-pocket.

Characterization of L. japonicus karrikin and strigolactone receptor mutants

To explore the roles of LjKAI2a and LjKAI2b in L. japonicus, we characterized mutants in these genes as well as in D14 and MAX2. We identified LORE1 retrotransposon insertions in L. japonicus KAI2a, KAI2b and MAX2 (kai2a-1, kai2b-3, max2-1, max2-2, max2-3, max2-4) in available collections [52,53] and nonsense mutations in D14 and KAI2b (d14-1, kai2b-1, kai2b-2) by TILLING [54] (Fig 6A, S1 Table). Since some of the max2 and kai2b mutants were impaired in seed germination or production (S1 Table) we continued working with kai2b-1, kai2b-3, max2-3 and max2-4. Quantitative RT-PCR analysis revealed that all mutations caused reduced transcript accumulation of the mutated genes in roots of the mutants except for d14-1 (S8 Fig). Furthermore, the transcript accumulation of LjKAI2a and LjKAI2b was not affected by mutation of the respective other paralog (S8A Fig).

Fig 6. Role of D14, KAI2a, KAI2b and MAX2 in shoot and hypocotyl development of Lotus japonicus.

(A) Schematic representation of the L. japonicus D14, KAI2a, KAI2b and MAX2 genes. Black boxes and lines show exons and introns, respectively. LORE1 insertions are indicated by red triangles and EMS mutations by red stars. (B) Shoot phenotype of L. japonicus wild-type and karrikin and strigolactone perception mutants at 8 weeks post germination (wpg). Scale bars: 7 cm. (C) Number of branches and of L. japonicus wild-type, karrikin and strigolactone perception mutants at 7 wpg (n = 12–21). (D) Leaf size of the indicated genotypes at 9 wpg (n = 12–15 plants with an average of 3 leaves). (E) Hypocotyl length of the indicated genotypes of L. japonicus under short day conditions (8h light/16h dark) at 1 wpg (n = 79–97). (C-E) Letters indicate different statistical groups (ANOVA, post-hoc Tukey test).

The LORE1 insertion in the kai2a-1 mutant is located close (19 bp) to a splice acceptor site. Since some LjKAI2a transcript accumulated in the mutant, we sequenced this residual transcript to examine the possibility that a functional protein could still be made through loss of LORE1 by splicing. We found that indeed a transcript from ATG to stop accumulates in kai2a-1 but it suffers from mis-splicing leading to a loss of the LORE1 transposon plus 15 bp (from 369–383), corresponding to five amino acids (YLNDV) at position 124–128 of the protein (S9A and S9B Fig). This amino-acid stretch reaches from a loop at the surface of the protein into the cavity of the binding pocket (S9C Fig). The artificial splice variant did not rescue the Arabidopsis kai2-2 hypocotyl phenotype, confirming that it is not functional in planta and showing that the amino acids 124-YLNDV-128 are essential for LjKAI2a function (S9D Fig).

Karrikin and rac-GR24 cause reduction in hypocotyl growth of L. japonicus in an LjKAI2a-dependent manner

The d14-1 and all max2 mutants displayed increased shoot branching, indicating that the L. japonicus strigolactone receptor components D14 and MAX2 are involved in shoot branching inhibition (Fig 6B and 6C), as for Arabidopsis, pea and rice [4,43,55,56]. In addition, d14 and max2 mutants had smaller leaves (Fig 6D), a phenotype that has not yet been associated with strigolactone signaling in other dicotyledon species. Surprisingly, kai2a and kai2b single mutants as well as kai2a-1 kai2b-1 double mutants or max2 mutants did not display the canonical elongated hypocotyl phenotype, which is observed in Arabidopsis [4] also in white light conditions (Figs 2, 3 and 5). If anything, the kai2a-1 kai2b-1 and max2 mutant hypocotyls were shorter than those of the wild type (Fig 6E). This indicates that the requirement of KL perception for suppression of hypocotyl elongation under white light is not conserved in L. japonicus and/or that KL may not be produced under these growth conditions.

To examine whether L. japonicus hypocotyls are responsive to karrikin treatment, we measured the dose-response of hypocotyl growth in wild-type to KAR₁, KAR₂ and also to rac-GR24. Hypocotyl elongation of wild type plants was progressively inhibited with increasing concentrations of all three compounds (S10A Fig). However, it was not suppressed by KAR₁ or KAR₂ treatment in the kai2a-1 kai2b-1 double mutant and the max2-4 mutant (S10B and S10C Fig). This demonstrates that similar to Arabidopsis, the hypocotyl response to karrikin of L. japonicus depends on the KAI2-MAX2 receptor complex. We also examined the KAR₁ response of kai2a and kai2b single mutant hypocotyls and found that kai2a-1 did not significantly respond to KAR₁ and KAR₂, while the two allelic kai2b mutants showed reduced hypocotyl growth in response to both karrikins (S10B Fig). The transcript accumulation pattern of DLK2 (Lj2g3v0765370)–a classical karrikin marker gene in Arabidopsis [4,45]–was consistent with this observation and DLK2 was induced in hypocotyls by KAR₁ and KAR₂ in a LjKAI2a-dependent but LjKAI2b-independent manner (S10D Fig). rac-GR24 treatment induced an increase of DLK2 transcripts in a LjKAI2b-independent, partially LjKAI2a-dependent, and fully MAX2-dependent manner, suggesting that this induction is mediated via LjKAI2a (GR24^ent-5DS) and LjD14 (GR24^5DS), similar to Arabidopsis [45] (S10C Fig). In summary, LjKAI2a appears to be necessary and sufficient to perceive karrikins and GR24^ent-5DS in the L. japonicus hypocotyl, possibly because expression of LjKAI2b in hypocotyls is too low under short day conditions (S2B Fig).

L. japonicus root system architecture is modulated by KAR₁ but not by KAR₂ treatment

rac-GR24 treatment can trigger root system architecture changes in Arabidopsis and Medicago truncatula [57–59], and it has recently become clear for Arabidopsis that lateral and adventitious root formation is co-regulated by karrikin and strigolactone signaling [15,25]. We examined, whether L. japonicus root systems respond to rac-GR24, KAR₁ and KAR₂ (Fig 7A). Surprisingly, in contrast to Arabidopsis and M. truncatula, L. japonicus root systems responded neither to rac-GR24 nor to KAR₂. Only KAR₁ treatment led to a dose-dependent decrease in primary root length and an increase of post-embryonic root (PER) number, and thus to a higher PER density (Fig 7A, S12A Fig). PERs include lateral and adventitious roots that can be difficult to distinguish in L. japonicus seedlings grown on Petri dishes. The instability of rac-GR24 over time in the medium could potentially prevent a developmental response of the root to this compound in our experiments [60]. However, refreshing the medium with new rac-GR24 or karrikins at 5 days post- germination, did not alter the outcome (Fig 7B). Consistently, we observed DLK2 induction in roots after KAR₁ but not after KAR₂ treatment (Fig 7C).

Fig 7. Lotus japonicus root system architecture is affected specifically by treatment with KAR₁ but not KAR₂.

(A) Primary root length (PRL), post-embryonic root (PER) number and PER density of wild-type plants 2 wpg after treatment with solvent (M) or three different concentrations of KAR₁, KAR₂ or rac-GR24 (GR24) (n = 32–57). (B) PER density of wild-type plants at 2 wpg and treated with solvent (Mock) 1 μM KAR₁, 1 μM KAR₂, or 1 μM rac-GR24 (n = 43–51). Plants were transferred onto fresh hormone-containing medium after 5 days. (C-D) RT-qPCR-based expression of DLK2 normalized to Ubiquitin expression in roots at 2 wpg after 2 hours treatment with solvent (Mock), (C) 1 μM KAR₁ and 1 μM KAR₂, (D) 1 μM rac-GR24 (n = 4). (A and C) Letters indicate different statistical groups (ANOVA, post-hoc Tukey test). (B) Asterisks indicate significant differences (ANOVA, Dunnett test, N.S.>0.05, *≤0.05). (D) Asterisk indicate significant differences versus mock treatment (Welch t.test, *≤0.05, **≤0.01, ***≤0.001).

Together with the hypocotyl responses to KAR₁, KAR₂ and rac-GR24 this indicates organ-specific sensitivity or responsiveness to these three compounds in L. japonicus with a more stringent uptake, perception and/or response system in the root.

Surprisingly, we found that the roots responded to rac-GR24 treatment with increased DLK2 transcript accumulation (Fig 7D) although no change in root architecture was observed in response to this treatment (Fig 7A). This suggests that different ligands may be transported to different tissues or may have a divergent impact on receptor conformation, thereby mediating different downstream responses. To confirm the contrasting responses of L. japonicus root systems to KAR₁ and rac-GR24, and to test whether they result from divergent molecular outputs, we examined transcriptional changes after one, two and six hours treatment of L. japonicus wild-type roots with KAR₁ and rac-GR24 using microarrays. Statistical analysis revealed a total number of 629 differentially expressed (DE) genes for KAR₁-treated and 232 genes for rac-GR24-treated roots (S2 Table). In agreement with previous reports from Arabidopsis and tomato [44,61,62] the magnitude of differential expression was low. Most of the DE genes upon KAR₁ and rac-GR24 treatment responded solely after 2h (S11 Fig). Interestingly, only a minority of 48 genes responded in the same direction in response to both KAR₁ and rac-GR24, while the majority of genes responded specifically to KAR₁ (580 DEGs) or rac-GR24 (169 DEGs). If rac-GR24 were to simply mimic the effect of KAR (GR24^ent-5DS) and SL (GR24^5DS) on roots, one would have expected a large overlap with KAR₁ responses, and in addition a number of non-overlapping DEGs, regulated through D14. In summary, the microarray experiment confirmed largely non-overlapping responses of L. japonicus root response to KAR₁ and rac-GR24.

Both LjKAI2a and LjKAI2b mediate root architecture-responses to KAR₁ but only LjKAI2a mediates DLK2 expression in response to GR24^ent-5DS

To inspect which α/β-hydrolase receptor mediates the changes in L. japonicus root system architecture in response to KAR₁ treatment, we examined PER density in the karrikin receptor mutants. For the non-treated roots, PER density was significantly higher than wild type only for kai2b-1 (Fig 8A), possibly caused by the reduced primary root length of this line (S13 Fig). The Ljkai2a-1 kai2b-1 double mutant and the max2-4 mutant did not respond to KAR₁ treatment with changes in root system architecture (Fig 8A, S12B–S12D Fig). With 1 μM KAR₁, we obtained contradictory results for the single kai2a and kai2b mutants in independent experiments (S12B and S12D Fig). However, kai2a and kai2b single mutants but not the kai2a kai2b double mutant responded to a slightly higher concentration of 3 μM KAR₁ (Fig 8A), indicating that LjKAI2a and LjKAI2b redundantly perceive KAR₁ (or a metabolite thereof) in L. japonicus roots. This pattern was mirrored by DLK2 expression in roots: both kai2a and kai2b single mutants responded to KAR₁ with increased DLK2 expression, while the kai2a-1 ka2b-1 double mutant and the max2-4 mutant did not respond (Fig 8B). Since LjKAI2b did not respond to GR24^ent-5DS in vitro as well as in the heterologous Arabidopsis background (Figs 4B and 5, S6 Fig), we examined its ability to mediate DLK2 induction by GR24^ent-5DS in L. japonicus roots. Wild-type and kai2b mutant roots responded to GR24^ent-5DS with increased DLK2 expression, but this was not the case for kai2a roots confirming that LjKAI2b cannot bind and mediate responses to GR24^ent-5DS (Fig 8C). In summary, LjKAI2a and LjKAI2b act redundantly in roots in mediating responses to KAR₁ but only KAI2a can perceive GR24^ent-5DS.

Fig 8.

LjKAI2a and LjKAI2b operate redundantly in the response of roots to KAR₁ (A) Post-embryonic-root (PER) density of L. japonicus plants, 2 wpg after treatment with solvent (M) or 3 μM KAR₁ (n = 34–72). Letters indicate different statistical groups only for non-treated mutant roots (ANOVA, post-hoc Tukey test). (B-C) RT-qPCR-based expression of DLK2 in roots of L. japonicus plants at 2 wpg after 2 hours treatment with solvent (Mock) or (B) 3 μM KAR₁ or (C) 1μM GR24^ent-5DS. Expression values were normalized to those of the housekeeping gene Ubiquitin (n = 3–4). (A-C) Asterisks indicate significant differences versus mock treatment (Welch t.test, *≤0.05, **≤0.01, ***≤0.001).

Discussion

Gene duplication followed by sub- or neofunctionalization is an important driver in the evolution of complex signaling networks and signaling specificities during the adaptation to new or diverse environments. In legumes, the karrikin receptor gene KAI2 multiplied possibly during the whole genome duplication that occurred in the Papilionoidaea before the diversification of legumes 59 million years ago [63]. While the Mimosoids, Genistoids and Milletioids, contain three different KAI2 versions, the Hologalegina clade appears to have lost one of them, retaining the more closely related KAI2a and KAI2b versions. Here, we provide evidence that L. japonicus KAI2a and KAI2b diversified in their ligand-binding specificity as well as their requirement in hypocotyl vs. root system responses to ligands (Fig 9).

Fig 9. L. japonicus KAI2a and KAI2b display organ-specific redundancy and differ in their ligand-binding specificity.

(A) LjKAI2a is required to mediate inhibition of hypocotyl growth in response to KAR₁ and KAR₂. In roots LjKAI2a and LjKAI2b redundantly promote postembryonic root density, but only in response to KAR₁ treatment. (B) In the Arabidopsis kai2-2 background LjKAI2a mediates hypocotyl growth inhibition in response to KAR₁, KAR₂ and GR24^ent-5DS. In the same background, LjKAI2b mediates a stronger response to KAR₁ than to KAR₂ and no response to GR24^ent-5DS (indicated by a red cross). Three divergent amino acids at the binding pocket are indicated in white. (C) Swapping the three divergent amino acids in the binding pocket reconstitutes GR24^ent-5DS activity through LjKAI2b and abolishes GR24^ent-5DS activity through LjKAI2a. Among the three amino acids F157/W158 are decisive for GR24^ent-5DS binding (strong colors), while L160/M161 and S190/L191 play a weaker role (pale colors). Amino acids from LjKAI2a have a red/pale red and amino acids from LjKAI2b a violet/pale background.

LjKAI2a and LjKAI2b differ in their quantitative sensitivity to KAR₁ and KAR₂, which vary only by the presence of one methyl group in KAR₁ (Fig 3B). An increased hydrophobicity of the LjKAI2b binding pocket as compared to LjKAI2a may mediate the preference towards the more hydrophobic KAR₁, similar to the fire-following plant Brassica tournefortii [40]. The difference in ligand preference of LjKAI2a vs. LjKAI2b is more dramatic for GR24^ent-5DS, an enantiomer of the synthetic strigolactone analogue rac-GR24, which acts through Arabidopsis KAI2 when applied to plants, promotes interaction of KAI2 with SMAX1 in yeast and binds to AtKAI2 in vitro [8,15,34,45,46]. We show that LjKAI2a mediates strong hypocotyl growth responses to GR24^ent-5DS in Arabidopsis as well as transcriptional activation of DLK2 in Lotus japonicus roots. LjKAI2b is incapable of triggering these responses to the compound, while being able to induce the same responses upon KAR₁ treatment. The dramatic difference in the ability of LjKAI2a and LjKAI2b to bind GR24^ent-5DS is confirmed in vitro by DSF and intrinsic tryptophan fluorescence assays. Together, these results demonstrate that the individual α/β-fold hydrolase receptor is sufficient to explain ligand sensitivity in planta.

Identifying the determinants of ligand-binding specificity of D14 and different KAI2 and KAI2-like proteins is an area of active research. Binding specificity of D14 and KAI2 to SLs and KARs respectively has been associated with the geometry and size of the binding pocket [6,64]. Changes in amino acid residues located in the pocket of divergent KAI2 versions in parasitic weeds have enabled alterations in pocket architecture and evolution of a chimeric receptor that perceives strigolactones like D14 but mediates germination like KAI2 [38,39]. The rigidity of lid helices forming the tunnel of the binding pocket have been proposed to determine specificity of KAI2-like proteins for strigolactone-like molecules vs. KAR₁ in Physcomitrella patens [37].

We identified three amino acids at the ligand-binding pocket that differ between LjKAI2a and LjKAI2b. Two of these are conserved across the legume KAI2a and KAI2b clades, namely L160 and S190 in KAI2a and M161 and L191 in KAI2b. This pattern of conservation suggests functional relevance in maintaining flexibility for different KAI2 ligands in legumes. Indeed, exchanging these two amino acids slightly changes the thermal instability of the two KAI2 versions in the DSF assay. Neither of the two amino acid changes is predicted to substantially impact the pocket volume or geometry but the amino acids of LjKAI2b are more hydrophobic, which may explain the preference for the more hydrophobic KAR₁ over KAR₂. A similar phenomenon was observed in Brassica tournefortii, a fire-following weed that has two functional KAI2 genes [40]. Similar to the situation in L. japonicus, BtKAI2b mediated a greater sensitivity to KAR₁ over KAR₂ in the Arabidopsis background, while it was the reverse for BtKAI2a. This was explained by one amino acid polymorphism in the binding pocket towards a more hydrophobic amino acid (V98L) in BtKAI2b. Notably, this residue (V98L) is in a very different position than the polymorphic residues in L. japonicus KAI2a/KAI2b, suggesting that the receptors are highly plastic and that similar binding-specificities for a given ligand may be achieved by changing hydrophobicity in different positions of the pocket.

Exchanging L160/M161 and S190/L191 between L. japonicus KAI2a and KAI2b was sufficient to change their sensitivity to GR24^ent-5DS in the DSF in vitro assay. However, the developmental response of Arabidopsis hypocotyls was hardly changed, possibly because in vivo, suboptimal ligand binding to the receptor can be stabilized by interacting proteins. A third amino acid difference (F157/W158) between the two KAI2 proteins occurs in L. japonicus. This residue critically determines sensitivity to GR24^ent-5DS in vitro as well as in Arabidopsis likely because the bulky tryptophan may sterically hinder GR24^ent-5DS binding, while still allowing binding of the smaller karrikins. In fact, swapping F157 with W158 alone was sufficient to swap the ability to respond to GR24^ent-5DS in DSF as well as intrinsic fluorescence assays.

B. tournefortii is a fire-following plant, the seeds of which respond to karrikins with dormancy breaking and germination [40]. Therefore, it makes adaptive sense for B. tournefortii to maintain two copies of KAI2, one of which is specialized for KAR₁, the most abundant KAR in smoke, and the other of which may be specialized for the endogenously produced ligand. For L. japonicus, which is not a fire-follower, KAR₁, KAR₂ and GR24^ent-5DS are likely not natural KAI2 ligands. Nevertheless, the maintenance of two KAI2 genes in the Hologalegina legumes, each with amino acid polymorphisms conferring differences in binding preferences to artificial ligands, requires an adaptive basis. One possibility is that L. japonicus KAI2a and KAI2b have specialized to bind different ligands in planta, indicative of legumes producing at least two different versions of the as-yet-unknown KAI2 ligand. The distinct expression patterns and developmental roles of LjKAI2a and LjKAI2b might also be consistent with a tissue-specific diversity of ligands, or even an endogenous ligand versus an exogenous ligand derived from the rhizosphere. From our assays with artificial ligands we extrapolate that LjKAI2b has a higher ligand selectivity than LjKAI2a. The additional amino acid change that occurred in L. japonicus but not in the other examined legumes may indicate that the KL bouquet of L. japonicus has further diversified. Alternatively, the F to W substitution in LjKAI2b may confer resistance to (a) toxic allelochemical(s) that may be released into the rhizosphere by competing plants or microorganisms. This speculative hypothesis is consistent with the role of LjKAI2b in roots (but not in hypocotyls) and with the observation that the F157W exchange occurred in several unrelated plant species independently that may all encounter compounds capable of blocking KAI2a in their natural habitat. It will be exciting to investigate the biological significance of this receptor sub-functionalization and the putative diversity of their ligands, once the molecule class of KL and its variants have been identified.

In addition to ligand-binding specificity at the level of the receptor, we identified a surprising organ-specific responsiveness to synthetic KAI2 ligands in L. japonicus. While hypocotyl growth is inhibited in response to KAR₁, KAR₂ and rac-GR24, root systems only respond to KAR₁ with architectural changes (Fig 9A). To our knowledge such an organ-specific discrimination of different but very similar KAR molecules has not previously so clearly been observed. However, a similar scenario could be at play in rice, in which transcriptome analysis of KAR₂-treated rice roots identified no differentially expressed gene [16], whereas rice mesocotyls respond with growth inhibition to the same treatment [7,16]. Although KAI2 can be shown to bind KAR₁ in vitro by isothermal titration calorimetry or fluorescent microdialysis [5,6,65], there is evidence suggesting that KARs are not directly bound by KAI2 in vivo, but may be metabolized first to yield the correct KAI2-ligand, which may bind with higher affinity [34,46]. It is possible that substrate specificities differ among enzymes involved in KAR metabolism in hypocotyls vs. roots. This would imply that the single methyl group, which distinguishes KAR₁ from KAR₂, is sufficient to impact specialized metabolism of karrikins. Alternatively, the transport of KAR₂ or the KAR₂-derived metabolic product could be limited in the root system, or KAR₂-derivatives may be rapidly catabolised in roots, thus limiting their effect. While KAR₂ fails to induce increased PER density as well as DLK2 expression in L. japonicus roots, GR24^ent-5DS triggers DLK2 transcript accumulation albeit being unable to increase PER density. DLK2 induction by GR24^ent-5DS requires KAI2a, thus involvement of D14 can be excluded. Furthermore, LjKAI2a and LjKAI2b act redundantly in mediating KAR₁-induced root system changes, excluding the possibility that they are regulated exclusively by LjKAI2b, which cannot bind GR24^ent-5DS. It is tempting to speculate that conformational changes of KAI2 proteins may differ depending on the ligand and that the extend of the change may influence the interaction strength with the karrikin signaling repressor SMAX1, MAX2 and/or additional proteins [8,66]. Perhaps DLK2 expression is more sensitive to quantitative SMAX1 removal than genes required to be induced for root system changes, such as the ethylene biosynthesis gene ACS7 [66]. Alternatively, SMAX1 proteins inhibiting DLK2 expression are more accessible to the receptor complex, thereby allowing interaction even when the receptor binds a suboptimal ligand, as compared to SMAX1 individuals supressing transcriptional activity of genes involved in root system changes; or GR24^ent-5DS is only taken up into a subset cells, in which SMAX1 removal does not mediate root system changes.

We observed that KAR₁ treatment triggers increased PER density in L. japonicus. This is somewhat contradictory to kai2 and max2 mutants in Arabidopsis, which display an increased lateral root density [15]. The discrepancy may result from different physiological optima between the two species or from nutrient conditions in the two experimental systems. We observed the KAR₁ response of L. japonicus root systems in half-Hoagland solution with low phosphate levels (2.5μM PO₄^3-) and without sucrose, whereas the root assay in Arabidopsis was conducted in ATS medium (Arabidopsis thaliana salts) with 1% sucrose [15]. Phosphate and sucrose levels have previously been described to influence the effect of strigolactone and rac-GR24 on Arabidopsis root architecture [57,67,68].

In Arabidopsis and rice, KAI2/D14L is required to inhibit hypocotyl and mesocotyl elongation, respectively [3,4,16]. Since these two species are evolutionarily distant from each other, but have both retained a function of KL signaling in inhibiting the growth of similar organs, it seemed likely that this function would be conserved among a large number of plant species. Surprisingly, in L. japonicus, we observed no elongated hypocotyl phenotype for the kai2a-1 kai2b-1 double and two allelic max2 mutants (Fig 5). However, we could trigger a reduction of hypocotyl elongation by treatment with KAR₁, KAR₂ and rac-GR24 in the wild type and in a LjKAI2a and LjMAX2-dependent manner. Perhaps the endogenous KL levels in L. japonicus hypocotyls are insufficient to cause inhibition of hypocotyl elongation, at least under our growth conditions. Somewhat contradictory to the hypocotyl responsiveness to KAR₁, KAR₂ and rac-GR24 of wild type and kai2b mutants, untreated hypocotyls of both L. japonicus kai2 mutants as well as max2 mutants were slightly shorter than those of wild-type plants. We currently do not know the reason for this. Perhaps it is caused by small and undetectable differences in germination between the genotypes. It is difficult to precisely record germination rates of L. japonicus because seeds hardly germinate when they are not scarified, while scarification can abolish detectable differences in germination speed between mutants.

In summary, we have demonstrated sub-functionalization of two KAI2 copies in L. japonicus with regard to their ligand-binding specificity and organ-specific relevance. Furthermore, we find organ-specific responsiveness of L. japonicus to two artificial KAI2 ligands. A phenylalanine to tryptophan transition independently occurred in the KAI2-binding pocket in several angiosperms, while a leucine-to-methionine and a serine-to-leucine exchange are conserved in KAI2a and KAI2b across legumes. This conservation and independent multiple occurrence of specific amino acid polymorphisms suggests that they bear functional relevance for discriminating diverse KAI2 ligands. Our findings open novel research avenues towards understanding the diversity in KL ligand-receptor relationships and in developmental responses to, as yet, unknown natural as well as synthetic butenolides that influence diverse aspects of plant development.

Materials and methods

Plant material and seed germination

The A. thaliana kai2-2 (Ler background) and d14-1 (Col-0 background) mutants are from [4], the d14-1 kai2-2 double mutant from [45], the htl-2 mutant was provided by Min Ni [69] and the cross with K02821 is from [16]. Seeds were surface sterilized with 70% EtOH. For synchronizing the germination, seeds were placed on ½ MS 1% agar medium and maintained at 4°C in the dark for 72 hours.

The L. japonicus Gifu max2-1, max2-2, max2-3, max2-4, kai2a-1 and kai2b-3 mutations are caused by a LORE1 insertion. Segregating seed stocks for each insertion were obtained from the Lotus Base (https://lotus.au.dk, [70]) or Makoto Hayashi (NIAS, Tsukuba, Japan, [53] for max2-2). The d14-1, kai2b-1 and kai2b-2 mutants were obtained by TILLING [54] at RevGenUK (https://www.jic.ac.uk/technologies/genomic-services/revgenuk-tilling-reverse-genetics/). Homozygous mutants were identified by PCR using primers indicated in S3 Table. For germination, L. japonicus seeds were manually scarified with sand-paper and surface sterilized with 1% NaClO. Imbibed seeds were germinated on 1/2 Hoagland medium containing 2.5μM PO₄^3- and 0.4% Gelrite (www.duchefa-biochemie.com), at 24°C for 3 days in the dark, or on ½ MS 0.8% agar at 4°C for 3 days in dark (only for the experiment in Fig 6E).

Phylogenetic, synteny and protein sequence analysis

Lotus japonicus KAI2, D14 and MAX2 sequences were retrieved using tBLASTn with AtKAI2, AtD14 and AtMAX2, against the NCBI database, the plantGDB database and the L. japonicus genome V2.5 (http://www.kazusa.or.jp/lotus)). The presence of MAX2-like was identified by tBLASTn in an in-house genome generated by next generation sequencing using CLC Main Workbench [71]. Pea sequences were found by BLASTn on “pisum sativum v2” database with AtKAI2 as query (https://www.coolseasonfoodlegume.org)). For Fig 1, the MUSCLE alignment of the protein sequences was used to generate Maximum-likelihood tree with 1000 bootstrap replicates in MEGAX [72]. For the synteny analysis of MAX2 and MAX2-like, flanking sequences were retrieved from the same in-house genome [71]. For S7 Fig, KAI2 sequences across the plant phylogeny were retrieved by BLAST-P search against the EnsemblPlants, NCBI and 1KP databases [51], in addition, KAI2 sequences of the parasitic plants Striga hermonthica and Orobanche cumana were retrieved from Conn et al. 2015 [38]. The MUSCLE alignment, generated in MEGAX [72], was used to produce a tree with 1000 bootstrap replicates with IQTREE [73].

Structural homology modelling of proteins

Proteins were modelled using SWISS-MODEL tool (https://swissmodel.expasy.org) with the A. thaliana KAI2 (4JYM) templates [5].

Visualization of protein localization in Nicotiana benthamiana leaves and Western Blot

D14, KAI2a, KAI2b and MAX2 genes were amplified from L. japonicus genomic DNA by Phusion PCR using the primers shown in S3 Table and cloned in pENTR/D-TOPO (Invitrogen). They were then transferred by LR reaction (Invitrogen) into Gateway plasmids (described in [74,75]) 35S:TSaphire-GW-Nos (for MAX2 fusions) or 35S: mOrange-GW-Nos (for D14, KAI2a, KAI2b fusions). Nicotiana benthamiana leaves were transiently transformed by infiltration with Agrobacterium tumefaciens strain AGL1 containing the plasmids encoding TSaphire-MAX2, mOrange-D14, mOrange-KAI2a and mOrange-KAI2b fusion proteins. Three days after transformation transformed N. benthamiana leaf disks were cut and observed with an SP5 Confocal microscope (www.leica-microsystems.com). Overlays were generated using Fiji (http://fiji.sc/).

For Western Blots proteins were extracted from 3 pooled leaf disks according to Singh et al 2014 [74]. SDS page and protein blotting was performed as described [74]. Membranes were probed using anti-GFPmono monoclonal IgG from mouse (Roche) and anti-dsRed from mouse (Clontech) at a dilution 1:5000 and the secondary anti-mouse HRP antibody from Goat (Biomol).

Bacterial protein expression and purification

Full-length L. japonicus coding sequences were cloned into pE-SUMO Amp using primers in S3 Table. Clones were sequence-verified and transformed into Rosetta DE3 pLysS cells (Novagen). Subsequent protein expression and purification were performed as described previously [34], with the following modifications: the lysis and column wash buffers contained 10 mM imidazole, and a cobalt-charged affinity resin was used (TALON, Takara Bio).

Differential scanning fluorimetry

DSF assays were performed as described previously [34]. Assays were performed in 384-well format on a Roche LightCycler 480 II with excitation 498 nm and emission 640 nm (SYPRO Tangerine dye peak excitation at 490 nm). Raw fluorescence values were transformed by calculating the first derivative of fluorescence over temperature. These data were then imported into GraphPad Prism 8.0 software for plotting. Data presented are the mean of three super-replicates from the same protein batch; each super-replicate comprised four technical replicates at each ligand concentration. Experiments were performed at least twice.

Intrinsic tryptophan fluorescence (ITF) assay

The ITF assay was performed in 384-well format on a BMG Labtech CLARIOstar multimode plate reader, using black FLUOtrac microplates (Greiner 781076). Reactions (20 μL) were set up in quadruplicate and contained 10 μM protein, 20 mM HEPES pH 7.5, 150 mM NaCl, 1.25% (v/v) glycerol, and 0–500 μM ligand. Ligands were initially prepared in DMSO at 20x concentration, and therefore reactions also contained 5% (v/v) DMSO. Ligands were dissolved in buffer (20 mM HEPES pH 7.5, 150 mM NaCl, 1.25% (v/v) glycerol) at 2× concentration immediately before use, of which 10 μL per well was dispensed with a multichannel pipette. An equivalent volume of 2x solution of protein in buffer was prepared and then dispensed onto the plate using an Eppendorf Multipette with a 0.1 mL tip. The plate was mixed at 120 rpm for 2 min, centrifuged at 500x g for 2 min, and then incubated in the dark for 20 min at room temperature. Fluorescence measurements were taken first with fixed wavelength filters (excitation 295/10 nm; longpass dichroic 325 nm; emission 360/20 nm), followed by the linear variable filter monochromator for emission wavelength scans (excitation 295/10 nm, emission 334–400 nm, step width 2 nm, emission bandwidth 8 nm). Measurements were performed at 25°C using 17 flashes per well for fixed filters or 20 flashes per well for wavelength scans. Gain and focus settings were set empirically for each experimental run. Data were blank-corrected by subtraction of fluorescence values from an identical set of wells containing ligand and buffer but no protein. Data analysis was performed in Graphpad Prism v8.4. Best fit curves were generated from untransformed fluorescence readings using nonlinear regression and the in-built “One site—Total” model, with least squares regression as a fitting method and an asymmetrical (profile-likelihood) 95% confidence interval. As saturation was not reached, only ambiguous values for Kd were returned. For emission wavelength scans, fluorescence values at each wavelength were normalised by expressing as a percentage of the corresponding value from samples lacking ligand.

Plasmid generation

Genes and promoter regions were amplified using Phusion PCR according to standard protocols and using primers indicated in S3 Table. Plasmids were constructed by Golden Gate cloning [76] as indicated in S4 Table.

Plant transformation

kai2-2 and d14-1 mutants were transformed by floral dip in Agrobacterium tumefaciens AGL1 suspension. Transgenic seedlings were selected by mCherry fluorescence and resistance to 20 μg/mL hygromycin B in growth medium. Experiments were performed using T2 or T3 generations, with transformed plants validated by mCherry fluorescence.

Shoot branching assay

A. thaliana and L. japonicus were grown for 4 and 7 weeks, respectively in soil in the greenhouse at 16h/8h light/dark cycles. Branches with length >1cm were counted, and the height of each plant was measured.

Hypocotyl elongation assay

A. thaliana seedlings were grown for 5 days on half-strength Murashige and Skoog (MS) medium containing 1% agar (BD). L. japonicus seedlings were grown for 6 days on half-strength Hoagland medium containing 2.5μM PO₄^3- and 0.4% Gelrite (www.duchefa-biochemie.com), or on half-strength MS containing 0.8% agar (only for experiment in Fig 6D). Plants were grown in long day conditions in 16h/8h light/dark cycles for Fig 2A and in short-day conditions in 8h/16h light/dark cycles for all other hypocotyl assays. For Karrikin, rac-GR24, GR24^5DS and GR24^ent-5DS treatments the medium was supplied with KAR₁ (www.olchemim.cz), KAR₂ (www.olchemim.cz), rac-GR24 (www.chiralix.com) GR24^5DS and GR24^ent-5DS (www.strigolab.eu) or equal amounts of the corresponding solvent as a control. Karrikins were solubilized in 75% methanol and rac-GR24 and the GR24 stereoisomers in 100% acetone, at 10mM stock solution. After high-resolution scanning, the hypocotyl length was measured with Fiji (http://fiji.sc/).

Root system architecture assay

L. japonicus germinated seeds were transferred onto new plates containing KAR₁ (www.olchemim.cz), KAR₂ (www.olchemim.cz), rac-GR24 (www.chiralix.com) or the corresponding solvent. Karrikins were solubilized in 75% methanol and rac-GR24 in 100% acetone, at 10 mM stock solution. Plates were partially covered with black paper to keep the roots in the dark, and placed at 24°C with 16-h-light/8-h-dark cycles for 2 weeks. After high-resolution scanning, post-embryonic root number was counted and primary root length measured with Fiji (http://fiji.sc/).

Treatment for analysis of transcript accumulation

Seedling roots were placed in 1/2 Hoagland solution with 2.5 μM PO₄^3- containing 1 or 3 μM Karrikin₁ (www.olchemim.cz for qPCR analysis, synthesized according to [77] for microarray analysis), Karrikin₂ (www.olchemim.cz), rac-GR24 (www.chiralix.com) or equal amounts of the corresponding solvents for the time indicated in Figure legends and the roots were covered with black paper to keep them in the dark.

Microarray analysis

Three biological replicates were performed for each treatment. Root tissues were harvested, rapidly blotted dry and shock frozen in liquid nitrogen. RNA was extracted using the Spectrum Plant Total RNA Kit (www.sigmaaldrich.com). RNA was quantified and evaluated for purity using a Nanodrop Spectrophotometer ND-100 (NanoDrop Technologies, Willington, DE) and Bioanalyzer 2100 (Agilent, Santa Clara, CA). For each sample, 500 ng of total RNA was used for the expression analysis of each sample using the Affymetrix GeneChip Lotus1a520343 (Affymetrix, Santa Clara, CA). Probe labeling, chip hybridization and scanning were performed according to the manufacturer’s instructions for IVT Express Labeling Kit (Affymetrix). The Microarray raw data was normalized with the Robust Multiarray Averaging method (RMA) [78] using the Bioconductor [79] package “Methods for Affymetrix Oligonucleotide Arrays” (affy version 1.48.0) [80]. Control and rhizobial probesets were removed before statistical analysis. Differential gene expression was analyzed with the Bioconductor package “Linear Models for Microarray Data”(LIMMA version 3.26.8) [81]. The package uses linear models for parameter estimation and an empirical Bayes method for differential gene expression assessment [82]. P-values were adjusted due to multiple comparisons with the Benjamini-Hochberg correction (implemented in the LIMMA package). Probesets were termed as significantly differentially expressed, if their adjusted p-value was smaller than or equal to 0.01 and the fold change for at least one contrast showed a difference of at least 50%. To identify the corresponding gene models, the probeset sequences were used in a BLAST search against L. japonicus version 2.5 CDS and version 3.0 cDNA sequences (http://www.kazusa.or.jp/lotus/). If, based on the bitscore, multiple identical hits were found, we took the top hit in version 2.5 CDS as gene corresponding to the probe. For version 3.0 cDNA search we used the best hit, that was not located on chromosome 0, if possible. For probesets known to target chloroplast genes (probeset ID starting with Lj_), we preferred the best hit located on the chloroplast chromosome, if possible. Probeset descriptions are based on the info file of the L. japonicus Microarray chip provided by the manufacturer (Affymetrix).

qPCR analysis

Tissue harvest, RNA extraction, cDNA synthesis and qPCR were performed as described previously [71]. qPCR reactions were run on an iCycler (Bio-Rad, www.bio-rad.com) or on QuantStudio5 (Applied Biosystems, www.thermofisher.com). Expression values were calculated according to the ΔΔCt method [83]. Expression values were normalized to the expression level of the housekeeping gene Ubiquitin. For each condition three to four biological replicates were performed. Primers are indicated in S4 Table.

Statistics

Statistical analyses were performed using Rstudio (www.rstudio.com) after log transformation for qPCR analysis. F- and p-values for all figures are provided in S5 Table. Raw data are shown in S1 Data.

Supporting information

S1 Fig. MAX2-like underwent pseudogenization.

(A) Schematic representation of the syntenic regions containing the MAX2 and MAX2-like loci in L. japonicus. Coloured arrows and black lines show exons and introns respectively. (B) Protein alignment of LjMAX2, LjMAX2-like and an artificial LjMAX2-like with a deletion of the thymine at the position 453 in the coding sequence (LjMAX2-like ΔT453). Position of the nucleotide deletion is indicated in the translated sequence by a red triangle. Amino-acid conservation between MAX2 and MAX2-like is indicated by a dark background.

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S2 Fig. Organ-specific accumulation of D14, KAI2a, KAI2b and MAX2 transcripts.

(A-C) Transcript accumulation in wild-type of D14, KAI2a, KAI2b and MAX2 normalized to expression of Ubiquitin, in (A) leaf, stem, flower and root of plants grown in pots, and in (B) hypocotyl and roots of 1 wpg plants grown on Petri dishes in 8h light /16h dark cycles, and in (c) roots of 2 wpg plants grown on Petri dishes in 16h light/8h dark cycles (n = 3).

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S3 Fig. Subcellular localisation of LjD14, LjKAI2a, LjKAI2b and LjMAX2 in Nicotiana benthamiana leaves.

(A) Subcellular localization of LjD14, LjKAI2a, LjKAI2b and LjMAX2 in N. benthamiana leaf epidermal cells. LjD14, LjKAI2a and LjKAI2b are N-terminally fused with mOrange. LjMAX2 is N-terminally fused with T-Sapphire. Scale bars: 25 μm. (B) Western blot of protein extracts from N. benthamiana, showing that the mOrange tag fused with LjD14, LjKAI2a and LjKAI2b was not cleaved at detectable amounts.

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S4 Fig. SDS-PAGE of purified SUMO fusion proteins and DSF assay with GR24^5DS.

(A) 200 pmol (approx. 8 μg) of purified proteins were separated by 12% SDS-PAGE containing 2,2,2-trichlorethanol as a visualization agent. Below each lane is the calculated protein size in kilodaltons. S, protein size standards (Precision Plus Dual Color Standards, Bio-Rad #1610394) with corresponding sizes in kDa shown on the left. Optimal exposures of recombinant proteins and size standards were taken separately under UV transillumination and red epi-illumination, respectively. The two images were merged in post-processing, and the junction between them is indicated by a vertical line. (B) DSF curves of purified SUMO fusion proteins of wild-type LjKAI2a and LjKAI2b, and versions with swapped amino acids LjKAI2a^{W157,M160,L190}, LjKAI2b^{F158,L161,S191}, LjKAI2a^W157, LjKAI2b^F158, at the indicated concentrations of GR24^5DS. The first derivative of the change of fluorescence was plotted against the temperature. Each curve is the arithmetic mean of four technical replicates. Peaks indicate the protein melting temperature. There is no ligand-induced thermal destabilisation consistent with no protein-ligand interaction.

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S5 Fig. Amino acid differences between the legume KAI2a and KAI2b clades.

Protein sequence alignment of KAI2a and KAI2b homologs from the legumes Lotus japonicus, Pisum sativum, Medicago truncatula and Glycine max, in comparison with Arabidopsis KAI2 and rice D14L. Residues conserved within the KAI2a and KAI2b clades but different between these clades are coloured in green and blue. Residues of the catalytic triad are coloured in red. A non-conserved tryptophan in LjKAI2b located in the protein cavity is coloured in violet. Yellow triangles indicate amino acid residues located in the ligand-binding cavity of the proteins. Orange triangles indicate the three amino acids responsible for differences in GR24^ent-5DS-binding between LjKAI2a and LjKAI2b.

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S6 Fig. Intrinsic tryptophan fluorescence assay confirms inability of LjKAI2b to interact with GR24^ent-5DS.

Intrinsic tryptophane fluorescence of wild-type LjKAI2a and LjKAI2b, and protein versions with swapped amino acids LjKAI2a^M160,L190, LjKAI2b^L161,S191, LjKAI2a^{M160,L190,W157}, LjKAI2b^{L161,S191,F158}, LjKAI2a^W157, LjKAI2b^F158 measured with (A) fixed wavelength filters (excitation 295/10 nm; longpass dichroic 325 nm; emission 360/20 nm) and (B) with a linear variable filter monochromator for emission wavelength scans (excitation 295/10 nm, emission 334–400 nm, step width 2 nm, emission bandwidth 8 nm) at the indicated GR24^ent-5DS concentrations.

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S7 Fig. The F157 to W replacement occurred multiple times in angiosperm KAI2 proteins.

Phylogenetic tree of KAI2 proteins rooted with A. thaliana DLK2. The KAI2a and KAI2b clades in legumes are highlighted by red and blue branches. Monophyletic groups corresponding to a same order or clade are highlighted by coloured rectangular boxes. Amino-acids at the positions corresponding to AtKAI2 157, 160 and 190 are indicated with single-letter code. A black background indicates the presence of the most common residues in KAI2 proteins: F157, L160 and A190. A blue background indicates residues M160 and L190, conserved in legume KAI2b. A red background indicates S190, conserved in legume KAI2a. A green background indicates a W at position 157. A brown background indicates a different residue.

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S8 Fig. Transcript accumulation in the L. japonicus KAR and SL receptor mutants.

(A) qRT-PCR based transcript accumulation of LjKAI2a and LjKAI2b, in roots of wild type and kai2a-1, kai2b-1, kai2b-3, kai2a-1 kai2b-1 and max2-4 as well as LjMAX2 and LjD14 in max2-4 and d14-1, respectively (n = 4). Expression values were normalized to those of the housekeeping gene Ubiquitin. (B) LjKAI2b transcript accumulation in wild-type, kai2b-1 (stop codon) and kai2b-3 (LORE1 insertion) mutants by semi-quantitative RT-PCR using primer pairs located 5’ and 3’ of the mutations, as well as flanking (ML) the mutations. Transcript accumulation of the housekeeping gene Ubiquitin is also shown.

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S9 Fig. Characterisation of the kai2a-1 allele.

(A) Schematic representation of mis-splicing caused by the LORE1 insertion in the kai2a-1 mutant. (B) cDNA alignment showing the absence of nucleotides 369 to 383 in the kai2a-1 transcript, causing a deletion of amino acids 124 to 128 (orange). (C) Protein model of LjKAI2a based on the AtKAI2-KAR₁ complex 4JYM [5] showing KAR₁ in green, residues of the catalytic triad in red and the amino acids missing in a hypothetical LjKAI2a-1 protein in orange. (D) Hypocotyl elongation at 6 dpg in Arabidopsis kai2-2 mutants transgenically complemented with genomic and the cDNA of wild-type LjKAI2a and Ljkai2a-1 driven by the AtKAI2 promoter (n = 75–106). Plants were grown in 8h light/16h dark cycles. Letters indicate different statistical groups (ANOVA, post-hoc Tukey test).

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S10 Fig. Lotus japonicus hypocotyls respond to KAR₁ and KAR₂ in a LjKAI2a- and LjMAX2-dependent manner.

(A) Hypocotyls and (B) hypocotyl length of L. japonicus wild-type seedling at 1 wpg after treatment with solvent (M) or three different concentrations of KAR₁, KAR₂ or rac-GR24 (GR24) (n = 95–105). Letters indicate different statistical groups (ANOVA, post-hoc Tukey test). (C) Hypocotyl length of the indicated genotypes at 1 wpg after treatment with solvent (Mock), 1 μM KAR₁ or 1 μM KAR₂ (n = 73–107). (D) Hypocotyl length of wild-type and max2-4 seedlings 1 wpg after treatment with solvent (Mock), 1 μM KAR₁, 1 μM KAR₂ (n = 66–96). (E) RT-qPCR-based expression of DLK2 in hypocotyls at 1 wpg after 2 hours treatment with solvent (Mock), 1 μM KAR₁, 1 μM KAR₂, or 1 μM rac-GR24 (GR24) (n = 3). Expression values were normalized to those of the housekeeping gene Ubiquitin. (A-E) Seedlings were grown in 8h light/16h dark cycles. (C-E) Asterisks indicate significant differences of the compounds versus mock treatment (ANOVA, post-hoc Dunnett test, N.S.>0.05, *≤0.05, **≤0.01, ***≤0.001).

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S11 Fig. Small overlap between transcriptional responses of Lotus japonicus roots to KAR₁ and rac-GR24.

Number of differentially expressed genes (DEGs, adjusted p-value < 0.01) as assessed by microarray analysis. Left panel: DEGs responding to 1 μM KAR₁ after 1h, 2h and 6h incubation. Middle panel: DE genes responding to 1 μM rac-GR24 1h, 2, 6h incubation. Right panel: comparison of DE genes responding to 2 h treatment with KAR₁ and rac-GR24.

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S12 Fig. KAR perception mutants are less responsive to KAR₁ treatment.

(A) Image of Lotus japonicus seedling with indicated post-embryonic roots (PERs). (B-D) Post-embryonic-root (PER) density of L. japonicus plants, 2 wpg after treatment with solvent (Mock) or 1 μM KAR₁, of wild-type, (B) kai2a-1, kai2b-1 and kai2a-1 kai2b-1 (n = 32–50); (C) max2-4 (n = 34–43); (D) kai2a-1, kai2b-3 and kai2a-1 kai2b-1 (n = 37–72). (B-D) Asterisks indicate significant differences versus mock treatment (Welch t.test, *≤0.05, **≤0.01, ***≤0.001).

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S13 Fig. KAR₁ response in roots requires LjKAI2a or LjKAI2b and LjMAX2.

Primary-root length (PRL) and post-embryonic-root (PER) number of L. japonicus plants, 2 wpg after treatment with solvent (Mock) or 3 μM KAR₁ (n = 34–72) displayed in Fig 9A. Asterisks indicate significant differences versus mock treatment (Welch t.test, *≤0.05, **≤0.01, ***≤0.001).

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S1 Table. L. japonicus mutants used in this study and information on seed production.

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S2 Table. Microarray-based differentially expressed genes in Lotus japonicus wild-type roots after 1h, 2h and 6h of treatment with 1μM KAR1 or 1μM rac-GR24.

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S3 Table. Primers.

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S4 Table. Plasmids.

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S5 Table. Results of ANOVA for multiple comparisons.

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S1 Data. Raw data for all quantitative assays shown in the manuscript (except microarray data).

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Data Availability

Raw microarray data and CEL files are available at Gene Expression Omnibus (GEO) accession number GSE160075, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE160075.

Funding Statement

The study was supported by an Australian Research Council Future Fellowship (FT150100162) to MTW and initially by the SFB924 of the DFG to CG and subsequently by the Emmy Noether program of the DFG, grant GU1423/1-1 to CG. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.