Introduction

Repetitive elements (REs) comprise a considerable portion of plant genomes, even comprising > 85 % in some plant genomes (Schnable et al. 2009). Although considered ‘junk’ in the past, REs are now known as important players in genome function and structure, and species evolution (Fedoroff 2012; Wicker et al. 2007). REs are generated or produced by chromosomal rearrangements, which drive chromosome structure variations between closely related lineages (Murat et al. 2017; Schubert and Lysak 2011). Tracking the dynamics of various repeat families could therefore provide insights into the genome history of closely related taxa (Long et al. 2013; Waminal et al. 2018b).

REs can be categorized into two classes: tandem repeats (TRs) and dispersed repeats (Kubis et al. 1998). TRs follow a head-to-tail organization, whereas direct repeats, such as transposable elements. TRs can be further classified into three groups based on repeat unit length: microsatellites (2–5 bp repeats), minisatellites (6–100 bp repeats) and satellite DNA (satDNAs) (150–400 bp monomer length) (Mehrotra and Goyal 2014).

TRs are often distributed in distinct chromosomal regions, usually at pericentromeric and subtelomeric sites (Sharma et al. 2013), often in low copies forming a “library” of repeats (Fedoroff and Bennetzen 2013; Ruiz-Ruano et al. 2016). Due to sequence homologies in these chromosomal regions, they have been considered as hotspots for chromosomal rearrangements during genomic perturbations such as those resulting from a genome merger (Hartley and O’Neill 2019; Rosato et al. 2018; Schubert and Lysak 2011).

Often, these chromosomal rearrangements could amplify a single or few TR families, and when reproductive barriers are formed, new species may develop with an altered chromosomal number, organization, or TR abundance (Mandáková and Lysak 2018; Murat et al. 2017). Several basic chromosome numbers are present in a genus, which was described as dysploid (Winterfeld et al. 2020). Ascending dysploids, or species with more chromosomes, are formed when chromosomes are fragmented and when fragments maintain or develop centromeres. In contrast, descending dysploids are formed when chromosomes fuse (Winterfeld et al. 2020). As the differential abundance and distribution of TRs among species in a taxonomic group can vary (Perumal et al. 2017), TRs are used as cytotaxonomic markers to study phylogenetic relationships (Guerra 2008, 2012).

Fluorescence in situ hybridization (FISH) of TRs can provide essential information for understanding genome structure, chromosome evolution and phylogenetic relationships among related taxa (Iovene et al. 2008; Matsuda and Chapman 1995). This information complements the inference of phylogenetic relationships based on DNA markers such as the internal transcribed spacers (ITS) of 45S rDNA (Kim et al. 2015), which are used extensively because of their abundance of phylogenetically informative sites and easy amplification in the plant species (Farah et al. 2018). In addition, the intergenic spacers (IGS) of the 45S rDNA coding genes are known to “carry” different TRs during species evolution (Falquet et al. 1997; Almeida et al. 2012). Comparing the distribution of duplicated sequences in the S. tora IGS could provide important data for studying Senna evolution.

The genus Senna, formerly Cassia (family Fabaceae, subfamily Caesalpinioideae) comprises approximately 350 species of herbs, shrubs, and trees (Tucker 1996; Monkheang et al. 2011). Senna has varied economic and medicinal applications, and has been used not only as a natural pesticide but also for treating skin diseases, gastrointestinal disorders, and inflammation (Ongchai et al. 2019; Singh et al. 2013). A desire to further exploit these health benefits has prompted the genome sequencing of Senna tora, as a widespread and representative species, to better understand Senna biology and evolution.

The predominant chromosome number of the genus Senna is 2n = 28 (Rice et al. 2015), but species with descending dysploid karyotypes of 2n = 22–26 have also been identified, such as S. tora with 2n = 26 (Cordeiro and Felix 2018; Pellerin et al. 2019). To understand the dysploidization in S. tora, we examined its genome TR composition in our previous work (Waminal et al. 2021). We identified eight S. tora TRs, many of which showed unusual chromosomal distributions. For example, StoTR02_7_tel, which is the Arabidopsis-type telomeric repeat, showed highly amplified loci in the pericentromeric regions in all S. tora chromosomes in addition to signals at chromosome termini. Besides, StoTR05_180, which was observed in the subtelomeric region of all S. occidentalis chromosomes was absent in these regions but highly amplified in the pericentromeric regions in S. tora chromosomes.

The classification of Senna is not yet fully understood, and no comparative cytogenetics have been performed to examine chromosome evolution in the genus. Here, to understand the dynamics of S. tora TRs and their role in S. tora dysploidy, we performed comparative FISH among nine Senna species. We analyzed the chromosomal distribution patterns of these TRs in a cyto-phylogenetic context based on the ITS1-5.8S-ITS2 sequences.

Materials and methods

Plant material

Root tips were collected from germinated seeds of nine Senna species, which were provided by the National Plant Germplasm System (USDA, USA), Department of Herbal Crop Research (NIHHS, RDA, Korea), and Rare Palm Seeds (Germany). Roots were treated with 2 mM 8-hydroxyquinoline for 5 h at 18 °C to arrest cells at metaphase, and then fixed in Carnoy’s solution and stored in 70 % ethanol until used for chromosome preparation.

Chromosome preparation

Chromosome spreads were prepared according to Waminal et al. (2012) and Eliazar et al. (2019). Briefly, the meristematic tips were immersed in an enzyme solution consisting of 1 % pectolyase Y-23 (Duchefa Biochemie, Netherlands) and 2 % cellulase R-10 (Duchefa Biochemie, Netherlands) for 60–90 min at 37 °C. Next, chilled Carnoy’s solution was added, and after centrifugation, the precipitate was pipetted and dropped onto pre-warmed glass slides in a humid chamber at 70 °C and then air-dried.

Probes preparation and fluorescence in situ hybridization (FISH)

S. tora TRs were identified using low-coverage sequences and short-read clustering with TAREAN (Novák et al. 2017) in our previous study (Waminal et al. 2018a, 2021). All pre-labeled oligonucleotide probes (PLOPs) used in this study are listed in Table 1.

Table 1 List of pre-labeled oligonucleotide probes used in this study

For the FISH procedure, a total of 40 µL hybridization mixture containing 100 % formamide, 50 % dextran sulfate, 20× SSC, 50 % dextran sulfate, 20× SSC, 50 ng/µL of each probe, and Sigma water were added to each slide and then denatured at 80 °C and kept in a humid chamber at 37 °C overnight. After hybridization, the slides were washed with 2× SSC at room temperature (RT) and then dehydrated through ethanol 70 %, 90 %, and 100 % for 3 min each. Finally, the slides were counterstained with a DAPI-Vectashield solution and captured under Cytovision ver 7.2 software with an Olympus BX53 fluorescence microscope system, equipped with a Leica DFC365 FS CCD camera. The images were enhanced using Adobe Photoshop CS6. Chromosomes were measured using the IdeoKar 1.2 software (Mirzaghaderi and Marzangi 2015), and chromosome typing was performed according to the method of Levan et al. (1964). Chromosomes were arranged in pairs depending on their FISH signals, length, and other chromosome features as described in our previous work (Pellerin et al. 2019; Youn and Kim 2018).

Genomic DNA extraction and sequencing of ITS sequences

Genomic DNA of nine Senna species was extracted from young leaves by using the cetyltrimethylammonium bromide (CTAB) method (Allen et al. 2006). The ITS primer pairs (F: GTCGCTCCTACCGATTGAA; R: TCTTTTCCTCCGCTTATTGA) were designed based on the 45S rDNA sequence of S. tora by using Primer3 software. PCR was performed by initial denaturation at 95 °C for 3 min, followed by 30 cycles of denaturation at 95 °C for 30 s, annealing at 60 °C for 30 s, and extension at 72 °C for 30 s, followed by a final extension at 72 °C for 5 min. Amplicons were ethanol purified and sequenced by Bionics (South Korea).

Phylogenetic analysis

The Senna ITS sequences were aligned using CLC Main Workbench version 5.5, then confirmed through MEGA X. Genetic distance was calculated using the Kimura 2 parameter formula (K2P), and the phylogenetic tree was constructed by MEGA X.

Results

Six of the eight S. tora TRs were detected in the nine Senna species

All Senna species in this study had 2n = 28 chromosomes (Fig. 1). In contrast, S. tora has only 2n = 26 chromosomes (Pellerin et al. 2019). To understand the impact of TRs in the karyotype dysploidy of S. tora, we performed FISH to analyze the presence or absence of signals and variations in chromosomal distributions to examine the dynamics of TRs identified in the S. tora genome.

Fig. 1
figure 1

FISH of S. tora TRs on root metaphase chromosomes of the nine Senna species. Six of the eight TRs, which showed signals from initial FISH screening, and StoIGS_463, are shown here. White arrows indicate the ITRs in S. candolleana, S. corymbosa, S. floribunda, S. occidentalis, and S. multiglandulosa. For signal patterns of individual probes, see supplementary data. Scale bar = 10 µm

Out of the eight S. tora TRs (Waminal et al. 2021), two were not detected by FISH in all nine Senna species (StoTR03_178 and StoTR04_55), while the other six were either present in all or only a few species (Table 2). StoTR02_7_tel, StoTR05_180, Sto_5S, and Sto_45S_CDS were detected in all species, whereas StoTR01_86 and StoTR06_159 were observed only in eight and four species, respectively (Fig. 1; Table 1). In addition, StoIGS_463 was also observed in only four species.

Table 2 Chromosomal distribution of major Senna tora tandem repeats in nine Senna species

StoTR02_7_Tel and StoTR05_180 were mostly colocalized

The StoTR02_7_Tel, which is an Arabidopsis-type telomere repeat sequence, was highly amplified in the interstitial regions of S. tora chromosomes in addition to the canonical sites at chromosome termini (Pellerin et al. 2019; Waminal et al. 2021). Likewise, StoTR05_180 was also mostly colocalized with StoTR02_7_Tel in S. tora in pericentromeric regions but absent in subtelomeric sites.

In the present study, all nine Senna species had StoTR02_7_Tel signals at the terminal region of all chromosomes (Fig. 1). However, in addition to these canonical sites, interstitial telomeric repeat (ITR) signals were also detected in S. candolleana, S. corymbosa, S. floribunda, S. multiglandulosa, and S. occidentalis (Figs. 2, 3 and 4; Table 2). In S. candolleana, chromosomes 1 and 7 had ITRs in the long arm. In S. corymbosa, ITRs were detected in the proximal region of the short arm of chromosomes 1, 2, and 3. In S. floribunda, three chromosomes had ITRs in the short arm; those in chromosomes 6 and 13 were in proximal regions while those in chromosome 11 were more interstitial. In S. occidentalis, ITRs were located at proximal regions in the short arm of chromosomes 1, 3, and 4.

Fig. 2
figure 2

FISH karyograms of the root metaphase chromosomes of the nine Senna species. StoTR01_86 was mostly colocalized at 45S rDNA sites in all species except S. siamea. StoTR05_180 was at subtelomeric sites in all species except in S. sulfurea, where it was localized at pericentromeric regions. The white arrows indicate the ITR in S. candolleana, S. corymbosa, S. floribunda, S. occidentalis, and S. multiglandulosa. The orange arrow shows the weak signal of StoTR01_86 in S. didymobotrya. For karyogram of each species showing individual TR distribution, see supplementary data. Scale bar = 10 µm

Fig. 3
figure 3

Karyotype idiograms showing the distribution of S. tora TRs in nine Senna species. Note the colocalization of StoTR01_86 and StoTR06_159 at the 45S rDNA loci in some species, and the unique distribution of StoTR05_180 at the pericentromeric regions of all chromosomes in S. sulfurea, contrary to subtelomeric location in other species

Meanwhile, StoTR05_180 signals were detected as colocalized signals with StoTR02_7_Tel in all species, except in S. sulfurea (Figs. 2, 3 and 4). In S. sulfurea, StoTR05_180 did not colocalize with StoTR02_7_Tel. StoTR02_7_Tel was exclusively distributed at chromosome termini in S. sulfurea, whereas StoTR05_180 was absent in these regions but was amplified in the pericentromeric regions with varied intensities in all chromosomes (Fig. 2).

The number of 45S rDNA loci was more diverse than that of 5S rDNA

Similar to S. tora, all nine species had only one pair of Sto_5S rDNA, whereas Sto_45S rDNA varied from one to four loci (Table 1). The 5S rDNA signals were localized in the short arms of the respective chromosomes in S. alata, S. candolleana, S. corymbosa, S. multiglandulosa, S. sulfurea, and S. siamea, and in the long arms in S. didymobotrya, S. floribunda, and S. occidentalis (Figs. 2, 3; Table 2).

Fig. 4
figure 4

Cyto-phylogenetic analysis among Senna species. The ten species, including S. tora, were grouped into four (I–IV). StoTR05_180 at the subtelomeric site is shared in all ten, and likely the primitive distribution pattern in, Senna. StoTR01_86 was shared by species in Groups II–IV. Independent chromosomal rearrangements involving several repeats and chromosomes have taken place in species Groups II–IV. Species in Group IV shared rearrangements involving the displacement of StoTR05_180 to the pericentromeric regions of chromosomes (pink box)

The Sto_45S_CDS signals were distributed only in the subtelomeric regions of the short arms of the respective chromosomes. One pair of 45S rDNA was detected in S. corymbosa, S. floribunda, S. multiglandulosa, and S. occidentalis, two in S. candolleana, three in S. alata, S. siamea, and S. sulfurea, and four in S. didymobotrya (Figs. 25; Table 2).

StoTR01_86 and StoTR06_159 colocalized at the 45S rDNA loci

The chromosomal distribution of StoTR01_86 in S. tora was in total contrast with that observed in the Senna species in this study. Although StoTR01_86 was localized in the pericentromeric regions in all S. tora chromosomes (Waminal et al. 2021), it was absent in the pericentromeric region in all currently investigated Senna species but colocalized at all 45S rDNA loci, except in S. siamea, which did not show any StoTR01_86 signal at all (Figs. 2, 3 and 4; Table 2).

On the other hand, StoTR06_159 was colocalized with 45S rDNA in S. tora, and also in S. alata, S. corymbosa, S. floribunda, and S. multiglandulosa (Figs. 2, 3 and 4; Table 2). However, the minor extra-NOR StoTR06_159 locus observed in S. tora was not detected in species with StoTR06_159 signals. None of the other species showed any StoTR06_159 signals (Table 2).

StoIGS_463 localized at extra-NOR loci

StoIGS_463 is a 463 bp duplicated sequence with two copies identified in the IGS region of S. tora 45S rDNA (Waminal et al. 2021). FISH also confirmed the exclusive localization of StoIGS_463 at the NOR site in S. tora. However, FISH on the nine Senna species showed no signals at NOR sites, but rather at subtelomeric or interstitial chromosomal regions in some species and were completely absent in some species (Figs. 2, 3; Table 2). While some distinct paired signals were observed, dispersed signals were also detected in many chromosomes, such as those in S. corymbosa, indicative of transposable element FISH signals.

Of the nine species, only S. alata, S. candolleana, S. corymbosa, and S. floribunda showed StoIGS_463 FISH signals (Figs. 2, 3 and 4; Table 2). Aside from chromosomes without signals, three StoIGS_463 distribution patterns were observed in these four species: (1) at the subtelomeric and interstitial regions, (2) only in the subtelomeric regions, and (3) only in the interstitial regions. In S. alata, there were ten, one, and three chromosomes that had the first, second, and third StoIGS_463 distribution patterns, respectively (Fig. 4; Table 2). In S. candolleana, only the first and third patterns were observed with eleven and three chromosomes bearing each pattern, respectively (Fig. 4; Table 2). In S. corymbosa, chromosome 4 did not show any StoIGS_463 signal, while four, five, and four chromosomes showed patterns i, ii and iii, respectively (Fig. 4; Table 2). Finally, in S. floribunda, there were 11, two, and one chromosomes that showed patterns i, ii and iii, respectively (Fig. 4; Table 2).

Chromosome rearrangement patterns support ITS-based phylogenetic tree

Since many TR loci formed from chromosomal rearrangements are not readily visible by FISH when these loci are shorter than the FISH detection threshold, grouping species based solely on FISH signal patterns could be misleading. Therefore, we compared the FISH distribution with the phylogenetic tree inferred using the entire ITS sequences (ITS1-5.8S-ITS2) of the Senna species, including S. tora data from our previous work (Waminal et al. 2021).

The Senna ITS length ranged from 632 bp in S. tora to 663 bp in S. corymbosa and had a mean of 649 bp. The ITS1 and ITS2 had relatively higher GC contents than those of 5.8S, and the GC content of the entire sequence ranged from 58.54–62.84 % and averaged 61.45 % (Table 3).

Table 3 Sequence length and GC content of the 45S rDNA ITS1-5.8S-ITS2 sequences of the 10 Senna species

These ITS sequences divided the Senna species into four (Fig. 4). Group I comprised only S. siamea, which showed the fewest FISH signals of the S. tora TRs, and the most primitive chromosomal distribution pattern, StoTR05_180, at the subtelomeric regions of all chromosomes. Groups II–IV all had StoTR01_86 signals, mostly at the 45S rDNA loci. Independent chromosomal rearrangements involving the other repeats have taken place in the species in these groups. The absence of FISH signals may either be short arrays that make these loci undetectable using FISH or indicate a lack of actual rearrangements. Additional chromosomal rearrangements involving StoTR05_180 occurred in Group IV. These rearrangements displaced the subtelomeric location of StoTR05_180 into the pericentromeric region, where they have been highly amplified in both S. sulfurea and S. tora. Additional rounds of rearrangements may have occurred in S. tora, as shown by several chromosomes with interstitial StoTR05_180 signals.

Discussion

In our study, we have compared the chromosomal distribution of the TRs identified from the S. tora genome with nine other Senna species in order to understand the impacts and evolutionary dynamics of these TRs in the dysploidization of the S. tora karyotype. Compared with the nine Senna species assessed in this study, S. tora had the most extensive chromosomal rearrangements and the only one with a descending dysploidy karyotype (Fig. 4), suggesting the involvement of these TRs in shaping the extant S. tora genome.

Interstitial telomeric repeats are evidence for Senna chromosomal rearrangements

In most eukaryotes, telomeric repeats are usually located at the terminal end of chromosomes and have a key function in preventing chromosomal damage (Muraki et al. 2012). However, telomeric repeats have also been found in interstitial regions, also known as interstitial telomeric repeats (ITRs) (Bolzan 2012). Several mechanisms have been postulated to explain the formation of ITRs. These include interchromosomal telomere fusion, DNA polymerase slippage, and double-strand break repair (Uchida et al. 2002; Lin and Yan 2008).

Of the ten Senna species, including S. tora, six had readily detectable ITR signals indicating shared chromosomal rearrangements involving StoTR02_7_Tel among these Senna species. The lack of ITR signals in the other species may indicate fixation and reduction of these repeat loci, rendering them undetectable by FISH, as has been previously observed in other plants (He et al. 2013). It is also possible that these StoTR02_7_Tel-mediated chromosomal rearrangements occurred independently in each species. The extreme contrast of the StoTR02_7_Tel distribution between S. siamea and S. tora suggests that S. siamea has a more primitive karyotype and that the massive chromosomal rearrangements in S. tora may have evolved relatively recently.

Concerted conversion of StoTR05_180 to (peri)centromeric TRs in S. sulfurea and S. tora

Species in Groups I–III carried StoTR05_180 in the subtelomeric regions, whereas those in Group IV (S. sulfurea and S. tora) have somehow managed to transpose these TR loci from the subtelomeric to the pericentromeric region in all chromosomes. We proposed the hypothesized that this transposition has been occurred involving all chromosomes of the group IV ancestral karyotype. As a result, the evidence indicated that StoTR05_180 presents in the pericentromeric region of all chromosomes in S. sulfurea and S. tora. The other scenario is likely given the relatively random process of chromosomal rearrangement events.

One possible mechanism for this concerted TR array transposition may involve chromoplexy, which is a massive chromosomal rearrangement event that involves several chromosomes (Comai and Tan 2019; Pellestor and Gatinois 2020). Microhomologies between telomeric and (peri)centromeric regions make these regions hotspots for chromosomal inversions (He et al. 2013).

While both S. sulfurea and S. tora had lost subtelomeric StoTR05_180 loci but amplified pericentromeric loci, only S. tora developed a novel centromeric repeat, StoTR03_178 (Fig. 5), which may have likely evolved from StoTR05_180 (Waminal et al. 2021). Disruption of the epigenetic makeup immediately after chromosomal rearrangements may have enabled StoTR05_180 to function as a novel centromeric repeat. This, in S. tora, may have eventually caused centromere positioning, and fixation of StoTR03_178 variants.

Fig. 5
figure 5

Comparative FISH with StoTR03_178 between S. sulfurea and S. tora. FISH signals were only detected in S. tora. Scale bar = 10 µm

The 45S rDNA IGS as repeat carrier during chromosomal rearrangements

45S rDNA is associated with genome rearrangements (Havlová et al. 2016). The sub-repeat elements in the IGS are considered important players in the dynamics of IGS (Jo et al. 2011). The elimination and reorganization of the IGS repeat elements were observed in Nicotiana tabacum after allopolyploidization which caused IGS length variation among Nicotiana species (Volkov et al. 1999). Although there is no exact mechanism to clearly explain the movement of TRs in and out of the 45S rDNA IGS, some authors have observed that TRs in the IGS moved out and amplified in another chromosomal region (Almeida et al. 2012). However, others also noted the opposite direction of IGS TR evolution in Phaseolus vulgaris, such that TRs moved into the 45S rDNA IGS from another region in the genome (Falquet et al. 1997). Our data suggest that the 45S rDNA IGS can act as TR “carrier” during chromosomal rearrangements, and that fragments of transposed TRs could sometimes get lodged and fixed in a taxon. Moreover, this observation suggests that TRs in the IGS are more like “footprints” of the recent involvement of the IGS in chromosomal rearrangements.

StoTR01_86, which was at the 45S rDNA locus in most Senna species except S. siamea and S. tora, suggests that 45S rDNA is involved in chromosomal rearrangement after the divergence of the Senna species from the ancestral karyotype S. siamea, which resulted in the fixation of StoTR01_86 in Group II-III species. Eventually, chromosomal rearrangement specific to S. tora may have caused more recent expulsion of the StoTR01_86 from the IGS and moved it into the pericentromeric regions of all chromosomes (Fig. 4) (Waminal et al. 2021).

StoTR06_159 also illustrates the movement of TRs in and out of the 45S rDNA IGS (Fig. 4). Moreover, StoIGS_463 explicitly showed the active role of the 45S rDNA IGS in homing repeats, which in this case is the subtelomeric ancestral repeat of StoIGS_463.

FISH data suggest the involvement of TRs in S. tora dysploidy

In Senna, the basic chromosome number is x = 14 (Waminal et al. 2021). Several species, however, have x = 11, 12, 13 resulting from descending dysploidization events (Elaine et al. 2005). Although various Senna species showed FISH signals from S. tora TRs, only S. tora had extensive genome rearrangements and dysploid karyotype (Fig. 4), suggesting the involvement of TRs in S. tora karyotype dysploidy.

Moreover, StoTR03_178 was observed in the interstitial region of S. tora chromosome 7, suggesting a relatively recent chromosome fusion (Waminal et al. 2021). Although we are not yet certain which ancestral chromosomes fused to form the S. tora chromosome 7, it is likely that orthologous S. sulfurea chromosomes 1 and 4 may have been involved. This hypothesis is based on the presence of subtelocentric S. sulfurea chromosomes 1 and 4, which were not detected in S. tora (Fig. 3). Moreover, subtelocentric chromosomes are often involved in interchromosomal fusion (Schubert and Lysak 2011).

Conclusions

We compared the chromosomal distribution of the eight S. tora TRs and a 45S rDNA IGS duplicated sequence, StoIGS_463, among nine Senna species. We have seen the dynamics of these TRs, which showed both shared and independent evolution. Importantly, we have shown cytogenetic evidence of the bidirectionality of TR movement into or out of the 45S rDNA IGS region, suggesting a role for 45S rDNA as a repeat carrier during chromosomal rearrangements. Moreover, these data also provide cytogenetic visualization of the expansion, contraction, and reorganization of repeat families in a repeat “library” of a lineage. Further studies should focus on characterizing the 45S rDNA IGS sequences of all Senna species to gain more insight into the role of the IGS in genome rearrangements.