- Research article
- Open Access
Genome constitution and evolution of Elytrigia lolioides inferred from Acc1, EF-G, ITS, TrnL-F sequences and GISH
BMC Plant Biologyvolume 19, Article number: 158 (2019)
Elytrigia lolioides (Kar. et Kir.) Nevski, which is a perennial, cross-pollinating wheatgrass that is distributed in Russia and Kazakhstan, is classified into Elytrigia, Elymus, and Lophopyrum genera by taxonomists on the basis of different taxonomic classification systems. However, the genomic constitution of E. lolioides is still unknown. To identify the genome constitution and evolution of E. lolioides, we used single-copy nuclear genes acetyl-CoA carboxylase (Acc1) and elongation factor G (EF-G), multi-copy nuclear gene internal transcribed space (ITS), chloroplast gene trnL-F together with fluorescence and genomic in situ hybridization.
Despite the widespread homogenization of ITS sequences, two distinct lineages (genera Pseudoroegneria and Hordeum) were identified. Acc1 and EF-G sequences suggested that in addition to Pseudoroegneria and Hordeum, unknown genome was the third potential donor of E. lolioides. Data from chloroplast DNA showed that Pseudoroegneria is the maternal donor of E. lolioides. Data from specific FISH marker for St genome indicated that E. lolioides has two sets of St genomes. Both genomic in situ hybridization (GISH) and fluorescence in situ hybridization (FISH) results confirmed the presence of Hordeum genome in this species. When E genome was used as the probe, no signal was found in 42 chromosomes. The E-like copy of Acc1 sequences was detected in E. lolioides possibly due to the introgression from E genome species. One of the H chromosomes in the accession W6–26586 from Kazakhstan did not hybridize H genome signals but had St genome signals on the pericentromeric regions in the two-color GISH.
Phylogenetic and in situ hybridization indicated the presence of two sets of Pseudoroegneria and one set of Hordeum genome in E. lolioides. The genome formula of E. lolioides was designed as StStStStHH. E. lolioides may have originated through the hybridization between tetraploid Elymus (StH) and diploid Pseudoroegneria species. E and unknown genomes may participate in the speciation of E. lolioides through introgression. According to the genome classification system, E. lolioides should be transferred into Elymus L. and renamed as Elymus lolioidus (Kar. er Kir.) Meld.
The taxonomic history of Triticeae mainly includes three stages, that is, artificial classification, natural or phonetic classification, and phylogenetic classification [1, 2]. Löve  divided Triticeae species into 37 genera according to the genomic system of classification, in which different species with the same genome or genome constitution were classified into one genus, although the justifiability of some genera remains controversial up to now. Many Triticeae species were reclassified into different genera on the basis of their genome constitutions [4,5,6,7]. However, the genome constitutions of many species with high ploidy in the genera Elytrigia, Elymus, and Roegneria in Triticeae still remain unknown or controversial.
Elytrigia lolioides (Kar. et Kir.) Nevski is a perennial, cross-pollinating wheatgrass that is distributed in Russia and Kazakhstan, has strong rhizomatous, and generally grows in stony mountain slopes, sandy land, and steppe [3, 8]. According to its morphological characteristics, E. lolioides is classified into different genera, including Triticum, Agropyron, Elytrigia, and Elymus, according to different classification systems [8, 9]. Cytological studies indicated that the chromosome number of E. lolioides is either 42 or 58 [10, 11]. It was suggested that this species contains St, E, and J genomes that are derived from Pseudoroegneria and Lophopyrum elongatum and L. bessarabicum, respectively, and is classified into Elytrigia . Dewey  supported this treatment but indicated that E. lolioides has St and unknown genomes, and the genome formula was designed as StX (X is undetermined genome). Yen and Yang  speculated that E. lolioides should be classified into genus Lophopyrum with E genome. Tao and Lin  suggested that E. lolioides contains StE genome. Therefore, the genome constitution and origin of E. lolioides remain controversial. According to the Dewey taxonomic principle, Elytrigia genus has five species, including E. repens, E. lolioides, E. pycnantha, E. pungens, and E. elongatiformis . Genome constitution of E. repens、E. pycnantha, and E. pungens were reported and these three species were classified into other genera . Therefore, investigating genome constitution of E. lolioides will be useful to investigate the taxonomic status of Elytrigia.
Chromosome pairing at meiosis in artificial hybrid is commonly used to detect the genome constitution of species [13,14,15,16]. Chromosome pairing at the metaphase I of meiosis is convincing step in determining the genome constitution of the target species. However, interpreting chromosome pairing at high ploidy levels is difficult because of the difficulty in distinguishing autosyndetic and homoeologous pairing in meiosis . Therefore, genomic in situ hybridization (GISH), specific molecular marker for genome or chromosome and phylogenetic analysis were used to investigate the genome constitution and origin of target species [18,19,20,21]. GISH is a fast and valuable tool to detect genome constitution and chromosomal translocation in species [22, 23]. Some genome-specific molecular and FISH markers were developed. These markers are stable and visual in detecting genome constitution and tracing target chromatin in wheat breeding program [24,25,26]. Phylogenetic analyses can identify the genome donors and introgression of polyploid. Single- or low-copy nuclear gene, multi-copy nuclear gene and cytoplasm gene have been successfully used to investigate parental and maternal origins [27,28,29]. Although undergoing concerted evolution, internal transcribed space (ITS) is a useful marker to conclude the genome origin of polyploid . Acetyl-CoA carboxylase (Acc1) gene, elongation factor G (EF-G), ITS, and the space between tRNA-Leu and tRNA-Phe gene (trnL-trnF region) sequences have been used to examine the phylogenetic relationship, hybridization events, parental donor, and maternal origin [31,32,33,34,35].
In the present study, the specific molecular markers for St genome, GISH, single-copy nuclear genes Acc1 and EF-G, multi-copy nuclear gene ITS, and chloroplast DNA trnL-F were used to investigate the genome constitution of E. lolioides. The objectives are as follows: (1) to detect the genome constitution and taxonomic treatment of E. lolioides, (2) to identify the maternal donor of E. lolioides, and (3) to clarify the origin of E. lolioides.
Phylogenetic analyses of ITS sequence
The length of E. lolioides ITS sequences ranged from 588 bp to 602 bp, and that of most sequences was ~ 601 bp. After multiple sequence alignments, the 13 bp deletion from 174 to 186 bp in the ITS1 region was found in an ITS sequence from E. lolioides (W6–26586, Fig. 1). The ITS data matrix of 79 sequences was analyzed based on maximum likelihood (ML) by using the GTR + I + G model (−Ln likelihood = 4280.8823). Brachypodium sylvaticum and Avena longiglumis were used as the outgroup. A total of 626 characters were used for phylogenetic analysis, in which 351 were constants, 112 were parsimony uninformative, and 163 were parsimony informative. Finally, a single phylogenetic tree was yielded with the following assumed nucleotide frequencies: A = 0.22610, C = 0.28870, G = 0.27680, T = 0.20840. The trees generated by Bayesian analysis and ML were similar to each other. The ML tree with bootstrap support (BS) values (above the branch) and Bayesian posterior probability (PP, below the branch) is displayed in Fig. 2.
The multiple copies of sequences from each E. lolioides accession were separated into two distinct clades. One clade contained 10 sequences each from E. lolioides and diploid Pseudoroegneria species (PP = 0.78). The other clade contained two sequences each from E. lolioides and diploid Hordeum species (BS = 98%, PP = 1.00).
Phylogenetic analyses of Acc1 sequence
The 31 and 38 positive clones were sequenced for the three accessions of E. lolioides. The length of these sequences ranged from 1400 bp to 1495 bp, and that of most sequences was ~ 1440 bp. All sequences contained eight exons and seven introns. These findings are similar to the results in a previous study . After multiple sequence alignments, 10 bp deletion was found in 43 sequences (17/31 in PI 440059, 14/38 in W6–26586, 12/28 in W6–26567) from the 110–119 position in intron 1 region. A 67 bp insertion at the 1015–1081 position in intron 5 region was found in two sequences from the two accessions of E. lolioides (PI440059 and W6–26586, Fig. 3). Blast search indicated that the 67 bp insertion belongs to Tc1 DNA transposon. Termination codon was found in the exon 5 of the two sequences from accession W6–26586, and these sequences were excluded in the phylogenetic analysis.
The phylogenetic analysis of the 82 Acc1 sequences was performed using Bromus inermis as the outgroup. The data matrix contained 1885 characters, 1353 of which were constants, 257 were parsimony uninformative, and 275 were parsimony informative. A signal phylogenetic tree generating by maximum likelihood analysis using the GTR + I + G model (−Ln likelihood = 8780.6729; assumed nucleotide frequencies: A = 0.25250, C = 0.18430, G = 0.21920, T = 0.34400) is shown in Fig. 4 with the BS from ML and PP values from Bayesian analyses.
Three distinct Acc1 copies of the sequences from each three accessions of E. lolioides were grouped into three different clades. The first clade was St clade, which included five diploid Pseudoroegneria species, tetraploid Elymus and Roegneria species, hexaploid species of Campeiostachys and E. lolioides (BS = 69%, PP = 1.00). In the St clade, Pseudoroegneria tauri, P. strigosa, P. stipifolia, Elymus sibiricus, Ely. trachycaulus, Roegneria caucasica, and three E. lolioides formed a paraphyletic grade. The second clade was the H genome clade, which contained the diploid species of Hordeum, tetraploid species of Elymus, hexaploid species of Campeiostachys and E. lolioides (BS = 100%, PP = 1.00). In the second clade, five E. lolioides sequences, two tetraploid species of Elymus (Ely. sibiricus and Ely. confuses) and Campeiostachys kamoji formed a subclade (PP = 56%, BS = 1.00). However, the third clade only contained sequences from E. lolioides without any diploid species (BS = 100%, PP = 1.00). One sequence each from the accession PI440059 of E. lolioides and L. bessarabicum was grouped together (BS = 56%, PP = 1.00). The Acc1 data displayed an evident Y genome clade (BS = 100%, PP = 1.00), and no sequences from E. lolioides were grouped in this clade.
Phylogenetic analysis of EF-G sequence
The EF-G matrix contained 71 taxa and 870 characters, 590 of which were constants, 127 were parsimony uninformative, and 153 were parsimony informative. HKY + G, as the best-fit model (−Ln likelihood = 3898.0823), was used in phylogenetic analysis. A single phylogenetic tree was yielded and the assumed nucleotide frequencies: A = 0.26340, C = 0.19760, G = 0.21780, T = 0.32120. The tree generated by Bayesian analyses and ML were similar to each other. The ML tree with BS values (above the branch) and Bayesian PP (below the branch) is displayed in Fig. 5.
The phylogenetic analyses of the EF-G sequence distinctly separated the three copies of sequences from the three accessions of E. lolioides into three different clades. The first clade was St clade, which included five Pseudoroegneria species, seven tetraploid Elymus species, five tetraploid Roegneria species and E. lolioides (PP = 93%, BS = 1.00). The second clade was the H clade, which contained the diploid of Hordeum species, seven tetraploid Elymus species and E. lolioides (PP = 99%, BS = 1.00). However, in the third clade, all sequences were only from E. lolioides that were grouped together (PP = 85%, BS = 1.00) and sisters to the sequences from diploid Aegilops, Triticum, Lophopyrum, Taeniatherum, and Crithopsis species. All these sequences had 7 bp deletion and 8 bp insertion in 164–172 and 215–224 bp positions, respectively (Fig. 6). Meanwhile, EF-G data displayed an evident Y genome clade (BS = 100%, PP = 1.00) and without any sequence from E. lolioides, which is similar to the results of the Acc1 phylogenetic tree.
Phylogenetic analyses of trnL-F sequence
A total of 42 trnL-F sequences were selected for ML analysis. B. tectorum was used as the outgroup. The data matrix contained 1013 characters, 884 of which were constants, 56 were parsimony uninformative, and 73 were parsimony informative. HKY + G as the best-fit model (−Ln likelihood = 2435.1624) was used in phylogenetic analysis, and a single phylogenetic tree was yielded. The assumed nucleotide frequencies were A = 0.33724, C = 0.15580, G = 0.13259, T = 0.37437. The tree generated by Bayesian analyses was similar to ML tree. The ML tree with BS values (above the branch) and Bayesian PP (below the branch) is shown in Fig. 7.
All trnL-F sequences were distinctly divided into five clades. The sequences from E. lolioides were grouped with diploid Pseudoroegneria, Lophopyrum, and Dasypyrum species (BS = 59%, PP = 0.99). In this clade, sequences from Lophopyrum species which contained E genome, formed a subclade (PP = 0.80).
In situ hybridization
Chromosome number analysis results indicated that E. lolioides is a hexaploid (2n = 6x = 42) wheatgrass. St2–80 is a FISH marker for St genome. Signals produced by St2–80 were present on the entire arm of the St genome chromosomes, except at the centromeric region. However, signals produced by St2–80 were present in the terminal region of the E and H genome chromosomes . This marker was used to detect St genome in the E. lolioides chromosomes. The signal on 28 chromosomes was displayed St type (Fig. 8a, b, and c). This result was confirmed by GISH, wherein 28 chromosomes were hybridized with the St probe from Pseudoroegneria libanotica (Fig. 8d). To detect the 14 other chromosomes, E (from Lophopyrum bessarabicum) and H (from Hordeum bogdanii) genomes were used as probes. After two-color GISH, no any E genome signals were displayed on the chromosomes (Fig. 8e). However, the chromosomes that did not hybridize with St genome displayed intense signals when probed by the H genome (Fig. 8f). Then, the test was performed using H genomes as probes in the three E. lolioides accessions (Fig. 8g, h, and i). Minor disparity was displayed in chromosome of W6–26586 that one chromosome which belongs to H genome did not hybridized H genome signals on the pericentromeric regions (Fig. 8i).
Maternal donor of E. lolioides
The chloroplast DNA (cpDNA) is maternally inherited in grasses . Several sequences, including space and coding regions (e.g., trnL-F, trnD-T, trnH-psbA, matK, Rps16, and rbcL) were used to identify the maternal donor of wheatgrass or genera in Triticeae [29, 32, 34, 38, 39]. In the present study, all sequences from E. lolioides with the sequences from the diploid Pseudoroegneria (St) and Dasypyrum (V) and the diploid and tetraploid Lophopyrum (E) formed a clade (BS = 59%, PP = 0.99) in trnL-F data. It seems to suggest that Pseudoroegneria, Dasypyrum, and Lophopyrum were the potential maternal donors of E. lolioides. In a previous study, close relationships among Pseudoroegneria, Dasypyrum, and Lophopyrum were discovered using the cpDNA data from diploid species in Triticeae [33, 40]. In contrast to the trnL-F data, Acc1 sequences from Pseudoroegneria, Dasypyrum, Lophopyrum, Hordeum, and other diploids were distinctly separated into different clades, and sequences from E. lolioides were placed into Pseudoroegneria, Lophopyrum, and Hordeum clades. No chromosomes that were hybridized with E probe were derived from L. bessarabicum in GISH. Thus, we infer Pseudoroegneria is a maternal donor of E. lolioides. Numerous studies indicated that Pseudoroegneria is a maternal donor of polyploid species containing St genome in Triticeae [41,42,43,44]. The female species in Triticeae carrying St genome are successful in terms of distant hybridization .
Origin of E. lolioides
Our results indicated that Pseudoroegneria is the major genome donor for E. lolioides. GISH and FISH indicated that E. lolioides had two sets of St genome. In strict consensus tree generated from the Acc1 sequence, several Acc1 sequences from the three accessions of E. lolioides formed a clade without any sequence from the diploid species in Triticeae. Meanwhile, all of these sequences had a 10 bp deletion that is absent in the other published Acc1 sequences of Triticeae species from the 110 to 119 positions in intron 1 region. Some non-synonymous substitutions were discovered in several of these sequences. One sequence that was placed into the St clade also had this deletion. The preliminary results in our laboratory also showed that the same deletion was found in Acc1 sequences from E. pungens, Psammopyrum athericum, and E. elongatiformis, which were collected from the Middle East (unpublished). Two of these sequences had 67 bp insertions at the 1015–1081 bp positions in intron 5. And in strict consensus tree generated from the EF-G sequence, three sequences from the three accessions of E. lolioides that formed a clade without other sequences were observed. Similarly as Acc1 sequences, these sequences also contained special insert fragments. Therefore, sequences with special indel may be derived from an independent diploid species, which is extinct or unknown. This hypothesis will be validated by checking whether Acc1 and EF-G sequences with special indel were obtained from Triticeae diploid species in the Middle East.
The contribution from Hordeum to the accessions of E. lolioides was indicated by the data of Acc1, EF-G, and ITS sequences with high support and also confirmed by GISH. However, the Hordeum-like copy of ITS sequence was not obtained from accessions PI 440059 and W6–26567 possibly due to concerted evolution. In the Acc1 data, E. lolioides and Elymus species (StH) formed a subclade without the diploid Hordeum species in H clade. It can be concluded that the tetraploid Elymus species was the direct donor during E. lolioides speciation. One chromosome had intensive hybridization signals derived from H. bogdanii on the arms but had clear signals derived from P. libanotica on the pericentromeric regions in GISH. Previous studies showed that these mosaic chromosomes are observed in Psammopyrum athericum (StEP/LEP) , E. pungens (StStEP/StLEP) , Elymus repens (StStH) , Thinopyrum intermedium (StEE) , and T. ponticum (StStEEE/EEEEE)  by genomic in situ hybridization. Thus, the chromosome rearrangement between St and the other genomes (i.e., E, H, and P) or the retrotransposon activity of St genome may lead to mosaic chromosomes after allopolyploidization. Interestingly, most of these mosaic chromosomes have the same character that St genome signal appeared on the centromeric or pericentromeric region of the other genomes. Redinbaugh et al.  found that the female species carrying the St genome are more successful in terms of distant hybridization. Those rearrangement or retrotransposon insertion may contribute to the stability of different genomes after allopolyploidization.
In the Acc1 data, one sequence from E. lolioides (PI440059) and L. bessarabicum formed a clade with moderate support (BS = 56%, PP = 1.00). Tao and Lin  produced a specific SCAR marker, which was used to detect StE genome in Triticeae, thereby indicating that E. lolioides contain StE genomes. However, parental donor from E genome was undiscovered by EF-G, ITS data, and GISH. The Lophopyrum-like Acc1 copy that was obtained from E. lolioides is likely caused by introgression . L. bessarabicum is a diploid species that is distributed in Mediterranean Sea, Azov Sea, and Euxine Sea. Therefore, overlapping the geographical area between L. bessarabicum and E. lolioides can increase the possibility for introgression.
The hypothetical scenarios of the origin of E. lolioides origin were suggested by combining the data of the four sequences and in situ hybridization. E. lolioides may have originated through the hybridization between tetraploid Elymus (StH) and diploid of Pseudoroegneria species, and then followed by whole genome duplication. After hybridization and polyploidy, the transposon or retrotransposon activation and E and unknown genome introgression may participate in E. lolioides speciation (Fig. 9).
Genomic constitution of E. lolioides
E. lolioides is a perennial wheatgrass that was first reported by Karelin and Kiriloff in 1841. The chromosome number of E. lolioides is controversial because different ploidy levels were reported. Schulz-Schaeffer and Jurasits  reported that the accession PI 223325 of Agropyron lolioides (= Elytrigia lolioides) has 58 chromosomes. However, when this accession was rechecked in the US National Plant Germplasm System, it was named as Elymus repens subsp. elongatiformis (https://npgsweb.ars-grin.gov/gringlobal/accessiondetail.aspx?id=1180280), which is an octaploid grass and distributed in Central Asia and southern Russia . Considering the report of Löve  and our present results, E. lolioides (2n = 42) is a hexaploid wheatgrass. In the present study, Pseudoroegneria and Hordeum were regarded as the major progenitors for E. lolioides as indicated by the data of the three nuclear gene (Acc1, EF-G, and ITS) sequences. Both GISH and FISH results indicated that E. lolioides had two sets of St genome and one set of H genome. However, in the strict consensus tree generated from EF-G and Acc1 sequences, several sequences from the three accessions of E. lolioides formed a clade without any sequence from the diploid species in Triticeae. All these sequences had a special deletion or insertion that is not present in other published sequences for Triticeae species. These sequences may be contributed by unknown species, which were extinct or undiscovered. The contribution from Lophopyrum to E. lolioides was only indicated by the Acc1 data with moderate support. However, parental donor from E genome was undiscovered by EF-G, ITS data, and GISH. The Lophopyrum-like Acc1 copy that was obtained from E. lolioides was likely caused by introgression. Our results indicated that E. lolioides contained two sets of St genome and one set of H genome, and the genome formula was designed as StStStStHH.
Classification status of E. lolioides
The main morphological characteristics of E. lolioides included long, creeping rhizome, long anther, apex subobtuse of lemmas, spikelet sessile, and one spikelet per node of rachis. The mid-nerve of lemma slightly extended and formed an extremely short point. According to the morphological characteristics, this species was successively classified into Agropyron, Elytrigia, and Elymus by an agrostologist with different classification systems . The problem on the classification of E. lolioides was mainly caused by the taxonomic status of Elytrigia genus that was established by Desvaux in 1810, and then treated as a genus, sectional status within Agropyron, subgenus of Agropyron or section of Elymus by different taxonomists, respectively  According to genome constitution, E. lolioides was classified into Elytrigia genus that genome constitution of either SJE  or SX . Yen and Yang  indicated that this species may be classified into Lophopyrum with E genome. Our results suggested that the genomic constitution of E. lolioides was StStStStHH. According to the genome classification system, this species should be transferred into Elymus L. and renamed as Elymus lolioidus (Kar. er Kir.) Meld..
According to our study, E. lolioides is a hexaploid wheatgrass. Pseudoroegneria and Hordeum are major genome donors. E and unknown genomes may participate in the speciation of E. lolioides through introgression. This species should be transferred into Elymus L by combining four sequences data and in situ hybridization. The results of this study will help in investigating the taxonomic status of Elytrigia genus.
Plant materials and DNA extraction
The seeds of the three E. lolioides accessions from Former Soviet Union and Kazakhstan were provided by the Germplasm Resources Information Network of the United States Department of Agriculture (USDA). The total genomic DNA was extracted from fresh leaf tissues by using the CTAB method . Three nuclear genes (Acc1, EF-G, and ITS) and one chloroplast trnL-F sequence from E. lolioides were amplified and sequenced. Acc1, EF-G, ITS, and trnL-F sequences from polyploid and diploid species representing A, S, D, E, W, St, V, K, Xp, Q, H, I, Ns, F, P, and Xe genomes in Triticeae were downloaded from GenBank (http://www.ncbi.nlm.nih.gov) and included in phylogenetic analysis. The basic information about these sequences, including genomic constitutions and GenBank identification numbers, are listed in Additional file 1: Table S1. The voucher specimens of E. lolioides were deposited in the Herbarium of Triticeae Research Institute, Sichuan Agricultural University, China.
Amplification and sequencing
Low-copy and multi-copy nuclear genes (Acc1, EF-G and ITS) and the chloroplast gene trnL-F sequences were amplified via polymerase chain reaction (PCR) by using the primers of cMWG699T3–2 and CMWG699T7–2 , AccF1 and AccF2 , ITSL and ITS4 , and c and f , respectively. The primers and PCR profiles for the Acc1, EF-G, ITS, and trnL-F genes are listed in Table 1. Sequences were amplified in a 25 μL reaction mixture containing 50 ng template DNA, 1× reaction buffer, 2 mM MgCl2, 0.4 μM of each primer, 200 μM dNTP, and 1.5 U ExTaq. In addition, 8% dimethylsulfoxide (DMSO) was added to avoid influence of higher GC content during ITS sequence amplification . The PCR products were detected on 1.0% agarose gels and then cloned into a PMD19-T vector according to the manufacturer’s instructions (TaKaRa, China). After white-blue plaque selection, 30–40 randomly selected clones of Acc1, EF-G, and ITS and 5 clones of trnL-F for each accession were sequenced in both directions by Shanghai Sangon Biological Engineering and Technology Service Ltd. (Shanghai, China).
Multiple sequence alignments were made using MAFFT 7.3  and adjusted manually. The phylogenetic analyses of Acc1, EF-G, ITS, and trnL-F data by using the ML method was performed using PAUP*4.0bet10 (Swofford DL, Sinauer Associates, http://www.sinauer.com). The best-fit evolutionary model for phylogenetic analysis was determined using ModelTest v3.7 with Akaike information criterion . ML heuristic searches were performed with 100 random addition sequence replications and Tree Bisection-Reconnection (TBR) branch swapping algorithm. As a measurement of the robustness of tree clades, the BS values were calculated with 1000 replications and displayed in figure (above the branch) if the BS values were > 50% .
In addition to ML analysis, Bayesian analyses were also performed using MrBayes 3.1 . The evolutionary model selected for Bayesian analyses was same as ML analysis. Two sets of four chains were run 3.3 million generations for Acc1 data, 4.2 million generations for EF-G data, 6.5 million generations for ITS data, and 0.54 million generations for trnL-F data, and samples were taken and saved every 100 generation under best-fit model. After discarding the first 25% samples as “burn-in”, a majority rule consensus tree with PP value (under the branch) was obtained.
Chromosome preparation, fluorescence, and multicolor genomic in situ hybridization
Rapidly growing roots were collected from adult plants. The roots were treated with N2O for 2 h at 0.1 MPa and then fixed for 5 min with 90% glacial acetic acid. Chromosomes were prepared for analysis by using a previously reported method . Plasmid DNA with St2–80 sequence was extracted using the EndoFree Plasmid Mini Kit (Tiangen, China), which was used to distinguish the chromosomes of St genome and others, including A, B, D, E, H, P, and Y genomes , according to the manufacturer’s instructions. The total genomic DNA of P. libanotica and plasmid (contained St2–80 sequence) were labeled with fluorescein-12-dUTP, and the genomic DNA of L. bessarabicum and H. bogdanii were labeled with Texas-red-5-dCTP by using the nick translation method. Hybridization procedure was performed according to the previously reported method . Slides were detected under an Olympus BX53 fluorescence microscope with camera. At least five metaphase cells for each accession were analyzed. Adobe Photoshop was used to proceed the color images.
- Acc1 :
Acetyl-CoA carboxylase 1
Akaike information criterion
elongation factor G
Fluorescence in situ hybridization
Genomic in situ hybridization
Internal transcribed space
Polymerase chain reaction
Sequence characterized amplified region
- TrnL-F :
Intergenic spacer between transfer RNA gene trnL (UAA) and trnF (GAA)
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We are very thankful to the US National Plant Germplasm System for providing the seeds, and sincerely thanks to Prof. Fangpu Han from Chinese Academy of Sciences for technology support for GISH and FISH.
This project was supported by the National Natural Science Foundation of China (Grant Nos. 31470305, 31270243, and 31200252), the National Key Research and Development of China (2016YFD0102000), and the fund from the Science and Technology Bureau and Education Bureau of Sichuan Province, China. Funds were used to design of the study and collection, analysis, and in writing the manuscript.
Availability of data and materials
All sequences data from this study were deposited in National Center for Biotechnology Information (NCBI) and the accession number from MK721792 to MK721830.
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Table S1. The related species in Triticeae used in this study. (XLSX 21 kb)