8urn:lsid:arphahub.com:pub:A71ED5FC-60ED-5DA3-AC8E-F6D2BB5B3573urn:lsid:zoobank.org:pub:C8FA3ADA-5585-4F26-9215-A520EE683979Comparative CytogeneticsCCG1993-07711993-078XPensoft Publishers10.3897/compcytogen.v16.i1.7905679056Research ArticlePlantaePoaceaePoalesEvolutionary biologyAfricaEuropeDistribution patterns of rDNA loci in the Schedonorus-Lolium complex (Poaceae)AnsariHelal Ahmad1EllisonNicholas1StewartAlan Vincent2WilliamsWarren Mervynwarren.williams@agresearch.co.nzhttps://orcid.org/0000-0002-3156-38211AgResearch Ltd, Grasslands Research Centre, Palmerston North 4412, New ZealandGrasslands Research CentrePalmerston NorthNew ZealandPGG Wrightson Seeds, Kimihia Research Centre, 1375 Springs Road, RD4, Lincoln 7674, New ZealandKimihia Research CentreLincolnNew Zealand
Corresponding author: Warren Mervyn Williams (warren.williams@agresearch.co.nz)
Academic editor: Ekaterina Badaeva
2022240320221613954C685D94C-AB76-5ACF-802B-E12042EE20B2EB6F2AC0-A868-4D61-9701-7DC4E2D0581B63858300912202129012022Helal Ahmad Ansari, Nicholas Ellison, Alan Vincent Stewart, Warren Mervyn WilliamsThis is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.http://zoobank.org/EB6F2AC0-A868-4D61-9701-7DC4E2D0581B
The Schedonorus-Lolium complex of the subtribe Loliinae (Poaceae) includes several economically important forage and turf grasses. This complex encompasses Lolium Linnaeus, 1753, Festuca Linnaeus, 1753 subgenus Schedonorus (P. Beauvois, 1824) Petermann, 1849 and Micropyropsis Romero Zarco et Cabezudo, 1983. New FISH results of 5S and 18S–26S rDNA sequences are presented for three species and the results are interpreted in a review of distribution patterns of 5S and 18S–26S rDNA sequences among other species in the complex. Micropyropsistuberosa Romero Zarco et Cabezudo, 1983 (2n = 2x = 14) displayed a distribution pattern of rDNA sequences identical to that of F.pratensis Hudson, 1762, supporting a close phylogenetic relationship at the bottom of the phylogenetic tree. “Loliummultiflorum” Lamarck, 1779 accessions sourced from Morocco showed a different pattern from European L.multiflorum and could be a unique and previously uncharacterised taxon. North African Festucasimensis Hochstetter ex A. Richard, 1851 had a marker pattern consistent with allotetraploidy and uniparental loss of one 18S–26S rDNA locus. This allotetraploid has previously been suggested to have originated from a hybrid with Festucaglaucescens (Festucaarundinaceavar.glaucescens Boissier, 1844). However, the distribution patterns of the two rDNA sequences in this allotetraploid do not align with F.glaucescens, suggesting that its origin from this species is unlikely. Furthermore, comparisons with other higher alloploids in the complex indicate that F.simensis was a potential donor of two sub-genomes of allohexaploid Festucagigantea (Linnaeus) Villars, 1787. In the overall complex, the proximal locations of both rDNA markers were conserved among the diploid species. Two types of synteny of the two markers could, to a considerable extent, distinguish allo- and autogamous Lolium species. The ancestral parentage of the three Festuca allotetraploids has not yet been determined, but all three appear to have been sub-genome donors to the higher allopolypoids of sub-genus Schedonorus. Terminal locations of both the markers were absent from the diploids but were very frequently observed in the polyploids.
FestucaFISHkaryotype evolutionLoliumrDNA locus evolutionspecies diversificationNew Zealand Ministry of Business, Innovation and EmploymentCitation
Ansari HA, Ellison N, Stewart AV, Williams WM (2022) Distribution patterns of rDNA loci in the Schedonorus-Lolium complex (Poaceae). Comparative Cytogenetics 16(1): 39–54. https://doi.org/10.3897/compcytogen.v16.i1.79056
Introduction
Ryegrasses of the genus Lolium Linnaeus, 1753 with ten diploid species and fescues of the genus Festuca Linnaeus, 1753 subgenus Schedonorus (P. Beauvois, 1824) Petermann, 1849 are closely related and, together with Micropyropsis Romero Zarco et Cabezudo, 1983, form the “Schedonorus-Lolium complex”, belonging to the family Poaceae Barnhart, 1895, subtribe Loliinae Dumortier, 1829 (Inda et al. 2013; Cheng et al. 2016). Several of these Lolium and Festuca species, which are native to temperate regions of Europe, Asia and Africa, are widely used for forage and turf purposes in all major temperate regions of the planet. Micropyropsistuberosa Romero Zarco et Cabezudo, 1983 (Romero Zarco and Cabezudo 1983) is the sole species of the genus and is diploid (Romero Zarco 1988).
Since the last major taxonomic revision of the genus Lolium by Terrell (1968), new species have been discovered and named, notably Loliumsaxatile H. Scholz et S. Scholz, 2005 (Scholz and Scholz 2005) and Loliumedwardii H. Scholz, Stierstorfer et van Gaisberg, 2000 (Scholz et al. 2000). Although Festuca has over 500 diploid to dodecaploid species, subgenus Schedonorus is limited to approximately 20 species, most from Europe, W Asia or N Africa. However, the broad-leaved Festuca species from highland tropical Africa, including Festucasimensis Hochstetter ex A. Richard, 1851 have also been shown to be part of the Schedonorus-Lolium complex (Namaganda et al. 2006; Inda et al. 2014; Minaya et al. 2015).
Several molecular genetic analyses involving DNA markers have been successfully carried out for the phylogenetic reconstruction of subtribe Loliinae. It has been shown that the Schedonorus-Lolium complex represents a monophyletic group, with Lolium clearly differentiated from Festuca (Charmet et al. 1997; Gaut et al. 2000; Catalán et al. 2004; Namaganda et al. 2006; Hand et al. 2010; Inda et al. 2014; Minaya et al. 2015; Cheng et al. 2016). Fertile hybrids formed between Lolium and Festuca species show chromosome pairing and recombination but the chromosomes can be distinguished using genomic in situ hybridization (Humphreys et al. 1995).
Karyological differences featuring chromosome number, structure and morphology have long been used to infer the systematic status and the evolutionary history of species divergence. However, in some groups of species conventionally stained chromosome preparations do not clearly delineate structural differences among chromosomes or species karyotypes. Molecular cytogenetic mapping of specific DNA sequences through fluorescence in situ hybridization (FISH) can overcome such problems, and provide enhanced pictures of chromosome architecture, leading to clear karyotype and genome discrimination (Albert et al. 2010; Chester et al. 2010; Xiong and Pires 2011). Two different families of multicopy and highly conserved ribosomal RNA genes (rDNA), one coding for 5S and the other for 35S rRNA arrays are universally present in plants. Tandemly repeated blocks of these genes are located independently at particular chromosomal sites and provide species-specific markers (Roa and Guerra 2015). Each 35S rDNA unit carries 18S, 5.8S and 26S RNA genes along with two internal transcribed spacers (ITSs) and tandemly repeated blocks of these units form the nucleolar organizer regions (NORs) or secondary constrictions on chromosomes. FISH mapping of 5S and 35S rDNA sequences is widely used to compare the chromosomal structural changes of related species and to infer the karyoevolutionary variations that accompany species diversification (Fukushima et al. 2011; Lan and Albert 2011; Roa and Guerra 2012, 2015; Jang et al. 2013).
Species of the Schedonorus-Lolium complex all share x = 7 as the base chromosome number and all have very similar biarmed chromosome morphologies and symmetrical karyotypes. Therefore, conventional karyological information is of little value for evaluating evolutionary changes (Malik and Thomas 1966; Namaganda et al. 2006; Kopecký et al. 2010). Molecular cytogenetic mapping of 5S and 35S rDNA has detected variations in the distributional patterns of the two rDNA markers among diploids and polyploids in this complex (Thomas et al. 1996, 1997; Ksia¸zczyk et al. 2010; Inda and Wolny 2013; Ansari et al. 2016; Ezquerro-López et al. 2017; Shafiee et al. 2020). Based on their report, Ezquerro-López et al. (2017) made a preliminary attempt to decipher the evolutionary relationships among Festuca species belonging to this complex.
In this study, we have mapped the chromosomal dispositions of 5S and 18S rDNA loci in five taxa, three of which were previously unmapped, and have discussed the evolutionary implications of the new results. Following this we have drawn together all the available information from disparate sources and have framed a more complete picture of rDNA chromosome patterns within the whole of this economically important complex. This is the first time such information has been integrated across numerous studies.
MethodsPlant materials and chromosome preparations
Seeds from five populations (Table 1) belonging to the Schedonorus-Lolium complex were accessed from the Margot Forde Forage Germplasm Centre at AgResearch Grasslands, Palmerston North and PGG Wrightson Seeds, Christchurch, New Zealand. Loliummultiflorum Lamarck, 1779 of Moroccan origin was designated MRCN to distinguish it from L.multiflorum material of European origin. Seeds were germinated and grown in a glasshouse. Somatic chromosome preparations were obtained from the meristematic tissue of actively growing root tips according to the flame-drying technique described earlier (Ansari et al. 1999, 2016). Good quality cytological preparations were selected after screening using phase contrast optics.
List of Schedonorus-Lolium complex taxa used in this study.
Taxon
Identity and source of seed
Festucasimensis Hochstetter ex A. Richard, 1851
BL 2043, Margot Forde Forage Germplasm Centre
Loliumperenne Linnaeus, 1753
Cv Impact, Margot Forde Forage Germplasm Centre
Loliummultiflorum Lamarck, 1779
B 3380, Margot Forde Forage Germplasm Centre
Loliummultiflorum MRCN
Cv. Barberia, PGG Wrightson Seeds
Micropyropsistuberosa Romero Zarco et Cabezudo, 1983
BZ 8319, Margot Forde Forage Germplasm Centre
Fluorescence in situ hybridization (FISH)
The DNA probes used for FISH were pTr18S (GenBank accession number AF071069), a 1.8 kb fragment from Trifoliumrepens Linnaeus, 1753 containing almost the entire 18S rDNA sequence representing the 35S rDNA and pTr5S (GenBank accession number AF072692), a 596 bp DNA fragment encoding the T.repens 5S rRNA. 35S and 5S rDNA probes were directly labelled with fluorochromes Fluor-X-dCTP and Cy-3-dCTP (GE Healthcare, NZ), respectively by nick translation according to manufacturer’s specifications. Double target FISH using the above DNA probes, post-hybridisation washing and counterstaining of somatic chromosomes with DAPI were carried out as described earlier (Ansari et al. 1999). Chromosome preparations were mounted in Vectashield (Vector Laboratories). Fluorescence images were acquired using a Zeiss monochrome MRm CCD camera on a Nikon epifluorescence microscope Microphot-SA and were processed with an ISIS FISH Imaging System (MetaSystems, Germany). At least five good quality early to late metaphase cells from each plant were used for analysing hybridization signals.
Results
Results of double colour FISH mapping using 35S and 5S rDNA sequences as probes on pro-metaphase or metaphase chromosomes of Loliumperenne Linnaeus, 1753 (2n = 2x = 14) are given in Fig. 1. Six 35S rDNA signals representing three loci were located proximally on three pairs of chromosomes (Fig. 1a, b). One locus was on the short arm of one chromosome pair, and the other two displayed hybridization on the long arms of two pairs of chromosomes. One of the chromosome pairs with 35S on the long arm displayed co-localization of the single 5S rDNA locus proximally on the short arm. The chromatin housing 35S rDNA regions, representing GC-rich nucleolus organizer regions (NORs) or secondary constrictions, were frequently decondensed and sometimes stretched in our flame-dried somatic chromosome preparations. These loci are positioned pericentromerically, and the cloudy decondensed and stretched 35S rDNAFISH signals could be observed joining the two condensed parts of NOR-bearing chromosomes (Fig. 1a, b). L.multiflorum (2n = 2x = 14) of north European/Mediterranean origin produced rDNAFISH signals identical to the pattern observed for L.perenne (Fig. 1c, d).
5670E179-BFCD-5DD8-A29F-44086E30C9A3
DAPI stained (grey scale) metaphase cells in the left column and the same cells in the right column displaying FISH mapping of 5S (red signals) and 35S rDNA sequences (green signals) in a, bL.perennec, dL.multiflorum, European origin e, fL.multiflorum MRCN Moroccan origin g, hM.tuberosai, jF.simensis. Dotted lines in a, c, e, g, and i denote decondensed 35S rDNA chromatin.
https://binary.pensoft.net/fig/663215
In contrast to L.perenne and L.multiflorum of north European origin, L.multiflorum (2n = 2x = 14) of Moroccan origin displayed only two pairs of NORs (Fig. 1e, f), each pair located proximally on the long arm. One of these NOR-bearing chromosome pairs co-localised 5S sequences proximally on the short arm.
Micropyropsistuberosa, 2n = 2x = 14, with a symmetrical karyotype, displayed one 5S and one 35S rDNA locus, each on separate chromosome pairs, and located proximally on the short arms (Fig. 1g, h). Co-localization of the two rDNA sequences on the same chromosome was not observed in M.tuberosa.
Festucasimensis, 2n = 4x = 28, displayed all biarmed chromosomes and a symmetrical karyotype. The eight FISH signals were distributed on separate chromosomes (Fig. 1i, j). One of the three pairs of 5S rDNA signals hybridized interstitially on the short arms. Each of the remaining two pairs of 5S signals were located distally in terminal regions, one in the short arm and the other in the long arm of two pairs of chromosomes. The only pair of 35S signals was located proximally on the short arms of a chromosome pair. Again, F.simensis did not show co-localization of the two rDNA sequences.
Discussion
We have mapped the diversity in the chromosomal locations of the two rDNA sequences for five taxa of the Schedonorus-Lolium complex. Three of these, M.tuberosa, L.multiflorum MRCN and F.simensis, were previously unmapped. The results for L.perenne and N European L.multiflorum agree with previous studies (Thomas et al. 1996; Ansari et al. 2016). The new results are discussed first and then rDNA chromosomal patterns across the complex are reviewed.
Micropyropsistuberosa exhibited single 5S and 35S rDNA loci positioned proximally on separate chromosomes as was also the case for F.pratensis (Thomas et al. 1997). In phylogenetic reconstructions within the Schedonorus-Lolium complex based on ITS and plastid DNA sequences, the divergence of M.tuberosa preceded the basal split between the diploid lineages of Festuca and Lolium (Torrecilla and Catalán 2002; Catalán et al. 2004; Inda et al. 2008, 2014; Šmarda et al. 2008). The similar arrangement of single 5S and 35S rDNA loci in M.tuberosa and F.pratensis is consistent with the interpretation that this was the ancestral diploid Schedonorus arrangement before the Lolium split.
The “L.multiflorum” of Moroccan origin is typical of the main Lolium lineage in having more than one 35S rDNA locus. One of these 35S loci has a syntenic 5S locus on the opposite chromosome arm, in common with L.perenne and L.multiflorum of Eurasian origin. However, compared with Eurasian L.multiflorum the Moroccan taxon has one fewer 35S locus. The Moroccan “L.multiflorum” could be a new and unique N African taxon that has chromosomal affinities with the allogamous Eurasian Lolium species.
A previous cytological analysis of the tropical African broad-leaved fescue, F.simensis, showed it to be tetraploid (2n = 4x = 28) and AFLP fingerprinting revealed a close phylogenetic relationship with European broad-leaved fescues, especially with hexaploid F.gigantea, (Namaganda et al. 2006). Nuclear and plastid DNA sequence studies also placed F.simensis in the Schedonorus-Lolium complex, close to Lolium (Inda et al. 2014). In this first molecular cytogenetics analysis of F.simensis, we have confirmed the tetraploidy, revealed a symmetrical biarmed karyotype and a distributional pattern of the two rDNA sequences consistent with allopolyploidy (Figs 1 and 2). In addition to two terminal 5S loci, on separate chromosomes, an interstitial 5S locus was observed on the short arm of a separate chromosome, a new location for this group of fescues. None of these 5S positions was consistent with the suggested close relationship with Lolium. On the other hand, the 35S rDNA locus was positioned proximally and could represent a link with a common ancestor to Lolium. Only one 35S locus was encountered in this allotetraploid, indicating uniparental loss during diploidisation. There are numerous examples of uniparental loss of 35S loci occurring in other allopolyploids (Ansari et al. 1999; Kotseruba et al. 2003, 2010; Williams et al. 2012; Kolano et al. 2016).
Based on a low-copy nuclear gene analysis, Minaya et al. (2015) suggested a Mediterranean origin of Afromontane F.simensis through hybridization between a diploid F.glaucescens and a Lolium-like diploid species. However, none of the distribution patterns of the two rDNA sequences in this allotetraploid align with F.glaucescens (Festucaarundinaceavar.glaucescens Boissier, 1844). Instead, the distribution patterns are consistent with the possible involvement of F.simensis in the formation of 6x F.gigantea (Linnaeus) Villars, 1787. Festucapratensis Hudson, 1762 is a putative diploid sub-genome donor of allohexaploid F.gigantea (Hand et al. 2010), but the sources of the other subgenomes remain unknown. We have noted a close similarity between the 5S and 35S patterns of allotetraploid F.simensis (present results) and F.gigantea (Thomas et al. 1997, Fig. 2). These species also show a close phylogenetic proximity based on DNA sequences (Namaganda et al. 2006; Inda et al. 2014). Hence, we infer that allotetraploid F.simensis could be a potential donor of the remaining two sub-genomes of allohexaploid F.gigantea (Fig. 2).
FD01947E-F586-5379-A8F7-14C4B7B61AB9
Schematic representation of the putative evolutionary lineages for chromosomes carrying 5S and 35S rDNA loci in the Schedonorus-Lolium complex. The numbers of marker and non-marker chromosomes are given inside the boxes. Red and black double circles represent 5S and 35S rDNA loci, respectively. *species in solid boxes were investigated during the present study; †synonym for L.rigidumvar.rottbollioides; ††synonym for F.arundinaceasubsp.fenas (Lagasca y Segura) Bornmüller, 1928 (Ezquerro-López et al. 2017).
https://binary.pensoft.net/fig/663216rDNA locus patterns across the diploid Schedonorus-Lolium taxa
All Lolium species, along with M.tuberosa and F.pratensis are natural diploids. The Lolium species, are evolutionarily more recent than the Festuca species based on DNA sequence phylogenies (Gaut et al. 2000; Catalan et al. 2004; Inda et al. 2014). All Lolium taxa studied so far, comprising eight of the ten extant species, displayed exclusively proximal chromosomal locations of both 5S and 35S rDNA sequences (Fig. 2). After the divergence from Festuca, the Lolium lineage invariably conserved the proximal locations of both the rDNA loci, but changes in the numbers and syntenic status of these loci apparently occurred later. The proximal localization of 5S rDNA in these diploids matches well with the general distribution pattern of this locus among angiosperms but contrasts with most Poaceae (Roa and Guerra 2015). The proximal mapping of 35S loci contrasts with more terminal localizations in the majority of angiosperms, including Poaceae (Roa and Guerra 2012; Garcia et al. 2017).
A single 5S rDNA locus (two FISH signals per cell) consistently occurred in all Lolium species. The number of 35S loci displayed has previously been noted as a distinguishing feature between F.pratensis (one locus) and Lolium species (more than one locus) (Thomas et al. 1996; Inda and Wolny 2013). All the Lolium taxa displayed increases in the number of 35S loci ranging from 2 to 5 (Fig. 2). Accordingly, there are two loci in L.multiflorum (Moroccan origin), L.persicum Boissier et Hohenacker, 1854, L.temulentum Linnaeus, 1753, L.remotum Schrank, 1789, L.rigidumvar.rottbollioides Heldreich ex Boissier, 1884 and L.canariense Steudel, 1855, three in L.perenne and L.multiflorum (European origin) to four or five in L.rigidumvar.rigidum Gaudin, 1811. These results were consistent with those of angiosperms in general, where numbers of 5S sites vary considerably less than 35S sites (Lan and Albert 2011; Garcia et al. 2017).
The two types of rDNA loci can be located on the same chromosome (syntenic) or on separate chromosomes (non-syntenic) (Morales et al. 2012; Barros e Silva et al. 2013; Olanj et al. 2015). The Macaronesian Lolium species, L.canariense, has no synteny of 5S and 35S loci (Inda and Wolny 2013). However, the remaining Lolium taxa (including both geographical races of L.multiflorum) have synteny (Fig. 2). The syntenic patterns can be differentiated into two groups. In one (allogamous) group, the two types of rDNA sequences were located proximally on either side of the centromere of the same chromosome, as represented by L.perenne and both geographical forms of L.multiflorum. In the other (largely autogamous) group, represented by L.persicum, L.temulentum, L.remotum, and subspecies and races of L.rigidum, both types of rDNA sequences were adjacent on the same chromosome arm, with 35S always distal to 5S. L.canariense shows the diploid Micropyropsis-F.pratensis arrangement with proximally located 5S and 35S rDNA loci on separate chromosomes as well as an additional pair of 35S loci (a Lolium characteristic, Fig. 2). On this basis, Inda and Wolny (2013) have suggested that L.canariense could be the link between the Festuca and Lolium lineages.
rDNA locus patterns among the polyploid Festuca species
The data presented in Fig. 2, based on the present investigation as well as earlier reports and analyses of DNA sequences (Thomas et al. 1997; Hand et al. 2010; Inda et al. 2014; Minaya et al. 2015; Ezquerro-López et al. 2017), summarise the patterns among polyploid species in subgenus Schedonorus. All the species are allopolyploid (Cao et al. 2000; Hand et al. 2010; Inda et al. 2014; Minaya et al. 2015; Ezquerro-López et al. 2017) and show no changes in the basic chromosome number (x = 7) and no apparent changes in the ancestral karyotype.
The numbers of 5S loci range from two in the tetraploids, F.mairei St. Yves, 1922 and F.glaucescens to eight in decaploid F.letourneuxiana (Festucaarundinaceavar.letourneuxiana (St. Yves) Torrecilla et Catalán, 2002) while 35S numbers ranged from one in tetraploid F.simensis to six in F.letourneuxiana (Fig. 2). Localisation of two 35S loci on the same chromosome, as in the tetraploids F.mairei and F.glaucescens (Thomas et al. 1997) is not frequently encountered in plants.
Seven of the eight Festuca polyploids had the 5S rDNA loci in the proximal region, either exclusively or in addition to other regions (Fig. 2). Terminal 5S loci were encountered in only three polyploid species and an interstitial 5S locus was found only in F.simensis (present study). In contrast, terminal 35S loci were more frequent. Five species mapped at least one 35S locus in the terminal region while four displayed exclusively terminal 35S loci (Fig. 2). Among these were tetraploids either with terminal 35S loci on each arm of one chromosome (F.glaucescens) or two 35S loci adjacent to each other on the same arm (F.mairei) (Fig. 2; Thomas et al. 1997). Three polyploids displayed exclusively proximal 35S hybridization signals including tetraploid F.simensis with only one 35S locus. The higher frequency of terminal 35S loci among the Festuca polyploids aligns well with the majority of angiosperms (Roa and Guerra 2012; Garcia et al. 2017). None of the Festuca species in the Schedonorus-Lolium complex studied so far have a syntenic arrangement of 5S and 35S rDNA loci, except for hexaploid F.corsica Salm-Reifferscheid-Dyck, 1840 which displayed synteny only in heteromorphic form (Ezquerro-López et al. 2017).
Two allotetraploids, F.mairei and F.glaucescens have been suggested as the ancestral parents of allo-octoploid F.atlantigena (Festucaarundinaceasubsp.atlantigena (St. Yves) Auquier, 1976) based on the formation of fertile interspecific hybrids between the two suggested ancestral parental species (Chandrasekharan and Thomas 1971) and FISH mapping of the two marker loci (Ezquerro-López et al. 2017). Six proximal 5S loci in the octoploid would reflect locus additivity from the ancestral parents while the elimination of one 35S locus may reflect genomic diploidisation. The ancestral parents of decaploid F.letourneuxiana could not be narrowed down by FISH mapping (Ezquerro-López et al. 2017). The allohexaploid species continental F.arundinacea Schreber, 1771 and F.corsica are hypothesised to share the same ancestral parents, viz., diploid F.pratensis and allotetraploid F.glaucescens (Humphreys et al. 1995; Thomas et al. 1997; Ezquerro-López et al. 2017; Fig. 2). Two distribution patterns of 5S and 35S rDNA sequences were observed in these allohexaploids, with differential losses of 35S loci and transpositions of both 5S and 35S loci. The display of two different trajectories of speciation in allopolyploids sharing the same lower-ploid ancestors has been proposed in other angiosperms (Bao et al. 2010; Weiss-Schneeweiss et al. 2012).
All four Festuca higher polyploids with putative parents reveal additivity of numbers of 5S loci, but, in three cases, losses of 35S loci, (Fig. 2). Diploidisation of polyploids may lead to the evolutionary loss of repetitive sequences and duplicate copies of genes (Renny-Byfield et al. 2013). Older polyploids often, but not always, show losses of copies of 35S rDNA genes and, in allotetraploids, uniparental losses of 35S loci are common (Leitch et al. 2008; Pellicer et al. 2010; Roa and Guerra 2012; Weiss-Schneeweiss et al. 2013; Garcia et al. 2017). Although there were positional shifts involving both 5S and 35S types, the results were consistent with the general observation for angiosperms that 5S loci are less variable than 35S loci (Lan and Albert 2011; Garcia et al. 2017).
The three allotetraploids (F.simensis, F.mairei and F.glaucescens), as the putative sub-genome donors to the allohexaploid and octoploid species, provide a novel example of sequential allopolyploidisation. The putative progenitors of all three allotetraploids remain unknown. However, nuclear and chloroplast DNA sequence analyses (Hand et al. 2010), supported by FISH mapping (Thomas et al. 1997) indicate that a diploid sub-genome is shared between F.mairei and F.glaucescens. The tetraploid species that became the sub-genome donors for higher ploidy fescues had terminal 5S and 35S loci that were largely conserved in the derivative species (Fig. 2). Among the Schedonorus-Lolium complex diploids studied so far, none have shown terminal localization of either marker, and neither were their DNA sequences consistent with them having been progenitors of these tetraploids (Hand et al. 2010). Harper et al. (2004) speculated on the basis of molecular cytogenetic findings, that diploid F.scariosa Lagasca y Segura ex Willkomm, 1861, belonging to the sub-genus Scariosae outside the Schedonorus-Lolium complex, was a potential ancestral parent for allotetraploid F.mairei. The likelihood of involvement of diploid sub-genome donor species from outside the Schedonorus-Lolium complex should be further explored using molecular and cytogenetic methods, including genomic in situ hybridization.
The variations in numbers of 35S sites in Lolium and the post-polyploidisation changes in the Festuca species have apparently occurred without any obvious changes in the symmetrical bi-armed karyotype that is a consistent feature of the Schedonorus-Lolium complex. Such lability in the absence of obvious structural changes might be attributable to paracentric chromosome rearrangements and/or the activity of transposable elements (Datson and Murray 2006; Raskina et al. 2008; Lan and Albert 2011; Barros e Silva et al. 2013; Weiss-Schneeweiss et al. 2013; Kolano et al. 2015).
Conclusion
This report has extended the distributional data on the rDNA sequences to seven of the ten known Lolium species and has added F.simensis to the list of seven polyploid fescue species already characterised. It has also explored the distribution patterns of rDNA loci within the Schedonorus-Lolium complex and considers some possible evolutionary trends. While these patterns can be used to deduce relationships among the higher polyploid Festuca species, the diploid progenitors of the allotetraploid species remain unidentified and enigmatic.
Author contributions
HAA designed the study with AVS and WMW. HAA performed the experiment, analysed the data and wrote the manuscript with co-writing from WMW. NWE isolated the DNA and labelled all the probes for FISH. AVS and NWE provided significant help in improving the manuscript. All authors read and approved the final manuscript.
Acknowledgements
We thank Joy Dick and Jaspreet Singh Sidhu for their help in formatting the manuscript for this journal. The work was supported by the New Zealand Ministry of Business, Innovation and Employment (contract no. C10X1202).
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
ReferencesAlbertPSGaoZDanilovaTVBirchlerJA (2010) Diversity of chromosomal karyotypes in maize and its relatives.129: 6–16. https://doi.org/10.1159/000314342AnsariHAEllisonNWBassettSAHussainSWBryanGTWilliamsWM (2016) Fluorescence chromosome banding and FISH mapping in perennial ryegrass, Loliumperenne L. BMC Genomics 17: e977. https://doi.org/10.1186/s12864-016-3231-zAnsariHAEllisonNWReaderSMBadaevaEDFriebeBMillerTEWilliamsWM (1999) Molecular cytogenetic organization of 5S and 18S–26S rDNA loci in white clover (Trifoliumrepens L.) and related species.83: 199–206. https://doi.org/10.1006/anbo.1998.0806BaoYWendelJFGeS (2010) Multiple patterns of rDNA evolution following polyploidy in Oryza.55: 136–142. https://doi.org/10.1016/j.ympev.2009.10.023Barros e SilvaAEdos Santos Soares FilhoWGuerraM (2013) Linked 5S and 45S rDNA Sites are highly conserved through the subfamily Aurantioideae (Rutaceae).140: 62–69. https://doi.org/10.1159/000350695CaoMSleperDADongFJiangJ (2000) Genomic in situ hybridization (GISH) reveals high chromosome pairing affinity between Loliumperenne and Festucamairei.43: 398–403. https://doi.org/10.1139/g99-129CatalánPTorrecillaPLópez RodríguezJÁOlmsteadRG (2004) Phylogeny of the festucoid grasses of subtribe Loliinae and allies (Poeae, Pooideae) inferred from ITS and trnL-F sequences.31: 517–541. https://doi.org/10.1016/j.ympev.2003.08.025ChandrasekharanPThomasH (1971) Studies in Festuca. 5. Cytogenetic relationships between species of Bovinae and Scariosae.65: 345–354.CharmetGRavelCBalfourierF (1997) Phylogenetic analysis in the Festuca-Lolium complex using molecular markers and ITS rDNA.94: 1038–1046. https://doi.org/10.1007/s001220050512ChengYMaXZhouKHumphreysMWZhangXQ (2016) Phylogenetic analysis of Festuca-Lolium complex using SRAP markers.63: 7–18. https://doi.org/10.1007/s10722-015-0324-5ChesterMLeitchARSoltisPSSoltisDE (2010) Review of the application of modern cytogenetic methods (FISH/GISH) to the study of reticulation (polyploidy/hybridisation).1: 166–192. https://doi.org/10.3390/genes1020166DatsonPMMurrayBG (2006) Ribosomal DNA locus evolution in Nemesia: transposition rather than structural rearrangement as the key mechanism? Chromosome Research 14: 845–857. https://doi.org/10.1007/s10577-006-1092-zEzquerro-LópezDKopeckýDIndaLA (2017) Cytogenetic relationships within the Maghrebian clade of Festucasubgen.Schedonorus (Poaceae), using flow cytometry and FISH.74: 1–9. https://doi.org/10.3989/ajbm.2455FukushimaKImamuraKNaganoKHoshiY (2011) Contrasting patterns of the 5S and 45S rDNA evolutions in the Byblisliniflora complex (Byblidaceae).124: 231–244. https://doi.org/10.1007/s10265-010-0366-xGarciaSKovaříkALeitchARGarnatjeT (2017) Cytogenetic features of rRNA genes across land plants: analysis of the Plant rDNA database.89: 1020–1030. https://doi.org/10.1111/tpj.13442GautBSTredwayLPKubikCGautRLMeyerW (2000) Phylogenetic relationships and genetic diversity among members of the Festuca-Lolium complex (Poaceae) based on ITS sequence data.224: 33–53. https://doi.org/10.1007/BF00985265HandMLCoganNOStewartAVForsterJW (2010) Evolutionary history of tall fescue morphotypes inferred from molecular phylogenetics of the Lolium-Festuca species complex. BMC Evolution Biology 10: e303. https://doi.org/10.1186/1471-2148-10-303HarperJAThomasIDLovattJAThomasHM (2004) Physical mapping of rDNA sites in possible diploid progenitors of polyploid Festuca species.245: 163–168. https://doi.org/10.1007/s00606-003-0110-2HumphreysMWThomasHMMorganWGMeredithMRHarperJAThomasHZwierzykowskiZGhesquiereM (1995) Discriminating the ancestral progenitors of hexaploid Festucaarundinacea using genomic in situ hybridization.75: 171–174. https://doi.org/10.1038/hdy.1995.120IndaLAWolnyE (2013) Fluorescent in situ hybridization of the ribosomal RNA genes (5S and 35S) in the genus Lolium: Loliumcanariense, the missing link with Festuca? Anales Jardin Botanico de Madrid 70: 97–102. https://doi.org/10.3989/ajbm.2329IndaLASanmartínIBuerkiSCatalánP (2014) Mediterranean origin and Miocene-Holocene Old World diversification of meadow fescues and ryegrasses (FestucasubgenusSchedonorus and Lolium).41: 600–614. https://doi.org/10.1111/jbi.12211IndaLASegarra-MoraguesJGMüllerJPetersonPMCatalánP (2008) Dated historical biogeography of the temperate Loliinae (Poaceae, Pooideae) grasses in the northern and southern hemispheres.46: 932–957. https://doi.org/10.1016/j.ympev.2007.11.022JangTSEmadzadeKParkerJTemschEMLeitchARSpetaFWeiss-SchneeweissH (2013) Chromosomal diversification and karyotype evolution of diploids in the cytologically diverse genus Prospero (Hyacinthaceae). BMC Evolutionary Biology 13: e136. https://doi.org/10.1186/1471-2148-13-136KolanoBSiwinskaDMcCannJWeiss-SchneeweissH (2015) The evolution of genome size and rDNA in diploid species of Chenopodiums.l. (Amaranthaceae).179: 218–235. https://doi.org/10.1111/boj.12321KolanoBMcCannJOrzechowskaMSiwinskaDTemschEWeiss-SchneeweissH (2016) Molecular and cytogenetic evidence for an allotetraploid origin of Chenopodiumquinoa and C.berlandieri (Amaranthaceae).100: 109–123. https://doi.org/10.1016/j.ympev.2016.04.009KopeckýDHavránkováMLoureiroJCastroSLukaszewskiAJBartošJKopeckaJDolezelJ (2010) Physical distribution of homoeologous recombination in individual chromosomes of Festucapratensis in Loliummultiflorum.129: 162–172. https://doi.org/10.1159/000313379KotserubaVGernandDMeisterAHoubenA (2003) Uniparental loss of ribosomal DNA in the allotetraploid grass Zingeriatrichopoda (2n = 8).46: 156–163. https://doi.org/10.1139/g02-104KotserubaVPistrickKBlattnerFRKumkeKWeissORuttenTFuchsJEndoTNasudaSGhukasyanAHoubenA (2010) The evolution of the hexaploid grass Zingeriakochii (Mez) Tzvel. (2n = 12) was accompanied by complex hybridization and uniparental loss of ribosomal DNA.56: 146–155. https://doi.org/10.1016/j.ympev.2010.01.003Ksia¸zczykTTaciakMZwierzykowskiZ (2010) Variability of ribosomal DNA sites in Festucapratensis, Loliumperenne, and their intergeneric hybrids, revealed by FISH and GISH.51: 449–460. https://doi.org/10.1007/BF03208874LanTAlbertVA (2011) Dynamic distribution patterns of ribosomal DNA and chromosomal evolution in Paphiopedilum, a lady’s slipper orchid. BMC Plant Biology 11: e126. https://doi.org/10.1186/1471-2229-11-126LeitchIJHansonLLimKYKovarikAChaseMWClarksonJJLeitchAR (2008) The ups and downs of genome size evolution in polyploid species of Nicotiana (Solanaceae).101: 805–814. https://doi.org/10.1093/aob/mcm326MalikCPThomasPT (1966) Karyotypic studies in some Lolium and Festuca species.19: 167–196. https://doi.org/10.1080/00087114.1966.10796216MinayaMDíaz-PérezAMason-GamerRPimentelMCatalánP (2015) Evolution of the beta-amylase gene in the temperate grasses: non-purifying selection, recombination, semiparalogy, homeology and phylogenetic signal.91: 68–85. https://doi.org/10.1016/j.ympev.2015.05.014MoralesAGAguiar-PerecinMLRMondinM (2012) Karyotype characterization reveals an up and down of 45S and 5S rDNA sites in Crotalaria (Leguminosae-Papilionoideae) species of the section Hedriocarpae subsection Macrostachyae.59: 277–288. https://doi.org/10.1007/s10722-011-9683-8NamagandaMLyeKAFriebeBHeunM (2006) AFLP-based differentiation of tropical African Festuca species compared to the European Festuca complex.113: 1529–1538. https://doi.org/10.1007/s00122-006-0400-5OlanjNGarnatjeTSonboliAVallèsJGarciaS (2015) The striking and unexpected cytogenetic diversity of genus Tanacetum L. (Asteraceae): A cytometric and fluorescent in situ hybridisation study of Iranian taxa. BMC Plant Biology 15: e174. https://doi.org/10.1186/s12870-015-0564-8PellicerJGarnatjeTHidalgoOTagashiraNVallèsJKondoK (2010) Do polyploids require proportionally less rDNA loci than their corresponding diploids? Examples from Artemisia subgenera Absinthium and Artemisia (Asteraceae, Anthemideae).144: 841–848. https://doi.org/10.1080/11263504.2010.522783RaskinaOBarberJCNevoEBelyayevA (2008) Repetitive DNA and chromosomal rearrangements: speciation-related events in plant genomes.120: 351–357. https://doi.org/10.1159/000121084Renny-ByfieldSKovarikAKellyLJMacAsJNovakPChaseMWNicholsRAPancholiMRGrandbastienMLeitchAR (2013) Diploidization and genome size change in allopolyploids is associated with differential dynamics of low- and high-copy sequences.74: 829–839. https://doi.org/10.1111/tpj.12168RoaFGuerraM (2012) Distribution of 45S rDNA sites in chromosomes of plants: structural and evolutionary implications. BMC Evolutionary Biology 12: e225. https://doi.org/10.1186/1471-2148-12-225RoaFGuerraM (2015) Non-random distribution of 5S rDNA sites and its association with 45S rDNA in plant chromosomes.146: 243–249. https://doi.org/10.1159/000440930Romero ZarcoC (1988) Números cromosomáticos de plantas occidentales, 472–486.45: 273–279.Romero ZarcoCCabezudoB (1983) Micropyropsis, género nuevo de Gramineae.11: 94–99.ScholzHStierstorferCGaisbergMV (2000) Loliumedwardii sp. nova (Gramineae) and its relationship with Schedonorussect.Plantynia Dumort.111(7–8): 561–565. https://doi.org/10.1002/fedr.20001110722ScholzSScholzH (2005) A new species of Lolium (Gramineae) from Fuerteventura and Lanzarote (Canary Islands, Spain).35: 281–286. https://doi.org/10.3372/wi.35.35208ShafieePAminiFMirzaghaderiGMortazavianSMMNooriSAS (2020) Karyotype analysis in six species of Lolium and Festuca (Poaceae).85: 281–288. https://doi.org/10.1508/cytologia.85.281ŠmardaPBurešPHorováLFoggiBRossiG (2008) Genome size and GC content evolution of Festuca: ancestral expansion and subsequent reduction. Annals of Botany 101: 421–433. https://doi.org/10.1093/aob/mcm307TerrellEE (1968) A taxonomic revision of the genus Lolium. Technical Bulletin 1392. United States Department of Agriculture, Washington.ThomasHMHarperJAMeredithMRMorganWGKingIP (1997) Physical mapping of ribosomal DNA sites in Festucaarundinacea and related species by in situ hybridization.40: 406–410. https://doi.org/10.1139/g97-054ThomasHMHarperJAMeredithMRMorganWGThomasIDTimmsEKingIP (1996) Comparison of ribosomal DNA sites in Lolium species by fluorescence in situ hybridization.4: 486–490. https://doi.org/10.1007/BF02261775TorrecillaPCatalánP (2002) Phylogeny of broad-leaved and fine-leaved Festuca lineages (Poaceae) based on nuclear ITS sequences.27: 241–251.Weiss-SchneeweissHEmadzadeKJangTSSchneeweissGM (2013) Evolutionary consequences, constraints and potential of polyploidy in plants.140: 137–150. https://doi.org/10.1159/000351727Weiss-SchneeweissHBlöchCTurnerBVillaseñorJLStuessyTFSchneeweissGM (2012) The promiscuous and the chaste: frequent allopolyploid speciation and its genomic consequences in American daisies (Melampodiumsect.Melampodium; Asteraceae).66: 211–228. https://doi.org/10.1111/j.1558-5646.2011.01424.xWilliamsWMEllisonNWAnsariHAVerryIMHussainSW (2012) Experimental evidence for the ancestry of allotetraploid Trifoliumrepens and creation of synthetic forms with value for plant breeding. BMC Plant Biology 12: e55. https://doi.org/10.1186/1471-2229-12-55XiongZPiresJC (2011) Karyotype and identification of all homoeologous chromosomes of allopolyploid Brassicanapus and its diploid progenitors.187: 37–49. https://doi.org/10.1534/genetics.110.122473ORCID