Author Correction: Mitochondrial plastid DNA can cause DNA barcoding paradox in plants

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

DNA barcoding may not be fit-for-purpose if there are misidentifications of commercial species in quality control systems. Identity testing methods must be able to accurately detect target ingredients to verify claims on labels. Accidental contamination and economically motivated adulteration (EMA) of herbal products have become common, serious threats to the herbal industries 15,16 . Such fraud costs the industry approximately $10-$15 billion globally every year due to the need to authenticate products and eliminate EMA targets 15 . More broadly, such fraud also damages the market for natural products by eroding consumer trust. DNA barcoding based on plastid (or chloroplast) and 45S nuclear ribosomal DNA (45 S rDNA) has been suggested as a credible, appropriate means to identify plant species ingredients in food and natural health products [17][18][19] . However, the misapplication of such DNA markers can be highly problematic for the industry. In February 2015, the New York State Attorney General's Office accused major herbal product retailers of selling adulterated products based on DNA barcode data and prohibited the retailers from selling the products 20 . However, the products were restored to market after an investigation determined that they had been produced in compliance with the guidelines of the US Food and Drug Administration and that barcode testing was not a scientifically validated test for regulatory or commercial identity testing applications. There is a considerable likelihood for both false positive and negative tests, as no guidelines have been published that address criteria such as specificity, sensitivity, limit of detection, applicability, repeatability and reproducibility 21 .
The commercial use of a scientific test method before it is validated can cause serious economic damage to specific brands, businesses and entire industries. For example, in April 2015, there was a false-positive ingredient identity test recorded in a Korean health functional food that has a label claim for an extract of the medicinal plant Cynanchum wilfordii (Cw), which is used to treat menopausal disorders 22 . Cw is an widely distributed herbal plant in Korea that is registered and approved as an ingredient for health functional foods by the Ministry of Food and Drug Safety in Korea 23 . Cw is reported to have several physiological effects such as enhancing immunity, inhibiting benign prostatic hyperplasia and anti-osteoporosis effects in animal models [24][25][26] . Cw has also been investigated as a functional food for reducing fat accumulation and liver damage 27 . An ethanol extract of Cw increased HDL-cholesterol levels and reduced the atherogenic index in rats and mice that were fed a high fat and high cholesterol diet 28,29 . Very recently, Youn et al. reported that an ethanol extract of Cw significantly reduced total cholesterol, apolipoprotein B and cholesteryl ester transfer protein levels in mild hypercholesterolemia subjects 30 . Cynanchum auriculatum (Ca) is a closely related plant species that is utilized as traditional Chinese medicine in China 31 . Ca has anti-tumor activity 32 with both gastroprotective 33 and antioxidant effects 34 . Ironically, Ca is not a desirable ingredient because it has not yet been registered as a food material in Korea. On the other hand, Ca has been used for local food and folk medicine in China 35,36 . Cw extract was a best-selling health functional food in Korea in 2012-2015. However, sales of the most popular Cw product plummeted after accusations of contamination with Ca instead of Cw, although both have similar functions and metabolite profiles 33,36 . At that time, two plastid DNA markers including intergenic targets between trnH and psbA genes as well as intron region of trnL were reported for discrimination of Cw and Ca 37,38 . The manufacturer of this product was sued and suffered public defamation for product adulteration by issuing from the Korea Consumer Agency who used one of the two DNA barcoding markers to make an adulteration claim. This adulteration claim was refuted, and the case was acquitted by the Korean Supreme Court due to the lack of properly validated scientific methods and the use of only one or two plastid DNA markers, which were inadequate for identifying these ingredients, as these barcodes could not discriminate these two closely related plant species. However, the industrial use of Cw products has sharply declined and its production has not yet recovered. Moreover, many innocent Cw farmers are still under suffering from an obligate regulation involving the use of a single real-time PCR marker, matK, with some false-positive detection defects derived from the plastid-mitochondrial genome flux in these taxa 39 .
The goal of the current study was to investigate plastid-mitochondrial genome flux and its impact on the herbal medicinal industry using ingredients from Cynanchum species as a case study. More specifically, we assembled the complete plastid and mitochondrial genomes of two Cynanchum species in order to assess the occurrence of plastid-mitochondrial genome flux in these species. In addition, we analyzed 81 mitochondrial genomes to explore lineage-specific MTPT patterns, which may contribute to mitochondrial genome diversity, as well as MTPTs capable of causing mis-authentications while employing DNA barcoding. Finally, we propose a set of recommended principals for developing guidelines for eliminating EMA using a multiple marker system.

Results plastid and mitochondrial genome sequences of C. wilfordii and C. auriculatum
We assembled the complete plastid 40,41 and mitochondrial genomes of Cw and Ca using low-coverage whole-genome sequencing (WGS) ( Table 1, Supplementary Fig. 1). For Cw, we obtained three type of circular forms of the mitochondrial genome. Type 1 and 2 shared 50% conserved downstream sequence, while type 3 shared no sequence homology with the other two. The total genome lengths were 379,601 bp, 352,774 bp and 111,332 bp for types 1, 2 and 3, respectively. The Ca mitochondrial genome was assembled into one linear major chromosome 652,279 bp in length, along with two minor types of circular forms derived from different recombination events of the three compartments. Both mitochondrial genomes showed large-scale collinearity with some structural rearrangement (Fig. 1a). The collinear regions showed high sequence similarity, and the sequences of all the mitochondrial genes were identical except for the copy number of the atp9 gene, which was two and one in Cw and Ca, respectively. The plastid genomes of both species showed overall collinearity, with 97.5% similarity (Fig. 2b).
Mtpts in the two Cynanchum species. In the plastid genomes, 34.3% and 37.7% of Cw and Ca sequences, respectively, showed homology with mitochondrial genome sequences of the same species (Fig. 1b). Almost 50% of plastid protein-coding genes-36 of the 75 genes-were identified in MTPTs of both Cynanchum species (Supplementary Table 2). Two universal DNA barcoding genes from the plastid genome, matK and rpoB, were also identified in MTPTs of both species: while rpoB was identified in the mitochondrial genomes in truncated forms, 135 bp and 297 bp, the complete genic region of matK was found in the mitochondrial genomes. Although the MTPT and its plastid counterparts showed relatively high diversity of insertions and deletions (InDels), the sequence similarity between homologous sequences in the two Cynanchum species was high (94.5%). The matK genes in the plastids of the two species shared 99.2% sequence similarity, and those in the MTPTs shared 99.6% sequence similarity (Supplementary Fig. 2a and Table 3). nucleotide substitution rates in the plastid and mitochondrial genomes. We calculated the nucleotide substitution rates of homologous genes (synonymous substitutions per synonymous site, Ks) between species in the plastid, mitochondrion and MTPT regions ( Fig. 1c and Supplementary Table 4). When we performed interspecies comparisons of each organelle genomic content between the two Cynanchum species, the mode of the Ks values of the 75 plastid genes was approximately 0.006-0.012 and that of the MTPT regions was ~0.001. The mitochondrial genes of both species were identical, and thus the Ks values were 0. However, when we performed intraspecies comparisons of plastid genes and their MTPT counterparts, the Ks values were much higher and broadly distributed (0.000-0.127) in both species.
We calculated the divergence times of the two Cynanchum species and members of two related genera, Asclepias syriaca and Rhazya stricta, based on the Ks values ( Fig. 1d) of their plastid and mitochondrial genes. The divergence rate calculated from the mitochondrial genome was much slower than that calculated from the plastid genome. R. stricta first diverged ~17.5-30.0 million years ago (MYA), and A. syriaca and the two Cynanchum species separated next at ~7.5-15.0 MYA. The two Cynanchum species were estimated to have diverged ~1.5-3.0 MYA based on plastid genome sequence divergence, although their mitochondrial genes are identical. The MTPT sequence showed 90% sequence similarity between A. syriaca and Cynanchum species and 99% sequence similarity between Cw and Ca. We found that a recent episode of elevated plastid-mitochondrial genome flux occurred ~10.7 MYA in the common ancestor of Cw and Ca based on Ks values between plastid and MTPT counterparts.  Table 4). All 78 protein-coding genes in the plastid genome of Arabidopsis thaliana were identified at least once as MTPTs among the 81 plant mitochondrial genomes examined (Fig. 2). rbcL was the most frequently detected MTPT, followed by atpB, psaA, psaB, psbC, psbD, rpl2, rpl23, rpoB, rps7, rps12 and ycf2, which were each identified in more than 20 plant species. The international recommendations for barcoding candidate regions for land plants include seven plastid targets, four genic and three intergenic regions 42 Among the four genic regions, rbcL and rpoB belonged to the most frequent MTPT group; rpoC1 was grouped in the moderately frequent group, as it was found in more than 10 species; and matK was rarely detected as an MTPT. The three intergenic regions (atpF-atpH, psbK-psbI and trnH-psbA) and their flanking genes were seldom identified as MTPTs.
The MTPT distribution was coincident with the taxonomical groupings based on mitochondrial genes for the 81 plant species. In addition, the same pattern of MTPT distribution was identified at the family or genus level, with some exceptions. Certain species, such as two Corchorus species and Capsicum annuum, showed unique, highly abundant MTPT patterns that were extremely different from those of closely related species (denoted with arrowheads on the phylogenetic tree in Fig. 2 and Supplementary Note S7). MTPTs corresponded to 5.7% and 33.1% of the plastid genome in the mitochondrial genomes of S. lycopersicum and C. annuum, respectively, indicating that there has been recent additional plastid-mitochondrial genome flux in C. annuum (Supplementary Figs. 3 and 4).

DnA barcode markers based on inter-and intra-species plastid polymorphism.
We identified polymorphic sites from the two Cynanchum species by performing pairwise alignment of the plastid genome sequences www.nature.com/scientificreports www.nature.com/scientificreports/ of both plants (Supplementary Table 5). Based on this information, we developed 12 DNA markers, including seven SNPs and five InDels, for the authentication of each species (Supplementary Table 6). We inspected three of these markers under different PCR conditions and found that two of them target the polymorphic plastid regions that are homologous to MTPT counterparts in the mitochondrial genomes of both species, while the third targets a polymorphic plastid region that has no MTPT counterpart (Fig. 3). The first marker is a Ca-specific marker derived from a SNP associated with matK that is currently used to detect Ca contamination in Cw products under obligate regulation by the Ministry of Food and Drug Safety of Korea 39,43 (Fig. 3a). The second is based on codominant primers targeting a 348-bp InDel polymorphism located in the intergenic spacer (IGS) region between rps2 and rpoC2, which produce a 481-bp band for Cw and a 135-bp band for Ca ( Supplementary Fig. 2a). The third marker is also based on codominant primers, in this case targeting the IGS region between rpoB and trnC-GCA and producing a 347-bp and 428-bp band for Cw and Ca, respectively. All three markers showed the expected genotype for the plastid genomes of both species using a moderate number of PCR amplification cycles (less than 25). However, for the first and second markers, unexpected bands were detected when we increased the number of PCR cycles or the amount  Fig. 3b,c). These bands were also amplified from all the 27 Cw collections in Korea ( Supplementary Fig. 5a). These unexpected bands were derived from MTPT targets. The MTPTs of both species are almost identical both to each other and to the matK gene of the Ca plastid ( Fig. 3a and Supplementary Fig. 2b). Furthermore, read mapping of WGS indicated that 88% and 12% of NGS reads were derived from the plastid and mitochondrial genomes, respectively (Supplementary Fig. 5 and Table 2). These numbers might represent the copy numbers of the plastid and mitochondrial genomes within a cell and might explain the different amounts of PCR products, i.e., the appearance of weaker bands derived from MTPTs compared to intense bands for the Ca_s_1 marker and Cw_i_1 marker in Cw and Ca, respectively (Fig. 3b,c and Supplementary Note 2). Finally, we designed nine additional DNA markers: three InDel and six SNP targets from plastids without MTPT homologs. All nine markers showed clear authentication of Cw and Ca without any noise, even following numerous PCR cycles, such as the third marker in Fig. 3b (Supplementary Fig. 6).
We assembled four more plastid genomes from different Cw collections and identified 11 targets, 6 SNPs and 5 InDel regions, showing intraspecies diversity among the five plastid genomes (Supplementary Fig. 8). We designed three intra-specific polymorphic markers from the InDel targets and inspected the 27 Cw and 26 Ca collections ( Fig. 4a and Supplementary Fig. 5b and Table 6). The three markers showed 2-3 haplotypes based on the copy numbers of tandem repeats. When we inspected the genotypes of 27 Cw collections using these markers, 12 showed the same genotype with Ca from at least one of the three markers.

Discussion
Plant mitochondrial genomes are extremely large, with sizes varying from 200 to 2000 kb ( Supplementary Fig. 9), i.e., 15-125 times larger than the conserved 16 kb animal mitochondrial genomes. Horizontal genome flux between the plastid, mitochondrial and nuclear genomes is an established but underappreciated phenomenon in plants. Cynanchum species harbor a single type of plastid genome but multi-chromosomal mitochondrial genomes, a type of structure that in other plant species is known to be derived from tandem repeat-mediated recombination [44][45][46] . Here, in a study of 81 angiosperm mitochondrial genomes, we detected varying degrees of plastid genome flux, with additional lineage-specific patterns, indicating that frequent plastid genome flux is quite common in angiosperms. Intriguingly, a very recent horizontal plastid genome transfer was detected in the mitochondrial genomes of some species, including C. annuum, indicating that plastid flux into the mitochondrial genome occurs more frequently during plant evolution 7,9,11,[47][48][49][50] (Supplementary Fig. 4). The C. annuum mitochondrial genome may have evolved independently through more than one period of genome flux after its divergence from the genus Solanum. The occurrence of multiple MTPT integration events has been inferred in several other plant lineages 19,[21][22][23][24] . Furthermore, since MTPT signals gradually disappear over evolutionary time due to the accumulation of mutations, the MTPTs of C. annuum may reflect recent transfers, which is also in accordance with the species' evolutionary history. Therefore, taking into account the case of C. annuum, it appears that the abundant, intact MTPT fragments in several species may result from multiple, recent species-specific horizontal plastid genome flux events 7 Table 2. Estimated proportions of NGS reads for the plastid and mitochondrial genomes of Cw and Ca. * Pt, Plastid; Mt, Mitochondria; † The genotype of each position is shown in parentheses, ' A' for adenine and 'G' for guanine. The proportion was calculated based on read depth for the polymorphic sites between the plastid and counterpart MTPT (Supplementary Fig. 5). The plastid and mitochondrial genome copy numbers are estimated to be 1,241 and 170 copies, respectively, in a somatic cell (2n).  Fig. 9). Plastid DNA copy numbers vary in different species and in different plant tissues. The plastid genome copy number declined rapidly, from 600 copies to fewer than 100 copies, during 5 days of dark treatment 51 . Plastid DNA is degraded by the organelle exonuclease DPD1 and contributes to phosphorus relocation 51 . When plastid DNA is not completely degraded, the abundant fragments of plastid DNA can occasionally be horizontally transferred into other cellular genomes via a mechanism involving the double-strand break repair system of the plant genome 52 .
To date, only 81 plant mitochondrial genome sequences have been reported, although thousands of plastid genomes have been characterized. This discrepancy is due to the complex mitochondrial genome structure, with an abundance of MTPTs, size variance and a high frequency of recombination. The current findings indicate that mitochondrial genomes, including MTPTs, exhibit low nucleotide substitution rates, showing more than three times slower evolution compared to plastid genomes 53 (Fig. 1c). Importantly, we demonstrated that plant barcoding targets are found in MTPTs (Fig. 2a) at meaningful frequencies in a diverse array of plants. Overall, we have uncovered a notable shortcoming of the common practice of barcode-based authentication of plant products by demonstrating that a wide range of horizontal transfer events involve MTPTs, which are likely to result in the co-amplification of unexpected bands (Fig. 3b,c and Supplementary Fig 5a). These promiscuous DNAs could affect molecular taxonomy by causing mis-positioning of species if the plastid DNA sequences used were confused with those of MTPTs 8 .
EMA is estimated to have cost the herbal supplement industry 10-15 billion dollars per year since 2010 15 . The impact of mis-authentication caused by the DNA marker paradox could have severe negative effects not only on the industry but also on all parties involved in the herbal supplement industry, from farmers to consumers and beyond, as demonstrated by the involvement of the New York State Attorney General's Office and the Korean Supreme Court in regard to Cynanchum products in 2015-2017. To avoid the incorrect application of DNA markers and thus to escape the DNA marker paradox, it is desirable to use multiple markers derived from different loci, which can credibly distinguish EMA from target plant products such as species-specific markers (Fig. S7, Supplementary Table 6) as the suggestion for DNA barcoding (Group et al. 42 ). How 42 the number of markers required to detect EMA does not need to be as high as that used in forensics to distinguish individuals of the same species (Homo sapiens).
Unlike major crops, herbal medicinal plants still have a wide range of natural intraspecies diversity because diverse collections are wildcrafted or undomesticated cultivated [1][2][3][4] . Therefore, there always be the possibility of false decision for the off-type individuals from molecular marker application as in the previous adulteration issue of Cw and Ca ( Supplementary Fig. 5a). We inspected the previously reported authentication markers for Cw and Ca in Korea. The psbA-trnH marker 37 identified both species almost correctly, but make a few case of false-negative (decide Ca plants as Ca-negative) detection that provide Cw genotype for a Ca collection. Another marker derived from SNPs in trnL loop 38 made false-positive (decide Cw plants as Ca-positive) errors for 2 of 27 Cw collections (Supplementary Fig 5a). Additionally, we inspected the haplotype diversity of Cw and Ca for 3 of the 11 intraspecies polymorphic sites revealed from a comparison of the five plastid genomes of Cw ( Fig. 4a and Supplementary Fig. 5b, 8 and Table 5). Based on the genotypes for the three markers, 27 Cw collections were classified into 5 groups, unlike Ca individuals, which are derived from a few Chinese collections and thus showed narrow genetic diversity. Notably, the application of the markers would place 12 of the 27 Cw collections as Ca and 1 of the 26 Ca collections as Cw if genotyping were based on data from individual negative genotypes. These findings emphasize the importance of marker choice and relying on more than one marker for authentication purposes.
To define the difficulty more generally, if the target species shows homogeneous genotypes for three loci, denoted A, B and C, the A 1 B 1 C 1 genotype can be clearly distinguished from the A 2 B 2 C 2 genotype. However, we found that many wild accessions have heterogeneous genotypes, such as A 1 B 1 C 2 or A 2 B 1 C 2 , as a result of intraspecies plastid genome diversity (Fig. 4) or plastid-mitochondrial genome flux (Fig. 3) 1,54 . If we were to focus only on the negative markers and assume that the heterogeneous genotypes represented counterfeit products (i.e., the negative detection method), the chance of detecting the counterfeits (the detection power) would be increased, but the possibility of a decision error that defines the genuine product as fake (the rate of false-positive, type I error) would also be increased. By contrast, if we were to focus on the positive markers and to assume that the heterogeneous genotypes represent the target product (i.e., the positive detection method), we could expect the opposite result: we would accept diverse genotypes as representing the target species and thereby reduce false-positive, but we would also reduce the detection power (Fig. 4b). Our analysis showed that 12 of the 27 Cw collections would be mis-authenticated if we applied the negative detection method. Conversely, the positive detection method would define all 27 Cw collections as genuine, and 1 of 26 Ca collections would be mis-authenticated as Cw (Fig. 4a). If we applied the negative detection method to increase the detection power of an assay, the false-positive error rate would be increased; likewise, if we applied the positive detection method to reduce the false-positive error rate, the detection power would be reduced.
In general, herbal plant resources are underdeveloped, and thus their genetic diversity is currently unknown or underestimated. Given this necessary balancing act, as long as the counterfeit plant is nontoxic, we propose that the positive detection method should be applied to reduce false-positive errors, even if the detection power is reduced and the false-negative rate (Type II error) is thereby increased. This approach could reduce unforced errors resulting in the sanctioning of genuine products and thereby protect the industry. However, in cases where there are safety concerns, such as toxicity associated with the EMA counterpart, the negative detection method should be applied to maximize the detection power even at the cost of more false-positive errors, because trace amounts of adulterant could pose a threat to both consumer health and the long-term success of the industry.
The raw materials for most herbal products are heterogeneous because they are collected from natural habitats or cultivated from wild collections. The breeding of superior cultivars and the establishment of quality management systems should be encouraged to produce consistent functional foods. The production of functional foods from specific cultivars managed from seed to final products with traceability will benefit from the development of scientifically well-supported cultivar-specific markers and minimize the damage from EMA, thus promoting the growth of the functional food and herbal supplement industry.

Materials and Methods
plant samples and DnA extraction. The 27 Cw materials for were collected from 6 different local-farming areas in Korea, and the 26 Ca materials were provided by the Rural Development Administration (RDA). Total genomic DNA was extracted from the samples using modified CTAB methods 55 for NGS analysis from 5 Cw samples and 1 Ca sample. For marker application, total genomic DNA was extracted from the samples using a Genomic Plus DNA Prep Kit (Inclone Biotech, Korea) following the manufacturer's instructions.
Assembly of plastid and mitochondrial genomes. We produced Illumina platform WGS Paired-End data using genomic DNA from individual Cynanchum wilfordii (Cw) and Cynanchum auriculatum (Ca) plants. We assembled the plastid genome sequence 40,41 (GenBank accession numbers NC_029459 and NC_029460) and mitochondrial genome sequence (GenBank accession numbers MH931257, MH931258, MH931259 and MH931260) using the WGS datasets. After trimming of low-quality reads, assembly was performed using CLC genome assembler (ver_4.01). The mitochondria-related contigs were extracted from the assembled contigs via comparison with the mitochondrial sequence of A. syriaca (NC_022796) using MUMmer 56 . Contigs showing over than 99% homology and overlap with the plastid genome were removed and the remaining mitochondrial DNA contigs were combined for each type of mitochondrial genome and validated by mapping of raw reads using the dnaLCW method 2,3 . Additionally, four independent Cw collections were sequenced on the MiSeq platform (Illumina, San Diego, CA), and their plastid genomes were also assembled following the methods described above (MK182385, MK182386, MK182387, MK182388).

Identification of MTPTs in the mitochondrial genome. To detect MTPTs in plant mitochondrial
genome sequences, we compared 81 mitochondrial genome sequences, including the newly assembled mitochondrial genomes of Cw and Ca and 79 published plant mitochondrial genomes (Supplementary Table 1) retrieved from the NCBI database. Each mitochondrial genome sequence was compared with the plastid genome sequence of A. thaliana (NC_000932) using BLASTN 57 based on more than 70% identity from at least 30 bp strands with an expectation value of 1E-10. The regions of the plastid genome matching transfer RNA (tRNA) or ribosomal RNA (rRNA) were ignored and excluded from this study because tRNA and rRNA are conserved in both organelle genomes.
Plastid marker design and PCR amplification. The plastid sequences of the Cynanchum species were aligned using MAFFT 58 . After identifying polymorphic regions by pairwise alignment of the Cw and Ca chloroplast genomes, we mapped each raw NGS read to the corresponding chloroplast genome to detect promiscuous regions including MTPT. SNPs or InDels showing heterogeneous genotypes for more than 3% of each read depth were eliminated. Primers for codominant markers and high-resolution melting curve (HRM) analysis were designed using Primer-BLAST 59 . We selected InDel polymorphic regions whose length was greater than 20 bp and converted these regions to the codominant marker. In the case of SNPs, we filtered out adjacent SNPs less than 150 bp long and designed primers flanking candidate SNPs with lengths ranging from 100 to 150 bp.
PCR was conducted using the following cycling program: pre-amplification at 95 °C for 5 min; 25-40 cycles of denaturation at 95 °C for 30S ec, annealing at 58 °C for 30 sec, and elongation at 72 °C for 30 sec; and a final elongation at 72 °C for 5 min. The mixture consisted of a total volume of 25 μL prepared using an Inclone TM Taq DNA Polymerase Kit (Inclone, South Korea) with 5-80 ng of template DNA, 1× PCR reaction buffer, 0.2 mM of each dNTP, 0.2 pmol of each primer (Bioneer, South Korea) and 0.4 units of Taq DNA polymerase. Ca-specific markers were amplified as described previously 38 . High-resolution melting-curve (HRM) analysis was performed via detection on a LightCycler 480 Real-time PCR Machine (Roche Applied Science, Indianapolis, IN, United States) under the following conditions: pre-amplification at 95 °C for 5 min followed by 45 cycles of 95 °C for 30 sec, 58 °C for 30 sec, and 72 °C for 30 sec. The reaction mixture (20 μL) contained 20 ng of template DNA, 0.5 pmol of each primer (Bioneer, South Korea) and a 1× Pre-mix of RealHelix TM Premier qPCR Kit (Nanohelix, South Korea). The uncropped gel images are shown in Supplementary Fig. 10.
KASP (Kompetitive allele-specific PCR) markers were designed from the same SNP positions used for HRM analysis with Kraken software (LGC Genomics, Hoddeson, UK). Thermocycling and endpoint genotyping for the KASP assays were applied to the Cw and Ca populations using a Roche LC480 (Roche Applied Science, Indianapolis, IN, United States) following the manufacturer's instructions in a total reaction volume of 10 μL containing 100 ng of template DNA, 0.14 μL of KASP assay mix and 5 μL of KASP reaction mix.
Ks value calculation for genes in plastid and mitochondrial genomes. We calculated the level of synonymous substitutions per synonymous site (Ks) between homologous genes in the plastid genomes (plastid genes, PT), mitochondrial genes (MT) and MTPTs of four Apocynaceae species, Cw, Ca, Asclepias syriaca 9 and Rhazya stricta 60 . Pairwise alignments of the coding sequences for common genes derived from each organelle were conducted using webPRANK 61 based on translated codons. After alignment, InDel regions and stop codons were trimmed using GBLOCKS 62 , and Ks values were calculated using CODEML from the PAML package 63 .