Undomesticated wild species, crop wild relatives, and landraces represent sources of variation for wheat improvement to address challenges from climate change and the growing human population. Here, we study 56,342 domesticated hexaploid, 18,946 domesticated tetraploid and 3,903 crop wild relatives in a massive-scale genotyping and diversity analysis. Using DArTseqTM technology, we identify more than 300,000 high-quality SNPs and SilicoDArT markers and align them to three reference maps: the IWGSC RefSeq v1.0 genome assembly, the durum wheat genome assembly (cv. Svevo), and the DArT genetic map. On average, 72% of the markers are uniquely placed on these maps and 50% are linked to genes. The analysis reveals landraces with unexplored diversity and genetic footprints defined by regions under selection. This provides fertile ground to develop wheat varieties of the future by exploring specific gene or chromosome regions and identifying germplasm conserving allelic diversity missing in current breeding programs.
Wheat is the world’s most widely grown crop, with annual production in excess of 600 million tons across the Americas, Europe, Asia, Australia, and Africa. Wheat provides 20% of the total protein and calories in human nutrition1, and supplies ~40% of the dietary intake of essential micronutrients, including zinc, iron, manganese, magnesium, and vitamins B and E for millions of people, who rely on wheat-based diets2. It is also an important energy source for farm animals3 and is processed for various other uses including fuel4,5. Approximately 95% of the global crop is hexaploid bread wheat (Triticum aestivum L. aestivum, genomic constitution AABBDD), whereas the remaining includes tetraploid durum wheat (Triticum turgidum L. durum, AABB) and other wheat types of smaller economic importance6.
Since its domestication >10,000 years ago, wheat cultivars have increased yields and adapted to a number of different climates and growing conditions7,8,9,10. This success, however, has resulted in a reduction of the genetic diversity in the elite gene pool11,12,13,14, This limits the development of new wheat varieties required to sustainably address the demands of the growing world population in a backdrop of climate changes, and abiotic and biotic stresses15,16. Wheat germplasm banks conserve ex situ ca. 560,000 accessions, including crop wild relatives (CWR) and landraces (as well as modern cultivars), which harbor untapped genetic diversity that will prove crucial for overcoming these challenges17,18,19,20. CWR and landraces have evolved mechanisms to survive or thrive in challenging environments through continuous cycles of natural and human selection. However, their resilience and adaptive mechanisms are poorly understood, which limits their use in breeding efforts12,15. Among the main challenges limiting the use of this germplasm in breeding is the need to efficiently identify accessions harboring advantageous genetic variants, and linkage drag associated with introgressing these desired genetic variants into elite germplasm20. Recent advances in genomics and molecular technologies, however, facilitate the characterization of the genetic diversity in large collections of accessions17,21,22, and increasingly provide strategies, e.g., gene editing, that avoid linkage drag23. For example, high-throughput genotyping can support the characterization of core subsets of accessions in a germplasm bank that capture most of the genetic diversity of larger germplasm groups24, and are a valuable starting point for phenotyping in search of diversity for use in breeding17,25,26,27,28.
The International Maize and Wheat Improvement Center’s (CIMMYT) germplasm bank is one of the largest wheat (and maize) germplasm providers worldwide, distributing ca. 20,000 packages of wheat seeds per year to ~100 countries. The Seeds of Discovery initiative (SeeD; http://seedsofdiscovery.org/), which aims to facilitate the effective use of genetic diversity of wheat and maize29, has characterized nearly 80,000 accessions from two of the world’s largest wheat germplasm banks: (i) CIMMYT, which hosts 140,812 wheat accessions, and (ii) the International Center for Agricultural Research in the Dry Areas (ICARDA), with 43,924 wheat accessions (https://www.genesys-pgr.org/welcome). Genotypic data from these germplasm banks have been used for a wide range of applications25,28,30,31,32.
The main objective of this work is to characterize the global genetic diversity of nearly 80,000 accessions from CIMMYT and ICARDA’s wheat collections, divided in three biological categories: (i) CWR, (ii) domesticated tetraploid taxa (AABB), and (iii) domesticated hexaploid (AABBDD) accessions. Secondly, we aim to understand this diversity and its possible use in breeding by mapping genetic variants (DArTseq-based SNP and SilicoDArT)33 to the IWGSC v1.0 reference genome34, to the Svevo (durum) tetraploid reference genome10, and against the DArT genetic map. Finally, we validate our approach by analyzing previously identified genomic regions associated with key agronomic traits, and we uncover regions or QTL associated with footprints of modern wheat breeding. This provides clues and targets for the wheat research and breeding community.
Diversity analysis of nearly 80,000 wheat accessions
We characterized the genetic diversity of 79,191 accessions from the CIMMYT and ICARDA germplasm banks: 56,342 domesticated wheat hexaploids, 18,946 domesticated wheat tetraploids, and 3903 CWR. These wheat accessions originated from 109 countries (passport data in Supplementary Data 1). For this analysis, we used high-quality SNPs and SilicoDArT (PAV (presence/absence variation)) markers generated independently for each of these three collections. As expected, there was a larger proportion (~50%) of common markers between the hexaploid and tetraploid accessions than shared between these and the CWRs (1–6%; Supplementary Fig. 1). After discarding markers with missing rate > 50% and minor allele frequency (MAF) ≤ 0.1%, markers with MAF between 0.1 and 1% constituted 41, 14, and 7% in the hexaploid, tetraploid, and CWRs, respectively (Table 1).
We aligned the SNPs and SilicoDArT markers to the hexaploidy wheat RefSeq v1.0 reference genome34, and to the durum wheat (Svevo) reference genome10 (Supplementary Table 1, Supplementary Fig. 2 for hexaploid, Supplementary Fig. 3 for tetraploid, and Supplementary Fig. 4 for CWR): 70% (66,067) of the markers mapped uniquely for the hexaploids on the RefSeq v1.0, 68% (30,806) and 69% (31,181) for the tetraploids, with the RefSeq v1.0 and Svevo genomes, respectively, and 50% (28,054) for the CWR on the RefSeq v1.0. As expected, most of the SNP markers were in intergenic regions, outside repeats (Supplementary Data 2 and detailed statistics in Supplementary Fig. 5).
The DArT genetic map (v4) (Supplementary Data 3, see “Methods” section) includes 105,122 markers distributed across the 21 hexaploid bread wheat chromosomes, with a mean of 5006 markers per chromosome. Positioning of SNPs and SilicoDArT markers on the DArT genetic map v4 resulted in a homogeneous distribution across all chromosomes (Supplementary Table 2). Totals of 44,501, 24,185, and 18,738 SNP markers have map positions, representing 52.03%, 53.29%, and 33.61% of all SNP markers for the hexaploid, tetraploid, and CWR data sets, respectively. Similarly, 23,571 (89.0%), 18,711 (70.5%), and 19,022 (30.9%) SilicoDArT markers aligned to the genetic map for the hexaploid, tetraploid, and CWR accessions, respectively. Supplementary Fig. 6 shows the complete distribution of the DArT genetic map markers for the hexaploid, tetraploid, and CWR, and the markers in common among pairs and all three groups of accessions.
We used this genotypic data to analyze each group independently. Accessions were classified as either hexaploid, tetraploid, or CWR based on their passport data. An iterative hierarchical clustering approach, based on modified Roger’s distance matrix (MRD), performed a stepwise branching of each group of accessions into subgroups or clusters of germplasm with maximum genetic diversity among and minimum genetic diversity within groups (see “Methods” section). In addition, we performed admixture analysis on a reduced number of markers (MAF > 5%, and linkage disequilibrium thinned), and admixture populations were compared to the MRD cluster approach. Below, we present the results of these analyses for each group.
Hexaploid analysis reveals unexplored genetic diversity
The 56,342 hexaploid accessions (81% from CIMMYT and 19% from ICARDA germplasm banks) encompass eight domesticated taxa (Supplementary Table 3), in which 99% are T. aestivum L. aestivum. We assigned these accessions to seven subgroups based on passport data: (1) landraces (40.3%), (2) cultivars, i.e., genotypes that are distinct, uniform, and stable, have been selected for desirable traits, and are widely cultivated (5.9%), (3) elite breeding lines (20.9%), (4) nursery lines, i.e., groups of distinct lines, assembled for comparative description, or evaluation (2.1%), (5) genetic stocks, i.e., typically lines resulting from the intercrossing of distinct species, with described whole chromosome or partial chromatin addition or deletion (1.9%), (6) primary synthetics (stable wheat genetic stocks, botanically named Aegilotriticum spp.) resulting from the crossing and chromosome doubling of tetraploid Triticum species (usually AABB genome durum wheat) with Triticum tauschii (DD genome; 0.25%), and (7) synthetic derivatives lines and their descendants resulting from crosses between a primary synthetic hexaploid and bread wheat (T. aestivum L. aestivum; 13.8%). We could not classify 8275 (14.7%) of the samples due to the lack of information in their passport data. The accessions originated from 105 countries, with greatest representation from Mexico (31.1%), Iran (8.1%), Turkey (4.4%), China (4.2%), Morocco (2.5%), Pakistan (2.1%), and Afghanistan (2.1%).
The multidimensional scaling (MDS) plots (Fig. 1a) illustrate distinct biological groupings within the hexaploid wheats and suggest that a large portion of the genetic diversity in the landraces has not been sampled in modern breeding (for more details see Supplementary Data 4 and Supplementary Movie 1): 70.1% of landraces are at >0.24 MRD distance from the average elite lines (Supplementary Fig. 7).
Admixture analysis at k = 8 (Fig. 1b and Supplementary Figs. 8–11) revealed a good fit of the hexaploid diversity into eight groups: (1) traditional landraces from Mexico (Mxn); (2) traditional landraces from Iran (Irn) and Turkey (Tur); (3) traditional landraces from Iran, Turkey, and Pakistan (Pak); (4) and (5) two groups of modern landraces from Mexico; (6) and (7) two groups of synthetic materials, one mainly from primary synthetics (Syn A) and the second with synthetic derivatives crossed with two and up to six elites lines (Syn B); and (8) a group of elite wheat germplasm. Within the large group of elite materials, we found 2260 elite lines, 4400 admixtures of elite with modern landraces, and a few traditional landraces from Iran and Turkey, and synthetics populations. The 2260 elite lines in this group contain in their pedigrees the varieties Kauz, Pastor, or Baviacora, which are progenies of Veery, a high-yielding CIMMYT line from the late 1970s, produced from a spring × winter wheat cross. Other studies have reported genetic separation of these varieties35,36, indicating that the 1B/1R translocated segment from rye, present in Veery and derived from Russian cultivar Kavkaz, markedly increases yield37.
Analysis of molecular variance (AMOVA) between clusters identified by the diversity analysis (FST values) indicated that grouping into 6 and 12 clusters were the most informative (Supplementary Fig. 12 and Supplementary Movie 2). At the level of 12 clusters, the traditional landraces are divided in four subgroups: traditional Mexican landraces (subgroup 5 in Fig. 1c), landraces from Iran and Pakistan (Lr Irn/Pak, 11), landraces from Iran (Lr Irn, 4), and landraces from Iran and Turkey (Lr Irn/Tur, 3). Two small subgroups (2 and 8), comprising 2.6% of the accessions, were separated from the Syn A group (10); based on their lack of markers on chromosome D, these two small subgroups are likely tetraploids that were originally miss-classified as hexaploids in their passport data and were identified by the analysis as outliers. The modern Mexican landraces were further subdivided, reflecting a greater contribution of elite germplasm to subgroup 7 compared with 1; subgroup 9 is too small to allow interpretation of its uniqueness. Supplementary Figs. 13–15 contains the FST distributions across all chromosomes and Supplementary Figs. 16–21 shows the distribution inside each chromosome. These results are consistent with the MRD analysis and support the idea that a large fraction of genetic variation present in landraces has not been incorporated into elite breeding programs.
Tetraploid analysis reveals breadth of diversity in durum elites
The 18,946 domesticated tetraploid accessions (20% from CIMMYT and 80% from ICARDA germplasm banks) encompass eight taxa Supplementary Table 4, in which 77.6% are T. durum. Based on passport information, we divided the accessions into four groups: landraces (55.8%), elite breeding lines (21.4%), cultivars (3.2%), and genetics stock (0.06%). We could not classify 19.6% of the accessions due to incomplete passport data, but we included those samples in the analysis. The accessions originated from 75 countries, with >50% coming from Ethiopia (18.1%), Turkey (16.7%), Mexico (7.7%), Iran (3.4%), Tunisia (2.8%), Morocco (2.7%), and Syria (2.5%). Analysis of the similarity matrix using MRD with an MDS plot (Fig. 2a) showed that the elite lines are distributed across almost the entire genetic diversity space of the landraces, with the notable exception of a genetically distinct group of several hundred Ethiopian landraces (Supplementary Data 5 and Supplementary Movie 3). Four distinct groups of landraces were identified based on MRD from the allelic frequencies of the group of 4048 elite breeding lines: 817 landraces (7.8%) were genetically close (MRD < 0.2) to the elite lines; 5918 landraces (55.9%) with MRD between 0.20 and 0.30, among which 29% are from Turkey and 10% from Iran; 3483 (32.9%) with MRD between 0.30 and 0.35, mostly (92%) from Ethiopia; and 356 (3.4%) with MRD > 0.35 from the elite lines, 42% of which are from Turkey (Supplementary Fig. 22).
The admixture analysis (K = 7) divided the diversity of the tetraploid accessions (Fig. 2b) into: (1) a remarkably distinct group of landraces from Ethiopia; (2) landraces mainly from northern Africa (Morocco, Algeria, and Tunisia) and Portugal; (3) landraces from Turkey, Iran, Jordan, and Syria; and (4) landraces from Turkey, Azerbaijan, Iran, and Russia. The analysis also identified a group (5) of the 3157 elite lines, 2279 (72%) of which were pure to this population, and 879 (28%) were admixtures of elites with landraces. Finally, we identified (6) a small group of accessions from Triticum diccocum, and (7) outliers that are potentially hexaploid accessions. All admixture figures from K = 2 to K = 7 are presented in Supplementary Figs. 23 and 24.
The cluster diversity analysis revealed a high FST value (0.307) at the level of seven clusters (Supplementary Fig. 25, Fig. 2c and Supplementary Movie 4). This analysis highlights the relative uniqueness of the diversity of Ethiopian landraces compared with all other tetraploid materials: tetraploid wheat has been cultivated in Ethiopia for thousands of years, and the area is considered a center of diversity for that species38. The FST analysis shows a substantial contribution to genetic diversity from the B genome (Fig. 2c and Supplementary Movie 4). Supplementary Figs. 26 and 27 contains the FST distributions across all chromosomes and Supplementary Figs. 28–30 shows the distribution inside each chromosome. This analysis also identified a group of 1008 accessions with 20% of their SNP markers mapping to D chromosomes, suggesting that they are hexaploids and demonstrating the value of genomic profiling to curate germplasm bank collections.
CWR analysis characterizes wheat sub-genomes diversity
The 3903 accessions of wheat wild relative species (21% from CIMMYT and 79% from ICARDA germplasm banks) include all known 27 wild species from the Aegilops–Triticum species complex (Fig. 3a, Supplementary Table 5, Supplementary Data 6 and Supplementary Movie 5). Aegilops comprises 23 annual species, of which 11 are diploid and 12 are allopolyploid39,40,41. The most represented species in this study were Aegilops tauschii (974 accessions), Aegilops triuncialis (661), Aegilops geniculata (401), Aegilops cylindrica (351), and Aegilops biuncialis (331). The 27 species comprised 11 genomic constitutions39. The accessions originated from 55 countries, with the largest representations from Turkey (17%), Iran (11%), Syria (10%), Lebanon (5%), Jordan (4%), and Greece (4%).
Both the MRD and admixture analysis grouped the accessions by similarity of genomes and then at species level (Fig. 3b, c). In the cluster analysis, the Aegilops accessions (1857 accessions of 11 species) containing genome UU at three ploidy levels (red bar in Fig. 3c), including D-genome-containing Aegilops juvenalis (DDMMUU), were separated from all other Aegilops and Triticum species (blue bar in Fig. 3c). Taxa with similar genomes clustered together (e.g., Aegilops kotschyi and Aegilops peregrina). The Aegilops and Triticum clusters were further differentiated into section Cylindropyron (Aegilops markgrafii and A. cylindrica) and most species of section Vertebrata (A. tauschii, Aegilops crassa, and Aegilops ventricosa) versus sections Sitopsis and Triticum. Section Cylindropyron are differentiated from section Vertebrata. The four wild Triticum species plus Aegilops speltoides (SS) initially grouped together with accessions from section Sitopsis (Aegilops bicornis, Aegilops longissima, and Aegilops sharonensis). Aegilops mutica clustered with section Comopyrum (Aegilops comosa and Aegilops uniaristata) and with A. uniaristata. Aegilops crassa (DDDDMM) and Aegilops vavilovii (DDMMSS) grouped together. Interestingly, the Aegilops neglecta were separated into two groups: (1) 49 potentially tetraploid samples (ssp. neglecta, UUMM) and (2) 76 potentially hexaploid (ssp. recta, UUMMNN) samples. These subspecies are difficult to distinguish phenotypically according to Van Slageren42. It was also interesting that A. biuncialis was separated into clusters of 261 and 46 samples. A total of 199 accessions (5.1%) were identified as outliers or potentially misclassified samples, and will be reanalyzed and evaluated to validate or correct their passport data.
Core set capture global diversity and misclassified accessions
Core germplasm subsets aim to eliminate redundancies and identify representative samples for use in various analyses. We formed core subsets that captured similar genetic diversity to their respective complete collections as indicated by values of expected heterozygosity (He2), inbreeding, and Shannon indices for both complete population and core subsets (Supplementary Fig. 31). The core subsets contained 20% of the complete populations, and consisted of 11,235, 3157, and 746 hexaploid, tetraploid, and CWR accessions, respectively (Supplementary Fig. 32).
We conducted a global diversity analysis for wheat by reanalysing the three core subsets together, obtaining 41,717 SilicoDArT and 112,748 SNP markers. The three groups were clearly differentiated using the SilicoDArT markers, and as expected from the results for individual group analyses, we found some outliers among putative tetraploids and hexaploids. We investigated the outliers by calculating the percentage of SilicoDArT markers located on the A, B, and D genomes (Supplementary Fig. 33). A total of 138 (4.4%) putative tetraploids had >10% of markers mapped to the D genome, and 97 of them had >20%. Similarly, among putative hexaploids, 273 (2.4%) had <20% of the markers mapped to the D genome. These observations suggest that 4.4% of tetraploid and 2.4% of hexaploid samples are misclassified in their passport information, a concern that is now being verified by the CIMMYT and ICARDA genebanks. With this analysis, we demonstrate the value of profiling using genomic tools to identified misclassification in germplasm banks.
Genomic regions under positive selection
Analysis of FST values on a variant per variant basis across the bread wheat genome highlights areas of positive selection. This is particularly informative when relatively high FST values are considered together with the backgrounds of the groups defined by the clusters (Supplementary Figs. 13–15). For each cluster split, the highest FST values reveal the genomic variants that contributed to the separation of the two subgroups, thereby identifying molecular footprints possibly associated with selective sweeps. We implemented this analysis across the full dataset, noting the genomic regions with high FST values (Supplementary Figs. 34–54). We illustrate the numerous potentially interesting analyses by focusing on two important cluster splits in the hexaploidy group: (1) the first split, which separates the accessions of traditional germplasm from the group that includes most of the elite lines, and (2) the third split, which consolidates the core cluster of elite lines by removing a large set of Mexican landraces (Supplementary Fig. 12). This analysis identified genomic regions that are known to be associated with key agronomic traits, but more importantly, we also uncovered many regions that could help explain the recent history of modern wheat breeding and offer target alleles for future breeding. For example, clusters of loci with high FST within a region of chromosome 3A associated with the well-characterized preharvest sprouting gene (TaMFT)43, are present in germplasm in cluster 2 (elite lines and Mexican landraces), but are absent in cluster 4 (elite lines and cultivars; Fig. 4).
GWAS analysis reveals loci associated with GPC and SDS
To conduct association scans with the DArTseq data, we phenotyped 3870 samples for two important traits for processing and end-use quality, grain protein content (GPC) and SDS sedimentation (Fig. 5 and Supplementary Table 6). We found 18 genomic regions associated with GPC on 12 chromosomes, with highest peaks on 4A and 4B, followed by 5A, 5B, 7A, and 7B. Similarly, Kumar et al.44 reported major and stable QTL for GPC on chromosomes 5B, 7A, and 7B of an exotic genotype, and indicated that these QTL were independent of grain yield. Such QTL could be useful to enhance GPC through marker-assisted selection (MAS), particularly if they do not compromise yield. Comparison with 49 GPC studies45 suggests that QGPC.ndsu.5B (located on 5BS) and QGPC.ndsu.7A.2 (located on 7AL) could be novel QTL, and the exotic germplasm could contribute to the wheat breeding gene pool for increasing GPC.
SDS sedimentation is a common test to determine overall gluten quality. High values on this test are associated with strong gluten (preferred for bread-making), while low values are associated with weak gluten (preferred for pastry products). Here, we report significant QTL for SDS sedimentation and putatively associate them with known storage protein genes. Specifically, high molecular weight glutenins, Glu-A1, Glu-B1, and Glu-D1 (located on the long arms of chromosomes 1A, 1B, and 1D), and low molecular weight glutenins, Glu-A3, Glu-B3, and Glu-D3 (located on the short arms of chromosomes 1A, 1B, and 1D) are candidate genes for the QTL on chromosomes 1A, 1B, and 1D, which had the largest effects on SDS sedimentation in this study. All these glutenin genes are well known, and their variability and effects on processing and end-use quality have been extensively reported46.
This diversity analysis for ca. 80,000 accessions from CIMMYT and ICARDA’s seed banks is likely the largest such analysis for any agricultural crop. The analysis of the 56,342 hexaploid accessions highlighted that relatively little of the genetic diversity available in landraces has been used in modern breeding. The largest genetic distance among the hexaploid samples was between elite germplasm and synthetic derivatives, the distinction being driven, as expected, by alleles introduced from A. tauschii, the D genome donor. The clustering analysis also identified landraces that have contributed to the genetic pool of modern breeding lines (e.g., landraces in clusters 6 and 7 in Fig. 2c), and landraces that host unexplored alleles/diversity (e.g., landraces from clusters 3, 4, 5, and 11), both presenting fertile ground for exploration and application in breeding programs.
Our diversity clustering analyses reveal genetic footprints defined by regions under selection. We describe the example of preharvest sprouting among hexaploids, for which genetic variants within the TaMFT gene (Chromosome 3A) are absent in the cluster of elite lines and cultivars, descendant from precursor cluster 2 that contains these variants. We envision numerous genetic studies that researchers may wish to conduct using the 231 FST chromosome profiles (2–12 cluster on 21 chromosomes) available in Supplementary Figs. 34–53. These data can be used, for example, to explore selective sweeps for any specific gene or chromosome region, analyze footprints defining divergence of landraces from distinct ecologies, or identify germplasm groups conserving allelic diversity missing in current breeding programs.
The analysis of 18,946 tetraploid accessions showed, and in contrast to the hexaploids, that much of the total genetic diversity is represented or explored by the elite durum accessions. There is, however, a large subset of accessions collected in Ethiopia that forms an isolated cluster, and whose genetic content is distinct from and largely unexplored by the elite materials. Analysis of the 3903 CWR highlighted the strong differentiation of sections, followed by species with similar genome constitution, and accurately identified subspecies ploidy level.
We anchored the genomic data to three genomic resources: the latest hexaploid and tetraploid wheat reference genomes and the DArT genetic map, to obtain both physical and genetic positions for the markers capturing the genetic diversity present in the hexaploid and tetraploid wheat accessions, and the CWRs. All the genotypic (DArTSeq) data, and two tools, the DArT genetic map, and CurlyWhirly, are available for use by the research community (see “Methods” section). The DArT genetic map enables confident localization of markers to genome-specific regions, avoiding the common problem in wheat (and other polyploids) of confounding effects among homologous chromosomal regions. CurlyWhirly is valuable for visualizing complex diversity data, e.g., Figs. 1–3. These resources should be useful in gene discovery, cloning, marker development, genomic prediction or selection (GS), MAS, genome-wide association studies (GWAS), and other applications.
These massive-scale genotypic data have already been used in several studies focused on enhancing the use of genetic diversity in wheat breeding. Singh et al.28 used DArTseq genotypic and multi-environment phenotypic data to demonstrate positive contributions of exotic germplasm to lines derived from crosses of exotics with CIMMYT’s best elite lines. Genomic-based prediction using 8416 Mexican and 2403 Iranian landraces from CIMMYT’s germplasm bank estimated prediction accuracies from 0.41 to 0.65 for Mexican, and from 0.18 to 0.65 for Iranian landraces31. Saint Pierre et al.32 characterized 803 spring wheat lines, including elite germplasm and diverse accessions, to develop models for genomic prediction of phenology traits and grain yield, and to predict performance of lines in environments where the lines were not tested. Sehgal et al.30 selected 200 diverse gene bank accessions out of 1423 spring bread wheat accessions for use in pre-breeding and allele mining for candidate genes for drought and heat stress tolerance. Finally, Sehgal et al.47 described efforts to identify genomic regions with stable expression and their epistatic interactions for grain yield and yield stability in a large panel of elite wheat under multiple environments via a genome-wide association mapping approach. These multiple studies exemplify the value of this germplasm that is now easier to utilize and exploit, thanks to the resources generated in the present study.
Rapid human population growth, climate change, and the need to balance increasing agricultural production with increased environmental sustainability make it necessary to optimize the use of available resources. Native allelic variation for relevant breeding traits is one such resource. The analysis provides a basis for targeted exploration and allele mining activities moving forward. Diversity per se is of limited value for breeding, instead the value lies in the understanding of diversity, and the identification and use of diversity associated with breeder relevant traits. There are a number of paradigms currently in use to better understand and identify breeder relevant diversity. Before the advent of widespread genomic characterization core collections were proposed as a model for mining representations of general diversity, these have evolved to use genomic data in their definition as more widespread characterization has become available48,49,50. Another approach, reflecting landrace adaptation to local environments, was the FIGS (Focused Identification of Germplasm Strategy)51 where passport derived collection site variables were used to identify materials of potential interest for phenotypic evaluation for specific environment-associated traits. More recent analysis has extended and revised these approaches to incorporate in-depth understanding and application of genomics. In maize, passport data, associated climate variables from collection sites are being used in conjunction with genome-wide fingerprint data to identify alleles from broad germplasm collections associated with breeder relevant parameters52,53. Using this information and screening against genomic profiles of existing elite germplasm enables the identification of both previously unhighlighted standing variation of breeding relevance existing within elite germplasm and also breeder relevant diversity that can then be introgressed into breeding pools using appropriate strategies (S. Hearne pers comm). Taking these parallels and moving forward with wheat, there is a clear opportunity to use the understandings derived from comprehensive genomic characterization, together with associated data, to define and implement clear strategies to explore, and use relevant genetic diversity for breeding in a more targeted data-driven manner.
The genomic data and analysis tools made public with this paper can assist wheat researchers to discover and use functional diversity that may be essential for meeting these challenges. The massive scale of the genotypic data, describing nearly 80,000 publicly available germplasm accessions, offer ample scope for further analyses, not only to understand selection footprints and possible genetic diversity bottlenecks in current elite germplasm, but to leverage relevant diversity from the shelves of germplasm vaults into the hands of breeders. The analyses conducted and described herein, plus examples cited from recent literature, demonstrate the value of molecular data to enrich current passport records and drive the transformation of germplasm banks from museums into strategically, effectively used genetic resource centers.
Plant material and DNA isolation
We explored a total of 79,191 wheat samples; 50,053 from the CIMMYT and 29,138 from the ICARDA germplasm banks. The material included landraces, elite breeding lines, cultivars, primary synthetics, synthetic derivatives, genetic stocks, and wheat wild relatives. The complete list of material is provided in Supplementary Data 1. We randomly selected five seeds of each accession number and grew them at CIMMYT greenhouses in Mexico for 2 weeks. We harvested young leaves of a single plant per accession number, froze them at −80 °C, and lyophilized for 24 h. To track and organize such a large number of accessions, we used CIMMYT’s DNA Sample Tracker System, a platform specifically developed to assist in the tracking of samples from seed to DNA. Genomic DNA was extracted in 96-well plate format from lyophilized leaves using a modified cetyltrimethyl-ammonium bromide method54. DNA quality and concentration were determined by electrophoresis on 1% agarose gels.
High-throughput genotyping using the DArTseq™
We use DArTdb (Diversity Arrays Technology’s database and Laboratory Information Management System) to track the DNA samples from wet lab analysis through to genotyping results. We employed a high-throughput genotyping method using DArTseq™ technology33 to genotype all samples. In this technology, the allele-calling pipeline does not require a reference genome that offers an unbiased method to assess genetic diversity in a large collection of accessions, as the one we have analyzed. It might not be the most suitable approach for other investigations, in which having a free reference calling or not using a fully repeatable method like a chip or array it could be a disadvantage. But, considering the objectives of this study and the exotic material we are analyzing, we found that DArTseq was the most appropriate genotyping approached to use at the beginning of the SeeD project. We genotyped ~20% of the samples at the DArT laboratory in Australia and 80% at the Genetic Analysis Service for Agriculture (Spanish acronym SAGA) in Mexico. The first step of library preparation is genomic complexity reduction of the samples through a digestion/ligation reaction using a combination of two restriction enzymes, PstI and HpaII. A PstI-compatible adapter include the Illumina flowcell attachment sequence, the sequencing primer (AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT), and varying length barcode regions. The reverse adapter contain the flowcell attachment region and the HpaII-compatible overhang sequence (CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCTCGG). Only fragments containing PstI-HpaII ends are amplified. After the PCR reaction, equimolar amounts of amplification products from each sample of the 96-well microtiter plate were bulked together, purified, and quantified, followed by sequencing of 77 cycles on Illumina Hiseq 2500 (Illumina Inc., San Diego, CA). The sequences were processed using proprietary DArT analytical pipelines. In the primary pipeline, the FASTQ files were first processed to filter poor-quality sequences by applying two filters: (1) a more stringent filter performed on barcode sequences using a Phred quality score of 30 (representing base call accuracy of 99.9% for at least 75% of the bases), and (2) on the rest of the sequence a Phred quality score of 10 (representing base call accuracy of 90% for at least 50% of the bases). The assignment of sequences to specific samples carried in the barcode split step is therefore very reliable. Approximately 2 million sequences per barcode/sample were used for marker discovery, of which 500,000 unique sequences collapsed into FASTQCOL files. The unique sequences were then identified and clustered by sequence similarity at a distance threshold of three base variations, using DArTsoft14 plugin in KDCompute application (http://www.kddart.org/kdcompute.html). The sequence clusters were then parsed into SNP and SilicoDArT markers using a range of metadata parameters derived from the quantity and distribution of each sequence across all samples in the analysis. One of the crucial parameters is balance of allele counts within the locus across the whole population under study, but there are many additional parameters involved in marker selection. The marker parsing algorithm was trained using data generated on DArTseq platform for over 1000 mapping populations across a broad range of species, including several hundred maps generated on wheat populations at three levels of ploidy reported in this paper. The training process enabled clear discrimination between allelic variants and sequence variation due to paralogous sequences, confirmed by segregation of markers in agreement with Mendelian distributions. DArTsoft14 enables additional tuning of the analysis process to specific material/genome, as it offers 43 parameters for sequence selection/filtering, SNP, and SilicoDArT marker selection and reproducibility calculations.
Most accessions were genotyped once, with a single representative plant per accession number. However, 23% (667 CWR, 4,057 tetraploid and 13,466 hexaploids) of the DNA samples were genotyped multiple times as technical replicates, which enabled calculation of reproducibility scores for each candidate marker. Thus, the total number of libraries analyzed was 97,381. The main parameters to select the markers were call rate (the proportion of samples with genotypic score, i.e. not recorded as missing data) with the threshold of 0.5, and average reproducibility (the proportion of technical replicate assay pairs for which the marker score is consistent) at least 0.95. Similar filtering parameters were used for SilicoDArT markers, but with call rate selection >80%.
DArTsoft14 exports two types of markers, SilicoDArT and SNP. SilicoDArT markers represent presence/absence of restriction fragments of a particular sequence in genomic representations. The PAV acronym has been used for these markers in some reports for genotyping-by-sequencing methods. However, as PAV is a commonly used term to describe presence/absence of a section of DNA in the genome, applying the same term to presence/absence of fragments in genomic representations is a source of confusion. SilicoDArTs are extracted from the sequence data using the DArT proprietary algorithm in DArTsoft14 software. SilicoDArTs are genetically dominant markers, analogous to microarray DArTs, but extracted in silico from sequences, hence the name. There are multiple molecular bases for SilicoDArT markers, with the PAV (absence of DNA sequence in the genome) being the least frequent one. SNPs in the recognition site of the restriction enzymes used in complexity reduction are usually the most common cause of SilicoDArT markers. Indels, both in recognition sites and within restriction fragments delineated by those sites, are also a frequent cause for SilicoDArTs. Cytosine methylation polymorphism within restriction enzyme recognition sites (when using methylation sensitive enzymes for complexity reduction) are responsible for varying proportions of SilicoDArTs, with the proportion of SilicoDArTs resulting from this type of molecular mechanism increasing with the genome size, with PstI site methylation being responsible for <10% of DArT markers small genome Arabidopsis thaliana55. SilicoDArT’s ability to detect methylation variation is very important as it complements the SNP-based genome profiling by providing some insight into epigenetic variation. SilicoDArTs also outperform SNPs in most deep phylogenetics analyses56.
SNP markers are identified de novo by comparing the sequences of fragments present in genomic representations (libraries) of samples processed in DArTsoft14. SNP markers are identified and called completely independently of any reference genome. These two elements (de novo calling and independence from the reference genome) make DArTseq SNP markers particularly robust and practically free from ascertainment bias that plagues many other genotyping technologies.
In the diversity analysis of hexaploid and tetraploid groups, we used SNP markers because it has more resolution for similar samples genetic background. Then, for CWR, which include more diverse germplasm with 11 different genome constitutions, we used SilicoDArT markers that perform better than SNP in deep phylogenetic studies.
Alignment on the genome references
The sequence data of molecular markers generated were processed with the dartR packagev1.0.5 (ref. 57) and converted to a SNPRelate CoreArray Genomic Data Structure (GDS)58 before exporting to plink bed format.
Nucleotide sequences for the DArT alleles were extracted from the markers sequence file and transformed into FASTA format using an in-house Python script. Adaptor trimming (performed by the same script) finds matches of at least 6 nt between the adaptor and the 3′ of both DArT allele sequences. The resulting FASTA was then used for downstream alignment.
A reciprocal Bowtie2 (ref. 59) alignment strategy was used to map the markers to the genomic sequences. Markers were first aligned to the bread wheat IWGSC RefSeq v1.0. for all three biological categories (domesticated hexaploids, domesticated tetraploids, and CWR) and to the durum wheat Svevo reference for the tetraploid group using end-to-end alignment. Unmapped reads were realigned using local alignment. Bowtie2 version 22.214.171.124 was used with default parameters with the following exceptions: –very-sensitive, -p 24 and –k 10, and –very-sensitive-local. Samtools 1.5 (ref. 60) was used to convert sam to bam, with the resultant files then merged using samtools merge and their output parsed with a Python script to extract the genomic alignment regions. Bowtie2 with –very-sensitive-local, -L 18, and –p 24 was then run to align these against the original reads. The output of this step was then parsed and compared to the alignments of the previous step. Alignments were parsed using the same Python script and only alignments where both DArT alleles agreed and the alignment was reciprocal were taken forward. For the remaining alignments, the number of mismatches was calculated (ignoring the SNP position) and the alignment with the least number of mismatches was written to a map plink file. A custom Python script was then used to extract the corresponding entries from the initially generated ped plink file using the recently created map file and produce a plink ped file containing genomic coordinates. Plink v1.90b4 was used to convert the ped file to vcf format, the vcf file was annotated using SnpEff61, and vcftools was used to generate SNP density coverage statistics.
Genetic consensus map
The genetic consensus map was built based on 81 individual genetic maps using a DArT markers consensus map software developed by F. Detering (DArT PL unpublished). The software requires the following inputs: (i) a reference map with one linkage group and marker positions per chromosome, and (ii) set of linkage groups from individual populations with marker positions and chromosome assignment for each group. The construction procedure uses the following pseudo-code algorithm: (i) initialize consensus map with the seed map and (ii) for each chromosome, find subset of linkage groups for this chromosome and repeat until subset is empty for each group in subset. The process requires at least three markers in common with the consensus map and correlates the positions of common markers with the consensus map. The group with the highest commonality (correlation × log [number of common markers]) is identified, and if the correlation is larger than 0.5, all markers are joined to the consensus map by linear interpolation. The group is removed from the subset and the process is repeated. Using this iterative process, DArT consensus map version 4 has 105,122 markers and is accessible at https://www.diversityarrays.com/technology-and-resources/genetic-maps/.
Data cleaning filters
After allele frequency estimation, three filters were applied to the SNP data: (1) selection of markers with proportion of missing values ≤0.50; (2) selection of markers MAF > 0.001; and (3) selection of accessions with proportion of missing values ≤0.50 (for hexaploids and tetraploids) or 0.75 (for wild relatives). In the case of SilicoDArT markers, we instead used a filter to select markers with proportion of missing values ≤0.80.
For the genetic diversity analysis we used the allele frequencies of the markers to calculate the expected and observed heterozygosity, inbreeding coefficient, Shannon entropy index, MRD for SNP data, and Jaccard distance for SilicoDArT data.
for an ith diploid marker (locus), and
the average over all loci for the population. The index summarizes genetic variation and it reaches a 0.5 value for diploid loci when the allelic frequencies are equal to 0.5, maximum of diversity. We used 2× he to describe the diversity on a 0 to 1 scale.
Observed heterozygosity, hoi, is the proportion of heterozygotes at locus ith, and it is averaged for the population characterization, ho. Inbreeding and other evolutionary processes affect ho, and comparison with he produces the inbreeding coefficient f for a locus:
and their average value for a population. The f coefficient is the maximum likelihood estimator of inbreeding under Hardy–Weinberg equilibrium63.
We used the Shannon diversity index for the ith locus:
and its average value for the population. We used the base-2 logarithm as when the allele frequencies are equal to 0.5 the index value is 1.0, maximum of diversity.
Genetic distances between individuals
Based on its good mathematical and genetic properties14, we selected the MRD to calculate the genetic distance between two individuals x and y, measured by a set of L SNP markers:
When using SilicoDArT data, we used the Jaccard distance, the ratio of number of agreements (present, present) divided by the total number of loci comparisons excluding the agreement (absent, absent):
where n is the number of agreements or disagreements.
We used the MDS statistical method to represent distances (measured into P > 3 dimensions) into three dimensions. MDS64 is a multivariate method for dimension reduction whose objective function, to be minimized, is the sum of squared differences of the distance between pairs of objects observed in P dimensions, minus an estimated distance between the same objects measured into two or three dimensions. We used two algorithms for the MDS analysis: (1) for hexaploids, we used the classical approach in which, to avoid computer memory issues, a matrix basic algorithm65 is applied to obtain a solution (60k × 60k distance matrix); and (2) the SMACOF66 solution (using a majorization algorithm, minimizing the same objective function as in the classical solution) was used with tetraploids (20k × 20k) and wild relatives (7k × 7k) matrices.
Cluster analysis and FST computation
We implemented an iterative hierarchical cluster analysis to group the accessions based on genetic diversity. This process starts by considering n (the size of the whole population being clustered) clusters. At each iteration, the method joins the nearest (minimum distance) two accessions, or a group and an accession, or two nearest groups to create n1, n2, …, 2, and 1 final cluster, where genetic distance is maximized between clusters and minimized within clusters. To identify the appropriate number of clusters that best explain the genetic distances in the original collection, we used the changes in pseudo F statistic67, i.e., the quotient between the variance between clusters divided by the variance within clusters. At each clustering level, we described the genetic diversity using the AMOVA both between and within clusters. For each clustering, we also analyzed the FST values using sliding window and considered their chromosome position to identify putative genomic regions driving the differences in the genetic diversity between and within clusters.
To understand which alleles contribute to the cluster subdivisions in each of the three main groups (CWR, tetraploids, and hexaploids), we computed FST calculation using vcftools v0.1.15 (ref. 68). For each cluster subdivision, a list of individuals was generated and calculations were performed, using FST window size of 1 Mb. Results were then loaded into R and plotted using the ggplot2 library. A scatter plot was generated, where x is the BIN_START, y is the WEIGHT_FST and each chromosome is plotted and colored separately. A geometric smooth was also added with a span = 0.1.
Building core subsets
Core subsets are a sampling solution to a germplasm bank manager’s challenge of managing big collections. The idea, from Brown24, is to look for a 10 or 20% subset of accessions representing the diversity of the whole collection. We followed the strategy proposed by Franco et al. (refs. 69,70) to form 20% subsets for genetic analyses, although the method allows formation of smaller or lager subsets according to the needs of the researcher. Briefly, accessions were grouped based on their pair distances (MRDs) and Ward71 minimum variance within groups clustering method, before assigning to each cluster a number of genotypes to be sampled that was proportional to the diversity of the cluster, measured as the average value of MRD distances within the group (D-method). Finally, 1000 candidate samples were extracted using stratified random sampling, and the most diverse candidate sample (the sample showing the maximum of average distance) was selected to be the core subset.
Analysis of molecular variance
The AMOVA analysis was challenging due to the specific markers, even after the filtering process. When comparing hexaploid, tetraploid, and CWR biological groups, we could use a defined number of markers that were informative for those three groups when together, but a different set of markers would be informative when comparing only a pair of them. To address this, we performed different AMOVA analyses: (1) analysis using all informative (polymorphic) markers for all comparisons, (2) analysis using only the informative markers for each specific comparison between pairs, even if a marker was not informative for one of the elements in the comparison, and (3) analysis using only the informative markers for all the groups or categories being compared.
AMOVA analyses were done both per locus (useful to identify different groups) and across all of them (a more general test). We used the AMOVA method as proposed by Nei72, and posteriorly described by Berg and Hamrick73. HT is defined as the genetic diversity in the whole populations, that is, the average value for he for the pooled population, and Hs is defined as the average value of the within subpopulation genetic diversity values:
is the among subpopulations genetic diversity, and the ratio:
is the proportion of the total diversity distributed among populations. FST does not own an identified statistical distribution, thus a way to determine its significance is using permutation tests, that is, obtaining an estimation of the FST statistic under the null hypothesis (H0: there are not biological subpopulations), and comparing the real observed value with the 90, 95, or another significant percentile of the null distribution. To obtain the null distribution, 1000 random permutations of genotypes (and their associated allelic frequencies) across biological groups were obtained and their FST values calculated.
Genome-wide association scans
We subsampled 3870 samples from the diversity analysis to phenotype for GPC and SDS sedimentation at the Wheat Quality laboratory at CIMMYT. We obtained a total of 145,422 SNPs by DArTSeq platform. We filtered to 46,594 SNPs that met the criteria RepAvg ≥ 0.95, MAF ≥ 0.01, missing rate ≤ 0.6, and heterozygosity rate ≤ 0.2. For high-quality 46,594 SNPs dataset, we firstly align it to the wheat reference genome, 31,694 SNPs across the wheat genome were obtained with 11,751, 13,441, and 6502 SNPs distributed on A, B, and D genome separately, secondly, the dataset was compared with consensus map, 3447 SNPs were obtained on A, B, and D genome with 1,234, 1,793, and 420 SNPs, finally, there are 8.62% SNPs couldn’t be mapped. Combined with the two mapped data sets, 35,141 SNPs across the wheat genome were retained for further study. We performed genome-wide association analysis on 35,141 SNPs dataset using an iterative usage of fixed and random model circulating probability unification74 implemented by R software with correction of kinship, including the first three PCA values as fixed effects.
In this study, we used visualization tools and interactive data repository to handle the large data volumes generated. One of the tools is Flapjack application that provides interactive visualizations of high-throughput genotypic data, allowing for rapid navigation and comparisons between lines, markers, and chromosomes. We exported data sets created in Flapjack or Germinate for visualization using CurlyWhirly (https://ics.hutton.ac.uk/curlywhirly), a tool that we hereby release for use by the research community. CurlyWhirly is a 3D visualization tool that handles large-scale genetic diversity data with plots containing hundreds of thousands of data points. To explore data sets in detail, a comprehensive hierarchical categorization and filtering system allows for fine-grained filtering and selection of data points. Furthermore, CurlyWhirly allows export of screenshots and videos of the data, with associated categorical color keys included. 3D-based multi-select functionality allows selection of data points within a given distance from a defined point, and export of these data points to a file. CurlyWhirly links smoothly with Germinate and Flapjack, providing many options for sub-setting, analysis, and visualization of large data sets.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Data supporting the findings of this work is available in the Supplementary Information files and CIMMYT Dataverse repository (https://data.cimmyt.org/dataset.xhtml?persistentId=hdl:11529/10548030). We also stored the same data into Germinate (http://germinate.cimmyt.org/wheat/), which are accessible after a brief registration in the website. All data sets generated and analyzed during the current study are available from the corresponding author upon request. The data sets created in Flapjack or Germinate can be visualized using CurlyWhirly (https://ics.hutton.ac.uk/curlywhirly). A reporting summary for this article is available as a Supplementary Information file. All biological material is available at the CIMMYT and ICARDA germplasm bank upon on-line request at https://www.cimmyt.org/resources/seed-request/ or https://indms.icarda.org/. Records for all germplasm accessions with DOIs included in this study can also be accessed through the Global Information System of the International Treaty on Plant Genetic Resources for Food and Agriculture at https://ssl.fao.org/glis/. Publicly available data used in this manuscript are IWGSC RefSeq v1.0 (https://wheat-urgi.versailles.inra.fr/Seq-Repository/Assemblies) and durum wheat genome (cv. Svevo) (https://www.interomics.eu/durum-wheat-genome). The detailed description of all parameters and settings used in the marker calling pipeline cannot be provided given the proprietary nature of the software, but access to the software can be negotiated and provided free for testing purposes by Diversity Arrays Technology Pty Ltd by contacting firstname.lastname@example.org. The source data underlying Figs. 1–5 are provided as a Source data file.
The CurlyWhirly visualization tool is described and available for download at https://ics.hutton.ac.uk/curlywhirly/ and the underlying code are available at GitHub (https://github.com/cropgeeks/curlywhirly). The Flapjack analysis and visualization tool is described and available for download at https://ics.hutton.ac.uk/flapjack/ and the underlying code are available at GitHub (https://github.com/cropgeeks/flapjack). Free R software environment used for the diversity and clustering analysis are available at GitHub (https://github.com/jfranco1951/Genetic-Diversity).
Goel, S., Yadav, M., Singh, K., Jaat, R. S. & Singh, N. K. Exploring diverse wheat germplasm for novel alleles in HMW-GS for bread quality improvement. J. Food Sci. Technol. 55, 3257–3262 (2018).
Velu, G., Singh, R. P., Huerta, J. & Guzmán, C. Genetic impact of Rht dwarfing genes on grain micronutrients concentration in wheat. F. Crop. Res. 214, 373–377 (2017).
Heuzé, V., Tran, G., Renaudeau, D., Lessire, M. & Lebas, F. Wheat Grain. Feedipedia, a Programme by INRA, CIRAD, AFZ and FAO https://www.feedipedia.org/node/223 (2015).
Talebnia, F., Karakashev, D. & Angelidaki, I. Production of bioethanol from wheat straw: an overview on pretreatment, hydrolysis and fermentation. Bioresour. Technol. 101, 4744–4753 (2010).
Swain, M. & Mohanty, S. Bioethanol Production From Corn and Wheat: Food, Fuel, and Future 1st edn, 45–59 (Academic, 2018).
Peng, J. H., Sun, D. & Nevo, E. Domestication evolution, genetics and genomics in wheat. Mol. Breed. 28, 281–301 (2011).
Kilian, B., Martin, W. & Salamini, F. in Evolution in Action: Case studies in Adaptive Radiation, Speciation and the Origin of Biodiversity (ed Glaubrecht, M.) 137–166 (Springer, Berlin Heidelberg, 2010).
Kilian, B., Özkan, H., Pozzi, C. & Salamini, F. in Plant Genetics and Genomics: Crops and Models 7 (eds Feuillet, C. & Muehlbauer, G. J.) 81–119 (Springer Science+Business Media, New York, 2009).
Kantar, M. B., Nashoba, A. R., Anderson, J. E., Blackman, B. K. & Rieseberg, L. H. The Genetics and Genomics of Plant Domestication. Bioscience 67, 971–982 (2017).
Maccaferri, M. et al. Durum wheat genome reveals past domestication signatures and future improvement targets. Nat. Genet. 51, 885–895 (2019).
Wang, S. et al. Characterization of polyploid wheat genomic diversity using a high-density 90 000 single nucleotide polymorphism array. Plant Biotechnol. J. 12, 787–796 (2014).
Tanksley, S. D. & McCouch, S. R. Seed banks and molecular maps: unlocking genetic potential from the wild. Science 277, 1063–1066 (1997).
Cox, T. S. Deepening the wheat gene pool. J. Crop Prod. 1, 1–25 (1997).
Reif, J. C. et al. Wheat genetic diversity trends during domestication and breeding. Theor. Appl. Genet. 110, 859–864 (2005).
McCouch, S. et al. Agriculture: feeding the future. Nature 499, 23–24 (2013).
Bhatta, M., Morgounov, A., Belamkar, V., Poland, J. & Baenziger, P. S. Unlocking the novel genetic diversity and population structure of synthetic Hexaploid wheat. BMC Genomics 19, 591 (2018).
Milner, S. G. et al. Genebank genomics highlights the diversity of a global barley collection. Nat. Genet. 51, 319–326 (2019).
Hajjar, R. & Hodgkin, T. The use of wild relatives in crop improvement: a survey of developments over the last 20 years. Euphytica 156, 1–13 (2007).
Maxted, N., Kell, S., Ford-Lloyd, B., Dulloo, M. & Toledo, Á. Toward the systematic conservation of global crop wild relative diversity. Crop Sci. 52, 774–785 (2012).
Dempewolf, H. et al. Past and future use of wild relatives in crop breeding. Crop Sci. 57, 1070–1082 (2017).
Müller, T. et al. Unlocking the diversity of genebanks: whole-genome marker analysis of Swiss bread wheat and spelt. Theor. Appl. Genet. 131, 407–416 (2018).
Langridge, P. & Waugh, R. Harnessing the potential of germplasm collections. Nat. Genet. 51, 200–201 (2019).
Pixley, K. V. et al. Genome editing, gene drives, and synthetic biology: will they contribute to disease-resistant crops, and who will benefit? Annu. Rev. Phytopathol. 57, 165–188 (2019).
Brown, A. Core collections: a practical approach to genetic resource management. Genome 31, 818–824 (1989).
Vikram, P. et al. Unlocking the genetic diversity of Creole wheats. Sci. Rep. 6, 23092 (2016).
Takenaka, S., Nitta, M. & Nasuda, S. Population structure and association analyses of the core collection of hexaploid accessions conserved ex situ in the Japanese gene bank NBRP-Wheat. Genes Genet. Syst. 93, 237–254 (2019).
Romay, M. C. et al. Comprehensive genotyping of the USA national maize inbred seed bank. Genome Biol. 14, R55 (2013).
Singh, S. et al. Harnessing genetic potential of wheat germplasm banks through impact-oriented-prebreeding for future food and nutritional security. Sci. Rep. 8, 12527 (2018).
Pixley, K. et al. CIMMYT’s seeds of discovery initiative: harnessing biodiversity for food security and sustainable development. Indian J. Plant Genet. Resour. 31, 1 (2018).
Sehgal, D. et al. Exploring and mobilizing the gene bank biodiversity for wheat improvement. PLoS ONE 10, 1–18 (2015).
Crossa, J. et al. Genomic prediction of gene bank wheat landraces. G3 6, 1819–1834 (2016).
Saint Pierre, C. et al. Genomic prediction models for grain yield of spring bread wheat in diverse agro-ecological zones. Sci. Rep. 6, 1–11 (2016).
Sansaloni, C. et al. Diversity Arrays Technology (DArT) and next-generation sequencing combined: genome-wide, high throughput, highly informative genotyping for molecular breeding of Eucalyptus. BMC Proc. 5, P54 (2011).
Appels, R. et al. Shifting the limits in wheat research and breeding using a fully annotated reference genome. Science 361, eaar7191 (2018).
Dreisigacker, S. et al. SSR and pedigree analyses of genetic diversity among CIMMYT wheat lines targeted to different megaenvironments. Crop Sci. 44, 381–388 (2004).
Dreisigacker, S. et al. Genetic structures of the CIMMYT international yield trial targeted to irrigated environments. Mol. Breed. 29, 529–541 (2012).
Villareal, R. L., Rajaram, S., Mujeeb-Kazi, A. & Toro, E. The effect of Chromosome 1B/1R translocation on the yield potential of certain spring wheats (Triticum aestivum L.). Plant Breed. 106, 77–81 (2006).
Harlan, J. R. Ethiopia: a center of diversity. Econ. Bot. 23, 309–314 (1969).
Kilian, B. et al. in Wild Crop Relatives: Genomic and Breeding Resources: Temperate Fruits (ed Kole, C.) 1–76 (Springer, Berlin, Heidelberg, 2011).
Keilwagen, J. et al. Separating the wheat from the chaff – a strategy to utilize plant genetic resources from ex situ genebanks. Sci. Rep. 4, 14–18 (2014).
Dorofeev, V., Filatenko, A., Migushova, E., Udaczin, R. & Jakubziner, M. Flora of cultivated plants of the USSR (Kolos, Leningrad, 1979).
van Slageren, M. W. & International Center For Agricoltural Research In the Dry Areas. Wild Wheats: a Monograph of Aegilops L. and Amblyopyrum (Jaub. & Spach) Eig (Poaceae), Vol. 9 (Wageningen Agricultural University Papers, 1994).
Nakamura, S. et al. A wheat homolog of MOTHER of FT and TFL1 acts in the regulation of germination. Plant Cell 23, 3129–3215 (2011).
Kumar, A. et al. Genome wide genetic dissection of wheat quality and yield related traits and their relationship with grain shape and size traits in an elite × non-adapted bread wheat cross. PLoS ONE 14, e0221826 (2019).
Kumar, J. et al. Genetics of Fe, Zn, β-carotene, GPC and yield traits in bread wheat (Triticum aestivum L.) using multi-locus and multi-traits GWAS. Euphytica 214, 219 (2018).
Wrigley, C., Bekes, F. & Bushuk, W. in Gliadin and Glutenin the Unique Balance of Wheat Quality (eds Wrigley, C., Bekes, F. & Bushuk, W.) 3–32 (2006).
Sehgal, D. et al. Identification of genomic regions for grain yield and yield stability and their epistatic interactions. Sci. Rep. 7, 1–12 (2017).
Holbrook, C. C., Anderson, W. F. & Pittman, R. N. Selection of a core collection from the U.S. germplasm collection of peanut. Crop Sci. 33 859–861 (1993).
Upadhyaya, H., Laxmipathi Gowda, C. & Dvssr, S. Plant genetic resources management: collection, characterization, conservation and utilization. J. SAT Agric. Res. 6, 1–12 (2007).
Xu, Y. in Molecular Plant Breeding, 151–194 (CAB International, Cambridge, 2010).
Khazaei, H., Street, K., Bari, A., Mackay, M. & Stoddard, F. L. The FIGS (Focused Identification of Germplasm Strategy) approach identifies traits related to drought adaptation in vicia faba genetic resources. PLoS ONE 8, e63107 (2013).
Romero Navarro, J. A. et al. A study of allelic diversity underlying flowering-time adaptation in maize landraces. Nat. Genet. 49, 476–480 (2017).
Gates, D. J. et al. Single-gene resolution of locally adaptive genetic variation in Mexican maize. bioRxiv 706739. https://doi.org/10.1101/706739 (2019).
Hoisington, D., Khairallah, M. & Gonzalez-de-Leon, D. CIMMYT Applied Molecular Genetics Laboratory (CIMMYT, México, 1994).
Wittenberg, A. H. J. et al. Validation of the high-throughput marker technology DArT using the model plant Arabidopsis thaliana. Mol. Genet. Genomics 274, 30–39 (2005).
Alam, M., Neal, J., O’Connor, K., Kilian, A. & Topp, B. Ultra-high-throughput DArTseq-based silicoDArT and SNP markers for genomic studies in macadamia. PLoS ONE 13, e0203465 (2018).
Gruber, B., Unmack, P., Berry, O. & Georges, A. in Beginning DAX with Power BI, Ch. 1, 1–25 (Apress, 2019).
Zheng, X. et al. A high-performance computing toolset for relatedness and principal component analysis of SNP data. Bioinformatics 28, 3326–3328 (2012).
Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357 (2012).
Li, H. et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics 25, 2078–2079 (2009).
Cingolani, P. et al. A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3. Fly 6, 80–92 (2012).
Berg, E. E. & Hamrick, J. L. Fine-scale genetic structure of a turkey oak forest. Evolution 49, 110–120 (1995).
Weir, B. S. Genetic Data Analysis II: Methods for Discrete Population Genetic Data, 150–156 (Sinauer Associates, Sunderland, MA, 1996).
Mardia, K. V, Kent, J. T. & Bibby, J. M. Multivariate Analysis (Academic, New York, 1979).
Dryden, I. L. & Mardia, K. V. Statistical Shape Analysis: With Applications in R (Wiley, 2016).
De Leeuw, J. & Mair, P. Multidimensional scaling using majorization: SMACOF in R. J. Stat. Softw. 31, 1–30 (2009).
Harabasz, J. A dendrite method for cluster analysis AU - Caliński, T. Commun. Stat. 3, 1–27 (1974).
Weir, B. S. & Cockerham, C. C. Estimating F-statistics for the analysis of population structure. Evolution 38, 1358–1370 (1984).
Franco, J., Crossa, J., Taba, S. & Shands, H. A sampling strategy for conserving genetic diversity when forming core subsets. Crop Sci. 45, 1035–1044 (2005).
Franco, J., Crossa, J., Warburton, M. L. & Taba, S. Sampling strategies for conserving maize diversity when forming core subsets using genetic markers. Crop Sci. 46, 854–864 (2006).
Ward, J. H. J. Hierarchical grouping to optimize an objective function AU - ward. Joe H. J. Am. Stat. Assoc. 58, 236–244 (1963).
Nei, M. Analysis of Gene Diversity in Subdivided Populations. Proc. Natl Acad. Sci. USA 70, 3321–3323 (1973).
Berg, E. E. & Hamrick, J. L. Quantification of genetic diversity at allozyme loci. Can. J. For. Res. 27, 415–424 (1997).
Liu, X., Huang, M., Fan, B., Buckler, E. S. & Zhang, Z. Iterative usage of fixed and random effect models for powerful and efficient genome-wide association studies. PLOS Genet. 12, e1005767 (2016).
This work was implemented by CIMMYT as part of the Seeds of Discovery, Sustainable Modernization of Traditional Agriculture (Mas-Agro), and CGIAR Research Program WHEAT, in collaboration with ICARDA, INIFAP, NIAB, EI, and DArT, and made possible by the generous support of the Secretariat of Agriculture and Rural Development (SADER), Mexico, and the Newton Fund—Biotechnology and Biological Research Council (BBSRC), United Kingdom. We thank Sarah Hearn, Mohamed Fawzy Nawar, Prashant Vikram, Masahiro Kishii, Julio Huerta, and Maria Itria Abba for their valuable suggestions and support. Our sincere gratitude and recognition go to colleagues who performed crucial work in DArT, SAGA, and CIMMYT laboratories and glasshouses. Any opinions, findings, conclusion, or recommendations expressed in this publication are those of the author(s) and do not necessarily reflect the views of SADER, BBSRC, CRP WHEAT, or our respective institutions.
The authors declare no competing interests, except A.K. and J.C. who works at DArT Company.
Peer review information Nature Communications thanks Simon Krattinger, Peter Langridge and Klaus Mayer for their contribution to the peer review of this work. Peer reviewer reports are available.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Sansaloni, C., Franco, J., Santos, B. et al. Diversity analysis of 80,000 wheat accessions reveals consequences and opportunities of selection footprints. Nat Commun 11, 4572 (2020). https://doi.org/10.1038/s41467-020-18404-w
This article is cited by
Single nucleotide polymorphism (SNP) markers for genetic diversity and population structure study in Ethiopian barley (Hordeum vulgare L.) germplasm
BMC Genomic Data (2023)
Selective sweeps identification in distinct groups of cultivated rye (Secale cereale L.) germplasm provides potential candidate genes for crop improvement
BMC Plant Biology (2023)
Scientific Reports (2023)
Genomic studies of the additive and dominant genetic control on production traits of Euterpe edulis fruits
Scientific Reports (2023)
Identification of novel putative alleles related to important agronomic traits of wheat using robust strategies in GWAS
Scientific Reports (2023)