Identification of a candidate dwarfing gene in Pallas, the first commercial barley cultivar generated through mutational breeding

Many induced mutants are available in barley (Hordeum vulgare L.). One of the largest groups of induced mutants is the Erectoides (ert) mutants, which is characterized by a compact and upright spike and a shortened culm. One isolated mutant, ert-k.32, generated by X-ray treatment and registered in 1958 under the named “Pallas”, was the first ever induced barley mutant to be released on the market. Its value was improved culm strength and enhanced lodging resistance. In this study, we aimed to identify the casual gene of the ert-k.32 mutant by whole genome sequencing of allelic ert-k mutants. The suggested Ert-k candidate gene, HORVU.MOREX.r3.6HG0574880, is located in the centromeric region of chromosome 6H. The gene product is an alpha/beta hydrolase with a catalytic triad in the active site composed of Ser-167, His-261 and Asp-232. In comparison to proteins derived from the Arabidopsis genome, ErtK is most similar to a thioesterase with de-S-acylation activity. This suggests that ErtK catalyzes post-translational modifications by removing fatty acids that are covalently attached to cysteine residues of target proteins involved in regulation of plant architecture and important commercial traits such as culm stability and lodging resistance.


Introduction
Barley (Hordeum vulgare L.) has a long history as crop plant and was domesticated about 10,000 years ago from its wild progenitor Hordeum vulgare ssp. spontaneum. This is based on archaeological findings from the Middle East, the area known as the fertile crescent (Badr et al., 2000;Mascher et al., 2016;Mascher et al., 2017). Barley is grown worldwide with a total production of around 150 million tons per annum (www.fao.org). Also barley breeding has a long history. Mutation breeding in barley was introduced shortly after the discovery that ionized irradiation could increase mutation frequencies in the fruit fly Drosophila melanogaster (Muller, 1927;Muller, 1928). First, the barley cultivars Gull and Danish Maja were used. However, the cultivar Bonus, which was known for its very high tillering capability and extremely high yield, soon became a favorite for mutation research (Gustafsson et al., 1971). Initially, chlorophyll mutants were used to optimize irradiation dosage and duration of irradiation. Chlorophyll mutants were useful since they have obvious visual phenotypes already at the seedling stage of the M 2 generation as, for example, yellow and white plants (Gustafsson, 1940). Due to the lack of chlorophyll, the chlorophyll mutations were lethal and the homozygous mutants died at the seedling stage. However, it was soon discovered that also viable mutations could be obtained, which were possible to have in homozygous form. The most common group was the so-called Erectoides (ert) mutants, which are characterized by an erect, compact and dense spike, and a straw that is often short and stiff (Lundqvist, 1992). Crosses were performed between different ert mutants that grouped 225 mutants to 31 different loci (Supplemented Table 1). The ert mutants were isolated during a time when agricultural practices were largely changed. A major difference was the use of fertilizers that greatly increased the yield of crops as fertilizers promote plant growth. However, the culms were not strong enough to hold the heavy spikes and as a result plants fell over. Therefore, introduction of stiff and short-culm mutant alleles in the breeding material was very important (Dockter and Hansson, 2015). An increased interest for lodging resistance has put many historic mutants with sturdy and shorter culms in focus since they represent valuable resources for plant breeding. Today, marker assistant breeding is widely used in breeding programs since a large number of traits can be followed in many individual plants. In addition, marker screening can be automated with robotic systems. Our goal is to identify mutated genes and the exact genetic identity of the mutant alleles since that will make them available for marker assistant breeding.
Mutant ert-k.32 was induced by X-ray in Bonus in 1947. This mutant, together with ert-a.23 (X-ray in Bonus 1944) and ert-a.28 (X-ray and FeSO 4 in Bonus 1944), was subjected to field trials and all three mutants showed increased lodging resistance in comparison to Bonus. Mutant ert-k.32 had superior stem stability and was accepted as a new cultivar in 1958 under the name Pallas. This was the first example of an induced barley mutant that was released as a commercial cultivar. Since then, plant breeders have used Pallas in crosses to develop other cultivars. For example, Pallas was crossed to Herta, which resulted in the cultivar Hellas (Gustafsson et al., 1971). Visir is another cultivar developed from Pallas through a cross with a "Long glume" barley landrace which improved resistance to powdery mildew (Gustafsson et al., 1971).
Today, short stem architecture in elite malting barley is often derived from a deficiency in the gibberellic acid hormone pathway with sdw1 alleles of the gibberellin 20-oxidase gene (HvGA20ox2) dominating in many barley breeding programs (Dockter and Hansson, 2015;Xu et al., 2017). However, breeders are looking for other genetic possibilities to provide lodging resistance and ert-k.32 could be an interesting alternative. In this work, we have identified a candidate gene, which we suggest is the Ert-k gene. We also describe the likely ert-k.32 mutation responsible for the Pallas phenotype. The finding will facilitate the use of this allele for efficient marker-assisted breeding and testing in today's elite germplasm. The Ert-k candidate gene encodes an alpha/beta-hydrolase, which has previously not been associated with changes in plant architecture.

Plant material and growth conditions
In this study, we used 14 barley spring cultivars (Supplementary  Table S2) and eight historic ert-k mutant lines (Supplementary Table  S3) obtained from the Nordic Genetic Resource Center (NordGen), Alnarp, Sweden (www.nordgen.org). These lines and F 1 plants obtained from allelism crosses were grown in greenhouses at the Department of Biology, Lund University, Sweden. Plants were grown in soil with article number 744704 from SW Horto (www. swhorto.se) in 5-L pots. Greenhouse conditions were set to 16-h light/8-h dark cycles and temperature 20°C during the day and 16°C during the night. All statistical data presented for phenotypic traits are based on measurement of 6-11 plants of each line.

General DNA methods
Genomic DNA for PCR reactions was extracted from fresh leaves using the REDExtract-N-AmpTM Plant PCR Kit (Sigma-Aldrich, St. Louis, MO, USA) according to the manufacturer's instructions. Sanger sequencing were performed by Eurofins Genomics, Germany. Used primers are shown in Supplementary Table S4. PCR were performed by initial denaturation at 94°C/3 min, followed by 35 cycles of 94°C/45 s, 56°C-62°C/45 s and 72°C/60-90 s, with a final extension step of 72°C/10 min.
Found mutations were confirmed by Sanger sequencing of at least two independent reactions.

RNA isolation and RT-PCR
In order to analyze whether the eight ert-k mutants are transcription deficient for the Ert-k candidate gene, RT-PCR (not qRT-PCR) was performed. Plants were grown in soil and 100 mg material from a single leaf was harvested and immediately frozen in liquid nitrogen. Porcelain mortar was used to homogenize leaf material under liquid nitrogen. Total RNA was isolated using Trizol reagent (Invitrogen Carlsbad, CA, USA) according to the manufacturer's instructions. Residual DNA was removed by DNAse I treatment (Thermo Fisher Scientific, USA). A 500 ng of total RNA was converted to single-stranded cDNA by using RevertAid First Strand cDNA synthesis kit (Thermo Fisher Scientific, USA) primed with (dT)15 in a 20 µL reaction volume (Stuart et al., 2021). Primers were designed to amplify a 1006 bp cDNA fragment. (Supplementary Table S4).

Allelism tests
The ert-k.32 mutant was used as male in each cross. Mutants ertk.76, and their mother cultivars Bonus and Foma were used as female. Pollination was performed 3 days after emasculation. F 1 plants were phenotyped and genotyped. For genotyping, specific primers were designed that could Frontiers in Genetics frontiersin.org 02 amplify either the wild type allele or the mutant allele (Supplementary  Table S4). 6-11 F 1 plants of each cross were evaluated. The statistical analyses were based on comparisons between a mutant and its mother cultivar, or comparisons between a mutant crossed to ert-k.32 and its mother cultivar crossed to ert-k.32.

Whole genome sequencing and data analysis
Genomic DNA for whole genome sequencing was extracted by a modified CTAB protocol (Doyle, 1991) as described in (Stuart et al., 2021). Genomic DNA was sent to the Earlham Institute (Norwich, UK, www.earlham.ac.uk) where DNA libraries were prepared and where DNA sequencing was performed on an Illumina HiSeq4000. 150 bp paired-end reads were obtained.
BWA mem (version 0.7.17) was used to align reads to the barley MorexV3 reference genome (Li and Durbin, 2010;Mascher et al., 2021). Samtools fixmate (samtools version 1.10) was used to fill in mate coordinates. Aligned reads were further processed to remove PCR duplicates by running Samtools markdup (Li et al., 2009). To get vcf files, bcftools mpileup (bcftools version 1.17) was used with the following filtering options: q 60 -Q 30 -D (where -q is mapping quality for the alignment, -Q is minimum base quality, -D is instruction to run the BAQ algorithm not only in problematic regions, but on all reads) (Li, 2011). To identify alleles observed in a mutant sample and not found in the control (mother cultivars Bonus or Foma), bcftools in combination with the "contrast" plugin was used. Bcftools view was used to exclude sites with heterozygous genotypes (-g^het), and to exclude sites with the reference genotype (-e 'GT = "ref"'). Functional annotation of variants was performed with Ensembl Variant Effect Predictor (McLaren et al., 2016).

Results
Genomic sequencing of ert-k mutants to identify an Ert-k candidate gene The Ert-k locus is represented by eight different alleles (Franckowiak and Lundqvist, 2012), which have been generated through treatment by X-rays, gamma-rays, neutrons and ethyl methanesulfonate of the cultivars Bonus and Foma (Supplementary Table S3). Early mapping experiments demonstrated that Ert-k is located on chromosome 6H (https:// bgs.nordgen.org/). More recently, mutant ert-k.32 was backcrossed to the cultivar Bowman to create a near-isogenic line; BW314. By genotyping BW314 with 3,072 single nucleotide polymorphisms markers (SNPs), the introgression region was defined by 14 SNP markers spanning 22.3 cM ( Figure 1) (Druka et al., 2011).
In our previous research, we further fine mapped the Ert-k locus by using three mapping populations; one double-haploid population derived from BW314 (ert-k.32) crossed to cultivar Quench, and F 2mapping populations derived from crosses of BW314 to Bowman and Quench. The analysis confirmed the centromeric location of Ert-k on barley chromosome 6H and mapped Ert-k to a 15.7 cM region between markers 2_0291 and 1_0040 (Skov Kristensen et al., 2016). With help of the barley reference genome sequence (Mascher et al., 2021), it is now possible to translate the genetic map to the physical map. The distance between 2_0291 and 1_0040 is more than 400 Mbp comprising 73% of chromosome 6H (Figure 1). There are 1,986 high-confident genes between markers 2_0291 and 1_0040. Since recombination events are less frequent in centromeric regions, fine mapping is problematic. We therefore decided to search for the Ert-k gene by whole genome sequencing of allelic ert-k mutants. Among the eight ert-k mutants, we selected the five mutants which had been induced by X-rays, gamma rays and ethyl methanesulfonate (Supplementary Table S3). In total, severe homozygous mutations were found in seven genes on chromosome 6H of the five mutants compared to their respective mother cultivar (Table 1). These mutations are likely to be caused by the mutagenic showing the introgression region between markers 1_029 and 1_ 0040, linked to ert-k.32 according to (Druka et al., 2011). The mapping was further improved by (Skov Kristensen et al., 2016) (marked in black). Ert-k candidate gene HORVU.MOREX.r3.6HG0574880 is located at position 161752829-161757701 Mbp in the physical map. Positions in Mbp are according to version 3 of the barley cultivar Morex (Mascher et al., 2021). Genetic position of SNPs is according to IBSC (2012) and name of SNP markers is according to (Close et al., 2009).
Frontiers in Genetics frontiersin.org 03 treatment and cause frameshifts or missense mutations changing amino-acid residues in their respective protein.
Since the ert-k mutants are supposed to be allelic, we especially looked for genes where all five mutants would have a mutation. Such gene was not found. However, the gene HORVU.MOREX.r3.6HG0574880 got our attention since this gene was mutated in the coding region of three of the five analyzed mutants (Table 1). The gene encodes an alpha/beta hydrolase of 399 amino-acid residues, has 6 exons and contains a fermentation-respiration switch protein FrsA domain ( Figure 2). Sanger sequencing of HORVU.MOREX.r3.6HG0574880 in all eight available ert-k mutants revealed an identical 4-bp deletion in exon 3 in both mutant ert-k.32 and ert-k.76, and a one-bp insertion in exon 5 in ert-k.309. In ert-k.32 and ert-k.76, the 4-bp deletion causes a truncated protein of 193 native amino-acid residues followed by an alanine residue. In ert-k.309, the one-bp insertion in exon 5 causes a frameshift. The truncated protein has 333 native amino-acid residues followed by glutamine and arginine ( Figure 2). No mutations in HORVU.MOREX.r3.6HG0574880 were found in ert-k.93, ert-k.302, ert-k.435, ert-k.459 or ert-k.477. We therefore analyzed whether we could detect any mRNA of the candidate gene in the eight mutants. mRNA was detected by RT-PCR in all ert-k mutants, which suggested that the mutants are not transcript deficient ( Figure 3). Since genomic DNA sequence information was available for ert-k.435 and ert-k.477, we looked for mutations in the intergenic regions in the vicinity of the candidate gene. In ertk.477, we found a "C/T" SNP variation at position 6H:161619756. The mutation was confirmed by Sanger sequencing. The SNP is 133,213 bp upstream from the start codon of HORVU.MOREX.r3.6HG0574880. Three genes are located between the SNP and HORVU.MOREX.r3.6HG0574880, namely, HORVU.MOREX.r3.6HG0574850, HORVU.MOREX.r3.6HG0574860 and HORVU.MOREX.r3.6HG0574870. It is known that enhancers can be located hundreds of thousands base pairs away from the target gene and do not necessarily operate on the closest promoter (Pennacchio et al., 2013).

Diallelic crosses to identify allelic ert-k mutants
In order to analyze if the eight ert-k mutants are truly allelic, we crossed ert-k.32 with the other seven ert-k mutants or with cultivars Bonus and Foma. Mutant ert-k.32 was used as father in the crosses and the success of the crosses was verified by the heterozygous presence of the ert-k.32 allele in the resulting F 1 plants. If two recessive mutants are deficient in the same gene, i.e., truly allelic, the F 1 generation will show the mutant phenotype. In contrast, if the two recessive mutants are deficient in two different genes, a wild-type phenotype is expected in F 1 plants. F 1 seeds were planted in the greenhouse together with Bonus, Foma and each of the eight ert-k mutants. The plants were phenotyped by visual inspection (Figure 4) and spike length and the length between rachis internodes 5 and 15 were measured ( Table 2). The allelism test suggested that mutants ert-k.93 and ert-k.302 might be non-allelic to ert-k.32, which would explain why no mutations in HORVU.MOREX.r3.6HG0574880 were found in these two mutants. Also ert-k.435 and ert-k.459 showed no mutations in this gene although the obtained F 1 plants displayed a mutant phenotype. Since we have no genome sequence data of ert-k.459, we could not analyze this mutant for intergenic SNP variation. In our previous work with barley mutants, we used to identify approximately 75% of the mutations in historic accessions that are supposed to be allelic (Zakhrabekova et al., 2012;Zakhrabekova et al., 2015;Matyszczak et al., 2020). Because the ert-k phenotype is similar to other ert phenotypes, we sequenced all ert-k mutants for the miRNA172 binding site of Ert-r (APETALA2)  (Houston et al., 2013). The reason why we sequenced only the miRNA172 binding site of Ert-r is that it is known that only mutations within this domain are causing a dwarf phenotype (Houston et al., 2013). No mutations were found (not shown).
Genotyping suggests that ert-k.32 and ertk.76 have different origin Mutants ert-k.32 and ert-k.76 were found to have the same 4-bp deletion, which was unexpected since the mutagenic process is random and they were induced with different mutagens and were isolated in different years (Supplementary Table S3). To rule out whether the two mutant lines have been mixed up over the years or if they represent two identical mutations generated independently of each other, we analyzed the SNP variation in a 40 Mbp region around the suggested Ert-k candidate gene HORVU.MOREX.r3.6HG0574880. Due to the tight linkage in the centromeric region around this gene, it is very likely that existing homozygous SNPs are inherited together. The presence of identical SNPs around the mutation would indicate a common origin of the mutants, i.e., seeds had been mixed up over the years. In contrast, the presence of unique SNPs would indicate that the two mutants are the results of two independent mutagenic events. In ert-k.32 and ert-k.76 we identified 17 and 12 SNPs, respectively, within the 40 Mbp region. Six of these were present in both mutants, whereas the remaining 11 and 6 SNPs were unique to each mutant ( Figure 5). The six common SNPs probably reflect differences between the Bonus line used for mutagenesis in 1947 and 1955 that generated ert-k.32 and ert-k.76, respectively, and the Bonus accession we sequenced in this experiment. The unique SNPs were likely obtained through the mutagenic treatment. In order to investigate whether the 4-bp deletion was a result of the mutagenic treatment or was already present in an "ancient" Bonus line, we sequenced the site of the 4-bp deletion from all Bonus accessions available at the Nordic Genetic Stock Center (www.nordgen.org) and the cultivars Gull, Opal Abed, Maja Abed, Binder Abed, Guld Svalöf, Seger and Hanna, which are in the pedigree of Bonus. None of the listed cultivars showed the 4-bp deletion, which supports that the deletion is a result of the mutagenic treatment.

Analysis of Pallas accessions and Pallas derived cultivars
Since Pallas was used in plant breeding shortly after it was released as a cultivar, we analyzed cultivars with Pallas in their pedigree and four accessions of Pallas that are available at the Nordic Genetic Stock Center (www.nordgen.org) (Supplementary Table S5). The 4-bp deletion seen in ert-k.32 and ert-k.76 was found in all cultivars except Jenny, which in addition did not show the characteristic compact spike phenotype of Pallas ( Figure 6). The fact that all four Pallas accessions and the cultivars Hellas, Senat and Visir contained the 4-bp deletion further supports that HORVU.MOREX.r3.6HG0574880 is the Ert-k gene.

Identification of a catalytic triad
Alpha/beta hydrolases are characterized by an active site composed of a catalytic triad of three involved amino-acid residues. Typically, a serine residue plays the role of a nucleophile in the reaction. The serine is activated by a catalytic base and a catalytic acid, which are typically a histidine and aspartate residue, respectively. To analyze if the ErtK candidate has a catalytic triad and to identify the involved residues, we performed an alignment of the ErtK candidate with several alpha/beta hydrolases with published protein structures (Mindrebo et al., 2016) (Figure 7). The alignment suggested that Ser-167, His-261 and D-232 are the essential aminoacid residues for the activity of the suggested ErtK hydrolase (Figure 7). The 4-bp deletion in ert-k.32 and ert-k.76 is located before the codon corresponding to His-261 and D-232, whereas the 1-bp insertion in ert-k.309 is located after.

Discussion
Genetic validation of genes and genomic regions associated with target traits for crop improvement is possible today thanks to recent advancements in genomic studies of cereals and other crop plants. Frontiers in Genetics frontiersin.org 05

FIGURE 3
RT-PCR analysis of HORVU.MOREX.r3.6HG0574880, suggested to be Ert-k. The gene can be amplified in all ert-k mutants and their mother cultivars.

FIGURE 4
Spike phenotypes of ert-k mutants, their mother cultivars Bonus and Foma, and F 1 plants from crosses. Scale bar 5 cm.

Frontiers in Genetics frontiersin.org 06
The game changer in barley research came in 2017 when the barley reference genome was published (Mascher et al., 2017). The aim of the current study was to identify and validate the genetic cause of the ert-k.32 mutation present in the cultivar Pallas, which was the first induced mutant to be released as a commercial barley cultivar on the market (in 1958). Pallas was known for its superior stem stability and increased lodging resistance. The reason to include semi-dwarf traits in plant breeding is to protect the plants against lodging under high nitrogenous fertilizer regimes. However, mutations providing a shorter and more sturdy plant architecture often have pleotropic effects, which affects other traits such as heading day (Kuczyńska et al., 2013) and malt quality (Hellewell et al., 2000). Therefore, mutations giving a mild short-culm phenotype have been favored by plant breeders over mutations giving a stronger phenotype (Vu et al.,TABLE 2 Phenotypic characters of F 1 plants obtained from crosses. The data is based on 6-11 plants of each line. The awns were not included in the spike length. The rachis internode length is the length between rachis node 5 and 15 as counted from the base of the spike. The p-values are based on comparisons between a mutant and its mother cultivar, or comparisons between a mutant crossed to ert-k.32 and its mother cultivar crossed to ert-k.32.

FIGURE 5
Location of homozygous SNPs in mutants ert-k.32 and ert-k.76 on chromosome 6H between Mbp 135 and 175. Black, SNPs common to ert-k.32 and ert-k.76; green, SNPs unique to ert-k.32; blue, SNPs unique to ert-k.76; red, the location of the 4-bp mutation at bp 161,755,966-161,755,969. Frontiers in Genetics frontiersin.org 07 2010; Dockter and Hansson, 2015). In certain barley types, breeders introgressed loss-of-function alleles of the semi-dwarfing gene Sdw1 (Dockter and Hansson, 2015;Xu et al., 2017). Other alleles, such as uzu1.a and ari-e.GP, are less widespread. The uzu1. a allele is a mutation in the brassinosteroid receptor and selected in East Asian cultivars (Chono et al., 2003;Dockter et al., 2014). The Scottish malting cultivar Golden Promise contains the ari-e.GP mutation, which is a one-bp insertion in the gene encoding the alpha-subunit of a heterotrimeric G protein, and the semi-dwarfing allele of HvAPETALA2 called Zeo2 (Houston et al., 2013;Braumann et al., 2018). In comparison, mutations in Ert-k are relatively mild and we therefore believe that ert-k mutant alleles would be good alternatives to sdw1 and other alleles to provide lodging resistance also in modern barley lines. Since the ert-k mutant phenotype is less obvious to recognize without training, the genetic validation of the Ert-k gene and the ert-k.32 allele is important to provide genetic markers that can be followed in breeding programs rather than tracking ert-k mutant alleles by phenotyping. We validated that the 4-bp deletion in HORVU.MOREX.r3.6HG0574880 of ert-k.32 was not present in any analyzed Bonus cultivar or any cultivar included in the pedigree of Bonus. Therefore, we suggest the 4-bp deletion to be the genetic deficiency responsible for the stem stability and increased lodging resistance of ert-k.32, Pallas, Hellas, Senat and Visir, which are carrying the mutation.
The suggested Ert-k gene (HORVU.MOREX.r3.6HG0574880) encodes a protein of the alpha/beta-hydrolase superfamily. Alpha/ beta-hydrolases have a broad range of functions. For example, they play important roles in primary and secondary metabolism as peptidases, lipases, peroxidases, esterases, thioesterases and dehalogenases (Ollis et al., 1992;Nardini and Dijkstra, 1999;Mindrebo et al., 2016;Dimitriou et al., 2017). Although the primary structure of alpha/beta-hydrolases differ significantly, the superfamily possesses a very conserved three-dimensional core structure. The core fold of alpha/beta-hydrolases is made by a beta-sheet, which consists of eight beta-strands and is surrounded by alpha-helices. The acid-base-nucleophile catalytic triad of alpha/beta hydrolases represent the most conserved elements of the alpha/beta hydrolase fold (Ollis et al., 1992;Mindrebo et al., 2016;Denesyuk et al., 2020). We identified Ser-167, His-261 and Asp-232 as the likely amino-acid residues to be involved in the catalytic triad. Interestingly, the fold of alpha/beta-hydrolases is also found in the major structure of phytohormone and ligand receptors of the gibberellin, karrikin and strigolactone signaling pathways in plants (Hotelier et al., 2004;Ueguchi-Tanaka et al., 2005;Ueguchi-Tanaka et al., 2007;Hamiaux et al., 2012;Waters et al., 2015). The receptors do not have the catalytic activity of a classic alpha/beta hydrolase. It was reported that loss-of-function mutations in the gibberellin receptor encoded by GID1, which is known to have the fold of an alpha/beta-hydrolase, produces a dwarf phenotype (Ueguchi-Tanaka et al., 2005). The gibberellin receptor lacks the histidine residue of the canonical catalytic triad and therefore does not have catalytic activity (Mindrebo et al., 2016). The finding of a complete catalytic triad in ErtK suggests that we have identified an enzymatically active alpha/beta hydrolase, which affects plant architecture. A search for proteins similar to ErtK in The Arabidopsis Information Resource (TAIR) database revealed AT3G01690 as the most similar protein (62% identical aminoacid residues). This protein is an Alpha/Beta Hydrolase Domaincontaining Protein 17-like acyl protein thioesterase (ABAPT), which functions as a de-S-acylation enzyme (Liu et al., 2021). A cyclic S-acylation and de-S-acylation is an important posttranslational modification of proteins in eukaryotes. In the S-acylation process, a fatty acid such as palmitate is covalently attached to a cysteine residue in the target protein via a thioester bond (Zaballa and van der Goot, 2018). The modification controls the localization and function of the target protein in the cell under Spike phenotype of cultivars with Pallas in their pedigree. Scale bar 5 cm.
Frontiers in Genetics frontiersin.org 08 different conditions (Lanyon-Hogg et al., 2017). The S-acylation is a reversible biochemical process that is mediated oppositely by S-acyltransferases and de-S-acylation enzymes. We believe that we have identified a gene putatively encoding a de-S-acylation protein with thioesterase activity that has a mild regulatory effect on plant architecture that we suggest is of relevance for plant breeding. In order to further understand the function of the suggested Ert-k candidate gene product, the target protein needs to be identified. It is possible that such protein is associated with the signaling or metabolism of the classic plant hormones regulating plant architecture such as culm length or inflorescence density.

Conclusion
In the present study, we have analyzed the genetic deficiency of Pallas (ert-k.32), which was the first induced barley mutant to be released on the market as a commercial cultivar. We suggest that the dwarf phenotype of Pallas is caused by a 4-bp deletion in the gene HORVU.MOREX.r3.6HG0574880, which encodes an alpha/betahydrolase. The identified gene can be used in marker assistant breeding for cultivars with improved lodging resistance based on the identified Ert-k candidate gene.

Author contributions
SZ and MH designed experiment. SZ, PE, KW, OS, AI, CD, MJ, and MH performed the research. SZ, QL, and PC analyzed data. SZ

Frontiers in Genetics
frontiersin.org and MH wrote the manuscript. All authors contributed to the article and approved the submitted version.

Funding
The study was supported by the Swedish Research Council (VR 2018(VR -05117, 2022, the Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning (FORMAS 2018-01026), the Erik Philip-Sörensen Foundation, the Royal Physiographic Society in Lund, the Swedish Institute Visby Programme 25896/2018, and GUDP under the Danish Ministry of Food. Agriculture and Fisheries.

Conflict of interest
Author PE is currently employed by Cirkulär AB. Authors CD, QL, MJ were employed by the Carlsberg Research Laboratory within the Carlsberg Group.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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