The endodermis is a key cell layer in plant roots that contributes to the controlled uptake of water and mineral nutrients into plants. In order to provide such functionality the endodermal cell wall has specific chemical modifications consisting of lignin bands (Casparian strips) that encircle each cell, and deposition of a waxy-like substance (suberin) between the wall and the plasma membrane. These two extracellular deposits provide control of diffusion enabling the endodermis to direct the movement of water and solutes into and out of the vascular system in roots. Loss of integrity of the Casparian strip-based apoplastic barrier is sensed by the leakage of a small peptide from the stele into the cortex. Here, we report that such sensing of barrier integrity leads to the rebalancing of water and mineral nutrient uptake, compensating for breakage of Casparian strips. This rebalancing involves both a reduction in root hydraulic conductivity driven by deactivation of aquaporins, and downstream limitation of ion leakage through deposition of suberin. These responses in the root are also coupled to a reduction in water demand in the shoot mediated by ABA-dependent stomatal closure.
Both Casparian strips and suberin lamellae, two extracellular hydrophobic barriers located in the wall of endodermal cells of the root, are thought to play important roles in restricting the free diffusion of solutes and water (reviewed in1,2). Casparian strips act as apoplastic barriers not only to block solutes moving into the xylem through the free space between cells, but also to prevent their backflow from the stele to the apoplast of the cortex3,4,5. Suberin lamellae, due to their deposition between the endodermal plasma membrane and secondary cell wall, do not block aploplastic transport but rather limit transcellular transport of nutrients6,7 and possibly water at the endodermis. Cross talk between the Casparian strip and suberin lamellae exists, with suberin being deposited in response to disruption of Casparian strips3,4,5,7,8. These extracellular barriers are therefore at a cross-road between control of mineral nutrient and water uptake. However, the mechanisms that allow plants to integrate both these barrier functions to enable the simultaneous uptake of sufficient water and mineral nutrients remain underexplored.
The dirigent-like protein Enhanced Suberin1 (ESB1) functions in the correct formation of Casparian strips by allowing the lignin, deposited at the Casparian Strip Domain through the action of Peroxidase64 (PER64) and the Respiratory Burst Oxidase Homolog F (RBOHF)9, to form into a continuous ring3. In the absence of this dirigent-like protein defective Casparian strips are formed along with enhanced and early deposition of suberin in the endodermis3. A similar pattern of Casparian strip disruption and response is also observed when the Casparian Strip Domain (CSD) is disrupted through the loss of Casparian Strip Domain Proteins (CASPs)3. These changes lead to systematic alterations in the profile of mineral nutrients and trace elements accumulating in leaves, and this phenotype provided the first tool for identification of genes involved in Casparian strip development10. Detection of the diffusible vasculature-derived peptides CASPARIAN STRIP INTEGRITY FACTORS 1 & 2 (CIF1 & 2) through interaction with the SCHENGEN3 receptor-like kinase is what drives this endodermal response to loss of Casparian strip integrity4,11,12.
Here, we report that detection of a loss of Casparian strip integrity at the root endodermis by the CIFs/SGN3 pathway leads to an integrated local and long-distance response. This response rebalances water and mineral nutrient uptake, compensating for breakage of the Casparian strip apoplastic seal between the stele and the cortex. This rebalancing involves both a reduction in root hydraulic conductivity driven by deactivation of aquaporins, and limitation of ion leakage through deposition of suberin in endodermal cell walls. This local root-based response is also coupled to a reduction in water demand in the shoot driven by ABA-mediated stomatal closure.
Results and Discussion
Loss of Casparian strip integrity leads to enhanced suberin deposition
The dirigent-like protein Enhanced Suberin1 (ESB1) functions in the formation of Casparian strips by allowing the correct deposition of lignin at the Casparian strip domain. The enhanced deposition of suberin in the esb1-1 mutant with disrupted Casparian strips can clearly be observed using the lipophilic stain Fluorol Yellow 088 (FY 088) close to the root tip (Fig. 1a), and this can be quantified by counting the number of endodermal cells after the onset of cell expansion to the first appearance of yellow fluorescence (Fig. S1a). This early deposition of suberin is also verified by the clear correspondence of FY 088 staining with enhanced promoter activity of known suberin biosynthetic genes13, including GPAT5 monitored through both GUS staining and GFP fluorescence (Fig. 1a), and also others through GUS staining (FAR1, FAR4, FAR5, GPAT5) (Supplementary Fig. S1a,b). This is further reinforced by the enhanced expression of known suberin biosynthetic genes (FAR1, FAR4, FAR5, GPAT5, HORST and MYB41) in esb1-1 relative to wild-type (Supplementary Fig. S1c).
To better understand the causal link between Casparian strip integrity and enhanced deposition of suberin, we performed a reciprocal grafting experiment that revealed that the esb1-1 mutation is only required in the root to drive enhanced deposition of suberin at the endodermis, placing the function of ESB1 and the driver for increased suberin in the same tissue (Fig. 1b and Supplementary Fig. S1d). To determine the cause and effect relationship between damaged Casparian strips and enhanced suberin we carefully monitored the first appearance of both Casparian strips and enhanced suberin in esb1-1. Using lignin staining in the Casparian strip marker line pCASP1::CASP1::GFP, we are able to observe that damaged Casparian strips are visible 2.5 days after sowing (Fig. 1c). This is at least 12 hr before the first indication of enhanced suberin biosynthesis, which we monitor using promoter activity of suberin biosynthetic genes GPAT5, FAR4, FAR1 and FAR5 (Fig. 1d; Supplementary Fig. S2a). This was also verified by the direct observation of suberin deposition with FY 088 (Supplementary Fig. S2b). The observation that treatment with the CIF2 peptide, normally leaked from the stele through loss of Casparian strip integrity, can enhance suberin deposition in wild-type plants11 supports our interpretation that enhanced suberin deposition is a response to loss of integrity of the Casparian strip-based apoplastic diffusion barrier. Furthermore, loss-of-function of the receptor-like kinase SGN3, required for sensing of CIFs, blocks the enhanced deposition of suberin in esb1-1 and casp1-1casp3-1 based on a chemical analysis of suberin in esb1-1 (Supplementary Fig. S3), and also on FY 088 staining4. We conclude that Casparian strip defects sensed by the CIFs/SGN3 surveillance system lead to enhanced deposition of suberin in the endodermis.
Enhanced suberin deposition limits solute leakage from the vasculature when Casparian strip integrity is lost
The observation that enhanced suberin is deposited as a response to loss of integrity of the endodermal-based diffusion barrier between stele and cortex, raises the question, what is the function of this increased suberin deposition? Previously, the extent of endodermal suberin has been shown to be part of the response to nutrient status6. We therefore tested the selectivity to solutes σNaCl, in roots varying in the extent of suberin deposition and the functionality of Casparian strips. For this, we measured solute leakage into xylem sap of pressurized roots at increasing sodium chloride concentrations in the solution bathing the roots. Taken individually, σNaCl of roots of esb1-1, sgn3-3 and wild-type were not significantly different from one another (Fig. 2a), which is surprising given the disruption of the Casparian strip-based apoplastic diffusion barrier in both mutants. However, removal of suberin in esb1-1, by endodermal-specific ectopic expression of a cutinase (CDEF1, CUTICLE DESTRUCTING FACTOR 1) (Supplementary Fig. S3)7, caused a significant decrease in σNaCl compared to wild-type plants (Fig. 2a), and a similar tendency when compared to esb1-1 (Fig. 2a). This supports the notion that enhanced suberin deposition at the endodermis helps prevent passive solute leakage caused by defects in the Casparian strips of the esb1-1 mutant. We also observed a significant decrease in σNaCl in the double mutant esb1-1sgn3-3 compared to both wild-type and sgn3-3 (Fig. 2a). It is known that SGN3 is required for the enhanced deposition of suberin that occurs at the endodermis in esb1-14 (Supplementary Fig. S3). Our observation that removal of this enhanced suberin in esb1-1sgn3-3 decreases σNaCl further supports our conclusion that the role of this increased suberin deposition is to limit solute leakage where Casparian strip barriers are disrupted.
Loss of Casparian strip integrity signals an inactivation of aquaporins responsible for reducing root hydraulic conductivity and enhanced suberin deposition
It has also been suggested that endodermal suberin may impact water permeability, though how is still unclear14. To further address the role of enhanced endodermal suberin, we investigated root hydraulic conductivity (Lpr) of esb1-1 and observed a significant reduction by 62% with respect to wild-type (Fig. 2b). Importantly, this difference in esb1-1 Lpr originates mainly from a reduction in an aquaporin-mediated (sodium azide sensitive) water transport pathway (20.8 ± 4.6 ml.g−1.h−1.MPa−1 in esb1-1 vs 91.2 ± 4.7 ml.g−1.h−1.MPa−1 for control plants, p < 0.001, Supplementary Fig. S4a). We also observed that the azide-resistant water transport pathway was lower in esb1-1 than in wild-type (Supplementary Fig. S4a), yet to a lesser extent than the aquaporin mediated pathway. The dramatic reduction in aquaporin-mediated Lpr in esb1-1 we observe is an intriguing finding, which led us to consider if this lack of aquaporin activity in esb1-1 roots is due to a direct output from the CIFs/SGN3 signalling pathway, or if it represents an effect downstream of enhanced suberin deposition. We found that removal of endodermal suberin in esb1-1 through expression of CDEF1 in the endodermis had no further effect on Lpr (Fig. 2b). This rules out a role for suberin in the reduced aquaporin-mediated Lpr of esb1-1. However, in the esb1-1sgn3-3 double mutant, as compared to esb1-1, we observed a full recovery of Lpr back to wild-type levels (Fig. 2b). Loss of Casparian strip integrity in esb1-1 therefore appears to be sensed by the CIFs/SGN3 signalling pathway, which leads to the inactivation of aquaporins, thereby reducing Lpr. To support this conclusion, we show that exogenous application of CIF2 to wild-type plants for 3 h induces a reduction in Lpr, and only in the presence of a functional SGN3 (Fig. 2c).
We have established the existence of two critical outputs of the CIFs/SGN3 diffusion-barrier surveillance system. These are enhanced deposition of endodermal suberin limiting solute leakage, and the inactivation of root aquaporin activity reducing Lpr. Do these two independent outputs of the CIFs/SGN3 diffusion barrier surveillance system work in parallel, or in series with one response leading to the other? The fact that removal of endodermal suberin in esb1-1 does not compensate for its reduced Lpr (Fig. 2b) suggests that enhanced suberin deposition is not the cause of the reduced aquaporin-mediated Lpr. However, reduced activity of aquaporins through loss-of-function of the two major aquaporins PIP2;1 and PIP2;2 in the pip2;1pip2;2 double mutant15, does cause significant increases in endodermal suberin deposition (Fig. 2d). A similar increase in suberin is also observed after treatment with the aquaporin inhibitor sodium azide through observation of the activity of the transcriptional reporter pGPAT5::mCITRINE-SYP122 for suberin biosynthesis6 (Fig. 2e). GPAT5 expression is observed to expand toward the root tip after 6 hours only of sodium azide treatment (Fig. 2e). Based on this evidence, we propose the following sequence of events. Casparian strip defects are detected by the apoplastic leakage of CIFs from the stele, being sensed by SGN3. Once activated, SGN3 signals the inactivation of aquaporins thereby reducing Lpr which in turn leads to the early and enhanced deposition of endodermal suberin. In such a model, SGN3 would inhibit aquaporin function, which may appear at variance with the usual activation of aquaporins through phosphorylation16. Yet, such an inhibition was recently described in the case of FERONIA, a protein kinase inactivating PIP2; 1 function through an as yet unknown mechanism17.
Activation of endodermal ABA signalling is not required for enhanced suberin deposition in responses to loss of Casparian strip integrity
Abscisic acid (ABA) has been shown to be involved in regulating both aquaporin activity reviewed in18 and suberin deposition6, making ABA an interesting candidate worth exploring for a role in downstream CIFs/SGN3 signalling. To probe this possibility we expressed the dominant negative allele of the regulator of ABA signalling ABA-INSENSITIVE 1 (ABI1) in the endodermis of esb1-1 using pELTP::abi1. This abi1 construct specifically blocks ABA signalling at the endodermis and delays suberisation in a wild-type background (Fig. 3 and Supplementary Fig. S4a) as previously shown in (6). In esb1-1, we observed abi1 to have no effect on either the inactivation of aquaporins or the enhanced deposition suberin (Fig. 3 and Supplementary Fig. S4a). We also observe that aquaporin inhibition with sodium azide in the pELTP::abi1-1 line still induces expression of the suberin biosynthesis gene GPAT5 toward the root tip in the pGPAT::mCITRINE-SYP122 line, as observed in wild-type (Supplementary Fig. S4b, Fig. 2e). Based on this, activation of ABA signalling in the endodermis does not link perception of Casparian strip defects with the downstream responses of reduced aquaporin-mediated Lpr or suberin deposition. Supporting this, we observe no significant difference in ABA concentration in roots of esb1-1 and wild-type (Fig. S4c). Interestingly, suppression of endodermal ABA signalling seems to contribute to the inactivation of aquaporin-mediated Lpr in a wild-type background (Supplementary Fig. S4a).
A root-based SGN3 derived signal mediates stomata closures by ABA locally in the leaves
The esb1-1 mutant is known to have reduced stomatal apertures and enhanced wilting resistance3,10. This suggests that the CIFs/SGN3 sensing system not only initiates a local root response to Casparian strip integrity but is also involved in initiating long-distance responses in the shoot. We observe reduced stomatal apertures in esb1-1 (Supplementary Fig. S5a), and an analysis of the expression of a set of known ABA signalling and response genes in leaves (Supplementary Fig. S5b–i) suggest that this stomatal closure is part of an ABA driven response. The aba1 mutation confers a strong ABA deficiency19. By generating an esb1-1aba1 double mutant, we investigated the ABA-dependent component in the leaf response we observe in esb1-1. ABA-deficiency in esb1-1aba1 suppressed both the reduced stomatal aperture (Supplementary Fig. S6a) and the activation of expression of ABA signalling and response genes (assayed as expression of RAB18, RD29B, CER1) that we observe in esb1-1 (Supplementary Fig. S6b–d). ABA is therefore necessary for the stomatal closure we observe in esb1-1. The elevated ABA concentration we observe in leaves of esb1-1 compared to wild-type (Supplementary Fig. S4d) supports this conclusion. We also used the esb1-1sgn3-3 double mutant to test if SGN3 is involved in initiating this leaf ABA response. In leaves of the esb1-1sgn3-3 double mutant the elevated expression of a set of ABA signalling and response genes observed in esb1-1 is reduced to below that of wild-type (Supplementary Fig. S5b–i). Further, the reduced stomatal aperture of esb1-1 is also recovered to wild-type levels in this double mutant (Supplementary Fig. S5a). SGN3 is therefore necessary for the ABA-dependent stomatal closure in response to the defective endodermal diffusion barrier in esb1-1.
This raises the question of what links detection of a break in the endodermal diffusion barrier with ABA-driven closure of stomates in the leaf? Removal of endodermal suberin in esb1-1 expressing CDEF1 revealed a significant reduction in ABA-regulated gene expression, and a tendency to increasing stomatal aperture towards wild-type (Supplementary Fig. S5). Thus, increased suberin deposition in the endodermis of the esb1-1 root appears to play a partial role in the ABA controlled reduction in leaf transpiration. We have ruled out a role of local ABA signalling in controlling enhanced suberin deposition at the endodermis in esb1-1 (Fig. 3). Using a similar strategy of expressing abi1 in the endodermis, in this case using the SCARECROW promoter (pSCR), primarily active in the endodermis20, we also show that in esb1-1 ABA signalling at the endodermis is not promoting stomatal closure (Supplementary Fig. S6e) or enhanced ABA signalling in leaves (assayed using expression of RAB18, RD29B and CER1) (Supplementary Fig. S6f–h). We note that pSCR is also active in bundle sheath cell21, and so ABA-signalling in these cells is also not involved in promoting stomatal closure in esb1-1.
Furthermore, enhanced ABA signalling in the endodermis is also not responsible for the initiation of the long-distance response of stomatal closure in leaves, and again it is more likely that suppression of ABA signalling is playing a role. This can be seen in the fact that expression of abi1 in the endodermis, blocking ABA signalling, mimics the effect of esb1-1 on Lpr and stomatal aperture closure (Supplementary Figs S4a and S6e). However, these possibilities remain to be further explored. In contrast to these root-based or long-distance effects, the closure of stomata in leaves in response to a root-based CIFs/SGN3 derived signal is mediated by ABA locally in the leaves. We also note that the long distance signal connecting CIFs/SGN3 in roots with reduced leaf transpiration is currently unknown. Interestingly, a root-derived peptide (CLE25) has been recently identified as involved in long-distance signalling22. In response to drought stress, CLE25 move from root to shoot and induces ABA accumulation in leaves and stomatal closure.
Output of CIFs/SGN3 surveillance compensates for loss of diffusion barrier function
Casparian strips have been suggested to play a critical role in forming a barrier to apoplastic diffusion to limit uncontrolled uptake and backflow of solutes from roots reviewed in1. However, most Casparian strip mutants only appear to show fairly subtle phenotypic effects, and this has been a source of continued puzzlement. Here, we show that sensing damage to Casparian strips via leakage of the vasculature-derived CIF peptides from the stele into the cortex triggers a mechanism that inactivates aquaporins, promotes enhanced deposition of suberin limiting solute leakage in roots, and reduces transpiration in leaves, which all contribute to increasing solute concentration in the xylem (Supplementary Fig. S7). The overall outcome of this integrated response is a rebalancing of solute and water uptake and leakage. These physiological compensation mechanisms mitigate the loss of Casparian strip integrity, allowing relatively normal growth and development. A key part of this compensation mechanism is the ability of esb1-1 to limit water loss by the shoot by reducing stomatal aperture, in an ABA-dependent manner. This is clearly established by our observation that the esb1-1aba1 double mutant has severely reduced growth and seed production compared to either of the single mutants, and these growth defects can be partially supressed by the exogenous application of ABA (Fig. 4, Supplementary Figs S8 and S9).
The mechanisms we have identified are triggered by the loss of Casparian strips integrity. Such an event can occur during biotic stress including root nematodes infestation, and also during developmental processes such as lateral root emergence (LRE) where Casparian strips are remodelled23, suberin deposition occurs7, and aquaporin expression is suppressed15.
Here, we describe novel outputs of the CIFs/SGN3 surveillance system that couple sensing of the integrity of the Casparian strip-based apoplastic diffusion barrier at the endodermis with pathways that regulate both solute leakage and hydraulic conductivity in the root (Fig. 5). Long distance signals then connect these root-based responses with compensatory mechanisms in leaves which are mediated by local ABA signalling (Fig. 5). Our discoveries provide a new framework which integrates our emerging understanding of the molecular development of the Casparian strip and suberin diffusion barriers with two of the major physiological functions required for plant survival – solute and water uptake.
The esb1-1 mutant was induced by fast neutron bombardment in a Col-0 background3, aba1 (N25407) generated by T-DNA insertion was provided by the Nottingham Arabidopsis Stock Centre (NASC). Marker lines for monitoring the suberin in the root of young seedlings including pFAR1::GUS, pFAR4::GUS, pFAR5::GUS, pCASP1::GFP and pGPAT5::NLS-GFP seeds with Col-0 background were provided by Domergue Frédéric24 and Niko Geldner6,25. To confirm the homozygous nature of the mutations in crosses between esb1-1 and the suberin reporter lines above, genotyping was done by PCR or sequencing. The seeds of sgn3-3, esb1-1sgn3-3, pCASP1::CDEF1 and esb1-1 pCASP1::CDEF1 for root hydraulic and suberin monomers measurement have been described in the references4,6, and were provided by Niko Geldner and Takehiro Kamiya7. The seeds of pELTP::abi1, pELTP::mCitrine-SYP122 and pSCR::abi1 was provided by Marie Barberon and José R. Dinneny. The pip2;1pip2;2 mutant was provided by Christophe Maurel15. The pELTP::abi1 line was crossed with pELTP::mCitrine-SYP122 and the T1 were analysed for mCitrine-SYP122.
Grafting of Arabidopsis
For grafting experiment, we used the protocol described in26. Arabidopsis seeds were sterilized and sowed in plates containing ½ MS, 1% Agar, and 0.5% sucrose. After 2 days of stratification at 4 °C, plants were grown in short-day conditions for one week (10 h. light/14 h dark) Then, the seedlings were cut as described in26. Shoots and roots were grafted in a new plate with the same medium and grown for 10 days. Then, adventitious roots emerging at or above the junction were removed from subsequent analyses.
Autofluorescence and FY 088 were detected with standard GFP filter with excitation at 488 nm and 500–600 nm band path filter by using a Zeiss LSM700 confocal microscopy3,27,28. Briefly, for observation of Casparian strips lignin with basic fuchsin and CASP1-GFP, 2.5 days old seedlings were grown on plates contatining ½ MS, 1% Agar. Seedlings were cleared and stained as described29. Suberin observation was done by FY 088 staining as described28. GUS-staining for observation of the early appearance of the expression of suberin biosynthesis gene was done as described25, and photos were taken by using stereo microscopes connected with a digital camera. For mounting root on glass slides, 50% glycerol was used. Quantification of the number of cells after the onset of elongation was done as described25. 2.5 days old plant were counted from the day when plates were taken out from the 4 °C and put into the growth chamber, with the 16 h. (light): 8 h. (dark) long-day conditions was set. Expression patterns of the suberisation reporter line pGPAT5::mCITRINE-SYP122 were observed using an epifluorescence microscope with GFP filter as described for FY 088 staining6. The length of the root and the length of the continuous suberisation zone were measured with the ImageJ software.
Real time quantitative RT-PCR analysis
qRT-PCR was done for the analysis of the transcript level of suberin biosynthesis genes and ABA-related genes in wild-type Col-0, esb1-1, esb1-1pCASP1::CDEF1, pCASP1::CDEF1, sgn3-3, esb1-1sgn3-3, pSCR::abi1, pSCR::abi1esb1-1, aba1, and aba1esb1-1. Two reactions were done per biological sample and 4 independent replicate samples per genotype were used to evaluate the transcript abundance of each genotype. Total RNA of leaves was extracted using TRIzol reagent (Invitrogen) and purified using RNeasy MinElute Cleanup Kit (Qiagen). After DNase treatment (Invitrogen), an equal amount of total RNA (1.5 μg) was used for RT with anchored Oligo(dT) 12–18 primer (Invitrogen). SuperScript®II reverse transcriptase was used for obtaining the first strand cDNA. FastStart Universal SYBR Green Master (ROX) (Roche) was used for Real time qRT-PCR. CT values were determined based on the efficiency of amplification and the mean CT values were normalized against the corresponding Ubiquitin10 gene (AT4G05320), and the expression of per genotype finally was calculated using the 2(−DDCT) method30.
Stomatal aperture measurements
Fully expanded leaves from 6–7 weeks old plant were grown in the greenhouse or growth chamber (80–100 μmol m−2 s−1 light intensity, a short-day photoperiod 10 h. light/14 h. dark). Leaves were harvested 3 to 5 h after lights were on. To determine stomatal aperture, we modified the protocol described in31. Nail polish was applied to the abaxial surface of leaves, when fully hardened a piece of transparent scotch tape was used to get out the film of clear nail polish from the surface of the leaf, the tape with the stomatal impression in the nail polish was placed onto a slide and observed under a light microscope (Zeiss Axioskop 40) at 20x objective and images were recorded digitally by ProgRes® CapturePro 2.9 Image Capture Software. Data were collected by measuring the maximum inner width of the stomatal pore from the captured photographs of a minimum of 50 stomata from 5 individual leaves per genotype and condition. Three independent measurements were done for the comparison between Col-0 and esb1-1, two independent measurements were done for the other mutant lines.
Exogenous ABA treatments
Seeds were sowed on the surface of the compost pots. After 2 days stratification in the 4 °C cold room, all the pots were transferred into the greenhouse with a controlled environment (250–300 μmol m−2 s−1 light intensity, a long-day photoperiod 16 h. light/8 h dark, 19 to 22 °C). Each pot contains two plants of the same genotype, and each genotype of Col-0, esb1-1, aba1 and aba1esb1-1 has four pots (N = 8 for each genotype were grown). About 100 mL of 10 µM exogenous ABA (Sigma, A1049) was sprayed onto the leaves of plants (Col-0, esb1-1, aba1 and aba1esb1-1) twice a week from the 8th day counted from the day when pots were transferred into the greenhouse from the 4 °C cold room. The control group was sprayed with the same amount of Milli-Q water. The treatment was continued until the 50th day, when the number of the siliques was quantified. Plants were bottom-watered twice per week with 0.25 × Hoagland solution.
Growth conditions for root hydraulic measurements and determination of ABA concentration. Seeds were surface sterilized and sowed into clear polystyrene culture plates (12 × 12 cm) containing ½ MS adjusted to pH 5.7. The plates were kept 2d at 4 °C and then incubated vertically for 10d under environmentally-controlled conditions: 60% relative humidity, 16 h/d of 250 µmol photons m−2 s−1 (long days) and 20 °C. Plants were later transferred into a hydroponic growth system consisting in a 35 × 35 cm plastic floating base over a basin filled with 8 L of hydroponic solution: 1.25 mM KNO3, 0.75 mM MgSO4, 1.5 mM, Ca(NO3)2, 0.5 mM KH2PO4, 50 mMFeEDTA, 50 mM H3BO3, 12 mM MnSO4, 0.70 mM CuSO4, 1 mM ZnSO4, 0.24 mM MoO4Na2, and 100 mM Na2SiO3. The different physiological determinations were done after 10–11 days of hydroponic culture.
Determination of plant water relations
Root hydrostatic conductance (Kr) was determined in freshly detopped roots using a set of pressure chambers filled with hydroponic culture medium32. Excised roots were sealed using dental paste (Coltène/Whaledent s.a.r.l., France) and were subjected to 350 kPa for 10 min to achieve flow stabilization, followed by successive measurements at pressures 320, 160, and 240 kPa. Root hydrostatic conductance (Kr) was calculated by the slope of the flow (Jv) to pressure relationship. The hydrostatic water conductivity (Lpr−h, ml H2O g−1 h−1 MPa−1) was calculated by dividing Kr by the root dry weight. For sodium azide (NaN3) experiments, Lpr−h was determined from continuous Jv measurement at 320 kPa as described33. The effect of the CIF2 peptide on the Lpr−h of Col-0 and sgn3-3 mutant was determined by subjecting the plants to 1 µM concentration of CIF2 (11) for 3 h, and afterwards determining its Lpr−h by using 320, 160, and 240 kPa in pressure chambers as explained before.
Selectivity to solutes
The passive leakage of solutes, and subsequent selectivity (σNaCl), of the root was tested by determining the osmotic potential of the xylem sap in plants under constant pressure of 300 kPa in the pressure chamber under a series of NaCl solutions from 0 to 150 mM. The osmotic potential of the sap was measured using a Vapro 5520 osmometer (Wescor, USA) and was plotted against the osmotic potential of each salt treatment concentration and its slope represented selectivity of the root to NaCl, or σNaCl.
Xylem sap osmotic potential
The plants were de-topped with a razor blade at the root – rosette junction and the isolated hypocotyl was immediately introduced into a 100 µl micro capillary. Dental paste (Coltène/Whaledent s.a.r.l., France) was used to ensure a proper seal between the hypocotyl and the capillary. We left the plants exuding for 10 min and later on the xylem sap was collected after another 45 min and its osmolality was measured using a Vapro 5520 osmometer (Wescor, USA).
Suberin Chemical Analysis
For quantitative chemical analysis suberin was extracted, depolymerised, derivatised and quantified as by GC-MS as previously described10.
Extraction and purification of indole-3-acetic acid (IAA) and abscisic acid (ABA) metabolites was done as described previously34 with minor modifications. Frozen samples were homogenized using a MixerMill (Retsch GmbH, Haan, Germany) and extracted in 1 ml 50 mM sodium phosphate buffer (pH 7.0) containing 1% sodium diethyldithiocarbamate and stable isotope-labelled internal standards (5 pmol of [13C6]-IAA and [6H2]-ABA per sample added). The pH was adjusted to 2.7 with 1 M hydrochloric acid, and the samples were purified by solid phase extraction. The extracts were purified on Oasis HLB columns (30 mg, Waters Corp., Milford, USA), conditioned with 1 ml methanol, 1 ml water, and 0.5 ml sodium phosphate buffer (pH 2.7). After sample application, the column was washed with 2 ml 5% methanol and then eluted with 2 ml 80% methanol. Eluates were evaporated to dryness and dissolved in 30 ul of mobile phase prior to mass analysis using a 1290 Infinity Binary LC System coupled to the 6490 Triple Quad LC/MS System with Jet Stream and Dual Ion Funnel technologies (Agilent Technologies)35.
The data were analysed using either analysis of variance (ANOVA) with the MIXED procedure or by using pair t-test in SAS (version 9.2, SAS Institute Inc., NC, USA). For ANOVA analyses, Tukey’s honest significant difference (HSD) or Duncan’s multiple range test (MRT) post-hoc adjustments were used to determine significant differences between treatments means at α = 0.05.
Geldner, N. The endodermis. Annu. Rev. Plant Biol. 64, 531–558 (2013).
Andersen, T. G., Barberon, M. & Geldner, N. Suberization — the second life of an endodermal cell. Current Opinion in Plant Biology 28, 9–15 (2015).
Hosmani, P. S. et al. Dirigent domain-containing protein is part of the machinery required for formation of the lignin-based Casparian strip in the root. Proc. Natl. Acad. Sci. USA 110, 14498–14503 (2013).
Pfister, A. et al. A receptor-like kinase mutant with absent endodermal diffusion barrier displays selective nutrient homeostasis defects. Elife 3 (2014).
Kamiya, T. et al. The MYB36 transcription factor orchestrates Casparian strip formation. Proc. Natl. Acad. Sci. USA 201507691, https://doi.org/10.1073/pnas.1507691112 (2015).
Barberon, M. et al. Adaptation of Root Function by Nutrient-Induced Plasticity of Endodermal Differentiation. Cell 1–35, https://doi.org/10.1016/j.cell.2015.12.021 (2016).
Li, B. et al. Role of LOTR1 in Nutrient Transport through Organization of Spatial Distribution of Root Endodermal Barriers. Curr. Biol. 1–9, https://doi.org/10.1016/j.cub.2017.01.030 (2017).
Kalmbach, L. et al. Transient cell-specific EXO70A1 activity in the CASP domain and Casparian strip localization. Nature Plants 1–9, https://doi.org/10.1038/nplants.2017.58 (2017).
Lee, Y., Rubio, M. C., Alassimone, J. & Geldner, N. A Mechanism for Localized Lignin Deposition in the Endodermis. Cell 153, 402–412 (2013).
Baxter, I. et al. Root Suberin Forms an Extracellular Barrier That Affects Water Relations and Mineral Nutrition in Arabidopsis. PLoS Genet 5, e1000492 (2009).
Doblas, V. G. et al. Root diffusion barrier control by a vasculature-derived peptide binding to the SGN3 receptor. Science 355, 280–284 (2017).
Nakayama, T. et al. A peptide hormone required for Casparian strip diffusion barrier formation in Arabidopsis roots. Science 355, 284–286 (2017).
Nawrath, C. et al. Apoplastic Diffusion Barriers in Arabidopsis. The Arabidopsis Book 11, e0167–36 (2013).
Ranathunge, K. & Schreiber, L. Water and solute permeabilities of Arabidopsis roots in relation to the amount and composition of aliphatic suberin. Journal of Experimental Botany 62, 1961–1974 (2011).
Péret, B. et al. Auxin regulates aquaporin function to facilitate lateral root emergence. Nature Cell Biology 14, 991–998 (2012).
Santoni, V. In Plant Aquaporins 285, 83–105 (Springer, Cham, 2017).
Bellati, J. et al. Novel Aquaporin Regulatory Mechanisms Revealed by Interactomics. Mol Cell Proteomics 15, 3473–3487 (2016).
Maurel, C. et al. Aquaporins in Plants. Physiological Reviews 95, 1321–1358 (2015).
Koornneef, M., Jorna, M. L., Brinkhorst-van der Swan, D. L. & Karssen, C. M. The isolation of abscisic acid (ABA) deficient mutants by selection of induced revertants in non-germinating gibberellin sensitive lines of Arabidopsis thaliana (L.) heynh. Theor. Appl. Genet. 61, 385–393 (1982).
Di Laurenzio, L. et al. The SCARECROW gene regulates an asymmetric cell division that is essential for generating the radial organization of the Arabidopsis root. Cell 86, 423–433 (1996).
Shatil-Cohen, A., Attia, Z. & Moshelion, M. Bundle-sheath cell regulation of xylem-mesophyll water transport via aquaporins under drought stress: a target of xylem-borne ABA? The Plant Journal 67, 72–80 (2011).
Takahashi, F. et al. A small peptide modulates stomatal control via abscisic acid in long-distance signalling. Nature 556, 235–238 (2018).
Vermeer, J. E. M. et al. A Spatial Accommodation by Neighboring Cells Is Required for Organ Initiation in Arabidopsis. Science 343, 178–183 (2014).
Domergue, F. et al. Three Arabidopsis Fatty Acyl-Coenzyme A Reductases, FAR1, FAR4, and FAR5, Generate Primary Fatty Alcohols Associated with Suberin Deposition. Plant Physiology 153, 1539–1554 (2010).
Naseer, S. et al. Casparian strip diffusion barrier in Arabidopsis is made of a lignin polymer without suberin. Proc. Natl. Acad. Sci. USA 109, 10101–10106 (2012).
Marsch-Martínez, N. et al. An efficient flat-surface collar-free grafting method for Arabidopsis thaliana seedlings. Plant Methods 9, 14 (2013).
Malamy, J. E. & Benfey, P. N. Organization and cell differentiation in lateral roots of Arabidopsis thaliana. Development 124, 33–44 (1997).
Lux, A., MORITA, S., Abe, J. & ITO, K. An Improved Method for Clearing and Staining Free-hand Sections and Whole-mount Samples*. Annals of Botany 96, 989–996 (2005).
Ursache, R., Andersen, T. G., Marhavy, P. & Geldner, N. A protocol for combining fluorescent proteins with histological stains for diverse cell wall components. The Plant Journal 93, 399–412 (2018).
Livak, K. J. & Schmittgen, T. D. Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method. Methods 25, 402–408 (2001).
Hilu, K. W. & Taxon, J. R. 1984. Convenient method for studying grass leaf epidermis. JSTOR 33, 413 (1984).
Javot, H. The Role of Aquaporins in Root Water Uptake. Annals of Botany 90, 301–313 (2002).
Sutka, M. et al. Natural variation of root hydraulics in Arabidopsis grown in normal and salt-stressed conditions. Plant Physiology 155, 1264–1276 (2011).
Novák, O. et al. Tissue-specific profiling of the Arabidopsis thaliana auxin metabolome. The Plant Journal 72, 523–536 (2012).
Floková, K. et al. UHPLC-MS/MS based target profiling of stress-induced phytohormones. Phytochemistry 105, 147–157 (2014).
We acknowledge support from the ERA-NET Coordinating Action in Plant Sciences program project ERACAPS13.089_RootBarriers, with support from Biotechnology and Biological Sciences Research Council (grant no. BB/N023927/1 to D.E.S.), the German Research Foundation (DFG; grant no. FR 1721/2-1 to R.B.F. and the AgreenSkills+ fellowship programme to MC-P which has received funding from the EU’s Seventh Framework Programme under grant agreement N° FP7-609398 (AgreenSkills+ contract). This work was also funded by the Ministry of Education, Youth and Sports of the Czech Republic (National Program for Sustainability I, grant no. LO1204), the Swedish Governmental Agency for Innovation Systems (Vinnova) and the Swedish Research Council (VR). We thank Kevin Mackenzie (University of Aberdeen–Microscopy Histology Facility) and Carine Alcon (BPMP-PHIV microscopy platform) for assistance using the confocal microscope and stereo microscope for observing the root samples, and the Swedish Metabolomics Centre (http://www.swedishmetabolomicscentre.se/) for access to instrumentation.
The authors declare no competing interests.
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Wang, P., Calvo-Polanco, M., Reyt, G. et al. Surveillance of cell wall diffusion barrier integrity modulates water and solute transport in plants. Sci Rep 9, 4227 (2019). https://doi.org/10.1038/s41598-019-40588-5
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