- Research article
- Open Access
DArT markers: diversity analyses, genomes comparison, mapping and integration with SSR markers in Triticum monococcum
© Jing et al; licensee BioMed Central Ltd. 2009
- Received: 09 February 2009
- Accepted: 30 September 2009
- Published: 30 September 2009
Triticum monococcum (2n = 2x = 14) is an ancient diploid wheat with many useful traits and is used as a model for wheat gene discovery. DArT (D iversity Ar rays T echnology) employs a hybridisation-based approach to type thousands of genomic loci in parallel. DArT markers were developed for T. monococcum to assess genetic diversity, compare relationships with hexaploid genomes, and construct a genetic linkage map integrating DArT and microsatellite markers.
A DArT array, consisting of 2304 hexaploid wheat, 1536 tetraploid wheat, 1536 T. monococcum as well as 1536 T. boeoticum representative genomic clones, was used to fingerprint 16 T. monococcum accessions of diverse geographical origins. In total, 846 polymorphic DArT markers were identified, of which 317 were of T. monococcum origin, 246 of hexaploid, 157 of tetraploid, and 126 of T. boeoticum genomes. The fingerprinting data indicated that the geographic origin of T. monococcum accessions was partially correlated with their genetic variation. DArT markers could also well distinguish the genetic differences amongst a panel of 23 hexaploid wheat and nine T. monococcum genomes. For the first time, 274 DArT markers were integrated with 82 simple sequence repeat (SSR) and two morphological trait loci in a genetic map spanning 1062.72 cM in T. monococcum. Six chromosomes were represented by single linkage groups, and chromosome 4Am was formed by three linkage groups. The DArT and SSR genetic loci tended to form independent clusters along the chromosomes. Segregation distortion was observed for one third of the DArT loci. The Ba (black awn) locus was refined to a 23.2 cM region between the DArT marker locus wPt-2584 and the microsatellite locus Xgwmd33 on 1Am; and the Hl (hairy leaf) locus to a 4.0 cM region between DArT loci 376589 and 469591 on 5Am.
DArT is a rapid and efficient approach to develop many new molecular markers for genetic studies in T. monococcum. The constructed genetic linkage map will facilitate localisation and map-based cloning of genes of interest, comparative mapping as well as genome organisation and evolution studies between this ancient diploid species and other crops.
- Simple Sequence Repeat Marker
- Hexaploid Wheat
- Polymorphism Information Content
- Segregation Distortion
- Simple Sequence Repeat Locus
Triticum monococcum (2n = 2x = 14), generally known as einkorn wheat, is an ancient diploid species domesticated in the Fertile Crescent ~10,000 years ago (. This species dominated human farming activities in the Neolithic period. However, the cultivation area gradually decreased during the Bronze Age due to domestication of tetraploid and hexaploid wheat . In modern times T. monococcum remains cultivated at low scale only in the mountainous areas of several Mediterranean countries. This species has not been bred intensively and therefore retained its genetic diversity .
Wild relatives of hexaploid wheat are known to be important sources of traits for wheat genetic improvement. T. monococcum (AmAm) is closely related to T. urartu (AuAu), the donor of the A-genome of hexaploid wheat [4–6]. Recently, T. monococcum has gradually been recognised as an attractive diploid model for exploitation of useful traits, discovery of novel genes and variant alleles, and functional genomics. Many traits have been examined in T. monococcum which can be useful for modern wheat breeding [7–9]. T. monococcum has also been successfully used for gene discovery in a subgenome map-based cloning approach, as exemplified by the cloning of the leaf rust resistance gene Lr10 [10, 11], the vernalisation genes VRN1 and VRN2 [12, 13], the domestication locus Q [14, 15], and a member of the senescence and nutrient remobilisation controlling NAC gene family . Natural and artificially mutagenised T. monococcum populations have been made available and were used to identify and map genes of agronomic importance [17, 18]. Furthermore, TILLING (Targeting Induced Local Lesions IN Genomes) and VIGS (Virus Induced Gene Silencing) platforms for functional genomics are under development in several laboratories (http://www.wgin.org.uk; http://www.plantsciences.ucdavis.edu/dubcovsky). Thus, in the foreseeable future T. monococcum is expected to play an important role in wheat genetic and genomic studies.
Globally, thousands of accessions of T. monococcum have been collected and retained in major germplasm stock centres. In order to use T. monococcum resources efficiently in programmes on genetic improvement of hexaploid wheat, it is necessary to assess diversity of this species at the genome level. For this, high-throughput molecular marker technologies are needed. T. monococcum has been shown to possess a high level of polymorphism at DNA marker loci. RFLP (Restriction fragment length polymorphism) and AFLP (Amplified fragment length polymorphism) markers have been developed and used for generating genetic linkage maps and for mutation mapping, map-based cloning, and genome synteny comparisons [4, 20–23]. These markers have also been used to resolve the site of the T. monococcum domestication . Microsatellite markers (also called simple sequence repeats or SSRs) have been tested in T. monococcum in comparison with hexaploid wheat and its A-genome donor diploid species T. urartu. This information has been used to produce a genetic map integrating RFLPs and SSRs [24, 25]. However, the aforementioned markers are primarily gel-based and sequence-dependent. The cost per data point, labour-intensive assay procedures and the limitation of polymorphism of the current marker technologies restricts their application to whole-genome scan approaches such as large-scale genotyping of germplasm collections, association mapping, pedigree analysis and QTL (Quantitative Trait Loci) Mapping As You Go .
Diversity Arrays Technology (DArT) has been developed as a sequence-independent and micro-array hybridisation-based marker system . DArT generates medium-density genome scans by scoring the presence versus absence of DNA fragments in representations of genomic DNA samples. It simultaneously determines hundreds to thousands of polymorphic loci in a single assay [27, 28]. Since its initial development in rice, DArT has been employed in genetic mapping, genotyping and diversity assessment in barley [28–31], Arabidopsis , cassava , sorghum , hexaploid and durum wheat [35–38], and approximately 30 other plant species (Diversity Arrays Technolgy P/L, unpublished data). DArT has also been used to study pan-genomic evolution in non-model organisms  because of its high-throughput and cost-effective nature.
We report here the results of a study aimed to (1) develop a T. monococcum diversity array (DArT) for high-throughput genome-wide genotyping, (2) assess the utility of the DArT technology for analysis of genetic diversity in a representative collection of T. monococcum accessions, (3) compare the relationships between the A m - genome and other Triticum genomes using DArT markers, (4) produce a genetic linkage map for T. monococcum integrating DArT and SSR markers, and (5) refine the genome locations of two morphological trait loci.
A total of 1536 DArT clones were developed from a Pst I/Taq I representation generated from a mixture of DNA of two T. monococcum accessions MDR002 and MDR308 . These two accessions were the parents for a large mapping population, which had previously been genotyped with SSR markers and used for mapping several agronomically important traits [8, 9]. In a parallel project, a substantial number of DArT clones were developed from genomic representations of other Triticum species with different ploidy levels (Triticarte P/L, unpublished). We combined clones from all projects to assemble a custom-designed array containing 1536 clones derived from the two T. monococcum accessions, 2304 clones derived from hexaploid wheats (including the Triticarte Wheat 2.3 array), 1536 clones derived from tetraploid durum wheat (including the Triticarte Durum 2.0 array), and 1536 clones derived from 15 Iranian accessions of T. boeoticum Boiss., which is the wild relative of T. monococcum (see Additional file 1; Ali Mehrabi, unpublished data).
Genetic diversity amongst T. monococcum accessions revealed by DArT
T. monococcum accessions used in this study
Year of collection
Transformable12, mapping population
EMS mutagenised population13
BAC library, genetic map, EST library, mapping populations
Polymorphism information content (PIC) values for 846 DArT markers developed from T. monococcum genome.
Number of DArTs
% total DArTs
The relationship between the quality and the performance of the 846 DArT markers developed from T. monococcum genome.
Number of markers
99.8 ± 1.2
98.8 ± 2.8
97.9 ± 3.7
99.0 ± 2.5
99.3 ± 2.0
99.2 ± 2.4
0.34 ± 0.14
0.32 ± 0.14
0.24 ± 0.14
0.13 ± 0.03
0.12 ± 0.02
0.31 ± 0.15
Relationships between the genomes of T. monococcum and related Triticum spp
Number and feature of polymorphic DArT markers identified in this study
Polymorphic among 16 accessions
Mean quality (%)
86.3 ± 9.6
86.7 ± 9.3
85.0 ± 10.6
88.7 ± 8.8
Mean call rate (%)
99.3 ± 2.1
99.1 ± 2.1
99.3 ± 2.1
99.1 ± 2.6
0.30 ± 0.14
0.32 ± 0.15
0.29 ± 0.15
0.32 ± 0.14
Polymorphic between MDR002 and MDR308
Mean quality (%)
84.1 ± 6.0
83.3 ± 4.6
82.3 ± 4.9
85.3 ± 5.6
Mean call rate (%)
93.8 ± 3.6
93.5 ± 2.8
93.1 ± 2.7
94.6 ± 3.0
0.42 ± 0.06
0.43 ± 0.05
0.43 ± 0.04
0.40 ± 0.07
Correlation between pairs of similarity matrices describing the relationships of T. monococcum accessions generated by using DArT markers from different origins.
Whole DArT set
Whole DArT set
Comparison of DArT markers hybridised to T. monococcum and hexaploid wheat genomes
Scored in T. monococcum
Scored in hexaploid wheat
Score in T. monococcum
Score in hexaploid wheat
Polymorphic in both ploidy
80.5 ± 6.9
96.6 ± 4.1
0.38 ± 0.1
0.51 ± 0.32
0.45 ± 0.33
Present in diploid, polymorphic in hexaploid
80.3 ± 7.4
97.9 ± 2.7
0.41 ± 0.11
1.00 ± 0.00
0.44 ± 0.27
Absent in diploid, polymorphic in hexaploid
82.0 ± 7.0
97.9 ± 2.5
0.44 ± 0.08
0.00 ± 0.00
0.67 ± 0.24
Present in hexaploid, polymorphic in diploid
78.3 ± 11.0
96.9 ± 5.7
0.27 ± 0.12
0.41 ± 0.29
1.00 ± 0.00
Absent in hexaploid, polymorphic in diploid
82.7 ± 10.0
96.9 ± 5.7
0.26 ± 0.11
0.57 ± 0.28
0.00 ± 0.00
Genetic mapping of DArT and microsatellite (SSR) loci
To confirm that DArT markers were inherited in a Mendelian manner, we constructed a linkage map for a cross between T. monococcum accessions MDR308 and MDR002 . Hybridising the array with a total of 94 F2 progeny from this cross as well as the two parental accessions identified 300 polymorphic DArT markers: 133, 71, 61 and 35 were derived from genomes of T. monococcum, hexaploid wheat, tetraploid wheat, and T. boeoticum, respectively (Table 4). The same T. monococcum mapping population was also genotyped using microsatellite markers mapped to the A sub-genome of hexaploid wheat . Out of 274 microsatellite markers analysed, 90 (32.8%) were polymorphic between the two parental T. monococcum accessions MDR002 and MDR308. Rates of polymorphism for different types of microsatellite markers were as follows: WMC - 41.9% (36 polymorphic markers out of 86 examined), CFA and CFD - 39.3% (11 out of 28), BARC markers - 38.2% (21 out of 55), GDM and WMS - 33.7% (28 out of 83), and DuPw - 13.6% (3 out of 22). The data for DArT and microsatellite markers were merged for construction of a genetic linkage map for T. monococcum.
Map length and genome coverage
Marker distribution amongst chromosomes
Features of a genetic linkage map for T. monococcum integrating DArT and SSR markers
Morphological trait locus
Distribution of DArT markers derived from genomes of different Triticum species
The distribution of DArT markers originated from genomes of various Triticum species across the seven chromosomes of T. monococcum.
Am map position
Fine-mapping of morphological trait loci
In T. monococcum, black awns and hairy leaves are two morphological traits known to be controlled by single dominant genes Ba and Hl, respectively. Our previous genetic study revealed a linkage between Ba and the SSR locus Xwmc336 on 1Am, and between Hl and the SSR locus Xcfd39 on 5Am . These two traits segregated in MDR002 × MDR308 F2 mapping population as single independent loci and therefore it was possible to refine the positions of Ba and Hl in T. monococcum genome. Previous estimations showed that the genetic distance was 21.5 cM between Ba and Xwmc336, and 17.4 cM between Hl and Xcfd39. Linkage analysis combining SSR and DArT markers confirmed that Ba was located at 80.09 cM on 1Am between the DArT marker locus wPt-2584 at 60.59 cM and the SSR locus Xgwmd33 at 83.76 cM, and Hl was located at 136.16 cM on 5Am between the DArT marker loci 376589 at 134.84 cM and 469591 at 138.77 cM.
The availability of a high density genetic linkage map for a species is essential for identifying QTLs of interest, isolation of genes by map-based cloning, comparative mapping, and genome organisation and evolution studies . We have developed polymorphic DArT markers from genome representations of two T. monococcum accessions, 15 T. boeoticum, and hexaploid and tetraploid Triticum species. The genetic linkage map of T. monococcum constructed in this study is the first map integrating DArT and SSR markers.
Determining genetic relationships between T. monococcum accessions and with hexaploid wheat varieties using DArT marker fingerprinting
DArT markers are typically developed from a representation which is generated from a pool of DNA samples from a number of accessions, cultivars or breeding lines which as a group cover the genetic diversity within a species or a group of closely related species . In the current study, DArT markers were initially generated from genomic representations of two T. monococcum accessions, parents of an F2 mapping population. In addition, this study took advantage of the existence of a large number of DArT markers previously developed from hexaploid, tetraploid and other diploid Triticum species.
The inclusion of DArT clones from various genomes meant the average PIC value of the data set (0.31) was lower than in comparable studies. For example, for barley, sorghum and cassava the values obtained were 0.38, 0.41 and 0.42, respectively [28, 33, 34]. However, the data provided useful information for comparison of Triticum genomes of different ploidy levels. In the genetic diversity assessment of 16 T. monococcum accessions, 20.6% (317 out of 1536) of the DArT markers developed from the two T. monococcum accessions were polymorphic. DArT markers developed from genomes of other Triticum species also displayed good polymorphism frequencies (10.68%, 10.22% and 8.2% for markers developed from hexaploid, tetraploid and diploid species, respectively) in T. monococcum. In hexaploid wheat, 15.3% (788 out of 5137) of DArT markers were found to be polymorphic when assessing the genetic diversity of 13 Australian cultivars . Similar studies in durum wheat and barley revealed only 9.6% and 10.4% of polymorphic DArTs, respectively [28, 36]. Thus, the group of 16 T. monococcum accession genotyped in this study appeared to be more genetically diverse than the bread and durum wheat collections assayed in those studies. Furthermore, most of the DArT markers whose genome locations have been determined in previous studies were located on homoeologous chromosomes of T. monococcum. Thus, DArT markers from related genomes were also useful in probing genetic diversity in T. monococcum. The custom-designed DArT array developed here can be used in studies focusing on comparison of the T. monococcum genome with genomes of other Triticum species.
Principal coordinate analysis of the 16 T. monococcum accession revealed that the site of collection is only partially correlated with genetic diversity. Most accessions used in this study have been genotyped with SSR markers in a previous study, and a similar pattern had been observed . Thus, DArT fingerprints are as useful for resolving the genetic relationships in T. monococcum as non-DArT based markers. One of the accessions, MDR650 (PI 355520) was found to be genetically distantly related to other T. monococcum accessions, which raised a question whether it is a true T. monococcum. However, MDR650 (PI 355520) possesses the three major traits of the domesticated einkorn wheat: larger and plumper seeds, a tough rachis preventing spikelets falling apart at maturity, and relatively easy threshing. These traits are absent in the wild species T. boeoticum. We have crossed MDR650 (PI 355520) with many other T. monococcum accessions and discovered that the crossability could reach 100% (data not shown). Furthermore, MDR650 (PI 355520) did not cluster with hexaploid wheat and was closer to the T. monococcum cluster. Thus, we still consider MDR650 (PI 355520) an accession of T. monococcum.
The relationships between the Am-genome of T. monococcum and those of hexaploid wheat T. aestivum and its sub-genome donor, T. urartu have been studied in different context. For instance, chromosome pairing and recombination were studied between homoeologous chromosomes 1A and 1Am, 3A and 3Am as well as 5A and 5Am and were shown to be collinear and differentiated at sub-structural level [20, 46]. Good micro-colinearity/colinearity at particular genetic loci has also been reported [47, 48]. Other studies as well as the present one demonstrate that many A-genome molecular markers could also be used for genetic studies in T. monococcum [24, 25]. However, their genome-wide use was not previously reported. The use of DArT markers allowed us to assess the relationships in a new perspective. We showed here that most of the DArT markers which are polymorphic in T. monococcum were either conserved or absent in hexaploid genomes, and vice versa, indicative of divergence of the Am-genome from the A-genome . On the other hand, many DArT markers originated from B- and D-genomes of hexaploid wheat could hybridise to the T. monococcum genomes and provide the polymorphism information in T. monococcum. Thus, at the homoeologous genomes level, there is a complex relationship between T. monococcum and hexaploid wheat.
T. monococcum genetic linkage maps
A T. monococcum genetic map has been previously constructed using MDR308 (DV92) as one of parental accessions by Dubcovsky et al (1996) . This map contains 335 markers, including RFLPs, isozymes, seed storage proteins, rRNA, and various morphological loci. The total length of this map is 1071.6 cM, the average chromosome length is 153.1 cM, and the average marker density is one marker per 3.2 cM. More recently, Singh et al (2007)  used a T. boeoticum × T. monococcum RIL population to construct another genetic linkage map integrating 177 SSR and RFLP markers, and two morphological trait loci. The total length of this map is 1262 cM, the average chromosome length is 180.3 cM, and the average marker density is one marker per 7.05 cM. In comparison, our current genetic map derived from linkage analysis of an F2 population from a cross between MDR308 and MDR002 integrates 274 DArT markers, 82 SSR markers and two morphological trait loci. This map spans over 1062.7 cM, with six chromosomes represented by single linkage groups and chromosome 4Am by three groups of linked markers. The average chromosome length is 151.8 cM, and the average marker density in the genome is one marker per 2.97 cM. Observed differences in lengths and marker densities for the three T. monococcum linkage maps may well be related to differences in the mapping populations, the types and error-rates of the genetic marker systems used, and/or the algorithms and mapping functions used to compute genetic distances. For example, Singh et al (2007)  used the Haldane's mapping function, whereas the Kosambi's mapping function was used in other cases.
The current genetic linkage is also very similar in length and in marker densities to the A-genome maps of hexaploid wheat constructed using the Kosambi's map function. In one case, 369 SSR markers were mapped onto a 944 cM A-genome with the marker density of one marker per 2.56 cM . In another study, 464 SSR markers were mapped onto a 1231 cM A-genome with the marker density of one marker per 2.65 cM . Recently DArT markers have also been developed and integrated with conventional markers i.e. SSRs, RFLPs and AFLPs in hexaploid wheat  and tetraploid wheat .
Genome organisation and segregation distortion
The Am-genome of T. monococcum is closely related to the Au-genome of T. urartu and to the A-genome of the hexaploid wheat [4–6]. This is reflected by the high transferability of SSR markers from hexaploid wheat to T. monococcum and the overall good colinearity of SSR arrangement along the chromosomes [8, 24]. Gaps are frequently observed in hexaploid wheat genetic linkage maps making use of SSR, RFLP and AFLP markers [49–52]. Similarly, Singh et al (2007)  observed four large gaps on linkage maps of chromosomes 2Am, 4Am and 7Am in T. monococcum. In contrast, in our current linkage map for T. monococcum there was only two gaps on chromosome 4Am. This suggests that DArT markers can be used to fill the gaps and help generate higher resolution genetic linkage maps.
Strong segregation distortion was observed during construction of our current genetic linkage map for T. monococcum. Over one third of the marker loci across the seven chromosomes displayed allele frequencies skewed from their Mendelian expectations. This was observed for both DArT and SSR markers, with preferences for both parental alleles. Segregation distortion has also been observed by Dubcovsky et al (1996)  and Singh et al (2007)  during construction of einkorn wheat genetic linkage maps, regardless of the type of populations used. In one study (Dubcovsky et al 1996)  15% of the marker loci displayed segregation distortion and were clustered on chromosomes 1Am and 7Am, while in other study (Singh et al 2007)  two major distorted regions were detected on chromosome 2Am. Strong segregation distortion has also been noted during the construction of durum wheat and bread wheat linkage maps integrating SSR and DArT markers .
Utility of DArT markers and the genetic linkage map in T. monococcum
The two parental T. monococcum lines, MDR308 and MDR002, used for developing the F2 mapping population had a number of contrasting traits including awn colour, leaf pubescence, grain hardness, salt tolerance, as well as resistance to the fungus Mycosphaerella graminicola and to soil-borne cereal mosaic viruses [8, 9, 53]. We demonstrated here that the constructed genetic linkage map helped refine the chromosome regions spanning the Ba and Hl trait loci. Also, this map was recently used to refine the TmStb1 locus conferring resistance to M. graminicola isolate IPO323 on chromosome 7Am, and to identify and map new QTLs conferring salt tolerance (HCJ and KHK, unpublished).
MDR308 (also known as DV92), one of the parental lines of the F2 mapping population used in this study, has previously been used for developing a range of molecular tools including a genetic linkage map integrating RFLPs, AFLPs and seed storage proteins , a BAC library , and several populations of chemically- and radiation-induced mutants http://www.wgin.org.uk. The availability of DArT marker information for MDR308 (DV92) further increases the utility of this accession.
In the near future it should be possible to link various available genetic linkage maps of T. monococcum thereby creating a frame work consensus map for wider applications in molecular genetics and genomics studies.
DArT is a rapid and efficient approach to develop many new molecular markers for genetic studies in T. monococcum. The constructed genetic linkage map will facilitate localisation and map-based cloning of genes of interest, comparative mapping as well as genome organisation and evolution studies between this ancient diploid species and other crops.
This study used 16 T. monococcum accessions and an F2 population of 98 individuals derived from a cross between accessions MDR002 and MDR308 . The detailed information about these accessions is also listed in Table 1. In addition, 23 hexaploid wheat varieties collected from UK, continental Europe, China and America, or developed at CIMMYT, Mexico were used for genetic diversity compassion. The information about these hexaploid wheat varieties is provided in Additional file 2.
The DNA was extracted from leaves of 2-week-old einkorn wheat seedlings using the DNeasy Plant Mini Kit (QIAGEN) according to manufacturer's instructions. A set of 1536 new DArT clones were generated from a Pst I/Taq I representation of the MDR002 and MDR308 accessions as described previously [28, 36]. The new clones were printed together with 2304 polymorphism-enriched clones from hexaploid wheat, 1536 from tetraploid wheat, and 1536 from a group of 15 Iranian accessions of diploid T. boeoticum (see Additional file 1). The resulting composite array was then used to genotype the T. monococcum samples using the standard DArT protocol [28, 36].
A total of 279 SSR markers mapped to the A-genome of hexaploid wheat were tested for polymorphism between the T. monococcum accessions MDR002 and MDR308. These SSRs originated from 5 groups: 57 BARC markers from the Beltsville Agricultural Research Centre, USA [56, 57], 29 CFA and CFD markers from INRA Clermont-Ferrand, France [52, 58, 59], 24 DuPw markers from DuPont company ( et al. 2002, DuPont, unpublished; Dreisigacker et al. 2005), 85 GDM and WMS markers from IPK Gatersleben, Germany [61, 62], and 89 WMC markers from the Wheat Microsatellite Consortium . For each SSR primer pair, the 5'-end of the forward primer was labelled with infra-red dye (IRD700 or IRD800, LI-COR Biosciences UK Ltd). The PCR were carried out using the PCR Master Mix (Promega) in a 10-μl reaction volume containing 1× PCR Master Mix buffer, 0.1 μM forward and reverse primers, and 20-30 ng plant DNA. Amplifications were carried out in 96-well microtiter plates using a G-storm Thermal Cycler (GS4/GS4s, Gene Technologies, Essex, England). The programmes were 2 min at 94°C, followed by 30-35 cycles of 30 s at 94°C, 30 s annealing at 50-60°C (depending on the primer pairs), and 1 min at 72°C, and a final extension of 5 min at 72°C. The final PCR products were diluted to 20-40 times using formamide Li-Cor loading dye, denatured for 5 min at 85°C and stored on ice before 0.5-0.8 μ1 of the reaction mix was loaded on Li-Cor 4300 DNA Analyser.
T. monococcum accession diversity analysis and comparison with hexaploid wheat
A group of 16 T. monococcum accessions were genotyped using the custom-built DArT array as described previously . The polymorphic DArT markers were scored, and used for clustering analysis using principal coordinate plots. For genome comparison, genome representations of nine T. monococcum accessions and 23 hexaploid wheat varieties were hybridised to a newly built DArT array and scored the same way. The ploidy levels did influence the scoring as envisaged in the raw data of the hybridisation intensity. Therefore, only the DArT markers which were not affected by this context-dependent scoring were scored. The nine T. monococcum accessions and 23 hexaploid wheat varieties were hybridised in duplicate.
Genetic mapping and integration of DArT and SSR markers
T. monococcum accessions MDR308, MDR002 and 94 F2 individuals derived from a cross between them were genotyped with the custom-built array as described previously . In total, 300 DArT markers, 90 SSR markers as well as two morphological trait loci (Ba, black awn; Hl, hairy leaf) were used for genetic linkage map construction using JoinMap® 4.0 (Van Ooijen, J.W., 2006, JoinMap® 4.0, Software for the calculation of genetic linkage maps in experimental populations. Kyazma B. V., Wageningen, The Netherlands). Because of the inherent dominant nature of DArT markers which separates the female and male markers in the repulsion phase, the linkage maps for maternal DArT markers (scored as a, c) and for parental DArT markers (scored as b, d) were initially constructed independently with SSR markers. The two maps for individual chromosomal linkage groups were then merged together using SSR markers as bridges. Assignment of markers to linkage groups was achieved using logarithm of the odds (LOD) threshold values ranging from 3.0 to 10.0. The Kosambi's map function was used to estimate genetic distances. In total, 358 markers including 274 DArT markers, 82 SSR markers and 2 morphological trait locus markers were integrated into nine linkage groups. Goodness of fit for all the loci to an expected 1:2:1 or 1:3 segregation ratio was tested using chi-square (χ2) analysis. The graphical representation of the map was drawn using GGT2.2 software .
All statistical analyses were carried out using GenStat (10th edition, VSN International, UK). For principal coordinate analysis Jaccard similarity matrices were generated using the DArT markers. Two-dimensional scores were calculated and used to generate scatter plot matrices of scores. For the Mantel test which looks for association between the off-diagonal values of two similarity (or distance) matrices, the correlation of the matrices were evaluated. The DArT markers were subdivided into four different categories depending on their genome origins and similarity matrices calculated. The similarity coefficients from these matrices were then compared pair by pair to form a new correlation matrix. The significance of each correlation was assessed using a randomisation test (with 1000 random permutations). The p-values were calculated and were always < 0.001 (where the null hypothesis is one of zero association). For the Kolmogorov-Smirnov test, the map position data of the DArT and SSR markers on individual chromosomes were fed into GenStat and the p-values were calculated. The Chi-square goodness-of-fit test was carried out to examine the random distribution of DArT markers of different origins across the genome, by calculating the association between the numbers of the markers of different origins the chromosomes.
The genetic marker and linkage map data, along with details and accession numbers for the deposition of raw data, are freely available at the UK WGIN http://www.WGIN.org.uk and Monogram http://www.monogram.ac.uk/services.php as well as the GrainGene http://wheat.pw.usda.gov/GG2/index.shtml websites.
This research is part of the core project of the Wheat Genetic Improvement Network which is supported by a grant from the Department for Environment, Food and Rural Affairs (Defra, AR0709). The Li-Cor 4300 DNA analysers were purchased with funds received from a BBSRC - REI grant (BB/C5111056/1). The hexaploid wheat genotypes selected for analysis were part of either the BBSRC-CASE studentship (BB/S/N/2002/846) awarded to KHK or the EU-FP6 Integrated Project BIOEXPLOIT (partner 007 KHK). We thank Dr. Sue Welham for her excellent statistical advice. We thank Daniel Jenk and Kim Oldham for their technical support in verifying SSR work. Rothamsted Research receives grant-aided support from the Biotechnology and Biological Sciences Research Council (BBSRC) of the UK.
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