Genome-wide introgressions of Thinopyrum bessarabicum into wheat resulted in 12 recombinant lines. Cytological and molecular techniques allowed mapping of 1150 SNP markers across all seven chromosomes of the J genome.
Thinopyrum bessarabicum (2n = 2x = 14, JJ) is an important source for new genetic variation for wheat improvement due to its salinity tolerance and disease resistance. Its practical utilisation in wheat improvement can be facilitated through development of genome-wide introgressions leading to a variety of different wheat–Th . bessarabicum translocation lines. In this study, we report the generation of 12 such wheat–Th . bessarabicum recombinant lines, through two different crossing strategies, which were characterized using sequential single colour and multi-colour genomic in situ hybridization (sc-GISH and mc-GISH), multi-colour fluorescent in situ hybridization (mc-FISH) and single nucleotide polymorphic (SNP) DNA markers. We also detected 13 lines containing different Th. bessarabicum chromosome aberrations through sc-GISH. Through a combination of molecular and cytological analysis of all the 25 lines containing Th. bessarabicum recombinants and chromosome aberrations we were able to physically map 1150 SNP markers onto seven Th. bessarabicum J chromosomes which were divided into 36 segmental blocks. Comparative analysis of the physical map of Th. bessarabicum and the wheat genome showed that synteny between the two species is highly conserved at the macro-level and confirmed that Th. bessarabicum contains the 4/5 translocation also present in the A genome of wheat. These wheat–Th . bessarabicum recombinant lines and SNP markers provide a useful genetic resource for wheat improvement with the latter having a wider impact as a tool for detection of introgressions from other Thinopyrum species containing the J or a closely-related genome such as Thinopyrum intermedium (JrJrJvsJvsStSt) and Thinopyrum elongatum (EeEe), respectively.
Genetic diversity in wheat was reduced during domestication resulting in a narrow gene pool hindering the development of superior wheat varieties especially in the current climate of plateauing crop yields and dynamic biotic threats. However, some genetic variation can be introduced through introgressions from its distant wild relatives (Able and Langridge 2006; Feuillet et al. 2008; Gill et al. 2011; Zhang et al. 2017). These wild relatives are a largely unexploited source of agronomically important traits (Danilova et al. 2017; Friebe et al. 1996; Jauhar and Chibbar 1999; Schneider et al. 2008).
Thinopyrum bessarabicum (Savul. and Rayss) A. Lӧve (2n = 2x = 14, JJ) is a perennial maritime wheatgrass reported to possess salt tolerance (King et al. 1997a) and disease resistance (Xu et al. 2009), making it a valuable source of genetic variation for wheat improvement. High-salinity tolerance was found in hexaploid amphiploids (2n = 6x = 42, AABBJJ) derived from Chinese Spring and Th. bessarabicum (Hassani et al. 2010; King et al. 1997b). Wheat–Th . bessarabicum chromosome addition lines have also been developed and studied allowing gene discovery for useful traits that can be further utilised in wheat improvement programmes (King et al. 1996; William and Mujeeb-Kazi 1993, 1995; Xu et al. 2009; Zhang et al. 2002) but such addition and substitution lines are generally unsuitable for agronomic purposes, as many unwanted genes are introduced along with those giving rise to the trait of interest.
Homoeologous recombination can reduce the size of the wild relative segment including the gene(s) of interest incorporated into the wheat chromosome. However, presence of the Ph1 locus makes it difficult to induce homoeologous recombination between chromosomes of wheat and its wild relatives, and therefore, there has been limited utilization of alien genes in wheat (Griffiths et al. 2006; Riley and Chapman 1958). Several approaches have been used to allow introgression of wild relative chromatin into wheat, including ph1 mutant (King et al. 2017; Zhao et al. 2013), irradiation (Bie et al. 2007; Chen et al. 2013), tissue culture (Banks et al. 1995; Lapitan et al. 1984; Larkin and Scowcroft 1981), spontaneous translocations (Liu et al. 2013) and gametocidal genes (Endo 2007; Masoudi-Nejad et al. 2002). A number of these approaches have also been used to develop wheat–Th. bessarabicum translocation and recombinant lines (Ardalani et al. 2016; Ghazali et al. 2015; King et al. 1993a; Qi et al. 2010; Zhuang et al. 2004). These translocations/recombinants have been further characterised using biochemical, cytological and molecular techniques (King et al. 1993b; Patokar et al. 2016; Pu et al. 2015; Shen et al. 2013; William and Mujeeb-Kazi 1993).
The major problem in developing wheat-wild relative introgressions is the selection of recombinants, which occur only at low frequency. Such selection would be greatly enhanced by the availability of genetic markers spaced along the wild relative chromosome since conventional cytological methods are difficult to use to identify small segmental recombinants. In previous studies, molecular resources used to characterise wheat–Th. bessarabicum recombinants and translocations have included random amplified polymorphic DNA (RAPD) markers (King et al. 1993b), expressed sequence tag (EST)-derived sequences (Chen et al. 2007; Luan et al. 2010; Shen et al. 2013) and PCR based Landmark Unique Gene (PLUG) markers (Ardalani et al. 2016; Ghazali et al. 2015). However, these techniques as well as just cytological detection are low-throughput and have limited success. The development of next-generation sequencing technologies and high-throughput single nucleotide polymorphism (SNP) markers and corresponding SNP-arrays, has enabled faster, more accurate detection of introgressions from wild relatives into wheat (King et al. 2017; Tiwari et al. 2014, 2015). This high-throughput genotyping approach can then be complemented by genomic in situ hybridization (GISH), which allows the direct visualization of alien chromatin (Schwarzacher et al. 1992).
In this study, we have developed a resource of SNP markers spread across all seven Th. bessarabicum chromosomes which were used to identify 12 wheat–Th. bessarabicum recombinants and detect intact Th. bessarabicum chromosomes alongside spontaneous structural aberrations in introgression lines. These wheat–Th. bessarabicum introgression lines were developed using two different crossing strategies (King et al., 2017). A combination of cytological methods and molecular marker analysis of these recombinants and aberrations allowed physical characterisation of all Th. bessarabicum chromosomes into 36 segmental blocks of 1150 SNP markers. Development and physical localisation of such resources of high-density molecular markers specific for wild relative chromosomes will greatly improve the efficiency of wild relative introgressions into wheat.
Materials and methods
To generate introgressions, two crossing strategies were employed as illustrated in Fig. 1. In the first (Crossing Strategy 1), hexaploid wheat Triticum aestivum cv. Paragon ph1/ph1 mutant (2n = 6x = 42) was pollinated with Th. bessarabicum (accession PI 531712, obtained from United Stated Department of Agriculture, USDA; 2n = 2x = 14) to produce F1 interspecific hybrids. The second crossing program (Crossing Strategy 2) exploited colchicine-doubled hybrids between tetraploid wheat Triticum turgidum L. cv. Creso ph1/ph1 mutant (2n = 4x = 28) and Th. bessarabicum (King et al. 1993a) obtained from the Germplasm Resource Unit (GRU) at the John Innes Centre. In this work, introgression of genetic variation from Th. bessarabicum into wheat was expected to occur when the chromosomes of the two species recombine in the absence of the Ph1 pairing locus during gametogenesis in these interspecific F1 hybrids. This recombination would result in the production of gametes which carry Th. bessarabicum/wheat recombinant chromosomes (the subsequent transmission of these recombinant chromosomes to their progeny leads to the generation of Th. bessarabicum/wheat introgressions). Hybrids from both strategies were grown to maturity and backcrossed. F1s from the first strategy were used as the female and backcrossed with Paragon, carrying the wild-type Ph1 locus intact, to generate a BC1 population. In the second strategy, the amphidiploids were used as the pollen donor and backcrossed onto hexaploid wheat Paragon Ph1/Ph1 to produce BC1 plants. The BC1 individuals from both strategies and their resulting progenies were then recurrently pollinated with Paragon Ph1/Ph1 to produce BC2, BC3 and BC4 populations. Three heads from each plant in each backcross population were bagged to allow self-fertilisation. Cross fertility was calculated as the number of crosses setting seed.
Thirteen wheat–Th. bessarabicum derivatives were used for allocating markers to their corresponding chromosomal locations in this study. Five of these derivatives were obtained from the GRU and included 4 disomic addition lines, DA1J-1 (WPGS id#28181), DA2J-1 (WPGS id#28183), DA4J-1 (WPGS id#28184), DA5J-1 (WPGS id#28185) and 1 ditelosomic addition line DtA5JS (WPGS id#28186). One translocation line, T2BS∙2BL-2JL [Line 1176; Patokar et al. (2016)], and 7 disomic addition lines DA1J-2 (GID: 1784842), DA2J-2 (GID: 184896), DA3J (GID: 1807809), DA4J-2 (GID: 1803509), DA5J-2 (GID: 1803460), DA6J (GID: 229186), DA7J (GID: 1803417) were kindly provided by Dr. Kishii Masahiro of the International Maize and Wheat Improvement Center (CIMMYT, Mexico). A further 3 wheat–Th. bessarabicum disomic addition lines WPGS id#28187, WPGS id#28188 and WPGS id#28189 were obtained from the GRU with unknown chromosome constitutions.
The protocol for genomic in situ hybridization (GISH) was as described in Zhang et al. (2013), Grewal et al. (2017) and in King et al. (2017). In summary, genomic DNAs from young leaves of the three putative diploid progenitors of bread wheat, i.e. T. urartu (A genome), Ae. speltoides (B genome), and Ae. tauschii (D genome) and of Th. bessarabicum, were isolated using extraction buffer [0.1 M Tris–HCl (pH 7.5), 0.05 M EDTA (pH 8.0), 1.25% SDS]. Samples were incubated at 65 °C for 1 h before being placed on ice and mixed with ice cold 6 M NH4C2H3O for 15 min. The samples were then spun down, the supernatant mixed with isopropanol to pellet the DNA and the isolated DNA further purified with phenol/chloroform. The genomic DNA of Th. bessarabicum and T. urartu were labelled by nick translation with Chroma Tide Alexa Fluor 488-5-dUTP (Invitrogen; C11397; green). Genomic DNA of Ae. tauschii was labelled with Alexa Fluor 594-5-dUTP (Invitrogen; C11400; red). Genomic DNAs of Ae. speltoides and T. aestivum cv. Paragon were fragmented to 300–500 bp in a heat block at 100 °C. Preparation of chromosome spreads was as described in Grewal et al. (2017) and in King et al. (2017).
Slides were initially probed, for single colour GISH (sc-GISH), using labelled genomic DNA of Th. bessarabicum (100 ng) and fragmented genomic DNA of Paragon (3000 ng) as blocker (1:30 per slide) to detect the Th. bessarabicum introgressions. The slides were bleached (dipped in 2 × SSC to remove the coverslip, transferred to 4 × SSC for 5 min and air dried in the light) and re-probed, for multi-colour GISH (mc-GISH) with labelled DNAs of T. urartu (100 ng) and Ae. tauschii (200 ng) and fragmented DNA of Ae. speltoides (3000 ng) as blocker (1:2:30 per slide) to detect the AABBDD genomes of wheat. All slides were counterstained with DAPI and analysed using a high-throughput, fully automated Zeiss Axio Imager.Z2 upright epifluorescence microscope (Carl Zeiss Ltd, Oberkochen, Germany) with filters for DAPI (blue), Alexa Fluor 488 (green) and Alexa Fluor 594 (red). Photographs were taken using a MetaSystems Coolcube 1 m CCD camera. Further slide analysis was carried out using Metafer (automated metaphase image capture) and ISIS (image processing) software (Metasystems GmbH, Altlussheim, Germany). This system enabled the fully automated capture of high and low power fluorescent images of root tip metaphase spreads. Where a sc-GISH image could not be obtained for the backcross line showing a Th. bessarabicum segment in the genotyping, its self-fertilised seed was used to obtain a sc-GISH image of the recombinant chromosome or structural aberration.
For multi-colour fluorescence in situ hybridization (mc-FISH), two repetitive DNA sequences pSc119.2 (McIntyre et al. 1990), and pAs.1 (Rayburn and Gill 1986) were labelled with Alexa Fluor 488-5-dUTP (green) and Alexa Fluor 594-5-dUTP (red), respectively, and hybridized to the slides prior to sc-GISH. Some slides were then bleached as described above and sequentially re-probed for sc-GISH and mc-GISH.
Genotyping via an Axiom® SNP array
The Nottingham/BBSRC Wheat Research Centre (WRC) is presently engaged in the genome-wide introgression of genetic variation from wild relatives into wheat. To detect introgressed chromosomes and chromosome segments from these wild relatives into wheat, an array of circa 35 K SNPs, known as the Axiom® Wheat-Relative Genotyping Array, has been developed (King et al. 2017; Winfield et al. 2016). In summary, the array is composed of SNPs each showing polymorphism for the wild relatives relative to the wheat genotypes under study. All the SNPs incorporated in this array formed part of the Axiom® 820 K SNP array (Winfield et al. 2016). The data-set for the Axiom® 820 K array is available from http://www.cerealsdb.uk.net (Wilkinson et al. 2012, 2016). Table 2 shows the number of putative SNPs, for each linkage group, between Th. bessarabicum and the wheat genotypes included on the array. This 384-format genotyping array facilitates cost-effective, high-throughput, high resolution screening of introgressions that are being generated from wild relatives, including Th. bessarabicum.
The Axiom® Wheat-Relative Genotyping Array was used to genotype 447 samples in total. Control samples included three replicates of each of the three parental lines, i.e. wheat cvs. Paragon and Creso and the wild relative Th. bessarabicum; one 2JL translocation line and 12 wheat–Th. bessarabicum disomic addition lines. Call rate for a sample was calculated as the percentage of the number of SNP probes on the array that resulted in a definitive genotype call (AA, AB, BB). The equipment, software, procedures and criteria used for this genotyping are as described by King et al. (2017).
Physical mapping of Th. bessarabicum chromosomes
Individuals from a backcross population between wheat and Th. bessarabicum were genotyped with the Axiom® Wheat-Relative Genotyping Array. Along with triplicates of all three parental lines from both crossing strategies, 422 lines comprising BC1, BC2, BC3 and BC4 populations of Th. bessarabicum and 16 wheat–Th. bessarabicum derivatives were genotyped altogether. As described in the methodology by King et al. (2017), only the Poly High Resolution (PHR) SNP markers, which were co-dominant and polymorphic and generated calls (that qualified as the minor allele) for at least 2 of the 3 replicates of Th. bessarabicum, were used for further marker analysis. SNP markers which showed (1) heterozygous calls for either parent(s), (2) no polymorphism between the wheat parents and Th. bessarabicum and/or (3) no calls for either parent(s) were removed using Flapjack™ (Milne et al. 2010; v.1.14.09.24). The resulting markers were sorted into linkage groups in JoinMap® 4.0 (Van Ooijen 2011) with a LOD score of 40 using the genotype classification code ‘(a,h)’, where ‘a’ is the genotype of the first parent and ‘h’ is the genotype of the F1. ‘BCpxFy’ was used as the population code for each dataset which donates an advanced backcross inbred line family, where the backcross parent p had genotype ‘a’, x is the number of backcrosses including the one for creating the BC1 and y is the number of selfings, i.e. BCa1F0 is equivalent to BC1. All markers that did not show any heterozygous call or were unlinked were ignored and only the highest-ranking linkage groups with more than 100 markers assigned were selected for downstream analysis. Linkage groups from all advanced backcross populations were integrated in JoinMap® to produce one set of seven linkage groups for Th. bessarabicum. These were exported and assigned to chromosomes using information from the Axiom® Wheat HD Genotyping Array (Winfield et al. 2012). Erroneous markers that had more than 20% missing data were removed. Each linkage group was divided into various physical segmental blocks based on genotyping and matching GISH data of introgression lines. To obtain the marker order within a segmental block, the marker sequences were used in BLAST against the IWGSC Chinese Spring survey sequence v2 (IWGSC CSS v2; IWGSC 2014) and contigs with the highest or a very high BLAST score on the most likely chromosome, where available for each of the three genomes of wheat, were selected manually from the BLAST output. The genetic positions of the contigs were obtained from the POPSEQ data (Chapman et al. 2015) and used to order the markers in each linkage group (Online Resource 3). The long and short arm of each chromosome was identified and groups were orientated to have the short arm above the long arm. A physical map with chromosome ideograms was produced through MapChart 2.3 (Voorrips 2002). Graphical genotype visualization was performed using Graphical GenoTypes 2.0 (GGT; van Berloo 2008).
Synteny analysis with wheat was carried out using the BLAST positions of the markers on the Th. bessarabicum map, obtained as described above. To generate the circos plots, markers on each of the chromosomes on the physical map of Th. bessarabicum were separated by an incremental distance of 1 unit. To be able to equate the units of comparison in both species, the marker distance (physical position) on the Th. bessarabicum linkage groups and the genetic position of their syntenic contigs in wheat were scaled up by a factor of 1,000,000. Markers corresponding to the same genetic position on a wheat chromosome were grouped at the same physical position within a Th. bessarabicum chromosomal segment. Figure 7 was visualized using Circos (v. 0.67; Krzywinski et al. 2009) to observe synteny between Th. bessarabicum (physical position in units) and the wheat genome (genetic position in cM).
Generation of wheat–Th. bessarabicum introgressions
A total of 1775 crosses were made between wheat and Th. bessarabicum and their derivatives, through both crossing strategies (Fig. 1), leading to the generation of 10,321 crossed seeds (an additional 10,387 self- fertilised seeds were also produced). The number of seeds germinated, plants crossed, cross fertility and seed set are shown in Table 1. Fertility in the backcrosses varied quite substantially among individuals, often ranging from 0% seed set to a high proportion of fertile florets.
Through crossing strategy 1, five F1 hybrid seeds were produced by crossing wheat Paragon ph1 mutant with Th. bessarabicum. All 5 F1 seeds were germinated and every year produced was crossed with wheat, i.e. since these amphihaploids were expected to show very little fertility no attempts were made to self-fertilise them. Only 5 BC1 seeds were generated, of which only 3 grew to maturity and set seed. Table 1 shows that the F1 hybrids had the lowest cross fertility of 1.6% as compared with the backcross generations.
In crossing strategy 2, thirty wheat–Th. bessarabicum F1 synthetic amphidiploids were germinated and of these, 19 plants reached maturity. The cross fertility of these F1 plants was much higher at 24%, compared to those from crossing strategy 1. The F1 hybrids also produced 231 self-fertilised seeds indicating a moderate level of male and female fertility.
Development of a FISH-based karyotype for Th. bessarabicum chromosomes
To develop a FISH karyotype for Th. bessarabicum, mitotic chromosome spreads of Th. bessarabicum were analysed by mc-FISH using the two probes Oligop-pAs-1 and Oligo-pSc119.2-1 (Fig. 2a). Results showed that all seven Th. bessarabicum chromosomes could be distinguished from each other (Fig. 2b). Allocation of each of the seven pairs of Th. bessarabicum chromosomes to Triticeae homoeologous groups was possible based on visual characteristics of mc-FISH patterns. This was done by comparing sequential mc-FISH and sc-GISH of the mitotic spreads of Th. bessarabicum disomic addition lines in wheat (Online Resource 1). An example of this comparison is shown for chromosome 2J in DA2J-1 where the mc-FISH banding pattern of 2J (Fig. 2d) could be assigned through identification of chromosomes 2J in the same metaphase spread through sequential sc-GISH analysis (Fig. 2e). After comparison with all disomic addition lines, a mc-FISH karyotype of Th. bessarabicum chromosomes was established (Fig. 2c) which will be helpful for the identification of Th. bessarabicum chromosomes in a wheat background. As discussed later in the results, the disomic addition line for chromosome 3J (DA3J) was found not to have a whole chromosome 3J and no other source for a 3J disomic addition line was available. Thus, to establish a mc-FISH pattern for 3J, a disomic addition line created through our crossing program was used (Online Resource 1).
mc-FISH showed that both probes, Oligop-pAs-1 and Oligo-pSc119.2-1, mainly hybridized to distal/terminal regions of Th. bessarabicum chromosomes (Fig. 2a–c; Online Resource 1). Chromosomes 1J, 3J, 4J, and 6J had Oligo-pSc119.2–1 signals (in green) on terminal regions of both arms, while 2J, 5J, and 7J only had Oligo-pSc119.2-1 signals on terminal regions of the short arms (Fig. 2a–c). Strong Oligo-pAs-1 signals (in red) were observed on the terminal and/or subterminal regions of the long arm of chromosomes 2J, 3J, 4J and 5J and on the subterminal regions of the short arm of chromosome 7J (Fig. 2a–c). In addition, dispersed labelling of Oligo-pAs-1 was also observed on some chromosomes, except for centromeric and most pericentromeric regions. For chromosomes 1J and 6J, this dispersed labelling of Oligo-pAs-1 on the terminal region of the long arm of chromosome 1J and on the terminal region of the short arm of chromosome 6J, is the only distinguishing characteristic apart from the slightly larger size of chromosome 1J (Fig. 2a–c) Therefore, through this mc-FISH hybridization pattern, five chromosome pairs of Th. bessarabicum can be confidently identified and two pairs of chromosomes can be reliably identified.
Cytogenetic analysis of wheat–Th. bessarabicum introgressions lines
To identify wheat–Th. bessarabicum recombinants in our crossing programme, metaphase spreads of root-tips from 281 lines spread across BC2, BC3 and BC4 generations, from both crossing strategies, were analysed with sequential sc-GISH and mc-GISH as shown in Fig. 3a–f. Most introgression lines were monosomic additions for one or multiple Th. bessarabicum chromosomes. Figure 3a, b show sequential GISH images of line BC4-127A that showed a Robertsonian translocation from Th. bessarabicum recombined with the A genome of wheat. Figure 3c, d show sequential GISH images of line BC4-120D that showed a Robertsonian translocation from Th. bessarabicum recombined with the B genome of wheat. Figure 3e, f show sequential GISH images of line BC3F1-178C that showed a large segmental translocation from Th. bessarabicum recombined with the D genome of wheat. In total, 12 wheat–Th. bessarabicum recombinants were identified, which are shown in Fig. 3g. In addition, 13 aberrations were also observed, via GISH, in various J chromosomes in the introgression lines and validated through genotyping with molecular markers (see below). Structural aberrations included deletions (del), telocentrics (tc), chromosome breakages (cb) and translocations between segments of different Th. bessarabicum chromosomes (Tb–Tb). Presence of the Th. bessarabicum segment was validated through genotyping as discussed below.
Molecular marker analysis of wheat–Th. bessarabicum introgression lines
22,606 SNPs on the Axiom array showed polymorphism between Th. bessarabicum and wheat (Table 2). The SNPs appeared to be relatively evenly spread over all seven linkage groups. The Axiom array was used to screen genomic DNA prepared from 422 backcross lines between wheat and Th. bessarabicum, from both crossing strategies and 3 wheat–Th. bessarabicum derivatives from the GRU along with control samples. Genotype calls were generated, and the sample call rate ranged from 87.2 to 99.7% with an average of 98.7% for the 447 samples. The lowest call rates were obtained for the three Th. bessarabicum samples with an average of 87.9%. Affymetrix software classified the scores for each of the probes into one of six cluster patterns. However, only those calls classified as PHR were used for genotyping as these are optimum quality.
JoinMap® (van Ooijen 2011) was used to analyse the genotypes of all lines for the PHR SNPs and this led to the establishment of seven linkage groups. In total, the linkage groups were composed of 1150 SNPs and represented the seven chromosomes of Th. bessarabicum (Table 2). Linkage group 5 had the highest number of SNPs (19.8%) while linkage group 6 had the lowest (9%).
Physical mapping of Th. bessarabicum chromosomes
sc-GISH analysis of wheat–Th. bessarabicum recombinants and structural aberrations was combined with the above genotyping results to establish and/or confirm the order of the markers within each linkage group of Th. bessarabicum as shown in Fig. 4a–g. Presence of a heterozygous call for a SNP marker, represented in red and depicted as ‘h’, indicated the presence of Th. bessarabicum in a wheat background and a homozygous call represented in blue and depicted as ‘a’, indicated the absence of Th. bessarabicum in wheat at that marker. For all linkage groups, genotypes of wheat cvs. Paragon and Creso along with Th. bessarabicum were used as negative controls, i.e. to show absence of heterozygous calls. Where possible genotypes of disomic addition lines for the linkage group were used as positive controls, i.e. to show presence of Th. bessarabicum via presence of heterozygous calls for the SNP markers of that linkage group. Chromosome segments in green represent Th. bessarabicum chromatin which fluoresces due to hybridisation with the Th. bessarabicum genomic DNA probe. Chromosome segments in blue represent wheat chromatin and in purple represent Th. bessarabicum chromatin from another linkage group. The latter forms part of a structural aberration (Tb–Tb).
Linkage group 1 Apart from various monosomic 1J addition lines generated through crossing, three wheat–Th. bessarabicum recombinant lines BC2F1-197J, BC4-127A and BC4-126, and two lines with structural aberrations BC2F1-197H (Tb–Tb), BC2F1-197E (tc) had chromosome 1J specific markers as shown in Fig. 4a. Chromosome 1J had 124 SNP markers, however, a subset of these markers distributed along the chromosome, that detect different introgressed segments of 1J, have been displayed in Fig. 4a. DA1J-2 line was used as the positive control in genotyping.
Linkage group 2 Chromosome 2J had recombined with wheat only once through our crossing programme resulting in a Robertsonian translocation line. To be able to order the 189 SNP markers on 2J, we used this translocation line, BC3-522C, along with two lines with structural aberrations in 2J, BC3-527F (cb) and BC3-516 N (del), and one wheat–Th. bessarabicum recombinant (T2BL∙2BS-2JS) obtained from CIMMYT as shown in Fig. 4b. Both DA2J-1 and DA2J-2 were used as positive controls in genotyping.
Linkage group 3 Chromosome 3J had 185 SNP markers on it and these were ordered through aligning the genotyping data of two wheat–Th. bessarabicum recombinants, BC3-400A and BC3F1-178C, and three lines with structural aberrations, BC2-231F (cb), BC3-458F (cb) and DA3J (found to be a Tb–Tb translocation of 4JS-3JL as described later and shown in Online Resource 4), with their sc-GISH images (could not be obtained for line BC2-231F) as shown in Fig. 4c. A disomic addition line for 3J (BC3F1-178D) generated through our crossing program and confirmed by mc-FISH (Online Resource 1) was used as the positive control for genotyping.
Linkage group 4 Two wheat–Th. bessarabicum recombinant lines, BC4-124B and BC3-403D, along with one line with a structural aberration, BC3-456C (tc) were used to order the 155 SNP markers on chromosome 4J as shown in Fig. 4d. DA4J-1 and DA4J-2 were used as the positive controls in genotyping.
Linkage group 5 Chromosome 5J had the most SNP markers (228) and these were ordered through combining genotyping and sc-GISH analysis of two wheat–Th. bessarabicum recombinant lines, BC3-401A and BC3F1-197A, and two lines with a structural aberration, BC3-516N (del) and DtA5JS (tc), as shown in Fig. 4e. Lines DA5J-1 and DtA5JS were used as positive controls in genotyping where the latter helped in identifying markers on the short arm of chromosome 5J.
Linkage group 6 104 SNP markers on chromosome 6J were ordered by aligning the genotyping results and the sc-GISH results from one wheat–Th. bessarabicum recombinant line showing a Robertsonian translocation, BC4-120D, and three lines with structural aberrations, BC4-123I (del), BC3F1-197H (Tb–Tb) and DA5J-2 (found to be a Tb–Tb translocation of 6JS-5JL as described later and shown in Online Resource 4), as shown in Fig. 4f. DA6J-2 was used as the positive control in genotyping.
Linkage group 7 Only one wheat–Th. bessarabicum recombinant line, showing a very small introgressed segment and detected with one SNP marker, was observed for chromosome 7J which had 165 SNP markers. These markers were ordered through a combined analysis of this recombinant line, BC3-406, with five other lines showing structural aberrations, BC3-528A (tc), BC3-415I (cb), BC4-128H (tc), BC3F1-194E (del) and BC3-402F (del), as shown in Fig. 4g. DA7J-2 was used as the positive control in genotyping.
Using this methodology, we were able to physically divide the SNP map of Th. bessarabicum chromosomes into 36 segmental blocks (Fig. 5). The number and distribution of the SNP markers in each segmental block for chromosomes 1J-7J are shown in Online Resources 2 and 3, respectively. Chromosome 4J was divided into the least number of segmental blocks, i.e. 3, whereas chromosome 7J has the most divisions with 8 segmental blocks. Assuming synteny is conserved to a large extent between wheat and Th. bessarabicum, the potential order of the SNP markers within each segmental block was determined through their corresponding POPSEQ genetic position (Chapman et al. 2015). This allowed generation of a putative physical map of Th. bessarabicum chromosomes as displayed in Fig. 5 with the short arms of all chromosomes being divided into 14 segmental blocks (JS) and the long arms of all chromosomes being divided into 22 segmental blocks (JL).
A physical SNP map of Th. bessarabicum allowed us to track Th. bessarabicum introgressions through the backcross generations. Visualisation of the Th. bessarabicum segments through sc-GISH validated the genotyping data (indicated through GGT bar diagrams) and the physical map as shown in Fig. 6a–d. A BC2 line showed three Th. bessarabicum segments in sc-GISH and in its genotyping (indicated in red segments of the GGT diagram in Fig. 6a). Two of these were recombinants with wheat and one was a whole chromosome addition, which were all passed into the BC3 plant that was derived from it (Fig. 6b). The wheat–Th. bessarabicum recombinant chromosomes segregated into different BC4 plants as shown in Fig. 6c, d showing recombinants from chromosome 1J and 4J, respectively. The GGT diagrams representing the genotyping results of the BC3 and BC4 plants match the corresponding sc-GISH images from these lines.
Comparative analysis of wheat and Th. bessarabicum chromosomes
A total of 1150 markers based on the physical map of Th. bessarabicum were used in BLAST against the wheat Chinese Spring genome assembly. Contig information for the top hit from each of the three wheat genomes, where available, and for the overall top hit (maximum sequence identity match) was obtained (Online Resource 3). The BLAST results showed that 92.7, 94.4 and 93.5% of the markers had a significant BLAST hit on the A, B and D genomes of wheat, respectively. Of these BLAST hits, 32.5, 37.8 and 32.5% of the markers had an overall top hit on the A, B and D genomes of wheat, respectively, with some showing the same score for the top hit for more than one genome.
Circos plots indicating a significant syntenic relationship between the seven linkage groups of Th. bessarabicum and their orthologous chromosomes from each of the three genomes in hexaploid wheat are shown in Fig. 7a–h. Closely spaced links between Th. bessarabicum and wheat were grouped together and displayed as ribbons. Chromosomes 1J and 3J show high collinearity between the order of the Th. bessarabicum markers and the contigs on the corresponding chromosome groups in wheat on all 3 genomes (Fig. 7a, c, respectively). Chromosome 2J maintained synteny with all three group 2 chromosomes in wheat but also had 2 markers that aligned back to the centromeric region of chromosome 5B in wheat (Fig. 7b) when used in BLAST against the wheat genome assembly. Chromosomes 4J and 5J of Th. bessarabicum also maintained synteny with groups 4 and 5 of wheat, respectively (Fig. 7d, e). However, both chromosomes showed an inter-chromosomal translocation on their long arms such as the 4A/5A translocation observed in wheat (Devos et al. 1995; Liu et al. 1992). In addition, chromosome 5J also had 2 markers that aligned to the centromeric region of chromosome 2D in wheat (Fig. 7e) when used in BLAST against the wheat genome assembly. A segment of non-collinear markers that blasted to another region in group 6 of wheat indicated that chromosome 6J showed a translocation within its long arm (Fig. 7f). Chromosome 7J showed an inversion of its short arm as compared to wheat (Fig. 7g) but no translocation with group 4 unlike wheat (Devos et al. 1995; Liu et al. 1992). A summary of all the chromosomal rearrangements in Th. bessarabicum is shown in Fig. 7h. This data demonstrates that there is a close syntenic relationship between the A, B and D genomes of wheat and the J genome of Th. bessarabicum.
Genotyping for seedbanks and centric fusions of Th. bessarabicum chromosomes
Three wheat–Th. bessarabicum disomic addition lines WPGS id#28187, WPGS id#28188 and WPGS id#28189 were obtained from GRU with unknown chromosome constitutions. After genotyping on the Axiom® Wheat-Relative Array it was found that WPGS id#28187 was a chromosome 7J disomic addition line and WPGS id#28189 was a chromosome 6J disomic addition line. Genotyping results combined with sequential sc-GISH and mc-FISH showed that WPGS id#28188 was a disomic addition line of a centric fusion of chromosome arms 1JS and 6JL, making it DA1JS·6JL (Online Resource 4).
Genotyping complemented by sc-GISH and mc-FISH analysis also showed that the wheat–Th. bessarabicum disomic addition lines DA3J and DA5J-2, obtained from CIMMYT, were centric fusions between the arms of chromosomes from different Th. bessarabicum groups. DA3J was found to be composed of a disomic addition of a Robertsonian translocation between 4JS and 3JL, whereas DA5J-2 was found to be Robertsonian translocation between 6JS and 5JL (Online Resource 4).
A centric fusion between Th. bessarabicum chromosomes was also obtained through our crossing programme where the short arm of chromosome 4J and the long arm of chromosome 7J fused at the centromere in line BC3-277C resulting in translocation line T4JS∙7JL as shown in Online Resource 4.
Th. bessarabicum is a potentially important source of genetic variation for a range of agronomically important traits (King et al. 1997a; Xu et al. 2009). Many techniques have been used to produce wheat–Th. bessarabicum translocation lines but here we have exploited the ph1 mutant approach. Two strategies were used (Fig. 1), one similar to that described by King et al. (2017) where an amphihaploid F1 of hexaploid wheat ph1/ph1 and Th. bessarabicum was created and further backcrossed with hexaploid wheat Ph1/Ph1 (crossing strategy 1) and the second used a durum wheat–Th. bessarabicum ph1/ph1 amphidiploid (King et al. 1993a) which was backcrossed with hexaploid wheat Ph1/Ph1 (crossing strategy 2). Previous studies have highlighted the benefits of the latter approach to obtain wheat–Th. bessarabicum translocation lines (Mujeeb-Kazi 2006; Mujeeb-Kazi et al. 2013). We modified this approach using a durum wheat instead of hexaploid wheat. This increased the possibility of pairing between the univalent Th. bessarabicum chromosomes and the univalent D genome chromosomes from hexaploid wheat used as the female parent in the backcross in the absence of the homologous pairing Ph1 locus. However, we did not observe any preference for recombination with the D genome in the wheat–Th. bessarabicum recombinant lines obtained through crossing strategy 2 possibly due to the use of Paragon with Ph1 locus intact as the first backcross parent in crossing strategy 2. We are currently generating new backcross populations using durum and hexaploid wheat–Th. bessarabicum ph1/ph1 amphidiploids and Paragon ph1/ph1 as the first backcross parent.
Cross fertility in the F1 hybrids was 1.6% in crossing strategy 1 which was very low as compared to the cross fertility in the F1 hybrids in crossing strategy 2 which was 24% (Table 1). This was expected since the inter-specific F1 hybrids generated in crossing strategy 1 were haploid for the A, B, D and J genomes and the frequency of recombination between chromosomes from different genomes is likely to be very low. This would lead to significant infertility in the F1, i.e. polyhaploidy would result in the failure of normal disjunction of chromosomes at anaphase I of meiosis leading to low recombination and the production of unviable, unbalanced gametes. Doubling of the chromosome number of sterile wheat–Th. bessarabicum amphihaploids through colchicine-treatment and their utilisation as the F1 plant for further backcrossing in crossing strategy 2 ensured that these synthetic F1 amphidiploid lines had much higher fertility than those produced in crossing strategy 1. However, the cross fertility and the average number of seeds set per crossed head in both crossing strategies increased remarkably through the backcross generations as shown in Table 1 indicating restoration of fertility through more stable chromosome numbers in the backcross lines.
The low fertility of the F1 hybrids in crossing strategy 1 resulted in the generation of only 5 BC1 seeds, of which only 3 grew to maturity and set seed. Hence, if recombination did not occur in later generations, i.e. in the gametes of the BC1, BC2, BC3 and BC4 generations, then the total number of introgressions that could be generated was limited to the 3 female F1 gametes giving rise to these 3 BC1 plants. However, 570 BC1 seeds were produced through crossing strategy 2 and even though 41 seeds were backcrossed, many of those BC1 seeds have yet to be sown and taken further through the backcrossing program. Due to the low number of BC1 plants exploited in this program, the level of interspecific recombination detected through genotyping was also very low such that it was possible to assemble the seven linkage groups of Th. bessarabicum (Table 2) but not to produce a genetic map. We identified 12 wheat–Th. bessarabicum recombinant lines and 13 lines with Th. bessarabicum chromosome aberrations through GISH (Figs. 3, 4). These results were combined with genotyping results obtained through the high-throughput Axiom® Wheat-Relative Genotyping Array (Fig. 4) to produce a physical map of Th. bessarabicum chromosomes (Fig. 5) consisting of 1150 SNP markers distributed along 36 segmental blocks along the seven J chromosomes of Th. bessarabicum (Online Resource 2). Using this physical map, we could further characterise the 25 introgression lines and track them through the backcross generations (Fig. 6). Generating more recombinant lines with different sizes of introgressed segments from Th. bessarabicum would facilitate the development of an even more detailed physical map of Th. bessarabicum.
Cytogenetic analyses of wheat–Th. bessarabicum introgression lines have mainly involved sequential sc-GISH and mc-FISH (Patokar et al. 2016; Pu et al. 2015; Qi et al. 2010; Shen et al. 2013) but these studies have used mc-FISH to primarily characterise the wheat chromatin in the introgression lines (Patokar et al. 2016; Qi et al. 2010). Where mc-FISH was used to identify Th. bessarabicum chromosomes, it was only reported in studies involving chromosome 4J (Pu et al. 2015; Shen et al. 2013). All Th. bessarabicum chromosomes have only been characterised through C-banding until now (Mirzaghaderi et al. 2010). Du et al. (2016) used multiplexing of synthetic FISH oligos to successfully distinguish Th. bessarabicum chromosomes from wheat. However, to utilise this kind of FISH technique to identify and characterise wheat-wild relative translocation lines is still quite labour-intensive and requires species-specific sequence information for the wild relative under study which is currently not widely available and is costly to obtain for polyploids. In this study, we used the popular mc-FISH technique with the double probe combination of Oligo-pAs-1 and Oligo-pSc119.2 to generate a FISH karyotype of all seven Th. bessarabicum chromosomes. We did this using sequential mc-FISH and sc-GISH on wheat–Th. bessarabicum disomic addition lines, obtained through seedbanks and validated with SNP markers, where the Th. bessarabicum chromosome constitution was known. This was followed by matching the resulting banding patterns to corresponding chromosomes obtained from Th. bessarabicum mitotic spreads, thereby assigning a unique mc-FISH pattern to each of the seven pairs of Th. bessarabicum chromosomes (Fig. 2; Online Resource 1). It should be noted that the Th. bessarabicum accession used in this study was PI 531712, whereas most of the recombinant/translocation lines produced in other studies and the disomic addition lines used for validation in this study were derived from Th. bessarabicum accession PI 531711 which could lead to slight variation in the mc-FISH banding patterns. This difference is noticeable in the mc-FISH patterns of chromosome groups 4J and 6J (Online Resource 1) since the Oligo-pAs-1 signals on both these chromosome groups were either very faint or missing as compared to what was expected for accession PI 531712. However, the mc-FISH patterns of 4J and 6J in some of the introgressions lines generated through our crossing programme (shown in insets in Online Resource 1) matched the expected patterns of these chromosome groups since they were generated using the same Th. bessarabicum accession (PI 531712) as the one for which the karyotype was being developed.
Comparative analysis between Th. bessarabicum and wheat chromosomes showed that macro-synteny between the two species is conserved and the majority of Th. bessarabicum chromosome arms are collinear with their orthologous chromosomes in all three genomes in hexaploid wheat. Figure 7d shows markers from the bottom of segmental block 4JL-1 with links to the distal regions of the long arms of chromosomes 5B and 5D and Fig. 7e shows markers from the bottom of segmental block 5JL-2 with links to the distal regions of the long arms of chromosomes 4B and 4D. This indicates a reciprocal translocation between the long arms of chromosomes 4J and 5J which confirms a previous report by King et al. (1994) that indicated that Th. bessarabicum has the 4/5 translocation along with T. urartu and Aegilops umbellulata which had only been previously reported in wheat and rye (Devos et al. 1995; Liu et al. 1992). Since wheat already has the 4A/5A/7B translocation, the links on the A genome of wheat in Fig. 7d, e corresponded to the same chromosome group as Th. bessarabicum. This also helped to show that Th. bessarabicum did not have the 4/7 translocation as shown in Fig. 7g. Instead chromosome 7J showed an inversion of the small arm as indicated by the twisted links to wheat chromosome 7A, 7B and 7D in Fig. 7g. A break in collinearity with wheat chromosomes 6A, 6B and 6D indicated that chromosome 6JL may have a potential translocation from the distal end of the arm to the proximal end closer to the centromere (Fig. 7f). Presence of markers at the centromeric region of chromosome 2J from the centromeric region of group 5 in wheat and vice versa indicated a potential reciprocal translocation between the centromeric regions of chromosome 2J and 5J as shown in summary Fig. 7h.
Analysis of wheat–Th. bessarabicum introgression lines have shown several occasions where the Th. bessarabicum chromosomes have broken at the centromere producing telocentrics. These telocentrics may recombine with wheat chromosomes to produce Robertsonian translocations, stay univalent as chromosome aberrations or even recombine with other telocentrics from a different chromosome group of Th. bessarabicum. We observed that 50% of our 12 wheat–Th. bessarabicum recombinant lines were Robertsonian translocations (Fig. 3g) with many others reported in the literature (Ardalani et al. 2016; Ghazali et al. 2015; Patokar et al. 2016; Pu et al. 2015). Of the 13 lines identified with chromosome aberrations, 5 had univalent Th. bessarabicum telocentrics (Fig. 4). We also observed 4 lines through genotyping and subsequent sequential in situ hybridisation studies where telocentrics from 2 different Th. bessarabicum chromosomes had fused at the centromere (Online Resource 4) and such translocations have also been reported in the literature (Chen et al. 2007; Pu et al. 2015; Shen et al. 2013). During meiotic meta-/anaphase I, univalents have a tendency to misdivide (break) across their centromeres. This centric misdivision followed by the fusion of the broken arms from different chromosomes leads to the formation of whole-arm Robertsonian translocations (Robertson 1916) and in wheat, this process has been described in significant detail (Friebe et al. 2005; Lukaszewski 2010; Sears 1952). Thus, potentially due to the monosomic condition of Th. bessarabicum chromosomes in most of our backcross lines, we have observed several occurrences of centric fusions between Th. bessarabicum and wheat chromosomes and between different Th. bessarabicum chromosomes. Due to the preference for small segment introgressions from wild relatives into wheat to avoid linkage drag of negative traits, these Robertsonian translocations can be further backcrossed with wheat to produce small introgressions from Th. bessarabicum into wheat (Qi et al. 2010).
We also observed that in the rest of the six wheat–Th. bessarabicum recombinant lines, that showed homoeologous recombination, 4 were interstitial and 2 were distal recombinants. It has been shown before that most of the recombination occurs in the distal ends of wheat chromosomes (Gill et al. 1993). However, in these limited number of recombinant lines, we observed more frequent recombination between the interstitial regions of wheat and Th. bessarabicum chromosomes. This shift of homoeologous recombination towards the centromere has been reported previously for wheat–rye chromosomes (Lukaszewski et al. 2004) and can potentially be a new source for introduction of genetic variation from wild-relatives into wheat.
In this study, we have reported the generation of a new resource of molecular markers that can be used to characterise wheat–Th. bessarabicum introgression lines and potentially other translocation lines that involve other Thinopyrum species containing the J or a closely related genome such as Thinopyrum intermedium (JrJrJvsJvsStSt) and Thinopyrum elongatum (EeEe) respectively. We have also generated 12 wheat–Th. bessarabicum recombinant lines that are currently being self-fertilised for further trait analysis. Once stable, homozygous lines have been produced from the recombinant lines, they will be bulked and then made available via the Nottingham/BBSRC Wheat Research Centre website at http://www.nottingham.ac.uk/wisp/index.aspx.
Author contribution statement
SG, CY, SHE, DS, SA, IPK and JK carried out the crossing programme. SG performed the in situ hybridisation experiments. SHE, DS, SA and CY prepared the samples for genotyping and AJB ran the samples on the array. SG analysed the genotyping data, constructed the physical map and performed the comparative genome studies. SG, IPK and JK conceived and designed the experiments. SG wrote the manuscript with assistance from JK and IPK. All authors read and approved the final manuscript.
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This work was supported by the Biotechnology and Biological Sciences Research Council [grant number BB/J004596/1] as part of the Wheat Improvement Strategic Programme (WISP). The funding body played no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript. We would like to thank Dr. Adrian Shaw of the Germplasm Resource Unit at John Innes Centre and Dr. Masahiro Kishii from CIMMYT for providing us with seeds of valuable wheat–Th. bessarabicum derivative lines.
Conflict of interest
On behalf of all authors, the corresponding author states that there is no conflict of interest.
Communicated by Steven S. Xu.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Online Resource 1 mc-FISH and sequential sc-GISH images of disomic addition (DA) lines of Th. bessarabicum chromosomes (indicated by arrows) in hexaploid wheat background (PDF 91 kb)
Online Resource 2 Number of SNP markers in each segmental block (SB) for each linkage group (LG) of the Th. bessarabicum physical map of the J genome (PDF 27 kb)
Online Resource 3 Distribution of SNP markers along each of the seven J chromosomes of Th. bessarabicum as depicted on the physical map. Markers within each segmental block were ordered through genetic positions (POPSEQ data; Chapman et al., 2015) of the wheat contigs, for each of the 3 genomes of wheat, obtained through using BLAST against the IWGSC CSS v2 (IWGSC 2014) (XLSX 150 kb)
Online Resource 4 sc-GISH and sequential mc-FISH images of chromosomes showing Robertsonian translocations (indicated by arrows) between telocentrics from different J chromosomes of Th. bessarabicum and validated by genotyping data shown as GGT diagrams in insets (PDF 110 kb)
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Grewal, S., Yang, C., Edwards, S.H. et al. Characterisation of Thinopyrum bessarabicum chromosomes through genome-wide introgressions into wheat. Theor Appl Genet 131, 389–406 (2018). https://doi.org/10.1007/s00122-017-3009-y