Rye (Secale cereale L.) is an exceptionally climate-resilient cereal crop, used extensively to produce improved wheat varieties via introgressive hybridization and possessing the entire repertoire of genes necessary to enable hybrid breeding. Rye is allogamous and only recently domesticated, thus giving cultivated ryes access to a diverse and exploitable wild gene pool. To further enhance the agronomic potential of rye, we produced a chromosome-scale annotated assembly of the 7.9-gigabase rye genome and extensively validated its quality by using a suite of molecular genetic resources. We demonstrate applications of this resource with a broad range of investigations. We present findings on cultivated rye’s incomplete genetic isolation from wild relatives, mechanisms of genome structural evolution, pathogen resistance, low-temperature tolerance, fertility control systems for hybrid breeding and the yield benefits of rye–wheat introgressions.
Rye (Secale cereale L.), a member of the grass tribe Triticeae and close relative of wheat (Triticum aestivum L.) and barley (Hordeum vulgare L.), is grown primarily for human consumption and animal feed. Rye is uniquely stress tolerant (biotic and abiotic) and thus shows high yield potential under marginal conditions. This makes rye an important crop along the northern boreal-hemiboreal belt, a climatic zone predicted to expand considerably in Eurasia and North America with anthropogenic global warming1. Currently, rye is produced on 4.1 million ha (http://www.fao.org/faostat/en/, accessed June 2020), 81% of which is in northeastern Europe. More importantly, however, rye chromatin is commonly introgressed into bread wheat varieties to improve yield and thus rye genetic material is present in a far greater proportion of cultivated land area2,3,4,5. Rye is a diploid with a large genome (~7–8 gigabases, Gb)6, 50% larger than the syntenic diploid barley and bread wheat subgenomes7. Like barley and wheat, rye entered the genomics era very recently. A virtual gene-order was released in 20138 and a shotgun de novo genome survey of the same line became available in 20179. Both resources have been rapidly adopted by researchers and breeders10,11,12 but cannot offer equivalent opportunities to the high-quality genome assemblies available for other Triticeae species7,13,14,15,16,17.
We report a short-read based chromosome-scale genome assembly for rye inbred line ‘Lo7’ and demonstrate the potential of this new genomic resource by dissecting the incomplete genetic isolation of rye from wild relatives. We showcase detailed analyses of the genomic organization and complexity of gene families implicated in stress tolerance and pollen fertility. This resource will guide future rye breeding and provide immediate benefit in managing the trade-offs of using rye as a genetic resource in wheat crop improvement.
Genome assembly, validation and annotation
We de novo assembled scaffolds representing 6.74 Gb of the estimated 7.9 Gb ‘Lo7’ genome from >1.8 Tb of short-read sequence (Methods; Supplementary Table 1 and Supplementary Note). These scaffolds were ordered, oriented and curated using: (1) chromosome-specific shotgun (CSS) reads8, (2) 10x Chromium linked reads, (3) genetic map markers9, (4) three-dimensional chromosome conformation capture sequencing (Hi-C)18 and (5) a Bionano optical genome map (Supplementary Tables 2–7). After intensive manual curation (Supplementary Note), 92% of this assembled sequence (~78% of the estimated genome size) was arranged first into super-scaffolds (N50 > 29 megabases, Mb) and then into pseudomolecules. Shotgun reads (~947 Gb of data, ~120× mean depth-of coverage) were mapped back to the assembly to confirm a near-unimodal coverage distribution consistent with a high-quality assembly (Supplementary Table 8 and Supplementary Note). De novo annotation (Methods; Supplementary Table 9) yielded 34,441 high-confidence (HC) genes, including 96.4% of the BUSCO (v.3) near-universal single-copy ortholog set (Supplementary Table 1), 19,456 full-length DNA long terminal repeat (LTR) retrotransposons (LTR-RTs) from six transposon families (Supplementary Table 10)19, 13,238 putative microRNAs (miRNAs) in 90 miRNA families (Supplementary Tables 11–17) and 1,382,323 tandem repeat arrays (Supplementary Tables 18 and 19). Full-length LTR-RTs represent a similar proportion of the total assembly in relation to genome size as shown by other recent Triticeae chromosome-scale assemblies (Supplementary Note and Supplementary Table 20) providing further evidence for high assembly quality and completeness20. Fluorescence in situ hybridization (FISH) to mitotic rye chromosomes confirmed agreement between in silico predicted and true physical distribution of distinct low- and high-copy probe sequences (Methods; Supplementary Note and Supplementary Table 21).
The rye genome follows similar organization as previously reported for other Triticeae genomes7,13 (Fig. 1 and Supplementary Note): chromosomes are lacking recombination over ~50% of their physical length (Fig. 1a) and gene density increases by a factor of >10 towards the telomeres (Fig. 1b).
Gene collinearity plots (Fig. 1c and Supplementary Notes) between rye (‘Lo7’), barley (cv. ‘Morex’) and wheat (cv. ‘Chinese Spring’), confirm, with the exception of the gene-scarce zones surrounding centromeres, extensive genome collinearity. Genome expansion occurred rather uniformly over most of the chromosome arms with some acceleration toward distal regions, reflected by collinearity plots curving towards the telomeres (Supplementary Note). This expansion might be attributed predominantly to activity of LTR-RT families affecting the intergenic space21,22. We therefore estimated the time of highest insertion activity for the most frequent rye LTR-RT families RLG_SABRINA, RLG_WHAM and RLC_ANGELA (Methods; Fig. 1d–g and Supplementary Note). RLC_ANGELA elements did recently target this genomic niche and older RLG_SABRINA and RLG_WHAM expansions affected more proximal parts of the chromosome arms. Two distal regions on the long arms of rye chromosomes 4R and 6R, however, differed by a lack of the more ancient activity of the RLG_SABRINA and RLG_WHAM families, possibly highlighting regions affected by ancient translocation events from a rye with a different retrotransposon landscape to ‘Lo7’ (Supplementary Note). RLG_CEREBA elements (Fig. 1g) were active in centromeres, acting more constantly over longer time scales than the other frequent LTR-RT families.
Rye genome evolution
Large structural variations—mechanisms of genetic isolation
Megabase-scale inversions are a common feature of structural variation (SV) in the related barley genome23. In the absence of multiple rye genome assemblies, we sought to make a first survey of large SV prevalence among rye cultivars and wild relatives using three-dimensional conformation capture sequencing (Hi-C; Methods; Supplementary Note)23. In the comparison between two cereal rye cultivars ‘Lo7’ and ‘Lo225’, representing the two distinct heterotic gene pools in hybrid-rye breeding, megabase-scale inversions are apparent on four of the seven rye chromosomes (Fig. 2a and Supplementary Note). Among them, a 50-Mb inversion (comprising 382 HC genes) on chromosome 5R (positions ~650–700 Mb), coincides with a region lacking genetic recombination (Fig. 2b), providing genetic corroboration for its presence. This observation points to a previously undocumented source of unwanted linkage drag potentially affecting rye breeding efforts. Large inversions between ‘Lo7’ and other Secale representatives in the sample increase in number dependent on the phylogenetic distance to S. cereale and occur preferentially in the pericentromeric low-collinearity regions (P < 0.001, one-tailed empirical distribution derived from 10,000 simulations; Supplementary Note). Large SVs therefore provide a potential mechanism for localized collinearity loss between the pericentromeric regions of Triticeae species. This collinearity loss provides, in turn, at least one mechanism for effective genetic isolation during speciation24.
Reticulate evolution of rye
Rye’s divergence from its close relatives wheat and barley has not been comprehensively resolved. Using a draft assembly, Martis et al.8 interpreted variation in sequence identity between rye and barley along chromosomes as a possible indicator of ancient species hybridization creating a ‘mosaic’ genome. Genome-wide estimations of fixation indices (Fst) and ABBA-BABA-based D-statistics have reflected varying levels of recent genetic exchange among Secale groups25. We confirmed, using D-statistics, that directional gene flow has occurred between rye groups (Methods; Supplementary Table 22). We then extended Martis et al.8 sequence identity approaches with higher resolution proxies measurable across the chromosomes. Reticulation reduces the evolutionary distance between individuals of each species at any site where chromatin was secondarily exchanged, causing phylogenetic discordance among loci. Using the sequence identity of reciprocal best BLAST matches between rye CDS sequences and CDS sequences from barley cv. ‘Morex’13 and wheat cv. ‘Chinese Spring’7(Methods; Supplementary Note), we found no strong evidence of discordance among these genera: rye is more closely related to the bread wheat genomes than to barley across the whole genome (Table 1).
We then produced an analogous analysis for Secale species by calculating identity-by-state (IBS) statistics between ‘Lo7’ and sequence data from a population of 955 cultivated and wild ryes (dataset of Schreiber et al.25, expanded here by a further 352 genotypes; Methods). We used k-means clustering to define seven rye genetic clusters (Fig. 2c,d). In contrast to the intergenus comparisons, recent reticulation among rye clusters was strongly supported. In general, ‘Lo7’ is most closely related to S. cereale and S. vavilovii-dominated clusters and successively less related to S. strictum-like clusters and most distant from the S. sylvestre-dominated cluster (Fig. 2d; Supplementary Note). However, clear departure from this pattern occurs frequently (Fig. 2e,f and Supplementary Note). For example, at regions on chromosomes 1R and 4R (marked on Fig. 2e,f), S. sylvestre-like individuals are closely related to ‘Lo7’, often more closely even than some S. strictum-like individuals, suggesting recent genetic exchange between S. cereale-like and S. sylvestre-like genotypes. Pairwise Fst was calculated to assess the proportions of genetic variability within and between cluster groups and shows considerable variability across the chromosomes, especially comparing within- and between-group variability among S. strictum-like and ‘domesticated’-like clusters (Fig. 2d–f). On chromosome 4R, for instance, Fst is almost 0.8 along the pericentromeric region (~200–400 Mb) but approaches zero at two interstitial positions (~600 and 720 Mb), corroborating incomplete genetic separation between these subgroups.
To investigate the effects of incomplete genetic isolation on recent selection pressures exerted on domesticated rye, we examined the ratio of nonsynonymous to synonymous mutations in exonic single nucleotide polymorphisms (SNPs) segregating among ryes (Pn/Ps) but which shared an allele with the consensus state of the three bread wheat genomes (a proxy for the ancestral state), thus surveying primarily recent mutations within rye lineages (Methods). Under equivalent selective regimes, Pn/Ps values for wild and domesticated ryes are expected to be approximately equal but we observed Pn/Ps divergence in the low-collinearity pericentromeric regions of chromosomes 1R, 3R and 4R. This divergence probably reflects the reduced efficacy of selection in such regions where recombination is limited (for example, by SVs).
On the basis of these collected observations, we concur with the Martis et al.8 hypothesis that the genome of cereal rye is a mosaic in the sense that different rye species are not completely reproductively isolated; however, we did not produce any evidence to suggest that the mosaic involves intergeneric hybridization.
Tracking the fate of rye chromatin in wheat improvement
The transfer of rye genetic material into bread wheat can provide substantive yield and stress tolerance benefits26, though at the expense of bread-making quality27. These transfers involved a single 1BL.1RS Robertsonian translocation originating from cv. ‘Kavkaz’ and a single 1AL.1RS translocation from cv. ‘Amigo’ (Fig. 3)3,4. Due to the trade-off between yield and quality, wheat breeders must screen their programs for rye introgressions. Taking advantage of the new rye assembly, we implemented a high-throughput sequencing-based approach on four expansive wheat germplasm panels (Kansas State University (KSU), United States Department of Agriculture Regional Performance Nursery (USDA-RPN), International Maize and Wheat Improvement Center (CIMMYT), Wheat and Barley Legacy for Breeding Improvement (WHEALBI); Methods) segregating for both 1AL.1RS and 1BL.1RS. Translocations can be observed as obvious changes in normalized read depth across both the translocated and replaced chromosomal regions (Fig. 3b and Supplementary Note).
Human classification of a whole panel of karyotypes is still costly in terms of time. To alleviate this bottleneck, we developed an automated support vector machine (SVM) classifier that replicates human assignment with over 97% accuracy (Methods; Fig. 3c,d). We then demonstrated that the automated classifications predict yield. A mixed-effects linear model applied to yield data available for the autoclassified individuals in the KSU (n = 19,677) and USDA (n = 29,035) breeding panels showed that 1R introgressions could increase average yields up to ~4.55% (Table 2; Methods; Supplementary Tables 23–25). The 1AL.1RS karyotype significantly outyielded 1BL.1RS in the KSU panel but the reverse was true of the USDA panel (Table 2). This is probably due to the effects of foreign chromatin being highly nonuniform and influenced by diverse factors (Supplementary Note), in particular the wheat genetic background27,28. Taking advantage of the ‘Lo7’ chromosome-scale assembly, tracking of rye chromatin in wheat breeding programs will now become more reliable and predictable.
Rye vigor is in the genes
Rye distinguishes itself from other Triticeae through strong allogamy, which facilitates commercial hybrid-rye breeding, as well as conferring resilience to biotic stress and extreme winter-hardiness, qualifying rye as an important plant genetic resource in wheat improvement. Here, we showcase how the high-quality genome assembly sheds light on the genetic control of these specific aspects of rye biology.
Fertility restoration in rye and wheat
Rye hybrid breeding relies on efficient cytoplasmic male-sterility (CMS)/restorer-of-fertility (Rf) systems; however, the underlying molecular mechanisms have yet to be elucidated. Known Rf genes belong to a distinct clade of the pentatricopeptide repeat (PPR) RNA-binding factor family, referred to as Rf-like (RFL)29,30. Members of the mitochondrial transcription TERmination factor (mTERF) family are probably also involved in male fertility restoration in cereals31,32. The ‘Lo7’ assembly reveals a PPR-RFL/mTERF hotspot on 4RL coinciding with known Rf loci for two rye CMS systems known as CMS-P (the commercially predominant ‘Pampa’-type) and CMS-C12,33,34,35(Methods; Fig. 4a–f, Supplementary Tables 26 and 27 and Supplementary Note). We determined, as previously suggested, that these two loci, Rfp and Rfc, are closely linked but physically distinct36 (Supplementary Table 28). Two members of the PPR-RFL clade reside within 0.186 Mb of the Rfc1 locus (Supplementary Tables 26–28). The Rfp locus, in contrast, is neighbored by four mTERF genes (Supplementary Tables 27–28), in agreement with previous reports that an mTERF protein represents the Rfp1 candidate gene in rye32,37.
The new assembly also helped to dissect a strong candidate gene for the wheat locus Rfmulti (Restoration-of-fertility in multiple CMS systems) on wheat chromosome 1BS. Replacement of the wheat Rfmulti locus by its rye ortholog using 1RS.1BL chromosome translocations produces the male-sterile phenotype38,39. At the syntenic position of Rfmulti, wheat and rye share a PPR-RFL gene cluster7 (Fig. 4k, Supplementary Table 26 and Supplementary Note). Only two wheat RFL-PPR genes in the cluster, TraesCS1B02G071642.1 and TraesCS1B02G072900.1, encode full-length proteins; only the latter corresponds to a putative rye ortholog (SECCE1Rv1G0008410.1). Thus, the absence of a TraesCS1B02G071642.1 ortholog in the nonrestorer rye suggest it as an attractive Rfmulti candidate. Current implementations of a wheat–rye Rfmulti CMS system involve 1RS.1BL translocations5,40,41, which are typically linked to reduced baking quality27. Efforts to break this linkage may now benefit from marker development and/or genome editing approaches targeting TraesCS1B02G071642.1 (ref. 42).
Divergence of disease resistance loci in Triticeae
Rye plays an important role as genetic resource of biotic stress tolerance in wheat varieties carrying rye chromatin insertions. Race-specific pathogen resistance is typically associated with members of the class of nucleotide-binding-site and leucine-rich repeat (NLR)-motif genes43. We annotated 792 full-length rye NLR genes, finding them enriched in distal chromosomal regions, similar to what has been seen recently in the bread wheat genome7,44 (Fig. 4e and Supplementary Tables 29 and 30). We compared the genomic regions in rye that are orthologous to mildew (Pm2, Pm3 and Mla) and rust (Lr10) resistance gene loci from wheat and barley (Fig. 4g–j, Supplementary Table 31 and Supplementary Note). All loci, except for Lr10, contained complex gene families with several subfamilies either present or absent in individual genomes, indicating either functional redundancy or the evolution of distinct resistance specificities or targets. For example, the wheat Pm3 and rye Pm8/Pm17 genes are orthologs and belong to a subfamily (clade A, Fig. 4i) which is absent in barley, whereas a different distinct subfamily (clade B, Fig. 4i) of the Pm3 genes is present in wheat and barley but absent in rye (Supplementary Note). In essence, the ‘Lo7’ assembly reveals the genomic organization of conserved or nonorthologous NLR gene clusters, which can be exploited in future rye and wheat improvement efforts.
Rye possesses superior low-temperature tolerance (LTT) to other Triticeae crops45. A syntenic locus Fr2 comprising a cluster of CBF (C-repeat/DRE-binding factor) genes is present on Triticeae group 5 chromosomes controlling LTT46 in rye47, T. monococcum48, bread wheat49,50 and barley51. In cold-tolerant varieties, LTT-implicated CBF genes of the Fr2 locus are transcriptionally upregulated52,53. In ‘Lo7’, the Fr2 locus comprises a cluster of 21 CBF-related genes at 614.3–616.5 Mb on 5R (Fig. 4f and Supplementary Table 32).
Since CBF gene family expansion correlates with increased LTT in other Triticeae54 (Supplementary Note), we analysed phased-linked-read (10x Genomics Chromium) data of an Fr2-homozygous line with exceptional LTT (‘Puma-SK’ derived from rye variety ‘Puma’) in comparison to ‘Lo7’ (low LTT). Four of the Fr2 CBF genes, all members of the same CBF subfamily (Supplementary Note) for which CNV has been previously implicated in LTT in wheat54, showed patterns of copy number variation (CNV) (SECCE5Rv1G030450, SECCE5Rv1G030460, SECCE5Rv1G030480 and SECCE5Rv1G030490; Supplementary Table 33 and Supplementary Note).
Transferring superior LTT from rye to wheat by translocation is an attractive breeding goal. We derived a 5A.5RL translocation line in winter wheat ‘Norstar’ using ‘Puma’ rye as the 5R donor, thus replacing the wheat 5A CBF cluster (Methods; Fig. 5a,b). LTT, however, was not notably altered by the translocation compared to ‘Norstar’ (Fig. 5c), suggesting that the rye CBF gene cluster is activated but, as previously suggested by Campoli et al.53, differently regulated in the wheat background. Gene expression of ‘Puma’ CBFs with CNV were indeed attenuated during treatments of cold stress in ‘Norstar5A:5R’ (Methods; Fig. 5c). Therefore, transferring LTT from rye into wheat will require indepth understanding of differences in the LTT regulatory network between rye and wheat.
The high-quality chromosome-scale assembly of rye inbred line ‘Lo7’ constitutes an important step forward in genome analysis of the Triticeae crop species and complements the resources recently made available for different wheat species14,55,56,57,58 and barley13,59. This resource will help reveal the genomic basis of differences in major life-history traits between the self-incompatible, cross-pollinating rye and its selfing and inbreeding relatives. Our evolutionary analyses demonstrate that rye subspecies are better conceptualized as a reticulated group of incipient species and that mechanisms such as transposable-element expansion and SV between genotypes are probably acting to bring about evolutionary divergence. The joint use of the rye and wheat genomes to characterize the effects of rye chromatin introgressions may provide a short-term opportunity to breeders as they continue to better separate confounding variables from the genetic combinations that best improve yield in various environments; but these benefits will ultimately be affected by negative linkage so long as whole chromosome arm translocations are involved. Discoveries at the single-gene level—such as the contributions offered here to pathogen resistance, LTT and male fertility restoration control—will be best tested and exploited by finer-scale manipulation in dedicated experiments12. This is an indispensable prerequisite for the development of gene-based strategies that exploit untapped genetic diversity in breeding materials and ex situ gene banks to improve small grain cereals and meet the changing demands of global environments, farmers and society.
Genome size estimation by flow cytometry
We characterized the landscape of S. cereale genome sizes to contextualize the size of the ‘Lo7’ genome and gain an impression of genome size variation within the species. Grains from 15 diverse rye accessions were from nine providers listed in Supplementary Table 1. Plants of pea (seeds provided by Semo breeding station, Smržice, Czech Republic) served as an internal reference standard in flow cytometric estimation of nuclear DNA content in all accessions, except of the tetraploid accession ACE-1, for which S. cereale line ‘Lo7’ was used as a reference. Plants were raised in garden compost in pots and maintained in a greenhouse until they reached a height of 10–20 cm. Nuclear genome size was estimated essentially as described by Doležel et al.60 using a CyFlow Space flow cytometer (Sysmex Partec) equipped with a 532-nm green laser. The gain of the instrument was adjusted so that the peak representing interphase first growth (G1) nuclei of the standard was positioned approximately on channel 100 on a histogram of relative fluorescence intensity when using a 512-channel scale. Five individual plants per test species were sampled and each sample was analysed three times, each time on a different day. A minimum of 5,000 nuclei per sample was analysed and 2C DNA contents in pg were calculated from the means of the G1 peak positions by applying the following formula:
Mean nuclear DNA content (2C) was then calculated for each accession. DNA contents in pg were converted to genome size in bp using the conversion factor 1 pg DNA = 0.978 Gb (ref. 61). Statistical analysis was performed using NCSS 97 statistical software package (Statistical Solutions). One-way analysis of variance and a Bonferroni’s (all pairwise) multiple comparison test were used for analysis of variation in monoploid (1C×) genome size. A significance level α = 0.01 was used.
‘Lo7’ genome assembly and gene annotation
Descriptions of the assembly methods, descriptions of the data generation and the annotation procedure for gene features, are given in the Supplementary Note.
Fluorescence in situ hybridization (FISH)
Three-day-old roots of the rye accession were pretreated in 0.002 M 8-hydroxyquinoline at 7 °C for 24 h and fixed in ethanol:acetic acid (3:1 v/v). Chromosome preparation and FISH were performed according to the methods described by Aliyeva-Schnorr et al.62. The hybridization mixture contained 50% deionized formamide, 2× SSC, 20% dextran sulfate and 5 ng µl–1 of each probe. Slides were denatured at 75 °C for 3 min and the final stringency of hybridization was 76%. We used 34–65 nucleotide-long 5′-labeled oligo probes designed for the in silico identified repeats and published probe sequence (Supplementary Table 21). Images were captured using an epifluorescence microscope BX61 Olympus equipped with a cooled CCD camera (Orca-ER, Hamamatsu). Chromosomes were identified visually on the basis primarily of morphology, heterochromatic DAPI + bands and the localization of probe pSc119.2.1 (ref. 63) (Supplementary Note).
Gene-level synteny and percentage identity scores between rye and other Triticeae species
HC gene sequences from the ‘Lo7’ gene annotation were aligned to the annotated transcriptomes of bread wheat7 (T. aestivum cv. ‘Chinese Spring’) and barley13 (H. vulgare cv. ‘Morex’) using BLASTn (v.2.9.0+)64 with default parameters. The lowest E-value alignment for each gene against the transcriptome associated with each subject genome (or subgenome) was selected, with the highest bitscore and then longest alignment chosen in the case of a tie. Only reciprocal best matches per (sub)genome were accepted. Relative evolutionary distances between rye, barley and the wheat subgenomes were estimated using the mean percentage identity scores of these filtered matches, calculated in bins of 100 reciprocal matches (in increments of 20 bins). The positions of the bins on the pseudomolecules were taken to be the mean match position of the matches within each bin.
Phylogenetic analyses, IBS statistics, F st, D-statistics and P n/P s
The genotyping-by-sequencing (GBS) dataset of 603 samples from Schreiber et al.25 was extended by a 347 further GBS samples from the IPK gene bank (mainly wild Secale taxa) and the five samples used in the Hi-C SV-detection study (‘Lo7’, ‘Lo225’, ‘R1003’, ‘R925’ and ‘R2446’). The resulting sample set (n = 955) and passport data are listed in Supplementary Table 34. DNA isolated from the five Hi-C samples was sent to Novogene (en.novogene.com/) for Illumina library construction and sequencing in multiplex on the NovaSeq platform (paired-end 150-bp reads, ~140 Gb per sample, S2 flow cell). Demultiplexing, adapter trimming, read mapping and variant calling correspond to the approach described in Schreiber et al.25, using the new reference for read mapping. The dataset was filtered for a maximum of 30% missing data and a minor allele frequency of 1% resulting in 72,465 SNPs was used (Supplementary Note). A neighbor joining tree was constructed with the R package ‘ape’65, on the basis of genetic distances computed with the R package SNPRelate66. Principal component analysis (PCA) was performed with smartPCA from the EIGENSOFT v.6.0.1 package (github.com/DReichLab/EIG) using least square projection without outlier removal. Seven rye genetic clusters were designated using the ‘kmeans’ R function, with default parameters, using the first three principal components from the PCA as input.
For IBS and Fst analyses, a more stringent filtering regime requiring read depth ≥ 6, maximum 5% missing data and call quality ≥ 250 (resulting in 9,538 SNPs) was selected (Supplementary Note). IBS scores between ‘Lo7’ and the other lines in the set were calculated in windows of 100 consecutive SNP loci (at intervals of 25 SNP loci) using the snpgdsIBS function in the R package SNPRelate. Fst was calculated in the same windows using the snpgdsFst function in the R package SNPRelate (using method=’W&H02’). The calculation was performed for every pairwise combination of the following groups: ‘Domesticated-like’ (cluster 3), ‘Wild–S. strictum-like’ (clusters 1, 5 and 6) and ‘Wild–S. sylvestre-like’ (cluster 4).
To assign ancestral states to variant SNPs segregating in rye, exonic variants identified in the GBS dataset were coupled to their orthologs alleles in the three bread wheat (‘Chinese Spring’)7 alleles using the rye-versus-wheat CDS BLAST alignments (see above) and parsing the BLAST alignment strings using the custom script blast_get_alleles_at_position.c (https://github.com/mtrw/tim_bioinfo_tools). Reciprocal best matches were calculated separately for the alignments between the rye CDS set and the set of CDSs from each wheat genome. The ancestral allele was assigned by consensus among the wheat genomes and, if no allele claimed a majority, the variant was omitted from the dataset. Genome-wide D-statistics were calculated according to the four-taxon ABBA-BABA method as described in ref. 67, with the wheat consensus allele as the outgroup and selections of the k-means-assigned clusters selected as the three test populations. Estimator variance was approximated via the block jackknife procedure, with 5 Mb exclusion bins. The effects of the rye-versus-wheat nucleotide differences falling within coding sequences were annotated using SnpEff (v.4, ‘ann’ function), with default parameters. Pn/Ps scores (the ratio of counts of nonsynonymous to synonymous differences to wheat in variants segregating in rye) were calculated using the same binning scheme as was used for Fst and IBS (see above). Pn/Ps scores were calculated separately for subgroups of rye clusters representing ‘wild-like’ and ‘domesticated-like’ ryes separately (see main text). Pn/Ps scores were only estimated for bins in which the combined number of rye-segregating variants exceeded nine.
Wheat–rye introgression haplotype identification and classification
We assayed for the presence of 1R germplasm in wheat genotypes in silico by mapping various wheat sequence data to a combined reference genome made up of the pseudomolecules of rye line ‘Lo7’ (this study) and wheat cv. ‘Chinese Spring’7. Publicly available data were obtained from WHEALBI project resources68 (n = 506), CIMMYT (n = 903) and KSU (n = 4,277). GBS libraries were constructed and sequenced for samples from USDA-RPN (n = 875; Supplementary Table 23) as described in Rife et al.69. On the basis of the approach described by Keilwagen et al.70, reads were demultiplexed with a custom C script (github.com/umngao/splitgbs) and aligned to the combined reference using bwa mem (v.0.7, arguments -M)71 after trimming adapters with cutadapt72. The aligned reads from all panels were filtered for quality using samtools73 (v.1.9, arguments -F3332 -q20). The numbers of reads aligned to 1 Mb nonoverlapping bins on each pseudomolecule were tabulated. The counts were expressed as rpmm ≡ log2(reads mapped to bin per million reads mapped). To control for mappability biases over the genome, the rpmm for each bin was normalized by subtracting the rpmm attained by the ‘Chinese Spring’ sample for the same bin to give the normalized rpmm, r.
To investigate the possibility of classifying the samples automatically, visual representations of r across the combined reference genome were inspected and obvious cases of 1R.1A and 1R.1B introgression were distinguished from several other karyotypes, including nonintrogressed samples and ambiguous samples showing a slight overabundance of 1RS reads but less discernible signals of depletion in 1A or 1B (Supplementary Note). We defined the following features for each sample: featureA = –log[(mean(r1AI) – mean(r1AN)) × (mean(r1RI) – mean(r1RN))] and featureB = –log[(mean(r1BI) – mean(r1BN)) × (mean(r1RI) – mean(r1RN))]. Whenever the term inside the log was negative (and would thus give an undefined result), the value of the feature was set to the minimum of the defined values for that feature. The quantity mean(r1RI) refers to the average value of r for all bins within the terminal 200 Mb of the normally introgressed (I) end of 1R (an N in the subscript denotes the terminal 300 Mb of the normally nonintrogressed (N) arm) and so forth for other chromosomes. This choice of feature definition meant that, wherever little difference in r occurred between 1RS and 1RL, suggesting no presence of rye, the factor mean(r1RI) – mean(r1RN) would pull the feature values close to the origin and differences between r on the long and short arms of 1A or 1B would pull the values of A or B respectively away from the origin, depending upon which introgressions are present. A classifier was developed by training an SVM to distinguish nonintrogressed, 1A.1R-introgressed, 1B.1R-introgressed and ambiguously introgressed samples, using the function ksvm (arguments Type=’C-svc’, kernel=‘rbfdot’, C=1) from the R package kernlab. Classification results are given in Supplementary Table 25. Testing was performed by generating sets of between 50 and 600 random samples from the dataset and using these to train a model, then using the kernlab::predict() to test the model’s accuracy of prediction on the remaining data not used in training. This was repeated 100 times for each training dataset size.
To confirm the common origin of the 1AL.RS and 1BL.1RS introgressions, predicted 1RS carriers were selected to form a combined 1RS panel (over 1,200 lines) to call SNPs. A total of over 3 million SNPs were called with samtools/bcftools v.1.9 (mpileup -q20, -r chr1R:1-300000000; call -mv). SNPs were filtered on the basis of combined minimum read depth of 25, minor allele frequency of 0.01. A total of >900,000 SNPs were obtained. All IBS percentages were calculated and the square root values of per cent different calls were used to derive a heatmap for all pairwise comparisons (Supplementary Note).
SV detection in ‘Puma-SK’ and ‘NorstarPuma5A:5R’
To characterize the Fr2 region in ‘Puma-SK’ and the introgression in ‘NorstarPuma5A:5R’, whole-genome sequencing was performed using the Chromium 10x Genomics platform. Nuclei were isolated from 30 seedlings and high molecular-weight genomic DNA was extracted from nuclei using phenol chloroform according to the protocol of Zheng et al.74. Genomic DNA was quantified by fluorometry using Qubit 2.0 Broad Range (Thermofisher) and size selection was performed to remove fragments smaller than 40 kb using pulsed field electrophoresis on a Blue Pippin (Sage Science) according to the manufacturer’s specifications. Integrity and size of the size-selected DNA were determined using a Tapestation 2200 (Agilent) and Qubit 2.0 Broad Range (Thermofisher), respectively. Library preparation was performed as per the 10x Genomics Genome Library protocol (https://support.10xgenomics.com/genome-exome/library-prep/doc/user-guide-chromium-genome-reagent-kit-v2-chemistry) and uniquely barcoded libraries were prepared and multiplexed for sequencing by Illumina HiSeq. Demultiplexing and the generation of fastq files were performed using LongRanger v.2.2.0 mkfastq (https://support.10xgenomics.com/genome-exome/software/pipelines/latest/using/mkfastq; default parameters).
Sequencing reads from ‘Puma-SK’ and ‘NorstarPuma5A:5R’ were aligned to the rye line ‘Lo7’ and bread wheat cv. ‘Chinese Spring’7 genome assemblies, respectively, using LongRanger WGS (https://support.10xgenomics.com/genome-exome/software/pipelines/latest/using/wgs; arguments -vcmode ‘freebayes’). Large-scale structural variants detected by LongRanger were visualized with a combination of Loupe (v.2.1.1; https://support.10xgenomics.com/genome-exome/software/visualization/latest/what-is-loupe; downloaded February 2019; Supplementary Table 33). Short variants were called using the Freebayes software (github.com/ekg/freebayes) implemented within the Longranger v.2.2.0 WGS pipeline. For determining the introgression, ‘NorstarPuma5A5R’ reads which did not map to the ‘Chinese Spring’ reference were aligned to the ‘Lo7’ assembly using the LongRanger align pipeline (https://support.10xgenomics.com/genome-exome/software/pipelines/latest/advanced/other-pipelines). Samtools (v.1.9)73 bedcov was used to calculate the genome-wide read coverage across both references. CNV between ‘Puma-SK’ and ‘Lo7’ was detected using a combination of barcode coverage analysis output by the Longranger WGS pipeline and read depth-of-coverage based analysis using CNVnator75 v.0.4 and cn.mops76 v.1.12.0.
Expression profiling of ‘NorstarPuma5A:5R’ and ‘Puma’
RNA from ‘NorstarPuma5A:5R’ and ‘Puma’ was isolated and sequenced as described above. Sequencing adapters were removed and low-quality reads were trimmed using Trimmomatic77. RNA reads from ‘NorstarPuma5A:5R’ and ‘Puma’ were aligned to the ‘Lo7’ reference using Hisat2 (ref. 78; v.2.1.0; default arguments) and transcripts were quantified with htseq (ref. 79; v.11.1; default parameters). Differential expression analysis was carried out using DESeq2 (ref. 80; v.3.11; default parameters).
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The ‘Lo7’ assembly and gene feature annotation data are available via e!DAL at https://doi.org/10.5447/ipk/2020/33 and https://doi.org/10.5447/ipk/2020/29. The visual suite of resources for assembly assessment are stored at https://doi.org/10.5447/ipk/2020/32. Raw sequence data generated in the course of the study are available at European Nucleotide Archive (ENA) with accession numbers PRJEB32636 (PE and MP data for assembly), PRJEB32574 and PRJEB34626 (Hi-C), PRJEB34439 (10x), PRJEB32587 (CSS), PRJEB35392 (GBS data) and PRJEB35461 (RNAseq and IsoSeq for annotation of ‘Lo7’). Chromium 10x and RNAseq data for ‘Puma’ and ‘Norstar’ are available at PRJNA564622. The SNP matrix used for rye population genetic analyses is available via e!DAL at https://doi.org/10.5447/ipk/2020/31. GBS and sequence data generated for the USDA and CIMMYT wheat diversity panels are available at ENA with accession numbers PRJNA566410, PRJNA566408 and PRJNA566409. Optical map data and alignments are available via e!DAL at https://doi.org/10.5447/ipk/2020/30. High-stringency transposable element annotations (used for evolutionary analyses) are given in Supplementary Table 10, while the larger, low-stringency annotations (used for assembly quality comparisons) are available via e!DAL at https://doi.org/10.5447/ipk/2020/34.
The custom miRNA manipulation scripts used in miRNA annotation (SumirFind.pl, SumirFold.pl, SumirLocate_v2.py and Sumircreen_v2.py) are available at https://github.com/hikmetbudak/miRNA-annotation. Two custom scripts used for parsing BLAST output (get_alleles_at_position.c and blast_to_snps.c) are available at https://github.com/mtrw/tim_bioinfo_tools and custom R functions extending or modifying functions of the TRITEX assembly pipeline (version corresponding to commit ID 2898e74) are available at https://github.com/mtrw/Sc_genome_assembly. The custom tool used to demultiplex wheat panel GBS data (splitgbs.c) is available at github.com/umngao/splitgbs.
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We are grateful to M. Knauft, I. Walde, S. Koenig, M. Ziems and S. Thumm (Leibniz Institute of Plant Genetics and Crop Plant Research, IPK), J. Ens (University of Saskatchewan), C. Uauy and J. Simmonds (John Innes Centre), S. Duncan (Earlham Institute), Z. Dubská and J. Weiserová (Institute of Experimental Botany), A. Hastie (Bionano Genomics), K. Baruch (NRGene) and S. Taudien (Universitätsmedizin Göttingen) for providing technical, laboratory, greenhouse or bioinformatics services. A. Fiebig, D. Arend, J. Bauernfeind, T. Münch and H. Miehe (IPK) provided IT services. We thank A. Graner for helpful advice. Research for this project was supported by funding from: the Czech Science Foundation (grant no. 17-17564S) to H.S.; the Agriculture and Agri-Food Canada International Collaboration Agri-Innovation Program to A.L.; the Natural Resources Institute Finland Innofood Stategic Funds program to A.S.; the Biotechnology and Biological Sciences Research Council Designing Future Wheat program (grant no. BB/P016855/1) to A. Hall; the German Federal Ministry of Education and Research (BMBF) to K.F.X.M. and U.S. (project de.NBI no. FKZ 031A536) and E.B. (project RYE-SELECT no. FKZ 0315946A); the German Federal Ministry of Food and Agriculture (BMEL) (WHEATSEQ no. 2819103915) to K.F.X.M.; HYBRO Saatzucht GmbH & Co. KG to D.S.; the European Regional Development Fund’s plants as a tool for sustainable global development project (grant no. CZ.02.1.01/0.0/0.0/16_019/0000827) to J.D.; the 2Blades Foundation to B.W.; the Julius Kühn-Institute to B.H. and F.O.; KWS SAAT SE & Co. KGaA to V.K.; the Deutsche Forschungsgemeinschaft (grant no. HO 1779/30-1) to A. Houben; the Montana Wheat and Barley Committee to H.B.; the Noble Research Institute, LLC to X.-F. M.; the Australian Research Council (grant no. CE140100008) to I.S. and J.M.; Genome Canada and Genome Prairie (grant no. CTAG2) to C.J.P.; the National Research Council Canada’s Wheat Flagship Program to D.K. and A.S.; the Province of Saskatchewan Agriculture Development Fund to D.B.F.; the Bundesamt für Landwirtschaft, Bern (grant no. PGREL NN-0036) to B.K.; the Polish National Science Centre (grant nos. DEC-2015/19/B/NZ9/00921, DEC-2014/14/E/NZ9/00285 and 2015/17/B/NZ9/01694) to M.R.-T., H.B.-B., S.S. and B.M.
V.K. is an employee of KWS SAAT SE & Co. KGaA. D.S. is an employee of HYBRO Saatzucht GmbH & Co. KG. All other authors declare no competing interests.
Peer review information Nature Genetics thanks Peter Morrell and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
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Rabanus-Wallace, M.T., Hackauf, B., Mascher, M. et al. Chromosome-scale genome assembly provides insights into rye biology, evolution and agronomic potential. Nat Genet 53, 564–573 (2021). https://doi.org/10.1038/s41588-021-00807-0
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