Guard Mother Cells Research Articles

ABA inhibits entry into stomatal‐lineage development in Arabidopsis leaves

The number and density of stomata are controlled by endogenous and environmental factors. Despite recent advances in our understanding of stomatal development, mechanisms which prevent stomatal-lineage entry remain unclear. Here, we propose that abscisic acid (ABA), a phytohormone known to induce stomatal closure, limits initiation of stomatal development and induces enlargement of pavement cells in Arabidopsis cotyledons. An ABA-deficient aba2-2 mutant had an increased number/proportion of stomata within a smaller cotyledon, as well as reduced expansion of pavement cells. This tendency was reversed after ABA application or in an ABA over-accumulating cyp707a1cyp707a3 doublemutant. Our time course analysis revealed that aba2-2 shows prolonged formation of meristemoids and guard mother cells, both precursors of stoma. This finding is in accordance with prolonged gene expression of SPCH and MUTE, master regulators for stomatal formation, indicating that ABA acts upstream of these genes. Only aba2-2 mute, but not aba2-2 spch double mutant showed additive phenotypes and displayed inhibition of pavement cell enlargement with increased meristemoid number, indicating that ABA action on pavement cell expansion requires the presence of stomatal-lineage cells.

A Dof Transcription Factor, SCAP1, Is Essential for the Development of Functional Stomata in Arabidopsis

Stomata are highly specialized organs that consist of pairs of guard cells and regulate gas and water vapor exchange in plants [1-3]. Although early stages of guard cell differentiation have been described [4-10] and were interpreted in analogy to processes of cell type differentiation in animals [11], the downstream development of functional stomatal guard cells remains poorly understood. We have isolated an Arabidopsis mutant, stomatal carpenter 1 (scap1), that develops irregularly shaped guard cells and lacks the ability to control stomatal aperture, including CO2-induced stomatal closing and light-induced stomatal opening. SCAP1 was identified as a plant-specific Dof-type transcription factor expressed in maturing guard cells, but not in guard mother cells. SCAP1 regulates the expression of genes encoding key elements of stomatal functioning and morphogenesis, such as K(+) channel protein, MYB60 transcription factor, and pectin methylesterase. Consequently, ion homeostasis was disturbed in scap1 guard cells, and esterification of extracellular pectins was impaired so that the cell walls lining the pores did not mature normally. We conclude that SCAP1 regulates essential processes of stomatal guard cell maturation and functions as a key transcription factor regulating the final stages of guard cell differentiation.

Antagonistic regulation of the meristemoid-to-guard mother-cell-transition.

The building of a multicellular organism from a single cell is the result of coordinated acquisition of different cell identities in an ordered spatial arrangement. But, how do cells learn about their identity? Stomatal development in Arabidopsis provides perhaps one of the most tractable contexts in which to examine concepts of cell fate determination, as a variety of lineage tracing techniques, including long-term confocal time lapse imaging (Peterson and Torii, 2012), can be deployed in different genetic contexts and environmental conditions to trace the history of only a few cell types. In this essay, I focus on the choice between meristemoid cell self-renewal, in which one of daughters of a dividing meristemoid retains the properties of the parent cell, and its transition through guard mother cell (GMC) fate to produce stomata.

Polarization of Subsidiary Cell Division in Maize Stomatal Complexes

Stomatal development is a useful model to study division asymmetry in plants ([Facette and Smith, 2012][1]). In maize ( Zea mays ), the stomatal complex consists of a pair of guard cells bracketed by a pair of subsidiary cells, which help regulate aperture size. The guard mother cell (GMC) is

Identification of PAN2 by quantitative proteomics as a leucine-rich repeat-receptor-like kinase acting upstream of PAN1 to polarize cell division in maize.

Mechanisms governing the polarization of plant cell division are poorly understood. Previously, we identified pangloss1 (PAN1) as a leucine-rich repeat-receptor-like kinase (LRR-RLK) that promotes the polarization of subsidiary mother cell (SMC) divisions toward the adjacent guard mother cell (GMC) during stomatal development in maize (Zea mays). Here, we identify pangloss2 (PAN2) as a second LRR-RLK promoting SMC polarization. Quantitative proteomic analysis identified a PAN2 candidate by its depletion from membranes of pan2 single and pan1;pan2 double mutants. Genetic mapping and sequencing of mutant alleles confirmed the identity of this protein as PAN2. Like PAN1, PAN2 has a catalytically inactive kinase domain and accumulates in SMCs at sites of GMC contact before nuclear polarization. The timing of polarized PAN1 and PAN2 localization is very similar, but PAN2 acts upstream because it is required for polarized accumulation of PAN1 but is independent of PAN1 for its own localization. We find no evidence that PAN2 recruits PAN1 to the GMC contact site via a direct or indirect physical interaction, but PAN2 interacts with itself. Together, these results place PAN2 at the top of a cascade of events promoting the polarization of SMC divisions, potentially functioning to perceive or amplify GMC-derived polarizing cues.

The development of stomata and other epidermal cells on the rice leaves

In the leaves of rice (Oryza sativa), stomatal initials arose from two asymmetric cell divisions and a symmetric division. Guard mother cells (GMCs) and long cells in stomatal files (LCSs) were formed through the first asymmetric division of the precursor cell of GMCs. Subsidiary cells (SCs) were produced by the second asymmetric division of subsidiary mother cells or LCSs. Following SC formation, GMCs divided once symmetrically to generate guard cells and then differentiated terminally to form mature stomata. The developmental patterns of long cells, prickle hairs and short cells (phellem cells and silica cells) were also examined. Interestingly, we found that the different developmental stages of stomata and epidermal cells occurred in the similar location of immature leaves of the same phyllotaxis. In addition, two spacing patterns ("one stoma, one long cell" and "one short cell row") probably exist in rice leaves.

Sequence and function of basic helix-loop-helix proteins required for stomatal development in Arabidopsis are deeply conserved in land plants.

Stomata are a broadly conserved feature of land plants with a crucial role regulating transpiration and gas exchange between the plant and atmosphere. Stereotyped cell divisions within a specialized cell lineage of the epidermis generate stomata and define the pattern of their distribution. The behavior of the stomatal lineage varies in its detail among different plant groups, but general features include asymmetric cell divisions and an immediate precursor (the guard mother cell [GMC]) that divides symmetrically to form the pair of cells that will differentiate into the guard cells. In Arabidopsis, the closely related basic helix-loop-helix (bHLH) subgroup Ia transcription factors SPEECHLESS, MUTE, and FAMA promote asymmetric divisions, the acquisition of GMC identity and guard cell differentiation, respectively. Genome sequence data indicate that these key positive regulators of stomatal development are broadly conserved among land plants. While orthologies can be established among individual family members within the angiosperms, more distantly related groups contain subgroup Ia bHLHs of unclear affinity. We demonstrate group Ia members from the moss Physcomitrella patens can partially complement MUTE and FAMA and recapitulate gain of function phenotypes of group Ia genes in multiple steps in the stomatal lineage in Arabidopsis. Our data are consistent with a mechanism whereby a multifunctional transcription factor underwent duplication followed by specialization to provide the three (now nonoverlapping) functions of the angiosperm stomatal bHLHs.

Plant cell biology. From astronomy to zoology

Plant cell biology. From astronomy to zoology

A view from the top: new ligands controlling stomatal development in Arabidopsis

A view from the top: new ligands controlling stomatal development in Arabidopsis

BASL and EPF2 act independently to regulate asymmetric divisions during stomatal development

The initiation of stomatal development in the developing Arabidopsis epidermis is characterized by an asymmetric ‘entry’ division in which a small cell, known as a meristemoid, and a larger daughter cell is formed. The meristemoid may undergo further asymmetric divisions, regenerating a meristemoid each time, before differentiating into a guard mother cell which divides symmetrically to form a pair of guard cells surrounding a stomatal pore. Recently EPF2 and BASL have emerged as regulators of these asymmetric divisions and here we present results indicating that these two factors operate independently to control stomatal development.

The Signaling Peptide EPF2 Controls Asymmetric Cell Divisions during Stomatal Development

Stomata are pores in the plant epidermis that control carbon dioxide uptake and water loss. They are major regulators of global carbon and water cycles [1]. Several signaling components that regulate stomatal development have been characterized. These include a putative secretory peptide EPF1, LRR receptor components TMM and ER, and a peptidase SDD1 [2-4]. We have identified EPF2, a peptide related to EPF1 that is expressed in proliferating cells of the stomatal lineage, known as meristemoids, and in guard mother cells, the progenitors of stomata. EPF2 expression during leaf development affects stomatal density on the mature leaf. In the absence of EPF2, excessive numbers of cells enter the stomatal lineage and produce numerous small epidermal cells that express stomatal lineage reporter genes, whereas plants overexpressing EPF2 produce virtually no stomata. Results from genetic experiments indicate that EPF2 regulates a different aspect of stomatal development to EPF1 and are consistent with EPF2 acting in a pathway to regulate stomatal density that involves ER and TMM, but not SDD1. We propose that EPF2 is expressed earlier in leaf development than EPF1 and is involved in determining the number of cells that enter, and remain in, the stomatal lineage.

Asymmetric Division in Plant Development

In plants, as in other multicellular eukaryotes, asymmetric divisions are used to generate pattern and diversity during development. Asymmetric divisions must be oriented properly within their developmental context, but very little is known about how this is accomplished in plants. Plants lack proteins universally employed for polarization of asymmetric cell divisions in animals and pathways involved in orienting animal cell polarity. About 50 years ago, it was proposed, based on observations of cell division patterns in developing grass leaves, that the asymmetric divisions of subsidiary mother cells, which give rise to subsidiary cells of the stomatal complex, are polarized by the adjacent guard mother cell, the precursor of stomatal guard cells. Cartwright et al . (see the Perspective by Sack and Chen) implicate a receptor-like protein, PAN1, in transmission of a guard mother cell–derived signal that polarizes subsidiary mother cells in preparation for their asymmetric division. Thus, asymmetric cell division can be polarized in response to an extracellular cue in plants. H. N. Cartwright, J. A. Humphries, L. G. Smith, PAN1: A receptor-like protein that promotes polarization of an asymmetric cell division in maize. Science 323 , 649–651 (2009). [Abstract][Full Text] F. D. Sack, J.-G. Chen, Pores in place. Science 323 , 592–593 (2009). [Summary][Full Text]

A Receptor-Like Protein That Promotes Polarization of an Asymmetric Cell Division in Maize

Polarization of cell division is essential for eukaryotic development, but little is known about how this is accomplished in plants. The formation of stomatal complexes in maize involves the polarization of asymmetric subsidiary mother cell (SMC) divisions toward the adjacent guard mother cell (GMC), apparently under the influence of a GMC-derived signal. We found that the maize pan1 gene promotes the premitotic polarization of SMCs and encodes a leucine-rich repeat receptor-like protein that becomes localized in SMCs at sites of GMC contact. PAN1 has an inactive kinase domain but is required for the accumulation of a membrane-associated phosphoprotein, suggesting a function for PAN1 in signal transduction. Our findings implicate PAN1 in the transmission of an extrinsic signal that polarizes asymmetric SMC divisions toward GMCs.

TOO MANY MOUTHS promotes cell fate progression in stomatal development of Arabidopsis stems

Mutations in TOO MANY MOUTHS (TMM), which encodes a receptor-like protein, cause stomatal patterning defects in Arabidopsis leaves but eliminate stomatal formation in stems. Stomatal development in wild-type and tmm stems was analyzed to define TMM function. Epidermal cells in young tmm stems underwent many asymmetric divisions characteristic of entry into the stomatal pathway. The resulting precursor cells, meristemoids, appropriately expressed cell fate markers such as pTMM:GFP. However, instead of progressing developmentally by forming a guard mother cell, the meristemoids arrested, dedifferentiated, and enlarged. Thus asymmetric divisions are necessary but not sufficient for stomatal formation in stems, and TMM promotes the fate and developmental progression of early precursor cells. Comparable developmental and mature stomatal phenotypes were also found in tmm hypocotyls and in the proximal flower stalk. TMM is also a positive regulator of meristemoid division in leaves suggesting that TMM generally promotes meristemoid activity. Our results are consistent with a model in which TMM interacts with other proteins to modulate precursor cell fate and progression in an organ and domain-specific manner. Finally, the consistent presence of a small number of dedifferentiated meristemoids in mature wild-type stems suggests that precursor cell arrest is a normal feature of Arabidopsis stem development.

Ontogenesis of stomata in Velloziaceae: paracytic versus tetracytic?

In Velloziaceae, the number of subsidiary cells has been used to characterize species and support groups. Nevertheless, the homology of the stomatal types have not been scrutinized. Stomatal ontogenesis of Vellozia epidendroides and V. plicata, assigned to have tetracytic stomata, and of V. glauca and Barbacenia riparia, assigned to have paracytic stomata, were investigated. In the four species studied, stomata followed perigenic development. Subsidiary cells arise from oblique divisions of neighbouring cells of the guard mother cell (GMC). These cells are elongated and parallel to the longer axis of the stoma. Polar cells show wide variation, following the shape and size of the epidermal cells in the vicinity. Hence, these cells cannot be called subsidiary cells. This wide variation is due to a much higher density of stomata in some regions of the leaf blade. This distribution of stomata forces the development of short polar cells, leading to an apparently tetracytic stomata. In regions of low concentration of stomata, higher spatial availability between the GMCs allows the elongation of polar cells, leading to evident paracytic stomata. Therefore, the four studied species are considered braquiparacytic, questioning the classification of stomata into tetracytic and paracytic in Velloziaceae.

The bHLH Protein, MUTE, Controls Differentiation of Stomata and the Hydathode Pore in Arabidopsis

Stomata are turgor-driven epidermal valves on the surface of plants that allow for efficient gas and water exchange between the plant and its environment. The Arabidopsis thaliana basic helix-loop-helix (bHLH) protein, MUTE, is a master regulator of stomatal differentiation where it is required for progression through the stomatal lineage and the differentiation of stomata. The genetic control of stomatal spacing across the epidermal surface is variable in different organs. For instance, a distinct suite of genes from those in leaves regulates stomatal patterning in hypocotyls. Here we report that regardless of organ type, MUTE controls downstream events directing stomatal differentiation, specifically the transition from meristemoid to guard mother cell. Ectopic MUTE expression is sufficient to over-ride cell fate specification in cell types that do not normally differentiate stomata. Furthermore, MUTE is required for the production of the structure evolutionarily related to stomata, the hydathode pore. Consistently, MUTE displays expression at the tip of cotyledons and leaves, thus co-localizing with the auxin maxima. However, MUTE itself was not regulated by the auxin, and the absence of hydathode pores in mute did not affect the auxin maxima. Surprisingly, our analysis revealed that the requirement for MUTE could be partially circumvented under conditions of compromised inhibitory signaling.

Evaluating the effects of stomata development and senescence on the seasonal variation in stomatal conductance

We examined the influence of phenological changes in stomata on the seasonal variation of stomatal conductance using a Jarvis-type conductance model that included functions representing the active stomatal density and chlorophyll concentration of leaves. We studied the leaves of three 12-year-old oak trees (Quercus serrata). Stomatal conductance was measured under controlled ambient conditions (i.e., photosynthetic photon flux density, leaf temperature, and specific humidity deficit) in a chamber. Our analyses showed that low stomatal conductance could not be explained by environmental variables alone. Stomatal conductance decreased with increasing stomatal density, where the number of stomata included guard mother cells (GMC), in spring. On the other hand, time series of stomatal conductance showed a correlation with the increases in active stomatal density. Chlorophyll concentration was a good index of the low conductance in autumn, and the active stomata density was a good index of the leaf-unfolding period. These results implied that phenological progress of stomata must be included in land surface models for the accurate prediction of seasonal variations in water, energy, and CO2 cycles.

Stomatal Development

Stomata are microscopic pores on the plant epidermis that act as a major passage for the gas and water vapor exchange between a plant and the atmosphere. A pair of specialized guard cells works in concert to adjust pore size to maintain gas exchange while minimizing the water loss. The formation of stomata requires a series of cell-fate transitions from an initial meristemoid mother cell (MMC), to a stem-cell-like precursor meristemoid, to a guard mother cell (GMC), and finally to terminally-differentiated guard cells. Three closely-related Arabidopsis basic helix-loop-helix (bHLH) genes SPEECHLESS (SPCH), MUTE, and FAMA act sequentially at each key step to direct cell-fate transitions during stomatal development. In this addendum, we propose that a three-step relay of the three bHLHs establishes the molecular framework for stomatal differentiation. Specific expression patterns as well as protein domain structure and dimerization partners of each stomatal bHLH protein may determine the specific function as a key switch in each regulatory node.

Plant Development: Three Steps for Stomata

Three basic helix-loop-helix proteins regulate sequential steps in the formation of stomata: SPEECHLESS initiates entry into the stomatal lineage; MUTE controls asymmetric divisions of stomatal precursor cells; and FAMA promotes guard cell differentiation.

Cytoskeletal asymmetry in Zea mays subsidiary cell mother cells: A monopolar prophase microtubule half‐spindle anchors the nucleus to its polar position

Double labeling of microtubules and actin filaments revealed that in prophase subsidiary mother cells of Zea mays a monopolar prophase microtubule "half-spindle" is formed, which lines the nuclear hemisphere distal to the inducing guard mother cell. The nuclear hemisphere proximal to the guard mother cell is lined by an F-actin cap, consisting of a cortical F-actin patch and actin filaments originating from it. The microtubules of the "half-spindle" decline from the nuclear surface and terminate to the preprophase microtubule band. After disintegration of the latter, a bipolar metaphase spindle is organized. The polar F-actin cap persists during mitosis and early cytokinesis, extending to the chromosomes and the subsidiary cell daughter nucleus. In oryzalin treated subsidiary mother cells the prophase nuclei move away from the polar site. Cytochalasin B and latrunculin-B block the polar migration of subsidiary mother cell nuclei, but do not affect those already settled to the polar position. The prophase nuclei of latrunculin-B treated subsidiary mother cells are globally surrounded by microtubules, while the division plane of latrunculin-B treated subsidiary mother cells is misaligned. The prophase nuclei of brick 1 mutant Zea mays subsidiary mother cells without F-actin patch are also globally surrounded by microtubules. The presented data show that the prophase microtubule "half-spindle"-preprophase band complex anchors the subsidiary mother cell nucleus to the polar cell site, while the polar F-actin cap stabilizes the one metaphase spindle pole proximal to the inducing guard mother cell.