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Wild diploid wheat Aegilops tauschii, the D-genome progenitor of common wheat, carries large genetic variation in spikelet and grain morphology. Two differentiated subspecies of Ae. tauschii, subspecies tauschii and strangulata, have been traditionally defined based on differences in spikelet morphology. Here, we first assessed six spikelet shape-related traits among 199 Ae. tauschii accessions, and found that the accessions belonging to TauL1major lineage produced significantly longer spikes, higher spikelet density, and shorter, narrower spikelets than another major lineage, TauL2, in which the strangulata accessions are included. Next, we performed quantitative trait locus (QTL) analysis of the spikelet and grain shape using three mapping populations derived from interlineage crosses between TauL1 and TauL2 to identify the genetic loci for the morphological variations of the spikelet and grain shape in Ae. tauschii. Three major QTL regions for the examined traits were detected on chromosomes 3D, 4D and 7D. The 3D and 4D QTL regions for several spikelet shape-related traits were conserved in the three mapping populations, which indicated that the 3D and 4D QTLs contribute to divergence of the two major lineages. The 7D QTLs were found only in a mapping population from a cross of the two subspecies, suggesting that these 7D QTLs may be closely related to subspecies differentiation in Ae. tauschii. Thus, QTL analysis for spikelet and grain morphology may provide useful information to elucidate the evolutionary processes of intraspecific differentiation.
Aegilops tauschii Coss. (formerly called Ae. squarrosa L.), the D-genome progenitor of common wheat, is a wild diploid wheat relative with a wide distribution range from northern Syria and southeastern Turkey to western China [1,2]. The genome of Aegilops tauschii was brought into common wheat through interspecific crossing to tetraploid emmer wheat and subsequent amphidiploidization about 8,000 years ago . This evolutionary process can be artificially reproduced by generation of synthetic wheat hexaploids, obtained through interspecific triploid hybrids from crosses between cultivated tetraploid wheat and Ae. tauschii [4,5]. Therefore, Ae. tauschii is an useful genetic resource for wheat breeding to transmit phenotypic variation to common wheat through synthetic wheat hexaploids [6–9].
Ae. tauschii populations provide large natural variation in spikelet and floral morphological traits as well as flowering time [2,10–12]. Two subspecies, Ae. tauschii Coss. subspecies tauschii and Ae. tauschii Coss. subspecies strangulata (Eig) Tzvel., have been recognized in Ae. tauschii based on spikelet morphology [13,14], whereas the two typical forms of subspecies tauschii and strangulata are connected by a continuous range of intermediate forms . Some reports indicated difficulty in distinguishing the two subspecies, suggesting a high level of gene flow between the subspecies [16–18]. On the other hand, subspecies divergence was observed using the sensu-stricto criteria for subspecies strangulata in the classification [10,11]. For the sensu-stricto classification, the subspecies was defined based on classical reports [13,14]; accessions of subspecies tauschii have elongated cylindrical spikelets, whereas subspecies strangulata is characterized by quadrate spikelets. Moreover, natural variation in spikelet-related traits of Ae. tauschii shows significant longitudinal and latitudinal clines for spikelet size, with spikelets tending to be small in eastern and southern regions [10,11]. Overall, spikelet morphology is the key characteristic not only for differentiation of the two subspecies but also for intraspecific diversification in Ae. tauschii, although the genetic basis of spikelet shape divergence has not yet been analyzed.
Recent Bayesian population structure analyses with genome-wide marker genotyping showed that Ae. tauschii could be divided into two major genealogical lineages, tauschii lineage 1 (TauL1) and TauL2, and a minor lineage, TauL3 [12,19–21]. The TauL1 accessions are distributed from western habitats in the Transcaucasian and northern Iran regions to eastern habitats such as Pakistan and Afghanistan, whereas TauL2 is restricted to western habitats and subspecies strangulata is involved only in TauL2 [19,22]. Thus, differentiation of subspecies strangulata is considered to have occurred in TauL2. Moreover, Bayesian structure analyses indicate that two sublineages have genetically diverged in each of the two lineages, TauL1 and TauL2 . The eastward species expansion appears to be driven by the broad habitat range of TauL1, especially by one of the sublineages, Tau1b (TauL1b), and the TauL1b accessions exhibit peculiar phenotypes with early flowering time, high seed production ability, and salt stress tolerance during seedling growth [12,23]. Such morphological and physiological divergence might also underlie other traits that differ between TauL1 and TauL2 or among sublineages, because spikelet size tends to be small and density high in the eastern habitats [10,11]. Early-flowering accessions also have spread mainly in the eastern habitats [2,12], and genetic variation related to the early flowering phenotype have been partly studied [24–26]. However, no loci related to intraspecific divergence, especially for the Ae. tauschii morphology, have been identified.
Wheat spikelet morphology is related to grain shape and size, and spikelet shape-controlling genes pleiotropically affect grain shape [27,28]. Grain shape and size have been two of the main targets for wheat domestication and breeding [29,30], and thus understanding the genetic mechanisms controlling spikelet morphology is important for wheat breeding as well as intraspecific diversification in wheat relatives. The aims of the present study were (1) to clarify the relationships of the natural variation in spikelet and grain shape with the genetic lineages and (2) to elucidate the genetic loci controlling the morphological differences between the two subspecies and between the lineages in the wild D-genome progenitor of common wheat. In the present study, therefore, we conducted quantitative trait locus (QTL) analysis for spikelet shape-related traits using three mapping populations to identify the genetic loci for morphological variation in Ae. tauschii. Based on results of the QTL analyses, the evolutionary processes of lineage divergence and subspecies differentiation in Ae. tauschii were reevaluated.
Phenotypic data on spikelet morphology-related traits of the 199 accessions of Ae. tauschii were based on our previous reports [10,11]. The Ae. tauschii accessions were genealogically divided into two major intraspecific lineages, TauL1 and TauL2, and a minor lineage, TauL3, and TauL1 and TauL2 were each further divided into two sublineages; TauL1a and TauL1b, and TauL2a and TauL2b [12,21]. For comparison of the examined traits between the lineages and among the sublineages, data points on the TauL3 accessions and admixtures in TauL1 and TauL2 were omitted due to their limited numbers. The genealogical lineage and sublineage information of each Ae. tauschii accession was based on our previous report [12,21]. The phenotypic data and lineage information are represented in S1 Table.
Three F2 mapping populations of Ae. tauschii were used: KU-2078/PI499262, KU-2003/KU-2124, and PI476874/IG47182. In the parental accessions of the mapping populations, KU-2003, PI476874, and PI499262 belong to TauL1, and KU-2124, IG47182, and KU-2078 belong to TauL2 (Fig 1). The parental cross-combinations of all three populations were selected from interlineage pairs TauL1 and TauL2. KU-2078 is classified in subspecies strangulata, and the other five accessions are in subspecies tauschii. Therefore, the first population (KU-2078/PI499262) resulted from an intersubspecies cross between subspecies strangulata and subspecies tauschii, and the second and third (KU-2003/KU-2124 and PI476874/IG47182) populations were derived from intrasubspecies crosses of subspecies tauschii.
Plants were arranged randomly and grown in the experimental field of Kobe University. Seeds of the first F2 population (KU-2078/PI499262) were sown in November 2012, with a population size of 95. The second population (KU-2003/KU-2124) contained 116 F2 individuals and was grown in the 2011–2012 season . The last population (PI476874/IG47182), with 104 F2 individuals, was grown in the 2008–2009 season .
For 39 randomly selected accessions from the 199 Ae. tauschii accessions, four grain shape-related traits, grain length (GL), grain width (GW), grain height (GH), and length-to-width ratio of the grain (LWr), were measured. For each accession grown under field conditions at Kobe University in the 2009–2010 season, the grain shape-related traits of more than 20 seeds were measured, and the averages and standard deviations were calculated for each measurement. The phenotypic data for spikelet and grain morphology-related traits of the 199 accessions were statistically analyzed using RStudio ver. 0.99.902  in R software ver. 3.3.1  for Welch’s t test, Steel-Dwass test, and principal component analysis (PCA), and R package ‘ggplot2’  for PCA ploting.
For the first and second mapping populations, KU-2078/PI499262 and KU-2003/KU-2124, eight spikelet-related traits, i.e. spike length (SL), number of spikelets per spike (NSp), number of immature spikelets per spike (NISp), spikelet density (SpD), spikelet length (SpL), spikelet width (SpW), empty glume length (EGL), empty glume width (EGW), and four grain-related traits of GL, GW, GH, and LWr were evaluated. For the last population (PI476874/IG47182), six spikelet-related parameters (SL, NSp, SpD, SpL, EGL, and EGW) were measured. The three tillers that headed earliest for each F2 individual were used to measure the morphological traits, and the averages and standard deviations were calculated for each. The phenotypic data were statistically analyzed using R software.
To amplify PCR fragments of single sequence repeat (SSR) markers, total DNA was extracted from leaves of the parental Ae. tauschii accessions and F2 individuals. Information on SSR markers and the respective annealing temperatures was obtained from the National BioResource Project (NBRP) KOMUGI web site (http://www.shigen.nig.ac.jp/wheat/komugi/strains/aboutNbrpMarker.jsp) and the GrainGenes web site (http://wheat.pw.usda.gov/GG2/maps.shtml). For SSR genotyping, 2x Quick Taq HS DyeMix (TOYOBO, Osaka, Japan) was used as a master mix for the reactions under the following conditions: 40 cycles of 10 s at 94°C, 30 s at the annealing temperature for each SSR marker, and 30 s at 68°C. Information on the ‘kupg’ SSR markers on chromosome 7D is in our previous reports [35,36]. Six PCR-based landmark unique gene (PLUG) markers, TNAC, on chromosomes 3D and 7D were used additively according to a previous report . Genotyping with 16 ‘ctg’ single nucleotide polymorphism (SNP) markers were conducted according to our previous report .
For a cleaved amplified polymorphic sequence (CAPS) marker, Bd50050 on chromosome 7D, PCR products amplified with the primer set 5’-CTGCTGCGCCATTCTATTC-3’ and 5’-TAGAATGCAAGGGTGGCAAT-3’, then digested by the 4-bp cutting restriction enzyme HhaI. For mapping of the leaf rust-resistance locus Lr34 on 7DS , the primer set 5’-TGCGGCGATTCTATACTACT-3’ and 5’-CCGACATCAAGAACCTCC-3’ was used, and the PCR-amplified products were digested by the 4-bp cutting enzyme TaqI.
PCR products and their digests were resolved in 2% agarose or 13% nondenaturing polyacrylamide gels, stained with ethidium bromide, and visualized under UV light.
A phenotypic difference for hairy character on the flag leaf was observed between the parental accessions of the first mapping population, and the causal gene, tentatively named hfl, was used as a genetic marker for chromosome 3D.
The MAPMAKER/EXP version 3.0 package was used for construction of genetic maps with the genotyped markers . The threshold for log-likelihood (LOD) scores was set at 3.0, and genetic distances were calculated with the Kosambi function . QTL analyses were carried out by composite interval mapping with Windows QTL Cartographer version 2.5 software  using the forward and backward method. A LOD score threshold for each trait was determined by computing a 1000 permutation test. The percentage of phenotypic variation explained by a QTL for a given trait and any additive effects were also estimated.
Large divergence in spikelet shape-related traits has been observed between subspecies tauschii and strangulata [10,11]. Floral organ shape and culm-related traits also diverge between the subspecies . The six spikelet shape-related traits, SL, NSp, SpD, SpL, EGL, and EGW, analyzed in the present study showed large natural variation in 199 accessions of Ae. tauschii [10,11]. Morphological variation was assessed based on lineage and sublineage groups for the six spikelet shape-related traits. Significant differences (Welch’s t-test, P < 0.001) were observed between TauL1 and TauL2 for five traits, SL, NSp, SpD, SpL, and EGW, but not for EGL (Fig 2). Multiple comparisons among the four sublineages (TauL1a, TauL1b, TauL2a, and TauL2b) showed significant differences (Steel-Dwass test, P < 0.05) in the six traits even within the same lineages. The SpL value differed significantly between all four sublineages. Although there was no significant difference in EGL between the lineages, the sublineages TauL1b and TauL2a showed significantly higher EGL values than TauL1a. Significant differences were found between TauL1 sublineages for EGW and between TauL2 sublineages for SL and NSp. No significant difference for SpD was observed within the two sublineages in each lineage.
To clarify the relationship between spikelet shape and the sublineages, PCA was conducted based on the correlation matrix among the Ae. tauschii accessions. The first principal component (PC1) explained 50.3% of the total variance, and the variation in PC1 values had major effects on NSp, SpD, SpL and EGW (Table 1). PC2 explained 28.0% of the total variance, and high eigenvector values for PC2 were found in SL, NSp and EGL. PC3 contributing 10% of the variance was mainly derived from eigenvectors of SpD and EGW. The plot of the 169 accessions using their PC1 and PC2 values showed that the TauL1 accessions had generally larger PC1 values than the TauL2 accessions (Fig 3A), indicating that TauL1 tended to have longer spike, more spikelets per spike, and smaller spikelet than TauL2, which was consistent with the previous report . The PC2 values in TauL2 were more widely distributed than those in TauL1. Two sublineages of TauL2, TauL2a and TauL2b, were slightly differentiated, whereas the sublineage diversification was not clear in TauL1. Although the subspecies differentiation was not found in the graph of the first two axes from the PCA, subspecies strangulata formed a cluster in a graph using the PC1 and PC3 values (Fig 3B). The PC1-PC3 graph showed the differentiation of subspecies strangulata from subspecies tauschii in TauL1. These results indicated that these spikelet shape-related traits were related to the sublineage divergence and subspecies differentiation of Ae. tauschii.
Four grain shape-related traits, GL, GW, GH and LWr, varied in the randomly selected 39 accessions of Ae. tauschii, and significant differences (Welch’s t-test) were observed between TauL1 and TauL2 for GW and GH (P < 0.001) and for LWr (P < 0.01) (Table 2 and S1 Table). Grain size tended to be larger and LWr was smaller in TauL2 than in TauL1. The two sublineages of each lineage showed similar values for the four traits, although the number of examined accessions of each sublineage was limited (Fig 4). Three of the four grain shape-related traits also showed significant divergences (Welch’s t-test, P < 0.001) between the two subspecies (Table 2). GL was longer in subspecies tauschii than in subspecies strangulata, whereas GW was wider in subspecies strangulata than in subspecies tauschii. LWr was significantly smaller in subspecies strangulata than in subspecies tauschii, indicating that grains of subspecies strangulata were more spherical than those in subspecies tauschii.
PCA was performed for the grain shape-related traits of 37 TauL1 and TauL2 accessions, and PC1 and PC2 respectively explained 56.5 and 39.6% of the total variance (Table 3). A graph using the PC1 and PC2 values showed that the 37 accessions were grouped into TauL1, subspecies tauschii in TauL2, and subspecies strangulata in TauL2 (Fig 3C). TauL1 tended to have less than −0.5 of the PC1 values, and the subspecies tauschii and strangulata accessions in TauL2 generally had plus and minus values for PC2, respectively. As well as the spikelet shape-related traits, the grain shape traits were closely associated with intraspecific diversification of Ae. tauschii.
Twelve and six spikelet and grain shape-related traits were respectively evaluated in the first two F2 populations and the third population of Ae. tauschii. Each trait showed widely distributed variation in the populations, and transgressive phenotypes were observed in each population (Tables (Tables44 and and5),5), implying that several loci are contributed in the phenotypic variation. Parental accessions of TauL1 showed higher values for SL, NSp, SpD, GL, and LWr and lower values for NISp, SpL, SpW, EGL, GW, and GH than those of TauL2 in the three populations.
SL had higher positive correlation coefficients with SpL, SpW, EGL, and EGW in the first F2 population (KU-2078/PI499262) than in the other two populations (S2–S4 Tables). SpD was more negatively correlated with SL, SpL, SpW, EGL, and EGW in the first F2 population, whereas it correlated positively with NSp in the other populations. These results indicated that longer spikes and larger spikelets reduced spikelet density in this population, while the number of spikelets per spike contributed to low spikelet density in the others. Positive correlations between SpL, SpW, EGL, EGW, GL, and GW were commonly found in the three populations. However, strong or moderate positive correlations between GH and these six traits were observed only in the first F2 population, which might reflect the quadrate spikelets and spherical grains of subspecies strangulata. LWr was negatively correlated with SpW, EGW, and GW both in the first and second (KU-2003/KU-2124) F2 populations, but positively correlated with GL in the second F2 population.
In the first population, KU-2078/PI499262, 160 D-genome markers formed seven linkage groups, and total map length was 1250.7 cM with an average spacing of 7.85 cM between markers. The second mapping population, KU-2003/KU-2124, contained eight linkage groups, with two groups involved for chromosome 7D, and the total map length was 1455.4 cM with an average spacing of 13.2 cM between markers. In the third population, PI476874/IG47182, 158 markers were assigned to seven linkage groups, and the total map length was 1513.0 cM with an average spacing of 9.56 cM between markers.
QTLs for all examined traits were detected using the three linkage maps. In the first F2 population, KU-2078/PI499262, 41 QTLs for the twelve examined traits were assigned to the seven Ae. tauschii chromosomes (Table 6). QTLs for NSp, SpD, SpL, SpW, EgW, GL, GW, and GH were detected on a similar proximal region of chromosome 3D, and QTLs for NISp, SpD, SpW, and GW overlapped on chromosome 4D (Fig 5). While, QTLs for four spikelet- and three grain-related traits were found within the interval between Xbarc352 and Xcfd46 on chromosome 7D (Fig 6).
In the second population (KU-2003/KU-2124), 36 QTLs for these traits, except for GH, were assigned to the seven chromosomes (Table 7). QTLs for SpD, SpL, and EGL were found at a similar region of chromosome 3D, and six spikelet- and two grain-related QTLs were piled in the same region of the short arm of chromosome 4D (Fig 5).
Comparison of the linkage maps and the QTL locations revealed that many spikelet- and grain-related QTLs were commonly detected on similar regions of chromosomes 3D and 4D in the three linkage maps (Fig 5). The spikelet- and grain-related QTLs on chromosome 7D were peculiar to the first population, KU-2078/PI499262, out of the three mapping populations (Fig 6). Several spikelet- and grain-related QTLs were found on the other four chromosomes; on chromosomes 1D, 5D and 6D in the first population and on chromosome 2D in the second population (Tables (Tables66 and and7).7). Most of these QTLs covered different chromosomal regions in each mapping population and had no overlaps among the three populations. The SpL QTLs were found on chromosome 5D in all of the three mapping populations, whereas their locations on 5D were apparently distinct.
The genotypes of the F2 individuals at these QTLs on chromosomes 3D, 4D, and 7D were deduced from genotyping data on the surrounding markers, and the genotypic effects of these QTLs were compared. Significant differences (Tukey-Kramer HSD test, P < 0.05) were observed between the F2 individuals carrying alleles from TauL1 and TauL2 at the 29 QTL regions (Figs (Figs77 and and8).8). This observation was consistent with additive effects at each of the 29 QTLs, 27 of which coincided with the differences between the parents (Tables (Tables66 and and7).7). No significant differences were observed between the F2 individuals with TauL1 type-homozygous, heterozygous, or TauL2 type-homozygous alleles at each of the following 5 QTLs; the 3D QTL for NSp and the 4D QTLs for SpD and GW in KU-2078/PI499262, the 4D QTL for LWr in KU-2003/KU-2124, and the 4D QTL for NSp in PI476874/IG47182. At the QTLs for GL, the 7D QTL in KU-2078/PI499262 and the 4D QTL in KU-2003/KU-2124, heterozygous individuals showed significantly higher values than TauL1 type -homozygous ones.
The parental accessions of the KU-2078/PI499262 population showed a distinct spikelet phenotype; SpW of the subspecies strangulata accession KU-2078 was much larger than that of the subspecies tauschii accession (Fig 9A). From the F2 individuals of KU-2078/PI499262, four F2 plants (#7, #27, #63 and #85) were selected based on genotyping data on the surrounding markers and their spikelets were compared (Fig 9B). An F2 plant (#27) with KU-2078-homozygous alleles for both the 3D and 7D QTLs exhibited larger SpW than the other three F2 plants. The spikelets of F2 plants (#7 and #63) with either the KU-2078-homozygous allele for the 3D or 7D QTL were wider than those with the PI499262-homozygous alleles (#85).
The wheat diploid D-genome progenitor, Ae. tauschii, carries large genetic variation in spikelet and grain morphology. Here, highly significant correlations among spikelet and grain shape-related traits were observed in the two mapping populations, which indicated a tight relationship between spikelet and grain shape (S2 and S3 Tables). In Ae. tauschii, the widths of spikelets, empty glumes, and grains determine sphericalness of grains. Similar observations have been reported in wheat and its relatives, and subspecies differentiation-related genes dramatically affect grain shape, accompanied by alteration of spikelet morphology in tetraploid and hexaploid wheat [27,42,43].
We detected a lot of QTLs on all seven chromosomes of Ae. tauschii for the analyzed traits, and assembled most to three chromosomal regions on chromosomes 3D, 4D and 7D. In the three mapping populations, the 3D and 4D QTL positions for the spikelet shape-related traits were consistent (Figs (Figs55 and and6).6). Since the three populations were derived from interlineage crosses between TauL1 and TauL2, the 3D and 4D QTLs should contribute to intraspecific variation and lineage divergence of the spikelet morphology in Ae. tauschii. The TauL1 accessions provided longer spikes, higher spikelet density, and shorter and narrower spikelets than the TauL2 accessions (Fig 2), so intraspecific lineage divergence could be mainly caused by the genetic differences in the 3D and 4D QTL regions.
The three parental TauL1 accessions of the mapping populations were from TauL1b, which is considered to have spread eastward from the Transcaucasus and Middle East . The TauL1a, TauL2 and TauL3 accessions are restricted to the Transcaucasus/Middle East region. Longitudinal clines for the spikelet morphology were observed in Ae. tauschii, and Ae. tauschii accessions in the eastern habitats tend to have the small-spikelet-size phenotype [10,11]. The TauL1b accessions showed different spike and spikelet shape-related traits from the TauL2 accessions (Figs (Figs22 and and3),3), suggesting that the morphological clines, at least for spike and spikelet shape, could be due to the eastward expansion to Asia of TauL1b. Together with TauL1b, TauL1a also showed significant differences in spike and spikelet morphology compared with TauL2, and thus the morphological differences between the eastern and western accessions of Ae. tauschii might have arisen in the Transcaucasus/Middle East region before the TauL1b eastward expansion. The two QTL regions on chromosomes 3D and 4D should have the main contribution to the morphological divergence between the eastern and western accessions, and the effect of the 7D QTL region on the divergence could be additive.
Distinct spikelet and grain morphology of the two subspecies, tauschii and strangulata, is caused by genetic differences in the limited number of QTL regions (Table 6). The three QTLs on chromosomes 3D, 4D and 7D apparently mainly contribute to the morphological differentiation of the two subspecies (Figs (Figs55 and and6).6). However, overlap of QTLs on chromosome 7D was found only in the intersubspecies population (subspecies strangulata and tauschii), not in intrasubspecies populations (subspecies tauschii), suggesting that these 7D QTLs are closely related to subspecies differentiation in Ae. tauschii. Within TauL2, therefore, the 7D QTL contributed to the morphological differentiation of the subspecies. The subspecies strangulata accessions are unevenly distributed in only the TauL2b and TauL2 admixture but not in TauL2a (S1 Table). The TauL2b accessions exhibited shorter spikes and spikelets and fewer spikelets per spike than the TauL2a accessions, whereas no clear difference for EGW was found between TauL2a and TauL2b (Fig 2). The limited effects of the 7D QTLs on the intersublineage divergence appear to be due to coexistence of the two subspecies within TauL2b, so the genetic difference in the 7D QTL region in TauL2 might have arisen within TauL2b.
Some spikelet- and grain-related QTLs were additionally found on chromosomes 1D, 2D, 5D and 6D (Tables (Tables66 and and7),7), while the chromosomal regions for these QTLs showed few or no overlaps among the three mapping populations. These spikelet- and grain-related QTLs may reflect the morphological differences specific to the parental accessions and not be related to the lineage divergence and subspecies differentiation in Ae. tauschii. Therefore, other mapping populations derived from different parental combinations might allow us to detect additional QTLs for spikelet and grain shape in Ae. tauschii.
Genotypic differences in the 3D and 7D QTL regions additively affected the spikelet width (Fig 9), suggesting that the effects of the three QTLs on spikelet and grain morphology were additive. Addition of the genetic differences in the 7D QTL region to those of the 3D and 4D QTLs could more clearly have led to the subspecies differentiation in the spikelet and grain morphology. Due to the existence of morphological and genetic intermediates [16,44], the two subspecies were not formally described in a recent monograph . In our previous reports [10,11], these subspecies can be separated when the sensu-stricto identification criteria are used. The Transcaucasian and Iranian accessions contain intermediates that should be assigned to subspecies tauschii. The intermediates are predicted to belong to TauL2 lacking the subspecies strangulata-type alleles at the 7D QTL regions, similarly to the TauL2 parental accessions of the second and third mapping populations, KU-2124 (TauL2a) and IG47182 (TauL2x). Thus, the genotype of the 7D QTL region could be a critical point to distinguish subspecies strangulata from subspecies tauschii. This assumption should be tested by construction of a fine map around the 7D QTL region and development of molecular markers closely linked to the 7D QTLs in further studies. Thus, QTL analysis for spikelet and grain shape of wild plant species provides useful information to elucidate the evolutionary processes leading to intraspecific differentiation.
Subspecies strangulata produces wider and more spherical grains than subspecies tauschii, and the three QTL regions of chromosomes 3D, 4D and 7D control the sphericalness of grains in subspecies strangulata. The birthplace of common wheat supposedly been restricted to a narrow distribution range within the western habitats of Ae. tauschii , and the D-genome donor accessions putatively belong to TauL2 or undiscovered populations [16,19,20]. Our previous study on the chromosomal region of Iw2, a repressor of glaucousness, suggests that the subspecies strangulata accessions do not represent the direct descendants of the ancestral populations that gave rise to common wheat . Therefore, the 3D and 4D QTL regions could have been transmitted from the putatively ancestral TauL2 populations to common wheat, whereas the 7D QTLs might not have been integrated in the common wheat genome. Barley spike density is partly under the control of dense spike-ar (dsp.ar), assigned to the centromeric region of chromosome 7H . The 7D QTL region we identified is apparently positioned on the short arm, distal to the centromere (Fig 6), indicating that the 7D QTLs might be not orthologous to barley dsp.ar.
Up to now, many QTLs for grain size and shape have been detected on various chromosomes of common wheat [30,47,48], whereas the 3D, 4D and 7D QTLs detected in the present study might be novel. No data have yet indicated that homoeologous loci of the 3D, 4D and 7D QTLs can be found on the A and B genomes of common wheat. To elucidate the homoeologous relationship to previously reported QTLs for grain size and shape, fine mapping of these QTLs will likely be required. Our previous study using synthetic wheat hexaploids derived from crosses between a tetraploid cultivar and some Ae. tauschii accessions showed the presence of several QTLs for grain size and shape on various D-genome chromosomes , whereas no QTL appears to correspond to these new 3D, 4D and 7D QTLs. The disappearance in the mapping populations of synthetic wheat might be due to suppression of the QTL effects by homoeologous loci of the A and B genomes in the hexaploid genetic background, although the reason is not clear. Therefore, simple introgression of the 7D QTL region through synthetic wheat might not be effective in significantly altering the grain shape of modern common wheat cultivars. For dramatic alteration of the grain shape, changes of the homoeologous alleles on the A and B genomes should be required along with the D-genome QTLs.
Levels of significance are indicated by asterisks (* P < 0.05, ** P < 0.01, *** P < 0.001).
Levels of significance are indicated by asterisks (* P < 0.05, ** P < 0.01, *** P < 0.001).
Levels of significance are indicated by asterisks (* P < 0.05, ** P < 0.01, *** P < 0.001).
We thank Dr. Yoshihiro Matsuoka for his providing the lineage information of the Ae. tauschii accessions and critical reading of the manuscript.
This work was supported by grants from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan (Grant-in-Aid for Scientific Research (B) Nos. 21380005 and 16H04862) to ST, and by a Research Fellowship from the Japan Society for the Promotion of Science for Young Scientists to RN.
All relevant data are within the paper and its Supporting Information file.