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Control of Stomatal Distribution on the Arabidopsis Leaf Surface

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Science  31 May 2002:
Vol. 296, Issue 5573, pp. 1697-1700
DOI: 10.1126/science.1069596

Abstract

Stomata regulate gas exchange and are distributed across the leaf epidermis with characteristic spacing. Arabidopsisstomata are produced by asymmetric cell divisions. Mutations in the gene TOO MANY MOUTHS (TMM) disrupt patterning by randomizing the plane of formative asymmetric divisions and by permitting ectopic divisions. TMM encodes a leucine-rich repeat–containing receptor-like protein expressed in proliferative postprotodermal cells. TMM appears to function in a position-dependent signaling pathway that controls the plane of patterning divisions as well as the balance between stem cell renewal and differentiation in stomatal and epidermal development.

Stomata allow gas exchange and thus are key to the survival of land plants, yet the genes controlling stomatal development are poorly understood (1,2). Both the number and distribution of stomata are regulated during leaf development. Stomata are formed after a series of asymmetric divisions of transiently self-renewing precursors termed meristemoids [fig. S1 (3)]. Stomata are continually produced during the mosaic development of the leaf, and many form by division of cells next to preexisting stomata (Fig. 1A). Correct spacing results when the plane of formative asymmetric divisions is oriented so that the new precursor, the satellite meristemoid, does not contact the preexisting stoma or precursor (1, 4). Intercellular signaling provides spatial cues that regulate division orientation and may also block asymmetric division in cells adjacent to two stomata or precursors (4). The recessive too many mouths (tmm) mutation randomizes the plane of asymmetric division in cells next to a single stoma or precursor and permits asymmetric divisions in cells next to two stomata or precursors, thus producing clusters of stomata (Fig. 1, A and C). Also,tmm meristemoids divide fewer times before assuming the determinate guard mother cell fate. These phenotypes suggest that TMM is required for cells to respond appropriately to their position during stomatal development and that TMM participates in intercellular signaling.

Figure 1

Stomatal pattern development. (A) An idealized wild-type (WT) series (top) compared to an actual series from a tmm mutant plant (bottom). Methods are given in (4). Asymmetric division of a meristemoid mother cell (yellow) produces a meristemoid (red). An oriented division in a neighbor cell places the satellite meristemoid away from the preexisting stoma. tmm disrupts this division orientation, permits cells next to two stomata/precursors (*) to divide asymmetrically, and reduces the number of meristemoid divisions. (B and C) Cell membrane–localized GFP (PIP2A) in developing wild-type (B) and tmm-1 (C) leaves. Meristemoids (arrowheads) are normally placed in the wild type and can be ectopically placed in tmm mutants. The young stoma [arrow in (B)] probably formed after three asymmetric divisions that also produced the three surrounding epidermal cells (the cell labeled 1 is most recent). The tmm stoma [arrow in (C)] was produced after a single asymmetric division. Division of a cell next to two stomata/precursors produced an ectopic satellite meristemoid (arrowhead left of cell 1).

With the use of positional cloning (3), TMMwas found to encode a leucine-rich repeat (LRR)–containing receptor-like protein of 496 amino acids with a molecular weight of ∼54 kD (Fig. 2A). The predicted protein product contains 10 uninterrupted plant-type LRRs (5) and a putative COOH-terminal transmembrane domain. TMM encodes a predicted signal peptide of 23 amino acids and is most likely targeted to the plasma membrane (6). The LRR motif is found in proteins with a variety of functions in prokaryotes and eukaryotes, where it facilitates protein-protein or protein- ligand interactions. In transmembrane receptors, the LRR motif typically recognizes an extracellular signal and transduces information across the membrane through activation of a cytoplasmic kinase domain. Plant LRR receptor-like kinases (LRR-RLKs) participate in signaling during plant development, including meristem maintenance by CLAVATA1 (CLV1), hormone perception by BRASSINOSTEROID INSENSITIVE1 (BRI1), regulation of organ shape, and abscission zone formation (7–10); they also function in disease resistance (11, 12).

Figure 2

Molecular analysis of TMM. (A) The mature protein includes 10 LRRs, an NNL, a COOH-terminal non-LRR domain (CNL), a predicted transmembrane domain (TD), and no apparent cytoplasmic residues. (B) Alignment of the NNL domain of Arabidopsis TMM (At) with putative orthologs from Lycopersicon pennelli (Lp) andOryza sativa cv. Nipponbare (Os). GenBank accession numbers are NC003070, AW160186, and AP002819, respectively. Gray shading indicates conserved residues; black shading shows identical residues (22). (C) Northern analysis of TMMexpression in developing rosette leaves of 3-week-old Columbia (Col) wild-type, tmm-1, and tmm-2 plants, and roots and shoots from 9-day-old agar-grown wild-type seedlings, shows a transcript of ∼1.6 kb. TMM signal was not detected in roots. Actin serves as a loading control.

TMM lacks a cytoplasmic kinase domain and thus is similar to LRR-containing receptor-like proteins (LRR-RLPs), including CLV2 (13). Overall homology to previously described LRR-RLPs is relatively low, with the most homology between TMM and tomato disease resistance proteins, encoded by Cf-2 and Cf-9(14, 15), even though TMM has no known role in disease resistance. TMM contains paired cysteines in the NH2- and COOH-terminal non-LRR regions (four and two cysteines, respectively) that may form intra- or intermolecular disulfide linkages with a partner such as an LRR-RLK, similar to the association of CLV1 with CLV2 in a receptor complex (16). Presumably, interaction with additional factors would be necessary for TMM to participate in a signaling cascade, because it lacks a cytoplasmic domain.

The ethyl methane sulfonate–induced tmm-1 mutation (17) involves an insertion of a single thymidine in position 986 of the TMM coding region, and the fast-neutron mutagenized tmm-2 mutation has a deletion of a single thymidine at position 992. These mutations result in 33 and 14 missense residues, respectively, before premature termination that removes two-and-a-half LRR repeats and the transmembrane domain. Although it is likely that these mutant proteins do not function, shortened versions of TMM could be secreted from cells and may retain some activity. This possibility is supported by partial activity of the truncated protein product encoded by the rice disease resistance gene Xa21D, which lacks the normal transmembrane and kinase domains (18).

Monocot and other dicot species each encode TMM-like gene products. These proteins are most similar to TMM in the NH2-terminal, non-LRR–encoding domain (NNL) (Fig. 2B). In this region, the tomato protein is 75% and the rice protein is 60% identical to TMM, whereas they are 65 and 51% identical, respectively, to TMM within the LRR region. In contrast, the Arabidopsis genome encodes a small family of TMM-like RLPs, but these proteins are no more than 32% identical overall, and the NNL domain is not well conserved. Strong conservation of TMM-like proteins, especially the NNL, suggests that a biochemical function arose before the divergence of monocots and dicots, although grasses lack satellite meristemoids. Becausetmm eliminates stomata in several Arabidopsisorgans (19), TMM may participate in the initiation of asymmetric divisions that form stomata in all plants.

TMM transcripts are present in developing shoots but not in roots (Fig. 2C). The absence of transcripts from roots and the normal phenotype of tmm roots suggest that TMM does not participate in patterning asymmetric divisions of the root. As shown by hybridization to RNA isolated from rosette leaves of Columbia wild-type, tmm-1, and tmm-2 plants,TMM is transcribed at roughly equivalent levels in wild-type and mutant plants.

The cellular pattern of expression was determined by means of TMM translational fusions with green fluorescent protein (GFP) driven by the native TMM promoter (Fig. 3). Both COOH- and NH2-terminal TMM fusion proteins mostly or completely complemented the tmm phenotype, indicating that both the pattern of expression and protein activity are sufficient to restore developmental function (table S1). Expression was found in shoot epidermal cells and not in the shoot apical meristem, in subepidermal layers of the shoot, or in roots. In developing leaves, expression was first detected in young leaf primordia (Fig. 3A), and then migrated basipetally during development. The number of GFP-TMM–positive cells declined as leaves matured, and none were observed in fully expanded leaves. The absence of shoot apical meristem defects in tmmmutant plants, coupled with the lack of TMM expression in L1 cells of the meristem or incipient leaf primordia, indicates that TMM is not involved in protodermal cell development but instead defines a postprotodermal phase of epidermal development.

Figure 3

TMM expression pattern in wild-type plants. All fluorescence images are confocal micrographs of the developing abaxial leaf epidermis. (A) The TMMpromoter drives expression in developing leaves (L3 through L5) but not in the shoot apical meristem or incipient primordia. GUS staining is from TMMpro::GUS-GFP. (B) Control (CaMV 35S::GFP) showing constitutive cytoplasmic and nuclear fluorescence. Fluorescence appears localized to the cell periphery because of the large vacuole present in epidermal cells. (C) Cell-specific expression including that in a stoma (S) and meristemoid (M) from TMMpro::GUS-GFP [see supporting online text (3)]. (D through I)TMMpro::TMM-GFP fusion protein. (D) Young leaf undergoing the initial asymmetric divisions that form meristemoids (M), which are brighter. Meristemoids, as well as isolated cells (arrow), may later host an asymmetric division. Fluorescence appears diffuse in very young cells because of the distribution of endoplasmic reticulum. Paired fluorescence (E) and bright-field (F) images of a guard mother cell (GMC) complex with two TMM-GFP–positive neighbor cells and one negative neighbor cell (*). Stomatal (S) fluorescence is absent. (G) Intermediate stage leaf showing dispersed TMM-GFP–positive cells, many produced by asymmetric divisions. A satellite meristemoid (SM) was formed by division of the neighbor cell adjacent to a guard mother cell (GMC). Cells next to more than one stoma or precursor rarely divide (*). Cell walls were visualized with propidium iodide. Paired fluorescence (H) and bright-field (I) micrographs showing stomatal complexes in which only the most recently formed sister cell to a stoma (S) is TMM-GFP–positive. Two cells that are not adjacent to stomata or precursors are also fluorescent [arrowheads in (H)]. Scale bars, 14 μm.

Because tmm disrupts the plane and frequency of asymmetric divisions in neighbor cells (cells next to stomata, meristemoids, or guard mother cells), TMM expression was analyzed in these locations. TMM is expressed in many neighbor cells (Fig. 3, C through I). This localization is consistent with phenotypic data (4), suggesting that TMM functions in an intercellular signaling pathway in which neighbor cells receive cues about the position of an adjacent stoma or precursor. A putative receptor complex containing TMM could transduce extracellular spatial information into a signaling cascade that orients the plane of asymmetric division, thus generating the minimal one-celled stomatal spacing pattern.

Although TMM is expressed in neighbor cells, not all such cells were fluorescent (Fig. 3, C through I). To determine whether this reflects a developmental pattern, TMM expression was quantified as a function of neighbor cell age (Fig. 4). Expression was highest in the neighbor cell most recently produced by asymmetric division and declined progressively with age. Because young neighbor cells are more likely to divide asymmetrically than older ones (1,2), TMM expression correlates positively with division competence and negatively with the terminal differentiation of neighbor cells as pavement cells. TMM is also expressed in some cells adjacent to two stomata and/or precursors (asterisks in Fig. 3G), suggesting that TMM may help prohibit their division. TMM expression does not, however, predict the formative asymmetric division of neighbor cells. About 40% of complexes do not produce any satellite meristemoids, and only 12% of all complexes produce more than one satellite meristemoid (20), but most complexes exhibit TMM-GFP fluorescence in more than one neighbor cell (Fig. 4). This indicates that TMM is not restricted to cells committed to asymmetric division but is expressed in some cells that remain nonproliferative or divide symmetrically.

Figure 4

TMM-GFP expression as a function of neighbor cell size and location next to meristemoids, guard mother cells, or stomata. Expression was most frequent in the smallest neighbor cell (NC1) at all stages and decreased in all NCs with age. Data were collected from the abaxial epidermis of intermediate-stage second leaves.

Smaller cells in developing leaves can divide either symmetrically or asymmetrically, and only the latter produces a meristemoid (4). TMM was often expressed in relatively small cells that were not neighbor cells (arrow in Fig. 3D; arrowheads inFig. 3H). These cells did not appear to be meristemoids because of their shape and because there was no adjacent larger sister cell. TMM expression may thus mark a population of division-competent stem cells from which the stomatal lineage may be selected. This hypothesis is supported by the observation that larger epidermal cells, which are known to divide rarely if at all (4, 21), usually did not express TMM (Fig. 3, C through I).

TMM is also expressed in stomatal precursor cells. Expression is highest in meristemoids, less abundant in guard mother cells, and absent from mature guard cells (Fig. 3, D through I). Meristemoids have only a limited capacity for self-renewal and ultimately differentiate into guard mother cells. TMM regulates meristemoid self-renewal, because tmm reduces the number of meristemoid asymmetric divisions (4). In addition, meristemoids that occasionally form in contact divide away from each other in the wild type but not in tmm mutants (4). These phenotypes and the strong expression of TMM in meristemoids suggest that TMM regulates proliferation and positional responses in meristemoids as well as in division-competent cells that may enter the stomatal pathway.

On the basis of these observations and the identity of TMM as an LRR-RLP, we propose that TMM is a component of a receptor complex whose function is to sense positional cues during epidermal development. The interspersion of proliferating and differentiating cells during this phase requires that spatial information be integrated to appropriately pattern cell types. TMM controls the orientation of asymmetric divisions that create the minimal one-celled stomatal spacing pattern and may also participate broadly in regulating cell proliferation and differentiation based on positional context. The latter function appears analogous to the CLV1/CLV2 signaling pathway that regulates the balance between stem cell maintenance in the central shoot apical meristem and cell differentiation at the meristem flanks (9). In contrast, TMM functions in cells that are dispersed within the developing epidermis and have different fate potentials, ranging from multipotent stem cells that may undergo a formative asymmetric division to meristemoids that invariably mature into stomata.

Additional support for the importance of position-dependent cell proliferation in epidermal patterning comes from theSTOMATAL DENSITY AND DISTRIBUTION 1 locus, which encodes a processing protease likely to participate in cell signaling (1). The control of cell division relative to nearby differentiating cells is likely to be a recurring theme in plant development.

  • * To whom correspondence should be addressed. E-mail: sack.1{at}osu.edu

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