A dirigent family protein confers variation of Casparian strip thickness and salt tolerance in maize

Wang, Yanyan; Cao, Yibo; Liang, Xiaoyan; Zhuang, Junhong; Wang, Xiangfeng; Qin, Feng; Jiang, Caifu

doi:10.1038/s41467-022-29809-0

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Published: 25 April 2022

A dirigent family protein confers variation of Casparian strip thickness and salt tolerance in maize

Nature Communications volume 13, Article number: 2222 (2022) Cite this article

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Abstract

Plant salt-stress response involves complex physiological processes. Previous studies have shown that some factors promote salt tolerance only under high transpiring condition, thus mediating transpiration-dependent salt tolerance (TDST). However, the mechanism underlying crop TDST remains largely unknown. Here, we report that ZmSTL1 (Salt-Tolerant Locus 1) confers natural variation of TDST in maize. ZmSTL1 encodes a dirigent protein (termed ZmESBL) localized to the Casparian strip (CS) domain. Mutants lacking ZmESBL display impaired lignin deposition at endodermal CS domain which leads to a defective CS barrier. Under salt condition, mutation of ZmESBL increases the apoplastic transport of Na⁺ across the endodermis, and then increases the root-to-shoot delivery of Na⁺ via transpiration flow, thereby leading to a transpiration-dependent salt hypersensitivity. Moreover, we show that the ortholog of ZmESBL also mediates CS development and TDST in Arabidopsis. Our study suggests that modification of CS barrier may provide an approach for developing salt-tolerant crops.

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Introduction

Salt stress is one of the widely spread abiotic stresses, which affects about 20 million hectares of cultivated lands all over the world, and the area of the salt-affected farmland is increasing year by year due to the drastic climate change as well as the irrigation-dependent cultivating practice^1,2. Given the fact that most crops are glycophytes, the salinization of farmland has emerging as a major environmental stress restricting global agriculture^3,4,5. Under salt-affected farmland, crops take up excessive cations and anions (mainly Na⁺ and Cl^-), thereby leading to ion toxicity and impairments of various physiological processes. Meanwhile, high concentration of soil salts decreases osmotic potential of soil solution, and then causes osmotic stress². The salt-stress-induced osmotic stress, ion toxicity, and various subsequent effects (e.g. oxidative stress) together decline the quantity and quality of agricultural products^6,7. In order to secure the sustainability of global agriculture, there is an urgent need of investigating the mechanisms underlying crop salt tolerance.

During the long course of evolution, plants have evolved a variety of mechanisms to adapt the salted land on which they lives, including osmotic adjustment, regulation of ion content, activation of ROS scavenging mechanism, growth reprograming, and so forth². In the last decades, a number of factors associating with a specific or multiple salt-tolerance processes have been identified^2,8,9,10. The regulation of Na⁺ transport at cellular, tissue and whole-plant levels are essential for plant salt tolerance. Various Na⁺ transporters have been identified from different transporter protein families, for example, the Na⁺/H⁺ antiporter SOS1 pumps Na⁺ out of the cell^7,11, the HKT1 family transporters retrieve Na⁺ from the xylem vessels then promote shoot Na⁺ exclusion^12,13,14, the HAK family Na⁺ transporters are associated with the regulation of root Na⁺ concentration and root-to-shoot Na⁺ translocation^15,16,17. These transporters together with their regulators form a complex network regulating the uptake, transport and compartment of Na⁺^2,6,18,19. Also, previous studies have shown that shoot Na⁺ exclusion is substantially associated with the transpiring status. For instance, AtRBOHF-mediated ROS production promotes shoot Na⁺ exclusion and salt tolerance only under high transpiring condition, thereby mediating transpiration-dependent salt tolerance (TDST)^20,21. Up to this day, the exact mechanism of TDST remains largely unclear, especially in major crops (e.g. maize, wheat, and rice). As most crops are farmed under high transpiring environment, it is valuable to investigate the mechanisms underlying TDST in crops, thus to facilitate the breeding of crops with improved salt tolerance in agricultural relevant transpiring environments.

Casparian strips (CS) are lignin-based cell-wall modification in the root endodermis of vascular plants, which is a tight barrier blocking the non-selective apoplastic transport of solutes and water^22,23. It has been shown that the formation of CS is a highly ordered process. In the early stage, EXO70A1-mediated exocytosis localizes the Casparian strip membrane domain proteins (CASPs) into the CS domain to form discontinuous protein scaffolds^24,25, which are then linked together to form a continuous CASPs scaffold with the action of CIF1/2-SGN3-SGN1 complex (a peptide-receptor like kinase-coreceptor complex)^26,27,28. Meanwhile, other factors essential for the formation of CS are recruited to the CS domain (e.g. RBOHF, PER64, ESB1)²⁹, and then the monolignol oxidation and polymerization occurred to form Casparian strip^29,30. During the maturation of endodermis, MYB36 directly regulates the expression of the main genes involving the formation of Casparin strip³¹, and the dirigent family protein ESB1 is suggested to mediate bimolecular coupling during the lignin biosynthesis³². It has also been shown that the development of endodermal Casparian strip and suberin lamellae shows large plasticity in response to environmental clues^22,33,34. For instance, the biosynthesis and degradation of endodermal suberin lamellae are modulated by various plant hormones (e.g., ABA and ethylene) in response to nutrient stresses³³, and the endodermal CS barrier integrity is constantly checked by two CIF peptides and its maturation can be accelerated by low-K⁺ signaling^26,35,36. It is noteworthy that previous studies have also shown that the endodermal CS barrier matures closer to the root apex under salt stress^33,37,38, and the natural diversities of salt tolerance in rice are likely associate with the variations of the CS barrier³⁴, indicating the association between the CS barrier and crop salt tolerance. However, as the factors regulating the development of Casprin strip in crops are largely unidentified, and the genetic basis underlying the natural variations of CS barrier in crops remains unknown, making it challenging to clarify the role of endodermal CS barrier in crop salt tolerance.

Maize is one of the major cereal crops, and soil salinization is one of the major abiotic stresses restricting maize production worldwide^39,40. Therefore, there is an urgent need of investigating the mechanism underlying maize salt tolerance. Previous studies have shown that natural maize inbred lines displayed large diversities of salt tolerance^17,41, and the diversities were partially ascribed to the QTL regulating the shoot Na⁺ exclusion^14,17,42. In this work, we investigate maize salt tolerance by focusing on the identification and functional study of the genes underlying the natural variation of transpiration-dependent salt tolerance (TDST). We show that the inbred line CIMBL45 confers a transpiration-dependent salt hypersensitive phenotype, due to the loss of function of ZmSTL1. ZmSTL1 encodes a dirigent family protein designated as ZmESBL, which likely regulates the formation of endodermal Casparian strip (CS) by mediating the lignin deposition at the endodermal CS domain. Under high salt (NaCl) condition, the mutants lacking ZmESBL increase the apoplastic transport of Na⁺ across the endodermis to reach vasculature, and then lead to an increased root-to-shoot Na⁺ transport via the xylem-based transpiration flow, thereby leading to a transpiration-dependent salt hypersensitivity. In addition, we show that ESBL (the ortholog of ZmESBL in Arabidopsis) also mediates CS formation and salt tolerance in transpiring plants, and reveal that the lignin-based Casparin strip but not the suberin lamella promotes the shoot Na⁺ exclusion and TDST. Overall, we identify a gene underlying the natural variations of crop endodermal CS barrier, and demonstrate that the lignin-based CS barrier substantially promotes shoot Na⁺ exclusion and salt tolerance under high transpiring environment, hence providing valuable knowledge for developing salt-tolerant crops.

Results

ZmSTL1 underlies the salt hypersensitivity of CIMBL45

In this study, we aimed to investigate the genetic basis underlying the natural diversities of transpiration-dependent salt tolerance (TDST) in maize. We compared the salt sensitivity of ~200 maize inbred lines under high (50% relative humidity, RH) and low (95% RH) transpiring environments, subsequently identified an inbred line CIMBL45 showing a salt hypersensitive phenotype under 50% RH condition, but not under 95% RH condition (Fig. 1a–d). More specifically, the salt-grown CIMBL45 plants were yellowish and showed a significant decrease of leaf SPAD (soil plant analysis development) value under 50% RH condition, but not under 95% RH condition (Fig. 1a–d). By contrast, the salt-grown 3H-2 (a salt-tolerance inbred line) showed an undetectable change of leaf SPAD value under either high or low transpiring conditions (Fig. 1a–d). These results indicated that CIMBL45 showed a transpiration-dependent salt hypersensitive phenotype, thus provided a genetic material to investigate TDST in maize.

**Fig. 1: CIMBL45 shows a transpiration-dependent salt hypersensitive phenotype.**

We next determined the genetic basis underlying the transpiration-dependent salt hypersensitivity of CIMBL45. We generated F1 seeds by crossing CIMBL45 and 3H-2, and then obtained the F2 population by selfing of the F1 plants. The F2 plants were grown under 100 mM NaCl condition with low (50%) atmospheric relative humidity to analyze the salt sensitivity. Subsequently, we observed that about 25% of the F2 plants showed a yellowish phenotype comparable with that of the CIMBL45 (Fig. 1e, f), indicating that the transpiration-dependent salt hypersensitivity of CIMBL45 is conferred by a single recessive gene. We designated the casual gene as ZmSTL1 (Salt-Tolerant Locus 1).

ZmSTL1 is a dirigent family gene

We next identified the genetic identity of ZmSTL1 by a combined application of bulked segregant analysis (BSA) based rough mapping and marker-based fine mapping. Firstly, we generated two DNA samples from the bulked salt-tolerant and salt-sensitive F2 progenies, and then produced 40-Gb whole-genome-sequencing data for each sample using Illumine Hiseq 3000 system (see methods). The subsequent ΔSNP index analysis mapped ZmSTL1 to a 20-Mb region on Chromosome 1 (Fig. 2a) (see method). Secondly, we developed 11 markers (Supplementary Table 1), with which we mapped ZmSTL1 to a 110-kb region using 876 salt-sensitive F2 progenies (Fig. 2b). There were two genes (Zm00001d033941 and Zm00001d033942) within the 110-kb candidate region (Fig. 2b), with Zm00001d033941 encoded a protein with unknown function and Zm00001d033942 encoded a dirigent (DIR) family protein.

**Fig. 2: The dirigent family gene *Zm00001d033942* is the candidate of *ZmSTL1*.**

To validate the candidates, we used the CRISPR-Cas9-based approach to generate mutants lacking the candidate genes, and obtained two independent mutants for each candidate (Supplementary Figs. 1 and 2) (see Method). Zm00001d033941^crispr-1, Zm00001d033941^crispr-2, Zm00001d033942^crispr-1 and Zm00001d033942^crispr-2 respectively conferred a 7-, 2-, 10- and 23-bp InDel, all of which caused frameshifting (Supplementary Figs. 1, 2). We then analyzed the salt sensitivity of these mutants (Fig. 2c–f), and unraveled that Zm00001d033942^crispr-1 and Zm00001d033942^crispr-2, but not Zm00001d033941^crispr-1 and Zm00001d033941^crispr-2, displayed a salt hypersensitive phenotype under 100 mM NaCl condition with 50% RH (Fig. 2c, e; Supplementary Fig. 3), suggesting that Zm00001d033942 is the most likely candidate of ZmSTL1. Such a conclusion was supported by an allelism test, in which we took CIMBL45 and Zm00001d033942^crispr-1 alleles to be the loss-of-function alleles, and took the wild-type (WT) progenitor allele of Zm00001d033942^crispr-1 as the functional Zm00001d033942 allele, then generated two F1 hybrids (CIMBL45/Zm00001d033942^crispr-1 and CIMBL45/WT). Follow-up analysis found that CIMBL45/Zm00001d033942^crispr-1 but not CIMBL45/WT was hypersensitive to salt stress under 50% RH condition (Supplementary Fig. 4). Moreover, we observed that Zm00001d033942^crispr mutants showed salt hypersensitive phenotype under 50% RH but not under 95% RH condition (Fig. 2c–f), which was similar to that of CIMBL45 (Fig. 1a–d). These results confirmed that the genetic variation at the dirigent family gene Zm00001d033942 accounted for the transpiration-dependent salt hypersensitivity of CIMBL45.

A 1-bp insertion truncates ZmSTL1 protein in CIMBL45

We next identified the genetic variation underlying the functional variation of ZmSTL1/Zm00001d033942. We amplified and sequenced the genomic fragment covering Zm00001d033942 (including 5’- and 3’- UTRs) using the primers 033942-G-F and 033942-G-R (Supplementary Table 1), subsequently identified 4 SNPs (SNP503, SNP507, SNP514 and SNP515) and one InDel (Ins512) variants between the DNA sequences of the 3H-2 and CIMBL45 (Supplementary Table 2), among which SNP503 leaded to an amino acid change from leucine to proline, and Ins512 (a 1-bp insertion) leaded to a frameshifting and truncation of Zm00001d033942 in CIMBL45 (Supplementary Table 2; Fig. 2g). As CIMBL45 conferred a functional null allele of ZmSTL1/Zm00001d033942 (Fig. 2; Supplementary Fig. 4), we suggest that the frameshifting insertion (Ins512) is the most likely genetic variant underlying the functional variation of ZmSTL1/Zm00001d033942 in CIMBL45, and the allele without Ins512 is the salt-tolerant allele of ZmSTL1/Zm00001d033942.

ZmESBL is predominantly located in the Casparin strip domain

ZmSTL1/Zm00001d033942 belongs to the DIR gene family. The phylogenetic analysis of the DIR family proteins from maize (n = 33), rice (n = 20), soybean (n = 44), and Arabidopsis (n = 26) indicated that these proteins were grouped into five families (Family I-V), and Zm00001d033942 fell into Family V (Fig. 3a). Zm00001d033942, OS01G0879300, GLYMA_11G085200, GLYMA_05G242100, and AT5G42655 were grouped together to form a subfamily (Fig. 3a). As a previous study has designated AT5G42655 as Enhanced Suberin Like (ESBL) in Arabidopsis³¹, accordingly, we named Zm00001d033942 as ZmESBL (Zea may L. Enhanced Suberin Like), and ZmSTL1/Zm00001d033942 is referred to as ZmESBL for the remainder of this manuscript.

**Fig. 3: Phylogenetic analysis, expression pattern and the subcellular localization of Zm00001d033942/ZmESBL.**

The DIR family proteins have been shown to mediate regio- and stereoselectivity of bimolecular coupling during lignan and lignin biosynthesis⁴³, however, the physiological roles of ZmESBL and its orthologs remain unclear. Considering that previous studies have showed that ESB1 (a Family V member) plays a role in the development of the endodermal Casparian strip (CS) barrier in Arabidopsis, and the loss-of-function of ESB1 leads to an ectopic deposition of suberin and lignin in endodermis³², we then speculated that ZmESBL might also play a role in the regulation of endodermal CS development and/or suberin deposition. To address this hypothesis, firstly, we analyzed the tissue specificity of ZmESBL expression, and observed that ZmESBL mainly expressed in root tissue (Fig. 3b, c), and its transcripts were predominantly detected in the endodermis and the stele cells adjacent to the endodermis (Fig. 3d). Secondly, we determined the subcellular localization of ZmESBL by generating and analyzing the Arabidopsis plants expressing GFP-ZmESBL under the control of the ESBL (the ortholog of ZmESBL in Arabidopsis) promoter and the endodermal-specific ESB1 promoter³² (see methods). The results indicated that the GFP-ZmESBL was predominantly detected at the endodermal CS domain of pESBL-GFP-ZmESBL and pESB1-GFP-ZmESBL plants (Fig. 3e; Supplementary Fig. 5). These observations suggest that ZmESBL likely plays a role in the regulation of endodermal Casparian strip formation and/or suberin deposition.

Lacking of ZmESBL impairs lignin deposition at the CS domain

We next compared the endodermal suberin deposition and Casparian strip formation between wild-type and ZmESBL^crispr plants. In order to make a proper comparison, firstly, we analyzed whether the loss-of-function of ZmESBL affects root development, and found that the primary root of the wild-type and ZmESBL^crispr plants showed comparable meristem size (~4.0 mm), elongation zone length (~3.0 mm), and a comparable length of the elongated endodermal cell (~125 μm) (Supplementary Fig. 6a–e), suggesting that ZmESBL unlikely regulates the aspects of root cell division and elongation. We then analyzed the pattern of the endodermal suberin deposition using a fluoral yellow 088 staining-based assay (see “Methods”). The results indicated that both the wild-type and ZmESBL^crispr plants started to form suberin lamellae in endodermis at ~5.0 cm from the root apex (~ the 344^th elongated endodermal cell), and the intensities of the fluoral yellow 088 staining were comparable (Supplementary Fig. 7), indicating that ZmESBL is unlikely associated with the regulation of endodermal suberin deposition.

Previous studies have shown that the CS diffusion barrier is made of a lignin polymer⁴⁴. We next compared the endodermal Casparian strip in the primary root of ZmESBL^crispr and wild-type plants using the basic fuchsin staining of lignin (see methods). We showed that, under control condition, the discontinuous lignin deposition at the endodermal CS domain started at 1.5 cm to the root apex (~ the 64^th elongated endodermal cell) in the wild-type root, and then developed into ring-like continuous Casparin strips at 2.5 cm from the root apex (~ the 144^th elongated endodermal cell) (Fig. 4a; Supplementary Fig. 6f). In contrast, the CS staining can be detected until at 2.5 cm from the root apex (~ the 144^th elongated endodermal cell) in the ZmESBL^crispr root, and the fluorescence intensity was detected at significantly lower levels as compared with that of the wild-type control (Fig. 4a). We also showed that the control-grown and salt-grown root segments (2.0–2.5 and 2.5–3.0 cm from the root apex) of the ZmESBL^crispr mutants respectively displayed a ~15% and ~25% reduction of lignin content under control and salt conditions (Fig. 4b). Strikingly, we found that the Casparin strips of ZmESBL^crispr mutants were not fully continuous even at 3.0 cm from the root apex (~ the 184^th elongated endodermal cell) (Fig. 4a). These observations indicated that lacking ZmESBL function leaded to defective Casparian strips with reduced and discontinuous lignin deposition. Moreover, we compared the CS structure of the wild-type and ZmESBL^crispr plants using a transmission electron microscopy assay, which permits us to analyze the CS structure in more detail. The results indicated that the wild-type root formed later Caparian strips that likely can function as an apoplastic barrier³³ at 2.5 cm from the root apex (~ the 144^th elongated endodermal cell) (Fig. 4c), and the Caparian strip was located at the pericycle side of the endodermal cell-cell contact site (Supplementary Fig. 8a). In contrast, although ZmESBL^crispr can form Casparian strips at the similar position, the Casparian strips were incomplete and less organized (Fig. 4c; Supplementary Fig. 8b), which expanded to a wider domain at the elder root region (e.g. 4.0 cm from the root apex) (Supplementary Fig. 8c). Taken together, we conclude that ZmESBL plays an important regulatory role in maize CS development.

**Fig. 4: Lacking ZmESBL function leads to incomplete and less organized Casparian strips.**

Salt accelerates CS development by a ZmESBL-dependent manner

Previous studies have observed that the development of the endodermal Casparian strips shows large plasticity in response to the environmental clues^22,33. We next investigated the salt-induced plasticity of endodermal CS development and its association with ZmESBL. We observed that the discontinuous and continuous staining of CS lignin was respectively detected at 1.0 and 1.75 cm from the root apex (~ the 36^th and 105^th elongated endodermal cell) in the salt-grown wild-type root, being detected in younger cells as compared with that of the control-grown wild-type root (Fig. 4a). In addition, we observed by electron microscopy that the later Casparin strips of the salt-grown wild-type root were 25% wider than that of the control root (Fig. 4d). These results indicated that salt stress not only accelerates the development of Casparian strip, but also leads to the formation of a wider Casparian strip. By contrast, the salt-grown ZmESBL^crispr root conferred defective Casparian strips comparable with that of the control-grown ZmESBL^crispr root (Fig. 4a–c), suggesting that the salt-induced plasticity of Casparian strip is dependent upon the function of ZmESBL. Moreover, we observed that ZmESBL was mainly expressed in root tissue and its expression was induced 2–6 h following the onset of salt (100 mM NaCl) treatment (Fig. 4e). Notably, the root segments (up to 2.0 cm to root apex) where the onset and maturation of Casparian strip occurs displayed higher ZmESBL transcription (Fig. 4f), suggesting that the salt-induced reprograming of the endodermal CS development might be associated with the increased transcript levels of ZmESBL.

Salt-induced strengthen of CS barrier is dependent on ZmESBL

We next compared the function of the endodermal CS barrier in the primary roots of ZmESBL^crispr and wild-type plants using the apoplastic tracer propidiumiodide (PI). The results indicated that, in the root tip region (up to 2.0 cm from the root apex), PI penetrated the endodermis and entered into root stele both in ZmESBL^crispr and wild-type plants (Fig. 5a), indicated that the endodermal apoplastic barrier was not fully function. The PI penetration was completely blocked at about the 144^th elongated endodermal cell (2.5 cm to root apex) of the wild-type root, by contrast, PI penetration was detectable even at 3.5 cm from the root apex (~ the 224^th elongated endodermal cell) in ZmESBL^crispr root (Fig. 5a), indicating that loss-of-function of ZmESBL leads to a defective endodermal CS barrier. Moreover, we examined the effect of salt stress on the endodermal CS barrier (Fig. 5b). The results indicated that PI penetration was blocked at 2.0 cm from the root tip (~ the 127^th elongated endodermal cell) in the salt-grown wild-type root (Fig. 4a–c), suggesting that the CS barrier become functional in younger endodermal cells under salt condition. By contrast, PI penetration was detectable at 3.5 cm from the root apex (~ the 264^th elongated endodermal cell) in the salt-grown ZmESBL^crispr root, which was comparable with that of the control-grown ZmESBL^crispr root (Fig. 4a–c). Taken together with the observations that salt accelerates the development of Casparian strips and leads to the formation of wider Casparian strips, these results indicate that the salt-induced reprograming of CS development increases the function of endodermal CS barrier, and such a reprograming is dependent upon the function of ZmESBL.

**Fig. 5: Lacking ZmESBL function leads to a defective endodermal CS barrier.**

ZmESBL reduces the apoplastic loading of Na⁺ into stele

Shoot Na⁺ exclusion is essential for crop adaptation to salt stress, and reducing the stele Na⁺ loading provides a major mechanism of shoot Na⁺ exclusion^2,6. Considering that the endodermal CS barrier is able to block the excessive apoplastic transport of mineral elements across the endodermis to reach root stele²², we then investigated the role of ZmESBL-mediated CS formation for preventing the stele Na⁺ loading. We exposed the roots of the wild-type and ZmESBL^crispr plants to salt solution (200 mM NaCl) for a short time (15 min), then collected the root segments 2.0–3.0 and 3.0–4.0 cm from the root apex (at where the CS barrier of ZmESBL^crispr was less functional than that of the wild-type plants), and then separated the stele from the outer part tissues to analyze the Na⁺ content (Fig. 5d). The results indicated that, while the outer part samples with different genotypes showed comparable Na⁺ concentrations, the stele samples of ZmESBL^crispr mutants showed higher Na⁺ concentrations as compared with that of the wild-type plants (Fig. 5e), suggesting that the loss-of-function of ZmESBL increases the apoplastic transport of Na⁺ across endodermis, thereby increasing the stele Na⁺ loading.

ZmESBL promotes shoot Na⁺ exclusion in transpiring plants

To further clarify the role of ZmESBL in regulating Na⁺ delivery and salt tolerance, we compared the Na⁺ concentrations in the root, xylem sap and shoot tissues of ZmESBL^crispr and wild-type plants. The results indicated that the Na⁺ contents in the root and xylem sap of the salt-grown ZmESBL^crispr plants were respectively ~20% and ~50% higher than that of the wild-type plants, and the differences were identified both under 50% and 95% RH conditions (Fig. 5f, g). These observations supported the perspective that lacking ZmESBL function increases the appoplastic transport of Na⁺ across endodermis to root stele and to be loaded into the xylem flow, and the effects were irrelevant to the transpiring status. Intriguingly, we found that the salt-grown ZmESBL^crispr mutants accumulated 6 times more shoot Na⁺ than the wild-type plants under high transpiring condition (50% RH), and the transpiration-restricting high RH (95%) reduced the accumulation by ~65% (Fig. 5h). These observations suggested that the disruption of ZmESBL function increases the apoplastic transport of Na⁺ across endodermis, thereby leading to the excessive loading of Na⁺ into root stele, nevertheless, the stele Na⁺ can be excessively delivered to shoot and causes salt hypersensitivity only under high transpiring environment, which explains the transpiration-dependent salt hypersensitivity of ZmESBL^crispr mutants. In addition, while previous studies have shown that Na⁺/K⁺ ratio is important for plant salt tolerance⁶, and the impairment of Casparian strip is associated with a decreased tissue K⁺ content^33,45, we found that the loss-of-function of ZmESBL leaded to a significant reduction of K⁺ content under both control and salt conditions, and under both high and low humidity conditions (Supplementary Fig. 9a, b). Specifically, the salt-grown ZmESBL^crispr plants under low RH (50%) condition conferred ~17% less shoot K⁺ than that grown under high RH (95%) condition (Supplementary Fig. 9b), which probably also made a contribution to the transpiration-dependent salt hypersensitivity of ZmESBL^crispr mutants.

Arabidopsis ESBL regulates endodermal CS formation

The orthologs of ZmESBL were identified in most of the higher plants, and ESBL is the ortholog of ZmESBL in Arabidopsis (Fig. 3a). We then determined whether ESBL also regulates the formation of the endodermal CS barrier. We generated two independent mutants lacking ESBL function (esbl-1 and esbl-2) using the CRISPR-Cas9 based approach, with both of them conferred frameshifting mutations (Supplementary Fig. 10) (see method). Follow-up assay observed that the CS autofluorescence of the esbl-1 and esbl-2 mutants were significantly (~60%) weaker than that of the wild-type plants (Fig. 6a), and esbl-1 and esbl-2 showed a significant (~8%) reduction of root lignin content as compared with that of the wild-type plants (Supplementary Fig. 11). Meanwhile, the esbl-1 and esbl-2 mutants ectopically deposited a small amount of lignin at the cortex face of the endodermal cell-cell contact site. These observations suggest that lacking ESBL function impairs the lignin deposition at the normal CS domain (Fig. 6a). Nevertheless, the impairment was different from that of the esb1 mutant, which deposited lignin in patches in the CS domain and displayed an ectopic deposition of lignin in the corners of the endodermal cells on both the pericycle and cortex faces³² (Fig. 6a, b). In addition, while previous study have shown that esb1 root displays ectopic suberin deposition in younger endodermal cells as compared with the wild-type root³²(Fig. 6c–e), we observed that the suberin deposition in the endodermis of the wild-type and esbl roots started at the same position (~ the 36^th endodermal cells from the onset of elongation) (Fig. 6c), and the amount of suberin deposition in esbl root was comparable with that of the wild-type root (Fig. 6d, e). These observations suggest that ESBL and ESB1 regulate lignin deposition and CS formation via distinct mechanisms. We next compared the function of the endodermal CS barriers in esbl-1, esbl-2, esb1 and the wild-type plants using the PI penetration assay (Fig. 6f, g). To quantify the barrier function, we counted the number of the endodermal cells from the onset of elongation to the site where the PI fluorescence was undetectable in root stele, and observed that the PI penetration was fully blocked at ~ the 13^th endodermal cell from the onset of elongation in the wild-type root, but at ~ the 35^th cell in esbl-1, esbl-2 and esb1 roots (Fig. 6g). These observations indicated that the function of the endodermal CS barrier was disrupted in esbl-1 and esbl-2 plants, which was comparable with that of esb1 plants.

**Fig. 6: Arabidopsis ESBL is essential for CS development and salt tolerance under high transpiring condition.**

We next determined the mechanism by which ESBL orthologs regulate CS development. Firstly, as the above studies have shown that lacking of ZmESBL leaded to a reduction of lignin content (Fig. 4b), we then investigated the relationship between the Casparin strip defect and the reduction of lignin content in esbl plants, and found that the monolignol treatment (20 μM coniferyl alcohol plus 20 μM sinapyl alcohol) can neither restored the formation of Casparian strip nor rescued the function of the endodermal barrier of esbl mutant (Supplementary Fig. 12), suggesting that the Casparian strip defect of esbl is unlikely ascribed to the decrease of lignin content. Secondly, previous studies have shown that the exocytosis of CASP proteins into the CS domain to form discontinuous protein scaffolds occurs at the early (onset) stage of CS formation^24,25, and then form a continuous CASP scaffolds at the later stage^26,27,28. We then investigated whether ESBL is associated with the formation of CASP scaffolds. To do this, we generated pCASP1-CASP1-GFP lines in the esbl and wild-type background, and observed that neither the formation of the early stage discontinuous CASP1 scaffolds nor the formation of the later stage continuous CASP1 scaffolds was affected in esbl mutant (Supplementary Fig. 13). These observations suggest that ESBL is unlikely associated with the onset of CS formation, hence suggesting that ESBL might be part of the machinery regulating the later CS formation processes.

ESBL promotes salt tolerance in transpiring plants

We further determined whether ESBL associates with the transpiration-dependent salt tolerance (TDST) by comparing the salt sensitivity and shoot Na⁺ content of esbl-1, esbl-2, esb1 and wild-type plants under the high and low transpiring conditions (Fig. 6h–j). We found that, while salt (150 mM NaCl) treatment leaded to an undetectable change of the leaf SPAD values of the wild-type plants under both 50% and 95% RH conditions (Fig. 6h, i), it caused a ~55% reduction of the SPAD values of esbl-1 and esbl-2 plants under 50% RH condition, but not under 95% RH condition (Fig. 6h, i), demonstrated that lacking ESBL function caused a transpiration-dependent salt hypersensitivity. esb1 also displayed a transpiration-dependent reduction of leaf SPAD value following the onset of salt treatment, but the reduction was less apparent as compared with that of the esbl-1 and esbl-2 plants (Fig. 6h, i). We next observed that, under 50% RH condition, the salt-treated esbl-1 and esbl-2 plants showed a ~150% increase of shoot Na⁺ content as compared with that of the wild-type plants, with esb1 showed only a ~20% increase of shoot Na⁺ content (Fig. 6j). We also observed that the transpiration-restricting high atmospheric relative humidity (95%) substantially reduced the shoot-Na⁺ accumulation of the salt-treated esbl-1 and esbl-2 mutants (Fig. 6j). Taken together, we concluded that ESBL substantially confers shoot Na⁺ exclusion and salt tolerance under high transpiring condition in Arabidopsis. Moreover, we observed that esbl mutants showed 6–26% reduction of shoot K⁺ content as compared with that of the wild-type plants, depending upon the growth conditions (Supplementary Fig. 14). Specifically, the salt-grown esbl mutants conferred ~26% less shoot K⁺ than that of the wild-type plants under 50% RH condition (Supplementary Fig. 14), which likely also made a contribution to the transpiration-dependent salt hypersensitivity of esbl mutants.

CS barrier confers salt tolerance in transpiring plants

As above observations have shown that mutants lacking ESBL and ESB1 both conferred a defective CS barrier, it is probably a surprise to unravel that esb1 is more tolerant to salt stress than esbl mutant under 50% RH condition (Fig. 6h–j). The discrepancies could be ascribed either to the ectopic suberization of endodermal cells, or to the compensatory lignin deposition at the endodermal cell-cell contact sites of esb1 mutant³². To test these possibilities, we analyzed the salt sensitivities of additional CS formation-associated mutants, including myb36-1, casp1-1 caps3-1 and rbohf-F3. Previous studies have shown that all of these mutants confer defective Casparian strips. In the meantime, these mutants show distinct pattern of ectopic suberin and/or lignin accumulation at endodermis, with casp1-1 caps3-1 ectopically accumulates both suberin and lignin²⁵, myb36-1 ectopically accumulates suberin but not lignin³¹, rbohf-F3 ectopically accumulates neither suberin nor lignin³⁰. We found that myb36-1 and rbohf-F3 showed a comparable transpiration-dependent excessive shoot-Na⁺ accumulation and salt hypersensitivity (Fig. 7a–c), by contrast, casp1-1 caps3-1 was more tolerant to salt stress than myb36-1 and rbohf-F3 under 50% RH condition (Fig. 7a–c). These observations support the notion that the ectopic endodermal lignin deposition (in casp1-1 caps3-1 and esb1) but not the ectopic endodermal suberin lamella deposition (in myb36-1) can partially complement the function of CS barrier in terms of promoting shoot Na⁺ exclusion and salt tolerance. These discoveries also suggest that the transpiration-dependent salt hypersensitive phenotype of the plants lacking RBOHF function is substantially ascribed to the impairment of the CS barrier²¹.

**Fig. 7: The lignin deposition at CS domain confers shoot Na⁺ exclusion and salt tolerance in transpiring plants.**

Furthermore, we analyzed the salt sensitivity of the mutants deficient of endodermal suberin lamella deposition (daisy-1 and gpat5-1)^46,47, discovered that the salt-treated daisy-1, gpat5-1, and wild-type plants displayed comparable shoot Na⁺ contents and salt sensitivity both under high and low transpiring conditions (Fig. 7d–f), which supported the notion that the suberin lamella deposition was less relevant to shoot Na⁺ accumulation and salt tolerance. Taken together with the observations that the mutants (ZmESBL^crispr, esbl-1, esbl-2, myb36-1 and rbohf-F3) with a severe defect of lignin deposition in endodermal CS domain accumulated several times more shoot Na⁺ and were hypersensitive to salt stress under high transpiring condition (Figs. 2c, 5h, 6h, 6j, 7a, 7c), these results demonstrated that the lignin-based endodermal CS barrier but not the endodermal suberin lamella conferred an important mechanism of shoot Na⁺ exclusion and salt tolerance in transpiring plants.

Discussion

The soil salinity is one of the major abiotic stress hindering the productivity and quality of agricultural products worldwide², thus there is an urgent need of characterizing salt-tolerant mechanisms that can be used to developing salt tolerant crops. Nevertheless, decades of efforts have made little progress, due to the complexity of salt response and its interaction with the variable environmental factors^2,8,20. For this reason, the studies of salt tolerance using the plants growing in the physiologically realistic conditions are recommended. Previous studies have showed that the AtRBOHF-mediated ROS production confers salt tolerance under high transpiring conditions, mediating transpiration-dependent salt tolerance (TDST)^20,21. As most crops are farmed under high transpiring environments, it is therefore valuable to investigate the molecular mechanism of crops TDST. Here we have shown that the dirigent (DIR) family protein ZmESBL underlies the natural variations of TDST in maize (Figs. 1 and 2). A 1-bp insertion causes the frameshifting and truncation of ZmESBL in the maize inbred line CIMBL45, and then leads to transpiration-dependent salt hypersensitivity (Figs. 1, 2). ZmESBL provides an important genetic target for improving maize salt tolerance in the agricultural relevant transpiring environments.

DIR proteins were originally identified to regulate regio- and stereoselectivity of phenoxy radical coupling reactions⁴³, and the follow-up studies have revealed that the plant DIR proteins involve in a wide range of developmental processes and plant responses to various environmental signals. For instance, AtDIR6 is associated with secondary cell-wall formation⁴⁸; AtDIR12 is likely associated with the synthesis of seed-specific neolignans⁴⁹; AtDIR10/ESB1 is required for the formation of the endodermal Casparian strip (CS)³²; a DIR-like protein PDH1 regulates soybean pod dehiscence likely by mediating lignin deposition⁵⁰. In this study, we have observed that the DIR protein ZmESBL is associated with the lignin deposition at the endodermal CS domain in maize (Figs. 3e and 4a–c), the loss-of-function of ZmESBL leads to a defective CS barrier (Fig. 5a). In addition, we have shown that the Arabidopsis mutants lacking ESBL (the ortholog of ZmESBL) also confer a defective endodermal CS barrier due to the deficiency of lignin deposition (Fig. 6a, b, f, and g). Moreover, while previous studies have shown that the DIR protein ESB1 also involves in the regulation of endodermal CS formation in Arabidopsis, our study has revealed that ESBL and ESB1 regulate the CS development likely via distinct mechanisms. These discoveries provide an important demonstration that ZmESBL and its orthologs likely mediate a conserved mechanism of lignin deposition at the endodermal CS domain across monocot and dicot species, and across C4 and C3 species. In this regard, we showed that the loss-of-function of ESBL didn’t affect the formation of the dot-like CASP1 scaffolds during the onset of CS formation (Supplementary Fig. 13), indicating that ESBL is less relevant to the onset of CS formation. Given the fact that the DIR family proteins have been shown to mediate regio- and stereoselectivity of bimolecular coupling during lignan and lignin biosynthesis⁴³, it remains highly possible that ESBL ortholog mediate bimolecular coupling during the polymerization of monolignol in the endodermal CS domain.

Sodium (Na⁺) is the most abundant soluble cation in many saline farmlands, and shoot Na⁺ exclusion is important for crop salt tolerance^{12,13,51,52,53}. Our previous studies have shown that natural maize population displays large diversity of shoot Na⁺ exclusion, which is partially ascribed to the variations of ZmHKT1- and ZmHAK4-mediated retrieving of Na⁺ from the xylem flow, and the variation of ZmNSA1-mediated regulation of SOS1 activity^14,17,42. Here we have shown that, under salt (NaCl) condition, loss-of-function of ZmESBL increases the apoplastic transport of Na⁺ across endodermis to reach stele, then increases Na⁺ content in xylem-based transpiration flow (Fig. 5e), and then causes excessive root-to-shoot delivery of Na⁺ under high transpiring condition (Fig. 5g), which in turn leads to a transpiration-dependent salt hypersensitive phenotype. Taken together with the regulatory role of ZmESBL in CS development, these observations indicate that endodermal CS barrier provides a major mechanism preventing excessive stele-Na⁺ loading, and that ZmESBL-mediated CS formation underlies natural variation of shoot Na⁺ concentration and salt tolerance in transpiring maize plants. Intriguingly, it was previously shown that the functional variation of CS barrier is likely associated with the diversities of salt tolerance in rice^54,55, thus suggesting that the functional variation of CS barrier might underlies natural variation of salt tolerance in a wide range of crops. Nevertheless, such a perspective needs to be addressed in future study.

The maturation of endodermis cells involves the lignin deposition at Casparin strip domain at the early stage and the formation of suberin lamella at the later stage^22,23, with the lignin-based CS barrier prevents apoplastic delivery of minerals⁵⁶, and the suberin lamella establishes a barrier for uptake of minerals from the apoplast into the endodermis³³. Previous studies have shown that the maturation processes of endodermis are genetically regulated and influenced by environmental signals³³. Previous studies have also shown that salt stress promotes maturation of the lignin-based Casparin strip and increases suberin lamella deposition in the endodermis cells^33,37,55, however, the molecular basis and the physiological significance of these processes are less understood. Here we have shown that salt stress accelerates the development of the lignin-based Casparin strips, as well as leads to the formation of wider Casparian strips. Intriguingly, the salt-induced reprograming of CS development is dependent upon the function of ZmESBL (Fig. 4a–c), more specifically, might be associated with the increase of ZmESBL transcription (Fig. 4e, f). Given the fact that the salt-grown ZmESBL^crispr mutants accumulated 6 times more shoot Na⁺ than that of the wild-type plants under high transpiring condition, we suggest that the endodermal CS barrier and its plasticity providing a major mechanism of shoot Na⁺ exclusion and salt tolerance in transpiring plants. By contrast, the endodermal suberin lamella is less relevant to Na⁺ hemostasis and salt tolerance (Fig. 7d–f). These observations also suggest that the physiological role of CS-mediated regulation of salts and probably other nutrients uptake should be determined in transpiring plants.

In summary, our study has identified ZmESBL, a dirigent family gene underlying the natural variation of salt tolerance under high transpiring condition. ZmESBL and its orthologs mediate a conserved mechanism of lignin deposition at the endodermal Casparian strip domain, with which we have demonstrated that the lignin-based Casparian strip barrier provides a major mechanism regulating stele-Na⁺ loading, thereby promoting shoot Na⁺ exclusion and salt tolerance in transpiring plants, suggesting that the genetic engineering of endodermal lignin deposition might provide a strategy for improving the salt tolerance of a wide range of crops.

Methods

Plant growth and salt treatment

The maize inbred lines (3H-2 and CIMBL45) were obtained from National Maize Improvement Center of China at China Agricultural University. Pots with a height of 12 cm and a diameter of 10 cm were used for the growth of maize plants. In essence, the pots were filled with uniformly mixed Pindstrup substrate (www.pindstrup.com) and watered to soil saturation with water or salt (100 mM NaCl) solution. Ten seeds were planted in each pot, grown in the controlled environments with indicated atmospheric relative humidity for analyzing the salt sensitivity, measuring the leaf SPAD value, and collecting samples for the measurement of ion contents. For the growth and salt treatment of Arabidopsis plants, Seven-day-old plants grown on MS agar plates were transferred to pots filled with Pindstrup substrate, grown for 3 weeks in controlled environments (16/8-h light/dark cycle, 22 °C, ~50% relative humidity), then watered once to soil saturation with 150 mM NaCl solution or water (control). Seven days later, the plants were photographed, the SPAD values of the 4^th leaf were measured, and the shoot samples were collected for the measurement of ion contents.

Rough mapping and fine mapping of ZmSTL1

The bulked DNA samples were extracted using DNAsecure plant kit (TIANGEN DP320-03), and then sequenced at Novagene, using the high-throughput sequencing platform highseq3000. The reads with more than 10% of missing bases and more than 50% of bases with Q-score lower than 20 were filtered, and the clean reads were mapped to the Maize reference genome (Zm-B73-REFERENCE-GRAMENE-4.0) using Burrows-Wheeler-Alignment Tool software (version 0.7.12)⁵⁷. The alignment files were converted to SAM/BAM files for SNP-calling using SAMtools (version 1.11)⁵⁸. SNP-index was calculated using host python and shell scripts. The SNPs detected in both bulked DNA samples were used for calculating Δ(SNP-index). Sliding window analysis was applied with 2-Mb window size and 10-Kb steps using BEDTools (version 2.29.2)⁵⁹, and Fig. 2A were generated using the R package CMPlot (version 3.7.0). Following the BSA-based rough mapping of ZmSTL1, we developed 11 markers, and used 876 salt hypersensitive F2 plants to conduct the fine mapping of ZmSTL1, and mapped ZmSTL1 locus to a ~110-kb region between markers M9 and M10.

Generation of the CRISPR/Cas9 knockout mutants

The method of generating ZmESBL^crispr mutants was generated using a CRISPR-Cas9 based approach⁶⁰. A pCAMBIA-derived CRISPR/Cas9 binary vector with two gRNA expression cassettes targeting two adjacent sites of ZmESBL was generated and transformed into Agrobacterium strain EHA105, and then into the immature embryos of the maize inbred line 32990700 (wild type). In order to identify the positive mutants, the PCR products encompassing the gRNA-targeted sites for each of the transgenic plants were sequenced by capillary sequencing. To generate the CRISPR-Cas9 knockout mutants of ESBL in Arabidopsis, a pCAMBIA-derived CRISPR/Cas9 binary vector pHSE401–2gR with two gRNA expression cassettes was generated and transformed into Agrobacterium strain GV3101, and then transformed into Arabidopsis Col-0. The mutants were identified by amplifying and sequencing the genomic region encompassing the gRNA-targeted sites.

Generation of pESB1 -GFP-ZmESBL transgenic plant

Approximately 1.5-kb DNA upstream of Arabidopsis ESB1 was amplified from Col-0 genomic DNA using the primers pESBl-F and pESBl-R (Supplementary Table 1). The GFP coding sequence was amplified using the primers GFP-F and GFP-R (Supplementary Table 1). The ZmESBL coding sequence was amplified using the primers ZmESBL-F and ZmESBL-R (Supplementary Table 1). Those fragments were cloned into pGoldenGate-MCY2⁶¹ to generate pESBl-GFP-ZmESBL construct, which was then introduced into Agrobacterium strain GV3101 and transformed into the Col-0 laboratory strain to generate pESB1-GFP-ZmESBL transgenic plant.

Microscope observation of Casparian strip

We used a lignin staining-based assay to observe endodermal Casparian strip in maize. In essence, the plants were grown under control or salt conditions for 4 days, then the cortex cells were carefully removed from the root with dissecting needles under stereoscope, and then the root was stained with the basic fuchsin solution (0.005% w/v in water; Sigma 857343) overnight at room temperature. The samples were rinsed in autoclaved deionized water for three times (5 min each) for observation. Confocal microscope setting for basic fuchsin was excitation 561 nm, and emission was 591–649 nm, and representative images are shown. The observation of Casparian strip in Arabidopsis was performed as follows. Five days old seedlings were incubated in solution containing 0.24 mol/L HCl and 20% methanol for 15 min at 57 °C, then incubated in solution containing 7% NaOH and 60% ethanol for 15 min at room temperature, then rehydrated by sequential incubating in 40%, 20%, 10%, 5% ethanol solutions (5 min each), and then keep in 25% glycerol for microscope observation of Casparian strip. Confocal microscope setting was excitation 488 nm, and emission was 493–537 nm. To obtain the z-stack images of Casparian strip, 0.95-μm step-size confocal microscope images were taken, and then radial optical sections were constructed. For the transmission electron microscope assay of Casparian strip³⁰, the root samples were fixed for 1 h at room temperature in fixative containing 2.5% (v/v) glutaraldehyde and 2% (v/v) formaldehyde in 0.05 mol/L phosphate buffer (PB; pH6.8), and then post-fixed for 1 h in 2% (w/v) osmium tetroxide in PB. Then, the samples were washed two times with distilled water, dehydrated through a gradient series of ethanol, infiltrated with Spurr’s embedding medium, and then polymerized for 48 h at 60 °C. Ultrathin sections (100 nm) were prepared from the embedded samples and observed with the transmission electron microscope (Hitachi HT7800).

PI penetration assay and suberin staining

PI penetration assay of the barrier function of maize Casparian strips was conducted as follows. The root of three days old maize seedlings were incubated in the staining solution containing (2 µg/mL PI) (Sigma P4170) for 24 h, then rinsed in water twice and transversely sliced the sample, the sections were analysis with a Zeiss LSM710 confocal microscopy (excitation 561 nm, emission 591–649 nm). The barrier function of Arabidopsis Casparian strips is quantified using the PI penetration assay⁵⁶. The endodermal suberin deposition was determined using fluoral yellow 088 staining⁶².

Determination of Na⁺ and K⁺ content

Na⁺ contents in shoot, root and xylem sap were determined using a 4100‐MP AES device (Agilent, Santa Clara, CA, USA). In order to measure the Na⁺ and K⁺ contents in the root and shoot tissues, samples were oven-dried at 80 °C to constant weight, then incinerated at 300 °C for 3 h and 575 °C for 6 h. The ashes were dissolved in 10 mL 1% hydrochloric acid, diluted with an appropriate volume of 1% hydrochloric acid, and then the ion contents were measured. For the analysis of ion content in the xylem sap, 2-weeks-old seedlings were de-topped with a sharp blade, the xylem sap exuding at the cut surface was collected by a micropipette every 15 min for 1 h, and then the ion contents were measured.

Generation of the phylogeny tree

The phylogeny tree of DIR proteins was generated using Clustalx 2.1⁶³. The sequences of Arabidopsis, maize, rice and soybean DIR proteins (accession numbers as shown in Fig. 3a) were downloaded from TAIR (https://www.arabidopsis.org/), MaizeGDB, RAP (https://rapdb.dna.affrc.go.jp/) and SoyBase, respectively.

Data availability

The genome sequencing data generated in this study have been deposited in the NCBI database under BioProject number PRJNA706836 and BioSample number SAMN18146009 and SAMN18146011. All the raw images have been deposited to the BioImage Archive in BioStudies database under accession code S-BIAD390. Source data are provided with the paper. Source data are provided with this paper.

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Acknowledgements

The authors thank Xiangdong Fu and Wenkun Zhou for stimulating discussions. The authors acknowledge financial support from Beijing Outstanding Young Scientist Program (BJJWZYJH01201910019026 awarded to F.Q.), and the National Natural Science Foundation of China (Grant 32071933 and 31470350 awarded to C.J.).

Author information

These authors contributed equally: Yanyan Wang, Yibo Cao.

Authors and Affiliations

State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, 100193, Beijing, China
Yanyan Wang, Yibo Cao, Xiaoyan Liang, Junhong Zhuang, Feng Qin & Caifu Jiang
Key Laboratory of Forest Silviculture and Conservation of the Ministry of Education, College of Forestry, Beijing Forestry University, 100083, Beijing, China
Yibo Cao
Center for Crop Functional Genomics and Molecular Breeding, China Agricultural University, 100193, Beijing, China
Junhong Zhuang, Feng Qin & Caifu Jiang
National Maize Improvement Center of China, Department of Plant Genetics and Breeding, China Agricultural University, 100193, Beijing, China
Xiangfeng Wang

Authors

Yanyan Wang
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Yibo Cao
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Xiaoyan Liang
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Junhong Zhuang
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Xiangfeng Wang
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Feng Qin
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Caifu Jiang
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Contributions

Y.W., Y.C., X.L., F.Q., X.W., and C.J. designed the experiments. Y.W. conducted the fine mapping of ZmSTL1, and worked together with Y.C. and J.Z. to generate the CRISPR/Cas9 knockout lines, and to study the function of ZmSTL1/ZmESBL and ESBL. X.L. and X.W. carried out the bioinformatics analysis. Y.W. and C.J. wrote the manuscript, with the other authors’ contributions.

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Correspondence to Caifu Jiang.

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Wang, Y., Cao, Y., Liang, X. et al. A dirigent family protein confers variation of Casparian strip thickness and salt tolerance in maize. Nat Commun 13, 2222 (2022). https://doi.org/10.1038/s41467-022-29809-0

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Received: 22 February 2021
Accepted: 31 March 2022
Published: 25 April 2022
DOI: https://doi.org/10.1038/s41467-022-29809-0

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