Hordeum murinum L. is a species complex composed of related taxa, including the subspecies glaucum, murinum and leporinum. However, the phylogenetic relationships between the different taxa and their cytotypes, and the origin of the polyploid forms, remain points of controversy. The present work reports a comparative karyotype analysis of seven accessions of the H. murinum complex representing all subspecies and cytotypes. The karyotypes were determined by examining the distribution of the repetitive Triticeae DNA sequences pTa71, pTa794, pSc119.2, pAs1 and pHch950, the simple sequence repeats (SSRs) (AG)10, (AAC)5, (AAG)5, (ACT)5, (ATC)5, and (CCCTAAA)3 via in situ hybridization. The chromosomes of the three subgenomes involved in the polyploids were identified. All tetraploids of all subspecies shared the same two subgenomes (thus suggesting them to in fact belong to the same taxon), the result of hybridization between two diploid ancestors. One of the subgenomes present in all tetraploids of all subspecies was found to be very similar (though not identical) to the chromosome complement of the diploid glaucum. The hexaploid form of leporinum came about through a cross between a tetraploid and a third diploid form. Exclusively bivalent associations among homologous chromosomes were observed when analyzing pollen mother cells of tetraploid taxa. In conclusion, the present results identify all the individual chromosomes within the H. murinum complex, reveal its genome structure and phylogeny, and explain the appearance of the different cytotypes. Three cryptic species are proposed according to ploidy level that may deserve full taxonomic recognition.
Citation: Cuadrado Á, Carmona A, Jouve N (2013) Chromosomal Characterization of the Three Subgenomes in the Polyploids of Hordeum murinum L.: New Insight into the Evolution of This Complex. PLoS ONE 8(12): e81385. https://doi.org/10.1371/journal.pone.0081385
Editor: Christos A. Ouzounis, The Centre for Research and Technology, Hellas, Greece
Received: May 10, 2013; Accepted: October 13, 2013; Published: December 13, 2013
Copyright: © 2013 Cuadrado et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was funded by grants from the Spanish Ministry of Science and Innovation (AGL 2009-10373 and AGL2012-34052). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The author have declared that no competing interests exist.
Polyploidy has been particularly important in the evolution of the family Poaceae . Certainly, it has played an important role in the diversification of the genus Hordeum, which contains diploid, tetraploid and hexaploid taxa. C-banding karyotypes and the meiotic behaviour of Hordeum hybrids suggest the existence of four basic diploid genomes –: H, I, Xa and Xu (following the nomenclature of Wang et al.  and Linde-Laursen et al. ). Accordingly, molecular phylogenies cluster Hordeum species into four groups . The species H. murinum L., which possesses the Xu-genome, is usually recognized as having three subspecies: glaucum (Steud.) Tzvelev (2n = 2x = 14), murinum (2n = 4x = 28), and leporinum (Link) Arcang. (2n = 4x = 28, 2n = 6x = 42) . However, since there is no single diagnostic morphological characteristic that distinguishes the three forms - which are easily confused - most authors refer to the murinum complex , .
For many years it remained unclear whether the polyploid forms of H. murinum were auto- or allopolyploids –. Recently, however, allopolyploidy has been strongly supported by molecular phylogenetic analyses that differentiate 2x, 4x and 6x forms –. Indeed Jakob and Blattner  indicate that glaucum was involved in the formation of the tetraploids together with a now likely extinct taxon belonging to the same Hordeum Xu genome group, and that a third, closely related taxon contributed to the formation of the hexaploid leporinum. Nevertheless, additional cytogenetic analyses are needed to reveal the true genomic constitution of the different H. murinum taxa and cytotypes.
The aim of the present work was to examine the karyotypes of a representative sample of H. murimum accessions covering all subspecies and cytotypes. If the diploid glaucum was involved in the origin of the polyploid cytotypes, its chromosomes should be present in them. The same is true if tetraploid forms were involved in the origin of the hexaploid forms.
Materials and Methods
Material representing all three subspecies and cytotypes of the H. murinum complex was obtained from the IPK Germplasm Bank (Gatersleben, Germany). Table 1 provides information on the accession numbers and places of origin of the material used.
Root tips were obtained from seedlings and exceptionally from plants grown in pots in a greenhouse. Meiotic divisions were observed in pollen mother cells. Chromosome preparations were obtained as previously described .
Probes, labeling and in situ hybridization
Five probes containing repeated DNA sequences were used to characterize chromosomes by FISH: pTa794 and pTa71 (respectively containing 5S rDNA and 45S rDNA from Triticum aestivum L.), pSc119.2 and pAs1 (tandem repeat sequences obtained from Secale cereale L. and Aegilops tauschii Coss respectively) and pHch950 (a dispersive, repetitive sequence derived from Hordeum chilense Roem. & Schult.). Full probe descriptions, probe labelling procedures and the FISH conditions used have been described in earlier work . To detect telomeric repeats (Tel.), the oligomer (5′-CCCTAAA-3′)3, synthesized with Dy547 (red) (Isogen Life Science) at both ends, was used according to Cuadrado et al. . Five other synthetic oligonucleotides - (AG)10, (AAC)5, (AAG)5, (ACT)5 and (ATC)5 - synthesized with biotin (Roche Applied Science) at both ends - were used to detect their respective SSRs by ND (non denaturing)-FISH, as previously described .
Fluorescence microscopy and imaging
Slides were examined using a Zeiss Axiophot epifluorescence microscope. Biotin/Cy3, digoxigenin/FITC and DAPI stained images were recorded with each filter set using a cooled CCD camera (Nikon DS). The localization of the signals relative to the DAPI staining pattern was resolved by merging images using Adobe Photoshop, employing only those functions that applied equally to all pixels.
Ploidy level of H. murinum taxa
In agreement with previous chromosome counts for H. murinum taxa, diploid (2n = 2x = 14), tetraploid (2n = 4x = 28) and hexaploid (2n = 6x = 42) cytotypes were detected among the examined accessions (Table 1). However, accession GRA2735 - supposedly glaucum - was found to have 2n = 28 instead of the expected 2n = 14. Further, accession GRA1183 – supposedly murinum – was found to have 2n = 42 instead of the expected 2n = 28. Individuals of these accessions were therefore grown in the field and identified morphologically following the key provided by Bothmer et al. . Accession GRA2735 showed features diagnostic of glaucum, including pedicelate central spikelets longer than the lateral spikelets, and anthers with purple dots (Fig. S1). This is the first report of a tetraploid form of glaucum. Accession GRA1183, however, showed the diagnostic characteristics of leporinum (pedicelate central spikelets shorter than the lateral spikelets).
Karyotype analysis of diploid H. murinum
Figure 1 shows the distinctive hybridization patterns obtained with a number of repetitive probes in metaphase chromosomes of the H. murinum diploid accession BCC2002.
Each panel shows merged images to facilitate the visualization of the in situ signals with respect to DAPI (blue) staining (a). In a, the arrows point to the two pairs of satellited chromosomes; in h, the arrows and arrowheads point to 5S rDNA and 45S rDNA loci respectively. In i and j, the arrows point to the pair of chromosomes carrying interstitial telomeric repeats and both ribosomal sequences. (k) Karyotypes showing one chromosome of each homologous group chosen from the metaphases shown in g–h (top and two bottom rows) and a–f (the remaining rows). Scale bar = 10 µm.
FISH analysis using probe pTa71 revealed four signals at the secondary constriction of the two satellited chromosome pairs (Fig. 1a). One of these chromosome pairs also carried a pTa794 signal in a more proximal position (Fig. 1d). Another pair of chromosomes carrying a pTa794 signal in a distal position on the short arm was detected (Fig. 1d and j). Thus, the combination of pTa71 and pTa794 easily distinguishes three chromosome pairs (Fig. 1k, top row). The pAs1 probe returned similar banding patterns for different chromosomes, making clear identifications very difficult (Fig. 1f). No signals were observed with probe pSc119.2.
The most clear, intense and rich pattern of signals was obtained with probe (AAG)5, which clearly identified the seven homologues chromosome pairs (Fig. 1e). (AAC)5 produced similar though slightly less diagnostic patterns (Fig. 1h). Most of the AAC sites co-localized with AAG in the pericentromeric regions. Well defined and intense signals were observed with (AG)10 near the centromeres of four chromosome pairs (Fig. 1c). In contrast (ATC)5 (Fig. 1b) and (ACT)5 (Fig. 1g) only revealed signals of weak intensity that were little suitable as diagnostic markers. Finally, the expected signals for the telomeric probe were seen at the ends of all chromosome arms. In addition, interstitial telomeric repeats were found in the satellited chromosome pair carrying both pTa71 and pTa794 signals (Fig. 1i–j).
Once the hybridisation pattern of each probe was analysed, multiple target in situ experiments using two-by-two combinations of the probes (reprobing the same chromosome preparations) allowed the characterization of the seven chromosome pairs (e.g., Fig. 1a–f). Following the classical nomenclature used for Triticeae chromosomes with unknown homoeology, karyotypes were constructed arranging chromosomes A to G in order of decreasing length with the satellited chromosomes at the end (Fig. 1k).
Chromosome identification and karyotype diversity within tetraploid H. murinum
Figures 2 shows the distinctive hybridization patterns obtained with several repetitive probes in metaphase chromosome preparations of five tetraploid accessions covering all H. murinum subspecies.
In a, the arrows point to (AG)10 signals in five pairs of chromosomes. One pair carrying weak signals is shown in the insets. In b and e, the arrows point to pSc119.2 signals. The arrowheads in f point to the 14 chromosomes labeled with pHch950. In g, the arrows and arrowheads point to minor pTa794 and pTa71 sites respectively. In h, the arrows and arrowheads point to interstitial telomeric repeats and stronger, derived pTa71 signals (see g) respectively. The satellited chromosome pair belonging to subgenome Xu carrying pTa71, pTa794 and interstitial telomeric sequences is amplified in g′ and h′. Scale bar = 10 µm.
In all tetraploid accessions, probe pHch950 hybridized in a dispersed fashion with seven chromosome pairs (Fig. 2a and f). Six intense pTa71 signals were detected at the secondary constriction of the three satellited chromosome pairs. Two further minor pTa71 signals were seen on the long arms of a small metacentric chromosome pair (Fig. 2g). Six pTa794 signals were detected, the four strongest in two satellited chromosome pairs (Fig. 2g). Besides those expected at both chromosome ends, telomeric interstitial signals were observed on one of the two satellited chromosome pairs carrying (as in diploids) pTa71 and pTa794 signals (Fig. 2g–h).
pSc119.2 revealed subtelomeric signals of different intensity ranging in number from four on two chromosome pairs in accessions GRA1021 and BCC2007, to ten on four chromosome pairs in accession GRA2894 (compare Fig. 2b and e). This indicates diversity among the 4x accessions for the presence/absence of this repetitive sequence. Similarly, (AG)10 showed well defined signals of different intensity in different chromosomal regions (from the centromere to a subtelomeric position) in five or six chromosome pairs, depending on the accession analyzed (Fig. 2a).
The pAs1 probe revealed a rich pattern of signals on all chromosome arms, making individual chromosome identification very difficult (Fig. 2d and f). However, all 14 chromosomes pairs were easily identified on the basis of the chromosomal location of (AAG)5 (Fig. 2c–e and Fig. 3a). The (AAC)5 probe mostly co-localized with (AAG)5 but produced a less diagnostic pattern (Fig. 2b). Finally, as in the diploids, no reliable (ATC)5 or (ACT)5 signals were observed; no attempt was therefore made to characterize their in situ patterns in detail.
The results obtained with the pHch950 probe were particularly important for identifying the chromosomes of the two subgenomes involved in the tetraploids (Fig. 2a and f). Firstly, the seven chromosome pairs revealed with the pHch950 probe were analyzed in detail with the diagnostic pTa71, pTa794 and (AAG)5 probes. With the exception of the non-satellited chromosome pair carrying the minor 45S rDNA locus, the chromosomes showed sizes, morphologies and hybridization patterns similar to those seen for the chromosomes of diploid H. murinum (compare Fig. 1k and Fig. 3a). The above seven pairs were identified as belonging to subgenome Xu and were arranged in the karyotypes according to the nomenclature system previously employed for the diploids. The pair with no counterpart in the diploid was identified as G Although other minor differences were found between the Xu subgenome and the genome of the diploids (for example, FISH with the probe pTa794 returned no signal on chromosome E of the tetraploids), the physical map returned by the probes revealed great similarities between the diploid glaucum and the subgenome Xu of the tetraploids (compare Fig. 1k and Fig. 3b). For example, the satellited chromosome pair of this subgenome carries both 45S rDNA and 5S rDNA loci and interstitial telomeric sequences, just like the satellited chromosome F of diploids (compare Figs. 1j and 2g–h).
Once the identity of the Xu chromosomes was established, the seven chromosome pairs without pHch950 signals were characterized. These chromosomes should not share the same Xu genome, and the provisional designation of subgenome Xv is here proposed. Among the Xu and Xv chromosomes, homoeology relationships could be established for the two pairs of satellited chromosomes: chromosomes F (which, like chromosome F of diploids and subgenome Xu of tetraploids, carries both rDNA sequences) and G (which, like chromosome G of the diploids has a large satellite on the long arm) (Fig. 2g). The remaining chromosomes of subgenome Xv (A to E) were arranged in decreasing order of the length; however, no homoeologies can be established between these chromosomes and their counterpart in the subgenome Xu without further genetics analysis.
Finally, the easy identification of all 14 chromosome pairs after ND-FISH with (AAG)5 allowed chromosome-by-chromosome analysis of the hybridization patterns of the remaining probes (Fig. 2 e–f), and the assessment of cytogenetic diversity by comparing the homologous chromosomes of the five tetraploid accessions (Fig. 3a). Accession GRA2894, which showed the largest number of pSc119.2 and (AG)10 signals among the tetraploids, was chosen to represent the karyotypes based on probes pTa71, pTa794, pAs1, pSc119.2 and (AG)10 (Fig. 3b). The results are summarized in Table 2.
Identification of the three subgenomes presents in hexaploid H. murinum
Each panel shows merged images to facilitate the visualization of the signals with respect to the blue DAPI staining. In a, the arrows point to the 14 chromosomes revealed with pHch950. In c, the arrows and arrowheads point to the 5S rDNA and 45S rDNA minor loci respectively. In d, the arrows point to interstitial telomeric repeats (enlarged in the insets). In e, the arrowheads indicate pTa71 signals derived from previous hybridizations. (g) The four chromosome pairs carrying pSc119.2 signals were chosen from the metaphase shown in e–f. Scale bar = 10 µm.
Chromosomes of each karyotype were chosen from the same metaphase (that shown for [AAG]5 in Fig. 4b). Note that the pTa71, pTa794 and pSc119.2 signals were drawn over the DAPI-stained chromosomes. The orange signals in the pAs1 karyotype are the stronger red signals observed in the (AG)10 karyotype.
As in the tetraploids, seven chromosomes pairs were distinguished using pHch950 (Fig. 4a). The pTa71 probe revealed 10 strong signals at the secondary constriction of the five satellited chromosome pairs. Two minor pTa71 signals were also seen on a small metacentric chromosome pair (Fig. 4c). Eight pTa794 signals were detected, the six strongest in three satellited chromosomes pairs (Fig. 4c). As in the diploid and tetraploid taxa, one satellited chromosome pair (carrying both ribosomal loci) showed interstitial telomeric signals (Fig. 4d). The chromosomal distribution revealed by pAs1 was coincident with that seen for the diploids and tetraploids, although in the hexaploids (with more chromosomes of similar morphology and in situ patterns) it was very hard to identify individual chromosomes (Fig. 5). Ten pSc119.2 signals of different intensity were localized in subtelomeric regions of four chromosome pairs (Fig. 4g).
Once again, among the SSR probes investigated, the richest pattern of signals was obtained with probe (AAG)5 (Fig. 4b and f). (AAC)5 signals mostly co-localized with clusters of AAG repeats, although some chromosome were very enriched in (AAG)5 signals and showed no accompanying (AAC)5 signal (compare Fig. 4e–f). As in the diploid and tetraploid accessions, no very reliable signals were observed with (ACT)5 and (ATC)5. Finally, discrete (AG)10 signals were observed in different locations in 12 chromosome pairs (Fig. 5).
The same strategy used for the characterization of the subgenomes in the tetraploids was followed in the hexaploids. Firstly, the seven chromosome pairs revealed with pHch950 were analyzed in detail with the diagnostic probes pTa71, pTa794 and (AAG)5. This set of chromosomes has the same morphology and in situ patterns as the chromosomes of the Xu subgenome of the tetraploids. The 14 chromosome pairs that showed no hybridization with probe pHch950 were easily separated into two groups of seven chromosome pairs. One group showed the same morphology and in situ patterns as the chromosomes of the subgenome Xv observed in the tetraploids, and was easily identified (Fig. 4b). The other group, whose members were very enriched in (AAG)5 signals, belongs to a related genome here named subgenome Xw (Fig. 5). Probes pTa794 and pTa71 diagnostically identified two chromosomes belonging to subgenome Xw. Like F chromosomes belonging to subgenomes Xu and Xv, the pair of satellited chromosomes carrying proximal 5S rDNA sites was identified as chromosome pair F. The other pair of Xw satellited chromosomes carrying only 45S rDNA was identified as chromosome pair G (Fig. 4c). The remaining chromosomes belonging to the Xw subgenome (A to E) were arranged in the karyotype on the basis of chromosome size. Once again, no homoeologies could be established between these chromosomes and the respective Xu and Xv chromosomes.
Finally, the identification of chromosomes with (AG)10 and pSc119.2 signals was performed after reprobing with (AAG)5 (Fig. 4g). (AG)10 was found on chromosomes belonging to all three subgenomes (the positions on Xu and Xv were the same as seen on the chromosomes of the tetraploids). It is noticeable that, as in the diploids (genome Xu), no signals were observed with the probe pSc119.2 on chromosomes belonging to subgenome Xw (Fig. 5, Table 2)
Meiotic behaviour of chromosomes
The meiotic behaviour of the chromosomes was analyzed in pollen mother cells at metaphase I in tetraploids BCC2007 and GRA2735. Only bivalents were formed (mostly ring-type); no univalents, multivalents or other chromosome associations were observed. Sequential experiments using two-by-two combinations of the probes unequivocally identified the seven bivalents. In both accessions, the bivalents only involved homologous chromosomes (Xu-Xu and Xv-Xv) (Fig. 6).
The chromosome identities present as bivalents Xu-Xu and Xv-Xv are indicated in white and yellow letters, respectively. In a, the arrows point the seven bivalents revealed with pHch950 (some of them in the inset). In c, the arrows point the bivalents carrying pSc119.2 signals. In d, the arrows and arrowheads point to the (AG)10 and 45S rDNA signals respectively. In f, the arrowheads point to the pSc119.2 signals. Scale bar = 10 µm.
Identification of H. murinum chromosomes
The first step in understanding the genome structure and evolution of a species is the unambiguous discrimination of its chromosomes. The identification of each H. murinum chromosome pair, including its hexaploids, is here reported for the first time. As indicated by other authors, the five Triticeae probes used (pTa71, pTa794, pAs1, pHch959 and pSc119.2) were insufficient for the reliable identification of most chromosomes , , . However, the pattern of distribution of several SSRs was shown very useful in chromosome identification. Indeed, the use of (AAG)5 in combination with the morphology of DAPI-stained chromosomes was enough to easily distinguish all individual chromosomes. The use of a single probe for chromosome identification facilitates the co-localization of other probes carrying different fluorochromes in two-colour in situ experiments. With the exception of (ACT)5 and (ATC)5 (which were ineffective as chromosome markers), the probes used in the present work provided a saturated physical map of H. murinun with a rich set of cytogenetic landmarks distributed throughout all chromosome arms.
It is well documented that several members of the tribe Triticeae commonly show 5S rDNA loci in homoeologous group 5 (e.g., wheat, rye and H. bulbosum), while 45S rDNA loci are commonly present in homoeologous groups 5 and 6 (e.g., barley and H. chilense) –. On the basis of the location of rDNA loci, chromosomes F and G of (sub)genomes Xu, Xv and Xw should be assigned respectively to the Triticeae homoeologous groups 5 and 6. However, homoeologies can only be fully supported by demonstrating conserved synteny in further analysis. Since H. murinum chromosomes can be identified when in bivalent configuration (Fig. 6), the analysis of meiotic pairing in the hybrids of H. murinum with H. vulgare should allow homoeologous relationships to be established between the species, as reported for H. bulbosum when analyzing its hybrids with H. vulgare .
The origin of polyploids in the H. murinum complex
The confluence of distinguishable groups of seven chromosome pairs in the tetraploids and hexaploids contributes to our knowledge on the origin of the polyploid forms of H. murinum. The present results show the morphology and in situ patterns of the chromosomes in the diploid glaucum to be very similar to a set of 14 chromosomes in the tetraploid and hexaploid cytotypes. This supports the idea that glaucum was the diploid donor of the subgenome Xu present in H. murinum polyploids, and agrees with the assumption of Rajhathy and Morrison  (based on studies of meiosis) that one of the genomes of the murinum tetraploid cytotypes is that of diploid glaucum.
Nearly nothing is known about the identity of the non-glaucum diploid progenitors. Recent molecular phylogenies have shown that ancient H. murinum diploid progenitors involved in the origin of polyploids should belong, along with glaucum, to the same Xu genome group of Hordeum species that became isolated after the separation of their sister group, i.e., the H genome lineage of H. vulgare and H. bulbosum , , . The present results seem to reflect the existence of substantial differences in the amount and distribution of certain repeat DNA sequences among the subgenomes present in polyploids. Thus, even assuming that the Xu, Xv and Xw genomes have a monophyletic origin, their separation from a common ancestor must have occurred at a relatively early stage. A detailed chromosome analysis of other diploid forms of Hordeum and closely related Triticeae species might provide new clues regarding the identity of the Xv and Xw donor progenitors, or support the hypothesis suggested by Jacob and Blattner  that these genomes belong to extinct species. Irrespective of the identity of the non-glaucum parents, the donor species of the subgenome Xv must have been common to all tetraploids of all subspecies. Indeed, only minor differences were seen when comparing karyotypes for the analyzed probes of the five tetraploid accessions examined. The in situ patterns of the Xu and Xv subgenome chromosomes of the hexaploids are almost identical to the corresponding chromosomes present in tetraploids, indicating a common origin and low divergence after the addition of the third Xw subgenome at the hexaploid level.
Genome remodelling and polyploidy
Allopolyploidy has been an important mechanism in the rapid genomic evolution of the members of Triticeae –. The present work contributes to our understanding of the coevolution of the Xu, Xv and Xw subgenomes following the polyploidization process. In general, the chromosomes of the same (sub)genome at different ploidy levels are very similar, suggesting that no great karyotypic alteration occurred after polyploidization. Only chromosome G of subgenome Xu present in the polyploids appears to have no definitive counterpart in diploid glaucum. This agrees with the fact that diploid glaucum has two pairs of satellited chromosomes (F and G), as revealed by the presence of secondary constrictions and major 45S rDNA signals (Fig. 1k, ), while only one such pair (chromosome F) is present in the Xu subgenome of the polyploids , . Genome remodelling after polyploidization could have led to the replacement of the satellited chromosome G observed in the diploids (with major 45S rDNA sites) by the small metacentric chromosome with only minor 45SrDNA signals found in the tetraploid and hexaploid cytotypes. Deletion of the 45S rDNA genes is likely the main cause of this karyotypic difference. In fact, deletion or inactivations of ribosomal genes are common in hybrid and polyploid members of Triticeae. Intergenomic translocations are also common structural changes detected in allopolyploids. An example of this is the well characterized cyclic translocation of chromosomes 4A, 5A and 7B in tetraploid and hexaploid wheats . No large translocations were detected in the present study. However unlike diploid glaucum, which shows no pSc119.2 signals , , pSc119.2 signals were observed in subtelomeric positions on one Xu chromosome arm of three tetraploids and the hexaploid accessions analyzed in the present work. This suggests the presence of a terminal translocation or perhaps simply the jumping of transposable elements after allopolyploidization. The presence of the pSc119.2 signals in the same location on chromosome FXu as seen in two leporinum accessions (from Italy and France) might indicate a common origin for these samples. In contrast, the interstitial telomeric repeats on chromosome FXu, invariably found in the seven accessions here analyzed, suggest that this chromosomal rearrangement must be an ancient characteristic of the Xu genome. This may have occurred before the diversification of the H. murinum species but after the diversification of genomes Xu and H since no interstitial telomeric repeats are seen in barley .
Taxonomy of the H. murinum complex
The H. murinum complex is probably one of the best studied groups in the genus Hordeum. However, the taxonomic treatment of H. murinum taxa has always been controversial. Although it is well accepted that H. murinum can be split into three subspecies - glaucum, murinum and leporinum  – their geographical and ecological distinctiveness has led some authors to contemplate three separate species: H. glaucum Steudel, H. murinum sensu stricto and H. leporinum Link , . Another problem of the complex is the taxonomic status of the different cytological forms of leporinum (which are not recognized as distinct taxa since they show no distinctive morphological traits). An unexpected result of the present work was the finding of 28 chromosomes in accession GRA2735, classified as glaucum by the seed bank delivery information and confirmed as such by the information in Fig. S1. This is the first report of a tetraploid form of glaucum, which further reflects the difficulties encountered in dealing with the complex.
The present cytogenetic results showed no greater similarity to exist between the three leporinum tetraploid accessions than between tetraploids of the different subspecies. This agrees with many phylogenetic studies that have been unable to separate tetraploids of leporinum and murinum. Indeed, populational analyses of several quantitative and qualitative features, and indeed of different molecular markers, have revealed no significant differentiation between tetraploid populations morphologically classified as different taxa , –. Some authors suggest that the different subspecies form a continuous morphological cline strongly correlated with bioclimatic variables . Others suggest the existence of hybrids of murinum and leporinum , while yet others indicate the separation of these taxa must have occurred relatively recently . The present results suggest that all murinum tetraploids should be included within the same species.
In conclusion, this study reveals the origin of the polyploids of the H. murinum subspecies and highlights their phylogenetic relationships. It is here suggested that the members of the complex be divided into three subgroups according to their ploidy level: 2x-murinum, 4x-murinum and 6x-murinum. 2x-murinum with the haploid genome formula Xu, should include the diploid form of glaucum; 4x-murinum, with the haploid genome formula XuXv, should include the currently recognized murinum and the tetraploid cytotypes of glaucum and leporinum. Finally, 6x-murinum with the haploid genome formula XuXvXw, should include the hexaploid cytotypes of leporinum. Certainly, the taxonomic treatment of H. murinum based exclusively on morphological criteria would appear to be questionable.
Spikelets and anthers from the tetraploid accessions GRA2735 as distinctive features of glaucum. a) Pedicelate central spikelet longer than its lateral counterparts. b) The three anthers from a central spikelet showing characteristic purple spots.
Conceived and designed the experiments: A. Cuadrado. Performed the experiments: A. Cuadrado A. Carmona. Analyzed the data: A. Cuadrado. Contributed reagents/materials/analysis tools: A. Cuadrado NJ. Wrote the paper: A. Cuadrado NJ.
- 1. Van de Peer Y, Maere S, Meyer A (2009) The evolutionary significance of ancient genome duplications. Nat Rev Genet 10: 725–732.
- 2. Bothmer RV, Flink J, Landström T (1986) Meiosis in interspecific Hordeum hybrids. I. Diploid combinations. Can J Genet Cytol 28: 525–535.
- 3. Bothmer RV, Flink J, Landström T (1987) Meiosis in interspecific Hordeum hybrids. II. Triploid combinations. Evol. Trends Plants 1: 41–50.
- 4. Linde-Laursen I, Bothmer RV, Jacobsen N (1992) Relationships in the genus Hordeum: Giemsa C-banded karyotypes. Hereditas 116: 111–116.
- 5. Wang RRC, Bothmer RV, Dvorak J, Fedak G, Linde-Laursen I, et al.. (1996) Genome symbols in the Triticeae. In: Wang RRC, Jensen KB and Jaussi C (eds) Proceedings of the 2nd International Triticeae Symposium, Utah State University, Logan, pp 29–34
- 6. Linde-Laursen I, Heslop-Harrison JS, Shepherd KW, Taketa S (1997) The barley genome and its relationship with the wheat genomes. A survey with and internationally agreed recommendation for barley chromosome nomenclature. Hereditas 123: 1–16.
- 7. Blattner FR (2009) Progress in phylogenetic analysis and a new infrageneric classification of the barley genus Hordeum (Poaceae:Triticeae). Breeding Science 59: 471–480.
- 8. Bothmer RV, Jacobsen N, Baden C, Jorgensen RB, Linde-Laursen I (1995) An ecogeographical study of the genus Hordeum. 2nd ed. IPGRI, Rome, p, 129
- 9. Giles BE, Lefkovitch LP (1986) A taxonomic investigation of the Hordeum murinum complex (Poaceae). Pl Syst Evol 153: 181–197.
- 10. Jacobsen N, Bothmer RV (1995) Taxonomy of the Hordeum murinum complex (Poaceae). Nord J Bot 15: 449–458.
- 11. Rajhathy T, Morrison JW (1962) Cytogenetic studies in the genus Hordeum. 6. The murinum complex. Canad J Genet Cytol 4: 240–247.
- 12. Gupta PK, Fedak G (1985) Intergeneric hybrids between Hordeum californicum and Triticum aestivum. J Hered 76 (5) 365–368.
- 13. Bothmer RV. Flink J, Landström T (1988) Meiosis in interspecific Hordeum hybrids. III. Tetraploid (2x×6x) hybrids. Hereditas 108: 141–148.
- 14. Jahan B, Vahiny AA, Ali SI (1992) Chiasma frequency and chromosome associations in sixteen taxa of Hordeum species. Cytologia 57: 51–57.
- 15. de Bustos A, Cuadrado A, Soler C, Jouve N J (1996) Physical mapping of repetitive DNA sequences and 5S and 18S–26S rDNA in five wild species of the genus Hordeum. Chromosome Res 4: 491–499.
- 16. Taketa S, Harrison GE, Heslop-Harrison JS (1999) Comparative physical mapping of the 5S and 18S.25S rDNA in nine wild Hordeum species and cytotypes. Theor Appl Genet 98: 1–9.
- 17. Tanno K, Bothmer RV, Yamane K, Takeda K, Komatsuda T (2010) Analysis of DNA sequence polymorphism at the cMWG699 locus reveals phylogenetic relationships and allopolyploidy within Hordeum murinum subspecies. Hereditas 147: 34–42.
- 18. Ourari M, Ainouche A, Coriton O, Huteau V, Brown S, et al. (2011) Diversity and evolution of the Hordeum murinum polyploidy complex in Algeria. Genome 54: 639–654.
- 19. Brassac J, Jakob SS, Blattner FR (2012) Progenitor-Derivative relationships of Hordeum polyploids (Poaceae, Triticeae) inferred from sequences of TOPO6, a nuclear low-copy gene region. PLoS One 7 (3) e33808.
- 20. Jakob SS, Blattner FR (2010) Two extinct diploid progenitors were involved in allopolyploid formation in the Hordeum murinum (Poaceae:Triticeae) taxon complex. Mol Phylogenet Evol 55: 650–659.
- 21. Cuadrado A, Jouve N (2007) The non-random distribution of long clusters of all possible classes of tri-nucleotide repeats in barley chromosomes. Chromosome Research 15: 711–720.
- 22. Cuadrado A, Hieronim G, Jouve N (2009) A novel, simple and rapid nondenaturing FISH (ND-FISH) technique for the detection of plant telomeres. Potential used and possible target structures detected. Chromosome Res 17: 755–762.
- 23. Cuadrado N, Jouve N (2010) Chromosomal detection of simple sequence repeats (SSRs) using nondenaturing FISH (ND-FISH). Chromosoma 119: 495–503.
- 24. Taketa S, Ando H, Taketa K, Harrison GE, Heslop-Harrison JS (2000) The distribution, organization and evolution of two abundant and widespread repetitive DNA sequences in the genus Hordeum. Theor Appl Genet 100: 169–176.
- 25. Cuadrado A, Jouve N (1994) Mapping and organization of highly-repeated DNA sequences by means of simultaneous and sequential FISH and C-banding in 6x-triticale. Chromosome Research 2: 331–338.
- 26. Cabrera A, Friebe B, Jiang J, Gill BS (1995) Characterization of Hordeum chilense chromosomes by C-banding and in situ hybridization using highly repeated DNA probes. Genome 38: 435–442.
- 27. Pickering R, Klatte S, Butler RC (2006) Identification of all chromosome arms and their involvement in meiotic homoeologous associations at metaphase I in 2 Hordeum vulgare L.×Hordeum bulbosum L. hybrids. Genome 49: 73–78.
- 28. Kakeda K, Taketa S, Komatsuda T (2009) Molecular phylogeny of the genus Hordeum using thioredoxin-like gene sequences. Breed Sci 59: 595–601.
- 29. Ozkan H, Feldman M (2009) Rapid cytological diploidization in newly formed allopolyploids of the wheat (Aegilops-Triticum) group. Genome 52: 926–934.
- 30. Shaked H, Kashkush K, Ozkan H, Feldman M, Levy AA (2001) Sequence elimination and cytosine methylation are rapid and reproducible responses of the genome to wide hybridization and allopolyploidy in wheat. Plant Cell 13: 1749–1759.
- 31. Han F, Fedak G, Guo W, Liu B (2005) Rapid and repeatable elimination of a parental genome-specific DNA repeat (pGc1R-1a) in newly synthesized wheat allopolyploids. Genetics 170: 1239–1245.
- 32. Naranjo T (1990) Chromosome structure of durum wheat. Theor Appl Genet 79: 397–400.
- 33. Gupta PK, Fedak G, Molanar SJ, Wheatcroft R (1989) Distribution of a Secale cereale DNA repeat sequence among 25 Hordeum species. Genome 32: 383–388.
- 34. Smith DF (1972) Hordeum species in grasslands. Herbage Abstracts 42: 213–223.
- 35. Baum BR, Bailey GL (1990) Key and synopsis of North American Hordeum species. Can J Bot 68 (11) 2433–2442.
- 36. Savova-Bianchi D, Keller-Senften J, Felber F (2002) Isozyme variation of Hordeum murinum L. in Switzerland and test of hybridization with cultivated barley. Weed Res 42 (4) 325–333.
- 37. El-Rabey HA, Badr A, Schäfer-Pregl R, Martin W, Salamini F (2002) Speciation and species separation in Hordeum L. (Poaceae) resolved by discontinuous molecular markers. Plant Biol 4 (5) 567–575.