The patterning of the Arabidopsis root epidermis depends on a genetic regulatory network that operates both within and between cells. Genetic studies have identified a number of key components of this network, but a clear picture of the functional logic of the network is lacking. Here, we integrate existing genetic and biochemical data in a mathematical model that allows us to explore both the sufficiency of known network interactions and the extent to which additional assumptions about the model can account for wild-type and mutant data. Our model shows that an existing hypothesis concerning the autoregulation of WEREWOLF does not account fully for the expression patterns of components of the network. We confirm the lack of WEREWOLF autoregulation experimentally in transgenic plants. Rather, our modelling suggests that patterning depends on the movement of the CAPRICE and GLABRA3 transcriptional regulators between epidermal cells. Our combined modelling and experimental studies show that WEREWOLF autoregulation does not contribute to the initial patterning of epidermal cell fates in the Arabidopsis seedling root. In contrast to a patterning mechanism relying on local activation, we propose a mechanism based on lateral inhibition with feedback. The active intercellular movements of proteins that are central to our model underlie a mechanism for pattern formation in planar groups of cells that is centred on the mutual support of two cell fates rather than on local activation and lateral inhibition.
The patterning of the Arabidopsis root epidermis depends on a genetic regulatory network that operates within and between cells. Genetic studies have identified a number of key components of this network, but the functional logic of the network has remained unclear. In this work, we integrate genetic and biochemical data in a mathematical model that we use to explore both the sufficiency of known network interactions and the extent to which additional assumptions about the model can account for wild-type and mutant data. Our model shows that an existing hypothesis concerning the autoregulation of the transcription factor WEREWOLF does not account fully for observed expression patterns, and we confirm the absence of autoregulation experimentally in transgenic plants. We propose an alternative mechanism centred on the movement of transcriptional regulators between epidermal cells, and present experimental support for this mechanism. These movements underlie a novel mechanism for pattern formation in planar groups of cells, centred on mutual support of two cell fates rather than local activation and lateral inhibition.
Citation: Savage NS, Walker T, Wieckowski Y, Schiefelbein J, Dolan L, Monk NAM (2008) A Mutual Support Mechanism through Intercellular Movement of CAPRICE and GLABRA3 Can Pattern the Arabidopsis Root Epidermis. PLoS Biol 6(9): e235. doi:10.1371/journal.pbio.0060235
Academic Editor: Detlef Weigel, Max Planck Institute for Developmental Biology, Germany
Received: February 1, 2008; Accepted: August 18, 2008; Published: September 23, 2008
Copyright: © 2008 Savage et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by Human Frontier Science Project research grant RGP0012/2005 (to NAMM and LD) and the U.S. National Science Foundation grant IOS-0744599 (to JS).
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: LALI, local activation and lateral inhibition; LIF, lateral inhibition with feedback
The cells of the Arabidopsis root epidermis emerge from the initial cells in the root meristem with the potential to adopt either of two cell fates—trichoblasts (cells that can go on to differentiate as root hair cells) or atrichoblasts (that differentiate into non–hair-bearing epidermal cells). In the wild-type seedling, the two cell types are arranged in a stereotyped spatial pattern, with files of trichoblasts overlying two cortical cells (the H position) separated by files of atrichoblasts in contact with only one underlying cortical cell (the N position) (Figure 1) [1,2]. This fixed pattern does not result from lineage restriction, but depends on a combination of positional information from the cortex and the operation of a genetic regulatory network within the epidermis [3–5]. At the core of this network lie protein complexes centred on the basic helix-loop-helix proteins GLABRA3 (GL3) and ENHANCER OF GLABRA3 (EGL3) and the WD40-repeat–containing protein TRANSPARENT TESTA GLABRA (TTG). These proteins can bind to the MYB proteins WEREWOLF (WER) and CAPRICE (CPC) to form two protein complexes (the WER- and CPC-complexes, respectively).
The epidermis is the outer ring of large cells. Trichoblasts (marked by blue GUS staining) are located over the clefts between underlying cortical cells (the H position). Atrichoblasts (no staining) touch only one cortical cell (the N position). Note that trichoblasts are sometimes separated by more than one atrichoblast. This is a result of occasional anticlinal cell divisions in the epidermis, which increase the number of epidermal cells in a ring (newly formed epidermal rings in the apical meristem contain 16 cells).
Genetic and biochemical studies have highlighted a number of basic features of the epidermal interaction network. First, the WER-complex represses GL3/EGL3 transcription and enhances CPC transcription [6–8]. The CPC-complex is believed to lack transcriptional activity, but CPC has been reported to repress WER transcription . Second, the CPC and GL3 proteins exhibit striking mobility, moving freely between epidermal cells [9–11]. Third, the SCRAMBLED (SCM) receptor-like kinase is believed to play a role in the interpretation of a cortical signal that biases pattern formation by repressing WER transcription in the H position [12,13]. These network features have been proposed to underlie a pattern-forming mechanism based on lateral inhibition , but a detailed investigation of their sufficiency to account for experimental data has not been carried out. It has been suggested on theoretical grounds, however, that autoregulation of WER activity is necessary for epidermal pattern formation [14,15], although experimental support for this proposal is lacking . In this paper, we show by a combination of mathematical modelling and experimental studies that WER autoregulation does not play a significant role in the epidermal patterning network, and propose a mechanism for patterning that depends on the mutual support of the two epidermal cell fates.
Mathematical Representation of the Epidermal Patterning Network
We have developed a mathematical model representing the core epidermal interaction network, in order to investigate the regulatory logic of epidermal patterning. Our model seeks to capture all key interactions and protein movements identified in experimental studies (Figure 2). The nature of the regulation of WER transcription is central to our model. WER transcription is repressed by both SCM and CPC, but no specific activators of WER transcription have been identified. To address directly the open question of the necessity for WER autoregulation, we consider two alternative forms of WER regulation. In the first version, we assume local WER self-activation, implemented by the enhancement of WER transcription by WER-complex (Figures 2A and 3A). In this scenario, CPC down-regulates WER indirectly via competition for TTG/GL3/EGL3. In the second version, we do not include local WER self-activation, assuming instead that WER transcription is activated uniformly in all epidermal cells, with both CPC and SCM (in the H-position cells) repressing WER transcription directly (Figures 2B and 3B). We refer to the genetic regulatory network containing the first version of WER regulation as the “local WER self-activation model,” and the regulatory network containing the second version as the “mutual support model.”
Cell-nets are labelled j−1, j, j+1 according to their position in an epidermal ring (epi-net). mRNAs are represented by ellipses, and proteins by rectangles. All components of a cell-net are shown in cell-net j, but for clarity, only mobile proteins (and their corresponding mRNAs) are shown in cell-nets j−1 and j+1. Arrows between components represent regulatory interactions, with pointed and blunt ends representing activation and repression, respectively. The interactions that differ between the two networks are shown in red. The parameters ci determine the relative strengths of key interactions, and are shown alongside the arrows representing these interactions.
(A) The local WER self-activation model.
(B) The mutual support model.
(A) The local WER self-activation model.
(B) The mutual support model.
In order to focus more clearly on the core logic of the epidermal patterning network, the model incorporates a number of simplifying assumptions. First, since the expression pattern of TTG within the epidermis is not known, we assume that it is expressed uniformly and that it plays only a permissive role in allowing the formation of WER and CPC protein complexes with GL3/EGL3. On the basis of this assumption, we do not include an explicit TTG variable in our mathematical model. TTG is, however, present implicitly in all the cells of our model epidermis. Second, we do not include the CPC-complex explicitly in the model; rather, we represent the ability of CPC to compete with WER for binding to TTG/GL3/EGL3  by a direct inhibition of WER-complex formation by CPC. The CPC-complex is implicitly present in all model cells that express both CPC and GL3/EGL3. Third, GL3 and EGL3, which act in a partially redundant manner , are represented by a single network component. Similarly, the three MYB proteins CPC, TRIPTYCHON (TRY), and ENHANCER OF TRY AND CPC1 (ETC1), which act in a partially redundant manner , are also represented by a single network component (denoted by CPC).
In order to incorporate the observed intercellular movement of the CPC and GL3/EGL3 proteins, we have imposed a specific mechanism in our model: both CPC and GL3/EGL3 proteins are moved actively out of the cells in which they are produced (translated). We adopt this active mechanism to reflect the observed accumulation of these proteins in the nuclei of cells neighbouring the cells in which they are produced. A GL3-YFP fusion protein, expressed under the GL3 promoter in a gl3 mutant background, accumulates in the nuclei of N-position cells, even though the corresponding mRNA is restricted to H-position cells . Similarly, a HA-tagged CPC protein, expressed under the CPC promoter in a cpc mutant background, accumulates in the nuclei of H cells, even though its mRNA is restricted to N cells . A CPC-GFP fusion protein can be observed in the nuclei of both cell types [9,10]. However, this protein is expressed at much higher levels than the endogenous CPC protein (due perhaps to protein stabilisation) and causes numerous cells in the N position to adopt the trichoblast fate . These experimental results demonstrate that both CPC and GL3 proteins move away from their sites of production, but the mechanism by which they do this is not known. Given this uncertainty, we have incorporated in our model a simple movement scheme that captures the observed complementary patterns of protein production and accumulation. Possible molecular mechanisms underlying this scheme are discussed below.
We simulate a ring of 16 epidermal cells (which we refer to as the epi-net) following its emergence from the meristem. This represents the stereotypical number of cells found in each epidermal ring in the apical region of the seedling root in which patterning takes place [1,2]. As the cells age (and so move further away from the root apex), occasional anticlinal cell divisions can occur, increasing the number of cells in an epidermal ring [4,5] (the cross-section in Figure 1 shows an example of an older epidermal ring in which this has occurred). However, since we are here modelling the earliest stages of patterning in the epidermis, we do not consider these later events explicitly. Each simulated cell (referred to as a cell-net) contains all the components of the Arabidopsis root hair patterning network shown in Figure 2, and so in a simulated cell, any combination of components can be expressed, including the combinations specific to trichoblast or atrichoblast cells. Figure 3 shows the network state (expression of network components and active interactions) in cell-nets corresponding to epidermal cells that have adopted either a stable trichoblast or atrichoblast fate. The mechanistic differences between the local WER self-activation and mutual support models are clearly visible in Figure 3.
Since mechanistic details (such as rate laws and the corresponding kinetic parameters) of the epidermal interaction network are not known, a model based on differential equations would involve a large number of unknown parameters. Instead, we adopt a modelling framework that encodes the logical form of interactions. At a given time, the components of a cell-net are either expressed or not. Components that have only positive regulatory inputs (WER, GL3/EGL3, CPC, CPC, GL2, and GL2—see Figure 2) are expressed if their direct positive regulators are expressed. For example, if WER (mRNA) is expressed in a cell-net, then WER (protein) will be expressed. GL3/EGL3 has one negative input (the WER-complex) and is expressed if its input is not. To specify similar logical rules for the expression of the two components (WER and WER-complex) whose production is regulated by a combination of positive and negative regulators would involve making arbitrary assumptions about the dominance of activators or repressors (see Protocol S1). To avoid this, and to allow scope for investigating the effects of any assumptions we make about dominance, we adopt a stochastic formalism in which these components each have a time-evolving probability of expression. The probability of a component being expressed corresponds to the average abundance of that component in the cell. In our formalism, the change in probability over time is determined by the expression of the component's direct regulators and the corresponding activation/inhibition “rates” (which encode the relative strengths of the regulatory interactions). For example, the probability of the WER-complex being expressed is increased by a small amount if both GL3/EGL3 and WER are expressed, and decreased by a small amount if both GL3/EGL3 and CPC are expressed. The incorporation of stochasticity in our model not only increases the investigative scope, but also supplies a form of noise, which is an inherent feature of biological systems and is an integral part of cell differentiation. Furthermore, this stochasticity plays an important role in triggering fate assignment in our model of the scm mutant, which lacks positional cues from the cortical cells (see Protocol S1). However, the formalism that we adopt is not intended to provide a detailed representation of the stochastic nature of molecular dynamics in a cell. A detailed description of the modelling formalism and equations can be found in Materials and Methods.
Our stochastic Boolean formalism provides a versatile setting in which to investigate the effects of the relative strengths of combinatorial regulators for a specified regulatory logic. However, the results that we obtain from the model are not dependent on the use of this specific formalism. In particular, the behaviour of the model epidermis can be produced using Boolean models with appropriately chosen deterministic logical functions. In this case, the stochasticity needed to trigger patterning in the scm mutant epidermis can be introduced by adopting an asynchronous update scheme (see Protocol S1).
Simulation of Wild-Type and Mutant Epidermal Cell Fate Patterning
To assess the ability of the model networks to account for observed wild-type expression patterns, we simulated epi-nets in which all network components (except SCM) were initially expressed at the same level in all cells (i.e., all cell-nets are initially identical). To represent the positional bias received from the underlying cortex, SCM was set to be active only in cells located in the H position, resulting in a lower transcription rate of WER than in the N position. In an epi-net, H and N positions alternate: odd-numbered cell-nets are in the H position, while even-numbered cell-nets are in the N position (see Figure 4). With this imposed positional bias, both the local WER self-activation and mutual support models are capable of generating stable expression patterns that agree with the expression patterns observed in experimental data (Figure 4).
Time (in arbitrary units) is displayed on the vertical axis and cell position in the epidermal ring along the horizontal axis (the cells at the left- and right-hand ends are actually neighbours in the epidermal ring). For the two network components whose expression is probabilistic (WER mRNA and the WER-complex), the graphs show the probability of expression ranging from 0 (black) to 1 (green). All other components are either expressed (1) or not (0) at any given time. Odd-numbered cell-nets are in the H position, indicated by a dash on the bottom horizontal axis; even-numbered cell-nets are in the N position. Only CPC and GL3/EGL3 are expressed in cell-nets in the H position, in accordance with experimental data.
In scm mutant plants, experimental data show that epidermal cells adopt well-defined fates, but in a pattern that is not strictly correlated with position relative to the cortex [12,13]. To assess whether the model networks can also account for this phenotype, we set SCM to be inactive in all cells. In these simulations, the only patterning cues come from the stochasticity inherent in our modelling approach (we do not incorporate stochasticity in the initial conditions). Figure 5 shows a composite of the steady states resulting from 15 independent simulations in rings of cell-nets, aligned vertically to produce a virtual epidermis. However, it is important to note that such a picture does not represent the result of a full two-dimensional simulation, including aging and longitudinal signalling between cell rings. Both the local WER self-activation and mutual support models develop stable patterns in which each cell-net adopts a coherent state (either trichoblast or atrichoblast). For both models, the patterns produced are qualitatively comparable to those observed in scm mutant roots [12,13]. The total removal of cortical bias in our simulations may not be entirely equivalent to the situation pertaining in scm mutant roots, as the phenotypes of existing scm alleles suggest that some cortical positional information persists in these cases . However, our simulations show clearly that both forms of the epidermal patterning network are capable of spontaneous pattern formation, even in the absence of spatial bias. For both local WER self-activation and mutual support, the stochasticity in our modelling formalism acts to break symmetry allowing a spatially patterned state to emerge from a spatially uniform initial state.
The graphs show composites of the steady states resulting from 15 independent simulations in rings of cell-nets, aligned vertically to produce a virtual epidermis. Note that the layers in the simulations are independent (no “longitudinal” signalling or cell aging is included). As observed experimentally, each cell-net adopts a coherent set of expression levels, corresponding to either the trichoblast or atrichoblast fate, but the positions of the two cell fates are not strictly correlated with the H and N positions [12,13].
(A) The local WER self-activation model.
(B) The mutual support model.
To simulate the effect of other mutations, we set the corresponding cell-net components to be inactive in all cell-nets. Simulations of a wer mutation (unpublished data) result in identical expression patterns for both models, in agreement with experimental data (namely, the uniform expression of GL3/EGL3) [8,11,17]. We simulate WER overexpression by imposing uniform expression of both WER mRNA and WER protein throughout the epi-net. The epi-net steady states resulting from 15 independent simulations of the two versions of the epidermal patterning networks are shown in Figure 6. The expression pattern of all network components other than WER mRNA and WER are as in the simulated scm mutant (Figure 5), with each cell-net adopting a coherent state corresponding to either a trichoblast or atrichoblast. This mirrors the expression patterns reported in [8,14] and reflects the fact that WER, when overexpressed uniformly, is no longer able to respond to an imposed cortical bias.
As in Figure 5, the expression patterns for 15 independent simulations are shown.
(A) The local WER self-activation model.
(B) The mutual support model.
WEREWOLF Does Not Autoregulate during Epidermal Cell Fate Assignment
Figure 7 shows the expression of WER mRNA and WER protein in a simulated cpc mutant. Although both the local WER self-activation and mutual support models generate expression patterns for most network components that are in line with experimental data , they generate significantly different patterns of WER expression. In the local WER self-activation model (Figure 2A), the activation of WER expression by the WER-complex results in a wild-type pattern of WER expression even in the absence of CPC (Figure 7A, cf. Figure 4A). In contrast, the loss of CPC-mediated repression of WER in the mutual support model (Figure 2B) results in an increase in WER expression in the H positions, as it is only being repressed by SCM in the absence of CPC (Figure 7B). This corresponds to the pattern of WER expression observed experimentally . This result suggests that the mutual support model, which does not incorporate local WER self-activation, more accurately reflects events occurring during the patterning of the epidermis.
Other network components (not shown) have identical expression for both mechanisms.
(B) In the mutual support model of Figures 2B and 3B, the loss of CPC-mediated repression of WER results in an increase in WER expression in the H positions because it is only being repressed by SCM. This is also observed experimentally .
Since the local WER self-activation model fails to reproduce the observed pattern of WER expression in the cpc mutant, we tested the ability of the WER-complex (or WER) to enhance WER expression by examining the expression of GFP driven by the WER promoter (WERpro::GFP) in a wer mutant background (using a null mutant in which no functional WER protein is produced). We found GFP expression to be the same in wild type and the wer mutant, showing that WER transcription does not depend on the presence of functional WER protein (Figure 8A and 8B). To test directly our alternative assumption that WER transcription is activated uniformly in all epidermal cells, we carefully examined WER promoter activity (as visualised by WERpro::GFP) in wild-type seedlings. Whereas WERpro::GFP is preferentially expressed in the N cell file in less apical cells of the meristem, it exhibits uniform activity between N and H cell positions in cells proximal to the initials (Figure 8C). These results show that the initially uniform activity of the WER promoter throughout the epidermis resolves rapidly into a pattern matching that of WER transcription in wild-type roots even in the absence of WER protein. This strongly suggests that the establishment of patterned WER transcription—a key event in epidermal patterning—does not depend on local WER self-activation. Since the pattern of WER promoter activity in both wild-type and wer mutant roots corresponds to the wild-type pattern of cell fate in the epidermis, there is no obvious role for posttranscriptional regulation of WER activity (since posttranscriptional regulation of WER can only occur in cells in which WER is transcribed). Taken together, our modelling and experimental results show that WER is initially activated uniformly in the epidermis, and suggest that its rapid repression in emerging trichoblasts is controlled by a combination of SCM-mediated positional information and CPC.
(A and B) WERpro::GFP activity in wild-type (A) and wer mutant (B) backgrounds. The preferential activity of the WER promoter in N-position cell files (marked N) as opposed to H-position cell files (marked H) is maintained in the wer background. WT, wild type.
(C) WERpro::GFP activity in a H cell file in a wild-type root meristem. Near the apex of the root (bottom of the image), WER promoter activity is uniformly high throughout the epidermal rings. WER promoter activity gradually decreases in H position cells as they move away from the meristem.
To explore further the differences between the two model networks, we simulated mutants that are incapable of forming the WER-complex. Since GL3/EGL3 and TTG are required for complex formation, both the gl3 egl3 double mutant and the ttg mutant should lack WER-complex. In this scenario, the local WER self-activation and mutual support models predict different patterns of WER expression. In the local WER self-activation model, the failure of WER-complex formation results in a uniform loss of WER expression in the model epidermis (Figure 9A). However, since WER expression does not depend on local self-activation in the mutual support model, WER is expressed in an essentially wild-type pattern in the model epidermis (with an increased probability of expression in cells in the H position due to the lack of CPC-mediated repression) (Figure 9B). To test this prediction experimentally, we examined the expression of GFP driven by the WER promoter (WERpro::GFP) in these mutant backgrounds. As predicted by the mutual support model, GFP expression is essentially the same in the wild-type and mutant epidermis (Figure 10). This supports our finding that WER self-activation does not play a significant role in the early stages of epidermal patterning, and provides direct experimental validation of the predictions of the mutual support model of epidermal patterning.
Other network components (not shown) have identical expression patterns for both mechanisms.
(A) Local WER self-activation model (Figures 2A and 3A): Since WER is no longer up-regulated by the WER-complex (as the WER-complex cannot form in a gl3 egl3 double mutant), the probability of WER expression reduces to zero in all cells.
(B) Mutual support model (Figures 2B and 3B): In this mechanism, WER is up-regulated uniformly in all cell-nets, and down-regulated by CPC and SCM in cells in the H positions. However, as there is no WER-complex, there is no CPC, and so WER is down-regulated by SCM alone, resulting in patterned WER expression with an increased probability of expression in the H positions (compared to wild type). The magnitude of this increase depends on the relative strengths of WER down-regulation by CPC and SCM. This pattern mirrors the pattern of expression of GFP driven by the WER promoter shown in Figure 10.
The preferential activity of the WER promoter in N-position cell files (marked N) as opposed to H-position cell files (marked H) is maintained in both mutant backgrounds. No reduction in the level of promoter activity is observed in the mutant lines. WT, wild type.
Taken together, our modelling and experimental studies support a mechanism for spatial pattern formation in the Arabidopsis root epidermis that depends critically on the movement of mobile proteins between cells—a lateral inhibition with feedback (LIF) mechanism. Importantly, this mechanism does not depend on local WER self-activation, but relies instead on the repression of WER transcription in emerging trichoblasts by CPC protein. Previous theoretical discussions of epidermal patterning [14,15] have suggested that local WER self-activation is a necessary feature of the patterning network—a local activation and lateral inhibition (LALI) mechanism [18,19].
Although both the LALI and LIF mechanisms can generate similar stable patterns of cell fate, the logical structure of the underlying networks is quite different. LALI mechanisms depend on interlinked positive feedback (short range) and negative feedback (long range) whereas LIF depends on a single “double-negative” feedback loop, mediated by intercellular signalling, and does not depend on local self-activation. The logical structure of the LIF mechanism is analogous to the Delta-Notch signalling system in animal epithelia, in which proneural activity in one cell represses proneural activity in its neighbours through the transmembrane ligand Delta and its receptor Notch, ensuring directional signalling. Models of the Delta-Notch system exhibit spontaneous patterning that does not depend on any local self-activation [20,21].
In the LALI mechanism, the “activated” cell state (atrichoblast) inhibits its neighbours, which adopt an alternative fate (trichoblast). In contrast, in the LIF mechanism, cells adopting one of the two epidermal fates are mutually supporting, producing factors required by cells adopting the alternative fate. Adoption of the atrichoblast fate (high WER-complex) requires GL3/EGL3 from neighbouring cells; adoption of the trichoblast fate (low WER-complex) requires CPC from neighbouring cells (to prevent accumulation of WER-complex). In other words, a cell can only have high levels of WER-complex if a neighbouring cell has a low level of WER-complex and vice versa. This model therefore predicts that “runs” of three or more epidermal cells with similar levels of WER-complex should not occur. In the root apical meristem, where the early patterning of gene expression in the epidermis occurs, each ring of epidermal cells contains 16 cells, with alternating cells in H and N positions, as encoded in our model . We therefore observe a strict alternating pattern in our wild-type simulations that incorporate a positional bias from the cortex. In the simulated scm mutant, which lacks cortical bias, we do not observe more than two cells of the same fate neighbouring each other. In growing roots, the number of cells in an epidermal ring tends to increase as cells move away from the root apical meristem, due to occasional anticlinal cell divisions [4,5]. This is shown clearly in Figure 1, in which most H-position cells are separated by two N-position cells. In older epidermal rings, three or more adjacent cells are sometimes observed to have the same pattern of gene expression, which cannot be accounted for by our early patterning network in its current form. However, it is likely that once the basic pattern of expression of the core epidermal patterning components has been established, cell fate is stabilised by additional factors such as chromatin modification [23–25]. Such fate stabilisation mechanisms would allow cells to maintain their network state even when no longer supported by a neighbouring cell of the alternate fate.
We have shown by model simulation that the LALI mechanism (incorporating local WER self-activation) fails to account fully for the previously reported phenotype of a cpc mutant root, and by experiment that a specific form of local self-activation (WER-mediated up-regulation of WER transcription) does not operate in the early patterning of the root epidermis. Our combined modelling and experimental results favour an alternative mechanism (LIF) in which the two emerging cell fates mutually support each other through the active exchange of the mobile proteins CPC and GL3. The mutual support model predicts patterns of WER promoter activity in wer, gl3 egl3, and ttg mutant roots that are similar to wild type. We have verified these predictions experimentally, providing validation for the model and further support for our proposed patterning mechanism. Importantly, the model based on the LALI mechanism does not account for these new observations.
The mutual support model incorporates the active movement of the CPC and GL3 proteins from the cells in which they are produced to neighbouring cells. Such an active mechanism is suggested by the previously reported complementary patterns of production and accumulation of these proteins in the epidermis. We have adopted a modelling formalism based on binary states of expression (“on” or “off”). In this formalism, the patterning of the model epidermis depends on this active mechanism of protein movement. However, the possibility remains that the observed complementary patterns of protein production and accumulation could result from simple diffusion of the proteins between cells, together with sequestration of the proteins into nuclear-localised protein complexes (as occurs in the directed movement of the SHORTROOT protein in the root apical meristem ).
Previous theoretical discussions of epidermal patterning have proposed that local self-activation is a necessary feature of a patterning mechanism [14,15]. This conclusion is based on the theory of two-component activator–inhibitor models in which movement is purely diffusive. To explore the validity of this conclusion for the root epidermal patterning network, we have analysed two different mathematical representations of the mutual support model. First, we have developed a logical state (Boolean) model in which CPC and GL3 protein movement depends on a movement parameter, allowing both active and passive (diffusion-like) movement to be represented. Analysis of this model shows that passive GL3 movement is sufficient to account for patterning, so long as CPC moves actively (see Protocol S1). Second, we have developed a reaction–diffusion analogue of our logical model in which both GL3 and CPC move between cells by simple diffusion alone (see Protocol S1). When reduced to an effective two-component model for GL3 and CPC (by assuming that protein complex formation and WER dynamics reach equilibrium much faster than diffusive processes), we show that the model can take the form of a cross activator–inhibitor system, which is capable of spontaneous pattern formation via diffusion-driven instability . This analysis shows that the mutual support mechanism we propose can generate pattern spontaneously by diffusive protein movement and protein complex formation, in the absence of any local self-activation reaction. Numerical simulation of both the full and reduced models confirms that the diffusive mechanism generates stable patterns with protein distributions that match those observed in the root epidermis (see Protocol S1).
Our results serve to highlight the importance of a detailed investigation of the mechanisms of the intercellular movement of proteins such as CPC and GL3/EGL3 . A number of simple mechanisms might underlie an effective directionality of protein movement away from producing cells. For example, the movement of proteins through plasmodesmata could be dependent on a chaperone protein that is produced only in cells producing the mobile protein. Alternatively, passage through plasmodesmata could depend on localisation of the protein in the endoplasmic reticulum, which would favour movement away from the cells in which the protein is translated. An intriguing parallel is provided by the movement of small metabolites through small intercellular pores (microplasmodesmata) in the filamentous cyanobactoria Anabaena. A recent study has shown that the permeability of pores (and hence the mobility of metabolites) mirrors the states of differentiation of the two cell types in this system . In particular, as individual cells in the filament move towards a differentiated heterocyst fate, the permeability of pores between emerging heterocysts and neighbouring vegetative cells decreases compared to that between two vegetative cells. Thus, in this very different system, differential permeability of intercellular channels, dependent on cell fate, can establish spatially patterned protein distributions. The widespread occurrence of cell-to-cell trafficking of macromolecules in plant and animal tissues  suggests that mechanisms of the type we describe—centred on mobile proteins that can be sequestered in protein complexes—may play a role in a range of pattern-forming processes operating in planar groups of cells.
Materials and Methods
WERpro::GFP analysis in mutant roots.
The WERpro::GFP construct was previously reported in . Briefly, it included a 2.5-kb WER promoter fragment 5′ to the GFP coding sequence and a 1.1-kb 3′ WER fragment, and faithfully reported the WER transcription pattern. To examine the expression of WERpro::GFP in the wer, gl3 egl3, and ttg mutant backgrounds, we used the published wer allele, wer-1 , the gl3–1 egl3–1 line , and the ttg1–13 mutant . Plants homozygous for the WERpro::GFP insertion were crossed to plants homozygous for one of the mutant alleles. The resulting plants were self-pollinated, and F2 plants that were homozygous for the wer-1, gl3–1 egl3–1, or ttg1–12 mutations and the WERpro::GFP transgene were selected. These plants were in turn self-pollinated to produce a population of seed that were homozygous for the desired mutant allele and the WERpro::GFP transgene.
For confocal microscopy imaging, 4- or 5-d-old roots were stained with 10 μg/ml propidium iodide and visualised on a Leica TC5 SP confocal microscope. Images were assembled using Adobe Photoshop.
Mathematical formalism—epidermal patterning network.
In our models, a ring of 16 epidermal cells (the stereotypical number found in the apical region of the seedling root in which patterning takes place) is represented by an epi-net comprising 16 identically composed cell-nets, indexed by the integer j = 1, 2, …, 16. The set of components in each cell-net, together with their interactions, is shown schematically in Figure 2. In the mathematical model, the state of mRNAs is represented by the corresponding gene name abbreviation (for example, CPCtj represents the state of CPC mRNA at time t in cell-net j). The state of the corresponding protein carries an appended “p” (for example, WERptj represents the state of WER protein at time t in cell-net j). The state of the WER-complex is denoted by WERc. In order to capture what we believe to be the essential logic of the epidermal patterning network, while keeping the number of distinct molecular species in the model to a minimum, a number of known network components have been left out of the model, or combined into a single model variable. Both GL3 and EGL3 are represented jointly by a single model element GL3 (comprising variables for mRNA and protein). We justify this simplification by noting that all published data suggest that GL3 and EGL3 are regulated similarly and exhibit functional redundancy. Similarly, we represent the three single-repeat R3 MYB proteins CPC, TRIPTYCHON (TRY), and ENHANCER OF TRY AND CPC1 (ETC1) by a single model element CPC, since experimental evidence supports the idea that they act collectively and redundantly to specify the trichoblast fate . Furthermore, in the absence of experimental data to the contrary, we assume that the WD-repeat protein TRANSPARENT TESTA GLABRA (TTG), an essential component of the WER-complex, is expressed uniformly throughout the epidermis. This assumption renders the explicit representation of TTG in the models unnecessary, and our models do not contain TTG variables (although the protein is implicitly assumed to be present in all cells).
To investigate the patterning potential of the local WER self-activation and mutual support models (Figure 2), we use a discrete-time logical formalism. In this approach, the state of each network component is represented by a binary variable taking either value 1 (component expressed) or 0 (not expressed). Time evolution of the network state is modelled by the synchronous update of the state of each network component at equally spaced time points (t, t+1, t+2, …). For the network components whose state is regulated by only one other component type (WERp, GL3, GL3p, CPC, or CPCp), we adopt a conventional deterministic Boolean update formalism . For the two components whose state is regulated by more than one input (WER and WERc), we adopt a novel formalism based on the probability Ptj[X] that the state of component Xtj will be 1 at time t. Rather than specifying a deterministic function for the time evolution of the states of these components, we instead specify a deterministic rule for the time evolution of the probability of expression. This form of update allows us both to vary the relative strengths of the inputs and to incorporate stochasticity in the update process. Although this approach directly introduces stochasticity into the evolution equations of only two network variables, the stochasticity filters through to the other components. Thus, whereas all components could be represented probabilistically, this would necessitate the introduction of many more undetermined parameters without adding further functionality to the model. In a simulation of the network, the actual values (0 or 1) of WERtj and WERctj are determined stochastically at each time step according to the probability of expression, P tj[WER] and P tj[WERc].
The parameters in our probabilistic update functions (see below) allow us to explore the robustness of patterning to changes in the relative strengths of the inputs. Furthermore, the incorporation of stochasticity into the system is important, since stochasticity is an inherent feature of biological networks and is required in our models to initiate patterning in the simulated scm mutant. However, our approach does not attempt to mimic any specific form of stochasticity found in biological systems, and we have shown that the results obtained using our probabilistic formalism can be reproduced by using a deterministic Boolean model with stochasticity introduced in the form of asynchronous state update (see Protocol S1).
Our probabilistic Boolean formalism provides a simple way of exploring the consequences of specific assumptions about the regulatory logic of the epidermal patterning network. However, the use of a logical (on/off) representation of the network state assumes that the regulatory interactions represented in the model (e.g., transcription and translation) are essentially “all or nothing.” Since our primary objective is to explore the differences between two alternative network structures, we believe that this assumption is appropriate. Other approaches to modelling regulatory networks, such as those based on differential equations, do not depend on such an assumption being made. However, these models require the specification of many more parameters than our model, to represent the details of specific interaction kinetics. Such models can provide more-realistic representations of the dynamical evolution of the state of the network. Given that there are currently no data, either from which appropriate parameters can be specified, or against which detailed network dynamics can be validated, we do not believe that these approaches currently have a significant advantage over our logical formalism.
The local WER self-activation and mutual support models are defined in Equations (1) and (2), respectively. The models are identical apart from the equation encoding the time-evolution of WER mRNA. The symbol ∨ represents the logical “inclusive OR” function (i.e., A∨B = 0 if and only if A = B = 0). c0, c1,...c5, are positive parameters that determine the relative strengths of the inputs in the probabilistic multi-input update functions for WER and WERc (Figure 2). The constant terms c1 and c5 represent either constitutive production or degradation, depending on their preceding signs. The regulatory inputs to WER and WERc specify the amount by which the probability of expression of these components changes during a single time step. This form of update rule is similar to the rate equations that form the basis of differential equation models (in which the rate of change of a component is determined by the values of its direct regulators). Values within the brackets ⌊ ⌋ are forced to remain between 0 and 1.
A positional bias from the underlying cortex is incorporated in the models via the state of the SCRAMBLED (SCM) receptor-like kinase, which is taken to be 1 in cell nets occupying the H position and 0 in cell-nets occupying the N position. Activity of SCM results in a reduction in the rate of transcription of WER, determined by the parameter c0. We assume the two positions to be arranged alternately, as is typically the case in the apical root epidermis (anticlinal cell divisions in the epidermis, which can increase the spacing between H-position cells, typically occur further from the meristem, where the expression pattern of network components has already stabilised).
The initial state of all components, bar SCM (see above), is identical in all cell-nets, representing the fact that the final stable state of each cell-net is determined by its position relative to the underlying cortical cells rather than cell lineage. As the state of each cell-net evolves in time, the cell-nets adopt stable patterns of expression corresponding to either the trichoblast or atrichoblast cell fate (Figure 4). A detailed discussion of the dependence of the behaviour of the models on initial conditions and parameter values can be found in Protocol S1.
Protocol S1. Protocol S1 Contains Parameter and Initial Condition Analysis of the Mathematical Models, and Details of a Reaction–Diffusion Model for Epidermal Patterning
This file includes nine supporting figures and four supporting tables.
NSS, TW, JS, LD, and NAMM conceived and designed the experiments. NSS, TW, YW, and NAMM performed the experiments. NSS and NAMM analyzed the data. NSS, LD, and NAMM wrote the paper.
- 1. Dolan L, Duckett MD, Grierson C, Linstead P, Schneider K, et al. (1994) Clonal relationships and cell patterning in the root epidermis of Arabidopsis. Development 120: 2465–2474.
- 2. Galway ME, Masucci JD, Lloyd AM, Walbot V, Davis RW, et al. (1994) The TTG gene is required to specify epidermal cell fate and cell patterning in the Arabidopsis root. Dev Biol 166: 740–754.
- 3. Dolan L (2006) Positional information and mobile transcriptional regulators determine cell pattern in the Arabidopsis root epidermis. J Exp Bot 57: 51–54.
- 4. Berger F, Haseloff J, Schiefelbein J, Dolan L (1998) Positional information in plants is defined during embryogenesis and acts throughout plant life as domains with strict boundaries. Curr Biol 8: 421–430.
- 5. Kidner C, Sundaresan V, Roberts K, Dolan L (2000) Clonal analysis of the Arabidopsis root confirms that position, not lineage, determines cell fate. Planta 211: 191–199.
- 6. Koshino-Kimura Y, Wada T, Tachibana T, Tsugeki R, Ishiguro S, et al. (2005) Regulation of CAPRICE transcription by MYB proteins for root epidermis differentiation in Arabidopsis. Plant Cell Physiol 46: 817–826.
- 7. Ryu KH, Kang YH, Park Y, Hwang I, Schiefelbein J, et al. (2005) The WEREWOLF MYB protein directly regulates CAPRICE transcription during cell fate specification in Arabidopsis root epidermis. Development 132: 4765–4775.
- 8. Lee MM, Schiefelbein J (2002) Cell pattern in the Arabidopsis root epidermis determined by lateral inhibition with feedback. Plant Cell 14: 611–618.
- 9. Wada T, Kurata T, Tominaga R, Koshino-Kimura Y, Tachibana T, et al. (2002) Role of a positive regulator of root hair development, CAPRICE, in Arabidopsis root epidermal cell differentiation. Development 129: 5409–5419.
- 10. Kurata T, Ishida T, Kawabata-Awai C, Noguchi M, Hattori S, et al. (2005) Cell-to-cell movement of the CAPRICE protein in Arabidopsis root epidermal cell differentiation. Development 132: 5387–5389.
- 11. Bernhardt C, Zhao M, Gonzalez A, Lloyd A, Schiefelbein J (2005) The bHLH genes GL3 and EGL3 participate in an intercellular regulatory circuit that controls cell patterning in the Arabidopsis root epidermis. Development 132: 291–298.
- 12. Kwak S, Shen R, Schiefelbein J (2005) Positional signaling mediated by a receptor-like kinase in Arabidopsis. Science 307: 1111–1113.
- 13. Kwak S, Schiefelbein J (2006) The role of the SCRAMBLED receptor-like kinase in patterning the Arabidopsis root epidermis. Dev Biol 302: 118–131.
- 14. Pesch M, Hülskamp M (2004) Creating a two-dimensional pattern de novo during Arabidopsis trichome and root hair patterning. Curr Opin Genet Dev 14: 422–427.
- 15. Benítez M, Espinosa-Soto C, Padilla-Longoria P, Díaz J, Alvarez-Buylla ER (2007) Equivalent genetic regulatory networks in different contexts recover contrasting spatial cell patterns that resemble those in Arabidopsis root and leaf epidermis: a dynamic model. Int J Dev Biol 51: 139–155.
- 16. Esch JJ, Chen M, Sanders M, Hillestad M, Ndkium S, et al. (2003) A contradictory GLABRA3 allele helps define gene interactions controlling trichome development in Arabidopsis. Development 130: 5885–5894.
- 17. Kirik V, Simon M, Hülskamp M, Schiefelbein J (2004) The ENHANCER OF TRY AND CPC1 gene acts redundantly with TRIPTYCHON and CAPRICE in trichome and root hair cell patterning in Arabidopsis. Dev Biol 268: 506–513.
- 18. Gierer A, Meinhardt H (1972) A theory of biological pattern formation. Kybernetic 12: 30–39.
- 19. Oster GF (1988) Lateral inhibition models of developmental processes. Math Biosci 90: 265–286.
- 20. Collier JR, Monk NAM, Maini PK, Lewis J (1996) Pattern formation by lateral inhibition with feedback: a mathematical model of Delta-Notch intercellular signalling. J Theor Biol 183: 429–446.
- 21. Meir E, von Dassow G, Munro E, Odell GM (2002) Robustness, flexibility, and the role of lateral inhibition in the neurogenic network. Curr Biol 12: 778–786.
- 22. Dolan L, Janmaat K, Willemsen V, Linstead P, Poethig S, et al. (1993) Cellular organisation of the Arabidopsis thaliana root. Development 119: 71–84.
- 23. Xu C, Liu C, Wang Y, Li L, Chen W, et al. (2005) Histone acetylation affects expression of cellular patterning genes in the Arabidopsis root epidermis. Proc Natl Acad Sci U S A 102: 14469–14474.
- 24. Costa S, Shaw P (2006) Chromatin organization and cell fate switch respond to positional information in Arabidopsis. Nature 439: 493–496.
- 25. Caro E, Castellano MM, Gutierrez C (2007) A chromatin link that couples cell division to root epidermis patterning in Arabidopsis. Nature 447: 213–217.
- 26. Cui H, Levesque MP, Vernoux T, Jung JW, Paquette AJ, et al. (2007) An evolutionarily conserved mechanism delimiting SHR movement defines a single layer of endodermis in plants. Science 316: 421–425.
- 27. Murray JD (2003) Mathematical biology, 3rd edition. Volume 2. New York: Springer. pp. 82–90.
- 28. Jorgensen RA (2000) Directed cell-to-cell movement of functional proteins: do transcription factors double as signalling molecules in plants. Sci STKE 2000: PE2.
- 29. Mullineaux CW, Mariscal V, Nenninger A, Khanum H, Herrero A, et al. (2008) Mechanism of intercellular molecular exchange in heterocyst-forming cyanobacteria. EMBO J 27: 1299–1308.
- 30. Gallagher KL, Benfey PN (2005) Not just another hole in the wall: understanding intercellular protein trafficking. Genes Dev 19: 189–195.
- 31. Lee MM, Schiefelbein J (1999) WEREWOLF, a MYB-related protein in Arabidopsis, is a position-dependent regulator of epidermal cell patterning. Cell 99: 473–483.
- 32. Kauffman SA (1969) Metabolic stability and epigenesis in randomly constructed genetic nets. J Theor Biol 22: 437–467.