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In the growing apex of Arabidopsis thaliana primary roots, cells proceed through four distinct phases of cellular activities. These zones and their boundaries can be well defined based on their characteristic cellular activities. The meristematic zone comprises, and is limited to, all cells that undergo mitotic divisions. Detailed in vivo analysis of transgenic lines reveals that, in the Columbia-0 ecotype, the meristem stretches up to 200 µm away from the junction between root and root cap (RCJ). In the transition zone, 200 to about 520 µm away from the RCJ, cells undergo physiological changes as they prepare for their fast elongation. Upon entering the transition zone, they progressively develop a central vacuole, polarize the cytoskeleton and remodel their cell walls. Cells grow slowly during this transition: it takes ten hours to triplicate cell length from 8.5 to about 35 µm in the trichoblast cell files. In the fast elongation zone, which covers the zone from 520 to about 850 µm from the RCJ, cell length quadruplicates to about 140 µm in only two hours. This is accompanied by drastic and specific cell wall alterations. Finally, root hairs fully develop in the growth terminating zone, where root cells undergo a minor elongation to reach their mature lengths.
During their lifetime, plant cells progress through a series of distinct developmental phases. Most of them originate from apical meristems,1 where mother cells continuously generate new cells. Each cell undergoes several mitotic cycles before leaving the meristem and embarking for irreversible postmitotic expansion. Initially, this cellular expansion is slow and accomplished in the three dimensions. Soon afterwards, however, cells effectively polarize their growth and start fast anisotropic cell growth, commonly known as cell elongation along the apical-basal polarity axis.2
A long-held view is that cells initiate cell elongation immediately after leaving the apical meristem. This view is based primarily on static pictures of longitudinal root sections and the accompanying statements are perpetuated in textbooks for more than a century.3,4 In fact relatively little attention has been paid to those changes cells undergo while leaving the meristem and heading for the more mature parts of the root apex.
This dogmatic idea in plant biology was questioned in 1990 by demonstrations that cells of maize root apices undergo slow isotropic-like growth after leaving the meristem.5 This root apex zone was initially named the post-mitotic ‘isodiametric’ growth zone,5–7 and later renamed into the ‘distal elongation zone’ (DEZ) by Ishikawa and Evans.8 Nevertheless, it is noteworthy that cells in this zone still do not elongate at high rates and, in fact, resemble meristematic cells in many aspects.2,7,9 In this zone, cells undergo a series of fundamental changes in their cytoarchitecture and physiology, and accomplish dramatic rearrangements of the actin cytoskeleton.7,10,11 For this reason, the term transition zone was coined to describe this unique part of the root apex.2,10,12
Arabidopsis root apices are very well-described regarding division patterns and radial organisation.13–15 In sharp contrast, there is a lack of solid data regarding the longitudinal (axial) zonation of Arabidopsis root apices. As a consequence, the traditional anatomical view on the longitudinal zonation of the root apex, inherited from early anatomists of the 19th century,3,4 segregated into meristematic, elongation, and differentiation zones, is preserved up to the present date (reviewed in ref. 13 and 16). Although some authors acknowledge the transition zone (often termed DEZ) in root apices of Arabidopsis,17–20, and some even describe cell wall markers for this zone,21 the overwhelming majority adhere to the classical text-book model. Typically, the transition zone (or DEZ) is overlooked and considered part of the meristem.15,22–30
To address these controversial issues, we have analyzed in detail steadily growing root apices of Arabidopsis with special attention to the level of individual epidermal cells. Here, we provide evidence from in vivo experiments for the existence of three clear-cut zones Arabidopsis roots, namely division, transition, and of fast elongation, similar to those described for maize root apices (see below). In this treatise, we do not discuss the nongrowing differentiation zone, as this has been done elsewhere.31,32 Published data corroborate the fact that the early postmitotic root cells first traverse the transition zone, and only then they are released into the rapid cell elongation zone. In the transition zone, root cells acquire unique physiological properties, the most relevant being their high sensitivity to diverse environmental factors such as gravity, humidity, light, and oxygen all of which have fundamental consequences for both the signal-mediated tropisms as well as morphogenesis of roots.
Especially authors who used kinematic approaches to study root surfaces, but not cells directly, preferred to call this root region the distal elongation zone (DEZ).6,7,8,18,33–39 The cellular concept of the transition zone12 is based on findings that postmitotic root cells leaving the meristem show more similarities to interphase cells of the meristem than to elongating cells.2,5,7,12 In fact, cells leaving the meristem are not able to start elongating immediately. Cells become competent for fast elongation only after spending some time within the transition zone, acquiring the necessary cytoarchitecture and metabolic properties.2,12 For instance, cells leaving the apical meristem do not have the necessary vacuoles that would drive the extremely fast cell elongation and do not have the necessary mechanical properties of cell walls which would allow their rapid yielding.
In postmitotic maize root cells leaving the meristem, the cortical microtubules are not completely ordered in transverse arrays,40 while their actin filaments are not organized into longitudinal bundles yet.10,41 Importantly, all postmitotic cells in the transition zone perform a drastic reorganization of their cytoskeletal elements.2,10,40 This extensive rearrangement of the cytoskeleton is essential for the developmental switch into rapidly elongating root cells which expand strictly uniaxially.2,9,10,42
Arabidopsis root apices were analyzed in vivo and in vitro against a background of the above the maize information. As guidance for the information to follow, a representative root apex of a five-day-old Col-0 Arabidopsis seedling is shown in Figure 1, in which an epidermal trichoblast cell file is highlighted. This confocal micrograph of a live root stained with propidium iodide clearly shows the cell walls. In plant tissues, there is no movement of cells relative to each other. Therefore, cell growth measured for one cell layer is by definition also indicative for the other neighboring cell layers of the organ, unless cell division occurs which is not the case here. In earlier work,43 we have introduced the stage of root hair bulging in trichoblasts as a new useful marker for time-related cellular development. Cells passing this critical developmental stage are extremely sensitive to both auxin44 and ethylene.43,45
During steady-state growth of Arabidopsis roots used in our experiments, a new cell reaches this stage of root hair bulging in each thrichoblast cell row every 30 minutes (see the video sequence at: http://webhost.ua.ac.be/fymo/Root.avi). Knowing the regular timing of development in the trichoblast cell file, it is easy to measure and calculate the course of cells throughout root apices. Obviously, the small size and simple anatomy of Arabidopsis roots makes this model object extremely useful for the detailed in vivo characterization of individual root zones of cellular activities as well as for their easy localization in root apices (Table 1).
There are almost no reports that describe the basal (proximal) limit of the apical meristem in root apices of Arabidopsis. Classical cytological studies using pulse-labeled (usually with tritiated thymidine) samples did not include Arabidopsis as object of interest.46 This species only acquired the status of model plant more recently.1,13,14,47 Fortunately, current molecular biology techniques allow a direct approach to answer the question of meristem length. One can easily visualize the expression of proteins which are exclusively confined to dividing cells, such as cyclin B1 using (CYCB1;1) promoter-GUS lines.48–50 Hauser and Bauer30 used this rather elegant technique and reported that the proximal (basal) limit of the meristematic zone is situated at about 160 µm from the RCJ, and that the zone contained an average of about eight mitotic cells per cell file. There are several other reports, all of which did not specifically focus on the size of the meristem, but that did make use of the same CYCB1;1 transgenic line. All these data reveal invariably that the most proximal cell divisions are localized somewhere between 100 and 200 µm from the RCJ, depending on growth conditions and seedling age.29,51–55 During our studies of the cytoskeleton in Arabidopsis roots,45 we have performed a detailed analysis of the occurrence of mitotic and cytokinetic figures along the apex (Le J, unpublished data). Our observations are in accordance with the data published with the CYCB1;1 line, as we never detected preprophase bands, mitotic spindles or phragmoplasts farther than 200 µm from the RCJ.
Our values observed in vivo are in contrast to those indirectly computed from kinematic analysis of Arabidopsis root growth, localizing the proximal limit of the meristem between 488 and 713 µm from the RCJ, encompassing some 43 to 70 meristematic cells for one cortical cell file.24,25,56,57 On the contrary, calculations performed on longitudinal root sections correspond well with data from work with the cyclin reporter gene constructs. Using the longitudinal section through the Arabidopsis root apex (Fig. 2) published by Ishikawa and Evans,35 one can approximately calculate the number of cells in a cell file. In the left epidermal file, which is intact throughout this section, there are about 22 cells in the meristem (the first 200 µm from the RCJ) and about 20 cells in the transition zone (between 200–400 µm from the RCJ; for the determination of the basal limit of the transition zone see below). Kidner et al15 calculated the average number of dividing cells from longitudinal sections of 3 days old Arabidopsis root apices. These authors counted the number of cells within particular cell files from the initial cells towards the nondividing cells. They reported that the number of cells forming the apical root meristem varies between 18 (stele, atrichoblast) up to 35 (trichoblast) cells. From these data, it is clear that the indirect kinematic technique2,24,25,57 shifts the basal border of the meristem into the transition zone or even beyond (see later). The problems arising with such kind of indirect analysis might be the consequence of noise-rich smoothening and curve-fitting procedures.
Thus, root cells leave the meristem somewhere between 150–200 µm from the RCJ (Fig. 1) in roots of Arabidopsis thaliana ecotype Col-0 seedlings grown in vitro at 23°C, 16 h/8 h light/dark cycle, on agarose for about five days. However, this value is not absolute for all Arabidopsis roots grown under other conditions, as the size of the meristem varies according to factors regulating plant development. During plant growth, the increase in the rate of root growth is accompanied by an enlargement of the apical meristem.24 Also, it is known that apical root cells are monitoring signals arriving from older more proximally located cells.58 Among these signals, sucrose and auxin are the most likely candidates. For instance, addition of 4.5% sucrose to the medium of growing Arabidopsis roots increased the number of dividing cells and enlarged the size of the apical meristem, shifting its proximal limit from about 162 to about 300 µm from the RCJ.30
Similar to sucrose, auxin increased the size of root meristems, while addition of cytokinin resulted in a decrease in the size of apical meristems of Arabidopsis roots.25 In accordance with this effect of cytokinin, genetically engineered tobacco plants with a reduced cytokinin content due to expression of cytokinin oxidase genes from Arabidopsis, showed substantially enlarged root meristems.59,60 A more recent report confirmed that cytokinins control the exit of cells from the root meristem in Arabidopsis.61 Besides these signal-mediated changes in the size of the apical meristem, ectopically expressed mitotic cyclins are known to increase the size of the root meristem48 while dominant-negative forms of Cdc2a kinase lower the population of dividing cells in Arabidopsis root apices.62 Therefore, these core cell cycle molecules appear to act as apparent targets for signal-transduction cascades regulating the cell cycle during growth and development of plant roots. In fact, tight correlations were reported between cell production rates and activities of cyclin-dependent kinases between roots of several Arabidopsis ecotypes.21
In spite of the wide availability and usage if the CYCB1;1 line, it is rather surprising that the basal border of the Arabidopsis root meristem is still an controversial issue in the current literature. Many authors simply ignore the transition (or the DEZ) zone and consider the onset of rapid cell elongation as the basal limit of the root meristem.63–65 On the basis of the CYCB1;1 line, as well as of the careful analysis of the MAP4-GFP line (Le J, unpublished data), the proximal (basal) limit of the meristem is at about 200 µm from the RCJ. The subsequent growth zone, about 320 µm long, corresponds to the transition zone.
At about 520 µm from the root cap junction, cell length increases noticeably (Fig. 1). This zone of rapid cell elongation will be discussed later. The cells distal to the zone of fast cell elongation (approximately between 200 to 520 µm from the RCJ) belong to the transition zone.
At 200 µm from the RCJ, cells enter the transition zone with an average cell length of 8 µm. During the subsequent 10 hours, their length increase is negligable reaching only 9 µm at 280 µm from the RCJ, although cell width increases from 14 to 16 µm. This section of the trichoblast cell file is not within the focus plane in the micrograph (Fig. 1). However, in the same cell file, a row of 17 cells covering the distance from 280 to 520 µm from the RCJ (distal to the arrowhead mark) can clearly be discerned: in that row, the elongation from 9 µm to 30 µm takes 8.5 hours. Furthermore, elongation is not homogeneously spread. In the the youngest six cells (three hours of development), no increase in cell length can be measured, while in the oldest six cells the growth in length is much more substantial. It is precisely in the latter part of the transition zone that trichoblast cells develop a central vacuole (upper asterisk in Fig. 3), while this feature is completely absent in the more distal part (younger cells, lower asterisk in Fig. 3) of the transition zone. In Figure 3, the arrowhead marks the end of the transition zone and the arrow the end of the elongation zone. This allows direct comparison with the (Fig. 1).
Cells in the proximal part of the transition zone are competent for the onset of fast cell elongation while cells in the distal part are competent to return back to the cell cycle activity. This finding coincides with the expression of cdc2 also in cells of the apical part of the transition zone (see Fig. 2F in ref. 66), suggesting that cells of the distal part of the transition zone maintain competence for cell division. All this renders the transition zone a kind of dynamic reservoir of developmentally plastic cells allowing rapid adjustment of both growth speed as well as direction of root growth according to demands of the actual environmental challenges.
As mentioned earlier, the development of trichoblast cell files mirrors somehow the development occurring in other cell types. Atrichoblasts are longer than trichoblasts (in general about 15%). This feature is seen throughout the transition zone. Vacuolization in this cell-type, as well as in the cortex cells, starts closer to the RCJ than in trichoblast cells, as illustrated in Figure 2. Cortex cells, on the other hand, are good markers for following increases in cell widths that occur in the transition zone. The final width of the cortex cells is only reached at the proximal end of the transition zone at about 520 µm from the RCJ. This is fully in accordance with the situation in maize root apices7 and can serve as another indication of the limit of the transition zone.
Based on kinematographic analysis of the root surface extension, several authors have defined the border between slow cytoplasmic growth and fast cell elongation arbitrarily as the point where the relative elemental growth rate reached 30% of its maximum value.18,35,37,38 Incidentally, this indirect approach fits well with results of our in vivo cytological analysis reported here.
As a matter of fact, the concept of slow cell growth preceding the abrupt acceleration driving the fast cell elongation was confirmed also for Arabidopsis hypocotyl cells.67 Here, cells elongate synchronously during the first 48 hours at a low rate, before the first cells at the base of the hypocotyl start their fast elongation. During the first 48 hours, these slowly elongating cells can be compared with cells passing through the transition zone. Thus, in the root apex transition zone, cell expansion is slow and occurs not only in the longitudinal (axial), but also to a certain extent in the transverse direction. At the basal limit of the transition zone, cells abruptly enter the phase of fast cell elongation and stop their widening. This corresponds exactly to the situation in maize root apices.5 The onset of rapid cell elongation is accompanied by impressive changes in structure and function of vacuoles and cell walls.
In the growing root apex, maturation of the protophloem elements occurs within the transition zone, approximately at 250 µm from the root cap junction,68,69 allowing local unloading of phloem-transported sugars into this growth zone.68,69 As illustrated before, the central vacuole of trichoblasts develops only in the proximal part of the transition zone. This morphological characteristic is corroborated by the finding that the expression of the tonoplast aquaporin γ-TIP starts abruptly at the proximal border of the transition zone.70
Concomitant with these changes in the cytoplasm, the cell wall undergoes specific adaptations. In vivo localization of XET action highlighted its maximal values at the proximal end of the transition zone.71 Xyloglucan endotransglucosylase/hydrolase (XTH) is an enzyme that modifies the cellulose-xyloglucan network, the load-bearing structure in plant cell walls. XTHs can cleave xyloglucans and subsequently rejoin the newly formed ends to available xyloglucan chains or oligosaccharides.72 This activity creates the opportunity for a turgor-pressure driven increase of the distance between two adjacent cellulose microfibrils, leading to growth. Cells within the transition zone are characterized by a progressive increase of the XET activity in their cell walls.71 This XET activity reaches its maximum values at the end of cell growth in three dimensions, at the basal limit of the transition zone, and heralds the onset of strictly polarized rapid cell elongation (no further cell expansion in width).71 In fact, the XET activity can be taken as a physiological marker of the proximal part of the transition zone in root apices of Arabidopsis. McCartney et al.21 reported the occurrence of a cell wall pectic (1 → 4)-β-D-galactan in the transition zone of Arabidopsis roots. This points again to fundamental changes in cell wall properties occurring at the border between the transition zone and the zone of fast cell elongation. In order to loosen cell walls effectively, the cellulose and xyloglucan network is also affected by expansins which are expressed and localized to cells of the transition zone too.73,74 The idea of structural changes occuring in the cell wall at this ‘no return’ developmental point is further stressed by the detection of an increase in cellulose, xyloglucan and methylesterified pectins at the onset of fast cell elongation using FT-IR (De Cnodder T et al., unpublished results).
In a recent study, we have shown that cortical microtubules in the epidermis of Arabidopsis roots have a strictly transverse orientation at the basal limit of the transition zone.45 It was reported that the cessation of radial expansion in postmitotic root cells of Arabidopsis was closely associated with the strict alignment of cortical microtubules into transverse arrays.75 When cortical microtubules do not accomplish this redistribution, postmitotic cells fail to restrict their radial expansion and increase in width even throughout the elongation region as was described in bot1 and fra2 mutants of Arabidopsis.75,76 Similar links between cortical microtubules and cell polarity were indicated by several other mutants of Arabidopsis.77–79 However, other mutants showed a reduced cell polarity, with thicker and shorter root cells, although their cortical microtubules were arranged in highly ordered transverse arrays. In this regard, we can mention CORE mutants,80 the kor mutant75 and rsw4/rsw7 mutants.81 Evidently, besides ordered cortical microtubules, also the correct in muro localization of wall metabolic events is critical. In this respect, the cell wall has a pivotal role.75,76,83–86
At the plasma membrane-cell wall interface,87 COBRA could potentially be involved in establishing polarity of cell growth of postmitotic root cells.88 COBRA is a member of glycosylphosphatidylinositol (GPI) anchored proteins, which are anchored to the outer plasma membrane leaflet and with putative interactions with cell wall molecules. COBRA mRNA levels were shown to be dramatically upregulated in cells located around 200 µm (see Fig. 4D and E in ref. 88) from the RCJ interpreted by the authors as rapidly elongating cells. Both, from distances from the RCJ as well as from the shapes of these cells (see Fig. 4D and E in ref. 88) it is obvious that COBRA mRNAs and proteins are located abundantly within the transition zone. Root cells of the cobra mutant have a reduced content of cellulose and fail the polarization of cell expansion as they expand too much in width and do not achieve proper elongation.88 Nevertheless, mutant root cells reach normal volumes. This phenotype suggests that COBRA could be important for the acquisition and maintenance of the nongrowing status of cross-walls which is the most critical event in the polarization of postmitotic root cells during their switch into the rapid cell elongation.42
In the Arabidopsis root, fast cell elongation starts when cells leave the transition zone and slows down when trichoblasts initiate outgrowths of root hairs.45 In the example shown in Figure 1, cells increase their length from about 35 µm (arrowhead) to 135 µm (arrow) in two hours. There is some variability in the elongation rate, but the whole process is always terminated in less than three hours as can be seen in other cell files (Fig. 1). Along the root axis, the end of the fast elongation is situated at about 900 µm from the RCJ. In normal growing conditions, additional increase in cell length occurs up to about 1500 µm from the RCJ. Further on, the relative elemental growth rate of the root is not statistically different from zero.45
Fast cell elongation is based on, and accomplished by, processes clearly different from the slow cell growth in the transition zone. In situ analysis of cell wall composition by FT-IR spectroscopy reveals a unique character for this part of the root (De Cnodder T et al., unpublished results). The β-glucosyl Yariv reagent was found to inhibit specifically the fast cell elongation.89 It affects fucosylated arabinogalactan-proteins which are required for full cell elongation in root apices as deduced from the mur1 phenotype of Arabidopsis.90 In the epidermis wall, the cellulose fibrils are oriented parallel and strictly transverse to the root axis.91 The cortical microtubules mirror this organisation and are aligned strictly parallel and transverse to the root axis.45 The rate of cell elongation is inversely related to the endogenous ethylene concentration.43 Under saturating conditions, the fast cell elongation is completely abolished, as is the residual elongation in the growth-ceasing zone, and cells never elongate beyond the length reached at the basal limit of the transition zone. For trichoblasts this is 35 µm, a length also reported for dwarfed phenotypes like the ctr1-1 mutant that expresses a constitutive ethylene response. On the contrary, it was found that cells have the potential to elongate beyond their normal length as trichoblasts elongated up to 200 µm in the absence of ethylene, a cell size also found in ein2-1, an ethylene insensitive mutant.43 Fast elongation is also very sensitive to other hormone signals. In the root apices of the stunted plant 1 mutant of Arabidopsis, rapidly elongating root cells were affected while slowly expanding more apical cells were unaffected.25,56 In this particular mutant, cell elongation defects are mediated via cytokinin-based signaling as cytokinin-treated wild type seedlings truly phenocopied this mutant.25 Moreover, auxin is also known to preferentially affect the fast cell elongation.8,44,92
The basal limit of the fast cell elongation zone is marked by the disturbance of the transverse arrays of the cortical microtubules.45 This feature is evident when the fast elongation is blocked by a high dose of ethylene (for maize roots see ref. 92). However, the microtubule reorientation is not causally linked to the observed stop in cell elongation. Primary are events in the cell wall, including a rise in apoplastic pH, callose deposition and cross-linking events steered by reactive oxygen species.93 The transit from pure cell elongation to differentiation is highlighted by the expression of a fucose-containing epitope in the cell wall of epidermal cells.90 Furthermore, epidermal cells become symplastically isolated when leaving the fast elongation zone.94 Another marker for the end of rapid elongation is the accumulation of myosin VIII along the cross walls of the epidermal cells exactly where in the trichoblasts root hairs start to develop rapidly (Verbelen et al., unpublished results).
Intriguingly, cells in the transition zone continue their growth also under osmotic stress, while the growth in the fast elongation region is irreversibly stopped.2,96–98 This reaction is dependent on ABA accumulation and lowering of ethylene production.97,98 Several other hormones differentially affect the two zones. As mentioned before, the endogenous cytokinin level specifically affects cells in the fast elongation zone,25,56 as is the case with ethylene.43 Exogenous auxin inhibits cell growth in the zone of fast elongation, but it can stimulate cell growth within the transition zone upon gravistimulation.2,5,8 Furthermore, the transition zone is the unique site for perception and response to a range of (external) factors. Local application of extracellular calcium inhibited cell growth specifically within the transition zone but exerted only weak responses in the zone of fast elongation.8 Moreover, calcium waves spread through the transition zone of Arabidopsis root apices (Fig. 8 in ref. 99 and Fig. 3D in ref. 100). Differential passage of cells through opposite sides of the transition zone95 allows growing root apices to initiate their curvature culminating in root tropisms in response to gradients of external factors as diverse as gravity, temperature, moisture, salinity, oxygen availability, electric fields, and heavy metals.2,5,39,100 Transition zone cells are also sensitive towards mechanical stimuli6 and to aluminum toxicity,101–103 which is mediated by glutamate receptors.104 Aluminum was shown to inhibit the basipetal auxin transport in the distal part of the transition zone103 and to induce, like the auxin transport inhibitor NPA, cell divisions within the transition zone.105 That aluminum targets specifically cells of the transition zone was also reported in the recent study which showed that aluminum is not only internalized into these cells but it also inhibits endocytosis and vesicle recycling, as well as NO production.106
This unique signalling profile and sensory status is an additional and important characteristic of cells building up the transition zone. This was already shown in maize root apices where cells of the transition zone proved to have unique cytological and metabolical properties allowing them to sense diverse environmental factors and endogenous cues.2,7
Since 1993, it has been clear that the transition zone is very special from the standpoint of auxin-mediated cell growth control.8 The authors made the very peculiar observation: exogenous auxin inhibits root growth but induces a burst of cell growth in the cells of the transition zone at the top of the gravistimulated roots, resulting in rapid gravibending of these roots.8 Adaptation of roots to high auxin was well documented in older literature,107–109 but Ishikawa and Evans8 discovered that the transition zone plays a key role in this respect. Such recovery of root growth in a high auxin environment is associated with a complete reconstruction of microtubules.44 Recently, a new technique was introduced which allows in vivo monitoring of auxin influx into maize root apices, revealing that external auxin is preferentially taken up in the transition zone.110 Subsequent application of this technique to roots of Arabidopsis revealed that the distal portion of the transition zone, which has been defined here on the basis of cytological characteristics (150–350 µm), corresponds precisely with the peak of auxin influx.111–113
This observation is in agreement with the situation in maize root apex where the distal portion of the transition zone also shows the highest uptake of external auxin.110 Recent advancements in the understanding of the polar auxin transport in Arabidopsis allowed to indentify unique loops of auxin streams, driven by at least five PINs including PIN1, PIN2, PIN3, PIN4 and PIN7, specifically for the root apex.113,114 Moreover, four of five PINs expressed in root apices (PIN1, PIN2, PIN4, PIN7) localize polarly at the cell peripheries, which are rich in actin,41 preferentially in cells of the transition zone.114–117
Shoot apex lacks such complex auxin flow and uses just PIN1 for the polar auxin transport (reviewed in ref. 118).
Root apex streams are driven by cells of the stele transporting auxin towards the root apex (PIN1, PIN4), and by cells of the lateral root cap and epidermis supporting the basipetal transport stream (PIN2) which then joins the apical one again (PIN4, PIN7) at the basal limit of the transition zone.114 The latter authors interpreted the root apex zone where the basipetal stream loops back into the acropepal stream, as the elongation zone (see the Fig. 5C in ref. 114). However, actual viewing of Figures 2A–H (see especially the Fig. 2A in ref. 114) makes it quite evident that they, are not aware of the precise root apex zonation. This urges for caution in many situations where authors made claims about root apex zones in Arabidopsis.
In root apices of Arabidopsis thaliana, four distinct and successive zones can be clearly discerned: the meristematic zone, the transition zone, the zone of fast cell elongation and the growth terminating zone. Each of these zones is characterized by a specific set of cellular activities as well as by specific responses towards plant hormones and signals. Between the apical meristematic zone and the region of fast cell elongation, a relatively large zone of developmentally plastic cells is located within the transition zone. While the apical (distal) part119 of this region contains cells that optionally can reenter the cell cycle, cells of the basal (proximal) part of this zone are optimized for a sudden signal-mediated entry into the fast cell elongation region. As this developmental passage of cells can be differentially regulated at the opposite root flanks, this unique zone provides the root apices with an effective mechanism to reorientate growth in response to environmental stimuli (Fig. 4). Importantly, the transition zone is easily recognized by simple features such as positions of nuclei, cell shapes, and and organization of vaculoes (Table 1). The definition of these four growth zones in vivo challenges the widespread classic view3,4 of meristematic, elongation, and differentiation zone that is mainly based on the traditional post mortem morphological observations of root apices.
Authors acknowledge the financial support of the Research Foundation-Flanders (FWO), grants G0345.02, G0034.97 and G0281.98. K.Vissenberg is a post-doctoral fellow of the Research Foundation-Flanders (FWO). Financial support by grants from the Bundesministerium für Wirtschaft und Technologie (BMWi) via Deutsches Zentrum für Luft und Raumfahrt (DLR, Cologne, Germany; project 50WB 0434), from the European Space Agency (ESA-ESTEC Noordwijk, The Netherlands; MAP project AO-99-098), and from the Ente Cassa di Risparmio di Firenze (Italy) is gratefully acknowledged. F.B. receives partial support from the Slovak Academy of Sciences (Grant Ageny VEGA, Bratislava, Slovakia; project 2/5085/25).
Previously published online as a Plant Signaling & Behavior E-publication: http://www.landesbioscience.com/journals/psb/abstract.php?id=3511