Symbiosis Receptor-like Kinase (SYMRK) is indispensable for the development of phosphate-acquiring arbuscular mycorrhiza (AM) as well as nitrogen-fixing root nodule symbiosis, but the mechanisms that discriminate between the two distinct symbiotic developmental fates have been enigmatic. In this study, we show that upon ectopic expression, the receptor-like kinase genes Nod Factor Receptor 1 (NFR1), NFR5, and SYMRK initiate spontaneous nodule organogenesis and nodulation-related gene expression in the absence of rhizobia. Furthermore, overexpressed NFR1 or NFR5 associated with endogenous SYMRK in roots of the legume Lotus japonicus. Epistasis tests revealed that the dominant active SYMRK allele initiates signalling independently of either the NFR1 or NFR5 gene and upstream of a set of genes required for the generation or decoding of calcium-spiking in both symbioses. Only SYMRK but not NFR overexpression triggered the expression of AM-related genes, indicating that the receptors play a key role in the decision between AM- or root nodule symbiosis-development.https://doi.org/10.7554/eLife.03891.001
Like all plants, crop plants need nutrients such as nitrogen and phosphate to grow. Often these essential elements are in short supply, and so millions of tons of fertiliser are applied to agricultural land each year to maintain crop yields. Another way for plants to gain access to scarce nutrients is to form symbiotic relationships with microorganisms that live in the soil. Plants pass on carbon-containing compounds—such as sugars—to the microbes and, in return, certain fungi provide minerals—such as phosphates—to the plants. Some plants called legumes (such as peas, beans, and clovers) can also form relationships with bacteria that convert nitrogen from the air into ammonia, which the plants then use to make molecules such as DNA and proteins.
To establish these symbiotic relationships with plants, nitrogen-fixing bacteria release chemical signals that are recognized via receptor proteins, called NFR1 and NFR5, found on the surface of the plant root cells. These signals trigger a cascade of events that ultimately lead to the plant forming an organ called ‘root nodule’ to house and nourish the nitrogen-fixing bacteria. A similar signalling mechanism is thought to take place during the establishment of symbiotic relationships between plants and certain soil fungi.
A plant protein called Symbiosis Receptor-like Kinase (or SYMRK for short) that is also located on the root cell surface is required for both bacteria–plant and fungi–plant associations to occur. However, the exact role of this protein in these processes was unclear. Ried et al. have now investigated this by taking advantage of a property of cell surface receptor proteins: if some of these proteins are made in excessive amounts they activate their signalling cascades even when the initial signal is not present.
Ried et al. engineered plants called Lotus japonicus to produce high levels of SYMRK, NFR1, or NFR5. Each of these changes was sufficient to trigger the plants to develop root nodules in the absence of microbes. Genes associated with the activation of the signalling cascade involved the formation of root nodules were also switched on when each of the three proteins was produced in large amounts. In contrast, only an excess of SYMRK could activate genes related to fungi–plant associations. Ried et al. also found that, while SYMRK can function in the absence of the NFRs, NFR1 and NFR5 need each other to function. These data suggest that the receptor proteins play a key role in the decision between the establishment of an association with a bacterium or a fungus.
As an excess of symbiotic receptors caused plants to form symbiotic structures, Ried et al. propose that this strategy could be used to persuade plants that usually do not form symbioses with nitrogen-fixing bacteria to do so. If this is possible, it might lead us to engineer crop plants to form symbiotic interactions with nitrogen-fixing bacteria; this would help increase crop yields and enable crops to be grown in nitrogen-poor environments without the addition of extra fertiliser.https://doi.org/10.7554/eLife.03891.002
Plants circumvent nutrient deficiencies by establishing mutualistic symbioses with arbuscular mycorrhiza (AM) fungi or nitrogen-fixing rhizobia and Frankia bacteria (Gutjahr and Parniske, 2013; Oldroyd, 2013). One of the first steps in the reciprocal recognition between rhizobia and the legume Lotus japonicus is the perception of bacterial lipo-chitooligosaccharides, so called nodulation factors, by the two lysin motif (LysM) receptor-like kinases (RLKs) Nod Factor Receptor 1 (NFR1) and NFR5 (Madsen et al., 2003; Radutoiu et al., 2003, 2007; Broghammer et al., 2012). Nodulation factor application induces two genetically separable calcium signatures in root hair cells; an early transient influx into the cytoplasm and within minutes calcium-spiking - periodic calcium oscillations in and around plant cell nuclei (Ehrhardt et al., 1996; Miwa et al., 2006; Oldroyd, 2013). (Lipo)-chitooligosaccharides have also been isolated from AM fungi (Maillet et al., 2011; Genre et al., 2013) and a NFR5-related LysM-RLK from Parasponia has been pinpointed as a likely candidate for their perception (Op Den Camp et al., 2011). The common symbiosis genes of legumes are required for AM and root nodule symbiosis. A subset of these genes is essential for either the generation or the decoding of calcium-spiking. In L. japonicus, the former group encodes the RLK Symbiosis Receptor-like Kinase (SYMRK; Stracke et al., 2002; Antolín-Llovera et al., 2014), two cation-permeable ion channels CASTOR and POLLUX (Imaizumi-Anraku et al., 2005; Charpentier et al., 2008; Venkateshwaran et al., 2012) as well as the nucleoporins NUP85, NUP133, and NENA (Kanamori et al., 2006; Saito et al., 2007; Groth et al., 2010). The latter group encodes Calcium Calmodulin-dependent Protein Kinase (CCaMK; Tirichine et al., 2006; Miller et al., 2013) and CYCLOPS (Yano et al., 2008), which form a complex that has been implicated in the deciphering of calcium-spiking (Kosuta et al., 2008). Phosphorylation by CCaMK activates CYCLOPS, a DNA-binding transcriptional activator of the NODULE INCEPTION gene (NIN; Schauser et al., 1999; Singh et al., 2014). NIN itself is a legume-specific and root nodule symbiosis-related transcription factor and regulates the Nuclear Factor-Y subunit genes NF-YA1 and NF-YB1 that control the cell division cycle (Soyano et al., 2013; Yoro et al., 2014). The paradigm of a common signalling pathway for both symbioses bears important open questions about the molecular mechanisms that ensure the appropriate cellular response for AM fungi on the one hand and for rhizobia on the other hand.
SYMRK carries an ectodomain composed of a malectin-like domain (MLD), and a leucine-rich repeat (LRR) region that experienced structural diversification during evolution (Markmann et al., 2008) and is cleaved to release the MLD (Antolín-Llovera et al., 2014). Although SYMRK has been cloned several years ago (Stracke et al., 2002), its precise function in symbiosis is still enigmatic. While nfr mutants lack most cellular and physiological responses to rhizobia (Radutoiu et al., 2003), including nodulation factor-induced calcium influx and calcium-spiking, root hairs of symrk mutants respond with calcium influx to nodulation factor but not with calcium-spiking, and do not develop infection threads with rhizobia (Stracke et al., 2002; Miwa et al., 2006). Based on these phenotypic observations, SYMRK was positioned downstream of the NFRs (Radutoiu et al., 2003; Miwa et al., 2006). Importantly, it has not been conclusively resolved whether SYMRK plays an active signalling role in symbiosis or, alternatively, is involved in mechanical stress desensitisation (Esseling et al., 2004). To approach this issue, we built on the observation that specific mutations in, or over-abundance of mammalian receptor tyrosine kinases on the cell surface is linked with the development of some cancers caused by spontaneous receptor complex formation and inappropriate initiation of signalling (Schlessinger, 2002; Wei et al., 2005; Shan et al., 2012). We hypothesized that similar behaviour could be triggered by overexpression of symbiosis-related plant RLKs, providing a tool to further dissect the specific signalling pathways they address.
To achieve overexpression, we generated constructs expressing functional SYMRK (Antolín-Llovera et al., 2014), NFR5, or NFR1 under the control of the strong L. japonicus Ubiquitin promoter and added C-terminal mOrange fluorescent tags for detection purposes (pUB:SYMRK-mOrange, pUB:NFR5-mOrange, pUB:NFR1-mOrange). The functionality of the NFR constructs was confirmed by their ability to restore nodulation in the corresponding, otherwise nodulation deficient, nfr mutant roots to the level of L. japonicus wild-type roots transformed with the empty vector (Figure 1—figure supplement 1). Intriguingly, transgenic expression of any of the three symbiotic RLK versions in L. japonicus roots was sufficient to spontaneously activate the entire nodule organogenesis pathway as evidenced by the formation of nodule-like structures in the absence of rhizobia (Figure 1; Figure 1—figure supplement 2). The presence of peripheral vascular bundles instead of a central root vasculature unambiguously identified these lateral organs as spontaneous nodules (Figure 1C). Spontaneous nodule primordia or nodules were present on 90% (116 out of 129), 23% (30 out of 133), 11% (16 out of 182), and 0% (0 out of 164) of L. japonicus root systems at 60 days post transformation (dpt) with, respectively, pUB:SYMRK-mOrange, pUB:NFR5-mOrange, pUB:NFR1-mOrange, or the empty vector (Figure 1A; Figure 1—figure supplement 2). A total of 810 empty vector roots generated throughout the course of this study did not develop spontaneous nodules in any of the genetic backgrounds and time points tested. Roots expressing functional SYMRK-RFP from its native promoter (pSYMRK:SYMRK-RFP; Kosuta et al., 2011) and grown in the absence of rhizobia did not develop spontaneous nodules, indicating that spontaneous nodulation was triggered by SYMRK expression from the Ubiquitin promoter and not by the addition of a C-terminal tag alone (Figure 1—figure supplement 3). Moreover, the expression of non-tagged SYMRK under the control of the Ubiquitin promoter triggered the formation of spontaneous nodules. In comparison to roots transformed with the tagged SYMRK version, a lower number of roots transformed with non-tagged SYMRK contained spontaneous nodules (Figure 1—figure supplement 4). One explanation for this observation is that the C-terminal mOrange tag might result in alterations in the relative amount of signalling-active SYMRK. Another possibility is that the presence of the tag improves homo- and/or hetero-dimerization, which subsequently leads to downstream signalling. Our results demonstrate that overexpression of NFR1-mOrange, NFR5-mOrange, or SYMRK results in the activation and execution of the nodule organogenesis pathway in the absence of external symbiotic stimulation.
To establish whether the development of nodule-like structures was associated with nodulation-related gene activation, we analysed the expression behaviour of marker genes induced during root nodule symbiosis (NIN and SbtS; Kistner et al., 2005) via quantitative real-time PCR (qRT-PCR; Figure 2A). The SbtS gene is also induced during AM symbiosis (Kistner et al., 2005). In comparison to control roots transformed with the empty vector, the SYMRK construct resulted in a highly significant increase in NIN and SbtS transcript levels (mean fold increase of 137 and 24, respectively). A slighter but statistically significant increase in transcript levels could be observed in roots overexpressing either NFR1-mOrange (NIN, mean fold increase 3; SbtS, mean fold increase 7) or NFR5-mOrange (NIN, mean fold increase 8; SbtS, mean fold increase 15) (Figure 2A).
To monitor the spontaneous activation of NIN and SbtS by an independent and histochemical method, we made use of stable transgenic L. japonicus reporter lines carrying either a NIN promoter:β-glucuronidase (GUS) fusion (pNIN:GUS; Radutoiu et al., 2003) or a SbtS promoter:GUS fusion (pSbtS:GUS; Takeda et al., 2009) (Figure 2B). In addition, we employed the symbiosis-reporter line T90 that was isolated in a screen for symbiosis-specific GUS expression from a promoter-tagging population (Webb et al., 2000) (Figure 2B). The T90 reporter is activated in roots treated with nodulation factor or inoculated with Mesorhizobium loti and—similar to pSbtS:GUS—also shows GUS expression during AM (Radutoiu et al., 2003; Kistner et al., 2005). GUS activity was determined in roots by histochemical staining with 5-bromo-4-chloro-3-indolyl glucuronide (X-Gluc; Figure 2B). Either of the three symbiotic RLKs but not the empty vector activated the pNIN:GUS, the pSbtS:GUS, as well as the T90 reporter in the absence of M. loti or AM fungi (Figure 2B).
This histochemical analysis of GUS activity, in combination with the qRT-PCR results, provide strong evidence that overexpression of symbiotic RLKs leads to the activation of nodulation-related genes in the absence of external symbiotic stimulation (Figure 2). However, the three RLK genes were not equally effective in inducing the symbiotic program: NFR5 or NFR1 overexpression resulted in a lower percentage of root systems showing promoter activation and formation of spontaneous nodules when compared to SYMRK overexpression (Figure 1; Figure 1—figure supplement 2; Figure 2B). Interestingly, SYMRK- as well as NFR5-mediated T90 or NIN promoter activation was first observed in the root and retracted to nodule primordia and nodules over time, while NFR1-mediated T90 or NIN promoter activation could only be detected in nodule primordia or in nodules (Figure 2B). The Ubiquitin promoter drives expression of the receptors in all cells of the root (Maekawa et al., 2008), which is in marked contrast to the highly specific and developmentally controlled expression patterns of the marker genes observed. These incongruences thus reveal the presence of additional layers of regulation, operating downstream of the receptors, which dictate the precise expression patterns of the reporters.
Since SYMRK is not only required for nodulation but also for AM symbiosis, we investigated the potential of dominant active RLK alleles to spontaneously activate AM-related marker genes or a promoter:GUS reporter (Figure 3). Blue copper-binding protein 1 (Bcp1) and the subtilisin-like serine protease gene SbtM1 are induced during AM symbiosis (Liu et al., 2003; Kistner et al., 2005; Takeda et al., 2009), and both genes are predominantly expressed in arbuscule-containing and adjacent cortical cells (Hohnjec et al., 2005; Takeda et al., 2009, 2012). Furthermore, in L. japonicus, SbtM1 expression marks root cells that contain an AM fungi-induced prepenetration apparatus (Takeda et al., 2012)—an intracellular structure that forms prior to invasion by fungal hyphae (Genre et al., 2005). Transcript levels of SbtM1 and Bcp1 were determined via qRT-PCR, and both were significantly increased in roots transformed with pUB:SYMRK-mOrange compared to the empty vector control (Figure 3A). To determine SbtM1 activation by an independent, histochemical approach, we employed a stable transgenic L. japonicus line harbouring a SbtM1 promoter:GUS fusion (pSbtM1:GUS; Takeda et al., 2009). In line with the results from the qRT-PCR experiments, overexpression of SYMRK-mOrange in roots of the pSbtM1:GUS reporter line resulted in activation of the SbtM1 promoter at 40 and 60 dpt (Figure 3B). In contrast, no SbtM1 promoter activation or AM-related gene induction could be detected upon overexpression of either of the NFRs (Figure 3). The absence of AM-related gene expression in NFR5-expressing roots is not a consequence of the overall lower induction power of the NFR5 construct. In SYMRK- vs NFR5-expressing roots, the relative ratio of transcripts was 1.6:1 for SbtS and 17:1 for NIN (Figure 2A). In contrast, SbtM1 was undetectable in NFR5- but more than 1100-fold above detection limit in SYMRK-overexpressing roots (Figure 3A). These data clearly demonstrate a strong difference in the gene repertoire activated by SYMRK vs NFR5. Together with the spontaneous nodulation, these results demonstrate that overexpression of NFR1-mOrange, NFR5-mOrange, or SYMRK-mOrange activates the nodulation pathway as evidenced by spontaneous organogenesis and gene expression results at the level of endogenous transcripts as well as promoter:GUS expression. In contrast, only the SYMRK construct but neither of the NFR constructs induced AM-related gene expression. This suggests that signalling specificity towards the two different symbiotic programs is achieved at the level of the receptors.
Spontaneous receptor complex formation caused by overexpression offers itself as a likely explanation for the observed activation of symbiosis signalling in the absence of an external trigger or ligand. This is a scenario described in the context of cancer formation, where receptor tyrosine kinase overexpression or specific mutations in the receptor lead to receptor dimerization in the absence of a ligand, which results in ectopic cell proliferation (Schlessinger, 2002; Wei et al., 2005; Shan et al., 2012). Upon expression in Nicotiana benthamiana leaves in the absence of symbiotic stimulation, we observed previously weak association between full-length SYMRK and NFR1 as well as NFR5, but not between SYMRK and the functionally unrelated RLK Brassinosteroid Insensitive 1 (BRI1; Li and Chory, 1997; Antolín-Llovera et al., 2014; Figure 4—figure supplement 1). To test whether overexpression is associated with receptor complex formation in L. japonicus roots, we employed the overexpression constructs of NFR1, NFR5, or the unrelated EF-Tu receptor kinase (EFR; Zipfel et al., 2006) for co-immuno-enrichment experiments. The EFR construct did not interfere with nodulation in wild-type plants (Figure 1—figure supplement 1). Endogenous full-length SYMRK was co-enriched with NFR1 and NFR5, but not with EFR demonstrating association of SYMRK and both NFRs (Figure 4). However, it should be noted that the expression strength of EFR was lower than that of NFR1 and NFR5. SYMRK-NFR association was detected in the absence of nodulation factor. We did not observe an effect of M. loti on this association at 10 days post inoculation (Figure 4).
The availability of dominant active receptor gene alleles offers an attractive tool for their positioning in the genetic pathway required for nodule organogenesis and symbiosis-related gene expression. We asked whether the pUB:SYMRK-mOrange construct induced spontaneous nodules or the symbiosis-specific T90 reporter in mutants of common symbiosis genes (Figure 5; Figure 5—figure supplement 1 and 4). SYMRK-induced spontaneous nodules were absent from pollux-2, castor-12, nup133-1, or ccamk-13 mutant roots. Likewise T90 reporter (GUS) activation was not detectable in the castor-2 x T90 (Kistner et al., 2005) or ccamk-2 x T90 (Gossmann et al., 2012) lines (Figure 5—figure supplement 4). This epistasis revealed that the ion channel genes CASTOR and POLLUX, the nucleoporin gene NUP133, and the calcium- and calmodulin-dependent protein kinase gene CCaMK, operate downstream of SYMRK in a pathway leading to spontaneous nodulation and activation of T90 (Figure 5; Figure 5—figure supplement 1 and 4). In contrast, SYMRK induced spontaneous nodules on cyclops-3 mutant roots (Figure 5; Figure 5—figure supplement 1). Spontaneous nodule formation on the cyclops-3 mutant (Figure 5; Figure 5—figure supplement 1) corresponds to the formation of bump-like structures upon inoculation with M. loti on cyclops mutants (Yano et al., 2008). While bacterial infection is strongly impaired in L. japonicus cyclops or M. truncatula ipd3 mutants, nodule primordia or nodules, respectively, develop upon rhizobia inoculation (Yano et al., 2008; Horvath et al., 2011; Ovchinnikova et al., 2011). Furthermore, an autoactive version of CCaMK is able to induce the formation of mature spontaneous nodules in cyclops mutants (Yano et al., 2008). The ability of SYMRK to mediate spontaneous nodule organogenesis in the cyclops mutant is consistent with these results and points towards the existence of redundancies in the genetic pathway leading to organogenesis at the level of CYCLOPS (Singh et al., 2014).
We used the dominant active alleles to determine the hierarchy of the symbiotic RLK genes in the spontaneous nodulation and T90 activation pathways. Control roots of mutant lines transformed with the empty vector (218 root systems) or SYMRK driven by its own promoter (33 root systems) did not carry spontaneous nodules or nodule primordia (Figure 5; Figure 5—figure supplement 1–3). Expression of pUB:SYMRK-mOrange spontaneously activated the nodulation program in nfr1-1, nfr5-2, and symrk-3 mutant roots (Figure 5; Figure 5—figure supplement 1). Spontaneous nodules on nfr1-1 or nfr5-2 roots overexpressing SYMRK-mOrange indicate that the simultaneous presence of both NFRs is not necessary for spontaneous SYMRK-mediated nodulation (Figure 5; Figure 5—figure supplement 1). Consistent with this result, overexpression of SYMRK-mOrange resulted in spontaneous GUS expression in the nfr1-1 x T90 line (Gossmann et al., 2012) (Figure 5—figure supplement 4). NFR-mediated formation of spontaneous nodules could only be observed in the wild-type or the respective nfr mutant (Figure 5; Figure 5—figure supplement 2 and 3). Neither NFR construct spontaneously induced nodule organogenesis in a symrk-3 (null mutant) or symrk-10 (kinase dead mutant) background, indicating that the formation of nodules is depended on the presence of kinase-active SYMRK (Figure 5; Figure 5—figure supplement 2 and 3). Spontaneous NFR5-mediated nodulation was completely abolished in the nfr1-1 mutant, demonstrating that NFR1 is essential for this NFR5 function (Figure 5; Figure 5—figure supplement 2). This dependence of NFR5 on NFR1 is further supported by the observation that overexpression of NFR1-mOrange and SYMRK-mOrange but not of NFR5-mOrange activated the T90 reporter in the nfr1-1 mutant background (Figure 5—figure supplement 5). These results position SYMRK downstream of or at the same hierarchical level as NFRs. Moreover, while SYMRK-mediated spontaneous signalling does not require the simultaneous presence of NFR1 and NFR5, NFR5-mediated spontaneous signalling is dependent on the presence of NFR1.
A hallmark of the nitrogen-fixing symbiosis of legumes is the accommodation of rhizobia inside plant root cells in specialised organs—the nodules—that provide a favourable environment for nitrogen fixation. Given that the common symbiosis pathway is operating in AM symbiosis in most land plants, the discovery that expression of either of the three symbiotic RLK constructs from the strong Ubiquitin promoter leads to the spontaneous formation of nodules in transgenic L. japonicus roots (Figure 1, Figure 1—figure supplement 2; Figure 1—figure supplement 4; Figure 2; Figure 5, Figure 5—figure supplement 1–5) could pave the way towards the synthetic transfer of nitrogen-fixing root nodules to important non-leguminous crop species. As the symbiotic RLKs act at the entry level of root nodule symbiosis signalling, auto-active versions provide a valuable tool to study the entire nodulation pathway uncoupled from bacterial infection. Furthermore, dominant active RLK versions could be useful for probing and dissecting the symbiotic signalling pathway, also in those plant lineages that are presently unable to develop nitrogen fixing root nodule symbiosis.
It has been observed that cytoplasmic streaming in root hairs of a symrk-3 mutant did not resume after mechanical stimulation, which raised the possibility that the absence of calcium-spiking upon injection of calcium-sensitive dyes into mutant root hair cells was a pleiotropic effect of this increased touch sensitivity (Esseling et al., 2004; Miwa et al., 2006). If touch desensitisation was the only function of SYMRK, its overexpression would not lead to spontaneous nodule formation. We therefore unambiguously demonstrated a direct role of SYMRK in symbiosis signalling, while eliminating the possibility that the symbiosis defects of symrk mutants are due to pleiotropic effects only.
Mutants defective for either of the common symbiosis genes SYMRK, CASTOR, POLLUX, NENA, NUP85, or NUP133 produce very similar phenotypes in symbiosis, in that they abort infection at the epidermis and are impaired in calcium-spiking (Kistner et al., 2005; Miwa et al., 2006; Groth et al., 2010), which placed them at the same hierarchical level. Consequently, a genetic resolution of the relative position of the common symbiosis genes upstream of calcium-spiking was missing. Epistasis tests revealed that SYMRK initiates signalling upstream of other common symbiosis genes implicated in the generation and interpretation of nuclear calcium signatures (Figure 5, Figure 5—figure supplement 1 and 4). These findings support the conceptual framework in which SYMRK activates the calcium-spiking machinery and consequently the CCaMK/CYCLOPS complex, a central regulator of symbiosis-related gene expression and nodule organogenesis (Gleason et al., 2006; Tirichine et al., 2006; Singh and Parniske, 2012; Singh et al., 2014). This is in line with the observation that dominant active variants of CCaMK were able to restore nodulation and infection in symrk mutant backgrounds, indicating that a main function of SYMRK in symbiosis is the activation of CCaMK (Hayashi et al., 2010; Madsen et al., 2010).
We observed association between SYMRK and either NFR1 or NFR5 upon NFR overexpression in L. japonicus roots (Figure 4). Interestingly, under these conditions, the SYMRK-NFR association was detected in the absence of nodulation factor (Figure 4). In mammalian receptor tyrosine kinases as well as plant RLKs, ligand-induced receptor dimerization is the single most critical step in signal initiation (Li et al., 2002; Nam and Li, 2002; Schlessinger, 2002; Chinchilla et al., 2007; Schulze et al., 2010; Liu et al., 2012; Sun et al., 2013a, 2013b). However, ligand-independent dimerization of receptor tyrosine kinases mediated by specific mutations in the kinase domain (Shan et al., 2012) or by overabundance of receptor tyrosine kinases (Wei et al., 2005) results in signalling activation and is a scenario well described in the context of cancer formation (Schlessinger, 2002). Similarly, overexpression of symbiotic RLKs might trigger ligand-independent receptor complex formation and activation of downstream signalling, thus providing an explanation why the interaction was also detected in the absence of external symbiotic stimulation. Unfortunately, we could not address the question whether SYMRK-NFR interaction is ligand-induced at endogenous levels of NFR expression since NFR1 and NFR5 were difficult to detect under these conditions.
We observed that NFR5 requires NFR1 as well as SYMRK for the spontaneous initiation of symbiosis signalling. This provides support for a model first put forward by Radutoiu et al. (2003), in which NFR1 and NFR5 engage in a nodulation factor perception complex. This model has received additional support through their synergistic effect on promoting cell death in N. benthamiana (Madsen et al., 2011; Pietraszewska-Bogiel et al., 2013). The finding that NFR1 and NFR5 interact with SYMRK upon overexpression suggests that the three RLKs engage in a receptor complex (Antolín-Llovera et al., 2014; Figure 4, Figure 4—figure supplement 1), and that this interaction might activate SYMRK for signal transduction. The observation that SYMRK operates independently of NFR1 or NFR5 brings about a new twist into current models of the signalling pathway (Downie, 2014) (Figure 5; Figure 5—figure supplement 1 and 4). NFR1 and NFR5 are only essential in the epidermis (Madsen et al., 2010; Hayashi et al., 2014), and it is likely that—at least partially—other members of the LysM-RLK gene family of L. japonicus (Lohmann et al., 2010) take over their role in the root cortex. NFR1 or NFR5 dispensability may be explained by other LysM-RLKs that might engage in alternative receptor complexes with SYMRK. Alternatively, spontaneous SYMRK-mediated signalling might be independent of any LysM-RLK, however, given the large number of LysM-RLKs in legumes (17 in L. japonicus; Lohmann et al., 2010), it is difficult to test the latter hypothesis conclusively.
SYMRK undergoes cleavage of its ectodomain, resulting in a truncated RLK molecule called SYMRK-ΔMLD (Antolín-Llovera et al., 2014). In competition experiments in N. benthamiana leaves, NFR5 binds preferentially to SYMRK-ΔMLD, which experiences rapid turnover in N. benthamiana and in L. japonicus (Antolín-Llovera et al., 2014). As our SYMRK antibody does not recognise endogenous SYMRK-ΔMLD, we were not able to assess whether overexpressed NFR1 or NFR5 also associates with this truncated SYMRK variant in L. japonicus roots. In a hypothetical scenario, the SYMRK-ΔMLD complex with NFR5 forms constitutively to prevent inappropriate signalling, for example in the absence of rhizobia. The recruitment of NFR1, a hypothetical signal initiation event, would be promoted by the presence of nodulation factor. Our observation that upon overexpression in L. japonicus both NFR1 and NFR5 seem to interact with full-length SYMRK (Figure 4) suggests the formation of a ternary complex. This hypothetical complex has dual functionality: it signals through SYMRK on one hand to activate CCaMK and through the NFR1-NFR5 complex on the other hand to trigger the infection-related parallel pathways discovered by Madsen et al. (2010) and Hayashi et al. (2010). It is possible that SYMRK has a dual—positive and negative—regulatory role: on the one hand SYMRK promotes signalling but on the other hand SYMRK-ΔMLD may be involved in preventing inappropriate signalling. A negative regulatory role would explain the exaggerated root hair response of symrk mutants to rhizobia (Stracke et al., 2002), since NFR1–NFR5 interaction is no longer under governance by SYMRK-ΔMLD. It has been demonstrated recently that expression of the intracellular kinase domain of SYMRK (SYMRK-KD) from Medicago truncatula or Arachis hypogaea in M. truncatula roots from the CaMV 35S promoter induces nodule organogenesis in the absence of rhizobia (Saha et al., 2014). However, in the presence of Sinorhizobium meliloti, nodules on plants overexpressing AhSYMRK-KD were poorly colonized and bacteria were rarely released from infection threads (Saha et al., 2014).
The origin of AM dates back to the earliest land plants (∼400 mya) and recent angiosperms maintained a conserved genetic program for the intracellular accommodation of AM fungi (Gutjahr and Parniske, 2013). During the evolution of the nitrogen-fixing root nodule symbiosis, this ancient genetic programme has been co-opted, as evidenced by the common symbiosis genes (Kistner et al., 2005). The discovery that the ancient SYMRK might act as a docking site for the recently evolved nodulation factor perception system (Antolín-Llovera et al., 2014; Figure 4, Figure 4—figure supplement 1), highlights the role of this putative interface during the recruitment of the ancestral AM signalling pathway for root nodule symbiosis. Since a LysM-RLK closely related to NFR5 has been implicated in AM signalling (Op Den Camp et al., 2011), this finding also provides a conceptual mechanism for the integration of signals from the rhizobial and fungal microsymbiont through alternative complex formation between SYMRK and NFRs or AM factor receptors.
One question that has puzzled the community since the postulate of a common symbiosis pathway is how the decision between the developmental pathways of AM or root nodule symbiosis is made when the signalling employs identical signalling components. Models proposed involved different calcium-spiking signatures with symbiosis-specific information content (Kosuta et al., 2008) or additional yet unidentified pathways that operate in parallel to the common symbiosis pathway to mediate exclusive and appropriate signalling (Takeda et al., 2011). Our observation of differential gene activation triggered by NFRs and SYMRK provides evidence that an important decision point is directly at the level of the receptors (Figure 2 and 3). Moreover, the observation that the dominant active SYMRK allele activates both pathways, which is not detected by stimulation with AM fungi or rhizobia, implies the existence of negative regulatory mechanisms that prevent the activation of the inappropriate pathway upon contact with either bacterial or fungal microsymbiont. The SYMRK-mediated loss of signalling specificity may be explained by simultaneous complex formation of SYMRK with NFR1 and NFR5, and related LysM-RLKs that mediate recognition of signals from the AM fungus (Maillet et al., 2011; Op Den Camp et al., 2011), which results in the release of both negative regulatory mechanisms, or by an unbalanced stoichiometry of SYMRK and putative specific negative regulators of AM- and root nodule symbiosis signalling. Candidates for such regulators include the identified interactors of the kinase domains of NFR1, NFR5, and SYMRK (Kevei et al., 2007; Zhu et al., 2008; Lefebvre et al., 2010; Mbengue et al., 2010; Chen et al., 2012; Den Herder et al., 2012; Ke et al., 2012; Toth et al., 2012; Yuan et al., 2012). The loss of signalling specificity upon SYMRK overexpression is reminiscent of expression of the deregulated CCaMK314 deletion mutant that also induces spontaneous nodules and AM-related gene activation (Takeda et al., 2012). It is therefore possible that SYMRK overexpression imposes a deregulated state on CCaMK that is otherwise attainable artificially through the deletion of its regulatory domain.
For a detailed description of the constructs and primers used in this study, please see Supplementary file 1.
Transient transformation of N. benthamiana leaves was performed as described previously (Antolín-Llovera et al., 2014).
L. japonicus seed germination (Groth et al., 2010) and hairy root transformation (Charpentier et al., 2008) were performed as described previously. Plants with emerging hairy roots systems were transferred to Fahraeus medium (FP) plates containing 0.1 µM of the ethylene biosynthesis inhibitor L-α-(2-aminoethoxyvinyl)-glycine at 2.5 weeks after transformation. For spontaneous nodulation experiments, promoter activation assays, or qRT-PCR experiments, plants were transferred to sterile Weck jars containing 300 ml dried sand/vermiculite and 25 ml FP medium at 23 dpt. For co-enrichment experiments, plants were transferred to sterile Weck jars containing 300 ml dried sand/vermiculite at 23 dpt, mock treated with 20 ml FP medium or inoculated with 20 ml of a M. loti MAFF303099 DsRED suspension in FP medium set to an OD600 of 0.05, and incubated for 10 days. Plants for the SYMRK- and CCaMKT265D-mediated T90 activation in the nfr1-1, cyclops-2, and ccamk-2 mutants were transferred to FP plates containing 0.1 µM of the ethylene biosynthesis inhibitor L-α-(2-aminoethoxyvinyl)-glycine at 21 dpt and kept on FP plates for 17 days. Transformants of the pSbtM1:GUS line were directly transferred to Weck jars containing 300 ml dried sand/vermiculite and approximately 25 ml ddH2O at 2.5 weeks after transformation. It is important to avoid free water at the bottom of the Weck jar. Plants were grown in Weck jars in a growth chamber (16 hr light/8 hr dark; 24°C) for 1.5–6 weeks. For complementation experiments, plants were transferred from FP plates to open pots containing 300 ml dried sand/vermiculite and 75 ml FP medium at 23 dpt. After 1 week, plants were inoculated with 25 ml per pot of a M. loti MAFF303099 DsRED suspension in FP medium set to an OD600 of 0.05. Roots were phenotyped 15 days after inoculation.
Protein extraction and immunoprecipitation was performed as described previously (Antolín-Llovera et al., 2014).
Plant tissue was ground to a fine powder in liquid nitrogen with mortar and pestle. Proteins were extracted by adding 200 µl extraction buffer per 100 mg root tissue (50 mM Hepes, pH 7.5, 10 mM EDTA, 150 mM NaCl, 10% sucrose, 2 mM DTT, 0.5 mg/ml Pefabloc, 1% Triton-X 100, PhosSTOP [Roche, Germany], Plant Protease Inhibitor [P9599; Sigma–Aldrich, Germany], 1% polyvinylpolypyrrolidone). Samples were incubated for 10 min at 4°C with 20 rpm end-over mixing, and subsequently centrifuged for 15 min at 4°C and 16,000 RCF. 30 µl of each protein extract was mixed with 10 µl 4× SDS-PAGE sample buffer (input; 25% (vol/vol) 0.5 M Tris–HCl (pH 6.8), 35% (vol/vol) 20% SDS, 40% (vol/vol) 100% Glycerol, 0.03 g/ml DTT, dash of Bromphenol blue). For immuno-enrichment procedures, 30 µl RFP binder coupled to magnetic particles (rtm-20; Chromotek, Germany) were washed in wash buffer (WB; 50 mM Hepes, pH 7.5, 10 mM EDTA, 150 mM NaCl, 1% Triton-X 100). Between 500 and 1000 µl of the protein extract was added to the beads and immuno-enrichment was performed for 4 hr at 4°C with 20 rpm end-over mixing, followed by 15 min magnetic separation at 4°C. Supernatant was removed and beads were washed twice with WB. 40 µl 2× SDS-PAGE sample buffer was added to the beads and both beads and input were incubated 10 min at 56°C. After heating, beads were magnetically collected at the tube wall for 5 min and 40 µl of the supernatant (eluate) was taken. For SDS-PAGE, 20 µl of the input or eluate were loaded on each gel.
Western blot analysis was performed as described previously (Antolín-Llovera et al., 2014).
GUS activity originating from the activation of promoter:GUS reporters was visualized by X-Gluc staining as described previously (Groth et al., 2010).
Transgenic root systems of L. japonicus plants were harvested 40 dpt. 80 mg root fresh weight per sample was applied for total RNA extraction using the Spectrum Plant Total RNA kit (Sigma–Aldrich, Germany). For removal of genomic DNA, RNA was treated with DNase I (amplification grade DNase I, Invitrogen, Germany). RNA integrity was verified on an agarose gel and the absence of genomic DNA was confirmed by PCR. First strand cDNA synthesis was performed in 20 µl reactions with 600 ng total RNA using the SuperScript III First-Strand Synthesis SuperMix (Invitrogen, Germany) with oligo(dT) primers. qRT-PCR was performed in 20 µl reactions containing 1× SYBR Green I (Invitrogen, Germany) in a CFX96 Real-time PCR detection system (Bio-Rad, Germany). PCR program: 95°C for 2 min, 45 × (95°C for 30 s; 60°C for 30 s; 72°C for 20 s; plate read), 95°C for 10 s, melt curve 60°C–95°C: increment 0.5°C per 5 s. Expression was normalized to the reference genes EF-1alpha and Ubiquitin, and EF-1alpha was used as a reference to calculate the relative expression of the target genes. The empty vector samples were used as negative control. Three biological replicates were analysed in technical duplicates per treatment. A primer list can be found in the supplementary files (Supplementary file 1B).
All statistical analyses and data plots have been performed and generated with R version 3.0.2 (2013-09-25) ‘Frisbee Sailing’ (R Development Core Team, 2008) and the packages ‘Hmisc’ (Harrell, 2014), ‘agricolae’ (Mendiburu de, 2014), ‘car’ (Fox and Weisberg, 2011), ‘multcompView’ (Graves et al., 2012) and ‘multcomp’ (Hothorn et al., 2008). For statistical analysis of the numbers of nodules, nodule primordia, or total organogenesis events, a Kruskal–Wallis test was applied followed by false discovery rate correction. Quantitative real-time PCR data were power transformed with the Box–Cox transformation and a one-way ANOVA followed by a Dunnett's test was performed, in which every treatment was compared to the empty vector samples.
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- Martin Parniske
- Martin Parniske
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We thank Michael Bartoschek for technical support as a student helper and Verena Klingl for technical assistance. This work was supported by the DFG priority program SPP1212 ‘Microbial Reprogramming of Plant Cell Development’ and the European Research Council (ERC).
- Maria J Harrison, Boyce Thompson Institute for Plant Research, United States
© 2014, Ried et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.