Research Article

ESKIMO1 Disruption in Arabidopsis Alters Vascular Tissue and Impairs Water Transport

  • Valérie Lefebvre,

    Affiliation: Institut Jean-Pierre Bourgin UMR1318 INRA-AgroParisTech, INRA Centre de Versailles-Grignon, Versailles, France

  • Marie-Noëlle Fortabat,

    Affiliation: Institut Jean-Pierre Bourgin UMR1318 INRA-AgroParisTech, INRA Centre de Versailles-Grignon, Versailles, France

  • Aloïse Ducamp,

    Affiliation: Institut Jean-Pierre Bourgin UMR1318 INRA-AgroParisTech, INRA Centre de Versailles-Grignon, Versailles, France

  • Helen M. North,

    Affiliation: Institut Jean-Pierre Bourgin UMR1318 INRA-AgroParisTech, INRA Centre de Versailles-Grignon, Versailles, France

  • Alessandra Maia-Grondard,

    Affiliation: Institut Jean-Pierre Bourgin UMR1318 INRA-AgroParisTech, INRA Centre de Versailles-Grignon, Versailles, France

  • Jacques Trouverie,

    Affiliation: Ecophysiologie Végétale, Agronomie et nutritions N, C, S, UMR INRA-UCBN, Université de Caen Basse-Normandie, Caen, France

  • Yann Boursiac,

    Affiliation: Biochimie et Physiologie Moléculaire des Plantes, Institut de Biologie Intégrative des Plantes, UMR 5004 CNRS/UMR 0386 INRA/Montpellier SupAgro/Université Montpellier 2, Montpellier, France

  • Gregory Mouille,

    Affiliation: Institut Jean-Pierre Bourgin UMR1318 INRA-AgroParisTech, INRA Centre de Versailles-Grignon, Versailles, France

  • Mylène Durand-Tardif mail

    Affiliation: Institut Jean-Pierre Bourgin UMR1318 INRA-AgroParisTech, INRA Centre de Versailles-Grignon, Versailles, France

  • Published: February 01, 2011
  • DOI: 10.1371/journal.pone.0016645


Water economy in agricultural practices is an issue that is being addressed through studies aimed at understanding both plant water-use efficiency (WUE), i.e. biomass produced per water consumed, and responses to water shortage. In the model species Arabidopsis thaliana, the ESKIMO1 (ESK1) gene has been described as involved in freezing, cold and salt tolerance as well as in water economy: esk1 mutants have very low evapo-transpiration rates and high water-use efficiency. In order to establish ESK1 function, detailed characterization of esk1 mutants has been carried out. The stress hormone ABA (abscisic acid) was present at high levels in esk1 compared to wild type, nevertheless, the weak water loss of esk1 was independent of stomata closure through ABA biosynthesis, as combining mutant in this pathway with esk1 led to additive phenotypes. Measurement of root hydraulic conductivity suggests that the esk1 vegetative apparatus suffers water deficit due to a defect in water transport. ESK1 promoter-driven reporter gene expression was observed in xylem and fibers, the vascular tissue responsible for the transport of water and mineral nutrients from the soil to the shoots, via the roots. Moreover, in cross sections of hypocotyls, roots and stems, esk1 xylem vessels were collapsed. Finally, using Fourier-Transform Infrared (FTIR) spectroscopy, severe chemical modifications of xylem cell wall composition were highlighted in the esk1 mutants. Taken together our findings show that ESK1 is necessary for the production of functional xylem vessels, through its implication in the laying down of secondary cell wall components.


The environmental conditions in which plants live vary constantly, during the day, with the seasons and as a consequence of climate. Plants are sessile organisms that are constrained to complete their live-cycle in one place and therefore must protect themselves against adverse conditions: their growth depends on their responses to the environment.

Plants perceive variations in the environment and react, in accordance to the nature and the intensity of the stress (reviewed in [1]). In response to abiotic stress, many genes are either down-regulated, mostly genes involved in growth, or activated at the transcriptional level [2], [3], [4], [5], [6]. Up-regulated genes can propagate the stress signal (transcription factors, hormone synthesis…), be involved in homeostasis (osmoticum synthesis, ions and water transport, molecule protection by chaperones…) or damage limitation (detoxification, antioxidants…) (reviewed in [7], [8]). As a result, there is a constant readjustment of the balance between growth arrest in order to protect and save the organism and growth maintenance at the risk of exhausting water or nutrient supplies (e.g. [9]). The regulation of stomata aperture according to water availability is a good illustration of this equilibrium. Stomata are the pores through which plants lose water through evapo-transpiration and acquire CO2 for carbon fixation by photosynthesis: closing stomata economizes water, but reduces growth as CO2 influx is limited. Water depletion induces stomata closure, through an increase of the stress hormone ABA [10], [11].

The ESK1 gene was initially identified by map-based cloning of the Arabidopsis thaliana esk1-1 mutation obtained using an in vitro screen for constitutive freezing tolerance [12]. Subsequently, it was shown that when esk1 plants were grown in soil, they were more tolerant to freezing than wild type after a period of acclimation [13], [14]. esk1 mutant phenotypes are those of a stressed plant: reduced stature and relative water content (RWC) compared to wild type [12], [14], [15], it accumulates high levels of stress metabolites that are thought to maintain the internal osmotic status, such as the osmoticum proline [12], [15] and its transcriptome resembles that of drought-stressed wild type plants [14]. Furthermore, the evapo-transpiration of esk1 mutants is severely reduced and their water use efficiency (WUE) i.e. the amount of carbon incorporated in biomass per water used, is higher than wild type.

The stressed phenotypes of esk1 led us to examine whether ESK1 was implicated in the action of the stress hormone ABA. We have examined ABA production in esk1 mutants and the phenotypes of double mutants affected in ABA responses and esk1. Then, we addressed the origin of the very low evapo-transpiration of esk1. We observed that cross sections of esk1 vascular tissue had an “irregular xylem” (irx) phenotype. Analysis of the xylem cell wall in esk1 mutants highlighted significant modifications in chemical composition compared to the wild type. Furthermore, we assessed esk1 root-hydraulic conductivity. Taken together, our results indicate that ESK1 is necessary for the formation of the functional xylem required for water transport to aerial plant tissues.


ABA levels are altered in esk1 plants

esk1 mutants were previously described as freezing [12], cold and salt tolerant [14], [15]. A common factor in these stress responses is the accumulation of the phytohormone ABA [16]. In order to determine whether ABA was implicated in inducing the stressed esk1 state, ABA contents were measured in rosettes of wild type and two esk1 mutants (esk1-4 and esk1-5) submitted or not to mild drought (Figure 1) and compared to the ABA-deficient mutant aba3-1, affected in the sulfuration of the molybdenum cofactor required for the last steps of ABA biosynthesis [17], [18]. ABA measurements from the two esk1 mutants were similar as expected for null mutant, with or without drought treatment (Table S1, LSD tests).


Figure 1. Basal ABA levels are high in esk1 mutants.

Box-plot of [ABA] determined for wild type Col-0 (wt), aba3-1, esk1-4 and esk1-5 under control and mild drought conditions. The [ABA] is reported as pg/mg of dry weight. Each box-plot was produced from results for 11 or 12 measurements. Red * indicates significant difference with wild type for the same treatment and black * indicates significant genotype x treatment interaction (p-value<0.05) for each pair of wild type and the other three genotypes.


In control conditions, ABA contents were significantly higher in esk1 mutants than either wild type or aba3-1, the latter being due to its defect in ABA biosynthesis [17]. Increased in ABA production is associated with stress and is in accord with esk1 mutants being stressed per se. As previously described, ABA contents were significantly higher in drought conditions for wild type and aba3-1, however, ABA levels in esk1 mutants were the same as those in non-stressed conditions (Table S1, 1D ANOVA). The slight increase in ABA levels in aba3-1 plants in these conditions is probably because this is not a null allele [19].

We found significant genotype x treatment interactions for the wild type and the other three genotypes (Figure 1, black stars and Table S1, 2D ANOVA), but no interactions were significant when analyzing esk1 and aba3-1 (Table S1, 2D ANOVA). These results demonstrate that esk1 mutants respond differently to drought stress than wild type.

ESK1, ABA3 and likely OST1 act in independent pathways

To determine whether the higher ABA levels observed in esk1 mutants were a direct or indirect consequence of ESK1 function, double mutants were generated with either aba3-1 or the ABA signaling mutant ost1/snrk2e. OST1 is a SnRK2 protein kinase that acts in an early step of the ABA signaling pathway in guard cells [20]. Water loss in double mutants was examined either indirectly as leaf temperature differences visualized using infrared thermal imaging of detached leaves, or by rapid dehydration of rosettes (Figures 2 and 3).


Figure 2. esk1-5 ost1 double mutant phenotypes.

A. Two representative plants of each genotype grown in standard non-stressed conditions: wild type (wt), ost1, esk1-5 and esk1-5 ost1 double mutant. B. False color infrared image of detached leaves from 4 week-old plants, 2 leaves from 2 plants were observed for each genotype. C. Rapid dehydration of detached rosettes from 4 week-old plants. Water loss was determined as % of initial fresh weight. Error bars represent standard error values (n = 4).


Figure 3. esk1 aba3-1 double mutants phenotypes.

A. Two representative plants of each genotype grown in standard non-stressed conditions: wild type (wt), aba3-1, esk1-4, esk1-5, esk1-4 aba3-1 and esk1-5 aba3-1 double mutants. B. False color infrared image of detached leaves from 4 week-old plants, 2 leaves from 2 plants were observed for each genotype. C. Rapid dehydration of detached rosettes from 4 week-old plants. Water loss was determined as % of initial fresh weight. Error bars represent standard error values (n = 4).


The aba3-1 and ost1/snrk2e single mutants displayed lower leaf temperatures than wild type due to their increased water loss upon dehydration, as previously reported [17], [20], [21] (Figures 2B and 3B). For the aba3-1 mutant, this was due to its impaired ability to synthesize ABA, whereas the ost1 mutant is affected in the ABA signaling pathway that induces stomata closure, downstream of ABA production. In contrast, esk1 leaves were hotter and water loss was reduced compared to wild type, in accordance with the reduced evapo-transpiration reported by Bouchabke-Coussa and co-workers [14] (Figures 2B, C and 3B, C). Both esk1-5 ost1 and esk1-5 aba3-1 had leaf temperatures that were intermediate of those for the parental genotypes, as expected if the mutations affected independent pathways (Figures 2B and 3B). Nonetheless, intermediate leaf temperatures could also be obtained if the two genes act in partially overlapping pathways that modulate stomata opening. Similar results were obtained in water loss measurements on rapid dehydration of detached rosettes (Figures 2C and 3C). The esk1 mutant plants lost only 30% of their weight as water, whereas ost1 and aba3-1 lost over 70%. Water loss from the esk1-5 ost1, esk1-5 aba3-1 and esk1-4 aba3-1 double mutants was always between these extremes.

As shown in Figure 2A, esk1-5 ost1 and esk1-5 mutant plants were the same size. As the ost1 mutation does not affect plant stature, despite having open stomata, this indicates that the factor influencing plant size is not the degree of stomata opening. In contrast, both esk1 and aba3-1 mutants display dwarf phenotypes and the double mutant plants were even smaller (Figure 3A), indicating that the growth limitations caused by these mutations are additive. Thus, ABA3 and ESK1 are independent in the determination of plant size and act in different pathways. The small size of esk1 is not, therefore, directly due to the high levels of ABA accumulation. Taken together the double mutant phenotypes demonstrate that ESK1 does not intervene in growth regulation and water loss through ABA and the high ABA levels in mutants is an indirect consequence of esk1 mutation.

Hydraulic conductivity is reduced from the esk1 root apparatus

The major driving force of plant water uptake is transpiration, which is controlled by stomata aperture. Entry of water into the plant is also regulated by the hydraulic conductance of the root apparatus and can potentially limit water availability in the shoots [22]. Given the reduced water loss, high leaf temperature and low RWC of esk1 mutants [14] (Figures 2 and 3), we hypothesized that the overall water flux supplied by the xylem sap is reduced in esk1 plants. In order to test this hypothesis, esk1 root hydraulic conductance was measured and compared to wild type (Figure 4).


Figure 4. Hydraulic parameters of the root apparatus are modified in esk1.

A. Root hydraulic conductance Lo is expressed as ml of sap exudate per hour and per unit of exerted pressure. B. Root/rosette dry weight ratio. C. Root hydraulic conductivity is expressed as Lo per unit of root mass. Wild type (wt). Black * indicates significant difference with wt (p-value<0.05).


The root hydraulic conductance, or Lo, represents the overall capacity of the root apparatus to transport water from the soil to the shoot. The root hydraulic conductivity, or Lpr, is the conductance of a root surface unit: Lo = Lpr*S, with S related to the surface of exchange between the root and its substrate. Lo and Lpr have been measured for wild type and two esk1 mutants, as well as the root/rosette dry weight ratio (Figure 4). Despite the small size of the esk1 lines, the dry matter allocation between the root apparatus and the rosette was similar to that of wild type. The Lo of esk1 lines was exceptionally low: 6% and 5% of wild type for esk1-1 and esk1-5 respectively. Part of this low root conductance can be explained by the small biomass of the root apparatus. Nonetheless, the Lpr values for the esk1 lines were also extremely low, indicating that the mutant root system produced a higher resistance to water transport from the soil to the hypocotyl. Thus, water transport is impaired in esk1 mutants in comparison to wild type and probably induces the low evapo-transpiration and the reduced RWC observed in the mutants.

The ESK1 promoter specifically drives expression in vascular tissue

To determine the site of ESK1 gene function, expression analyses were carried out using a 1 kb ESK1 promoter region fused to the GUS reporter gene.

Seven independent insertion lines were analyzed and similar results for seedlings and mature plants were obtained: in all cases, expression was restricted to the vascular tissue and was initially observed a few days after germination, just after the appearance of the first differentiated vascular tissues, in the radicle and cotyledons (Figure 5A1, A3). In roots, GUS staining was absent from the meristematic and elongation zone and was only apparent in the differentiation zone (Figure 5A2). At ten days after germination, expression profile is still restrained to vascular tissues of all organs (Figure 5A3–A5).


Figure 5. Histochemical analysis of GUS reporter gene expression from the ESK1 promoter.

A. Expression in whole plantlets 4 days after germination (A1, A2) and 10 days after germination (A3, A4, A5) with magnification of root (A4) and leaf (A5). B. Transverse section of hypocotyls, before (B1, B2) and after floral transition (B3, B4). C. Transverse section of stem (C1, C2). Double-headed arrow indicates the position of cross-section in B2. Red arrowheads indicate interfascicular fibers (B3) or sclerenchyma (C1, C2) and black arrowheads indicate newly-formed xylem cell (B1, B2, B4, C1, C2). X, xylem; P, phloem.


More detailed characterization of ESK1-promoter driven expression within the vascular tissue was performed on three independent homozygous transgenic lines, using sections of hypocotyls and stems. As shown in Figure 5 (B1, B2, C1), GUS staining was restricted to the cells undergoing xylem vessel differentiation, in both hypocotyls and stems. Furthermore, ESK1 also appeared to be expressed in the interfascicular parenchyma in the stem (Figure 5C1, C2). After floral induction, GUS staining was also observed in the fibers of the hypocotyls as well as xylem vessels (Figure 5B3, B4).

These results reveal that the ESK1 gene is specifically expressed in tissues undergoing secondary cell wall deposition.

esk1 mutants show altered vascular apparatus morphology

As ESK1 expression was specific to vascular tissue and esk1 mutants were defective in water transport, we conducted a detailed analysis of vascular tissue structure in different esk1 mutants.

Similar results were obtained with the three mutants studied and results obtained with esk1-1 are presented. Transverse sections were performed on hypocotyls, roots and stems of 6 week-old plants grown on soil without water deficit (Figure 6). Xylem in vascular bundles of esk1 roots and hypocotyls appeared collapsed (Figure 6A1, B). In hypocotyls, fibers also seem to be affected: cells appeared angular and the ring of fibers that surrounded xylem vessels seemed less regular than in wild type (Figure 6A2). This phenotype was reminiscent of the irx mutants that have collapsed xylem [23]. When stems were only a few centimeters high, their xylem vessels seemed unaffected (Figure S1). However, at later stages, when they developed lateral branches, irregularly shaped cells and collapsed xylem elements were observed in stems at both the base (Figure 6C1) and mid-height level (Figure 6C2).


Figure 6. Comparison of vascular tissue of esk1-1 and wild type, in hypocotyls, roots and stems.

Vascular tissue is shown for esk1-1 on the left hand side and for wild type (wt) on the right hand side. A. Transverse section of hypocotyl observed under UV light. A1, fibers (fib); A2, xylem cells (X). B. Transverse section of root observed under UV light. C. Transverse section of the stem base (C1) and at mid-height (C2) observed under UV light. Arrowheads indicate collapsed xylem.


In view of this phenotype, we hypothesized that the very low esk1 root hydraulic conductivity was due to restricted water transport through collapsed vessels. This is defined by Poiseuille's law, in which the major factor affecting the hydraulic conductance of a tube is its diameter. The theoretical conductivity of root tracheary elements (TE) was calculated for esk1 mutant and wild type, based on maximal diameter measurements obtained from transverse sections of root. As shown in Table 1, the flux calculated for esk1 mutants is approximately five-fold lower than that of wild type. This establishes a direct consequence of the irx phenotype observed for esk1 mutants on hydraulic conductivity through the root apparatus.


Table 1. Low esk1 root hydraulic conductivity is mainly explained by a reduction in tracheary element diameter.


The chemical composition of esk1 xylem is different from wild type

The chemical composition of the vascular tissue of hypocotyls at two developmental stages and the stem base was examined using FTIR spectral analysis performed on the xylem of transverse sections. Two representative esk1 null mutants were analyzed and a Student's t-test was performed, corresponding to the differences between wild type and esk1 spectra. For graphical representation, t-values were plotted against wave numbers to determine the significance of the differences at each wavelength (Figure 7B and 8B).


Figure 7. The structure and composition of esk1 xylem is modified in hypocotyls.

A. Transverse section of hypocotyls from 3 week-old (3 wo) and 6 week-old (6 wo) esk1-1 and esk1-5 plants, with lignin stained in green with Carmine-green (3 wo), or lignin fluorescing under UV light (6 wo). B. Comparison of FTIR spectra obtained from xylem in hypocotyl sections of 3 week-old (3 wo) or 6 week-old (6 wo) wild type and esk1 plants. A Student's t-test was performed on absorbance values of wild type versus mutant and plotted against wave numbers. The grey zone, between -2 and +2, corresponds to non-significant differences (p-value<0.05) between the two genotypes tested. Significant positive t-values indicated a higher absorbance value in wild type than in esk1 mutants.


In accordance with the severe vascular tissue defects observed in both hypocotyls (Figure 7A) and stems (Figure 8A), the infrared absorbance spectra from esk1 mutants were different from those of wild type. Furthermore, esk1-1 FTIR profiles obtained from stems (Figure 8B) and from hypocotyls before and after fiber appearance (Figures 7B) presented the same differences to wild type indicating that the composition of the xylem cell walls was modified in a similar manner in these different tissues.


Figure 8. The structure and composition of esk1 xylem is modified in stems.

A. Transverse section of stems from esk1-1 and esk1-5 plants, with lignin fluorescing under UV light. B. Comparison of FTIR spectra obtained from xylem in basal stem sections of wild type and esk1 plants. A Student's t-test was performed on absorbance values of wild type versus mutant and plotted against wave numbers. The grey zone, between −2 and +2, corresponds to non-significant differences (p-value<0.05) between the two genotypes tested. Significant positive t-values indicated a higher absorbance value in wild type than in esk1 mutants.


Significant differences were observed in the absorption at wavelengths from 1800 cm−1 to 1700 cm−1, which correspond to ester linkages [24] or esterified pectins [25]: esk1 absorbance was reduced compare to wild type. In addition, a highly significant peak was observed at wavenumbers around 1240 cm−1, assigned to C-O vibrations in pectic polysaccharides [25]. Other major differences were in a series of wavelengths between 1000 cm−1 and 830 cm−1, associated with crystalline polysaccharide components such as cellulose, and suggest a reduction in the amount of crystalline cellulose [24]. For example, 898 cm−1 corresponds to the β-linked glucan polymers [25]. A direct measurement of crystalline cellulose carried out on 6 week-old hypocotyls and stems confirmed that the esk1 mutant contains lower levels of cellulose than the wild type (Figure 9 and data not shown). In addition, significant differences were noted between wild type and esk1 mutants at the wavelengths around 1370 cm−1 that are associated with CH2 stretches of cellulose and 1157 cm−1, attributed to cellulose C-O-C linkages [25]. Finally, significant differences in absorbance at other non-assigned wavelengths were also observed between wild type and mutants.


Figure 9. Crystalline cellulose content is reduced in esk1-5 hypocotyl.

Cellulose contents expressed as % of hypocotyl dry weight. Data from 4 measurements are plotted. The decrease in esk1-5 cellulose content compared to wild type (wt) was significant using Mann and Whithney non parametric test (p-value<0.05).


Interestingly, in the transcriptome data previously obtained for esk1-5 [14], no “core genes” participating directly in cellulose, hemicellulose, pectin or lignin biosynthesis or modification were down-regulated in esk1-5 background. However, At1g23205, annotated as a pectin methyl esterase inhibitor (PMEI) was expressed 6.6 times less in esk1-5 than in wild type, in accordance with the reduction in esterified pectins indicated by FTIR analysis.


esk1 mutants were initially described as freezing tolerant without cold acclimation [12] and ESK1 was proposed to be a negative regulator of freezing tolerance [26]. Later studies also revealed altered responses to other stresses such as drought and salt, thereby revoking the specificity of its action. Instead, ESK1 was proposed to play a role in water uptake or circulation [14], [15]. Nevertheless the precise function of ESK1 in these processes remained to be determined.

ESK1 plays a role in xylem layout

Xylem conducts water and nutrients from the soil to sink organs. Its differentiation occurs in two steps which seem to be coupled [27]. During the first step, only xylem vessels are generated, and in the second, corresponding to secondary growth, xylem and fibers are formed. TE then undergo programmed cell death (PCD), leading to functional cell corpses. These empty cells are connected end-to-end by perforated cell plates that allow fluid transport and can support the turgor pressure generated by transpiration without collapsing [28]. Thus, differentiation of TE involves several steps: cell expansion, followed by the deposition of a thick secondary cell wall and cell death [29].

In seedlings grown in vitro, GUS expression from the ESK1 promoter was observed in vascular tissue a few days after germination and may coincide with the occurrence of secondary cell wall deposition, even though the exact time point of the onset of secondary vascular development has not been determined in Arabidopsis [30]. A close inspection of ESK1-promoter driven staining pattern in the xylem of hypocotyl before floral induction revealed that (i) only the last cell of the xylem cell file was stained and (ii) stained cells presented morphological differences, from dense stained cells, to cell corpses possibly corresponding to different stages of xylem vessel differentiation, rather than PCD. Moreover, at later stages of development, staining was also apparent in interfascicular fibers suggesting that ESK1 expression occurs in tissues undergoing or that will undergo secondary cell wall deposition and not specifically in TE cell lines (Figure 5).

Cytological analysis revealed that esk1 mutants presented a strong irx phenotype in roots, hypocotyls and stems (Figure 6). The localization of ESK1-promoter driven expression in TE and fibers is in agreement with the collapsed xylem vessels and disorganized fibers observed for esk1 mutants. Several irx mutants have been shown to be affected in their secondary cell wall synthesis and some of them display reduced resistance to compressive force [23]. For instance, irx1/cesa8, irx3/cesa7 and irx5/cesa4 mutants are affected in subunits of the cellulose synthase complex [31], [32], [33], [34]; irx8 is deficient in hemicellulose [35]; cad-c cad-d double mutant is affected in cinnamyl alcohol dehydrogenase and has 40% less lignin than wild type plants as well as collapsed xylem elements [36]. These irx mutants, apart from cad-c cad-d, also have a reduced stature. Moreover irx3/cesa7 and cad-c cad-d have reduced rigidity, indicating the importance of the composition of the plant cell wall in determining the physical properties of the plants.

In addition, the expression patterns observed for ESK1 were similar to those for reporter genes under the control of transcription factor promoters that are involved in secondary cell wall synthesis [37]. Therefore, ESK1 may participate in the process leading to secondary cell wall deposition.

The esk1 rosette suffers from a defect in water supply from the root apparatus

As xylem vessels are conducting tubes that transport water, defects in their shape may have consequences on water distribution. Water supply is determined by the transport capacity of the root system, or root hydraulic conductance, with the degree of stomata opening controlling the rate of the transpiration driven water uptake into plants. The esk1-5 mutant had high levels of ABA, causing stomata closure and consequently low levels of evapo-transpiration (Figures 1, 2 and 3). In the esk1-5 ost1 and esk1-5 aba3-1 double mutants, water loss and leaf temperature, were intermediate between those of the single mutants (Figure 2B, C and 3B, C). This higher evapo-transpiration compared to esk1 single mutants was likely due to increased opening of stomata, which are, therefore, functional in esk1. Thus, the reduced levels of evapo-transpiration observed in esk1 mutants were not due to permanently closed stomata. We hypothesized that this could be because water uptake or transport to the vegetative tissues is reduced by the esk1 mutation.

When hydraulic conductivity was assessed, this was found to be lower for esk1 mutant roots (Figure 4 and Table 1). Water uptake by the roots occurs through radial transfer from the soil to the xylem vessels through the apoplast, the symplast or through the cell-to-cell pathway where it crosses cell membranes through water channels named aquaporins [38], [39]. Apoplastic, symplastic or aquaporin water transport modification could partly explain the lower Lpr measured for esk1 roots compared to wild type (Figure 4 and Table 1). Nonetheless, transcriptome analyses did not find significant alterations in aquaporin transcript abundance in esk1-5 plants [14]. A reduction in root system biomass could also cause a moderate decrease in water flow (Figure 4A, C), as would modifications to the root structure that generate resistance to water transport from the soil to aerial parts.

Once water has reached the xylem, its flux largely depends on the diameter of the vessels. The fact that the shape of the xylem vessels in esk1 roots was strongly altered could cause a higher resistance of esk1 vessels to water flow, independent of the water supply status, in agreement with the particularly low hydraulic conductivity measured for the esk1 lines (Figure 4C). The maximal conductivity calculated using Poiseuille's law predicts a decrease of 80% in esk1 compared to wild type due to decrease in the diameter of roots vessels (Table 1). This reduction is of the same order of magnitude as the decrease observed in root hydraulic conductivity measured. This suggests that the diameter of the xylem vessels is the main factor limiting water flux in xylem in esk1 mutants. By contrast, in maize the radial resistance is usually rate-limiting and not the longitudinal hydraulic resistance within the xylem [39]. These results suggest that the origin of the disrupted water uptake and water circulation through esk1 xylem would be the alterations observed in the vessels' structure. Therefore, ESK1 appears to be necessary for the correct formation of functional xylem vessels.

The esk1 stressed phenotype is likely due to its TE default

Our results tend to show that, as a result of collapsed TE, the overall volume of water circulating in esk1 xylem is greatly reduced.

In previous studies, the esk1-5 mutant was described as constitutively stressed with regard to its physiology: smaller stature of the plants, reduced RWC and transpiration rate, better WUE, similar transcriptomic profile and metabolomic data under control and drought conditions [14], [15]. The increased osmolyte concentrations observed in esk1 lines compared to wild type [14], [15] would explain the freezing-tolerant phenotype described by Xin and co-workers [26]. In the current study, we showed that ABA levels in esk1 mutants were higher than those of wild type in non-stressed conditions, which would be incoherent with a role for ESK1in stomata closure through ABA signaling downstream [40]. Analysis of the double mutant esk1-5 aba3-1 showed that this was not due to a direct role of ESK1 in ABA biosynthesis. Indeed, the double mutant phenotypes demonstrated that ESK1 did not intervene in growth regulation and water loss through ABA and that high ABA levels were an indirect consequence of esk1 mutation. Moreover, double mutant studies and root Lpr measurement confirmed that ESK1 could contribute to water circulation in the plant, as suggested earlier [14], [15]. This conclusion is consolidated by the fact that the size of esk1-5 ost1 double mutant is identical to esk1-5 (Figure 2A) and is, therefore, independent of the level of evapo-transpiration by the plant and only dependant on the amount of water in the plant. In addition, esk1-5 aba3-1 double mutants were smaller than both dwarf single mutants due to the combined effects of ABA deficiency and reduced water transport.

Like esk1, irx1/cesa8 has a reduced stature and high ABA levels, together with collapsed xylem and reduced water loss on detached leaves [32]. Chen and coworkers also observed an enhanced drought and osmotic stress tolerance in irx1/cesa8 mutant compared to wild type [32]. Moreover, irx14 mutant, affected in a glycosyl transferase involved in cell wall glucuroxylan biosynthesis, has recently been shown to exhibit drought tolerance [41]. It will be interesting to see whether this is a general phenomenon among irx mutants.

By integrating all the aspects of the esk1 phenotype, a model can be obtained were the low hydraulic conductance of the root apparatus, due to xylem vessels malformation, induces an hydraulic signal to the shoot, resulting in ABA synthesis [42]. The consequences of high ABA levels are well documented, and include stomata closure, low evapo-transpiration and synthesis of metabolites like soluble sugars and proline.

Xylem malformation in esk1 is accompanied by alterations in secondary cell wall composition

irx phenotypes have been reported for mutants affected in their cell wall composition. FTIR analyses were performed on esk1 sections targeting xylem, which are mainly composed of secondary cell wall. We observed differences between wild type and esk1 that were attributed to reduced pectin esterification and crystalline cellulose in the mutant. The later was confirmed by crystalline cellulose measurements (Figures 7, 8 and 9 and data not shown).

Although pectins are mainly present in primary cell walls [43], [44], pectin methylesterification appears to be a prerequisite for lignin modifications during secondary cell wall deposition in xylem cells [45]. A feedback loop which would interconnect the control of cellulose and pectin biosynthesis has already been suggested to participate in the homeostasis of wall rigidity [46]. Compensation mechanisms have also been observed between primary and secondary cell walls, when studying the irx3 mutant affected in a secondary cell wall specific cellulose synthase gene [31]. It is also worth noting that comparative FTIR spectroscopy performed on the irx1 mutant clearly demonstrated that the cell wall modifications encountered in esk1 mutants are not those of a cellulose synthase deficient mutant (Figure S2).

All the modifications observed in esk1 mutants would therefore be consistent with a role for ESK1 in the deposition or maintenance of a functional secondary cell wall, specifically in xylem and interfascicular fibers, its defect inducing a strong irx phenotype. Indeed, the altered secondary cell wall composition may result in a modification of the mechanical properties of the TE, so that resulting cell walls cannot provide enough strength to endure negative pressure, therefore inducing an irx phenotype [23].

Recently, sequence analysis predicted ESK1 to be part of a novel group of proteins named the PC(Pmr5-Cas-1p)-esterase family. Members of this family share a putative N-terminal acylesterase domain and ESK1 was proposed to modify cell wall glycans through carbohydrate acylation [47]. ESK1 also contains a C-terminal Domain of Unknown Function 231 (DUF231) [26]. Bischoff and co-workers found that members of the DUF231 gene family like POWDERY MILDEW RESISTANCE 5 (PMR5), TRICHOME BIREFRINGENCE (TBR) TBR-LIKE 3 (TBL3) and ESK1, harbor another plant-specific domain (TBL domain) that contains a conserved GDSL motif common to certain esterases and lipases [48]. Interestingly, FTIR analysis and PME activity measured for tbr and tbl3 etiolated seedlings also indicated reduced levels of esterified pectins in their cell walls compared to the wild type [48]. Moreover, secondary cell wall cellulose contents were reduced in tbr and tbl3. Bischoff and co-workers concluded that the TBL/DUF231 genes might be pectin-binding proteins that are involved in the overall cell wall chemical balance [49]. Bischoff and Scheible also propose that ESK1 should be renamed TBL29 (personal communication).

Nevertheless, we cannot exclude a more general action of ESK1 in xylem formation, as such broad impact on secondary cell wall chemical composition has not previously been reported for any cell wall mutant. The precise function of proteins harboring a DUF231 remains to be determined.


The data presented here demonstrate that ESK1 plays a major role in the formation of functional xylem vessels, which has dramatic consequences on water transport. ESK1 is expressed in cells that develop into xylem and TE are collapsed in esk1 mutants, a characteristic feature of irx phenotype. We establish for the first time in this study a clear link between this TE phenotype and the low water conductance, which explains their small stature, low evapo-transpiration, the stressed plant state and the stress tolerance previously reported [12], [14], [15]. Our results favor the hypothesis that ESK1 is a protein involved in cell wall deposition, maturation or regulation, as suggested for other members of the DUF231 family [47], [48], [49], [50]. It is also possible that the defect in ESK1 could influence earlier steps with consequences on the correct assembly of cell walls in xylem and interfascicular fibers.

Identification of the molecular function of ESK1, its involvement in stress responses and its potential role in cell wall formation will require further investigation.

Materials and Methods

Plant material and growth conditions

esk1-1 was isolated by Xin et al. [26] and esk1-4 and esk1-5 have been described by Bouchabke-Coussa et al. [14]. ost1/snrk2e [51] was kindly provided by Dr J. Leung, aba3-1 was identified by Leon-Kloosterziel et al. [17] and irx1-1 was described by Turner et al. [23]. esk1-1, esk1-4, esk1-5, ost1/srk2e and aba3-1 are in the Col-0 genetic background, irx1-1 is in the Ler background.

Abiotic stress

For ABA measurements, control culture conditions and mild drought stress were applied to individual plants, grown on Fertiss® propagation plugs. Seeds were stratified 3 or 4 days at 4°C in 0.1% (w/v) agar and then two seeds were sown onto each propagation plug. After the emergence of cotyledons, seedlings were removed to leave one plant on each plug. Plants were grown in controlled conditions in a growth chamber (22°C, light intensity 180 µmol m−2 s−1, 16 h photoperiod, 70% RH). Stress was applied at bolting: twenty-five days after sowing in our conditions. Each propagation plug was adjusted daily to the target substrate saturation with nutritive solution: 60% (w/v) for the control and 30% (w/v) for mild drought stress as previously described Bouchabke-Coussa et al. [14]. Plants were harvested after 7 days of stress implementation.

Infrared thermography and water-loss assays

Rapid dehydration assays were carried out using 3-week-old plants grown on propagation plugs in a growth-chamber (22°C, light intensity 180 µmol m−2 s−1, 16 h photoperiod, 70% RH). Four rosettes per genotype were cut from their root system and water loss was measured as described previously [52].

For leaf temperature measurements, plants were grown for 4 weeks in soil in a glasshouse (22°C, minimum 13 h photoperiod, maximum light intensity of 500 µmol m−2 s−1). In a growth chamber (25°C, 150 µmol m−2 s−1, 50% RH) leaves from well-watered plants were detached, placed abaxial-side uppermost and images acquired using an A320 infrared camera equipped with a 45° lens (FLIR Systems;

ABA content determination

Four independent experiments were carried out using plants at inflorescence emergence, either subjected to mild water deficit [14] or controls. Triplicate measurements were carried out for each condition and each measurement was performed using tissue from a pool of three rosettes. Tissue was freeze-dried prior to extraction of ABA.

Samples were weighed and 33 ng of a standard ABA-d4 (Euriso-Top SA, France) were added as an internal standard. Freeze-dried material was ground in 3 ml acetone/water/acetic acid (80/19/1; v/v/v), then centrifuged (4630 g, 4°C, 3 min). After re-extraction of the pellets with 1 ml of extraction solvent and sonication for 20 min (25 Hz), the supernatants were combined and concentrated under nitrogen. The dry extract was dissolved in 150 µl acetonitrile/water (50/50; v/v), filtered and analysed by HPLC–electrospray-tandom mass spectrometry (HPLC-ES-MSMS). Sample components were separated on a reverse-phase column (Uptisphere C18 5 µm, 150×2 mm i.d, Interchrom) using a Waters 2695 separation module (Alliance) (Waters, Milford, MA, USA) equipped with a Waters 2487 dual UV detector, with a flow-rate of 0.15 ml/min and a binary gradient: acetonitrile 0.5% acetic acid (v/v) (A) and acetic acid 0.5% (v/v) (B). Typically, the solvent gradient was programmed as following: 0–5 min 20% A, 5–15 min 65% A, 15–20 min 100% A, before returning to the initial composition at 30 min. Separated molecules were ionized in the ESI source and analyzed with a Waters Quattro LC triple quadrupole mass spectrometer (Waters, Milford, MA, USA) operating in a Multiple Reaction Monitoring (MRM) scanning mode. Instrument parameters were set as follows: capillary 2.75 kV (negative mode), extractor 2 V, source block and desolvation gas temperatures 120 and 350°C, respectively. Nitrogen was used to assist the nebulisation and the desolvation (250 and 450 L/h respectively), argon was used as collision gas at 3.5 10−3 mbar. The parameters used for MRM quantification of ABA-d4 and ABA in positive mode were: cone potential 16 V, collision energy 10 eV for two transitions used m/z 267>251 and 263>247 respectively. The limit of detection (LOD) and limit of quantification (LOQ) were calculated from calibration curve and sample using the Quantify module of MassLynx version 4.1 software. Typically, for a 5 µl injection of sample prepared with 33 ng internal standard and reconstituted in 150 µl of 50/50 acetonitrile/H2O (v/v), the respective LOD and LOQ are 1 and 3 pg/mg dry mass.

Data from the four independent experiments were combined for the statistical analysis. Multiple-samples comparisons were performed between genotypes for each treatment independently. Analysis of the effect of two variables, i.e. genotype and water treatment, and their interactions on the ABA concentration was performed by 2-D ANOVA for each pairs of genotypes. ANOVAs and multiple-samples comparisons were performed with the Statgraphics® software. Multiple-samples comparisons were carried out using the Fisher test (Least Significant Difference) at the 5% threshold. Box-plots graphs were performed with tools created by the Anastats association, available free at​ad.htm.

Reporter constructs, GUS assays and cytological observations

An approximately 1 kb fragment of the ESK1 promoter was amplified from wild type Col-0 genomic DNA using 5′ attB1-TGGTTGGTGCCGTATACATA 3′ and 5′ attB2-CCAAGGTTGCATCTGTTTGT 3′ primers, where attB1 and attB2 contain sequences complementary to the Gateway™ recombination sequences. The PCR product was cloned in the pDONR207™ gateway entry vector (Invitrogen™) via BP recombination reaction. Subsequently an LR recombination reaction was carried out to introduce the fragment into the pBI101-R1R2 binary destination vector (F. Divol, J.-C. Palauqui and B. Dubreucq, Institute Jean-Pierre Bourgin, INRA, Versailles, France, unpublished data) as a fusion with the GUS reporter gene. Electro-competent C58C1 Agrobacterium tumefaciens were transformed with this construct, which was then used for agroinfiltration of wild type Arabidopsis flower buds. Seven independent transgenic lines, each with a single homozygous T-DNA insertion, were retained for subsequent analyses.

Histochemical detection of GUS expression was performed as described by Jefferson et al. [53]. Potassium ferricyanide/potassium ferrocyanide was used and concentration adjusted (from 1 to 3 mM) depending on the insertion line, the organ and the developmental stage considered. Samples were observed by light microscopy (LEICA DMR B DIC). For observation of hypocotyls or stems or GUS stained, esk1 and wild type samples were embedded in 8% agarose and 70 µm sections cut using a vibratome. esk1 and wild type sections were observed under UV light, where lignified tissues appears fluorescent, or under white light when stained with carmine-green which gives green coloration to lignin and pink coloration to cellulose [54].

Hydraulic conductance

Root water transport measurements were performed essentially as described in Javot et al. [55]. Freshly excised root organs were inserted into a pressure chamber with the hypocotyls threaded through the lid of the chamber. Upon pressurization, the flow rate of the exuded sap was measured and plotted as a function of the pressure imposed. The gradient of the graph obtained provided the hydraulic conductance measure, or Lo, which was then adjusted with respect to root dry weight in order to obtain the root hydraulic conductivity, or Lpr. Data were obtained from 13 measurements for wild type, 9 measurements for esk1-1 and 5 measurements for esk1-5.

Box-plots graphs were performed with tools created by the Anastats association, available free at​ad.htm.

For calculation of root maximal conductivity, ImageJ software was used to measure the maximal radius of the 4 to 5 larger xylem vessels. 4 images of root sections observed under UV light, from 3 different plants were used. The maximal conductivity (g) of the vessels was calculated according to Poiseuille's law.

R = (8.η)/(π.r4) where g = 1/R (m2/s/MPa), η is the water viscosity coefficient (1E−9 MPa/s) and r is the maximal radius (µm).

FTIR spectroscopy

Analyses were carried out on xylem tissue from hypocotyls or the basal region of branched stems using 50 µm thick vibratome sections of agarose-embedded tissue. For each genotype, 5 to 6 sections from 3 different plants were analysed. FTIR spectra were collected from a 50 µm x 50 µm window targeting xylem vessels; normalization of the data and statistical analysis (Student's t-test) were performed as described in Mouille et al. [24].

Crystalline cellulose extraction and dosage

Plant material was harvested and stored in absolute ethanol. Hypocotyl or stem pieces were ground and incubated twice in 70% ethanol for 60 min at 70°C. Pellets were then washed in acetone for 2 min at room temperature then vacuum-dried. After weighing samples, crystalline cellulose content was determined as described in Scott and Melvin [56] and Updegraff [57]. Two independent experiments were carried out with two replicates in each. A Mann and Whitney non parametric test was used to compare cellulose content between the two genotypes.

Mann and Whitney non parametric test and box-plots graphs were performed with tools created by the Anastats association, available free at​ad.htm.

Supporting Information

Figure S1.

Vascular tissue structure in young stems of esk1 and wild type. Transverse section of young stems (2 to 3 centimeters high) from wild type (A, wt) and one representative esk1 mutant plant (B, esk1-1), with lignin stained in green with Carmine-green.



Figure S2.

The structure and composition of esk1-1 and irx1-1 xylem are different. Comparison of FTIR spectra obtained from xylem in basal stem sections of irx1-1 and esk1-1 plants and their respective wild types, Ler and Col-0, respectively. A Student's t-test was performed on absorbance values of wild type versus mutant and plotted against wave numbers. The grey zone, between −2 and +2, corresponds to non-significant differences (p-value<0.05) between the two genotypes tested.



Table S1.

Statistical comparisons of ABA measurements from wild type (wt), esk1 and aba3-1 mutants.




We thank Akira Suzuki, Georges Pelletier, Françoise Budar and Volker Bishoff for critical reading of the manuscript, and Liliane Laroche, Lilian Dahuron and Bernadette Trouve for plant culture. We are grateful to Richard Sibout, Jérôme Pelloux and Deborah Goffner for productive scientific exchanges.

Author Contributions

Conceived and designed the experiments: VL HMN JT YB MDT. Performed the experiments: VL MNF AD HMN AMG JT YB GM. Analyzed the data: VL MNF AD HMN AMG JT YB GM MDT. Contributed reagents/materials/analysis tools: VL MNF AD AMG. Wrote the paper: VL HMN AMG YB GM MDT.


  1. 1. Lefebvre V, Kiani SP, Durand-Tardif M (2009) A Focus on Natural Variation for Abiotic Constraints Response in the Model Species Arabidopsis thaliana. Int J Mol Sci 10: 3547–3582.
  2. 2. Desikan R, Mackerness SAH, Hancock JT, Neill SJ (2001) Regulation of the Arabidopsis transcriptome by oxidative stress. Plant Physiol 127: 159–172.
  3. 3. Seki M, Narusaka M, Abe H, Kasuga M, Yamaguchi-Shinozaki K, et al. (2001) Monitoring the expression pattern of 1300 Arabidopsis genes under drought and cold stresses by using a full-length cDNA microarray. Plant Cell 13: 61–72.
  4. 4. Seki M, Narusaka M, Ishida J, Nanjo T, Fujita M, et al. (2002) Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high-salinity stresses using a full-length cDNA microarray. Plant J 31: 279–292.
  5. 5. Kreps JA, Wu Y, Chang HS, Zhu T, Wang X, et al. (2002) Transcriptome changes for Arabidopsis in response to salt, osmotic, and cold stress. Plant Physiol 130: 2129–2141.
  6. 6. Kilian J, Whitehead D, Horak J, Wanke D, Weinl S, et al. (2007) The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV-B light, drought and cold stress responses. Plant J 50: 347–363.
  7. 7. Wang W, Vinocur B, Altman A (2003) Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance. Planta 218: 1–14.
  8. 8. Bray EA (2004) Genes commonly regulated by water-deficit stress in Arabidopsis thaliana. J Exp Bot 55: 2331–2341.
  9. 9. Hummel I, Pantin F, Sulpice R, Piques M, Rolland G, et al. (2010) Arabidopsis plants acclimate to water deficit at low cost through changes of carbon usage: an integrated perspective using growth, metabolite, enzyme, and gene expression analysis. Plant Physiol 154: 357–372.
  10. 10. Nilson SE, Assmann SM (2007) The control of transpiration. Insights from Arabidopsis. Plant Physiol 143: 19–27.
  11. 11. Wasilewska A, Vlad F, Sirichandra C, Redko Y, Jammes F, et al. (2008) An update on abscisic acid signaling in plants and more. Mol Plant 1: 198–217.
  12. 12. Xin Z, Browse J (1998) Eskimo1 mutants of Arabidopsis are constitutively freezing-tolerant. Proc Natl Acad Sci U S A 95: 7799–7804.
  13. 13. Reyes-Diaz M, Ulloa N, Zuniga-Feest A, Gutierrez A, Gidekel M, et al. (2006) Arabidopsis thaliana avoids freezing by supercooling. J Exp Bot 57: 3687–3696.
  14. 14. Bouchabke-Coussa O, Quashie ML, Seoane-Redondo J, Fortabat MN, Gery C, et al. (2008) ESKIMO1 is a key gene involved in water economy as well as cold acclimation and salt tolerance. BMC Plant Biol 8: 125.
  15. 15. Lugan R, Niogret MF, Kervazo L, Larher FR, Kopka J, et al. (2009) Metabolome and water status phenotyping of Arabidopsis under abiotic stress cues reveals new insight into ESK1 function. Plant Cell Environ 32: 95–108.
  16. 16. Thomashow MF (1994) 30 Arabidopsis thaliana as a Model for Studying Mechanisms of Plant Cold Tolerance. In: Cold Spring Harbor laboratory Monograph Archive 807–834. DOI:10.1101/087969428.27.807.
  17. 17. Leon-Kloosterziel KM, Gil MA, Ruijs GJ, Jacobsen SE, Olszewski NE, et al. (1996) Isolation and characterization of abscisic acid-deficient Arabidopsis mutants at two new loci. Plant J 10: 655–661.
  18. 18. Schwartz SH, Leon-Kloosterziel KM, Koornneef M, Zeevaart JA (1997) Biochemical characterization of the aba2 and aba3 mutants in Arabidopsis thaliana. Plant Physiol 114: 161–166.
  19. 19. Xiong L, Ishitani M, Lee H, Zhu JK (2001) The Arabidopsis LOS5/ABA3 locus encodes a molybdenum cofactor sulfurase and modulates cold stress- and osmotic stress-responsive gene expression. Plant Cell 13: 2063–2083.
  20. 20. Mustilli AC, Merlot S, Vavasseur A, Fenzi F, Giraudat J (2002) Arabidopsis OST1 protein kinase mediates the regulation of stomatal aperture by abscisic acid and acts upstream of reactive oxygen species production. Plant Cell 14: 3089–3099.
  21. 21. Merlot S, Mustilli AC, Genty B, North H, Lefebvre V, et al. (2002) Use of infrared thermal imaging to isolate Arabidopsis mutants defective in stomatal regulation. Plant J 30: 601–609.
  22. 22. Maurel C, Simonneau T, Sutka M (2010) The significance of roots as hydraulic rheostats. J Exp Bot 61: 3191–3198.
  23. 23. Turner SR, Somerville CR (1997) Collapsed xylem phenotype of Arabidopsis identifies mutants deficient in cellulose deposition in the secondary cell wall. Plant Cell 9: 689–701.
  24. 24. Mouille G, Robin S, Lecomte M, Pagant S, Hofte H (2003) Classification and identification of Arabidopsis cell wall mutants using Fourier-Transform InfraRed (FT-IR) microspectroscopy. Plant J 35: 393–404.
  25. 25. Kacurakova M, Smith AC, Gidley MJ, Wilson RH (2002) Molecular interactions in bacterial cellulose composites studied by 1D FT-IR and dynamic 2D FT-IR spectroscopy. Carbohydr Res 337: 1145–1153.
  26. 26. Xin Z, Mandaokar A, Chen J, Last RL, Browse J (2007) Arabidopsis ESK1 encodes a novel regulator of freezing tolerance. Plant J 49: 786–799.
  27. 27. Chaffey N, Cholewa E, Regan S, Sundberg B (2002) Secondary xylem development in Arabidopsis: a model for wood formation. Physiol Plant 114: 594–600.
  28. 28. Fukuda Y (2000) Interaction of nuclear proteins with intrinsically curved DNA in a matrix attachment region of a tobacco gene. Plant Mol Biol 44: 91–98.
  29. 29. Plomion C, Leprovost G, Stokes A (2001) Wood formation in trees. Plant Physiol 127: 1513–1523.
  30. 30. Elo A, Immanen J, Nieminen K, Helariutta Y (2009) Stem cell function during plant vascular development. Semin Cell Dev Biol 20: 1097–1106.
  31. 31. Bosca S, Barton CJ, Taylor NG, Ryden P, Neumetzler L, et al. (2006) Interactions between MUR10/CesA7-dependent secondary cellulose biosynthesis and primary cell wall structure. Plant Physiol 142: 1353–1363.
  32. 32. Chen Z, Hong X, Zhang H, Wang Y, Li X, et al. (2005) Disruption of the cellulose synthase gene, AtCesA8/IRX1, enhances drought and osmotic stress tolerance in Arabidopsis. Plant J 43: 273–283.
  33. 33. Taylor NG, Howells RM, Huttly AK, Vickers K, Turner SR (2003) Interactions among three distinct CesA proteins essential for cellulose synthesis. Proc Natl Acad Sci U S A 100: 1450–1455.
  34. 34. Taylor NG, Scheible WR, Cutler S, Somerville CR, Turner SR (1999) The irregular xylem3 locus of Arabidopsis encodes a cellulose synthase required for secondary cell wall synthesis. Plant Cell 11: 769–780.
  35. 35. Persson S, Caffall KH, Freshour G, Hilley MT, Bauer S, et al. (2007) The Arabidopsis irregular xylem8 mutant is deficient in glucuronoxylan and homogalacturonan, which are essential for secondary cell wall integrity. Plant Cell 19: 237–255.
  36. 36. Sibout R, Eudes A, Mouille G, Pollet B, Lapierre C, et al. (2005) CINNAMYL ALCOHOL DEHYDROGENASE-C and -D are the primary genes involved in lignin biosynthesis in the floral stem of Arabidopsis. Plant Cell 17: 2059–2076.
  37. 37. Zhong R, Lee C, Zhou J, McCarthy RL, Ye ZH (2008) A battery of transcription factors involved in the regulation of secondary cell wall biosynthesis in Arabidopsis. Plant Cell 20: 2763–2782.
  38. 38. Javot H, Maurel C (2002) The role of aquaporins in root water uptake. Ann Bot 90: 301–313.
  39. 39. Steudle E, Peterson C (1998) Review article. How does water get through roots? J Exp Bot 49: 775–788.
  40. 40. Xie X, Wang Y, Williamson L, Holroyd GH, Tagliavia C, et al. (2006) The identification of genes involved in the stomatal response to reduced atmospheric relative humidity. Curr Biol 16: 882–887.
  41. 41. Keppler BD, Showalter AM (2010) IRX14 and IRX14-LIKE, two glycosyl transferases involved in glucuronoxylan biosynthesis and drought tolerance in Arabidopsis. Mol Plant 3: 834–841.
  42. 42. Christmann A, Weiler EW, Steudle E, Grill E (2007) A hydraulic signal in root-to-shoot signalling of water shortage. Plant J 52: 167–174.
  43. 43. Sanchez-Rodriguez C, Rubio-Somoza I, Sibout R, Persson S (2010) Phytohormones and the cell wall in Arabidopsis during seedling growth. Trends Plant Sci 15: 291–301.
  44. 44. Wolf S, Mouille G, Pelloux J (2009) Homogalacturonan methyl-esterification and plant development. Mol Plant 2: 851–860.
  45. 45. Pelloux J, Rusterucci C, Mellerowicz EJ (2007) New insights into pectin methylesterase structure and function. Trends Plant Sci 12: 267–277.
  46. 46. Burton RA, Gibeaut DM, Bacic A, Findlay K, Roberts K, et al. (2000) Virus-induced silencing of a plant cellulose synthase gene. Plant Cell 12: 691–706.
  47. 47. Anantharaman V, Aravind L (2010) Novel eukaryotic enzymes modifying cell-surface biopolymers. Biol Direct 5: 1–8.
  48. 48. Bischoff V, Nita S, Neumetzler L, Schindelasch D, Urbain A, et al. (2010) TRICHOME BIREFRINGENCE and Its Homolog AT5G01360 Encode Plant-Specific DUF231 Proteins Required for Cellulose Biosynthesis in Arabidopsis. Plant Physiol 153: 590–602.
  49. 49. Bischoff V, Selbig J, Scheible WR (2010) Involvement of TBL/DUF231 proteins into cell wall biology. Plant Signal Behav 5 1057-1059:
  50. 50. Vogel JP, Raab TK, Somerville CR, Somerville SC (2004) Mutations in PMR5 result in powdery mildew resistance and altered cell wall composition. Plant J 40: 968–978.
  51. 51. Yoshida R, Hobo T, Ichimura K, Mizoguchi T, Takahashi F, et al. (2002) ABA-activated SnRK2 protein kinase is required for dehydration stress signaling in Arabidopsis. Plant Cell Physiol 43: 1473–1483.
  52. 52. Lefebvre V, North H, Frey A, Sotta B, Seo M, et al. (2006) Functional analysis of Arabidopsis NCED6 and NCED9 genes indicates that ABA synthesized in the endosperm is involved in the induction of seed dormancy. Plant J 45: 309–319.
  53. 53. Jefferson RA, Kavanagh TA, Bevan MW (1987) GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6: 3901–3907.
  54. 54. Cholet C, Mondolot L, Andary C (2002) New histochemical observations of shot grapevine berries. Australian Journal of Grape and Wine Research 8: 126–131.
  55. 55. Javot H, Lauvergeat V, Santoni V, Martin-Laurent F, Guclu J, et al. (2003) Role of a single aquaporin isoform in root water uptake. Plant Cell 15: 509–522.
  56. 56. Scott TA, Melvin EH (1953) Determination of dextran with anthrone. Anal Chemistry 25: 1656–1661.
  57. 57. Updegraff DM (1969) Semimicro determination of cellulose in biological materials. Anal Biochem 32: 420–424.