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. 2022 Jan 12;12(1):e8517. doi: 10.1002/ece3.8517

Morphological, cytological, and molecular evidences for natural hybridization between Roegneria stricta and Roegneria turczaninovii (Triticeae: Poaceae)

Chen Chen 1, Zilue Zheng 1, Dandan Wu 1,2, Lu Tan 1, Cairong Yang 3, Songqing Liu 3, Jiale Lu 2,4, Yiran Cheng 2, Lina Sha 2,4, Yi Wang 1,2, Houyang Kang 1,2, Xing Fan 1,2, Yonghong Zhou 1,2, Changbing Zhang 5,✉, Haiqin Zhang 2,4,✉
PMCID: PMC8809439  PMID: 35136562

Abstract

Some plants with low fertility are morphologically intermediate between Roegneria stricta and Roegneria turczaninovii, and were suspected to be natural hybrids between these species. In this study, karyotype analysis showed that natural hybrids and their putative parents were tetraploids (2n = 4x = 28). Meiotic pairing in natural hybrids is more irregular than its putative parents. Results of genomic in situ hybridization and fluorescence in situ hybridization indicate that natural hybrids contain the same genome as their putative parents. The nuclear gene DNA meiotic recombinase 1 (DMC1) and the chloroplast gene rps16 of natural hybrids and their putative parents were analyzed for evidence of hybridization. The results from molecular data supported by morphology and cytology demonstrated that the plants represent natural hybrids between R. stricta and R. turczaninovii. The study is important for understanding species evolution in the genus since it demonstrates for the first time the existence of populations of natural homoploid hybrids in Roegneria. The study also reports for the first time that the composition of the genomic formula of R. turczaninovii is StY, confirming that the current taxonomic status is correct.

Keywords: chromosome pairing, DMC1, FISH, GISH, natural hybrids, Roegneria, rps16

Our comprehensive analyses of natural hybrids, R. stricta, R. turczaninovii and the other Triticeae species, growing nearby from morphology, cytology, and molecular levels, provided support for the origin of natural hybrids. It demonstrates for the first time the existence of populations of natural homoploid hybrids in Roegneria.

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1. INTRODUCTION

Hybridization is the main driving force of plant evolution (Soltis & Soltis, 2009). It is estimated that about 25% of plant species are known to be involved in hybridization with other species (Mallet, 2005). These can provide source of genetic variation than on further evolution, through adaptation and selection leading to speciation (Arnold et al., 2012; Whitney et al., 2010). Hybridization can occur between species of the same ploidy level (homoploid hybridization) and between species of different ploidy levels (heteroploid hybridization). In plants, hybridization with an increase in ploidy (allopolyploidy) is associated with speciation much more commonly than homoploid hybridization, partly because of reproductive isolation between hybrids and parents with different ploidy (Soltis et al., 2014; Soltis & Soltis, 2009). So far, only about 20 cases of homoploid hybrids have been well documented in plants (Gross & Rieseberg, 2005; White et al., 2018).

The Triticeae (Poaceae) is an important economic gene pool for genetic improvement of cereal and forage crops, including about 450 diploid and polyploid species distributed in a wide range of ecological habitats over the temperate, subtropical, and tropical pine regions (Dewey, 1984). The majority of species are allopolyploids, and the ploidy levels range from diploid (2n = 2x) to dodecaploid (2n = 12x). With combining a wide variety of biological mechanisms and genetic systems, the tribe Triticeae is an excellent group for research in evolution, genetic diversity, and speciation in plant polyploids (von Bothmer & Salomon, 1994; Paštová et al., 2019).

Roegneria C. Koch is a relatively large perennial genus in Triticeae, and includes approximately 130 species, most of which are tetraploid with the StY genome, nearly 70 of which are found in China (Yang et al., 2008). Roegneria species not only provided genetic material for the improvement of forage crops but could also be used as potential contributors of genes for cereal crops (Keng, 1959), such as Roegneria stricta Keng and Roegneria turczaninovii (Drob.) Nevski. Predecessors have reported some studies on the hybrids of Roegneria, such as a hybrid of Roegneria and Hordeum (Zhou et al., 1995), a hybrid of R. ciliaris and Leymus multicaulis (Zhang et al., 2008). These hybrids were created by the artificial hybridization and could not replace the value of natural hybrids.

Early identification of hybridization is mainly based on morphological characteristics. However, the reliability of morphological markers is low, and morphological intermediacy is not always related to hybridization. It may also be caused by convergent evolution or environment (Rieseberg, 1995). Cytological markers have been used as important evidence for hybridization, including karyotype analysis, meiotic pairing analysis, Genomic in situ hybridization (GISH), and Fluorescence in situ hybridization (FISH) (Han et al., 2004; Mao et al., 2017). However, due to the high parental chromosome homology of interspecific hybrids, it is difficult to explore origin of hybrids by FISH and GISH (Soltis et al., 1992). Single‐ or low‐copy nuclear genes, which are less susceptible to concerted evolution, can serve as useful markers for studies of phylogenetic relationships (Lei et al., 2018; Sha et al., 2010). DNA meiotic recombinase 1 (DMC1) gene has been used to examine hybridization events (Tang et al., 2017). The chloroplast DNA (cp DNA) is maternally inherited in grasses (Smith et al., 2006), and ribosomal protein S16 (rps16) is used to identify the maternal donor of genera in Triticeae (Yan et al., 2014).

To cultivate new forage varieties, R. stricta and R. turczaninovii cv. Linxi were planted very close in Hong yuan Research Base of the Sichuan Academy of Grassland Science (SAGS), Sichuan Province, China (31.47°N, 102.33°E). We harvested the seeds of the two species and planted them individually. In these plants, we found that some plants grew stronger and had lower seed setting rate than the surrounding plants (Figure 1a‐c), and they had intermediate morphological characters of R. stricta and R. turczaninovii, such as pubescence of leaf, basal leaf sheath, and stem node (Figure 1d‐o). We suspected that these plants are natural hybrids between R. stricta and R. turczaninovii. To determine if this is indeed the case, we conducted different methods including morphological analysis, cytological analysis, and phylogenetic analysis in these putative hybrids and their accompanying plants.

FIGURE 1.

FIGURE 1

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Morphological characteristics of the natural hybrids and their parents. (a) – (c) Natural distribution of hybrids. (a) hybrid RH1 (arrowed). (b) hybrid RH2 (arrowed). (c) hybrid RH1 (arrowed). (d–g) Leaves of hybrids and parents. (d) R. turczaninovii (arrowed). (e) R. stricta (arrowed). (f) hybrid RH1 (arrowed). g: hybrid RH2 (arrowed). (h–k) Stem node of hybrids and parents. (h) R. turczaninovii (arrowed). (i) R. stricta (arrowed). (j) hybrid RH1 (arrowed). k: hybrid RH2 (arrowed). (l–o) Basal leaves of hybrids and parents. (l) R. turczaninovii (arrowed). (m) R. stricta (arrowed). (n) hybrid RH1 (arrowed). o: hybrid RH2 (arrowed)

2. METHODS AND MATERIALS

2.1. Plant materials

Seventeen hybrids of RH1 (plants found in R. stricta field) and 40 hybrids of RH2 (plants found in R. turczaninovii field) were randomly distributed in fields. The possible parents R. stricta and R. turczaninovii, and the other Triticeae species growing nearby were also obtained, including R. grandis (StY), E. sibiricus (StH), and Campeiostachys nutans (StYH). All of them were collected from Hong Yuan Research Base of SAGS. Twenty diploid species (representing the genomes St, H, Ee , Eb , W, P, Ta, V, Ns, A, B, and D), Roegneria species (StY), Elymus species (StH), and Campeiostachys species (StYH) from the tribe Triticeae were used for cytological analysis and phylogenetic analysis. The names of the sampled taxa, abbreviations, accession numbers, ploidy level, genomic constitution, and GenBank accession numbers were listed in Table 1. Materials with PI and W6 were kindly provided by American National Plant Germplasm System (Pullman, WA, USA). The authors of this study collected all other accessions, for which voucher specimens were deposited with the perennial nursery and herbarium of the Triticeae Research Institute, Sichuan Agricultural University, China (SAUTI).

TABLE 1.

Plant materials used in Phylogenetic analysis

Number Species/hybrids Genome 2n Accession Locality GenBank No.
DMC1 rps16
1 RH1‐3 StY 4x V 03 Sichuan, China MZ130351* MZ130373*
MZ130352*
2 RH1‐6 StY 4x V 06 Sichuan, China

MZ130353*

MZ130374*
MZ130354*
3 RH1‐8 StY 4x V 08 Sichuan, China MZ130355* MZ130375*
MZ130356*
4 RH1‐11 StY 4x V 11 Sichuan, China MZ130357* MZ130376*
MZ130358*
5 RH1‐14 StY 4x V 14 Sichuan, China MZ130359* MZ130377*
MZ130360*
6 RH2‐2 StY 4x V 19 Sichuan, China MZ130329* MZ130362*
MZ130330*
7 RH2‐5 StY 4x V 22 Sichuan, China MZ130331* MZ130363*
MZ130332*
8 RH2‐10 StY 4x V 27 Sichuan, China MZ130333* MZ130364*
MZ130334*
9 RH2‐12 StY 4x V 29 Sichuan, China MZ130335* MZ130365*
MZ130336*
10 RH2‐15 StY 4x V 32 Sichuan, China MZ130337* MZ130366*
MZ130338*
11 RH2‐17 StY 4x V 34 Sichuan, China MZ130339* MZ130367*
MZ130340*
12 RH2‐18 StY 4x V 35 Sichuan, China MZ130341* MZ130368*
MZ130342*
13 RH2‐30 StY 4x V 47 Sichuan, China MZ130343* MZ130369*
MZ130344*
14 RH2‐37 StY 4x V 54 Sichuan, China MZ130345* MZ130370*
MZ130346*
15 RH2‐39 StY 4x V 56 Sichuan, China MZ130347* MZ130371*
MZ130348*
16 Roegneria strictus (Keng) S.L. Chen StY 4x Y 2102 Sichuan, China MZ130327* MZ130361*
MZ130350*
17 Roegneria turczaninovii (Drobow) Nevski StY 4x ZY 11140 Inner Mongolia, China MZ130328* MZ130372*
MZ130349*
18 Elymus sibiricus L. StH 4x PI 619579 Xinjiang, China EU366409*
BOP 022815 KP211332* MK775250*
PI 372541
19 Elymus caninus L. StH 4x PI 314621 Former Soviet Union EU366407*
EU366408*
20 Elymus elymoides (Raf.) Swezey StH 4x PI 628684 United States FJ695161*
FJ695160*
21 Elymus glaucus Buckley StH 4x PI 593652 Oregon United States FJ695163*
FJ695162*
22 Elymus virginicus L. StH 4x PI 490361 United States GQ855195*
PI 882397 Sichuan, China GQ855196*
23 Elymus wawawaiensi StH 4x PI 506284 Sichuan, China
24 Roegneria caucasica K. Koch StY 4x H 3207 Xinjiang, Armenia HM770785*
HM770784*
25 Roegneria ciliaris (Trin.) Nevski StY 4x 87‐88 335 Sichuan, China KU160610*
88‐89‐238 KU160617*
26 Roegneria dura Keng StY 4x Y 2124 Neimenggu, China KX578879*
27 Roegneria grandis Keng StY 4x ZY 3189 Xizang, China KU160615* MN703669*
Y 3189 KU160618*
28 Roegneria hondai Kitagawa StY 4x Y 0362 Sichuan, China KX578840*
KX578841*
29 Roegneria longearistata (Boiss.) Drob. StY 4x Y 2259 Inner Mongolia, China KX578848
30

Roegneria shandongensis (B. Salomon)

J. L. Yang & C. Yen

 StY 4x ZY 3150 Shanxi, China KX578862*
31 Roegneria ugamica (Drob.) Nevski StY 4x Y 1698 Sichuan, China KX578877*
KX578878*
32 Campeiostachys nutans (Griseb.) J. L. Yang, B. R. Baum et C. Yen StYH 6x Y 2086 Sichuan, China
ZY 17101 KX578851*
ZY 17102 KX578852* MT385866*
S 22‐4 KX578853*
33 Pseudoroegneria libanotica (Hackel) D. R. Dewey St 2x PI 228389 Iran FJ695174*
PI 228392
34 Pseudoroegneria spicata (Pursh) A. Löve St 2x PI 547161 United States FJ695175* KY636118*
PI 632532
35 Pseudoroegneria stipifolia (Czern. ex Nevski) St 2x PI 325181 Stavropol, Russian FJ695176*
36 Pseudoroegneria strigosa (M. Bieb.) A. Löve St 2x PI 595164 Xinjiang, China FJ695177*
PI 499637
37 Pseudoroegneria tauri (Boiss.) A. Löve St 2x PI 401329 Iran KU160613
PI 380650
38 Agropyron cristatus (L.) Gaertn P 2x H 4349 China AF277241* KY126307*
PI 598628 Kazakhstan
39 Australopyrum retrofractum (Vickery) A. Löve W 2x H 6723 China AF277251* KY636080*
PI 531553 United States
40 Hordeum chilense Roem. & Schult. H 2x PI 531781 Chile FJ695173*
41 Hordeum pubiflorum Hook. f. H 2x BCC 2028 KY636108*
42 Hordeum bogdanii Wilensky H 2x PI 531761 China FJ695172* MH331641*
43 Hordeum vulgare L. I 2x H 3878 Italy EF115541*
44 Lophopyrum elongatum (Host) A. Löve Ee 2x PI 531719 Israel AF277246*
PI531718 MH331643*
45 Thinopyrum bessarabicum (Savul. & Rayss) A. Eb 2x PI 531711 Russia AF277254* KY636145*
W6 21890
46 Psathyrostachys huashanica Keng ex P.C Kuo Ns 2x PI 531823 Shanxi, China GU165826*
47 Aegilops speltoides Tausch. B 2x H 6779 DQ247833*
48 Aegilops tauschii Coss. D 2x H 6668 AF277235*
AE 429 JQ754651*
49 Dasypyrum villosum (K. Koch) Nevski V 2x H 5552 AF277236*
W6 7264 MH285850*
50 Secale cereale L. R 2x KC912691*
51 Taeniatherum copmedusae (L.) Nevski Ta 2x H 10254 AF277249*
PI 220591 MH285856*
52 Triticum urartu Tum. A 2x H 6664 DQ247826*
53 Bromus sterilis L. OSA 420 AF277234*
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1* Data from published sequences in the GenBank (http://www.ncbi.nlm.nih.gov).

2.2. Morphological analysis

Morphology among plants of putative hybrids, R. stricta, R. turczaninovii, R. grandis, E. sibiricus, and C. nutans, was measured for 21 characters. The Euclidean distance was calculated by the dist function in R. The hclust function in R was used to cluster. The tree was plotted by ggtree package in R.

2.3. Pollen fertility and seed set

The pollen grains from mature anthers were stained in an I2‐KI solution for pollen fertility study. Seed set was estimated from a 10‐spike sample per plant.

2.4. Karyotype and meiotic pairing analysis

Karyotype analysis was followed by Gill et al. (1991). The procedures of fixation, staining, and calculation of meiotic pairing followed Zhang and Zhou (2006).

2.5. Chromosome preparation and in situ hybridization

Chromosomes were prepared for GISH analysis according to the method of Han et al. (2004). Total genomic DNA was extracted from fresh leaves by the CTAB method (Murray & Thompson, 1980). Plasmids (from positive clones that are St genome) and the StY genome were labeled with fluorescein‐12‐dUTP or Texas‐red‐5‐dCTP using the nick translation method. Hybridization procedure, detection, and visualization were performed according to the method of Wang et al. (2017).

2.6. Amplification and sequencing

The DMC1 and rps16 gene were amplified using the primers listed in Table S1 (Petersen & Seberg, 2002; Shaw et al., 2005). All PCRs were conducted in a 50‐μl reaction volume, with 1.5 U Ex Taq polymerase (TaKaRa, Shiga, Japan). The PCR amplification protocols for the DMC1 and rps16 gene are presented in Table S1. PCR products were cloned into the pMD19‐T vector (TaKaRa). At least 15 random independent clones were selected for sequencing by Shanghai Sangon Biological Engineering and Technology Service Ltd. (Shanghai, China).

2.7. Phylogenetic analysis

DNA sequences were confirmed through BLAST nucleotide alignment in the NCBI database, and sequence alignments were made using MAFFT (Katoh & Standley, 2013). After preliminary phylogenetic analysis, the number of sequences is reduced. If there are more sequences of the same species form monophyletic groups, only one sequence is retained. ModelTest v3.06 (Posada & Crandall, 1998) was used to determine appropriate DNA substitution models and gamma rate heterogeneity using the Akaike information criterion (AIC).

The phylogenetic analyses of DMC1 and rps16 data were performed by using the maximum‐likelihood (ML) method in PhyML 3.0 (Guindon et al., 2009). The best‐fit evolutionary models determined were TPM1uf+G for DMC1 and TIM1+G for rps16. As a measurement of the robustness of tree clades, the bootstrap support (BS) values were calculated with 1000 replications and displayed in figure (above the branch) if the BS values were >50% (Felsenstein, 1985). Bayesian analyses were also performed using MrBayes 3.1 (Ronquist & Huelsenbeck, 2003). The evolutionary model selected default settings.

3. RESULTS

3.1. Morphological characteristics

The 57 natural hybrids were perennial grasses, which were similar in morphology and phenology to Roegneria species, such as one spikelet per node and palea equaling lemma. Most of hybrids were stronger than their surrounding plants (Figure 1a–c). These natural hybrids combined some unique characteristics of R. stricta and R. turczaninovii, such as leaf pubescence, stem node pubescence, and basal leaf sheath pubescence (Figure 1d‐o).

Morphology among plants of putative hybrids, R. stricta, R. turczaninovii, R. grandis, E. sibiricus, and C. nutans, was measured for 21 characters. Cluster analysis based on 21 morphological characters was shown in Figure 2. The results of cluster analysis indicated that 57 natural hybrids were closer to R. stricta and R. turczaninovii.

FIGURE 2.

FIGURE 2

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Cluster analysis of hybrids RH1, hybrids RH2, R. stricta, R. turczaninovii, R. grandis, E. sibiricus and C. nutans based on 21 morphological characters. Morphology including Top internodes length, First lemma length, Palea length, First glume length, First glume width, Second glume length, Second glume width, Flag leaf length and width, Top second leaf length and width, Spike length, Plant height, Awn length of first lemma, No. of spikelets per spike, No. of florets per spikelet, Hair on sheath, Hair on stem node, Hair on leaf, Awn

3.2. Evaluation of pollen fertility and seed set

The fertility, including pollen fertility and seed set, of R. stricta, R. turczaninovii, and putative hybrids, was shown in Figure 3. In R. stricta, the pollen fertilities were up to 92.05% and the seed sets were 90.02%. In R. turczaninovii, the pollen fertilities and seed set were high with 91.61% and 92.18%, respectively.

FIGURE 3.

FIGURE 3

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Pollen fertility and seed set of hybrids RH1, hybrids RH2, R. stricta and R. turczaninovii

As for the hybrids of RH1, the pollen fertilities varied from 1.01% to 8.09%, and the seed sets were lower than those of their possible parents, varying from 0.41% to 4.50% (Figure 3). As for the hybrids of RH2, the pollen fertilities varied from 0.83% to 13.63%, and seed set were lower, varying from 0.23% to 5.59% (Figure 3). It could be seen that the pollen fertilities and seed sets of putative hybrids were very low, indicating that they were hybrids and not stable species.

3.3. Karyotype analysis and chromosome pairing at metaphase I

Karyotype analysis showed that R. stricta, R. turczaninovii, and putative hybrids were tetraploids (2n = 4x = 28) (Figure 4).

FIGURE 4.

FIGURE 4

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Karyotype analysis of hybrids RH1, hybrids RH2, R. stricta and R. turczaninovii. (a) R. turczaninovii. (b) R. stricta. (c) RH1‐13. (b) RH2‐10

The meiotic configurations of the possible parent and the putative hybrids were listed in Table S2. Meiosis of R. stricta and R. turczaninovii were quite regular with 14 bivalents (Figure 5a–c, Table S2). Meiotic pairing in 17 hybrids of RH1 was comparatively high, with an average of 0.98 univalents and 13.52 bivalents per cell with c‐value of 0.89 (Figure 5d, e; Table S2). Chromosome pairing in 40 hybrids of RH2 was comparatively high with an average of 0.85 univalents and 13.55 bivalents per cell with c‐value of 0.90 (Figure 5g, h; Table S2). Except for hybrid RH2‐31, all hybrids had univalents.

FIGURE 5.

FIGURE 5

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Meiotic associations in PMCs of the parental species and hybrids. (a) and (b) R. turczaninovii with 14 II. (c) R. stricta with 14 II. (d) RH1‐15 with 14 II (12 ring + 2 rod). (e) RH1‐7 with 13 II (9 ring + 8 rod) + 2 I. (f) RH2‐38 lagging chromosomes. (g) RH2‐29 with 14 II (12 ring and 2 rod). (h) RH2‐11 with 13 II (11 ring and 2 rod) + 2 I. (i) RH2‐11 chromosome bridge

At the same time, some lagging chromosomes and chromosome bridges were observed at anaphase I (Figure 5f, i).

3.4. FISH and GISH analysis

To further explore the genomic constitutions of natural hybrids, we selected some hybrids for in situ hybridization. Since the suspected parents of natural hybrids were R. turczaninovii and R. stricta (StY), and meiotic pairing in natural hybrids were comparatively high, we speculated that genomic constitution of natural hybrids was StY. St2‐80 was a FISH marker for the St genome (Wang et al., 2017). Signals produced by St2‐80 were present on the entire arm of the St genome chromosomes, except at the centromeric region and near centromeric region (Wang et al., 2017). This marker was used to detect the St genome presented in the putative parents and hybrids.

St2‐80 signal pattern showed that 14 chromosomes of putative parents and hybrids were St type (Figures 6a, c, e and 7a, c, e). This result was confirmed by GISH analysis, where 28 chromosomes of putative parents and hybrids were hybridized with the StY probe from R. ciliaris (Figures 6b, d, f and 7b, d, f). The results of FISH and GISH indicated that the genomic constitution of putative parents and 11 hybrids (RH1‐3, RH1‐8, RH1‐11, RH1‐14, RH2‐2, RH2‐10, RH2‐12, RH2‐15, RH2‐17, RH2‐37, RH2‐39) was StY.

FIGURE 6.

FIGURE 6

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Analysis of FISH and GISH in R. stricta and R. turczaninovii. (a) and (b) R. stricta. (c–f) R. turczaninovii. (a), (c) and (e) Used St2–80 as probe (red), 14 chromosomes were labeled as St type (arrowed) and 14 chromosomes were labeled as non‐St type. (b), (d) and (f) With total genomic DNA of R. ciliaris (StY genome) was labeled with Texas‐red‐5‐dCTP (red) as probe, 28 chromosomes were labeled as red fluorescent signals

FIGURE 7.

FIGURE 7

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Analysis of FISH and GISH in hybrids. (a) and (b) RH1‐11. (c) and (d) RH2‐12. E and F RH2‐15. (a), (c), and (e) Using St2–80 as probe (green), 14 chromosomes were labeled as St type (arrowed) and 14 chromosomes were labeled as non‐St type. (b), (d) and (f) With total genomic DNA of R. ciliaris (StY genome) was labeled with fluorescein‐12‐dUTP (green) as probe, 28 chromosomes were labeled as green fluorescent signals

3.5. Phylogenetic analyses of the nuclear gene DMC1 and the chloroplast gene rps16 sequences

In order to analyze the possible parents of the hybrids, we analyzed the nuclear gene DMC1 and the chloroplast gene rps16 sequences of the hybrids and their associated species of Roegneria, Elymus, and Campeiostachys. The length of DMC1 sequences of hybrids ranged from 998 to 1004 bp. The data matrix contained 1166 characters, of which 267 characters were variable and 235 were parsimony informative. A single phylogenetic tree generated by maximum likelihood analysis using the TPM1uf + G model (−Ln likelihood = 4762.04) was shown in Figure 8.

FIGURE 8.

FIGURE 8

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Phylogenetic tree based on DMC1 sequences of hybrids using ML. Numbers with bold above nodes are bootstrap values, and numbers below nodes are Bayesian posterior probability values

The phylogenetic analyses of the DMC1 sequence were shown in Figure 8. In clade I (PP = 0.97), the St‐type sequences formed a strongly supported clade, which included diploid Pseudoroegneria (St) species, tetraploid Elymus (StH) and Roegneria (StY) species, hexaploid campeiostachys (StYH) species, and hybrids. The St‐type sequences of 15 hybrids and R. turczaninovii (StY) formed a subclade (BS = 54%, PP = 0.98). In clade Ⅱ (BS = 99%, PP = 1.00), the Y‐type sequences formed a strongly supported clade, which contained the tetraploid species of Roegneria (StY) and hybrids. The Y‐type sequences of 15 hybrids, R. turczaninovii (StY) and R. stricta (StY), formed a subclade (BS = 64%, PP = 0.84). In clade Ⅲ (BS = 83%, PP = 1.00), 10 diploid species contained 10 different basic genomes (Ee , Eb , W, P, Ta, V, Ns, A, B, and D). In clade IV (BS = 72%, PP = 1.00), the H‐type subclade included diploid Hordeum species and tetraploid Elymus (StH) species.

The length of hybrids of rps16 sequences varied from 830 to 831 bp. The data matrix contained 881 characters, of which 30 were variable characters and 30 were parsimony informative. TIM1 + G as the best‐fit model (−Ln likelihood = 1550.15) was used in phylogenetic analysis. The ML tree was displayed in Figure 9.

FIGURE 9.

FIGURE 9

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Phylogenetic tree based on rps16 sequences of hybrids using ML. Numbers with bold above nodes are bootstrap values, and numbers below nodes are Bayesian posterior probability values

The phylogenetic analyses of the rps16 sequence were shown in Figure 9. The rps16 sequences from hybrids of RH1 were grouped with R. stricta (BS = 62%, PP = 0.97). This clade contained 5 hybrids of RH1 sequences and R. stricta. The rps16 sequences from hybrids of RH2 were grouped with R. turczaninovii (BS = 86%, PP = 1.00). This clade contained 10 hybrids of RH2 sequences and R. turczaninovii. The above results showed that R. stricta was the maternal donor of the hybrids of RH1, while R. turczaninovii was the maternal donor of the hybrids of RH2.

4. DISCUSSION

4.1. Origin of natural hybrids

Natural hybrids are relatively common in flowering plants (Rieseberg & Ellstrand, 1993). Rieseberg (1997) reported that about 11% of plant species arose from interspecific hybridization. Artificial hybrids involving genus Roegeneria have been produced (Zhou et al., 1999), but there are no reports of natural hybrids. In this study, the low‐fertility plants were suspected natural hybrids because of their morphologically intermediate between R. stricta and R. turczaninovii. However, the natural hybrids had not been confirmed by cytological and molecular evidence. In this study, FISH and GISH analysis suggested that the genomic constitution of R. turczaninovii was StY. This result was further confirmed by molecular data. Phylogenetic analyses based on DMC1 sequence suggested that R. turczaninovii has St and Y genomes. It is the first report that the composition of the genomic formula of R. turczaninovii is StY, confirming that the current taxonomic status is correct. The natural hybrids were verified unambiguously because of morphological characteristics, and molecular sequences of natural hybrids were closer to those of R. stricta and R. turczaninovii in companion species (Figures 2 and 8). Phylogenetic analysis based on rps16 sequence showed that R. stricta was the maternal donor of the hybrids of RH1, R. turczaninovii was the maternal donor of the hybrids of RH2 (Figure 9). Thus, our results demonstrated that R. stricta and R. turczaninovii were the female and male parents, respectively, of the hybrids of RH1; R. turczaninovii and R. stricta were the female and male parents of the hybrids of RH2, respectively.

Additionally, meiotic pairing in 57 natural hybrids was comparatively high. This suggested that the genomes of their parents were homologous. This is consistent with our cytology and molecular data. Except for hybrid RH2‐31, all hybrids had univalent. This also provides evidence for the low pollen fertility and seed setting rate of hybrids. Pairing and recombination among homologous chromosomes are common in nascent allopolyploids (Gaeta & Pires, 2010). However, in the evolution of allopolyploids, homologous pairing is gradually eliminated and replaced by exclusive homologous pairing. R. stricta and R. turczaninovii contain the StY genome, but the genomes may have diverged in the two species, resulting in hybrids showing univalent at metaphase I. The chromosome bridge appeared to be in some natural hybrids at anaphase (Figure 5i). Such chromosome bridges might be formed by single‐ or three‐strand doubles within the reverse loop of a paracentric inversion heterozygote, and the chromosome bridge was a sign of inversion; these were important events in speciation.

4.2. Formation process of natural hybrids

Triticeae is a young group; there is a large possibility of random hybridization among the relative genera in the Triticeae (Barkwoth & Bothmer, 2009). In this study, different genera species with different genome constitutions in Triticeae were planted in the experiment base of the SAGS, such as Roegneria (StY), Elymus (StH), and Campeiostachys (StYH). R. stricta and R. turczaninovii have closer genetic relationship, the florescence was consistent, and they were planted together, which provided conditions for natural hybridization.

From the perspective of hybridization rate, there were 23 hybrids out of which about 400 were R. stricta plants, and the natural hybridization rate was about 5.75%, while among the 330 R. turczaninovii plants, there were about 54 hybrids, and natural hybridization rate was about 16.36%. It can be seen that natural hybridization rate of R. turczaninovii was about 3 times that of R. stricta. The reason may be that the source of the R. stricta parents was single and the genetic diversity was low, while the R. turczaninovii parent has higher genetic diversity. Large morphological differences were observed in the field of R. turczaninovii, which lead to a higher natural hybridization rate. The genetic diversity of the R. stricta parents and R. turczaninovii parents needed to be further verified by molecular markers or other methods.

4.3. Homoploid hybrid speciation

In the evolutionary history, many grasses from the Triticeae have undergone interspecific hybridization, resulting in allopolyploidy, which homoploid hybrid speciation (HHS) was found only in rye (Martis et al., 2013). Homoploid hybrid speciation is rare due to strongly reduced fitness of early generation hybrids and weak reproductive isolation with the progenitors (Mallet, 2007; Rieseberg & Willis, 2007). Our comprehensive analyses of natural hybrids, R. stricta, R. turczaninovii and the other Triticeae species growing nearby from morphology, cytology, and molecular levels provided support for the origin of natural hybrids. It demonstrates for the first time the existence of populations of natural homoploid hybrids in Roegneria. Analyses of hybrid swarms or young hybrid taxa can play an important role in elucidating the first steps toward hybrid species (Nolte & Tautz, 2010). Although such taxa may not eventually produce well‐differentiated hybrid species, they can facilitate testing key predictions from models of hybridization and hybrid speciation (Barton, 2001; Buerkle et al., 2000). In this study, the natural homoploid hybrids are good research material for elucidating the first steps toward homoploid hybrids species. They can facilitate testing of key predictions from hybridization and hybrid speciation models. It can provide some references for the formation mechanism of natural hybrids of Triticeae.

4.4. Utilization of natural hybrids

Hybridization among species can act as an additional, perhaps more abundant, source of adaptive genetic variation than mutation (Arnold & Martin, 2009; Kunte et al., 2011; Whitney et al., 2010). In this study, we found some natural hybrids with good forage traits in plant height, tillers, and leaf, but the fertility was very low. If these natural hybrids could be genetically improved to create new forage varieties, it would have good ecological and economic benefits. As a result of further reproduction, these hybrids could be a valid species because some highly sterile F1 hybrids become species through adopting a vegetative mode of reproduction (Brysting et al., 2000).

CONFLICT OF INTEREST

The authors declare no conflict of interest.

AUTHOR CONTRIBUTION

Chen Chen: Conceptualization (equal); Formal analysis (lead); Investigation (lead); Methodology (equal); Project administration (equal); Writing – original draft (lead); Writing – review & editing (equal). Zilue Zheng: Conceptualization (equal); Data curation (equal); Formal analysis (equal); Investigation (equal); Software (lead); Writing – original draft (equal); Writing – review & editing (equal). Dandan Wu: Conceptualization (equal); Data curation (equal); Formal analysis (equal); Resources (supporting); Software (equal); Supervision (equal); Visualization (equal). Lu Tan: Formal analysis (equal); Investigation (supporting); Software (equal). Cairong Yang: Conceptualization (supporting); Methodology (supporting). Songqing Liu: Resources (supporting). Jiale Lu: Project administration (supporting); Supervision (supporting); Validation (supporting). Yiran Cheng: Formal analysis (supporting); Methodology (supporting); Software (supporting). Lina Sha: Visualization (supporting). Yi Wang: Validation (supporting). Houyang Kang: Supervision (supporting). Xing Fan: Software (supporting). Yonghong Zhou: Validation (supporting). Changbing Zhang: Data curation (equal); Project administration (equal); Resources (equal); Supervision (equal). Haiqin Zhang: Conceptualization (equal); Funding acquisition (lead); Investigation (equal); Project administration (equal); Resources (equal); Supervision (lead); Writing – original draft (equal); Writing – review & editing (equal).

Supporting information

Table S1‐S2

Click here for additional data file. (24.1KB, docx)

ACKNOWLEDGMENTS

The authors are thankful to the National Natural Science Foundation of China (Grant Nos. 31870309 and 31670331) and the Science and Technology Bureau of Sichuan Province (2021NZZJ0010, R21YYJSYJ0014) for their financial supports.

Chen, C. , Zheng, Z. , Wu, D. , Tan, L. , Yang, C. , Liu, S. , Lu, J. , Cheng, Y. , Sha, L. , Wang, Y. , Kang, H. , Fan, X. , Zhou, Y. , Zhang, C. , & Zhang, H. (2022). Morphological, cytological, and molecular evidences for natural hybridization between Roegneria stricta and Roegneria turczaninovii (Triticeae: Poaceae). Ecology and Evolution, 12, e8517. 10.1002/ece3.8517

Chen Chen and Zilue Zheng contributed equally to this work.

Contributor Information

Changbing Zhang, Email: c.b.zhang@126.com.

Haiqin Zhang, Email: haiqinzhang@163.com.

DATA AVAILABILITY STATEMENT

Morphological data are available from the Dryad Digital Repository at https://doi.org/10.5061/dryad.0cfxpnw3c. The Bayesian trees are available from the Dryad Digital Repository at https://doi.org/10.5061/dryad.rv15dv48m. The haplotype sequences of our study involved are deposited in GenBank with accession numbers MZ130327‐MZ130377.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Table S1‐S2

Click here for additional data file. (24.1KB, docx)

Data Availability Statement

Morphological data are available from the Dryad Digital Repository at https://doi.org/10.5061/dryad.0cfxpnw3c. The Bayesian trees are available from the Dryad Digital Repository at https://doi.org/10.5061/dryad.rv15dv48m. The haplotype sequences of our study involved are deposited in GenBank with accession numbers MZ130327‐MZ130377.

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