Allelic variation of TaWD40-4B.1 contributes to drought tolerance by modulating catalase activity in wheat

Tian, Geng; Wang, Shubin; Wu, Jianhui; Wang, Yanxia; Wang, Xiutang; Liu, Shuwei; Han, Dejun; Xia, Guangmin; Wang, Mengcheng

doi:10.1038/s41467-023-36901-6

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Published: 02 March 2023

Allelic variation of TaWD40-4B.1 contributes to drought tolerance by modulating catalase activity in wheat

Nature Communications volume 14, Article number: 1200 (2023) Cite this article

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Abstract

Drought drastically restricts wheat production, so to dissect allelic variations of drought tolerant genes without imposing trade-offs between tolerance and yield is essential to cope with the circumstance. Here, we identify a drought tolerant WD40 protein encoding gene TaWD40-4B.1 of wheat via the genome-wide association study. The full-length allele TaWD40-4B.1^C but not the truncated allele TaWD40-4B.1^T possessing a nonsense nucleotide variation enhances drought tolerance and grain yield of wheat under drought. TaWD40-4B.1^C interacts with canonical catalases, promotes their oligomerization and activities, and reduces H₂O₂ levels under drought. The knock-down of catalase genes erases the role of TaWD40-4B.1^C in drought tolerance. TaWD40-4B.1^C proportion in wheat accessions is negatively correlative with the annual rainfall, suggesting this allele may be selected during wheat breeding. The introgression of TaWD40-4B.1^C enhances drought tolerance of the cultivar harboring TaWD40-4B.1^T. Therefore, TaWD40-4B.1^C could be useful for molecular breeding of drought tolerant wheat.

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Introduction

Drought is one of the main abiotic stresses and poignantly affects crop growth and yield. Wheat (Triticum aestivum L.), a staple crop, is mainly cultivated in arid and semi-arid regions worldwide, so its yield is frequently compromised by water scarcity¹. This circumstance is aggravated by the increasing water resource deficiency. It is therefore very crucial and urgent to build drought-tolerant germplasms and cultivars without yield penalty via efficient strategies such as molecular assistant breeding². This requires a comprehensive dissection of the genetic basis of drought tolerance, with the aim to mine excellent genes that directly and efficiently target the principal physiological basis of drought response and have no negative impact on growth and yield.

Drought tolerance is a complex trait controlled by many genes with minor effects. In the past several decades, some quantitative trait loci (QTLs) of drought tolerance have been mined through the linkage analysis of segregation populations^3,4. Genome-wide association study (GWAS) is a powerful tool for dissecting the genetic basis of complicated agronomic traits. It is especially efficient for mining the allelic variations that have been selected during domestication and breeding, which appears to avoid the trade-offs between tolerance and yield, and therefore has promising potential in germplasm improvement. Given genomic complexity and a high proportion of repetitive sequences, the application of GWAS in wheat lags behind other major crops such as rice and maize^5,6,7,8,9. Up to now, all of the QTLs controlling drought tolerance in wheat were present as genetic positions, except for a NAC transcription factor TaNAC071-A that was recently identified via GWAS¹⁰. Apart from those regulating transcriptional levels, the allelic variations causing the alteration of peptide sequences may be the other evolutionary force affecting phenotype and trait improvement, but this kind of allelic variations in drought-tolerant genes have been rarely identified via GWAS and other genetic analyses so far. On the other hand, a series of genetic analyses, derived from segregation populations and GWAS in the past fifteen years, identified a consistent major genomic region qDSI.4B.1 on the short arm of chromosome 4BS (see Fig S3 and the references therein). This region is responsible for up to 22% of phenotypic variation under drought stress¹¹. Several consistent meta-QTLs locate in this interval¹², one of which, the major-effect MQTL_1.4 is also present in chromosome 4BS of tetraploid durum wheat as well as drought tolerance QTL regions of maize and barley based on the syntenic analysis¹³, making this location even more interesting and important for further scrutiny¹⁴. As yet, the drought-tolerant allelic gene in this locus has not been cloned.

As a principal physiological response to drought and other abiotic stress, excessive accumulation of reactive oxygen species (ROS), including H₂O₂, causes oxidative damage in plants^15,16,17. On the other hand, H₂O₂ serves as a signaling molecule for modulating the signaling transduction network to enhance abiotic stress tolerance and modulate plant growth^18,19. Plants have evolved types of efficient regulatory machinery including ROS scavengers to fine-tune ROS homeostasis and avoid toxic ROS levels for adapting to abiotic stresses¹⁸. The transcriptional regulation of the activities of scavenging enzymes during the response to abiotic stress has been widely investigated^20,21,22,23, but the modulatory scenario at the post-transcriptional level is still not well addressed in plants. It has been found that catalase, the important H₂O₂ scavenger, can be regulated by interacting with chaperones such as AtNCA1, AtLSD1, small heat shock protein AtHsp17.6CII, natriuretic peptide AtPNP-A in Arabidopsis, and ROD1, NCA1 isoforms, UDP-xylose synthase OsUXS3 and SRL10 in rice, and Alpha-momorcharin (αMMC) in Momordica charantia^{24,25,26,27,28,29,30,31,32}, and through post-translational modifications such as phosphorylation by OsSTRK1, AtCPK8 and AtSOS2 and ubiquitination by OsAPIP6^33,34,35,36 in the response to abiotic and biotic stresses. The activity of catalase can also be directly modulated by the effectors such as AvrPiz-t, CMV2b, and triple gene block protein 1 (TGBp1) from pathogens^24,37,38,39. In animal cells, the common mechanism for activating catalase is proved to form oligomers (mostly tetramers) with high activity, while monomeric catalases have no or low activity⁴⁰. The oligomerization of catalases has been seldom reported in plants; a study in rice found that catalases form dodecameric holoenzymes containing 12 subunits, and holoenzyme has high catalase activity and a fast turnover rate for H₂O₂⁴¹. However, the factors (chaperones) modulate the oligomerization and therefore the activity of catalases has not been identified in plants.

WD40 domain-containing proteins (WD40) constitute a large gene family among eukaryote species⁴² and usually serve as the scaffolds and chaperones to regulate protein interaction and function⁴³. In plants, WD40 genes have been reported to modulate various biological processes, such as the grain yield of maize and rice^44,45 and the adaptation to drought and other abiotic stress^46,47, but the underlying mechanism has not been well unraveled. Whether WD40 proteins directly target the principal physiological responses upon drought and other abiotic stresses such as post-transcriptionally modulating catalase and other ROS scavenging enzymes is unknown so far.

In this work, we conduct a GWAS and identify a drought-tolerant WD40 gene TaWD40-4B.1 embedding in qDSI.4B.1 locus on chromosome 4BS of wheat. The allelic nonsense variation of TaWD40-4B.1 produces the allele TaWD40-4B.1^T encoding a truncated peptide which is associated with lower drought tolerance in the wheat accessions. The complete allele TaWD40-4B.1^C enhances drought tolerance and grain yield under drought stress but does not impose their trade-offs. TaWD40-4B.1^C but not TaWD40-4B.1^T strongly interacts with canonical catalases and promotes their oligomerization and activity under drought stress. Thus, our research reveals that the TaWD40-4B.1^C allele plays a significant role in wheat drought tolerance.

Results

GWAS for wheat drought tolerance at the seedling stage

In order to mine drought tolerance-associated genes, a diverse panel of 198 common wheat natural accessions representing the diversity of genetic structure and geographical distribution of the wheat population was used to evaluate the genetic basis controlling drought tolerance (Supplementary Data 1 and 2). These accessions were genotyped by the 660 K single-nucleotide polymorphism (SNP) genotyping array. A total of 419,606 high-quality SNP markers were retained for analysis after filtering (MAF < 0.05 and missing data > 0.1), and these SNP markers were located on 21 chromosomes (Supplementary Fig. 1a). These accessions were clustered into six subpopulations by population structure and kinship analyses based on these filtered SNPs (Supplementary Fig. 1b–d and Supplementary Data 2). Then, we phenotyped the drought tolerance of these accessions at the seedling stage using the drought tolerance (DT) index, which was defined as the grades ranging from one to six according to the wilting extent of the first to the fourth leaves of the seedlings (Supplementary Fig. 2a–c). The selected accessions exhibited diverse drought tolerance with a large variation in DT indices ranging from one to six (Supplementary Fig. 2d and Supplementary Data 1).

To dissect the genetic loci governing drought tolerance, we performed a GWAS based on the DT index dataset using the filtered SNPs. Through a Bonferroni-adjusted correction, we set the P-value for the suggestive threshold as 2.383 × 10⁻⁶. Under the mixed linear model (MLM) with correction of the population structure (Q) and kinship (K), 55 SNPs were identified to be significantly associated with drought tolerance (Fig. 1a, b), and they were distributed in four linkage disequilibrium (LD) blocks on chromosomes 4A, 4B, 7B, and 4D. Of them, the leading SNP, AX-109453581, at the position of 67352769 on the short arm of chromosome 4B (4BS) was identified (P = 4.181 × 10⁻⁸; Phenotypic variance explanation = 14.34%; Fig. 1a, b and Supplementary Data 3). The LD block on 4BS is embedded in the drought-tolerant locus qDSI.4B.1 that has been widely reported in the past 15 years (refer to Supplementary Fig. 3 for examples and references). The LD block containing the leading SNP harbored 12 genes (Fig. 1c and Supplementary Data 4), whose expression profiles were evacuated among 48 randomly selected wheat accessions with DT indices ranging from 1.2 to 3 as well as from 5 to 6 (24 for each) (Supplementary Data 5). Five genes were transcribed under the control and/or drought stress, three of which (TraesCS4B02G072100, TraesCS4B02G072200, TraesCS4B02G072300) were induced by drought stress, and TraesCS4B02G072200 showed the highest transcriptional level under the drought condition (Supplementary Figs. 2 and 4a). However, the change folds of their expression upon drought stress were comparable between the accessions with low (1.2–3) and high (5–6) DT indices (Supplementary Fig. 4b–f), indicating that drought tolerance is not associated with the transcriptional regulation of these genes in the LD block.

**Fig. 1: The allelic variation of *TaWD40-4B.1* is associated with drought tolerance in wheat.**

The leading SNP mentioned above was located at the 14th nucleotide of TraesCS4B02G072200’s 3’-UTR (Fig. 1d). TraesCS4B02G072200 is an intron-less gene and encodes a typic WD40-repeat protein containing seven WD40 domains, along with two adjacent paralogs TraesCS4B02G072100 and TraesCS4B02G072300 to form a WD40 gene tandem cluster (Supplementary Fig. 5), coinciding with the phenomenon that some of the WD40 genes are distinguished as tandem duplication in wheat⁴⁸. Besides the leading SNP at 3’-UTR, three SNPs in the coding sequence (CDS) of TraesCS4B02G072200 were excavated based on Sanger sequencing of 198 accessions, and they were all linked with the leading SNP (Fig. 1d and Supplementary Data 6). Of these four linked SNPs, SNP465 and SNP999 were synonymous, while SNP1274 (G → A) was nonsense and caused the substitution of Trp codon TGG to stop codon TAG (Fig. 1e). Thus, the allelic variations in CDS of TraesCS4B02G072200 resulted in two haplotypes, one encoding a complete peptide and the other encoding a truncated peptide (Fig. 1h). The truncated peptide had lower prediction confidence of the seventh WD40 domain, and its 3D structure was affected (Supplementary Fig. 6). The seedlings of wheat accessions possessing complete haplotype exhibited higher DT indices than those with truncated haplotype (Fig. 1f). Hence, TraesCS4B02G072200 was the most putative candidate drought-tolerant gene and was named TaWD40-4B.1. In comparison with the accessions with complete haplotype (TaWD40-4B.1^C), those with truncate haplotype (TaWD40-4B.1^T) produced comparable transcripts of TaWD40-4B.1 under both well-watered and water-limited conditions (Fig. 1g). Meanwhile, the expression levels of TaWD40-4B.1’s paralogs as well as the other two transcriptionally detectable genes in the LD block were also equivalently similar between the accessions with TaWD40-4B.1^C and TaWD40-4B.1^T alleles (Supplementary Fig. 4g–j), indicating that the allelic variation is not associated with the transcriptional regulation of these genes. In line with these results, we concluded that TaWD40-4B.1 was the candidate gene of the drought-tolerant locus on chromosome 4BS, and its complete and truncated alleles were associated with the variation in drought tolerance of the wheat accessions.

TaWD40-4B.1 ^C but not TaWD40-4B.1 ^T enhanced the drought tolerance of wheat seedlings

To confirm the role of TaWD40-4B.1^C and TaWD40-4B.1^T in drought tolerance, we selected two cultivars, Yangmai 20 (YM20) carrying the TaWD40-4B.1^T allele and Shanrong 3 (SR3) carrying the TaWD40-4B.1^C allele respectively, to construct transgenic lines. Of them, both TaWD40-4B.1^C and TaWD40-4B.1^T overexpression lines (labeled as OE-C and OE-T, respectively) of either YM20 or SR3 were transformed with TaWD40-4B.1^C and TaWD40-4B.1^T driven by the ubiquitin promoter (pUbi) respectively, and their knock-down lines were generated via the RNA interference (RNAi) strategy (labeled as RNAi lines). To avoid the influence of the transcript dosage effect, the overexpression (OE) lines that produced similar transcripts of TaWD40-4B.1^C and TaWD40-4B.1^T were selected for water-withholding assay (Fig. 2a, b). In these RNAi lines, the expression levels of TraesCS4B02G072100 and TraesCS4B02G072300, two paralogs of TaWD40-4B.1, were comparable to those of the wild-type (Supplementary Fig. 7), showing that RNAi did not affect the transcription of the paralogs.

**Fig. 2: *TaWD40-4B.1*^C but not *TaWD40-4B.1*^T enhances drought tolerance of wheat seedlings.**

Under the well-watered condition, there was no morphological difference between YM20 or SR3 and their corresponding TaWD40-4B.1^C/TaWD40-4B.1^T overexpression and RNAi lines (Fig. 2c, d). Drought stress stimulated by water withholding caused the seedlings to wilt (Fig. 2c, d). Both YM20 and the OE-T lines were wilted with the same strength, and their shoot fresh weights and relative water contents were significantly reduced; while in comparison with YM20 and the OE-T lines, the OE-C lines exhibited superior growth capacity, the leaf wilting was attenuated, and the fresh weights and relative water contents were higher (Fig. 2c, e–g). Consistently, TaWD40-4B.1^C overexpression enhanced drought tolerance, alleviated leaf wilting, and the reduction of shoot fresh weight and relative water content in SR3 after water-withholding, while TaWD40-4B.1^T overexpression had no visible effect (Fig. 2d, h–j). On the other hand, the knock-down of TaWD40-4B.1^C in SR3 reduced drought tolerance, while the knock-down of TaWD40-4B.1^T in YM20 did not visibly alter the tolerance (Fig. 2c–j). Collectively, these data indicate that the TaWD40-4B.1^C but not TaWD40-4B.1^T improves the drought tolerance of wheat.

TaWD40-4B.1^C had stronger interaction with canonical catalases than TaWD40-4B.1^T

To explore the mechanism of TaWD40-4B.1-mediated drought tolerance, we identified potential TaWD40-4B.1-interacting proteins through screening a yeast two-hybridization library of wheat. Among these, two proteins annotated as catalase 3A (TaCAT3A) and TaCAT3U were identified repeatedly. There have three catalase genes (TaCAT1, TaCAT2, and TaCAT3) in the wheat genome, and each of them has three alleles located in A, B, and D subgenomes (Supplementary Fig. 8a). CATs have three classes in plants; according to the phylogeny and synteny relationships between TaCATs and CAT orthologues of other plants, TaCAT1, TaCAT2, and TaCAT3 are categorized into classes I, III, and II, respectively (Supplementary Fig. 8b), and are concurrently clustered with orthologous AtCAT2, AtCAT3 and AtCAT1 of Arabidopsis^49,50. The yeast two-hybridization assay showed that both TaWD40-4B.1^C and TaWD40-4B.1^T interacted with TaCAT1s and TaCAT3s but not TaCAT2s (Fig. 3a). We confirmed the interaction by the bimolecular fluorescence complementation assay (BiFC) using the A subgenome alleles of TaCAT1, TaCAT2, and TaCAT3 because the alleles among three subgenomes share high identity (Supplementary Fig. 8a). The result also shows that TaWD40-4B.1^C and TaWD40-4B.1^T interacted with TaCAT1A and TaCAT3A but not TaCAT2A via the transient co-expression of N-terminal yellow fluorescence protein (nYFP) fused TaCAT and cYFP fused TaWD40-4B.1 in wheat protoplasts (Fig. 3b and Supplementary Fig. 9). These findings indicate that TaWD40-4B.1 specifically interacts with TaCATs in classes I and III rather than class II. Recently, AtCAT3 (Class II) was verified to be a non-canonical catalase that functions as a transnitrosylase, whose activity depended on the unique Cys-343 residue that is highly conserved in plants, while AtCAT1 and AtCAT2 (Classes III and I, respectively) were canonical catalases characterized as the Thr-343 residue⁵¹. Interestingly, three alleles (TaCAT2A, TaCAT2B, and TaCAT2D) of class II TaCATs carry the conserved Cys-343 residue, while class I and III TaCATs carry Thr-343 (Fig. 3c and Supplementary Fig. 8b). These findings indicate that both TaWD40-4B.1^C and TaWD40-4B.1^T interacts with canonical catalases in class I and III rather than non-canonical catalases in class II in wheat.

**Fig. 3: TaWD40-4B.1^C has a stronger interaction capacity with canonical catalases than TaWD40-4B.1^T.**

Transient co-expression of GFP-fused proteins and peroxisome marker DsRed-SKL (SKL is a peroxisome targeting sequence) in wheat protoplasts showed that GFP-TaWD40-4B.1^C and GFP-TaWD40-4B.1^T did not localize in the peroxisomes but dispersed in the cells as GFP alone (Supplementary Fig. 10a). Alike rice CATs⁴¹, canonical TaCAT1 and TaCAT3 possess a peroxisomal targeting signal (PTS1) with the signaling motif (SRL) localized at −7 to −9 upstream of the C terminus, but noncanonical TaCAT2A has no PTS1 (Supplementary Fig. 8c); GFP-TaCAT1A and GFP-TaCAT3A majorly accumulated close to the peroxisomes, but GFP-TaCAT2A dispersed in the cells with no obvious fluorescence signal around the peroxisomes (Supplementary Fig. 10). The place of TaWD40-4B.1 and TaCATs in cells was further confirmed by the western blot assay using the total, cytoplasmic and peroxisomal proteins extracted from the protoplasts (Supplementary Fig. 10b). In wheat protoplasts, the YFP fluorescence signals of the interaction between TaWD40-4B.1^C/TaWD40-4B.1^T and canonical TaCATs accumulated close to the peroxisomes (Fig. 3b and Supplementary Fig. 9).

Given that the truncation was predicted to affect the structure of TaWD40-4B.1 (Supplementary Fig. 6 and Supplementary Data 7), we compared the interaction capacity of TaWD40-4B.1^C and TaWD40-4B.1^T with TaCATs using the split-luciferase complementation imaging (SLCI) assay (Fig. 3d). Both TaWD40-4B.1^C and TaWD40-4B.1^T interacted with TaCAT1A and TaCAT3A rather than TaCAT2A in Nicotiana benthamiana leaves, further confirming the specific interaction between TaWD40-4B.1 and canonical catalases. Moreover, the fluorescence signal densities produced by the interaction of TaWD40-4B.1^C and TaCAT1A/TaCAT3A were stronger than those between TaWD40-4B.1^T and TaCAT1A/3 A, showing TaWD40-4B.1^C had a higher affinity with canonical TaCATs. Because the expression of TaCAT3s instead of TaCAT1s was increased under drought stress⁴⁹, which indicates the close association between TaCAT3 and drought response, we chose TaCAT3A to further confirm the difference in interaction affinity. Firstly, TaCAT3A fused with GFP (TaCAT3A-GFP) and TaWD40-4B.1^C fused with cMyc tag (TaWD40-4B.1^C-cMyc)/TaWD40-4B.1^T-cMyc were transiently co-expressed in N. benthamiana leaves to conduct the co-immunoprecipitation assay. TaCAT3A-GFP was precipitated by either TaWD40-4B.1^C-cMyc or TaWD40-4B.1^T-cMyc, but the abundance of TaCAT3A-GFP precipitated by TaWD40-4B.1^C-cMyc was higher than that by TaWD40-4B.1^T-cMyc (Fig. 3e). Moreover, His-TaWD40-4B.1^C/His-TaWD40-4B.1^T and MBP-TaCAT3A being expressed, respectively, in E. coli were purified for the pull-down assay. After in vitro incubation, His-TaWD40-4B.1^C/His-TaWD40-4B.1^T were both pulled down by MBP-TaCAT3A, but not MBP alone, and pulled-down His-TaWD40-4B.1^C had a higher abundance than His-TaWD40-4B.1^T (Fig. 3f). These data demonstrate that TaWD40-4B.1^C has a stronger interaction capacity with canonical TaCATs than TaWD40-4B.1^T does.

TaWD40-4B.1^C but not TaWD40-4B.1^T promoted in vitro and in vivo catalase activity

Given that TaWD40-4B.1^C was more prone to interact with canonical TaCATs than TaWD40-4B.1^T, we compared the effects of the two haplotypes on catalase activity. First, we found that both the overexpression and RNAi lines of TaWD40-4B.1^C/TaWD40-4B.1^T had comparable expression levels of TaCAT1 and TaCAT3 to either SR3 or YM20 under either well-watered or drought conditions (Supplementary Fig. 11), showing the genetic manipulation of TaWD40-4B.1 did not affect the expression of catalase genes. The lines of TaWD40-4B.1^C and TaWD40-4B.1^T overexpression and TaWD40-4B.1^C RNAi possessed comparable catalase activities to SR3 in the whole leaves of seedlings under the well-watered condition (Fig. 4a). After exposure to drought stress, the catalase activities were elevated; in comparison with SR3, TaWD40-4B.1^C overexpressors had higher activities, its knock-down lines lower, but TaWD40-4B.1^T overexpression lines were comparable. A similar result was obtained in YM20 and its transgenic lines (Supplementary Fig. 12a). Then, we used a yeast fast-heterologous model system to further analyze the effects of TaWD40-4B.1^C and TaWD40-4B.1^T on in vivo catalase activity (Fig. 4b–d). The yeast cells expressing either TaWD40-4B.1^C or TaWD40-4B.1^T alone possessed catalase activity similar to the control transformed with an empty vector (Fig. 4c), showing recombinant TaWD40-4B.1^C or TaWD40-4B.1^T had no effect on the activity of yeast catalase. The expression of TaCAT3A increased the total catalase activity in yeast; in comparison with the yeast cells expressing TaCAT3A alone, those co-expressing TaWD40-4B.1^T had similar catalase activity, while those co-expressing TaWD40-4B.1^C had obviously higher catalase activity (Fig. 4c). Consistently, all the recombinants had similar growth rates to the control under the non-stressful condition (Fig. 4d). The exposure to 3 mM H₂O₂ slowed down the growth rates of all yeast lines. In comparison with the control, the yeast expressing TaWD40-4B.1^C or TaWD40-4B.1^T alone had a comparable growth rate. The yeast producing TaCAT3A exhibited more vigorous growth capacity than the control, in accord with the role of durum wheat TdCAT1⁵², and co-expression of TaWD40-4B.1^C but not TaWD40-4B.1^T promoted the positive effect of TaCAT3A on the growth ability (Fig. 4d). This indicates the increase in the in vivo catalase activity of TaCAT3A by TaWD40-4B.1^C enhanced the tolerance to oxidative stress in yeast. Meanwhile, we measured the role of TaWD40-4B.1^C and TaWD40-4B.1^T using the in vitro catalase activity assay (Fig. 4e). TaCAT3A alone had quite weak catalase activity and the presence of TaWD40-4B.1^T had no distinguishable effect on the activity of TaCAT3A. The application of TaWD40-4B.1^C triggered the in vitro activity of TaCAT3A, and the elevation of activity became more drastic following the increase of TaWD40-4B.1^C concentration.

**Fig. 4: TaWD40-4B.1^C but not TaWD40-4B.1^T promotes in vivo and in vitro activity and oligomerization of catalase.**

It has proved that oligomerization of catalases is crucial for activating their activities⁴⁰, and catalases oligomerize to dodecameric holoenzyme containing 12 units with high activity in rice⁴¹. First, the SLCI assay revealed that the homo-interaction occurred between TaCAT1A and TaCAT1A as well as between TaCAT3A and TaCAT3A, and the presence of TaWD40-4B.1^C but not TaWD40-4B.1^T promoted the homo-interactions (Fig. 4f, g). Then, the proteins of wheat leaves were cross-linked by dithiobis (succinimidyl propionate) (DSP) for immunoassay to detect the effect of TaWD40-4B.1 on the oligomerization of catalases using the antibody of TaCAT3 (56.4 kDa). Under both well-watered and drought conditions, in comparison with SR3, the abundances of dimeric and oligomeric catalases were increased by the overexpression of TaWD40-4B.1^C rather than TaWD40-4B.1^T, but decreased by the RNAi of TaWD40-4B.1^C (Fig. 4h). When the cross-links between proteins were cleaved by β-mercaptoethanol (β-ME) to destroy the protein-protein interaction, only monomeric catalases were detected with similar abundances among SR3 and the transgenic lines under either well-watered or drought condition (Fig. 4h), showing that TaWD40-4B.1 does not affect the expression of catalases. We further analyzed the role of TaWD40-4B.1 in the oligomerization of TaCAT3A in the reaction system of in vitro catalase activity assay using the same methodology (Fig. 4i). In the absence of TaWD40-4B.1, the MBP-fused TaCAT3A (104.6 kDa) was not oligomerized. The addition of TaWD40-4B.1^C induced the oligomerization of TaCAT3A, and the abundance of TaCAT3A oligomers became more pronounced with the rise of TaWD40-4B.1^C concentration, while the promotion to TaCAT3A oligomerization caused by TaWD40-4B.1^T turned out to be negligible. Different from the in vivo assay, dimerized TaCAT3A could hardly be detected in the in vitro system. These data indicate that TaWD40-4B.1^C rather than TaWD40-4B.1^T contributes more to the oligomerizations of canonical catalases and therefore increases their activities in wheat.

TaWD40-4B.1 ^C enhanced the tolerance to oxidative stress in wheat

Given that TaWD40-4B.1^C enhanced catalase activity, we further analyzed the role of TaWD40-4B.1^C and TaWD40-4B.1^T in the tolerance of wheat seedlings to oxidative stress simulated via supplying exogenous H₂O₂ in a liquid medium (Fig. 5a, b). In the absence of H₂O₂ treatment, the seedlings of SR3 and its transgenic lines were comparable to each other. When supplied with 100 mM H₂O₂, the growth of SR3 seedlings was affected, and the plant height was reduced. TaWD40-4B.1^C overexpression alleviated the growth restriction of SR3, and its knock-down aggravated the effect of oxidative stress; while TaWD40-4B.1^T overexpression had no obvious performance. We then measured the H₂O₂ level in the leaves of wheat seedlings planted in soil using the DAB staining assay (Fig. 5c). Under the well-watered condition, the H₂O₂ levels were similar among SR3 and all lines. Under drought stress, the H₂O₂ levels were increased; in comparison with SR3, the increase was weaker in TaWD40-4B.1^C overexpression lines, more significant in the knock-down lines, but similar in the TaWD40-4B.1^T overexpression lines. Consistently, the contents of malonaldehyde (MDA) representing the extent of in vivo oxidative damage were comparable among all plants under the well-watered condition (Fig. 5d). After exposure to drought stress, the MDA contents were increased significantly, and TaWD40-4B.1^C overexpression attenuated the accumulation of MDA, its knock-down had the opposite effect, while TaWD40-4B.1^T overexpression did not influence the MDA contents. The parallel analysis using YM20 and its TaWD40-4B.1^C/TaWD40-4B.1^T overexpression lines confirmed the role of TaWD40-4B.1^C and TaWD40-4B.1^T on oxidative stress and H₂O₂ levels as well (Supplementary Fig. 12b–e). Because ROS are often produced under all kinds of abiotic stresses, we measured the role of TaWD40-4B.1 in the tolerance to salt, alkali, and heat, the major abiotic stresses during the life course of wheat (Supplementary Fig. 13). TaWD40-4B.1 that constitutively expressed at the young and reproductive stages was induced by dehydration in leaves but not roots (Supplementary Fig. 13a, b). Thus, we measured the expression profiles of TaWD40-4B.1 upon these stresses and H₂O₂ treatment in leaves, and found that TaWD40-4B.1 was also induced by the stimuli (Supplementary Fig. 13c). In comparison with SR3, the TaWD40-4B.1^C overexpression and RNAi lines had higher and lower tolerance respectively to salt, alkali, and heat stress, while the TaWD40-4B.1^T overexpressors had similar tolerance capacities (Supplementary Fig. 13d–f). These data demonstrate that TaWD40-4B.1^C can avoid the over-accumulation of H₂O₂ (ROS) to enhance drought tolerance.

**Fig. 5: *TaWD40-4B.1*^C but not *TaWD40-4B.1*^T enhances tolerance to oxidative stress and reduces H₂O₂ level under drought stress.**

TaWD40-4B.1 ^C enhanced drought tolerance via catalase to avoid ROS over-accumulation

To confirm whether the role of TaWD40-4B.1^C in drought tolerance is due to promoting catalase activity, we conducted a genetic analysis using the TaCAT knock-down (RNAi) lines of SR3 that the expression of canonical catalase genes TaCAT1 and TaCAT3 was obviously reduced (Supplementary Fig. 14a). TaCAT knock-down slightly restricted the growth under the well-watered condition (alike CATB mutation in rice²⁴), and promoted the leaf wilting when the seedlings suffered from drought stress (Fig. 6a). The RNAi line had lower catalase activity than SR3, and the difference was more significant under drought (Fig. 6e), showing the decrease in catalase activity by TaCAT knock-down reduced drought tolerance. Then we crossed the TaCAT RNAi line and the TaWD40-4B.1^C/TaWD40-4B.1^T overexpression lines to construct the TaWD40-4B.1 genetic lines in the catalase knock-down background (Supplementary Fig. 14b–d). Under the well-watered condition, the seedlings of the cross lines were slightly shorter than those of the TaWD40-4B.1^C/TaWD40-4B.1^T overexpression lines (Fig. 6d). After exposure to drought stress, as observed above, the TaWD40-4B.1^C overexpression line exhibited superior drought tolerance than SR3 and the TaWD40-4B.1^T overexpression line; knock-down of TaCATs reduced the drought tolerance of SR3 and its TaWD40-4B.1 transgenic lines, and almost abolished the positive role of TaWD40-4B.1^C in drought tolerance (Fig. 6b–d). Consistently, the role of TaWD40-4B.1^C in promoting catalase activity under drought was also lost when TaCATs were knocked down (Fig. 6e). High light intensity induces photorespiration, which leads to the generation of large amounts of H₂O₂ in the peroxisomes, resulting in severe plant growth retardation⁵³. Catalase is a direct target of hydroxyurea, and hydroxyurea inhibits catalase activity⁵⁴. Under the high light intensity, SR3 had superior growth capacity than the TaWD40-4B.1^C RNAi lines in the absence of hydroxyurea, whilst the growth difference became weaker in the presence of low concentration (1 mM) of hydroxyurea, and comparable when applied high concentration (2 and 3 mM) of hydroxyurea (Supplementary Fig. 15). On the other hand, we randomly selected 24 wheat accessions harboring TaWD40-4B.1^C and 24 wheat accessions harboring TaWD40-4B.1^C to compare their catalase activities (Supplementary Data 5), and found that the accessions harboring TaWD40-4B.1^C had higher catalase activities than those with TaWD40-4B.1^T under drought (Fig. 6f). These data indicate the contribution of TaWD40-4B.1^C to drought tolerance is, at least in large part, achieved through its direct promotion of catalase activity to reduce ROS over-accumulation.

**Fig. 6: The role of *TaWD40-4B.1*^C in drought tolerance is dependent on catalases.**

TaWD40-4B.1 ^C overexpression enhanced grain yield under water-withheld conditions

As TaWD40-4B.1^C enhanced drought tolerance at the seedling stage, we further analyzed its role in grain yield by the water-withholding assay with plants at the reproductive stage grown in pots. Under the well-watered condition, SR3 and its transgenic lines showed similar growth ability during the whole life cycle, while under the water-withheld condition, in comparison with SR3, TaWD40-4B.1^C overexpression lines had a less wilting extent, TaWD40-4B.1^C knock-down lines exhibited an opposite phenotype and TaWD40-4B.1^T overexpression lines had no obvious difference (Fig. 7a), consistent with the difference in drought tolerance at the seedling stage. The grain sizes were comparable under the well-watered condition; water-withholding reduced the grain sizes, in comparison with SR3, the grain sizes of TaWD40-4B.1^C overexpression and knock-down lines became larger and smaller respectively, but those of TaWD40-4B.1^T overexpression lines were comparable (Fig. 7b–d). Consistently, 1000-grain weights (TGWs) were similar to each other under the well-watered condition, and water-withheld treatment reduced TGWs and differentiated them among the lines, with the highest in TaWD40-4B.1^C overexpression lines, the lowest in the knock-down lines (Fig. 7e). The other yield-associated indices including spike number, grain number per ear, and plant height, respectively, had no difference among SR3 and its transgenic lines under both well-watered and water-withheld conditions (Fig. 7f–h). Under the well-watered condition, there was no difference in grain yield; under the water-withheld condition, TaWD40-4B.1^C overexpression alleviated the decrease in grain yield and the overexpression lines had higher grain yields than SR3, TaWD40-4B.1^C knock-down exhibited an opposite effect, and TaWD40-4B.1^T overexpression lines had similar grain yields to SR3 (Fig. 7i). We also measured the effect of TaWD40-4B.1^C genetic manipulation on water use efficiency (WUE). SR3 and all the transgenic lines had comparable CO₂ assimilation rates, transpiration rates, and WUE under the well-watered condition (Fig. 7j–l). Under the water-withheld condition, in comparison to SR3, TaWD40-4B.1^C overexpression lines had a lower transpiration rate but higher CO₂ assimilation rate and WUE, its knock-down lines opposite, and these indices of TaWD40-4B.1^T overexpression lines were similar. The parallel yield trial using YM20 and its transgenic lines phenocopied the results of SR3 (Supplementary Fig. 16a–k).

**Fig. 7: *TaWD40-4B.1*^C enhances grain yields under the water-withheld condition.**

We further compared the yield of YM20 and its transgenic lines in the field with two irrigation conditions (Supplementary Fig. 16l–o). In the field irrigated with 1500 m³ ha⁻¹ of water, spike densities, and grain numbers per spike were comparable among YM20 and all lines, but TGWs of TaWD40-4B.1^C overexpression lines were higher (>2%) than those of YM20 and TaWD40-4B.1^T overexpression lines; in the field not irrigated with water, TaWD40-4B.1^C overexpression lines had similar grain numbers per spike but higher spike densities (~5%) and TGWs (5.5 and 6.0%) than YM20 and TaWD40-4B.1^T overexpression lines (Supplementary Fig. 16l–n). Under two irrigation conditions, in comparison with YM20, TaWD40-4B.1^T overexpression lines had comparable grain yields, but TaWD40-4B.1^c overexpression lines had higher by 6.9−7.9% and 12.9−16.3%, respectively (Supplementary Fig. 16o). In line with these, we found that TaWD40-4B.1^C but not TaWD40-4B.1^T enhances grain yield under water-withheld conditions.

The introduction of TaWD40-4B.1 ^C enhanced drought tolerance

Given the overexpression of TaWD40-4B.1^C but not TaWD40-4B.1^T enhanced tolerance and yield of wheat under drought stress, we further analyzed whether these two haplotypes could alter drought tolerance each other via introducing TaWD40-4B.1^C of drought tolerant cultivar Luyuan301 into drought sensitive cultivar Chuanmai36 harboring TaWD40-4B.1^T allele as well as introducing TaWD40-4B.1^T of Chuanmai36 into Luyuan301 through successive backcrossing to construct near-isogenic lines (NILs). Under the well-watered condition, there had no difference between Chuanmai36 and its NIL^TaWD40-4B.1C as well as Luyuan301 and its NIL^TaWD40-4B.1T; after water-withholding, Chuanmai36 exhibited lower drought tolerance than its NIL^TaWD40-4B.1C, oppositely Luyuan301 possessed higher drought tolerance than its NIL^TaWD40-4B.1T (Fig. 8a, b). This indicates that the introgression of TaWD40-4B.1^C indeed enhances drought tolerance, while TaWD40-4B.1^T in replacement of TaWD40-4B.1^C decreases drought tolerance. On the other hand, we analyzed the distribution of two TaWD40-4B.1 haplotypes using 600 accessions from different districts in China (Supplementary Data 8). The wheat accessions possessing TaWD40-4B.1^C (80.8%) were more than those carrying TaWD40-4B.1^T (19.2%) (Fig. 8c). Of them, the cultivars and breeding materials had lower proportions of TaWD40-4B.1^C, but the landraces had higher. Then, 584 of 600 accessions from 16 provinces/cities (the main districts of wheat production) of China were used to evaluate the relationship between the proportion of TaWD40-4B.1 haplotypes and annual rainfall (Supplementary Data 8). There were less accessions carrying TaWD40-4B.1^T in northern districts with lower annual rainfalls but fewer ones in southern districts with higher annual rainfalls, and the proportions of TaWD40-4B.1^T exhibited a close positive correlation with the annual rainfalls (Fig. 8d and Supplementary Data 9). In line with the public SNP information^55,56,57,58, we further found that there also had two haplotypes of TaWD40-4B.1 in the accessions around the world (Supplementary Fig. 17 and Supplementary Data 10 and 11). In consistency with the accessions in China, the proportions of accessions with TaWD40-4B.1^C were higher than those with TaWD40-4B.1^T. Comparatively, the proportions of TaWD40-4B.1^C in Asia and Oceania were higher, but those in America, Africa, and Europe were lower, and the proportion in West Europe was the lowest (Supplementary Fig. 17 and Supplementary Data 11). In comparison with total accessions, the cultivars and breeding lines had higher TaWD40-4B.1^T proportion, but the old cultivars had lower, close to the proportion of the landraces (Supplementary Fig. 17b).

**Fig. 8: The Introgression of *TaWD40-4B.1*^C enhances drought tolerance and the *TaWD40-4B.1*^C proportion is correlative with annual rainfall.**

Discussion

Natural variation offers the elite agricultural traits during the domestication and breeding of crops. Thus, to mine the elite allelic variations of stress-tolerant genes that do not impose the trade-offs between the yield and tolerance⁵⁹ is meaningful for dealing with adverse environmental stimuli. In this study, we performed a GWAS and identified a drought tolerance-associated locus qDT4B with the highest significant confidence on chromosome 4BS (Fig. 1). This locus is embedded in a consistent major genomic region qDSI.4B.1 of drought tolerance in both bread and durum wheat, as well as some other crops, that have been widely reported (see Supplementary Fig. 3 and the references therein), showing it is an important drought-tolerant locus of wheat and other crops. The drought tolerance of qDT4B locus owes to the WD40 gene TaWD40-4B.1, because the wheat accessions carrying truncated allele TaWD40-4B.1^T exhibit lower drought tolerance capacity than those with complete allele TaWD40-4B.1^C (Fig. 1), and TaWD40-4B.1^T is deficient in the role of enhancing drought tolerance, water use efficiency, and grain yield under the water-withheld condition that is performed by the TaWD40-4B.1^C (Figs. 2, 7, and 8 and Supplementary Fig. 16). More importantly, both overexpression and knockdown of TaWD40-4B.1^C have no adverse effect on plant growth and grain yield under the well-watered condition (Figs. 2, 5, and 7 and Supplementary Fig. 16). This indicates that TaWD40-4B.1^C is an elite gene (haplotype) for molecular breeding of drought-tolerant cultivars without imposing the trade-offs between grain yield and drought tolerance and has the potential in water-saving agriculture for coping with the increasing circumstance of global water resource deficiency. Besides, given its contribution to the tolerance to high salt, alkali, and heat (Supplementary Fig. 13), TaWD40-4B.1^C appears to have the potential for breeding germplasms with broad-spectrum tolerance to multiple abiotic stress.

As members of a large family, WD40 proteins participate in multiple processes such as development, metabolite biosynthesis, and immune and stress responses^60,61,62. It has been reported that WD40 proteins perform modulatory roles by serving as scaffolds for protein-protein interactions^42,63. For instance, maize WD40 proteins KRN2 and Shrek1 modulate grain development via interacting with a DUF1644-containing protein and regulating pre-rRNA processing, respectively^44,45; Arabidopsis WD40 protein COP1 regulates photomorphism by cooperating with a series of regulatory factors⁶⁴. WD40 proteins are involved in the MYB-bHLH-WD40 complex to transcriptionally modulate the biosynthesis of anthocyanins and other flavonoids, the secondary metabolites with non-enzymatic antioxidant capacity, which contribute to the tolerance for drought and other abiotic stress via decreasing ROS level^65,66. In this work, we found TaWD40-4B.1^C interacts with canonical catalases and promotes their activity, reduces H₂O₂ levels under drought, and the knock-down of catalase genes abolishes the role of TaWD40-4B.1^C in drought tolerance (Figs. 3–6 and Supplementary Fig. 12). Catalase, a crucial enzymatic scavenger for removing excessive H₂O₂, is closely associated with drought stress⁶⁷. Especially, the catalase coding gene of CAT2 (grouped in class I canonical catalase) is identified as an eQTL of drought tolerance in maize based on the eGWAS⁶⁸. Thus, apart from modulating protein-protein interactions such as MYB and bHLH transcriptional factors’ interaction, the WD40 protein (TaWD40-4B.1^C) offers drought tolerance by promoting catalase activity to avoid H₂O₂ (ROS) over-accumulation, the typical and principal physiological response to adverse environmental stimuli.

Among the catalase-interacting proteins, AtLSD1 interacts with all of the three catalases²⁹, OsROD1 and AtNCA1 interact with canonical OsCatB and AtCAT2 respectively, but whether they can interact with other canonical and non-canonical catalase (OsCatC/AtCAT1 and OsCatA/AtCAT3, respectively) have not been detected^24,25. In our research, TaWD40-4B.1 interacts with canonical TaCAT1s and TaCAT3s but not non-canonical TaCAT2s (Fig. 3), and appears to be chaperone specific to canonical catalase in plants, providing further evidence for its crucial contribution to excessive H₂O₂ scavenging. The active catalases are matured through heme acquisition and oligomer (majorly tetramer in animal cells) formation and are modulated by phosphorylation and ubiquitination^33,34. Here, TaWD40-4B.1^C can promote the in vitro activity of catalase (Fig. 4e) in the solution not adding heme and lacking the condition for catalase modification (TaWD40-4B.1 has no property for catalyzing the modification). Thus, TaWD40-4B.1^C promotes catalase activity largely by helping catalases oligomerize (Fig. 4f–i). It has proved that catalases form dodecameric holoenzymes with high catalase activity and fast turnover rate of H₂O₂ in rice⁴¹, and the molecular weight of oligomeric TaCATs is larger than that of tetrameric forms (Fig. 4h, i), so it is speculated that TaWD40-4B.1^C can promote the formation of dodecameric catalase holoenzymes and, consequently, enhance catalase activity and lower H₂O₂ levels under drought (Figs. 4a and 5 and Supplementary Fig. 12). In line with these data, the maturation of catalases is achieved via forming oligomerized (dodecamerized) holoenzymes instead of tetramers in plant cells, indicating the distinguishable mechanisms of catalase maturation between plants and animals. TaWD40-4B.1^C is therefore a factor modulating catalase oligomerization and provides a target for further understanding the molecular basis of catalase maturation.

Functional WD40 proteins require at least seven WD40 domains to form the structure of seven-bladed beta-propellers with a funnel-like shape stabilized by the disulfide bond connection between the first and last blades⁶⁹. TaWD40-4B.1^T deficient C-terminus starting from the last bipeptide of the seventh WD40 domain (Fig. 1h) has a slight difference in structure from TaWD40-4B.1^C (Supplementary Fig. 6). Thus, TaWD40-4B.1^T may lose chaperone function, so it can’t interact with canonical catalases and promote their oligomerization and activity to enhance drought tolerance (Figs. 2–7). On the other hand, besides as a toxic molecule resulting in oxidative damage when over-accumulation, H₂O₂ serves as an important signaling molecule to modulate the signaling transduction networks of abiotic stress response and growth and reproduction. To fine-tune ROS (H₂O₂) homeostasis through orchestrating ROS production and/or scavenging machineries will balance plant growth and stress tolerance. TaWD40-4B.1^C does not affect catalase activity, H₂O₂ level, growth ability, and grain yield under the well-watered condition (Figs. 4, 5, and 7 and Supplementary Fig. 12). This indicates the complicated modulation mechanisms of TaWD40-4B.1 in catalase activity in planta, and other unknown factors along with TaWD40-4B.1 may orchestrate ROS homeostasis and avoid imposing the trade-offs between grain yield and drought tolerance. Further exploration is needed to uncover the molecular and structural mechanisms underlying the interaction of TaWD40-4B.1^C with canonical catalases to promote their activities and identify its co-factors, which could provide clues for precisely modifying TaWD40-4B.1 to fine-tune catalase activity and promote its application potential in molecular breeding.

Wheat is an allohexaploid, possessing A, B, and D subgenomes, formed via two inter-species cross and genome duplication of three diploid progenitors. Our Sanger sequencing indicates the alleles of TaWD40-4B.1 in the A and D subgenomes (TraesCS4A02G242800 and TraesCS4D02G071100) also have no truncated haplotype. The collinearity analysis shows that TaWD40-4B.1 appears to be the duplicated copy of TraesCS4B02G072300, and the duplication occurred during the formation of the tetraploid progenitor of wheat (Supplementary Fig. 18). TaWD40-4B.1 is identical to the homologs (TRIDC4BG011100 and TRITD4Bv1G024340) of tetraploid emmer and durum wheat. Previous studies found that both TRIDC4BG011100 and TRITD4Bv1G024340 have no truncated haplotype based on genome resequencing and whole-exome capture methods^70,71,72,73 (Supplementary Data 12). Oppositely, in hexaploid wheat, the TaWD40-4B.1^T allele is present in approximately 20% of cultivars, but in 7.9% of Chinese and 15.4% of worldwide landraces (Fig. 8c and Supplementary Fig. 17). This suggests that the allelic variation may occur in hexaploid wheat, but it could not be excluded that the variation may occur in the tetraploid progenitor of wheat because there are fewer tetraploid wheat accessions in public genetic variation databases^70,71,72,73. Consequently, the allelic variation may be possibly selected during the breeding of hexaploid wheat cultivars with high yield and suitable height, which is partially associated with that the drought-tolerant QTL qDSI4B.1 in chromosome 4BS is highly linked with the QTLs and genes (e.g., Rht1) governing grain yield and plant height (Supplementary Fig. 3), the major agronomic traits of wheat breeding. Consistent with this, the leading cultivars such as Jimai 22 and Yangmai 18 in China carry the TaWD40-4B.1^T haplotype (Supplementary Data 8). On the other hand, the proportion of TaWD40-4B.1^C is negatively correlated with the annual rainfall, and more accessions carrying TaWD40-4B.1^C have been bred in the districts with less annual rainfall and abundant water resource (Fig. 8d, e). This indicates that the drought-sensitive haplotype appears to be less selected in the districts with more serious water deficiency, and TaWD40-4B.1^C contributes to the drought tolerance of wheat. Given the introgression of TaWD40-4B.1^C enhances wheat drought tolerance and has no trade-offs effect (Fig. 8a, b), the TaWD40-4B.1^T allele is a candidate target for both precise genomic editing and TaWD40-4B.1^C replacement to breed new cultivars and improve leading cultivars with higher water-saving capacity and water use efficiency following the increasing deficiency of water resources. A recent study proved that a WD40 gene KRN2 was convergently selected to improve grain yield via allelic variation in the upstream sequence to reduce expression in maize and rice⁴⁴. And as mentioned above, the syntenic drought tolerance QTL qDT4B.1 are involved in the maize and barley¹³. Thus, the members of the WD40 family may be selected for the improvement of drought and yield-related traits during crop domestication and breeding.

Methods

Phenotyping of drought tolerance for GWAS

The association-mapping panel composed of 198 wheat accessions was used for drought tolerance (Supplementary Data 1). The drought tolerance assay was conducted in a greenhouse under 16-h light/8-h dark and 16 °C/14 °C with a relative humidity of 40%. For each entry, 15 uniform seedlings were planted in a soil-filled plastic cone of 9.0 cm in diameter and 23.5 cm in depth. Each accession had five replicates. All of the accessions were randomly placed according to the completely randomized design. Water was withheld once the seedlings reached the three-leaf stage. The plants were re-watered until approximately 2/3 of entries were wilted when soil water content decreased to 15–20%. Two days after rewatering, a drought wilting score was assigned using a 1–6 scale illustrated in Fig S2, where score 1 represented a completely wilted plant, 2 a plant in which the first three leaves were fully wilted and the fourth was partially wilted, 3 a plant in which the first three leaves were fully wilted, 4 a plant in which the first two leaves were fully wilted and the third leaf was partly wilted, 5 a plant in which the first two leaves were fully wilted and the third not wilted, and 6 a plant in which only the second leaf was partly or hardly wilted. The index of drought tolerance was recorded according to the wilting score as illustrated in Supplementary Fig. 2. The DT index that was extremely deviated from those of the other replicates was considered as the outlier and excluded from the analysis.

Genome-wide association study

All of the 198 accessions were profiled using the wheat 660 K genotyping array by Capital Bio Technology Co. Ltd. (Beijing, China). The polyploid version of the Affymetrix Genotyping Console software (Affymetrix, Santa Clara, CA) was used to conduct SNP allele clustering and genotype calling on the raw SNP data. The physical locations of SNPs were identified based on the IWGSC wheat genome sequence (IWGSC RefSeq v1.0). After filtering SNPs with a missing rate of more than 10% or with a minor allele frequency (MAF) of <5% using the PLINK software⁷⁴, the filtered SNPs were 419,606 retained for GWAS with the whole population¹⁰. Population structure was investigated using the ADMIXTURE software⁷⁵ and evaluating each K from 2 to 5. The stack graphs visualizing the population structure data were generated using the R script. The stack graphs visualizing the population structure data were generated using the R script. Principal components and kinship analysis (PCA) of the population were performed using the software GCTA⁷⁶. Heat maps of kinship were generated based on the K-matrix using the pheatmap R package. The SNP genotypes, Q matrix, and trait scores for 198 accessions were incorporated into a compressed mixed linear model⁷⁷ implemented in the GAPIT R package⁷⁸. The Phenotypic Variance Explanation (PVE) of each SNP and the kinship matrix used in this analysis were also automatically generated by GAPIT. Manhattan plots and quantile–quantile plot (Q–Q plot) were plotted by the qqman package in R script to present the results of association with the individual trait and important P value distributions, respectively. After a Bonferroni-adjusted correction, the P value for the suggestive threshold was set to 2.3832 × 10⁻⁶ (1/419,604). LD and haplotype blocks were constructed using the LDBlockShow software⁷⁹.

Quantitative real-time PCR

The leaves and/or roots of young seedlings with and without treatment of water-withholding, H₂O₂, salt, alkali, and heat as well as the flag leaves, spikes, and grains of plants at the reproductive stage were sampled for RNA extraction. Total RNA was extracted using TRIzol reagent (Invitrogen, now ThermoFisher Scientific) following the supplier’s protocol. Total RNA was treated with DNase I to remove DNA and then used to synthesize the first strand of cDNA using the FastKing RT Kit (Tiangen, https://en.tiangen.com). The single-strand cDNA was used as the template for quantitative real-time (qRT)-PCR based on TransStart® Green qPCR SuperMix (Transgen, AQ101). The gene encoding the β subunit of tubulin (TaTub-β, TraesCS3D02G326900) was used as the reference sequence. The relevant primer sequences are given in Supplementary Data 13.

Vector construction and wheat transformation

The coding sequences of TaWD40-4B.1^C and TaWD40-4B.1^T were amplified with the cDNAs of cv. ShanRong 3 (SR3) and cv. YangMai 20 (YM20) as the template, respectively. To generate the overexpression lines, the coding sequences of TaWD40-4B.1^C and TaWD40-4B.1^T were ligated into the pGA3426 vector driven by the Ubiquitin promoter of Zea mays⁸⁰. To generate the RNAi lines of TaWD40-4B.1, the sense and antisense fragment (532nd−1001st nt) of TaWD40-4B.1 CDS was inserted into the pTCK303 vector driven by the Ubiquitin promoter of Zea mays. To generate the RNAi lines of canonical TaCATs, the sense and antisense fragments covering the conserved CDS regions of TaCAT1s (1070th–1350th nt) and TaCAT3s (430th−724th nt) in series were inserted into vector pTCK303. These constructs were transformed into Agrobacterium tumefaciens strain GV3101, and all of these transformants were transformed into both SR3 and YM20 with the A. tumefaciens–mediated shoot apical meristem transformation method⁸¹. The positively transformed lines were detected via genomic PCR with the total DNA extracted from the leaves as the template. The RNAi lines of TaCATs were crossed with TaWD40-4B.1^C and TaWD40-4B.1^C OE lines to generate TaWD40-4B.1^C OE/TaCATs RNAi lines and TaWD40-4B.1^T OE/TaCATs RNAi lines. The expression of TaCAT1s, TaCAT3s, TaWD40-4B.1^C and TaWD40-4B.1^T were measured with qRT-PCR as mentioned above.

Water-withholding assay, H₂O₂, salt, alkali, heat, and hydroxyurea treatments

Equal weights of dry soils were placed in cuboid plastic pots of 12 cm in width and 10 cm in height. The soils were watered adequately, and fifty seeds were sawed in each pot. The pots were placed in the greenhouse under 16-h light (200 μmol m⁻² s⁻¹)/8-h dark and 22 °C/20 °C with a relative humidity of 40%. When wheat seedlings grew to approximately 5 cm in height, 25 uniformed seedlings were retained, and the other seedlings were removed. After growing in well-watered conditions for 2 weeks, the wheat seedlings were subject to water withholding for a further 14 days. After rewatering for 3 days, the seedlings were phenotyped, and the area and water content of wilted leaves as well as the shoot weight were measured.

The other treatments were conducted using the seedlings raised by hydroponics. Grains were imbibed on moist filter paper at 20 °C for 3 days, and the seedlings were removed to half-strength Hoagland’s liquid medium (pH 6.0) in a greenhouse under 16-h light (200 μmol m⁻² s⁻¹)/8-h dark and 22 °C/20 °C with a relative humidity of 40%, and the medium was replaced every two days to keep fresh. The seedlings at the three- or one-leaf stage were used for phenotyping. For the treatments of H₂O₂, salt, and alkaline salt stress, wheat seedlings at three-leaf stage were transferred to the medium with or without 100 mM H₂O₂, 100 mM NaCl, and 50 mM NaHCO₃ (pH 10) for 7 days. For the treatment of heat stress, wheat seedlings at three-leaf stage were transferred into a growth chamber at 40 °C for 36 h followed by a 2-day recovery under the normal condition. For hydroxyurea treatment, wheat seedlings at one-leaf stage were transferred to medium with or without 1, 2, and 3 mM hydroxyurea (Beyotime, S1961) in a greenhouse under 16-h light (600 μmol m⁻² s⁻¹)/8-h dark and 22 °C/20 °C with a relative humidity of 40% for 5 days. After different periods (0–24 h) of treatment by H₂O₂, salt, alkaline salt, and heat stress, the leaves were sampled at the same time point for extracting RNA to avoid the influence of rhythm on the expression of genes. The seedlings raised in the medium were dehydrated by placing them in the air at room temperature for different periods (0–24 h), and the leaves and roots were sampled for extracting RNA at the same time point.

Expression of TaWD40-4B.1^C/TaWD40-4B.1^T and TaCAT3A in yeast

The vector pESC-HIS (Agilent, USA) was used to express cMyc-tagged TaCAT3A and FLAG-tagged TaWD40-4B.1^C/TaWD40-4B.1^T in yeast (Saccharomyces cerevisiae) strain AH109 MATa (trp1-901, leu2-3, 112, ura3-52, his3-200) under the control of the GAL1 and GAL10 promoters, respectively. The coding sequence of the cMyc epitope EQKLISEEDL was ligated into the multiple cloning sites (MCS) I downstream of the GAL1 promoter, and the open reading frame of TaCAT3A was inserted in front of the epitope sequence of cMyc. Similarly, the coding sequence of the FLAG epitope DYKDDDDK was ligated into the multiple cloning sites (MCS) II downstream of the GAL10 promoter, and the open reading frame of TaWD40-4B.1^C/TaWD40-4B.1^T was inserted in front of the epitope sequence of FLAG. The LiCl-PEG-based transformation and galactose-induced expression of the constructs ligated with cMyc-TaCAT3A alone, FLAG-TaWD40-4B.1^C/FLAG-TaWD40-4B.1^T alone, or cMyc-TaCAT3A and FLAG-TaWD40-4B.1^C/FLAG-TaWD40-4B.1^T were implemented according to the Instruction Manual of pESC Yeast Vectors. The Expression of TaCAT3A and TaWD40-4B.1^C/TaWD40-4B.1^T in yeast cells was detected via the Western-blot method with commercial c-Myc (ABclonal, AE010, 1:5000 (v/v)) and FLAG (ABclonal, AE005, 1:5000 (v/v)) antibodies.

The measurement of catalase activity and growth rate of yeast cells

To determine the effect of TaWD40-4B.1^C and TaWD40-4B.1^T on the activity of TaCAT3A in yeast, the yeast lines expressing cMyc-TaCAT3A and/or FLAG-TaDW40-4B.1^C/FLAG-TaWD40-4B.1^T were harvested. The total proteins of yeast lines were extracted using the One Step Yeast Active Protein Extraction Kit (Sangon Biotech, C500026), and the concentration of proteins was calculated via the Bradford method. Then 1 mg of total protein was used for measuring catalase activity using Catalase (CAT) assay kit (Nanjing Jiancheng Bioengineering Institute, A007-1-1). For the growth rate measurement, the yeast lines expressing the above-mentioned pESC vectors were incubated in liquid YNB-His⁻/Gal 2% medium at 30 °C till OD600 reached 0.1. Then H₂O₂ was added to the liquid medium to the final H₂O₂ concentration of 3 mM. The yeast lines were continued to incubate in the liquid medium with and without H₂O₂, and the OD600 values were recorded hourly. The curved lines based on OD600 values were drafted to mirror the growth rates.

Yeast two-hybridization assay

Yeast two-hybridization assays were performed in strain AH109 using the LiCl-PEG method based on the vectors pGADT7 and pGBKT7 according to the manufacturer’s protocol (Clontech). TaCATs was ligated into pGADT7, and TaWD40-4B.1^C/TaWD40-4B.1^T was ligated into pGBKT7. The pGADT7 and pGBKT7 constructs were co-transformed into AH109. Transformants were selected on the synthetic defined (SD) medium lacking Leu and Trp. Positive colonies were transferred to SD medium lacking Leu, Trp, and His.

Split-luciferase complementation imaging

To compare the interaction of TaCATs and TaWD40-4B.1, the CDS of TaCATs were ligated into the vector JW771 to construct N-terminus luciferase (nLuc)-TaCATs fused ORF, the CDS of TaWD40-4B.1^C/TaWD40-4B.1^T were ligated into the vector JW772 to construct C-terminus luciferase (cLuc)-TaWD40-4B.1^C/TaWD40-4B.1^T ORF, and nLuc-GFP and cLuc-GFP were constructed as the negative control. To analyze the effect of TaWD40-4B.1 on the interaction between TaCATs, nLuc-TaCATs and cLuc-TaCATs were constructed, and CDS of TaWD40-4B.1^C/TaWD40-4B.1^T and GFP were ligated into the vector pRI101-AN. Corresponding constructs were transformed into A. tumefaciens strain EHA105 and the transformants were infiltrated into the leaves of N. benthamiana plants under the condition of 16-h light/8-h dark and 22 °C/20 °C with a relative humidity of 80% for three days. Then, the leaves were incubated with 1 mM Dual-luciferin-free acid (GoldBio, L-123) dissolved in 0.01% (v/v) Triton X-100 and incubated for 5 min in the dark. The fluorescence image was acquired with a CCD camera (Tanon-5200). In this work, to compare the difference in interaction capacity of TaWD40-4B.1^C/TaCATs from TaWD40-4B.1^T/TaCATs, the respective constructs with the same amount were combined in a 1:1 ratio.

Co-immunoprecipitation assay

For the Co-IP assay, A. tumefaciens containing the various constructs were grown to an optical density (OD) of 0.8 and then infiltrated into the leaves of 4-week-old N. benthamiana plants. After 48–60 h of incubation, N. benthamiana leaves infiltrated with A. tumefaciens harboring either p35S::TaCAT-3A-GFP (driven by pRI101-GFPn) or p35S::TaWD40-4B.1^C/T-cMyc (driven by pRI101-cMyc) were harvested, snap-frozen, and ground to a powder. Proteins were extracted from the powdered material in Cell lysis buffer for Western and IP (Beyotime, P0013). Following centrifugation (20,000 × g for 10 min at 4 °C), the supernatant was incubated at 4 °C for 4 h in the presence of monoclonal anti-MYC antibody-conjugated beads (MYC-Trap, Chromotek, ytma-100). The beads were rinsed six times in Cell lysis buffer for Western and IP (Beyotime, P0013). Proteins were eluted from the beads by boiling in SDS-PAGE Sample Loading Buffer (Beyotime, P0015A) for 10 min followed by western blotting using anti-MYC (Abclonal, AE010, 1:5000 (v/v)) or anti-GFP (Abclonal, AE012, 1:5000 (v/v)) antibody.

Protein expression and purification

TaWD40-4B.1^C and TaWD40-4B.1^T were cloned into pET28a to generate TaWD40-4B.1^C-His and TaWD40-4B.1^T-His, while TaCAT3A was cloned into pMAL-C2X to get TaCAT3A-MBP. Escherichia coli strain DE3 was transformed using recombinant plasmids and the vector separately, and cultured at 37 °C in 500 mL LB. When the OD600 reached 0.6, protein expression was induced at 16 °C with 0.8 mM isopropyl β-D-1-thiogalactopyranoside (Beyotime, ST098) for 16 h. Purification of the recombinant proteins was performed following the manufacturer’s instructions.

Pull-down assay and the measurement of in vitro catalase activity

Two mg MBP or four mg MBP-tagged TaCAT3A proteins were immobilized on Amylose resins. Immobilized beads were incubated with 1 mg His-TaWD40-4B.1^C/T in 50 mM KH₂PO₄ (pH 7.4) for 1 h at 4 °C. After centrifugation at 60 × g at 4 °C for 1 min, the supernatant was removed, and the beads were washed six times with pre-cooled 50 mM KH₂PO₄ (pH 7.4). The resin-retained proteins were analyzed by immunoblotting using anti-His (Abclonal, AE003, 1:5000 (v/v)) or anti-MBP antibodies (Abclonal, AE016, 1:5000 (v/v)). To assess the effect of TaWD40-4B.1^C and TaWD40-4B.1^T on TaCAT3A activity, various concentrations of purified TaWD40-4B.1^C or TaWD40-4B.1^T proteins were mixed with TaCAT3A in 50 mM KH₂PO₄ (pH 7.4) for 1 h at 4 °C, and catalase activity was then determined using Catalase (CAT) assay kit (Nanjing Jiancheng Bioengineering Institute, A007-1-1).

TaCAT oligomerization assay based on cross-linked proteins

The SDS-PAGE electrophoresis using cross-linked proteins was implemented to reveal the attendance of oligomerized TaCATs in vivo and in vitro according to the previous report⁸² with slight modifications. Specifically, proteins were extracted from wheat seedlings at 4 °C in 50 mM KH₂PO₄ (pH 7.4) containing 1 mM PMSF (Beyotime, ST505) and 1× Protease inhibitor cocktail (Beyotime, P1005). After elimination of cell debris by centrifugation (12,000 × g) at 4 °C for 10 min, 2 mM dithiobis (succinimidyl propionate) (DSP; Sangon Biotech, C110213) was added to the extract, which was kept at 4 °C with shaking for 30 min. As for the analysis of in vitro oligomerization, the purified TaCAT3A-MBP by prokaryotic expression was mixed with various concentrations of purified TaWD40-4B.1^C or TaWD40-4B.1^T proteins in 50 mM KH₂PO₄ (pH 7.4) for 1 h at 4 °C, and DSP was added to cross-link the oligomeric proteins in the same way. The crosslinker was then quenched with 50 mM Tris buffer (pH 7.6) for 15 min at room temperature. Protein sample buffer containing 5% β-ME (reversal of crosslink) or without reducing agent (no reversal of crosslink) was added, and samples were boiled for 10 min before loading.

Subcellular localization and bimolecular fluorescence complementation (BiFC)

For subcellular localization, pBI221-GFP-TaCATs, pBI221-GFP-TaWD40-4B.1^C and pBI221-GFP-TaWD40-4B.1^T constructs were built, and each of them along with the plastid harboring peroxisome marker DsRed-SKL were introduced into wheat protoplasts by the PEG-mediated transfection⁸³. For BiFC, the coding sequence of TaWD40-4B.1^C/T and TaCATs was introduced into the pUC-SPYCE(MR) and pUC-SPYNE(R)173 vector, respectively⁸⁴, and GUS-YFPC was constructed as the negative control. Corresponding constructs along with the plastid harboring peroxisome marker DsRed-SKL were co-transformed into wheat protoplasts using the same method. Then the protoplasts were incubated in dark at 25 °C for 16–24 h. The confocal images were finally captured using the ZEISS LSM 900 system.

Isolation of intact peroxisomes

The protoplasts co-expressing GFP-tagged proteins and RFP-SKL mentioned above were harvested and peroxisomes were isolated as described⁸⁵ with some modifications. Briefly, 5 × 10⁶ intact peroxisomes were centrifuged at 5,000 × g for 1 min at 4 °C in grinding buffer (170 mM Tricine-KOH, 1 M sucrose, 1% [w/v] BSA, 2 mM EDTA, 5 mM DTT, 10 mM KCl, 1 mM MgCl₂, and 1× protease inhibitor cocktail, pH 7.5) to obtain the crude extract. The supernatant was loaded onto Percoll density gradients prepared in TE buffer (20 mM Tricine-KOH and 1 mM EDTA, pH 7.5)⁸⁵, and centrifuged for 12 min at 13,000 × g followed by centrifugation for 20 min at 27,000 × g. After centrifugation, peroxisomes are located at the bottom of the gradients. Fractions were collected from the top and bottom of the centrifugation tubes and washed in 36% (w/w) sucrose in TE buffer and centrifuged for 30 min at 39,000 × g. The top fraction was labeled as the cytosol and the pellet as the crude peroxisome. Subsequently, the crude peroxisome was loaded onto a sucrose density gradient (2 mL 41% [w/w], 2 mL 44% [w/w], 2 mL 46% [w/w], 3 mL 49% [w/w],1 mL 51% [w/w], 1.5 mL 55% [w/w], and 1 mL 60% [w/w] in TE buffer) and centrifuged at 80,000 × g for 2 h. After centrifugation, a white band appeared at the interface of 55 and 51% sucrose. The white band was collected and labeled peroxisome extract. These fractions were resuspended and boiled in the same volume of 1× SDS-PAGE Sample Loading Buffer (Beyotime, P0015A) and subjected to immunoblot analysis using anti-GFP (Abclonal, AE012, 1:5000 (v/v)) and anti-RFP (Abclonal, AE020, 1:5000 (v/v)) antibodies.

Analysis of MDA and H₂O₂ content, and catalase activity of wheat seedlings

Two-week-old seedlings grown in the soil were subject to water withholding for 1 week. The second leaves of water-withheld and well-watered seedlings were sampled for the following analysis. The relative quantification of H₂O₂ was manifested based on 3,3-diaminobenzidine (DAB) staining. The leaves were stained in 1 mg mL⁻¹ DAB (Coolaber, CD4181) solution in the dark for 12 h. After staining, the leaves were bleached with 85% ethanol in a water bath at 100 °C until chlorophyll completely faded. The leaves were snap-frozen in liquid nitrogen for the measurement of MDA content and in vivo catalase activity using the Lipid Peroxidation MDA Assay Kit (Beyotime, S0131) and Catalase (CAT) assay kit (Nanjing Jiancheng Bioengineering Institute, A007-1-1) according to the suppliers’ protocols.

The yield trail and the measurement of yield-associated traits

Germinated seeds of transgenic lines and non-transgenic controls by placing them at room temperature for 3 days were transferred into plastic pots (10 × 10 × 14 cm) containing an equal weight of soil. One seed was plated in one pot, and each line had twenty pots. Each pot was watered with the same amount of water to maintain the uniformity of soil-relative water content every 2 days until the beginning of jointing. Then, the seedlings were randomly separated into two groups for the parallel water-limited and well-watered treatment. The water-limited treatment was conducted via watering every ten days, while the well-watered treatment was performed by watering every two days. The watering was terminated at the beginning of senesced yellowing. After harvesting, the yield as well as the yield-associated indices including grain size and width, 1000-grain weight, grain number per spike/plant, and plant height were measured. During grain filling, CO₂ assimilation rate and transpiration rate were measured with an LI-6400XT Portable Photosynthesis System (Li-Cor, USA). The water use efficiency was calculated by dividing the CO₂ assimilation rate by the transpiration rate. The grain yield and yield-associated indices were recorded based on 10 seedlings per line, and the CO₂ assimilation rate and transpiration rate had approximately 20 replicates. The field water-saving trial was conducted at Shijiazhuang, China (E114°32′18″, N38°7′10″) from Oct, 2021 to Jun, 2022. In each irrigation field, all lines were planted randomly in blocks of 1.5 m × 9 m, and each line was planted in three blocks. Two irrigation treatments were conducted, one was that no water was irrigated during the whole life course, and the other was that 750 m³ ha⁻¹ water was irrigated at the sowing and reviving stages respectively (in total 1500 m³ ha⁻¹). The spike density was measured at the filling stage, and the grain yield and other indices were measured after harvesting.

Construction of near-isogenic lines

Drought-tolerant cultivar Luyuan 301 carrying the TaWD40-4B.1^C allele and drought-sensitive cultivar Chuanmai 36 carrying the TaWD40-4B.1^T allele were crossed each other to obtain F1 seeds. Then Luyuan 301 and Chuanmai 36 were used as recurrent parents to construct their near-isogenic lines (NILs) carrying TaWD40-4B.1^T and TaWD40-4B.1^C alleles, respectively. TaWD40-4B.1 was genotyped in each successive generation, and the heterozygous hybrids were backcrossed to create the BC5F1 population. Premature egg cells of BC5F1 populations were fertilized with maize pollen to construct haploid seedlings, which were used to construct double haploids by chromosome doubling. The near-isogenic lines of Luyuan 301 and Chuanmai 36 carrying TaWD40-4B.1^T and TaWD40-4B.1^C alleles, respectively, were genotyped from double haploids. The drought tolerances of NILs were detected by the water withholding assay as mentioned above.

Geographical distribution of wheat varieties

For the geographical distribution of wheat varieties, 1912 varieties were projected on the map according to their origin information^{55,56,57,58,86}, among which 600 were from China. The haplotypes of 600 varieties from China were confirmed via Sanger sequencing. The haplotypes of the other 1312 varieties were referred to the previous studies^55,56,57,58 that are integrated in SnpHub⁸⁷, and the haplotypes of 57 were confirmed via Sanger sequencing. The average annual rainfall (1973–2019) of provinces/autonomous regions of China were calculated according to the data provided by the National Centers for Environmental Information (https://www.ncei.noaa.gov/). Pearson correlation analysis was used to evaluate the association between TaWD40-4B.1^T allele frequency with average annual rainfall based on 583 wheat varieties from 16 provinces/cities of China.

Domain and 3D structure prediction and the phylogenetic analysis

The domain of TaWD40-4B.1^C/TaWD40-4B.1^T and the paralogs were analyzed with SMART (https://smart.embl-heidelberg.de/). Three-dimensional structures of TaWD40-4B.1^C and TaWD40-4B.1^T were predicted with SWISS-MODEL (https://swissmodel.expasy.org/). The peptide sequences of TaCATs were aligned in ClusterX2, and the phylogenetic tree was drafted with MEGA7.0.

Statistics and reproducibility

The normal distribution of the data was measured with the Shapiro–Wilk test. The difference among the data coinciding with normal distribution was conducted with a two-sided z-test, two-sample dependent two-sided t test, two-sample independent two-sided t test, or one-way ANOVA test. The post hoc comparison of one-way ANOVA was conducted with the Tukey method at a significance level of 0.05. The correlation between the proportion of TaWD40-4B.1^T and annual rainfall was conducted with the Pearson analysis. All experiments were repeated independently three times.

Reporting summary

Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.

Data availability

Data supporting the findings of this work are available within the paper and its Supplementary Information files. A reporting summary for this article is available as a Supplementary Information file. Source data are provided with this paper.

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Acknowledgements

We are grateful to Dr. Changle Ma from Shandong Normal University for presenting the plastid of peroxisome marker DsRed-SKL and Dr. Tongjin Zhao from Fudan University for the critical advice on this work. The work was supported by the National Key Research and Development Program (2022YFF1001600 to M.W.), the Key Project of Natural Science Foundation of Shandong (ZR202105200003 to M.W.), the National Natural Science Foundation of China (31870242 and 32170297 to M.W. and 31720103910 to G.X.), and the National Transgene Project (2020ZX08009-11B to M.W.).

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Authors and Affiliations

The Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, 266237, Qingdao, Shandong, P. R. China
Geng Tian, Shuwei Liu, Guangmin Xia & Mengcheng Wang
Institute of Vegetable Research, Shandong Academy of Agricultural Sciences, 250100, Jinan, Shandong, P. R. China
Shubin Wang
State Key Laboratory of Crop Stress Biology for Arid Areas, College of Agronomy, Northwest A&F University, 712100, Yangling, Shaanxi, P. R. China
Jianhui Wu & Dejun Han
Shijiazhuang Academy of Agriculture and Forestry Sciences, 050050, Shijiazhuang, Hebei, P. R. China
Yanxia Wang & Xiutang Wang

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Geng Tian
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Shubin Wang
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Jianhui Wu
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Yanxia Wang
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Xiutang Wang
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Shuwei Liu
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Dejun Han
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Guangmin Xia
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Mengcheng Wang
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Contributions

G.X. and M.W. conceived the work. G.T., S.W., M.W., Y.W., X.W., J.W., S.L., and D.H. conducted the experiment and analyzed the data. M.W., G.X., and G.T. wrote the paper. All authors read the manuscript.

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Correspondence to Guangmin Xia or Mengcheng Wang.

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Nature Communications thanks Ahmad Alqudah, Christine Foyer, Wen-Cheng Liu, and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.

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Tian, G., Wang, S., Wu, J. et al. Allelic variation of TaWD40-4B.1 contributes to drought tolerance by modulating catalase activity in wheat. Nat Commun 14, 1200 (2023). https://doi.org/10.1038/s41467-023-36901-6

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Received: 18 July 2022
Accepted: 22 February 2023
Published: 02 March 2023
DOI: https://doi.org/10.1038/s41467-023-36901-6

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