Development of stomata, valves on the plant epidermis for optimal gas exchange and water control, is fine-tuned by multiple signaling peptides with unique, overlapping, or antagonistic activities. EPIDERMAL PATTERNING FACTOR1 (EPF1) is a founding member of the secreted peptide ligands enforcing stomatal patterning. Yet, its exact role remains unclear. Here, we report that EPF1 and its primary receptor ERECTA-LIKE1 (ERL1) target MUTE, a transcription factor specifying the proliferation-to-differentiation switch within the stomatal cell lineages. In turn, MUTE directly induces ERL1. The absolute co-expression of ERL1 and MUTE, with the co-presence of EPF1, triggers autocrine inhibition of stomatal fate. During normal stomatal development, this autocrine inhibition prevents extra symmetric divisions of stomatal precursors likely owing to excessive MUTE activity. Our study reveals the unexpected role of self-inhibition as a mechanism for ensuring proper stomatal development and suggests an intricate signal buffering mechanism underlying plant tissue patterning.https://doi.org/10.7554/eLife.24102.001
Developmental patterning of multicellular organisms relies on positional cues as well as local cell-cell interactions. Development of stomata, turgor-driven cellular valves on the plant epidermis for optimal gas exchange while minimizing water loss, is coordinated by the intricate cell-cell signaling that impinges on the activity of cell-fate determinants (Pillitteri and Dong, 2013; Han and Torii, 2016). Stomatal development in Arabidopsis occurs through stereotypical cell-state transition events: a stomatal initial cell on the protoderm called a meristemoid mother cell (MMC) undergoes an asymmetric entry division to give rise to a meristemoid, a transient amplifying cell of the stomatal lineage. The meristemoid reiterates asymmetric divisions and renews itself, while creating surrounding stomatal lineage ground cells (SLGCs). Eventually, the meristemoid loses its stem-cell-like property and differentiates into a guard mother cell (GMC). The GMC executes a single round of symmetric division to form paired guard cells (GCs) surrounding a pore, thereby completing stomatal differentiation (Lau and Bergmann, 2012; Pillitteri and Torii, 2012; Han and Torii, 2016). These cell state transitions are directed by the sequential actions of three basic-helix-loop-helix (bHLH) proteins, SPEECHLESS (SPCH), MUTE, and FAMA, which determine the initiation and proliferation, meristemoid-to-GMC transition, and GMC-to-GC differentiation, respectively. These three bHLH proteins form heterodimers with the broadly expressed sister bHLH proteins SCREAM (SCRM: also known as ICE1) and SCRM2, both of which are absolutely required for the activities of SPCH-MUTE-FAMA (Lau and Bergmann, 2012; Pillitteri and Dong, 2013; Han and Torii, 2016).
The spatial control of stomatal differentiation processes is achieved by a family of secreted cysteine-rich peptides called EPIDERMAL PATTERNING FACTORS (EPFs) that are perceived by cell-surface receptors with extracellular leucine-rich repeat (LRR) domain: three ERECTA-family receptor kinases and their signal modulator LRR receptor-like protein TOO MANY MOUTHS (TMM) (Nadeau and Sack, 2002; Shpak et al., 2005; Hara et al., 2007, 2009; Hunt and Gray, 2009; Torii, 2012). These modules are conserved down to basal land plants (Caine et al., 2016). During the initiation of stomatal cell lineages, EPF2 peptide perception by ERECTA activates downstream intracellular signals mediated by the mitogen-activated protein kinase (MAP kinase) cascade, which inhibits the entry divisions of MMC by down-regulating SPCH protein (Lampard et al., 2008; Lee et al., 2012, 2015). As such, application of bioactive EPF2 peptide confers an epidermis solely composed of pavement cells, phenotypically identical to loss-of-function spch mutant (Lee et al., 2012). Recent studies established that EPF2 is a direct transcriptional target of SPCH and SCRM, therefore EPF2, ERECTA•TMM, and SPCH•SCRM modules constitute a negative feedback loop generating evenly distributed spatial patterns of stomatal initial cells (Lau et al., 2014; Horst et al., 2015). Furthermore, the decision of whether or not to enter the stomatal cell-lineage is fine-tuned by the competitive binding of EPF2 and its antagonistic peptide, EPF-LIKE9 (EPFL9), also known as Stomagen, to ERECTA (Kondo et al., 2010; Sugano et al., 2010; Lee et al., 2015). Unlike EPF2, the direct binding of Stomagen to ERECTA leads to the inhibition of receptor activation and signal transduction, therefore resulting in excessive stomatal clusters like erecta-family mutants (Lee et al., 2015).
The founding member of EPF/EPFL-family peptides, EPF1, enforces stomatal spacing and its loss-of-function mutation confers stomatal pairing and clustering (Hara et al., 2007). Both genetic and biochemical studies have placed ERECTA-LIKE1 (ERL1), a sister receptor of ERECTA, as well as TMM as a receptor module acting downstream of EPF1 (Hara et al., 2007; Lee et al., 2012). However, unlike EPF2, the exact action and function of EPF1 remain unclear. Early models predicted that the signal emanating from a meristemoid is perceived by the receptors in the neighboring cells to regulate stomatal patterning (Nadeau and Sack, 2003; Serna, 2004). However, both EPF1 and ERL1 promoter activities are the highest in the stomatal precursor cells, most notably in the late meristemoids and GMCs (Shpak et al., 2005; Hara et al., 2007). The inconsistency of their expression patterns and predicted functions adds to the conundrum as to how this ligand-receptor system operates. It is also unknown whether EPF1 signaling acts on any of the stomatal bHLH transcription factors. To address these questions, we investigated the in vivo dynamics and regulation of ERL1, the primary receptor of EPF1. We found that ERL1 and MUTE constitute a negative feedback loop, which, with co-expression of EPF1, elicits an autocrine inhibition of stomatal differentiation potential. Our study reveals the unexpected role of self-inhibition as a mechanism for ensuring timely transition of stomatal differentiation and proper stomatal patterning. Given that EPF1 peptide sources are shared by both autocrine and paracrine signaling, the intricate buffering mechanism may underpin proper stomatal patterning.
To clarify the role of EPF1-ERL1 signaling during stomatal development, we first examined the in vivo dynamics of ERL1-YFP fusion protein driven by its promoter expressed in erl1-2 null mutant background (ERL1pro::ERL1-YFP in erl1). This construct rescues the stomatal cluster phenotype in er erl1 erl2, indicating it is functional (Figure 1—figure supplement 1). Consistently, the expression level of the ERL1-YFP transgene is comparable to that of the endogenous ERL1 (Figure 1—figure supplement 1D). In early stomatal-lineage cells, including rectangular MMCs and early meristemoids, ERL1-YFP is localized sharply at the plasma membrane (Figure 1A–C,K,L; Video 1). During the asymmetric divisions of stomatal-lineage cells, ERL1-YFP exhibited striking accumulation at the newly-formed division site that separates the meristemoid and stomatal lineage ground cell (SLGC) (Figure 1D,F,M; Video 1).
Following the division, ERL1-YFP signals were detected in the plasma membrane of both the meristemoid and neighboring stomatal lineage ground cell (SLGC) (Figure 1E,G,N; Video 1). During the late meristemoid-to-GMC transition, ERL1-YFP showed transient yet high accumulation in the meristemoids while diminishing from the stomatal lineage ground cells (SLGCs), marking the late meristemoids the brightest (Figure 1G,H,N,O; Video 1). Expression of ERL1 disappears as the GMC divides symmetrically and differentiates into guard cells (Figure 1J,P,Q; Video 1).
It has been reported that ERL1 is a high-confidence SPCH target gene (Lau et al., 2014). While this is consistent with the early stomatal-lineage expression of ERL1, it does not explain the rapid boost in accumulation of ERL1 during the meristemoid-to-GMC transition (Figure 1). The transition from meristemoids to GMCs is specified by SPCH’s sister bHLH protein, MUTE (Pillitteri et al., 2007). We thus hypothesized that MUTE is driving the rapid increase of ERL1 in the late meristemoids. To address this, we first examined the MUTE and ERL1 proteins in the stomatal lineage cells using Arabidopsis lines co-expressing MUTE-tagRFP and ERL1-YFP driven by their own respective endogenous promoters (Figure 2A). As expected, early stomatal-lineage cells only express ERL1-YFP. However, all late meristemoids co-expressed MUTE-tagRFP in the nuclei and strong ERL1-YFP at the cell periphery (n = 270; 12 seedlings analyzed) (Figure 2A,B). MUTE-tagRFP was driven by the identical promoter (−1989 bp) used to express MUTE-GFP (Pillitteri et al., 2007). Both MUTEpro::MUTE-GFP and MUTEpro::MUTE-tagRFP exhibited transient signals during late meristemoid-to-GMC transition (Figure 2—figure supplement 1A), and their co-introduction into Arabidopsis seedlings further confirmed their co-expression (Figure 2—figure supplement 1B). Thus, the MUTE-tagRFP line accurately reflects the previously-documented MUTE dynamics.
Next, we used the estrogen receptor-based inducible overexpression system (XVE system) (Zuo et al., 2000) to address if ERL1 is upregulated by MUTE. The estradiol-inducible MUTE overexpression (iMUTE) line upregulates MUTE transcripts within two hours and remained high throughout the analyzed time course, with the maximum average fold increase of 1536 ± 79 after 8 hr (Figure 2C). iMUTE triggered rapid upregulation in ERL1 transcripts also within two hours, indicating that ERL1 is an early MUTE-induced gene (Figure 2D; Figure 2—figure supplement 2E). To unequivocally address whether ERL1 is a direct MUTE target, a chromatin immunoprecipitation (ChIP) assay was performed. For this purpose, we took advantage of the Arabidopsis scrm-D enabled line that vastly increases the stomatal-lineage cell population thereby enhancing the signals for ChIP assays (Horst et al., 2015). Our previous study has shown that the scrm-D-enabled transcriptomic profiling of meristemoids accurately reflects the meristemoid-specific gene expression during normal epidermal development (Pillitteri et al., 2011), further supporting the use of this genetic background. We introduced functional MUTE-GFP protein driven by its own promoter (MUTEpro::MUTE-GFP) (Pillitteri et al., 2007), into scrm-D mutant background. A robust binding of MUTE was detected within the ERL1 promoter at the region overlapping with the known SPCH binding site (Lau et al., 2014), which contains the predicted bHLH-binding E-box (Figure 2H,I; Figure 2—figure supplement 2A,B,D). Furthermore, the binding of MUTE-GFP at the ERL1 promoter region was also detected in the complemented genetic background, MUTEpro::MUTE-GFP expressed in mute, which exhibits wild-type phenotype (Pillitteri et al., 2007). As predicted, the fold-enrichment of signals were reduced in the absence of scrm-D mutation (Figure 2—figure supplement 2C). The data demonstrate the binding of MUTE-GFP during normal epidermal development. Collectively, the results indicate that MUTE induces ERL1 expression by directly associating with the ERL1 promoter region.
It has been reported that ERL1 primarily perceives EPF1 peptides (Hara et al., 2007; Lee et al., 2012). To clarify the spatiotemporal expression of EPF1 and MUTE, we next analyzed dual reporter seedlings expressing MUTEpro::MUTE-tagRFP and EPF1pro::erGFP. A population of meristemoids only exhibited nuclear RFP signals, suggesting that the onset of MUTE expression precedes that of EPF1 (14/180 cells expressed RFP only; from five seedlings) (Figure 2F,G). In the late meristemoids and GMCs, strong RFP and GFP signals co-exist, indicating that MUTE and EPF1 are co-expressed (Figure 2F,G). The EPF1 promoter activity remained very high in immature GCs, where MUTE-tagRFP signal was no longer detected (Figure 2F,G). We next analyzed whether EPF1 is also upregulated by MUTE. Unlike ERL1, however, iMUTE induction did not trigger any substantial changes in EPF1 expression (Figure 2E; Figure 2—figure supplement 2E), suggesting that EPF1 is not likely a MUTE target.
Our finding that MUTE directly induces ERL1 expression during meristemoid-to-GMC transition (Figure 2) implies a previously-undescribed role of the ERL1 receptor kinase in differentiating GMCs. EPF1 overexpression or exogenous EPF1 peptide application confers arrested meristemoids, a phenotype resembling mute, in ERL1-dependent manner (Lee et al., 2012). To understand the ultimate target of this EPF1-ERL1 signaling, we examined the effects of excessive EPF1 on transcription factors driving GMC differentiation, MUTE and SCRM. For this purpose, we first made use of our estradiol-induced EPF1 overexpression (iEPF1) line that rapidly upregulates EPF1 transcript amounts to the maximum fold increase of 407 ± 46 at 5 hr after estradiol treatment (Figure 3—figure supplement 1C). As reported (Hara et al., 2007; Lee et al., 2012), iEPF1 inhibits stomatal differentiation (Figure 3—figure supplement 1A,B). iEPF1 conferred a loss of signals from both MUTE transcriptional (MUTEpro::nucYFP) and translational (MUTEpro::MUTE-GFP) reporters 4 days after induction when arrested meristemoid phenotypes are evident (Figure 3A). By contrast, signals for SCRM transcriptional (SCRMpro::nucGFP) and translational (SCRMpro::GFP-SCRM) reporters remained in arrested meristemoids even after 4 days (Figure 3B). The effects of EPF1 peptide application mirrored iEPF1 (Figure 3—figure supplement 2). These results suggest that the EPF1 signal targets MUTE but not SCRM.
To understand the kinetics of MUTE disappearance, we next performed quantitative analysis of MUTE-GFP levels upon iEPF1 induction hourly (Figure 3C,D). The MUTE-GFP signals started to diminish at 15 hr after the iEPF1 induction and became barely detectable by 20 hr after the induction. By 24 hr, MUTE-GFP signals were undetectable (Figure 3C,D). In the mock-treated control, robust MUTE-GFP signals were detected throughout the 24 hr time course (Figure 3C,D). The timeframe is consistent with iEPF1 transcript accumulation (Figure 3—figure supplement 1C). Within the same timeframe, transcriptional and translational reporters of SCRM were not influenced by iEPF1 (Figure 3E,F). Gradual declines in GFP-SCRM signals were detected over time for both mock and iEPF1, which may be reflecting the developmental stage of the seedlings (Figure 3E,F).
To address the specificity of EPF1 signaling pathway, we further tested the effects of iEPF1 on SPCH promoter and SPCH-GFP protein accumulation. Strong GFP signals of both SPCHpro::nucGFP and SPCHpro::SPCH-GFP were detected even three days after iEPF1 overexpression (Figure 4A). By five days after iEPF1 overexpression, SPCH-GFP protein was no longer detected (Figure 4B). This likely reflects the developmental progression of all remaining stomatal-lineage cells beyond the SPCH-regulated steps. Further quantitative analysis of SPCH transcriptional and translational reporters showed that their signals are not changed by iEPF1 (Figure 4C,D). A steep decline in SPCHpro::nucGFP signals were detected within the first five hours in both mock and estradiol treatment for iEPF1 (Figure 4C). This may imply that SPCH promoter activity is sensitive to the liquid treatment. The overall decline of signals may also reflect the developmental stage of the seedlings (Figure 4C,D). On the basis of these findings, we conclude that MUTE, but not SPCH, is the specific target of EPF1-mediated signaling.
Our results indicate that ERL1 mediates extrinsic EPF1 peptide signaling, which in turn inhibits MUTE. Paradoxically, however, expression of the endogenous EPF1 coincides with MUTE (Figure 2). We thus postulated that expressing ERL1 only in the MUTE-expressing cells may lead to a loss of stomatal fate, in other words, having a secreted peptide, its receptor and target transcription factor only in the same cells will auto-inhibit stomatal differentiation. To test this hypothesis, we expressed the functional ERL1-YFP under the control of the MUTE promoter. MUTEpro::ERL1-YFP was introduced into er erl1 erl2 triple null mutants in order to ensure that ERL1 will be the only existing receptor pool that will perceive and transduce the signal (Figure 5). er erl1 erl2 cotyledon epidermis develops stomatal clusters (Figure 5A; Video 2) (Shpak et al., 2005). Strikingly, the expression of MUTEpro::ERL1-YFP in er erl1 erl2 conferred massive clusters of arrested meristemoids in the leaf epidermis (Figure 5B; Video 3). Consistently, stomatal index (SI=total number of stomata/total number of epidermal cells x100) underwent 14-fold reduction from 42.6 ± 5.3% to 2.9 ± 2.1% (mean ± standard deviation) (Figure 5C).
To test whether the meristemoid arrests are caused by the ERL1 signaling activated by the endogenous EPF1 peptides, we introduced MUTEpro::ERL1-YFP er erl1 erl2 into a mutant lacking functional EPF1. The epf1 epf2 double mutant was chosen in order to circumvent the complex effects of EPF-family peptides (Figure 5D,E). Indeed, MUTEpro::ERL1-YFP in er erl1 erl2 epf1 epf2 quintuple mutant background was not able to suppress stomatal differentiation, resulting in increased stomatal index (SI) (Figure 5C,E). The results suggest that the endogenous EPF peptides are required to elicit the inhibition of stomatal differentiation potential. However, the additional epf1 epf2 mutation did not fully revert the stomatal differentiation (Figure 5C), implying the possibility of further redundancy by EPF/EPFL genes.
The EPF-family peptide Stomagen positively regulates stomatal development via directly competing with EPF2 for the binding to ERECTA receptor (Kondo et al., 2010; Sugano et al., 2010; Lee et al., 2015). The Stomagen peptide also associates with ERL1 in planta (Lee et al., 2015). This prompted us to further test whether the excessive amounts of Stomagen could revert the fate of arrested meristemoids in MUTEpro::ERL1-YFP in er erl1 erl2. As control, mock treated leaf epidermis showed meristemoid arrests (Figure 5F). By contrast, application of bioactive Stomagen peptide (5 μM) to MUTEpro::ERL1-YFP er erl1 erl2 seedlings conferred clusters of mature stomata (Figure 5G). Therefore, Stomagen counteracts the EPF1-ERL1 autocrine signaling, likely via competing with EPF1 for the ERL1 binding. TMM forms a heteromer with ERL1 and is required for EPF1-ERL1 mediated signaling (Hara et al., 2007; Lee et al., 2012). Consistently, loss-of-function tmm mutation fully reverted the arrested meristemoid phenotype of MUTEpro::ERL1-YFP in er erl1 erl2 (Figure 5C, H, I). In all these cases YFP signals are detected in a subset of arrested meristemoids, confirming that the restoration of stomatal differentiation by epf1 epf2, Stomagen application, and tmm mutation is not due to the reduced expression of MUTEpro::ERL1-YFP (Figure 5E–I). On the basis of these findings, we conclude that the co-presence of EPF1, ERL1, and MUTE in the late meristemoids elicits autocrine inhibitory signaling, leading to a termination of stomatal fate.
It is well known that EPF1 signaling enforces asymmetric spacing division (Hara et al., 2007). To further address if the presence of the receptors in stomatal lineage ground cells (SLGCs) ameliorate the autocrine inhibition, we introduced MUTEpro::ERL1-YFP in seedlings that harbor wild-type copies of the three ERECTA-family genes. Indeed, the expression of MUTEpro::ERL1-YFP did not confer discernable phenotype (Figure 5—figure supplement 1). Our findings suggest that both a meristemoid and its neighboring cell share the same source of EPF1 signaling peptides, and a disproportionate balance of receptor pools between these two cell types evoke the self-inhibition of stomatal fate.
We have demonstrated that co-presence of EPF1, ERL1 and MUTE in the late meristemoids confers the developmental arrests of stomatal precursors (Figure 5). The important question, however, is the role of the EPF1-ERL1 autocrine inhibitory signaling during normal stomatal development. To address this question, a quantitative analysis of MUTE protein accumulation was performed in the presence or absence of TMM, which is required for the EPF1-ERL1 signal transduction. Specifically, we compared the MUTEpro::MUTE-tagRFP signals in the nuclei from the erl1 null mutant background fully rescued by ERL1pro::ERL1-YFP (hereafter referred to as ‘wild-type (WT)‘) and those from the erl1 tmm double null mutant background rescued by ERL1pro::ERL1-YFP (referred to as ‘tmm’) (Figure 6). The ERL1pro::ERL1-YFP transgene was introduced into tmm via genetic crosses. As shown in Figure 6A and C, MUTE-tagRFP signal intensity in each nucleus is substantially higher in tmm, with over 2.5-fold higher average total intensity in each nucleus compared to wild type. The result supports the hypothesis that endogenous autocrine EPF1-ERL1 signaling in the meristemoids prevents excessive MUTE protein accumulation. Also, compared to the wild-type epidermis, more cells express MUTE protein in tmm, consistent with the increase in stomatal precursor cells by tmm mutation (Figure 6C).
Next, we investigated the developmental consequence of excessive MUTE protein accumulation due to the loss of EPF1-ERL1 autocrine signaling. For this purpose, time-lapse live imaging of wild-type and tmm seedlings co-expressing MUTEpro::MUTE-tagRFP and ERL1pro::ERL1-YFP during stomatal development was performed (Figure 6D,E; Videos 4 and 5). Notably, the duration of proliferation-to-differentiation transition (i.e. hours from the last asymmetric division to the onset of symmetric division of a given stomatal precursor cell) is significantly shorter in tmm, with averages of 18.9 hr in wild type (n = 18) vs. 14 hr in tmm (n = 28) (Figure 6B). Moreover, we observed instances in tmm whereby the meristemoid accumulating high MUTE-tagRFP signals undergoes a symmetric division, giving rise to two daughter cells, both expressing MUTE-tagRFP, and eventually differentiating into paired stomata (Figure 6E, Video 5). It is well known that TMM is required for the asymmetric spacing division of a neighboring stomatal lineage ground cell (SLGC) (Nadeau and Sack, 2002; Lau and Bergmann, 2012; Han and Torii, 2016). On the contrary, the role of TMM in suppressing the symmetric division of a meristemoid has been overlooked. Taken together, our data suggest that loss of the autocrine EPF1-ERL1 signaling during normal stomatal development causes accelerated and dysregulated stomatal differentiation, likely as a ramification of excessive MUTE accumulation.
The EPF-family of secreted cysteine-rich peptides regulates multiple aspects of stomatal development and other developmental processes through the ERECTA-family receptors (Torii, 2012; Lee and De Smet, 2016). In this study, we discovered an unexpected role for EPF1 and ERL1 in the autocrine regulation of stomatal differentiation potential. The key framework is a negative feedback loop between MUTE and ERL1 whereby MUTE directly upregulates ERL1 expression (Figure 2), and in turn, ERL1 mediates EPF1-peptide signaling leading to inhibition of MUTE activity (Figure 3). ERL1 is also induced by SPCH in earlier stomatal-lineage cells, including MMCs, early meristemoids, and SLGCs (Figure 1) (Lau et al., 2014). While EPF1 expression is not regulated by MUTE, EPF1 turns on during meristemoid-to-GMC transition (Figure 2). Based on these findings, we proposed a coincidence model where the overlapping expression of EPF1, ERL1, and MUTE during a narrow developmental window in the late meristemoids triggers downregulation of MUTE (Figure 7), thereby ensuring timely transition to stomatal differentiation mediated by FAMA.
The co-expression of EPF1 and ERL1 triggering autocrine signaling challenges a traditional view of plant secreted peptide hormones as intercellular signals (Murphy et al., 2012). Known EPF/EPFL peptides function in a non-cell autonomous manner. For example, EPFL9/Stomagen secreted from internal mesophyll tissues is perceived by ERECTA in the protoderm (Lee et al., 2015). EPFL4 and EPFL6 are inter cell-layer signals between the stem endodermis and phloem to promote inflorescence elongation via ERECTA (Uchida et al., 2012). Recently, we have reported that EPFL2 peptide promotes leaf serration as a ligand for ERECTA-family (Tameshige et al., 2016). Interestingly, EPFL2 and its primary receptor, ERL2, exhibit inverse expression patterns: ERL2 shows the highest expression at the leaf teeth tips where EPFL2 expression is excluded. Therefore, EPF/EPFL-family peptides mediate signals both in autocrine and paracrine manners.
Both epf1 mutation and a dominant-negative ERL1 receptor confer a violation of one-cell spacing rule (Hara et al., 2007; Lee et al., 2012). Based on this phenotype, a paracrine model was proposed initially, whereby a signal (EPF1) emanating from the meristemoids/GMCs will be perceived by receptors (ERL1 and TMM) in the neighboring stomatal lineage ground cell (SLGC) to orient asymmetric spacing division (Figure 7A). However, based on the high expression of EPF1, ERL1, and TMM in the meristemoids/GMCs, an alternative autocrine model has been described (Figure 7B) (Facette and Smith, 2012). Here, EPF1 peptide is perceived by ERL1/TMM in the meristemoids/GMCs. A subsequent downstream signal transduction promotes the expression of a yet unidentified ligand X, which will be secreted and perceived by a yet unidentified receptor Y on the surface of neighboring stomatal lineage ground cells (SLGCs). This eventually leads to the oriented asymmetric spacing division (Figure 7B) (Facette and Smith, 2012). Our findings revise these models and propose a buffered system, whereby the pool of EPF1 is shared by both the meristemoid and its neighboring stomatal lineage ground cell (SLGC) (Figure 7C). ERL1 and TMM also accumulates at the plasma membrane of stomatal lineage ground cells (SLGCs), albeit in lesser amounts (Figure 1) (Nadeau and Sack, 2002; Horst et al., 2015). ERL1 in the stomatal lineage ground cells (SLGCs) most likely perceives the EPF1 peptides emitted from neighboring meristemoids, and this EPF1-ERL1 paracrine signaling orients the asymmetric spacing divisions. Based on this model (Figure 7C), the paracrine action of EPF1 also limits the inhibitory activity of EPF1-ERL1 autocrine signals in the meristemoids, since ERL1 in the meristemoids and in neighboring stomatal lineage ground cells (SLGCs) both share the same source of EPF1 signals.
It is important to note that the absolute co-expression of ERL1 and MUTE conferred severe meristemoid arrests due to excessive activation of ERL1 signaling pathway, when all three endogenous ERECTA-family receptors are missing (Figure 5). Indeed, MUTEpro::ERL1-YFP does not confer any discernable phenotype if the wild-type copies of the three ERECTA-family genes are present (Figure 5—figure supplement 1). It is therefore most likely that, in addition to ERL1, ERECTA and ERL2 receptor population expressed in stomatal lineage ground cells (SLGCs) buffer excessive EPF1 peptide ligands to ensure the proper and adequate level of MUTE inhibition. The idea of signal buffering by sister ERECTA-family receptors is supported by their known partial redundancy with complex genetic interactions (Shpak et al., 2004, 2005). Moreover, EPFL4/6 (CHAL/CLL1), which normally act as ligands for ERECTA-mediated inflorescence elongation, interfere with this buffering mechanism and confer stomatal clustering in the stems the absence of TMM (Abrash and Bergmann, 2010; Abrash et al., 2011; Uchida et al., 2012). Very recently, a VST-family of membrane-associated proteins was reported as a modulator of ERECTA-family signaling, via specifically interacting with ERL2 (Ho et al., 2016). Such factors may contribute to fine-tuning the EPF1-ERL1 signaling.
Our work also revealed that, while two paralogous ligand-receptor pairs, EPF2-ERECTA and EPF1-ERL1, enforce stomatal development via acting on the core stomatal bHLH proteins, the architectures of their regulatory framework are different. EPF2, but not its main receptor ERECTA, is the direct SPCH target (Lau et al., 2014; Horst et al., 2015). Conversely, ERL1, but not its main ligand EPF1, is the direct MUTE target (Figure 2). The biochemical mechanism of MUTE downregulation is unknown, but lines of evidence suggest the involvement of a MAP kinase cascade. First, YODA, MKK4/5, and MPK3/6 are genetically acting downstream of the three ERECTA-family RKs (Lampard et al., 2008; Bemis et al., 2013). Second, the expression of constitutively-active MKK4/5 by the MUTE promoter led to arrested meristemoids (Lampard et al., 2009), thus phenocopying EPF1 peptide application or overexpression (Hara et al., 2007; Lee et al., 2012). Unlike SPCH, however, MUTE does not possess a predicted MAP kinase target domain (Davies and Bergmann, 2014), raising a question of whether MUTE is a MPK3/6 substrate. In any event, functional specialization and re-wiring of regulatory circuits among the paralogs of EPF peptides, ERECTA-family receptor kinases, and stomatal bHLH transcription factors highlight the evolutionary mechanism underlying the sequential steps of stomatal differentiation steps.
Intrinsic polarity of meristemoids and asymmetric daughter cell fates are regulated by BASL (Dong et al., 2009). Recent studies have revealed that polarized BASL in the stomatal lineage ground cells (SLGCs) enhances the MAP kinase activity, resulting in lowered SPCH abundance (Zhang et al., 2015, 2016). In the absence of EPF1, GFP-BASL occasionally exhibits improper polar localization to the 'wrong' site within a periphery of the stomatal lineage ground cells (SLGCs), which predicts the mis-oriented site of asymmetric spacing division (Dong et al., 2009). It would be an interesting future question to address how the EPF1-ERL1 signaling pathway influences the location of BASL polarization and stomatal-lineage cell polarity.
It has become evident that plants make use of a myriad of peptide signals to regulate diverse developmental processes. Accumulating evidence suggest that plant peptide signals mediate both local cell-cell communications and long-distance root-to-shoot signaling (Brand et al., 2000; Searle et al., 2003; Hirakawa et al., 2008; Okamoto et al., 2013; Tabata et al., 2014). In most cases, however, the exact source and recipient cells of signals remains unclear. Previously studies have identified ligand-receptor systems that share the same expression domains. For instance, the tomato cysteine-rich secreted protein LAT52 and its receptor LRR-RK, LePRK2, are both expressed in pollen (Muschietti et al., 1998; Tang et al., 2002). It was speculated that pollen may monitor its germination state via LAT52-LePRKs autocrine signaling (Tang et al., 2002). Another example is CLE45-BAM3, a small secreted peptide ligand-LRR-RK pair: both CLE45 and BAM3 are expressed in protophloem tissue in roots, and their signal transduction leads to the inhibition of protophloem differentiation (Depuydt et al., 2013; Rodriguez-Villalon et al., 2014). It is not yet known whether these ligand-receptor signaling systems constitute feedback regulation with target transcription factors. In any event, the autocrine signaling may be a prevalent mode of peptide-receptor kinase signaling in plants. Here, focusing on stomatal development, where the differentiation potential of bipotent precursor cells can be monitored at a single cell resolution, one can decipher the contribution of autocrine peptide signaling and the buffering of autocrine vs. paracrine signals between two sister cells with different developmental fate. In animals, both paracrine and autocrine peptide signaling contributes to stem cell proliferation. For instance, Wnt, a key secreted cell-cell signal during animal development (Logan and Nusse, 2004), participates in the autocrine regulation of epidermal stem cell renewal in mice (Lim et al., 2013). A versatile use of peptide ligands for the maintenance and differentiation of adult stem cells may highlight yet another theme in the logic of development in multicellular organisms.
Arabidopsis thaliana Columbia (Col) accession was used as a wild type. The following mutants and reporter lines were reported previously: erl1-2, er-105 erl1-2 erl2-1 (Shpak et al., 2005); EPF1pro::erGFP, epf1, and tmm-KO (Hara et al., 2007); mute, MUTEpro::MUTE-GFP, SPCHpro::SPCH-GFP (Pillitteri et al., 2007); scrm-D, SCRMpro::GFP-SCRM (Kanaoka et al., 2008); epf1 epf2 er erl1 erl2 (Hara et al., 2009); ERL1pro::ERL1-YFP, Est::EPF1 (iEPF1) (Lee et al., 2012); and SCRMpro::nucGFP and SPCHpro::nucGFP (Horst et al., 2015). Plants were grown under the long-day condition.
The following plasmids were generated for this study: pAR202 (MUTE promoter), pAR205 (MUTE genomic sequence with no stop codon), pJSL105 (ERL1 genomic sequence with no stop codon), pBK5 (MUTEpro::ERL1-YFP), pJT163 (MUTEpro::MUTE-tagRFP), pLJP245 (Est::MUTE), and MUTEpro::nucYFP. To construct pBK5, three-way Gateway recombination was performed using pAR202, pJSL105, and R4L1pGWB540 (Nakagawa et al., 2008). To construct pJT163, three-way Gateway recombination was performed using pAR202, pAR205, and R4L1pGWB659 (Nakagawa et al., 2008). pGWB vectors are kind gift from Prof. Tsuyoshi Nakagawa (Shimane Univ.). For detailed information about the plasmids, see Supplementary file 1. Plasmids are transformed into Agrobacterium GV3101/pMP90 and subsequently to Arabidopsis by floral dipping. Over 10 lines were characterized for the phenotypes and reporter gene expressions. Established reporter lines were introduced into higher-order mutant backgrounds or dual reporter backgrounds via genetic crosses. The genetic crosses made in this study include: MUTEpro::MUTE-tagRFP x ERL1pro::ERL1-YFP erl1; MUTEpro::MUTE-tagRFP x EPF1pro::erGFP; MUTEpro::MUTE-GFP mute x MUTEpro::MUTE-tagRFP; Est::EPF1 x MUTEpro::nucYFP; Est::EPF1 x MUTEpro::MUTE-GFP mute; Est::EPF1 x SCRMpro::nucGFP; Est::EPF1 x SCRMpro::GFP-SCRM; Est::EPF1 x SPCHpro::nucGFP; Est::EPF1 x SPCHpro::SPCH-GFP spch; er erl1 erl2 x tmm; MUTEpro::ERL1-YFP er erl1 erl2 x Col-0 wild type; ERL1pro::ERL1-YFP erl1 tmm x MUTEpro::MUTE-tagRFP. The following transgenic lines in higher-order mutants were generated by floral dipping: ERL1pro::ERL1-YFP into er erl1 erl2; MUTEpro::ERL1-YFP into er erl1 erl2; MUTEpro::ERL1-YFP into epf1 epf2 er erl1 erl2; MUTEpro::ERL1-YFP into er erl1 erl2 tmm. For primer DNA sequence used for plasmid construction, see Supplementary file 2. Estradiol induction was performed as described previously (Lee et al., 2012).
EPF1 peptides were expressed, purified, and refolded as previously described (Lee et al., 2012, 2015). Stomagen peptide was custom synthesized (BioSynthesis, Lewisville, TX) and subjected to refolding. For quality control, the refolded peptides were analyzed by High Pressure Liquid Chromatography (Hewlett Packard 1100 Series) using ZORBAX 300 Extended-C18 column (Agilent), and each major peak was analyzed by Esquire-LC ion-trap mass spectrometer (Bruker Daltonics, Billerica, MA). The bioactivity of each refolded peptide batch was verified by seedling bioassays (Lee et al., 2015) prior to performing any experiments. For each peptide or mock treatment, at least three biological repeats were performed.
Homozygous transgenic lines for iMUTE were grown on ½ MS agar media for 4 days. 40–50 seedlings for each replicate were bathed in a ½ MS liquid media containing 10 μM estradiol or DMSO (mock). Total RNA was isolated from the seedlings using RNeasy Plant Mini Kit (Qiagen, 74904) and DNase I digestion (Qiagen, 79254) was performed on column during the RNA extraction according to the instructions of the manufacturer. 1 μg of RNA was converted to cDNA using iScript cDNA synthesis kit (Bio-Rad, 1708891) according to the instructions of the manufacturer. First-strand cDNA was diluted 1:7 in double distilled water and used as template for Real-time qPCR. qRT-PCR was performed as described below (see Chromatin immunoprecipitation section). At least four 10-fold dilution series were amplified by the same primers to set standard curve and calculate the quantity of the gene expression. Relative expression was calculated by dividing ACT2 gene expression over the specific-gene expression. Three biological replicates were performed. See Supplementary file 2 for oligo DNA primer sequence used for qRT-PCR.
160 mg seeds were sown on ½ MS agar media and seedlings were collected at 42 ~ 48 hr after germination in liquid nitrogen, which yields ca. 1.0 g of fresh weight. Frozen tissue was ground to fine powder and re-suspended in 20 ml of ChIP extraction buffer 1 (Bowler et al., 2004) containing 1% formaldehyde (Sigma, F1635). Samples were incubated at 4°C for 10 min for DNA-protein cross-linking. To quench the cross-linking 2 M glycine was added, then samples were incubated at 4°C for 5 min (Cui et al., 2016). The chromatin was extracted twice in ChIP extraction buffer 2 (Bowler et al., 2004). Isolated chromatin was lysed in 100 μl of Nuclei Lysis buffer on ice for 30 min with occasional stirring as described in Yamaguchi et al. (2014). Subsequently, volumes were brought up to 300 μl with ChIP dilution buffer with Triton X-100 (Yamaguchi et al., 2014). Sonication was performed to shear DNA using Bioruptor Plus UCD-300 sonicator (Diagenode), 30 s on/off cycles for 15 times at High power setting. After the sonication, samples were diluted up to 1 ml with ChIP dilution buffer with Triton and spun at full speed. The supernatant was precleared using Dynabeads protein G (Invitrogen, 10004D) for 1 hr at 4°C. Pre-cleared solution was subjected to overnight immunoprecipitation at 4°C. 2 μl of anti-GFP antibody (Ab290, Lot: GR278073-1) was added in 1 ml pre-cleared chromatin sample. Subsequent steps (capturing, washing, reverse cross-linking of immune-complex and DNA purification) were performed as described in Yamaguchi et al. (2014). Quantitative PCR (qPCR) was carried out using gene specific primers (Supplementary file 2). The qPCR was run using iTaq Universal SYBR Green Supermix on CFX96 real-time system (Bio-Rad, 1725121) with the following conditions: 95°C for 1 min; 45 cycles of 95°C for 5 s, 60°C for 30 s (Cycling Stage), 65–95°C 0.5°C increments at 5 s/step (Melting Curve Stage). At least three technical replicates were used for ChIP qPCR. Three biological replicates were performed. A dilution series of input was amplified simultaneously using the same primer pairs to calculate the quantity of the ChIPed DNA as % input (Yamaguchi et al., 2014).
The Zeiss LSM700 inverted confocal microscope (Thornwood, NY, USA) and the Leica SP5X-WLL inverted confocal microscope (Solms, Germany) were used for imaging. Time-lapse cotyledon imaging of ERL1-YFP was prepared as described previously with 20x/0.8 Apochromat lens (x1 zoom) on Zeiss LSM700 (Pillitteri et al., 2011; Peterson and Torii, 2012). For the multicolor images of YFP and RFP, transgenic seedlings were observed with a 63x/1.2 W Corr lens on Leica SP5X-WLL using Hy-D detector. 514 nm laser was used to excite YFP and 560 nm laser was used to excite RFP. The emission filter was 524–550 nm for YFP and 594–637 nm for RFP. For multicolor images of GFP and RFP, transgenic seedlings were observed with a 63x/1.2 W Corr lens on Leica SP5X-WLL using Hy-D detector. The 488 nm laser was used to excite GFP and the 560 nm laser was used to excite RFP. The emission filter was 500–515 nm for GFP and 594–637 nm for RFP. The Z-stack projection images were taken at the interval of 0.99 µm, covering the thickness of the entire cell. For qualitative image presentation, Adobe Photoshop CS6 was used to trim and uniformly adjust the contrast/brightness.
The Leica LAS AF software and Imaris ver. 8.1.3 (Bitplane) were used for post-acquisition image processing. Quantitative analysis of MUTE signal intensity was performed using Imaris ver. 8.1.3 briefly as the following. An extensive series of Z-stack confocal images covering the entire meristemoids (~17 layers) were subjected to surface rendering in red or green channel to capture MUTE-tagRFP, MUTE-GFP, SPCH-GFP, GFP-SCRM, SPCHpro::nucGFP, or SCRMpro::nucGFP expressing nuclei in the 3-D space (for each time point for time course). Cut-off value was set as 0.85 for sphericity, which effectively removed objects with non-specific signals. Intensity sum and standard deviation for each nucleus were subsequently calculated. Statistical analyses were performed using R ver. 3.3.1. Graphs were generated using R ggplot2 package or Microsoft Excel. See Supplementary file 4 for raw data for R-based analyses and actual R scripts.
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Sheila McCormickReviewing Editor; University of California-Berkeley, United States
In the interests of transparency, eLife includes the editorial decision letter and accompanying author responses. A lightly edited version of the letter sent to the authors after peer review is shown, indicating the most substantive concerns; minor comments are not usually included.
Thank you for submitting your article "Autocrine regulation of stomatal differentiation potential by EPF1 and ERECTA-LIKE1 ligand-receptor signaling" for consideration by eLife. Your article has been favorably evaluated by Christian Hardtke (Senior Editor) and three reviewers, one of whom, Sheila McCormick (Reviewer #1), is a member of our Board of Reviewing Editors. The following individual involved in review of your submission has agreed to reveal their identity: Eugenia Russinova (Reviewer #2).
The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.
This paper deals with the role of the secreted cysteine-rich peptide EPF1 in stomatal development. The authors present data supporting a negative feedback loop between ERL1 and MUTE. MUTE upregulates ERL1 expression and ERL1-mediated EPF1 signaling inhibits MUTE to specify the meristemoid-to-GMC transition switch. They further show that loss of EPF1-ERL1 signaling results in MUTE accumulation and stomatal development defects. The authors used an elegant combination of quantitative microscopy and genetic experiments to support this model. The work is novel, provides a function for EPF1 and is of interest to plant (and other) communities. Nonetheless, some aspects of the work are oversold. The authors need to improve the manuscript before publication in the following aspects:
1) Perform expression analyses to show that MUTE is induced after estradiol application and that this induction correlates with the increase and the decrease in expression of ERL1 and EPF1 respectively, hours after induction (Figure 2G and H). The same for the control treatment. Regarding Figure 3 and Figure 4; carry out expression analyses to show that EPF1 is induced after estradiol application. As in Figure 3D, they should also quantify the expression of pSCRM-GFP and SCRM-GFP fusion proteins in the nuclei and for the data presented in Figure 3—figure supplement 2 and Figure 4.
2) Provide information as to how the marker lines were generated (transformation or crossing), plant generation used, expression levels of the respective tagged proteins and background used (wild type, mutant). It is not always clear what was the genetic background used to express the tagged proteins, for example in Figure 2A, are ERL1-YFP and MUTE-tagRFP expressed in the Col-0 or erl1 background? Similarly for Figure 2E.
3) Fluorescently-tagged receptors are not always functional (sometimes they are only partially functional, for example BAK1, FLS2); therefore is important that the authors quantify the phenotypes of the rescued er erl1 erl2 triple mutant (Figure 5), in order to be more convincing that the ERL1-GFP fusion is functional (similar experiments were done for pMUTE::ERL1-YFP introduced in the er erl1 erl2 triple mutant). Also, the expression levels should be close to the endogenous, as even when using an endogenous promoter, overexpression of the transgene is frequently observed. Is the MUTE-GFP fusion functional?
4) TagRFP is a slowly maturing protein (100 min, in contrast to 10 min for GFP) and this might affect the co-localization dynamics shown in Figure 2A and B, Figure 5. Provide data or discuss this possibility.
5) It is not clear why MUTE-GFP in the scrm-D background was used for the ChIP assays and not MUTE-GFP in wild type. Is SCRM required for MUTE binding? Explain or discuss.https://doi.org/10.7554/eLife.24102.024
- Keiko U Torii
- Keiko U Torii
- Keiko U Torii
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We thank Tsuyoshi Nakagawa for the generous gift of Gateway cloning vectors; Lynn Pillitteri, Jin Suk Lee, Bob Kao, and Amanda Rychel for constructing the plasmids; Michal Maes for refolding Stomagen peptide; Kylee Peterson for assistance in genetic crosses and screening transgenic lines; University of Washington Chemistry Mass Spectrometry Facility for the Mass-spec analysis; Aarthi Putarjunan for commenting on the manuscript.
- Sheila McCormick, Reviewing Editor, University of California-Berkeley, United States
© 2017, Qi 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.