- Research article
- Open Access
Phylogeny and evolutionary history of Leymus(Triticeae; Poaceae) based on a single-copy nuclear gene encoding plastid acetyl-CoA carboxylase
BMC Evolutionary Biology volume 9, Article number: 247 (2009)
Single- and low- copy genes are less likely subject to concerted evolution, thus making themselves ideal tools for studying the origin and evolution of polyploid taxa. Leymus is a polyploid genus with a diverse array of morphology, ecology and distribution in Triticeae. The genomic constitution of Leymus was assigned as NsXm, where Ns was presumed to be originated from Psathyrostachys, while Xm represented a genome of unknown origin. In addition, little is known about the evolutionary history of Leymus. Here, we investigate the phylogenetic relationship, genome donor, and evolutionary history of Leymus based on a single-copy nuclear Acc1 gene.
Two homoeologues of the Acc1 gene were isolated from nearly all the sampled Leymus species using allele-specific primer and were analyzed with those from 35 diploid taxa representing 18 basic genomes in Triticeae. Sequence diversity patterns and genealogical analysis suggested that (1) Leymus is closely related to Psathyrostachys, Agropyron, and Eremopyrum; (2) Psathyrostachys juncea is an ancestral Ns-genome donor of Leymus species; (3) the Xm genome in Leymus may be originated from an ancestral lineage of Agropyron and Eremopyrum triticeum; (4) the Acc1 sequences of Leymus species from the Qinghai-Tibetan plateau are evolutionarily distinct; (5) North America Leymus species might originate from colonization via the Bering land bridge; (6) Leymus originated about 11-12MYA in Eurasia, and adaptive radiation might have occurred in Leymus during the period of 3.7-4.3 MYA and 1.7-2.1 MYA.
Leymus species have allopolyploid origin. It is hypothesized that the adaptive radiation of Leymus species might have been triggered by the recent upliftings of the Qinghai-Tibetan plateau and subsequent climatic oscillations. Adaptive radiation may have promoted the rapid speciation, as well as the fixation of unique morphological characters in Leymus. Our results shed new light on our understanding of the origin of Xm genome, the polyploidization events and evolutionary history of Leymus that could account for the rich diversity and ecological adaptation of Leymus species.
Leymus Hochst., a polyploid perennial genus in the wheat tribe (Poaceae: Triticeae), includes about 30 species that distribute in a wide range of ecological habitats over the temperate and subtropical and tropic alpine regions [1–3]. The natural habitats of Leymus species range from coastal to inland areas, including saline or alkaline lands, dry or semi-dry areas, as well as shady and moist forests. Morphologically, Leymus species exhibit large variation with absent (L. akmolinensis) to strong rhizomes (L. racemosus), single (L. ambiguus) to multiple spikelets (L. cinereus) per node, erectly involute (L. paboanus) to loosely flat (L. multicaulis) leaf, and subulate (L. innovatus) to lanceolate (L. arenarius) to absent (L. duthiei) glumes [1, 3–5].
The sectional delimitation of Leymus has been proposed by different scholars (See Table S1, Additional File 1). According to morphological characteristics, Tzvelev  and Löve  divided Leymus into four sections: sect. Leymus, sect. Anisopyrum, sect. Aphanoneuron, and sect. Malacurus. Barkworth and Atkins  suggested that the North American species of Leymus cannot be separated into sect. Anisopyrum and sect. Aphanoneuron and recognized Leymus as sect. Leymus and sect. Anisopyrum. Zhi and Teng  divided Chinese Leymus into three sections: sect. Racemosus, sect. Leymus, and sect. Anisopyrum, and suggested that central Asia might be the centre of diversity of the genus. Based on ecological habitats, Yen and Yang  defined three ecological sections of Leymus: sect. Arenarius, sect. Pratensus, and sect. Silvicolus. While these studies add to our understanding of subdivision of Leymus, phylogenetic relationships among its species remain unclear. Moreover, little is known about the evolutionary history of Leymus.
Cytologically, five ploidy levels were recognized in Leymus species: tetraploid (2n = 4x = 28), hexaploid (2n = 6x = 42), octoploid (2n = 8x = 56), decaploid (2n = 10x = 70) and dodecaploid (2n = 12x = 84) [1, 5]. Leymus has its origin through a typical polyploidization process, which might originate from allopolyploidy for ancestral entity and then continuous autopolyploidy for higher polyploids [1, 2]. All the Leymus species have two basic genomes, Ns and Xm . Previous studies based on morphology , cytogenetics , DNA hybridization patterns , and DNA sequences (nrITS, trnL-F) [10, 11] have revealed that the Ns genome of Leymus was originated from the genus Psathyrostachys. Despite decades of intensive efforts, there are still uncertainties regarding the origin of the Xm genome of Leymus. Based on morphological characteristics, the Xm genome was presumed to be the St genome of Pseudoroegneria  or the Eb genome of Thinopyrum bessarabicum . Cytogenetic analysis suggested that it was the Ee genome of Lophopyrum elongatum . However, cytogenetic and DNA hybridization analysis excluded the Eb and Ee genomes from the Leymus species [8, 9, 14]. Zhang and Dvorak  and Bödvarsdóttir and Anamthawat-Jónsson  advocated that tetraploid Leymus species were segmental autotetraploids with the genomes Ns1Ns1Ns2Ns2, derived from two distinct Psathyrostachys species. Wang et al.  designated the genomes of Leymus species as NsXm until the source of Xm is identified.
Polyploidy, including autopolyploidy and allopolyploidy, is a simple speciation process. The success of polyploids is often attributed to their genomic changes including genomic stability, chromosomal rearrangement, genome size and differential gene expression, which allows polyploids to adapt to new ecological niches or to be competitively superior to the parental diploids . A better understanding of the process of polyploidization and evolutionary history of polyploids is of widespread evolutionary interest . Phylogenetic analyses of chloroplast and nuclear DNA data have increased the possibility to recognize polyploidy and hybridization in plants [16–18]. However, the often relatively low variation in chloroplast DNA at the intraspecific level have limited the precision with which polyploidy can be identified [17, 19]. Single- and low- copy nuclear genes are less likely subject to concerted evolution, thus making themselves ideal tools for verifying the existence of suspected polyploids , identifying genome donors [18, 21], demonstrating multiple polyploid origins , clarifying hybridization events or introgression , and examining gene evolution in polyploids . Plastid acetyl-CoA carboxylase (ACCase) catalyzes the first step in de novo fatty acid biosynthesis. Southern hybridization and chromosome mapping indicate that a single copy of the Acc1 gene is present in each of the group 2 homoeologous chromosomes in hexaploid wheat . The Acc1 gene has been successfully used to study the phylogenetic relationships and evolutionary history of Triticum/Aegilops complex , and the evolution of Panicum virgatum L. .
In this study, we sequenced and analyzed the single-copy nuclear Acc1 gene for 29 Leymus polyploids and 35 diploid taxa representing 18 basic genomes in Triticeae. The objectives were (1) to elucidate the phylogenetic relationships of the Leymus species; (2) to demonstrate the evolution of Leymus; (3) to explore the origin of the unknown Xm genome in Leymus; (4) to estimate the divergence times for nodes within Leymus to document biogeographic diversification history of the genus.
Twenty-eight species and one variety of Leymus were included in this study. They were analyzed together with 35 diploid taxa representing 18 basic genomes in the tribe Triticeae. Sample information and GenBank accession data were listed in Table S2 (See Additional file 2). The seed materials of Leymus with PI and W6 numbers were kindly provided by American National Plant Germplasm System (Pullman, Washington, USA), and Leymus duthiei var. longearistata was kindly provided by Dr. S. Sakamoto (Kyoto University, Japan). The seed materials of Leymus with ZY and Y numbers were collected from the field by the authors of this paper. The plants and voucher specimens of the Leymus species are deposited at Herbarium of Triticeae Research Institute, Sichuan Agricultural University, China (SAUTI).
DNA Amplification, homoeologous sequence isolate, and sequencing
DNA extraction followed a standard CTAB protocol . The Acc1 gene was amplified with the Acc1-specific primers AccF1 (5'-CCCAATATTTATCATGAGACT TGCA-3') and AccF2 (5'-CAACATTTGAATGAAThCTCCACG-3'), and PCR was conducted under cycling conditions reported previously . To decrease the chance of PCR drift and PCR selection, a 75 μl reaction mixture was separated into five reactions, and PCR products were pooled together after amplification. The Acc1 sequence amplification was carried out in a 15 μl reaction mixture consisted of 0.3 U of high-fidelity Ex Taq DNA polymerase (TaKaRa Biotechnology Co. Ltd., Dalian, China), 1× reaction buffer, 1.5 mM MgCl2, 1.2 mM of each dNTP, 0.5 μM of each primer. PCR products were cloned into the pMD18-T vector (TaKaRa) following the manufacture's instruction.
Cloning of PCR amplicons from single-copy nuclear genes from allopolyploid species will isolate homoeologous sequences from each nuclear genome . Given that Leymus species contain the Ns and Xm genomes, PCR reactions will produce a heterogeneous mix of Acc1 sequences from each Leymus polyploid. To separate the homoeologous sequence of Acc1 gene from each accession, we performed the following process. Firstly, approximately 20 positive clones from each accession were screened by direct PCR using primer AccF1 coupled with M13R (on the side of the cloning site in the plasmid). Secondly, an Ns-type Acc1-specific primer, AccFn (5'-GAACCTGTGCTCATATGGTATATTA-3'), was designed and used together with the reverse primer AccF2 to screen the Ns-type Acc1 sequences from above 20 positive clones with Acc1 inserts. Thirdly, the rest of positive clones including the Xm-type Acc1 sequences were obtained. Finally, to determine whether the Xm-type of Acc1 sequences was the result of a biologically relevant recombination, an Xm-type Acc1-specific primer, AccFx (5'-ACTGCAGGTATGTTCTTTT-3'), was designed and used together with the primer AccF2 to amplify the Xm-type Acc1 sequences. The cloned PCR products were sequenced in both directions by TaKaRa Biotechnology Co. Ltd. (Dalian, China). All the sequences from Leymus species were determined at least 5 independent Ns-type clones and 5 independent Xm-type clones.
Alignments and test for substitution saturation
Multiple sequences were aligned using ClustalX , with default options (gap opening/gap extension: 15/6.66), and the alignments were refined manually in an effort to maximize the positional homology. To reduce the size of the matrixes and the possible impact of PCR artifacts, unique substitutions in single clones were ignored and several identical sequences were represented by a single original sequence in alignments. In the initial phylogenetic analysis, the number of sequences used for alignment was reduced by keeping only one sequence if more sequences of the same accession formed a monophyletic group. Substitution saturation in the alignments was estimated by plotting pairwise rates of transitions and transversions against sequence divergence calculated under TN93 model using the software DAMBE version 5.0.7 .
Nucleotide diversity estimate
To assess the divergence and genetic relationships between polyploids and its diploid progenitor, nucleotide diversity was estimated by Tajima's π , Watterson's θ , the number of fixed differences (SF) and the numbers of shared polymorphisms (SS). Tajima's π quantifies the mean percentage of nucleotide differences among all pairwise comparisons for a set of sequences, while Watterson's θ is simply an index of the number of segregating (polymorphic) sites. A fixed difference refers to the nucleotide site where all sampled sequences from one taxon are different from all sequences from another taxon, whereas a shared polymorphism occurs when two taxa have the same two bases segregating at the same site . Closely related taxa are expected to harbor a relative higher level of shared polymorphisms because the divergence event has not lasted long enough to erase all ancestral polymorphisms. Tests of neutrality including Tajima's and Fu and Li's D statistic were performed as described by Tajima , and Fu and Li . Significance of D-values was estimated with the simulated distribution of random samples (1000 steps) using a coalescence algorithm assuming neutrality and population equilibrium . These parameters were calculated with DnaSP 4.10.9  and ProSeq 2.0 .
We also examined demographic history in sampled Leymus lineages using mismatch distributions  and Fu's Fs statistics  in the program DnaSP 4.10.9 . Mismatch distributions are frequency distributions of observed nucleotide pairwise differences, and allow to infer whether lineages have undergone sudden or stepwise demographic expansion during historical periods . A unimodal mismatch distribution indicates a recent expansion, a multimodal (including bimodal) mismatch distribution indicates diminishing population sizes or structured size. The Fu's Fs statistic is very sensitive to demographic expansion . Significance of Fs-values was calculated with the simulated distribution of random samples (1000 steps) .
Three data matrixes, including exon + intron data, intron data and exon data, were used separately to carry out phylogenetic analyses. Phylogenetic analyses were conducted using maximum likelihood (ML) and Bayesian inference (BI). ML analysis was performed using PAUP*4.0b10 (Swofford D L, Sinauer Associates, http://www.sinauer.com). Bromus inermis Leyss. was used as the outgroup. The evolutionary model used for the three different data matrixes was determined using ModelTest v3.0 with Akaike information criterion (AIC) . The optimal models identified were GTR + G + I for the exon + intron data, GTR + G for the intron data, and TIM + G + I for the exon data. ML heuristic searches were performed with 100 random addition sequence replications and TBR branch swapping algorithm. The robustness of the trees was estimated by bootstrap support (BS) . ML bootstrapping was performed with 250 replicates, each with three replicates of stepwise random taxon addition, using the same model and parameters. BS-value less than 50% was not included in figures.
Bayesian inference (BI) analysis was performed using MrBayes v3.0 . BI analyses of the exon + intron and intron data matrixes were carried out under the same evolutionary model as ML analysis. For the exon data, because the TIM + G + I model is not implemented in MrBayes v3.0, we chose the closely related GTR + G + I model instead. Four MCMC (Markov Chain Monte Carlo) chains (one cold and three heated), applying MrBayes default heating values (t = 0.2), were run for 3,800,000 generations for the exon + intron data, 2,000,000 generations for the intron data, and 9,000,000 generations for the exon data, each sampling every 100 generations. The first 9500, 4200, and 23000 trees were stationary discarded as "brun-in" for the exon + intron, intron, and exon, respectively. The program Tracer v1.4  was used to examine the log likelihoods, ensuring that they were in the stationary "fury caterpillar" phase. The remaining trees were used to construct the 50%-majority rule consensus trees. Two independent runs were performed to check whether convergence on the same posterior distribution was reached. The statistical confidence in nodes was evaluated by posterior probabilities (PP). PP-value less than 90% was not included in figures.
Taking the potential for reticulation in closely related lineages into consideration, phylogenetic network reconstruction method was used to study relationships between ancestral and derived haplotypes. The median-joining (MJ) network method was performed for this study because of robustness compared to other network methods in simulation studies using known gene genealogies . MJ network has been successfully used to reveal specific progenitor-descendant relationships of polyploidy Triticum within Triticeae .
MJ network analysis was generated by the Network 126.96.36.199 program (Fluxus Technology Ltd, Clare, Suffolk, UK). As the program infers median-joining networks from non-recombining DNA , the test of recombination was performed using the GARD recombination-detection method within the HyPhy package . Building upon this test, the exon data was used to generate MJ network because of the absence of recombination signal in alignment (Log Likelihood = -1911.85; AIC = 4061.69), while the exon + intron and intron data were not used to reconstructed MJ network due to potential recombination signal.
The hypothesis of rate constancy was evaluated with a likelihood ratio test comparing the likelihood scores from the unconstrained and clock-constrained analyses. The molecular clock was rejected because constrained and unconstrained analyses differed significantly (χ2 = 205.94, df = 88, P < 0.0001). Therefore, divergence times with 95% confidence intervals (C.I.) were estimated using Bayesian relaxed molecular clock method, implemented in BEAST v1.4.6 . The lack of fossils for Triticeae precluded a direct calibration of tree topologies. Instead, node dating of the intron data was estimated on the basis of the intron region of the Acc1 gene clock of 0.0036 substitutions per site per MY (million year) . Two relaxed clock models, including uncorrelated lognormal and exponential branch length distribution models, were used to perform node dating. The final dating from the two models was compared. MCMC searches were run for 10,000,000 generations under GTR + G model (with the associated parameters specified by ModelTest as the priors), with the first 2,000,000 discarded as burn-in. The searches achieved adequate mixing as assessed by the high ESS values for all parameters, plateaus for divergence time estimates over generations after burn-in. For all analyses two independent runs were performed, the log files were combined to check for convergence on the same distribution and to ensure adequate sample sizes, and viewed using Tracer v.1.4 .
Screening of homoeologous Acc1 sequences in Leymus
About 20 forward (5'-3' direction) clones were screened from a plate of clones with putative Acc1 inserts by the primer AccF1 and M13R. The Ns-type Acc1 sequences were screened from above 20 forward clones by the primer AccFn and AccF2, and the rest of clones were the putative Xm-type Acc1 sequences. The primer AccFx and AccF2 were further used to verify the presence of the Xm-type Acc1 sequences. Consequently, two distinct types of Acc1 sequences (Ns- and Xm-type) were obtained from 24 Leymus species. Only one type of Acc1 sequence was detected from Leymus multicaulis (Ns-type), L. coreanus (Ns-type), L. ramosus (Xm-type), L. duthiei var. longearistata (Xm-type) and L. akmolinensis (Xm-type). For these five taxa, alternative genome type might be obtained by more screens with extensive positive clones if they were allopolyploidy origin. Another possibility is that one type has been pseudogenized so that they are undetectable by our primers. In addition, we also cannot rule out the possibility of autopolyploidy of all (or partial) five taxa with only one type of Acc1 sequence.
Acc1 sequence analyses
The DNA sequence of the Acc1 gene includes 8 exons and 7 introns, which was in agreement with previous studies . The sequence comparison from all the species studied here showed that the DNA sequence ranged in length from 1391 bp to 1470 bp, and the DNA sequences in most accessions were ~ 1440 bp in size. The aligned sequence length of the exon + intron, exon and intron data sets were 1549 bp, 696 bp and 857 bp, respectively. The alignment of the exon sequence was unambiguous without gaps. Many gaps, which resulted from indels (insertion/deletion) within intron regions, were found in the alignment of the exon + intron and intron data sets. In particular, apart from the single nucleotide acid substitution and deletion, the Xm-type sequences of Leymus species and the sequences from Agropyron species and Eremopyrum triticeum had a 4-bp TATA insertion at position 631-633 in the intron region compared to the remaining sequences (See Figure 1 and Additional file 3). A 33-bp insertion was detected for the Ns-type sequences at position 1187-1219 in the intron region from 11 Leymus species (L. flexus, L. qinghaicus, L. leptostachys, L. pseudoracemosus, L. ovatus, L. pendulus, L. secalinus, L. crassiusculus, L. duthiei, L. shanxiensis and L. yiwuensis) (See Additional file 3).
Features of the exon + intron, exon and intron data matrixes were listed in Table 1. As expected, due to strong functional constraint, the levels of nucleotide variation in exon region (150 variable characters, 9 transition mutations, and 3 transversion mutations) were lower than those in intron region (407 variable characters, 25 transition mutations, and 19 transversion mutations). The ratio of parsimony-informative characters and variable characters was 0.521 (intron), 0.496 (exon + intron), and 0.427 (exon), respectively. Plotting pairwise rates of transitions and transversions against sequence divergence calculated under TN93 model revealed a nearly linear regression, indicating that the three sequence data sets showed no saturation effects.
To reveal the putative genome donors of Leymus, the Acc1 gene sequences of all the polyploid species were included in the phylogenetic analyses, together with 35 diploid taxa representing 18 genomes in Triticeae (See Table S2, Additional file 2). At least 10 positive clones (including 5 Ns-type and 5 Xm-type clones) were sequenced. In cases multiple identical sequences resulted from cloned PCR products of one accession, only one sequence was included in the data set. Consequently, 89 unique sequences were obtained and used for the phylogenetic and network analysis.
Three data sets (exon + intron, intron, and exon) were used separately to perform phylogenetic analyses (ML and BI). ML analysis of the exon + intron data yielded a single phylogenetic tree (-Lnlikelihood = 8827.1373), with the following estimated ML parameters: the assumed nucleotide frequencies A: 0.2432, C: 0.1830, G: 0.2152, T: 0.3586, the proportion of invariable sites = 0.1926, gamma shape parameter = 0.8022. ML and Bayesian analyses of the exon + intron data recovered the same topology. The tree illustrated in Figure 2 was the ML tree of posterior probabilities (PP) above and bootstrap support (BS) below branches.
The phylogenetic tree showed that the Ns-type and Xm-type sequences from Leymus species were split into two well supported clades, clade I and clade II (See Figure 2 and Additional file 4). The clade I included the Xm-type sequences of Leymus and the sequences from Ag. cristatum, Ag. mongolicum, and Er. triticeum. Three subclades (A, B, and C subclade) with high statistical support were recognized in this clade. Subclade A included all the Leymus species from North America and the Qinghai-Tibetan Plateau, three Leymus species from other parts of central Asia and one Leymus taxa from East Asia (100% PP and 73% BS). Subclade B consisted of four Leymus species from Xiangjiang of China and one Leymus species from Kazakhstan (100% PP and 75% BS). Subclade C contained three Agropyron accessions and Er. triticeum (100% PP and 100% BS). Leymus komarovii was placed outside Subclade A, B, and C. The clade II contained the Ns-type sequences of Leymus and the sequences from Psathyrostachys. Two subclades (D and E subclade) with high statistical support were recognized within the clade II. Subclade D included four Psathyrostachys species and all the Leymus species except for those from the Qinghai-Tibetan Plateau (100% PP and 71% BS). Subclade E contained the Leymus species from the Qinghai-Tibetan Plateau (100% PP and 80% BS). It was worth mentioning that the sequence in subclade E had a 33-bp insertion at position 1187-1219 (See Additional file 4). Although subclade A, D and E were supported by high bootstrap values and posterior probabilities, the phylogenetic relationships among species within these subclades were considered unresolved due to a high number of zero-length branches.
ML analysis of the intron data yielded a single phylogenetic tree (-Lnlikelihood = 5903.3227), with the assumed nucleotide frequencies A: 0.2250, C: 0.1823, G: 0.1755, T: 0.4172, gamma shape parameter = 0.9703. ML and Bayesian analyses of intron data generated the same topology. The tree illustrated in Figure 3 was the BI tree of posterior probabilities (PP) above and bootstrap support (BS) below branches. This tree was highly congruent with the tree inferred from the exon + intron data except for some nodes presenting different statistical support (See Figure 3 and Additional file 5). Those polytomies observed in the tree inferred from the exon + intron data (within subclade A, D, and E) was not resolved with the use of intron data.
ML analysis of the exon data resulted in a single phylogenetic tree (-Lnlikelihood = 1877.7337), with the assumed nucleotide frequencies A: 0.2630, C: 0.1880, G: 0.2688, T: 0.2802, the proportion of invariable sites = 0.4451, gamma shape parameter = 0.9988. The ML trees showed that the Ns-type and Xm-type sequences from Leymus species were split into two clades but with weak bootstrap support (See Figure 4 and Additional file 6). BI and ML analysis of the exon data recovered the similar topology. Although basic topology based on the exon data was congruent with the tree inferred from the exon + intron and intron data, many low resolution branches were showed.
To get better insights into the number of haplotypes of the Acc1 sequence and their relatedness, the network reconstruction methods was employed. The exon data was used to generate MJ network because no recombination signal was detected in its alignment. Each circular network node represents a single sequence haplotype, with node size being proportional to number of isolates with that haplotype. Mv (median vectors representing missing intermediates) shows unsampled nodes inferred by MJ network analysis, and the number along the branches shows the position of mutations. Network loops represent either true reticulation events or alternative genealogies in closely related lineages.
Eighty-three haplotypes were derived from 89 sequences. MJ network revealed higher levels of haplotype diversity of exon region (See Figure 4 and Additional file 6). Two distinct types of haplotypes (Ns- and Xm-type) of Leymus species were recognized. The Ns haplotypes were four mutational steps (at position 267, 268, 306, and 615) away from the Xm haplotypes. In the Ns-type haplotype, Psa. juncea and L. paboanus were placed at central branching points, while the haplotypes from the Qinghai-Tibetan Plateau formed one distinct group. In the Xm-type haplotype, all the haplotypes from Leymus species formed one star-like radiation, and L. crassiusculus (LCRA2), L. leptostachys (LLEP2), L. innovatus (LINN2) and L. ambiguus (LAMB2) were placed at central branching points. The Xm-type haplotype was closely related to those from Ag. cristatum, Ag. mongolicum and Er. triticeum.
Nucleotide diversity between Leymus and its diploid progenitor
The greatest pairwise distance among the Ns-type sequences of Leymus ranged from 0.210 to 3.377%, while the greatest pairwise distance among the Xm-type sequences of Leymus ranged from 0.208 to 2.401%. The levels of divergence between the Xm-type sequences of Leymus and the sequences from Agropyron species and Eremopyrum triticeum was 4.477%. Sequence divergence between the Ns-type sequences of Leymus and Ns sequences of Psathyrostachys was 2.960%. The levels of divergence between Ns-type and Xm-type sequences within Leymus was 6.149%. These results indicated that the Ns- and Xm-type sequences in Leymus species were correspond to the two homoeologous Acc1 sequences.
Estimates of nucleotide polymorphism, π and θ, were shown separately for the Ns genome of Leymus and Psathyrostachys, and for Xm genome of Leymus (Table 2). The number of polymorphic sites in the Ns genome of Leymus was higher than that in the Ns genome of diploid Psathyrostachys. The estimates of Tajima's and Fu and Li's D statistic for Acc1 gene on the Ns genome of Leymus were -1.4676 (P < 0.05) and -2.5042 (P < 0.05), respectively, while Tajima's D estimate on the Ns genome of diploid species was 0.65817 (P > 0.10).
Thirteen shared polymorphisms and no fixed difference were observed at Acc1 locus between the Ns-type sequence of Leymus and that of Psathyrostachys, while equal numbers of shared polymorphisms and fixed differences (Ss = 8, SF = 8) were observed between the Xm-type sequence of Leymus and the sequences from Agropyron species and Er. triticeum. This indicated that Leymus are closer to Psathyrostachys than to Agropyron and Eremopyrum.
Mismatch distribution and Fs statistic
Mismatch distribution and Fu's Fs statistic were used to infer whether Leymus lineages within those terminal clades with low resolution branches have undergone sudden or stepwise expansion during historical periods. Observed pairwise differences (mismatch distributions) between Acc1 sequences within subclade A, D, and E were all unimodal (See Figure 2 and Additional file 4). Fu's Fs statistic of Acc1 sequences within subclade A, D, and E were -12.3070 (P < 0.001), -7.0359 (P < 0.001), and -3.6640 (P < 0.001), respectively. These results indicate that Leymus lineages species had undergone expansion during its evolutionary history.
Thirteen nodes were dated (nodes 1-13 in Figure 3 and Additional file 5) using the intron region of the Acc1 gene molecular clock of 0.0036 substitutions per site per MY. Two age estimates with 95% confidence intervals based on two different relaxed clock models were also presented in Figure 3 (See also Additional file 5). Under a lognormal relaxed clock, the coefficient of rate variation was estimated to be 0.752 (95% C.I., 0474-1.007), indicating that the intron data was not strictly clock-like and relaxed clock was appropriate. The age of divergence represent an interval depending on the model of branch length distribution (each with 95% C. I.). Time calibration analysis demonstrated that the age for the divergence of Leymus was dated to 10.8-12.4 MYA (node 1 and 8). Two extensive radiations of Leymus were dated to 3.7-4.3 MYA (node 4 and 11) and 1.7-2.0 MYA (node 5 and 13), respectively.
Phylogenetic relationships in Leymus species
Two types of Acc1 sequences, Ns- and Xm-type, were obtained from nearly all the polyploidy Leymus species in the present study. This allows phylogenetic relationships among Leymus species to be elucidated on the basis of orthologous comparison.
ITS data presented by Liu et al.  and Sha et al.  showed that the Leymus species from North America were grouped together with some Leymus species from central Asia. By analyzing random amplified polymorphic DNA polymorphism (RAPD), Yang et al.  suggested that the Leymus species from North America were scattered in different subclades and grouped with those species from central Asia. The present Acc1 gene data showed that the Leymus species from North America also did not group together but placed scatteredly into one subclade (subclade A and D) including the Leymus species from central Asia and East Asia. This indicates that the Leymus species from North America is closely related to those from central Asia and East Asia.
Based on ITS sequence data, Sha et al.  reported that L. racemosus, L. arenarius, L. ramosus and L. paboanus were nested into one group, while L. angustus, L. tiancshanicus, and L. karelinii were in another group. Anamthawat-Jónsson and Bödvarsdóttir  suggested that the northern European L. arenarius was closely related to the central Eurasian L. racemosus from fluorescence in situ hybridization (FISH) evidence. In this study, the Acc1 gene data revealed a close relationship of Xm genomes among L. racemosus, L. arenarius, L. angustus, L. tiancshanicus, and L. ramosus, which was partly congruent with previous study.
In the Acc1 gene tree, the Ns-type sequences of eleven Leymus species from the Qinghai-Tibetan Plateau were clustered distinctly in one clade, and the Xm-type sequences of most Leymus species from the Qinghai-Tibetan Plateau were also grouped together. Exon analysis showed that the Leymus species from the Qinghai-Tibetan Plateau were radiated from a putative unsampled node. These results suggest that the Ns-type sequences of Acc1 gene of Leymus species from the Qinghai-Tibetan Plateau and other parts of central Asia, East Asia and North America were evolutionarily distinct.
L. komarovii was previously described as Hystrix komarovii . Ellneskog-Staam et al.  advocated that L. komarovii most likely had one variation of StH genomes of Elymus. Yen and Yang  regarded L. komarovii as section Silvicolus of Leymus species (forest-dwelling) on the basis of ecological habitats. Morphylogically, L. komarovii is distinguished from other Leymus species by glume subulate, often reduced at top, and awn equaling lemma boby. Analysis of ITS sequences by Sha et al.  showed that L. komarovii was placed at the base of the clade including all sampled Leymus species. In this study, two distinct Acc1 sequences were obtained from L. komarovii. One sequence was sister to the sequences of Psathyrostachys species and the Ns genome sequence of Leymus species except for those from the Qinghai-Tibetean Plateau, while the other sequence was placed at the base of the clade I including all the Xm genome sequence of Leymus and P/F genome sequence. This result, in combination with morphological and ITS sequence data, suggested that L. komarovii has the NsXm genome of Leymus but with some variation.
Origin of Ns genome in Leymus
Meiotic pairing data from interspecific and intergeneric hybrids [2, 8] and molecular studies [5, 11, 52] had revealed that the Ns genome of Leymus (NsXm) was originated from Psathyrostachys. Wakeley and Hey  pointed out that closely related species are expected to harbor a relative higher level of shared polymorphisms than fixed differences. In this study, Leymus was grouped with Psathyrostachys species, and shared polymorphisms and fixed differences (Ss = 13, SF = 0) were observed. These results indicate that Leymus is closely related to Psathyrostachys. Combined with previous cytological and molecular studies, it can be concluded that the Psathyrostachys species served as the Ns genome donor during the polyploid speciation of the Leymus species.
The Ns genome is represented in all Leymus species. Psathyrostachys is the Ns haplome donor genus, which contains approximately eight diploids (NsNs) or tetraploids (NsNsNsNs) speices distributed in the Middle East, central Asia, and northern China . Based on DNA hybridization and FISH analyses, Wang et al.  suggested that the Ns genome of Leymus species may be originated from Psa. juncea and Psa. lanuginosa, while Psa. fragilis and Psa. huashanica were unlikely to be the donor species of the Ns genome in Leymus species. The present MJ analysis showed that all the exon haplotyes of Ns-type form a star-like radiation, and Psa. juncea was placed at central branching points, indicating that Psa. juncea is likely ancestral Ns-genome donor of Leymus species. The Acc1 gene genealogical structure may be related to the geographic ranges of Psathyrostachys species. Psa. juncea is widely distributed in the former USSR, Mongolia, and northwestern part of China, while Psa. fragilis, Psa. huashanica and Psa. lanuginosa is restrictly distributed in some regions of central Asia.
Polyploids often originate many times from independent populations of their progenitor, especially when polyploids and their parental species coexist on a large geographic scale . Wei et al.  reported that considerable genetic heterogeneity was exhibited in accessions of Psa. juncea that have different geographical origins. On the basis of our Acc1 sequences, nucleotide sequence diversity (π) of the Ns genome of Leymus was higher than in the Ns genome of diploid Psathyrostachys, indicating that the Acc1 sequence may evolve faster in the polyploid species than in the diploids. Considering a large-scale sympatric distribution between Leymus species and Psa. juncea, another possible explanation for greater diversity in the Ns genome of Leymus is that Leymus experienced recurrent hybridization with different populations of Psa. juncea. This possibility is further supported by tests of selection history at Acc1 locus. Significantly negative values of Tajima's and Fu and Li's D statistic for the Acc1 gene on Leymus Ns and Xm genome indicates that the observed number of rare variations exceeds the expected number in an equilibrium neutral model, which might suffer from a genetic bottleneck created by polyploidization. Whereas Tajima's D estimate for the Acc1 gene on diploid Ns genome was positive. These estimates are indicative of an excess of rare variants in Leymus that could be created by recurrent hybridization event or introgression of Ns-genome during polyploidization.
Possible Origin of the Xm Genome in Leymus
The genomic constitution of Leymus was assigned as NsXm, where Xm represented a genome of unknown origin . Three different genomes Ns [9, 50], St  and J(Eb) [1, 2] have been suggested as Xm genome. Sun et al.  suggested that Leymus secalinus might have 3-4 chromosomes from the Ee genome, and a very low homology existed between the Ee and Ns genomes. Southern hybridization of genomic DNA and meiotic pairing in hybrids of Leymus species confirmed that Th. bessarabicum (Eb) or Lo. elongatum (Ee) is not an ancestral genome of Leymus [8, 57].
In this study, the Xm-type Acc1 sequence, which is homoeologous sequences of the Ns-type Acc1 sequences, were obtained from nearly all the sampled Leymus species. Genealogical analyses of the Acc1 gene indicated that the obvious Xm genome specific clade (clade I) was distinct from the Ns clade (clade II). The Xm-type sequence of Leymus was grouped with the sequences from Agropyron species and Eremopyrum triticeum. They had a 4-bp TATA insertion, while this insertion was absent in the Ns-type sequence of Leymus and other diploid species in Triticeae. Recent genealogical analysis of chloroplast trnL-F sequence in Leymus species suggested that five Leymus species from North America (L. ambiguus, L. cinereus, L. innovatus, L. salinus and L. trticoides) and two Leymus species from East Asia (L. coreanus and L. komarovii) were clustered with Agropyron and Eremopyrum species (Sha et al., unpublished data). The close relationship between Agropyron and Eremopyrum species have been supported by morphological analysis  and several molecular data . Previous studies based on cytogenetics  and DNA sequence analyses  suggested the non-monophyletic origin of Eremopyrum. Our Acc1 sequence data showed that Eremopyrum distans is differentiated from Er. triticeum, and did not contradict the idea of paraphyly in Eremopyrum. Despite the non-monophyly of Eremopyrum, it is most likely that the Xm genome of Leymus species may be closely related to the P genome from Agropyron and the F genome of Eremopyrum. Equal numbers of fixed differences and shared polymorphisms (SF = 8, SS = 8) between the Xm-type sequence of Leymus and the sequences from Agropyron species and Er. triticeum were observed, which could be the result of incomplete lineage sorting of ancestral polymorphisms after speciation events. Molecular dating analyses suggested that the time to the most recent common ancestor (tMRCA) of Leymus (excluded L. komarovii), Agropyron and Er. triticeum was dated to 7.7-8.9 MYA, and the divergence of Agropyron and Er. triticeum was dated to 4.3-4.6 MYA, implying that the divergence between the Xm and P/F genomes might be prior to the divergence between the P and F genomes. Given the present data, it is hypothesized that the Xm genome of Leymus species might have been originated from an ancestral progenitor which was closely related to Agropyron species and Er. triticeum.
Colonization of Leymus
The present results substantiate that the Ns genome of Leymus is originated from Psathyrostachys and suggest that the Xm genome of Leymus is closely related to the P genome of Agropyron and the F genome of Eremopyrum. In fact, Psathyrostachys, Agropyron and Eremopyrum are all distributed in Eurasia (Most of species distributed in central Asia), and most species of Leymus are distributed in central Asia. Based on the morphological and geographic data, many scholars suggested that the origin of the genus Leymus was in central Asia [2–4, 6].
However, several Leymus species are found mainly in the mountains of North America [2, 4, 5]. Based on analysis of chloroplast trnL-F sequences, Sha et al.  suggested that the Xm genome lineages were suggested as the maternal donor of four Leymus species from North America and two Leymus species from East Asia. The present Acc1 gene data also indicated that the Leymus species from North America is closely related to those from central Asia and East Asia. The occurrence of similar maternal donor and close phylogenetic relationship between North American and East Asia Leymus species suggests a recent origin of North American plants. Molecular dating based on the intron data of the Acc1 gene suggested that the age of the most recent common ancestor (MRCA) of Leymus was dated to 11-12 MYA, and divergence time among East Asia, central Asia and North American species was dated to 6-8 MYA. Of interest, our estimated divergence time of 3.7-4.3 MYA (node 4 and 11) among most central Asia, East Asia and North America species was prior to the initial breakup of the Bering Land Bridge which was available for floristic exchanges until about 3.5 MYA . Therefore, it can be suggested that North American Leymus species might originate from recent colonization via the Bering land bridge.
Adaptive radiation of Leymus
Polyploids usually have an advantage in colonizing new habitats and ecological niches, a feature called adaptive radiation [16, 63]. Adaptive radiation are often characterized by short branch lengths, little sequence variation, rapid speciation, and diverse morphology and ecological habitats [63–67]. The present exon + intron and intron tree showed several star-like topology (many short internal branches connecting long external branches) within Leymus species (subclade A, subclade D, and subclade E). The Acc1 gene sequence divergence was also generally relatively low, ranging from 0.2% in many cases to 3.3% (subclade A, 0.3%-1.9%; subclade D, 0.2%-2.0%; subclade E, 0.3%-1.3%), which resulted in low branching resolution in the phylogenetic trees. The occurrence of a star-like radiation was presented in the ML tree and MJ network of the exon data. In addition, significantly negative values of Fs statistics and unimodal mismatch distributions within those polytomies observed in phylogenetic tree suggest rapid lineage expansions. These results, in combination with the fact that Leymus species exhibited large variation in morphological characteristics and habitats, indicate that adaptive radiation had occurred in Leymus.
Adaptive radiation might have been driven by specific geographical events and climate oscillations . Geological evidence indicates that extensive habitat changes occurred in the Qinghai-Tibetan Plateau and adjacent areas due to the recent large-scale upliftings of the Qinghai-Tibetan Plateau in Pliocene and climate oscillations in the Quaternary within 5 MYA (The most notable Pliocene/Pleistocene event is known as the Qingzang Movement occurred 3.4 MYA, 2.5 MYA and 1.7 MYA, respectively) . The present molecular dating suggested that Leymus have diverged in two extensive radiations during a period of 3.7-4.3 MYA and 1.7-2.1 MYA. Therefore, it is suggested that the radiation of Leymus might have been triggered by the recent uplifts of the Qinghai-Tibetan Plateau and the Quaternary climate oscillations. This hypothesis is further strengthened by the expansion of the habitats of its current species. The habitats preferred by most Eurasia Leymus species are cold and dry alpine meadow, steppe desert and dry slopes. However, L. duthiei grows in shady and moist forests in eastern part of the Qinghai-Tibetan Plateau (Hengduan Mountainous regions). Shi et al.  pointed out that both arid habitats at higher latitudes and warm and moist climate conditions at lower latitudes might result from the uplifting of the Qinghai-Tibetan Plateau. An et al.  suggested that the drier climate as well as biological and ecological diversity in central Asia also resulted from the uplifting of the Qinghai-Tibetan Plateau. Therefore, the rich geological and ecological diversity of the plateau and adjacent areas of central Asia, together with habitat isolation due to changing climatic conditions during and after the uplifts of the plateau, might well have promoted rapid speciation and radiation of Leymus in small, isolated populations. Wang et al.  considered that the rapid speciation and radiation could have resulted in small numbers of synapomorphic nucleotide substitutions and might promote the fixation of unique morphological characters in some species. In this study, the Ns-type sequences of Leymus species from the Qinghai-Tibetan Plateau have evolutionarily distinguished from those from other parts of central Asia, East Asia and North America. In particular, the species from the Qinghai-Tibetan Plateau shared a 33-bp insertion in the Ns-type sequences compared to Psathyrostachys species and other Leymus species. Morphologically, the Leymus species from the Qinghai-Tibetan Plateau are distinguished from the other Leymus species by leaf sheath glabrous, rachis and rachilla pubescent, and glume shorter than spikelet, while L. duthiei differs from the other species of subclade E by its highly reduced glumes and loosely flat leaf.
In this study, two homoeologues of the single-copy nuclear Acc1 gene were isolated from almost all the polyploid Leymus species and were analyzed with those of nearly all the diploid taxa in Triticeae. Sequence diversity patterns and genealogical analyses suggested that Leymus is closely related to Psathyrostachys, Agropyron, and Eremopyrum, which could shed new light on our understanding of the origin of Xm genome, the polyploidization events and evolutionary history of Leymus. Molecular dating, in combination with geographic evidence and the distribution of diploid donor of Leymus, indicated that North America Leymus species might originate from colonization via the Bering land bridge. The Acc1 gene data analyses also suggested that adaptive radiation might have occurred in Leymus within a relatively short timeframe. This might have promoted rapid sympatric or allopatric speciation, and allowed the fixation of unique morphological characters in Leymus. Adaptive radiation might have led to the rich diversity, the numbers of species and widely ecological adaptation of Leymus species.
Löve À: Conspectus of the Triticeae. Feddes Repert. 1984, 95: 425-521.
Dewey DR: The genomic system of classification as a guide to intergeneric hybridization with the perennial Triticeae. Gene Manipulation in Plant Improvement. Edited by: Gustafson JP. 1984, Plenem Press, New York, 209-279.
Yen C, Yang JL: Triticeae Biosystematics. 2008, Chinese Agricultural Press, Beijing, 4: In Chinese
Tzvelev NN: Zlaki SSSR (Grasses of the Soviet Union). 1976, Leningrad: Academiya Nauk SSSR, 176-189.
Barkworth ME, Atkins RJ: Leymus Hochst. (Gramineae: Triticeae) in North America: taxonomy and distribution. Am J Bot. 1984, 71: 609-625. 10.2307/2443358.
Zhi L, Teng ZH: Classification and geographic distribution of Leymus in China. Bull Bot Res. 2005, 25: 22-25.
Wang RR-C, Bothmer RV, Dvorak J, Fedak G, Linde-Laursen I, Muramatsu M: Genome symbols in the Triticeae (Poaceae). Proc 2nd Intern. Edited by: Wang RR-C, Jensen KB, Jaussi C. 1994, Triticeae Symp, Logan, Utah, USA, 29-34.
Wang RR-C, Jensen KB: Absence of the J genome in Leymus species (Poaceae: Triticeae): evidence from DNA hybridization and meiotic pairing. Genome. 1994, 37: 231-235. 10.1139/g94-032.
Zhang HB, Dvorak J: The genome origin of tetraploid species of Leymus (Poaceae: Triticeae) inferred from variation in repeated nucleotide sequences. Am J Bot. 1991, 78: 871-884. 10.2307/2445166.
Liu ZP, Chen ZY, Pan J, Li XF, Su M, Wang LJ, Li HJ, Liu GS: Phylogenetic relationships in Leymus (Poaceae: Triticeae) revealed by the nuclear ribosomal internal transcribed spacer and chloroplast trnL-F sequences. Mol Phylogenet Evol. 2008, 46: 278-289. 10.1016/j.ympev.2007.10.009.
Sha LN, Yang RW, Fan X, Wang XL, Zhou YH: Phylogenetic analysis of Leymus (Poaceae: Triticeae) inferred from nuclear rDNA ITS sequences. Biochem Genet. 2008, 46: 605-619. 10.1007/s10528-008-9175-5.
Shiotani I: Species differentiation in Agropyron, Elymus, Hystrix, and Sitanion (Abstract). Proceedings of the 12th Internaional Congress of Genetics, The Science Council of Japan, Tokyo. 1968, 184-
Sun GL, Wu BH, Liu F: Cytogenetic and genomic relationships of Thinopyrum elongatum with two Psathyrostachys species and with Leymus secalinus (Poaceae). Plant Syst Evol. 1995, 197: 225-231. 10.1007/BF00984641.
Zhang HQ, Yang RW, Dou QW, Tsujimoto H, Zhou YH: Genome constitutions of Hystrix patula, H. duthiei ssp. duthiei and H. duthiei ssp. longearistata (Poaceae: Triticeae) revealed by meiotic pairing behavior and genomic in-situ hybridization. Chromosome Res. 2006, 14: 595-604. 10.1007/s10577-006-1057-2.
Bödvarsdóttir SK, Anamthawat-Jónsson K: Isolation, characterization, and analysis of Leymus -specific DNA sequences. Genome. 2003, 46: 673-682. 10.1139/g03-029.
Soltis DE, Soltis PS, Tate JA: Advances in the study of polyploidy since plant speciation. New Phytol. 2003, 161: 173-191. 10.1046/j.1469-8137.2003.00948.x.
Sang T: Utility of low-copy nuclear gene sequences in plant phylogenetics. Crit Rev Biochem Mol Biol. 2002, 37: 121-147. 10.1080/10409230290771474.
Mason-Gamer RJ: Reticulate evolution, introgression, and intertribal gene capture in an allohexaploid grass. Syst Biol. 2004, 53: 25-37. 10.1080/10635150490424402.
Kim ST, Sultan SE, Donoghue MJ: Allopolyploid speciation in Persicaria (Polygonaceae): Insights from a low-copy nuclear region. Proc Natl Acad Sci USA. 2008, 105: 12370-12375. 10.1073/pnas.0805141105.
Smith JF, Funke MM, Woo VL: A duplication of gcyc predates divergence within tribe Coronanthereae (Gesneriaceae): phylogenetic analysis and evolution. Plant Syst Evol. 2006, 261: 245-256. 10.1007/s00606-006-0445-6.
Petersen G, Seberg O, Tde M, Berthelsen K: Phylogenetic relationships of Triticum and Aegilops and evidence for the origin of the A, B, and D genomes of common wheat (Triticum aestivum). Mol Phylogenet Evol. 2006, 39: 70-82. 10.1016/j.ympev.2006.01.023.
Sun GL, Daley T, Ni Y: Molecular evolution and genome divergence at RPB2 gene of the St and H genomes in Elymus species. Plant Mol Biol. 2007, 64: 645-655. 10.1007/s11103-007-9183-6.
Gornicki P, Fans J, King I, Podkowinski J, Gill B, Haselkorn R: Plastid-localized acetyl-CoA carboxylase of bread wheat is encoded by a single gene on each of the three ancestral chromosome sets. Proc Natl Acad Sci USA. 1997, 94: 14179-14184. 10.1073/pnas.94.25.14179.
Huang SX, Sirikhachornkit A, Faris JD, Su XJ, Gill BS, Haselkorn R, Gornicki P: Phylogenetic analysis of the acetyl-CoA carboxylase and 3-phosphoglycerate kinase loci in wheat and other grasses. Plant Mol Biol. 2002, 48: 805-820. 10.1023/A:1014868320552.
Huang SX, Su XJ, Haselkorn R, Gornicki P: Evolution of switchgrass (Panicum virgatum L.) based on sequences of the nuclear gene encoding plastid acetyl-CoA carboxylase. Plant Sci. 2003, 164: 43-49. 10.1016/S0168-9452(02)00327-8.
Doyle JJ, Doyle JL: A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull. 1987, 19: 11-15.
Doyle JJ, Doyle JL: Nuclear protein-coding genes in phylogeny reconstruction and homology assessment: some examples from Leguminosae. Molecular Systematics and Plant Evolution. Edited by: Hollingsworth PM, Bateman RM, Gornall RJ. 1999, Taylor and Francis, London, UK, 229-254.
Thompson JD, Plewniak F, Poch O: A comprehensive comparison of multiple sequence alignment programs. Nucleic Acids Res. 1999, 27: 2682-2690. 10.1093/nar/27.13.2682.
Xia X, Xie Z: DAMBE: Data analysis in molecular biology and evolution. J Hered. 2001, 92: 371-373. 10.1093/jhered/92.4.371.
Tajima F: Statistical method for testing the neutral mutation of hypothesis by DNA polymorphism. Genetics. 1989, 123: 585-595.
Watterson GA: On the number of segregation sites in genetical models without recombination. Theor Popul Biol. 1975, 7: 256-276. 10.1016/0040-5809(75)90020-9.
Hilton H, Kliman RM, Hey J: Using hitchhiking genes to study adaptation and divergence during speciation within the Drosophila melanogaster species complex. Evolution. 1994, 48: 1900-1913. 10.2307/2410516.
Fu YX, Li WH: Statistical tests of neutrality of mutations. Genetics. 1993, 133: 693-709.
Hudson RR: Gene genealogies and the coalescent process. Oxford Surveys in Evolutionary Biology. Edited by: Futuyma D, Antonovics J. 1990, Oxford University Press, New York, 1-44.
Rozas J, Sánchez-DelBarrio JC, Messeguer X, Rozas R: DNA sequence polymorphism, version 4.10.4.; DNAsp4 computer software. 2005, Barcelona Univ. Barcelona, Spain
Filatov DA: ProSeq: A software for preparation and evolutionary analysis of DNA sequence data sets. Mol Ecol Notes. 2002, 2: 621-624. 10.1046/j.1471-8286.2002.00313.x.
Rogers AR, Harpending H: Population growth makes waves in the distribution of pairwise genetic differences. Mol Biol Evol. 1992, 9: 552-569.
Fu YX: Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics. 1997, 147: 915-925.
Posada D, Crandall KA: Modeltest: testing the model of DNA substitution. Bioinformatics. 1998, 14: 817-818. 10.1093/bioinformatics/14.9.817.
Felsenstein J: Confidence limits on phylogenies: an approach using the bootstrap. Evolution. 1985, 39: 783-791. 10.2307/2408678.
Huelsenbeck JP, Ronquist FR: MrBayes: Bayesian inference of phylogenetic trees. Bioinformatics. 2001, 17: 754-755. 10.1093/bioinformatics/17.8.754.
Rambaut A, Drummond AJ: Tracer v1.4. 2007, [http://beast.bio.ed.ac.uk/Tracer]
Cassens I, Mardulyn P, Milinkovitch MC: Evaluating intraspecific "network" construction methods using simulated sequence data: do existing algorithms outperform the global maximum parsimony approach?. Syst Biol. 2005, 54: 363-72. 10.1080/10635150590945377.
Kilian B, Özkan H, Deusch O, Effgen S, Brandolini A, Kohl J, Martin W, Salamini F: Independent wheat B and G genome origins in outcrossing Aegilops progenitor haplotypes. Mol Biol Evol. 2007, 24: 217-227. 10.1093/molbev/msl151.
Bandelt HJ, Forster P, Röhl A: Median-joining networks for inferring intraspecific phylogenies. Mol Phylogenet Evol. 1999, 16: 37-48.
Pond SL, Frost SD, Muse SV: HyPhy: hypothesis testing using phylogenies. Bioinformatics. 2005, 21: 676-679. 10.1093/bioinformatics/bti079.
Drummond AJ, Rambaut A: BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol Biol. 2007, 7: 214-10.1186/1471-2148-7-214.
Chalupska D, Lee HY, Faris JD, Evrard A, Chalhoub B, Haselkorn R, Gornicki P: Acc homoeoloci and the evolution of wheat genomes. Proc Natl Acad Sci USA. 2008, 105: 9691-9696. 10.1073/pnas.0803981105.
Yang RW, Zhou YH, Ding CB, Zheng YL, Zhang L: Relationships among Leymus species assessed by RAPD markers. Biol Plant. 2008, 52: 237-241. 10.1007/s10535-008-0052-1.
Anamthawat-Jónsson K, Bödvarsdóttir SK: Genomic and genetic relationships among species of Leymus (Poaceae: Triticeae) inferred from 18S-26S ribosomal genes. Am J Bot. 2001, 88: 553-559. 10.2307/2657053.
Ellenskog-Staam P, Bothmer RV, Anamthawat-Jónsson K, Salomom B: Genome analysis of species in the genus Hystrix (Triticeae; Poaceae). Plant Syst Evol. 2007, 265: 241-249. 10.1007/s00606-006-0509-7.
Jensen KB, Wang RR-C: Cytological and molecular evidence for transferring Elymus coreanus and Elymus californicus from the genus Elymus to Leymus (Poaceae: Triticeae). Int J Plant Sci. 1997, 158: 872-877. 10.1086/297502.
Wakeley J, Hey J: Estimating ancestral population parameters. Genetics. 1997, 145: 847-855.
Wang RR-C, Zhang JY, Lee BS, Jensen KB, Kishii M, Tsujimoto H: Variations in abundance of 2 repetitive sequences in Leymus and Psathyrostachys species. Genome. 2006, 49: 511-519. 10.1139/G05-126.
Soltis DE, Soltis PS: Polyploidy: recurrent formation and genome evolution. Trends Ecol Evol. 1999, 14: 348-352. 10.1016/S0169-5347(99)01638-9.
Wei JZ, Campbell WF, Wang RR-C: Genetic variability in Russian wildrye (Psathyrostachys juncea) assessed by RAPD. Genet Resour Crop Evol. 1997, 44: 117-125. 10.1023/A:1008666908478.
Ørgaard M, Heslop-Harrison JS: Relationships between species of Leymus, Psathyrostachys, and Hordeum (Poaceae, Triticeae) inferred from southern hybridization of genomic and cloned DNA probes. Plant Syst Evol. 1994, 189: 217-231. 10.1007/BF00939728.
Clayton WD, Renvoize SA: Genera Gramineum. Grasses of the world. 1986, Royal Botanical Gardens, London, UK
Sakamoto S: Patterns of phylogenetic differentiation in the tribe Triticeae. Seiken Ziho. 1973, 24: 11-31.
Mason-Gamer RJ: The β-amylase genes of grasses and a phylogenetic analysis of the Triticeae (Poaceae). Am J Bot. 2005, 92: 1045-1058. 10.3732/ajb.92.6.1045.
Sha LN, Fan X, Yang RW, Kang HY, Ding CB, Zhang L, Zheng YL, Zhou YH: Phylogenetic relationships between Hystrix and its affinitive genera (Triticeae; Poaceae) based on nuclear Acc1, DMC1 and chloroplast trnL-F sequences. Mol Phylogenet Evol. 2009
Hopkins DM: The Bering Land Bridge. 1967, Stanford University Press, Stanford, CA, USA
Seehausen O: Hybridization and adaptive radiation. Trends Ecol Evol. 2004, 19: 198-207. 10.1016/j.tree.2004.01.003.
Richardson JE, Pennington RT, Pennington TD, Hollingsworth PM: Rapid diversification of a species-rich genus of neotropical rain forest trees. Science. 2001, 293: 2242-2245. 10.1126/science.1061421.
Wagstaff SJ, Breitwieser I: Phylogeny and Classification of Brachyglottis (Senecioneae, Asteraceae): An Example of a Rapid Species Radiation in New Zealand. Syst Bot. 2004, 29: 1003-1010. 10.1600/0363644042450991.
Wang AL, Yang MH, Liu JQ: Molecular phylogeny, recent Radiation and evolution of gross morphology of the Rhubarb genus Rheum (Polygonaceae) inferred from chloroplast DNA trnL-F sequences. Ann Bot. 2005, 96: 489-498. 10.1093/aob/mci201.
Linder HP: Plant species radiations: where, when, why?. Philos Trans R Soc B Biol Sci. 2008, 363: 3097-3105. 10.1098/rstb.2008.0075.
Li BY, Pan BT: Progress in paleogeographic study of the Tibetan Plateau. Geographical Research. 2002, 21: 61-70.
Shi YF, Li JJ, Li BY: Uplift and environmental changes of Qinghai-Tibetan Plateau in the late Cenozoic. 1998, Guangzhou: Guangdong Science and Technology Press
An ZS, Kutzbach JE, Prell WL, Port SC: Evolution of Asian monsoons and phased uplift of the Himalayan-Tibetan Plateau since late Miocene times. Nature. 2001, 411: 62-66. 10.1038/35075035.
The authors are thankful to the Excellent Doctoral Dissertation Fund of Sichuan Agricultural University (YBPY0803), the National Natural Science Foundation of China (Nos. 30870154, 30900087), and the Science and Technology Bureau and Education Bureau of Sichuan Province, China for the financial support. We are very grateful to American National Plant Germplasm System (Pullman, Washington, USA) providing the part seed materials. We also thank five anonymous reviewers for their very useful comments on the manuscript.
FX designed the study, designed allele-specific primer, carried out data analyses and wrote the manuscript; SLN, YRW and KHY carried out part of experiments; ZHQ, DCB and ZL collected seed materials; ZYL gave the good suggestions in the experiments and manuscript; ZYH planned the study, participated in the design of the experiments, and revised the manuscript. All authors approved the final manuscript.
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Fan, X., Sha, L., Yang, R. et al. Phylogeny and evolutionary history of Leymus(Triticeae; Poaceae) based on a single-copy nuclear gene encoding plastid acetyl-CoA carboxylase. BMC Evol Biol 9, 247 (2009). https://doi.org/10.1186/1471-2148-9-247
- Mismatch Distribution
- Acc1 Gene
- Acc1 Sequence
- Diploid Taxon
- Shared Polymorphism