Insight into chloroplast genome structural variation of the Mongolian endemic species Adonis mongolica (Ranunculaceae) in the Adonideae tribe

Adonis mongolica is a threatened species that is endemic to Mongolia. It is a medicinal plant from the Adonis genus and has been used to treat heart diseases. However, the genomics and evolution of this species have not been thoroughly studied. We sequenced the first complete plastome of A. mongolica and compared it with ten Adonideae species to describe the plastome structure and infer phylogenetic relationships. The complete plastome of A. mongolica was 157,521 bp long and had a typical quadripartite structure with numerous divergent regions. The plastomes of Adonideae had relatively constant genome structures and sizes, except for those of Adonis. The plastome structure was consistent across Adonis. We identified a 44.8 kb large-scale inversion within the large single-copy region and rpl32 gene loss in the Adonis plastomes compared to other members of the Adonideae tribe. Additionally, Adonis had a smaller plastome size (156,917–157,603 bp) than the other genera within the tribe (159,666–160,940 bp), which was attributed to deletions of intergenic regions and partial and complete gene losses. These results suggested that an intramolecular mutation occurred in the ancestor of the Adonis genus. Based on the phylogenetic results, Adonis separated earlier than the other genera within the Adonideae tribe. The genome structures and divergences of specific regions in the Adonis genus were unique to the Adonideae tribe. This study provides fundamental knowledge for further genomic research in Mongolia and a better understanding of the evolutionary history of endemic plants.

Adonis mongolica is a threatened species that is endemic to Mongolia.It is a medicinal plant from the Adonis genus and has been used to treat heart diseases.However, the genomics and evolution of this species have not been thoroughly studied.We sequenced the first complete plastome of A. mongolica and compared it with ten Adonideae species to describe the plastome structure and infer phylogenetic relationships.The complete plastome of A. mongolica was 157,521 bp long and had a typical quadripartite structure with numerous divergent regions.The plastomes of Adonideae had relatively constant genome structures and sizes, except for those of Adonis.The plastome structure was consistent across Adonis.We identified a 44.8 kb large-scale inversion within the large single-copy region and rpl32 gene loss in the Adonis plastomes compared to other members of the Adonideae tribe.Additionally, Adonis had a smaller plastome size (156,917-157,603 bp) than the other genera within the tribe (159,666-160,940 bp), which was attributed to deletions of intergenic regions and partial and complete gene losses.These results suggested that an intramolecular mutation occurred in the ancestor of the Adonis genus.Based on the phylogenetic results, Adonis separated earlier than the other genera within the Adonideae tribe.The genome structures and divergences of specific regions in the Adonis genus were unique to the Adonideae tribe.This study provides fundamental knowledge for further genomic research in Mongolia and a better understanding of the evolutionary history of endemic plants.
Adonis L., comprising 26-38 species, belongs to the Ranunculaceae family [1][2][3] .The higher classification of Adonis is the Adonideae tribe 4,5 .This genus is commonly distributed in southwestern Asia, Europe, Northern Africa, and the Mediterranean region 1,6 .The general morphology of Adonis is characterized by therophytes or perennials, compound leaves, 1-2 palmately or 2-3 pinnately dissected terminal inflorescences, and white, red, and yellow flowers 6,7 .The base number of chromosomes in the genus is x = 8.In perennial species, the somatic number of chromosomes is 2n = 16, and polyploid races with 2n = 24 and 2n = 32 have been identified 8,9 .Adonis is divided into two subgenera, Adonanthe and Adonis, which are perennial and annual species, respectively.
Adonis mongolica Simonovich is an important medicinal plant that is endemic to Mongolia 10,11 .Since 2000, it has been identified in only two locations in the country, which is of great concern 12 .The general morphology of A. mongolica is a plant height of 10-20 cm, with numerous white flowers and violet sepals (Fig. 1). A. mongolica inhabits a specific environment compared with other Adonis; however, previous studies on A. mongolica have primarily focused on its chemical components and medical usage [13][14][15] , in addition to its distribution and conservation 12,16 .However, the genetic background of A. mongolica, along with its phylogenetic relationships and classification, has not been determined.Similar to other Adonis species, A. mongolica has been used to treat heart failure with symptoms of tachycardia and edema 13 .Currently, A. mongolica is critically endangered globally because of overexploitation and loss of habitat 16 .Therefore, implementing programs for protecting and genetic breeding of threatened species is critical.Most Adonis species grow where topographical conditions allow for a water supply 17 , but A. volgensis, A. villosa, and A. mongolica grow mostly on drier montane and forb steppes, and these species show evidence of ecological vicariance [18][19][20][21] .The evolution of A. mongolica was most likely accompanied by the alteration and extension of its ecological constitution.
Over the past few decades, several researchers have studied the whole chloroplast genome (plastome) sequences of plants worldwide.This is because using the plastome sequences to resolve relationships between vascular plants at higher taxonomic levels is more successful than using short-sequence fragments 22,23 .Furthermore, in most angiosperm species, plastome inheritance is uniparental and highly conserved and provides important phylogenetic data 24 .The first detailed plastome study of Adonis in 1998 described the restriction site maps for the two species 25 .Currently, the plastomes of four Adonis species are available in the NCBI GenBank database [26][27][28] , accounting for only 2% of the total species diversity.According to previous plastome studies, the plastomes of the genus Adonis have large inversions and gene transpositions 25,27 , and the genus belongs to the Adonideae tribe along with Calathodes, Megaleranthis, and Trollius [26][27][28] .The Adonideae tribe was derived from its ancestor around 25.5 Mya 28 .In addition, phylogenetic relationships within the Adonis genus have been evaluated The plastome of A. mongolica was sequenced for the first time.A total of 8 Gb paired-end (150 bp) clean reads were generated.After trimming and normalization, a list of 22,993,276 paired reads was obtained for de novo assembly (Table S1).De novo assembly generated a single contig, 157,521 bp in length.The plastome of A. mongolica contained a large single-copy (LSC; 86,651 bp), a pair of inverted repeats (IR; 26,332 bp), and a small single-copy (SSC; 18,206 bp).The total GC content in A. mongolica was 37.9%.Particularly, the GC contents in the IR, LSC, and SSC regions were 43, 36.1, and 31.4%,respectively (Table 1), indicating that the IR region had a higher GC content than the SSC and LSC regions.Adonis mongolica contained 113 unique genes.The numbers of rRNA, tRNA, and protein-coding genes in the plastome were 4, 30, and 79, respectively (Fig. 2 and Table S2).Overall, the protein-coding sequences (CDS) were 78,470 bp long, whereas the non-coding sequences (including the intergenic spacer [IGS] and introns) were 79,051 bp long.

Organization of plastomes of the Adonideae tribe
The plastome sequences of 11   S3).The complete circular plastomes were 156,917-160,191 bp in length and included an LSC of 86,218-88,944 bp, an SSC of 18,067-18,532 bp, and a pair of IR regions of 26,087-26,632 bp (Table 1 and Table S4).The overall GC content was 37.9-38.1% and was slightly higher in the IR than in the LSC and SSC regions.The Adonideae plastomes contained 131 genes, including 80 protein-coding, 30 tRNA, and 4 ribosomal RNA genes (Fig. S1).Six protein-coding, seven tRNA, and four rRNA genes were duplicated within the IR regions.The complete plastome harbored 18 intron-containing genes, 16 of which had a single intron and two of which had two introns (Tables S5 and S6).Three intron-containing genes were found to be duplicated in the IR regions.The rps12 gene was a trans-spliced gene with the 5′-end located in the LSC and the 3′-end located in an IR region.
Analysis of codon usage and anticodon recognition patterns revealed 26,210-26,427 codons, of which leucine, serine, and isoleucine were the most abundant (Fig. S2).To identify codon patterns, we analyzed codon distribution in 11 plastomes (Fig. S3).Codons with A or T at the third position had a strong codon bias.Most Adonideae displayed a comparable pattern with high RSCU values for arginine (AGA), leucine (TTA), and alanine (GCT).

Repeat sequences
We investigated the repeat sequences of Adonideae species to determine their characteristics and proportions of repeat sequences within the tribe.Adonideae species had a similar number of forward, reverse, palindromic, and complementary repeats (Fig. 3a).For single-sequence repeats (SSRs), mononucleotide motifs were the most abundant in all species, followed by dinucleotide motif repeats (Fig. 3b).A total of 53-69 SSRs were identified, mostly in the LSC region and particularly within the IGS region.Most of the tandem repeats were located in the IGS region (Fig. 3c).We found 23-58 tandem repeats that were generally 9-68 bp long (Fig. 3d).Among the tandem repeats, three regions (rps16-ndhJ, ndhF-ccsA, ndhG-ndhI) in the IGS and the ycf2 gene in the LSC Table 1.Basic plastomes information of five Adonis species.

A. mongolica A. amurensis A. pseudoamurensis A. coerulea A. sutchuenensis
Nucleotide length (bp) region were common among the five Adonis plastomes.The number of repeat sequences was the highest in T. macropetalus (Fig. 3e).However, the tandem repeats were shorter than the other repeat sequences, and this pattern was similar in all the Adonideae examined (Fig. 3f).

Plastome comparison
The genome structure, gene order, and boundaries between IRs and single-copy regions were similar among Adonideae plastomes; however, genus-specific rearrangements in Adonis plastomes were revealed.Collinearity in gene placement among the 11 available Adonideae plastomes was assessed using AliTV (Fig. 4 and Fig. S4).
From the trnT-UGU to the rps16 genes, a 35-gene inversion (21 protein-coding genes and 14 tRNAs), 44.8 kb in length, evolved in Adonis.Furthermore, two deletion sites (844 and 524 bp) in the intergenic regions were found within the inversion region of the Adonis plastomes.This inversion was not detected in other available species within the tribe.In Adonideae, IR lengths ranged from 26,087 to 26,632 bp, but the borders between the IR regions and the two single-copy regions (LSC and SSC) were similar.The rps19 and ycf1 genes spanned the LSC/IRb and SSC/IRa junctions, respectively (Fig. S5).Only IR contraction was observed in A. coerulea because the rps19 gene was located entirely in the LSC region.The sequence identities of the 11 Adonideae were analyzed using mVISTA, with the A. mongolica plastome serving as a reference.We replaced the inversion of Adonis to calculate the sequence identity of each gene.As expected, the genic regions were more conserved than the intergenic regions when comparing the ten species (Fig. S6).This pair of IR regions was highly conserved, followed by the LSC and SSC regions.We analyzed the genetic divergence of genes and intergenic regions within Adonideae plastomes, and genus-related mutations were detected using pairwise comparisons.Overall, Adonideae plastomes had an average genetic diversity (Pi) value of 0.018.The highest Pi values of the IGS regions were observed for trnK-rps16 (0.102) in SSC (Fig. 5).The ycf1, rps16, ndhF, and matK genes are variable within the Adonideae species.Species-specific mutations of Adonis were detected using pairwise alignment.The highest Pi value was detected for psbT-psbN (0.104) in A. mongolica and A. coerulea (Fig. S7).In addition, the ndhF-trnL IGS showed considerable length variation in Adonideae because the rpl32 gene was completely lost in Adonis (Fig. S8).

Phylogenetic analysis
Two datasets were compiled to verify the phylogenetic relationships among members of the Adonideae tribe.The first dataset consisted of 80 conserved protein-coding sequences of 11 Adonideae species, obtained by aligning 87,075 bp, of which 82,024 bp (94.2%) were constant and 5051 bp (5.8%) were parsimony-informative.The second dataset contained the complete plastomes of 17 Ranunculaceae species.Due to the relatively high variation within the intronic and intergenic regions, the matrix contained 200,666 nucleotide sites, of which 152,797 bp (76.1%) were constant and 37,887 bp (18.9%) were parsimony-informative among Ranunculaceae.The Aconitum kusnezoffii Rchb.plastome served as the outgroup for both datasets.The Adonis species were distinct from other genera in the Adonideae tribe and were supported by strong bootstrap values and posterior probabilities (PPs) for the CDS and whole plastome datasets (Fig. 6 and Fig. S9).Adonis mongolica clustered with A. coerulea and A. sutchuenensis, whereas A. amurensis and A. pseudoamurensis were positioned as sister taxa in this cluster.However, the relationship between A. mongolica, A. coerulea, and A. sutchuenensis was differently positioned in the two datasets: in the whole plastome dataset, A. mongolica and A. coerulea were more closely related than A. sutchuenensis (Fig. 6); while, in the CDSs dataset, A. coerulea and A. sutchuenensis were more closely related than A. mongolica (Fig. S9).

Discussion
Plastomes have been widely used as models to elucidate patterns of genetic variation in space and time, as well as micro-and macro-evolutionary events across all plant lineages 32 .This is because the plastome is highly conserved, with evolutionary hotspots, such as gene insertions and deletions, IR contractions and expansions, inversions, and various repeat sequences 33 .We sequenced and characterized the plastome of A. mongolica and conducted comparative studies that included ten other species of the Adonideae tribe to identify genetic variations that could explain the evolutionary changes.The complete plastome of A. mongolica showed a typical quadripartite structure with one LSC, one SSC, and two IR regions, which was a highly conserved pattern.However, unique structural rearrangements were detected in the newly sequenced A. mongolica, as with other species of Adonis.Multiple inversions and transpositions have been detected in the LSC regions of Ranunculaceae plastomes 27,34 .The Adonis genus plastome includes a 44.8 kb inversion in the LSC region 25,27,28 .Inversions arise when two breaks occur within a DNA segment, and the segment between the two breaks inserts itself in the opposite direction, causing a 180° inversion relative to the adjacent region.Inversion breakpoints are frequently found in regions with repetitive nucleotides, and these regions may be reused in future inversions 35 .Repeated sequences have been discovered at the endpoints of several land plant plastome inversions, as well as in tRNA genes 36 .In the Adonis genus, the inversion reversed the order of genes between rps16 and trnT-UGU, placing trnK-UUU adjacent to trnT-UGU and rps16 adjacent to trnL-UAA.This inversion occurred between two tRNA genes; however, there was no repeat region near the endpoint of the inversion.This might have been caused by random changes in the Adonis plastome.Furthermore, large-scale inversion occurred in the ancestor of Adonis after being derived from the Adonideae tribe because this type of inversion was not observed in any other genus within the tribe.Plastome sequences have been used by many researchers to determine phylogenetic relationships at various taxonomic levels 37 .Early molecular phylogenetic studies have revealed that Adonis is related to Trollius 38 .Based on floral www.nature.com/scientificreports/development and phyllotaxis, Adonis was assigned to the Adonideae tribe and is closely related to the genus Calathodes 5 .In addition, the phylogenetic relationship of Ranunculaceae was revised using plastome analysis, revealing that Adonis belonged to the Adonideae tribe 27,28,39 .Our phylogenetic study revealed the same topology as previous studies; the Adonideae tribe formed a monophyletic clade, which includes Adonis, Calathodes, Megaleranthis, and Trollius based on whole plastome and protein-coding genes.Within this tribe, the Adonis genus formed a distinct monophyletic group (Fig. 6).
The plastome size of the Adonideae species investigated here varied slightly, with that of the Adonis genus being shorter (156,917-157,603 bp) than those of the other Adonideae species (159,666-160,940 bp).Adonis plastome size diversity was detected in LSC and IR.The IR contraction occurred due to a partial deletion (200 bp) of the ycf2 gene, reduction of the LSC region due to a ~ 2 kb nucleotide loss during large-scale inversion, and intergenic deletions in rps16-trnQ-UUG and psbM-trnD-GUC regions.The ycf2 gene is the largest plastid gene reported in angiosperms.The function of ycf2 is largely unknown; however, it does not appear to be related to photosynthesis 40 .The ycf2 gene within Ranunculaceae species shows genetic divergence with many repeat events and deletions 41,42 .The ycf2 gene could be an alternative to comprehensive genes for studying the relationships between Ranunculaceae species.More than 69 SSRs were identified in A. mongolica, and most repeats were in the ycf2 gene.This provides a rare opportunity to study the population genetics of this threatened plant, which is endemic to Mongolia.In addition, length variation was detected in the ndhF-trnL intergenic region within Adonideae.This spacer includes the gene rpl32, which produces the ribosomal protein L32 43 ; however, the gene has been completely deleted in the Adonis genus 27,34,39,44 .This spacer within the Ranunculaceae plastome is www.nature.com/scientificreports/either a pseudogene or absent and has a wide range of lengths with a 1.6 to 5.5-fold reduction compared to that of the full-length IGS of rpl32 45 .Due to various events of complete loss, this IGS region in Adonis is nearly 0.8 times shorter than that in other Adonideae genera.Transfer of rpl32 from the plastome to the nucleus has been observed in Euphorbiaceae 46 , Ranunculaceae 27,45 , Rhizophoraceae 47 , and Salicaceae 48 ; thus, the rpl32 may have been transferred to the nucleus or subjected to complete loss in the Adonis plastome.Furthermore, some coding regions had significantly high diversity, such as the ycf1, rps16, and matK genes (Fig. 5).These highly variable regions may be useful as specific DNA barcodes for species-level identification, as well as for providing genetic markers for resolving relationships among the Adonideae.Taxonomic studies of the Adonis genus have not been well revised; the species of sect.Adonanthe were mostly studied, including the nuclear ITS region 6,29,30 and the trnL-F 29 , atpB, and rbcL 38 regions of the plastome.In the present study, we estimated the genetic diversity of the plastomes of five species of sect.Adonanthe.The ccsA-ndhD, ndhD-ndhI, and trnD-trnY regions showed different haplotypes for each species (Fig. S7).These regions can be used to identify species within the Adonis genus.Among the modern barcoding markers, trnH-psbA (0.023) was highly variable for Adonis, whereas the previously used trnL-F (0.006), atpB (0.005), and rbcL (0.004) markers were relatively less variable.Based on our observations, partial genetic markers of the plastome are unsuitable for identifying species within the Adonis genus.Based on whole plastome sequences, A. mongolica clustered with A. coerulea and belonged to subg.Adonanthe sect.Adonanthe ser.Coerulea.The results revealed the morphological characteristics of petiolate leaves, rhizomes, trichomes on achenes, and white or purple petals 49 .The species of ser.Coerulea has numerous mixed light-purple and white flowers, whereas A. mongolica and A. davidii have only white flowers 7,18 .Interestingly, A. mongolica was a sister taxon to the cluster containing A. coerulea and A. sutchuenensis based on protein-coding genes.Specific mutations may have occurred in proteincoding genes of A. mongolica.Many studies have revealed that mutations in genes corresponding to flower color can affect adaptive success 50,51 .Future studies on the gene expression of flower color will be valuable for a better understanding of the adaptation and evolution of the Adonis genus.
The results of the present study expand the genetic information on medicinal plants endemic to Mongolia.In particular, A. mongolica has numerous genetic divergence regions; Adonis members show a genus-specific 44.8 kb inversion, several partial deletions, and complete gene loss.These changes have not been detected in other genera within the tribe; thus, they occurred in the ancestor of Adonis after its separation from the Adonideae tribe.This may have been caused by nonrandom recombination associated with climate change, making it an interesting topic for future evolutionary investigation.

Conclusions
The plastome of A. mongolica was sequenced and annotated for the first time.It included a highly conserved gene order, identical to that of the Adonis species, at 157 kb, and has a median plastome size for photosynthetic land plants.We identified important genetic resources for sequence divergence and phylogenetic inference of A. mongolica, providing a rare opportunity to study the genetic background of this threatened plant endemic to Mongolia.Comparative genomics indicated that Adonis plastomes were relatively conserved but included several genus-specific rearrangements and highly divergent locations.For instance, we identified a uniquely large inversion in the LSC region, complete gene loss from the SSC region, and some genes and intergenic regions with high sequence diversity.This study provides valuable genetic information to understand the evolutionary relationships of the genus Adonis within the Adonideae tribe.

Plant collection, DNA sequencing, and plastome assembly
The plant material used in this study was collected from natural populations in Argalant Soum, Tuv province (N47.887992 and E106.41658),Mongolia, and a voucher specimen (UBU0032866) was deposited in the herbarium of the National University of Mongolia, Mongolia.Total DNA was extracted from the tested species by using a modified CTAB method 52 .The library was prepared from total genomic DNA using the TruSeq DNA Nano Kit on the NextSeq 500 platform (Illumina, San Diego, CA, USA), following the manufacturer's protocol.Trimmomatic v. 0.36 53 was used to remove adapter sequences and low-quality reads to reduce biases in the analysis.The total number of bases, reads, GC (%), Q20 (%), and Q30 (%) for A. mongolica samples were calculated after filtering.A base quality plot generated using FastQC v. 0.11.5 54 was used to evaluate the overall quality of the data.This plot shows the range of quality values for each cycle.De novo assembly was performed with various k-mers using NOVOplasty 55 .The best k-mer was selected based on the assembly results, including the number of contigs, total contig length, and N50.Read sequences produced using the Illumina platform for plastome assembly were mapped to validate the assembly results, and the depth, coverage, and insert size were calculated.The raw data reads were mapped to an assembly result to identify the insert size of the raw data and the number of reads used in the assembly.The appropriate statistics were calculated after mapping.After the complete or draft plastome was assembled, BLAST analysis was performed to identify the species with which each contig (or scaffold) showed similarity.

Repeat analysis
We used REPuter to identify forward, reverse, palindromic, and complementary repeats with a minimum length of 20 bp, 90% identity, and a Hamming distance of 3 56 .SSRs were detected using MISA 57 with the minimum number of repeat parameters set to 10, 5, 4, 3, 3, and 3 for mono-, di-, tri-, tetra-, penta-, and hexanucleotides, respectively.Tandem repeats ≥ 20 bp were identified using the Tandem repeats finder 58 with a minimum alignment score of 50 and a maximum period size of 500; the identity of repeats was set to ≥ 90%.

Plastome annotation and comparative analysis
Plastome annotation of A. mongolica was performed using GeSeq 59 to predict the location, whereas BLAST 60 was used to determine the function of and identify the assembled sequences against nucleotide and protein sequence databases.The complete plastome sequence of A. mongolica has been submitted to GenBank (accession number: OQ569932).A total of 11 samples, representing five species from the genus Adonis, including A. mongolica, four species from the genus Trollius, and one species each from the genera Megaleranthis and Calathodes, were analyzed in this study.OrganellarGenomeDraw 61 was used to generate circular and linear plastome maps.The GC content and RSCU of the ten plastomes were analyzed using MEGA11 software 62 .The codon usage distribution of Adonideae plastomes was visualized using the Heatmapper tool with average linkage clustering and Euclidean distance measurement methods 63 .An RSCU < 1.00 indicated a codon that was used less frequently than expected, whereas an RSCU > 1.00 indicated a codon that was used more frequently than expected.Pairwise whole plastome alignments of the Adonideae plastomes were visualized using AliTV software 64 and MAUVE v2.3.1 65 .The SC/IR boundary shifts at four junctions (LSC/IRa, IRa/SSC, SSC/IRb, and IRb/LSC) of the sample plastomes were compared using IRscope 66 .The mVISTA program 67 in Shuffle-LAGAN mode 68 was used to detect species-specific genetic variation by comparing Adonideae plastomes with A. mongolica as a reference.DnaSP version 6 69 was used to calculate nucleotide variability (Pi) among plastomes.The CDS, intron, and IGS regions were analyzed separately to confirm the exact genetic variants.Statistical analysis was performed using XLSTAT 70 to test whether gene loss was related to IGS length.

Phylogenetic analysis
We constructed two datasets for phylogenetic analysis: CDSs of Adonideae species and complete plastomes of Ranunculaceae species.Complete plastomes and CDSs were individually aligned using MAFFT ver.7.388 71 .Alignment datasets were filtered to remove ambiguously aligned regions using GBlock ver.0.91.1 72 .The bestfitting model for nucleotide substitutions was determined using the Akaike information criterion in jModelTest v2.1.10 73, and the GTR + I + G model was selected for maximum likelihood (ML) analysis.The GTR + G model was selected for the Bayesian inference (BI) analysis.The maximum parsimony (MP) analysis was conducted using PAUP* v4.0b10 74 .The MP searches included 1000 random addition replicates and TBR branch swapping using the MulTree option.ML analysis was performed using RaxML v. 8.0.5 75 with 1000 bootstrap replicates.BI analysis was carried out using MrBayes 3.2.2 76, with two independent runs of four simultaneous chains executed for 5,000,000 generations using the Markov chain Monte Carlo algorithm.Trees were sampled every 5000 generations, and the first 25% were discarded as burn-in.The trees were determined using a 50% majority-rule consensus to estimate PPs.Reconstructed trees were visualized using FigTree version 1.4.2 77.

Figure 2 .
Figure 2. Circular gene map of the complete chloroplast genome of Adonis mongolica.Genes drawn inside the circle are transcribed clockwise, and those outside, counterclockwise.The darker gray in the inner circle represents GC content and light gray represents AT content.Intron containing genes are marked with a star.

Figure 3 .
Figure 3.The distribution of repeat sequences in of tribe Adonideae plastomes.(a) The number of repeat types in Adonideae plastome.(b) The number of simple sequence repeats (SSR) motifs and the distribution of SSRs in the genome regions.(c) Distribution of tandem repeats in intergenic region (IGS), intron, and exon.(d) Total number of tandem repeats.(e) Distribution of repeats in genomic regions.(f) Percentage of repeats in genomic regions.

Figure 4 .
Figure 4.The complete plastome structure of Adonideae species.Linear maps were built using the AliTV visualization software, based on whole genome alignment.Both panels depict pairwise comparisons, expressed as percentage of nucleotide similarity, that connect different homologous genomic regions.Genomes are completed in full and pictured in purple.

Figure 5 .
Figure 5.Comparison of the nucleotide diversity (Pi) values of intergenic regions among Adonideae.The mean Pi value of intergenic regions within the tribe Adonideae and the genera Adonis and Trollius is indicated by green, blue and orange lines, respectively.