- Open Access
Construction of the first high-density genetic linkage map and QTL mapping of flavonoid and leaf-size related traits in Epimedium
BMC Plant Biology volume 23, Article number: 278 (2023)
Leaves are the main medicinal organ in Epimedium herbs, and leaf flavonoid content is an important criterion of Epimedium herbs. However, the underlying genes that regulate leaf size and flavonoid content are unclear, which limits the use of breeding for Epimedium development. This study focuses on QTL mapping of flavonoid and leaf-size related traits in Epimedium.
We constructed the first high-density genetic map (HDGM) using 109 F1 hybrids of Epimedium leptorrhizum and Epimedium sagittatum over three years (2019–2021). Using 5,271 single nucleotide polymorphism (SNP) markers, an HDGM with an overall distance of 2,366.07 cM and a mean gap of 0.612 cM was generated by utilizing genotyping by sequencing (GBS) technology. Every year for three years, 46 stable quantitative trait loci (QTLs) for leaf size and flavonoid contents were discovered, including 31 stable loci for Epimedin C (EC), one stable locus for total flavone content (TFC), 12 stable loci for leaf length (LL), and two stable loci for leaf area (LA). For flavonoid content and leaf size, the phenotypic variance explained for these loci varied between 4.00 and 16.80% and 14.95 and 17.34%, respectively.
Forty-six stable QTLs for leaf size and flavonoid content traits were repeatedly detected over three years. The HDGM and stable QTLs are laying the basis for breeding and gene investigation in Epimedium and will contribute to accelerating the identification of desirable genotypes for Epimedium breeding.
For almost 2,000 years, plants of the genus Epimedium, which belongs to the family Berberidaceae, have been used in Chinese medicine to strengthen muscles and bones . Furthermore, Epimedium has a variety of biological actions, including anticancer, antioxidant, and antirheumatic effects [2, 3]. Previous studies have reported that most of these medicinal properties are attributed to leaf flavonoid glycosides . In China, the herb Epimedium, which is produced from wild resources, is offered using aerial plant parts, primarily dried leaves . Thus, wild Epimedium resources have gradually shrunk due to overexploitation in recent decades . Furthermore, the chemical synthesis of flavonoid glycosides was limited by the low rate of recovery . Epimedin C, a derivative of the phenylpropanoid pathway, is the major bioactive constituent of plant secondary metabolites in leaves. It has been recommended as a reference for the quality control of Epimedium herba [6, 7]. However, the complex biosynthesis process of secondary metabolites is not completely understood . To date, only some flavonoid biosynthetic process enzymes have been identified, such as EpPF3RT, EpRhS and Ep7GT from E. pseudowushanense . The leaf impacts plant development and biomass as the primary organ generated for consumption  and is the main medicinal organ in traditional herbals of Epimedium. At the molecular level, leaf size is generally coordinated and driven by multiple integrated signals of plant hormone production and signalling [9, 10]. The molecular mechanisms of leaf size have been revealed through a combination of genetic and intense analyses in Arabidopsis thaliana [10, 11], Medicago truncatula , Lactuca sativa  and Brassica  plant species. However, directional breeding of Epimedium for flavonoid glycoside content and leaf blade size is a substantial obstacle due to a lack of comprehension of the mechanisms of leaf blade generation and the flavonoid glycoside biosynthesis pathway. Therefore, it is essential to investigate the underlying QTLs governing leaf-size and flavonoid content features to develop novel varieties with high medicinal value.
Conventional breeding procedures are based on the phenotypic choice of genotypes from separated offspring generated by hybridization, which are usually limited by intensive labor, cost, and time efficiency . Marker-assisted selection (MAS), a methodology of species selection enabled by molecular markers, has the promise to replace phenotypic selection systems [15, 16]. Based on MAS, we might significantly accelerate the genetic improvement of desired agronomic qualities by selecting plants directly and effectively according to their genotypes [16, 17]. In molecular plant breeding, saturated HDGM employing molecular markers of great genome coverage is essential for MAS of advantageous alleles or traits [18, 16]. Quantitative trait locus (QTL) mapping based on HDGM is a technique used to discover closely affiliated molecular markers and to determine the genetic region linked to targeted phenotypes [19, 20]. Due to their abundance and density across the entire genome, single nucleotide polymorphism (SNP) loci offer an effective method for MAS, HDGM construction, and QTL mapping [21, 19]. Genotyping by sequencing (GBS) produces an enormous number of SNPs that are used to investigate species with large and complex genomes and has been extensively used in HDGM construction and QTL mapping of various species [15, 19, 16] including Momordica charantia , Cynodon dactylon Pers , and Schima superba . Thus, GBS techniques and QTL analysis associated with target traits could also be effective methods for the MAS of selective breeding for Epimedium.
An HDGM is essential for QTL evaluation ; however, no HDGM has been constructed for Epimedium. Therefore, HDGM is required for the discovery of important genes associated with phenotypes in Epimedium. In this study, SNPs were mapped to the E. sagittatum reference genome and were subsequently used to construct an Epimedium HDGM based on an F1 full-sib mapping family generated from a hybrid between E. leptorrhizum and E. sagittatum by utilizing SNP loci obtained by double-digest GBS technology. The leaf length (LL), leaf area (LA), Epimedin C (EC) and total flavone content (TFC) of individual plants were determined for three consecutive years. These phenotypic traits were then QTL evaluated to determine relevant SNP markers and potential positions on the HDGM. The development of an HDGM of Epimedium and QTL evaluation of economic traits can assist in clarifying the related genetic basis to improve MAS methods and Epimedium genetic improvements.
Variability characteristics of the four mapping traits in parents and progeny
The two parents showed unique characteristics in the EC, TFC, LL and LA traits (Fig. 1). Four traits from three separate years were subjected to analysis of variance (ANOVA), and the results indicated no discernible variation across the years (Supplementary Table S1). The skewness and kurtosis values were both less than one, except for the kurtosis values for TFC, which varied from 4.575 (2021) to 17.379 (2020). The descriptive statistical analysis of the four mapping traits showed that the coefficient of variation (CV%) varied from 14.636 (2021) to 17.195 (2019) for EC, from 12.247 (2020) to 19.712 (2019) for TFC, from 17.601 (2021) to 20.367 (2020) for LL, and from 31.637 (2021) to 31.946 (2019) for LA (Supplementary Table S2). Except for TFC, both the frequency distribution histogram and normality test results (Supplementary Table S3) among the three mapping traits for three consecutive years (2019–2021) showed a positive normal distribution. Despite the absence of a significant correlation between the other traits, the correlation analysis showed a significant association between LL and LA (Supplementary Fig. S1). Positively correlated traits (such as LL and LA) showed close relationships across genetic markers due to pleiotropic effects, which might benefit the prediction of candidate genes.
GBS library sequencing and SNP discovery
GBS sequencing provided 1,404,295,474 150 bp paired end reads and 186,913,974,238 bp clean reads (Supplementary Table S4). For the male and female parents, 106,416,658 (40.65% guanine-cytosine (GC) content with a Q30 of 94.75%) and 100,046,576 (40.65% guanine-cytosine (GC) content with a Q30 of 94.75%) reads were both aligned to the E. sagittatum genome, respectively. The F1 population had an average of 10,989,287 clean reads, with a range of 6,179,886 to 33,063,778. In addition, the average GC content of the 109 descendant sequences was 41.15%, and the Q30 score was 94.77% (Supplementary Table S4). In these reads, a total of 46,594 SNPs were obtained after comparison with the reference genome and filtering of SNPs. Given that the two parents were cross-pollinator lineages, 14,115 SNP markers from genotypes lm×ll (13,749), hk×hk (310), and ef×eg, (56) were employed to generate the HDGM (Supplementary Table S5).
Developing an HDGM based on the E. sagittatum reference genome
According to their location on the Epimedium sagittatum reference genome, 14,115 SNP markers were successfully allocated to six linkage groups (LGs). The paternal map comprised 5,269 markers distributed among six LGs, with an overall genetic length of 3246.91 cM and a mean marker gap distance of 0.84 cM. LG had a mean length of 541.15 cM, varying between 457.27 cM (LG2) and 785.62 cM (LG5) (Supplementary Table S6 and Fig. S2). On the maternal map, 392 markers were positioned in six LGs, with an overall genetic length of 985.82 cM and LG length varying from 131.02 cM (LG2) to 190.69 cM (LG4) (Supplementary Table S7 and Fig. S3). The consensus HDGM, which was generated by 5,271 SNPs, had a length of 2,366.07 cM and an average intermarker distance of 0.612 cM (Table 1; Fig. 2). The results showed that the most saturated chromosome was LG2, which contained 1,379 SNPs covering 317.03 cM with a mean intermarker distance of 0.23 cM. The longest LG5 included 442 markers, a total length of 555.66 cM, and an average gap of 1.30 cM, while the smallest LG6 had 365 markers, an overall distance of 369.142 cM, and a mean gap of 1.00 cM. The less than five cM gaps of a single LG ranged from 97.28% (LG5) to 99.69% (LG3). The longest gap in the consensus HDGM was 130.98 cM, which was present on LG5 (Table 1; Fig. 2).
HDGM quality assessment
To assure the quality of genotyping, an integrity evaluation of SNPs was performed among individuals of the mapping population with an average of 95.97% (Supplementary Fig. S4). The SNP marker was anchored to the reference genome of E. sagittatum to examine the collinearity between the HDGM and physical location. The results showed that the genetic arrangements of most markers were in the order of the physical map of the E. sagittatum genome, with the exceptions of LG1 and 2, which showed a minor departure in the collinearity test (Supplementary Fig. S5). Haplotype mapping was performed for the 109 F1 individuals and the parents using 5,271 SNPs to locate genotyping errors and double recombination. There was no crossover among the six linkage groups, and each individual recombination event was shown to be clear in the haplotype map (Supplementary Fig. S6). The highly purified interspecific F1 population, according to the above results, was appropriate for HDGM development and analysis.
QTL analysis for flavonoid flavonoids and phenotypes
Major-effect QTLs covering four traits were analysed separately on the HDGM. For three consecutive years (2019–2021), 31 stable QTLs associated with EC were detected on LG4 and LG6. Of these, 14 QTLs were detected on LG4, which ranged from 14.67 to 172.60 cM in length, with LOD values from 3.00 to 3.86 and explained variance from 4.00 to 11.40%. However, 17 QTLs were positioned on LG6 with a covered distance ranging from 232.40 to 309.57 cM and corresponded to LOD varying from 3.10 to 4.35, explaining variance spanning from 12.30 to 16.80% (Fig. 3 and Supplementary Table S8). For the TFC, only one stable QTL with one associated marker was mapped at 504.73 cM on LG5. The LOD estimate was 3.96, explaining 15.40% of the variance (Fig. 4 and Supplementary Table S8).
QTL analysis identified 12 QTLs targeting LL that were positioned on LG3 and LG5. Among the 12 QTLs, qELL-3-1 represented a stable QTL throughout the three individual years and was positioned at 210.02 cM onto LG3, with a corresponding LOD value of 3.68 and an explanatory variation of 16.80%. Moreover, 11 stable QTLs of LL were detected on LG5 over the three years (2019–2021), with genetic distances from 360.06 to 434.78 cM and LOD values between 3.26 and 3.80 along with explaining variation ranging from 14.95 to 17.34 (Fig. 5 and Supplementary Table S8). We observed that two LA controlling QTLs spanned LG3 and LG5, of which qELA-5-1 represented stable QTLs over the three years and covered genetic intervals ranging from 489.29 to 489.99 cM with LOD values of 3.26 and explained a variance of 15.05% (Fig. 6 and Supplementary Table S8). qELA-3-1 was identified as an important QTL, explaining 16.8% of the variation, and had an LOD value of 3.67. Due to the significant correlation between both LL and LA, QTLs for LL (qELL-3-1) and LA (qELA-3-1) were discovered in the same regions on LG3 (210.02 cM) (Supplementary Table S8).
GBS sequencing and the development of markers
HDGM based on molecular marker development is an important foundational study for plants to perform molecular breeding . The distribution and abundance of markers developed from the plant genome influence the regularity and coverage of markers for HDGM . GBS sequencing is an accurate, economical, and efficient method for the acquisition of many SNPs and genotyping in comparison to traditional methods of marker generation . For simplified genome sequencing, it has been suggested that the fragment produced by digestion of the genome with a suitable restriction enzyme can better represent the genome . However, species genome specificity has been neglected in previous studies, and there is usually only one common restriction endonuclease (e.g., EcoRI, SbfI, MseI and SacI) to digest genomes of various species [27, 28]. Early studies showed that the application of inappropriate single restriction endonucleases to genome digestion may initiate a maldistribution of identified fragments throughout the plant genome, reducing both the markers generated and the dependability of HDGM [28, 26]. This is consistent with our results that the fragments we harvested for sequencing could better represent the Epimedium genome after applying the two restriction endonuclease combinations (MseI and SacI) to genome digestion. This study used the GBS method to generate 46,594 SNPs from the genome, and 14,115 SNP markers were recognized to be considered effective markers for the construction of HDGM for Epimedium (Supplementary Table S5). The GC percentage of the sequencing dataset varied from 40.14 to 47.51% (Supplementary Table S4), which was higher than the values obtained from the five Epimedium (E. koreanum, E. pseudowushanense, E. lishihchenii, E. dolichostemon and E. acuminatum) chloroplast genomes (the average percentage of GC was 38.77%)1. This might be due to the diverse sources of DNA sequences analysed. Moreover, the GBS sequencing results generated an abundance of genomic information for the species Epimedium, which precisely reflects its genomic traits. These results indicate that the GBS approach is a viable method for genotyping and marker generation, which could be adapted in HDGM construction of Epimedium.
Construction of the HDGM of Epimedium
High-density consensus genetic maps are a prerequisite for QTLs to identify tightly linked molecular markers and the location of genes that control quantitative traits and are useful for MAS breeding . The HDGM also provides information about the genome of the assessed population and facilitates recombination landscape analysis within species . Although the consistency of the HDGM is important, there is currently no map available for Epimedium. Epimedium species have an outbreeding system and lack an internal barrier to hybridization (high incompatibility and crossover ability) , and perennial plants are more complicated to construct HDGM than homozygous annual herbaceous plants due to their lengthy generation spacing and high heterozygosity [30, 31]. In this study, an F1 family generated from a hybrid between E. leptorrhizum and E. sagittatum was employed to develop Epimedium HDGM. We used the GBS protocol to generate abundant SNPs and utilized the Epimedium genome to call SNPs. The number of molecular markers in the HDGM is one of the important indicators to assess its quality . Since the construction of the first genetic map, most genetic maps have been based on traditional markers such as simple sequence repeats (SSRs), the number of available markers is small, and their mapping resolution accuracy is limited . A total of 14,115 SNP markers were detected, of which 5,271 were mapped on the first consensus HDGM of Epimedium, and the mean distance between markers was 0.61 cM (Fig. 2; Table 1). Compared with the linkage map constructed based on traditional markers (e.g., SSR), the Epimedium consensus HDGM added more than 3,000 markers, and the mean marker distance was reduced by 10.21 cM (the shortest average distance between traditional markers is 10.82 cM) . Haplotype maps, the integrity of mapping individuals on the HDGM, and collinearity were used to assess HDGM reliability [14, 32]. The haplotype maps and the integrity of the individuals on the HDGM and the collinearity revealed that the high-density SNPs were accurately arranged within LGs (Supplementary Figs. S4-S6), which indicated the consistency of the HDGM. The consensus HDGM is the first Epimedium high-accuracy map with a large number of SNP markers, suitable distance, high resolution, and balanced various Epimedium HDGM indices, which can be used to identify QTLs for important Epimedium traits.
The F1 cross-pollinated (CP) model differs from the backcross, recombinant inbred lines, and double haploid populations used for mapping. The MapQTL program with interval mapping (IM) is appropriate technology for performing QTL evaluation in the CP model , and it has been effectively used in various species, such as pepper  and goji berry . QTL mapping analysis for secondary metabolite and leaf size-related traits using HDGM is an effective prediction method for quantitative trait mapping . Although specific secondary metabolites have important medicinal and commercial value, few QTLs related to modifying secondary metabolite content in Epimedium have been identified. Epimedin C is a glycosylated kaempferol derivative, and it is known that most GT proteins are related to glycosylation in plant secondary metabolism [33, 34]. Using QTL analysis, we evaluated two Epimedium secondary metabolite traits and discovered that EC had a significant correlation with its genetic variation. The identification of 31 stable QTLs associated with EC varied in both their proportion of phenotypic variance explained and significance, indicating that the content of EC in Epimedium is affected by quantitative genetics (Fig. 3 and Supplementary Table S8). These results are in line with genetic analyses of metabolites in eucalyptus  and hops . However, only one stable QTL for the TFC trait on LG5 was discovered (Fig. 4 and Supplementary Table S8). The identification of only one TFC related QTL site might be due to TFC being composed of multiple compounds or to slight variations in the TFC among the mapping populations.
Leaf size affects plant biomass  and is also an essential economic trait of Epimedium, and the leaves are the major organs used as Epimedium medicinal herbs . QTLs have been successfully used to discover candidate genes for plant leaf traits, including those of goji berry , grape  and wolfberry . In the three years, 12 stable QTLs for LL were discovered, with LG3 and LG5 regarded as hotspot locations for LL-related traits (Fig. 5 and Supplementary Table S8). In addition, we observed one LA related QTL in LG3 and LG5 (Fig. 6 and Supplementary Table S8). A significant correlation was found between LL and LA, and it is interesting that we also observed a colocalization phenomenon in LG3, although there was only one marker for this locus. Additionally, QTLs corresponding to LA and LL shared common positions on LG3 and LG5 throughout the three years. The colocalization of traits associated with QTLs usually reflects dual genomic regions in addition to positive significant correlations among different traits . Colocalization among different traits has also been found in other species, such as the fruit diameter and pericarp thickness of peppers, which have three common locations on the genetic map . In addition, LL, LA, fruit length, and leaf diameter of goji berries have also been observed to colocalize , indicating that the colocalization phenomenon of QTLs for various traits discovered in the common genomic area may be due to linkage or pleiotropy [38, 14]. In Epimedium, these markers might be used for leaf size and flavonoid content related trait breeding.
Materials and methods
Mapping population sampling
To construct an HDGM, E. leptorrhizum (female) and E. sagittatum (male) with significant differences in flavonoid content and leaf size were used as the hybrid parents. E. sagittatum, flowers white or yellow, ca. 8 mm or less in diam; yellow petals; leaflets ovate to ovate-lanceolate, 5–19 × 3–8 cm. E. leptorrhizum, flowers white, tinged with rose or deep rose, large, 3.5-4 cm in diameter; leaflets narrowly ovate or ovate, 3–10 × 2–5 cm (Fig. 1). The TFC of the male parent was higher than that of the female parent, and the content of EC was lower (Fig. 1). The hybrid parents were discovered in the field and cultivated in Wuhan Botanical Garden. In February-April 2017, a cross between E. leptorrhizum and E. sagittatum produced 109 hybrid seedlings. Hybrid seedlings were cultivated in a common garden with the hybrid parents for two years. To determine the purity of the offspring, four pairs of EST-SSR primers (Supplementary Fig. S7a) with amplified homozygous bands in the parents and hybrid progenies were used. Genotyping results showed that all 109 progenies were true hybrids and were used for subsequent analysis (Supplementary Fig. S7b). Every year from 2019 to 2021, the leaf tissues of the 109 F1 offspring plants and the two parents were sampled at the flowering stage and then frozen and stored at -80 °C for future evaluation.
Extraction of flavonoids and analysis
The leaves of the 109 F1 hybrid seedlings and the two parents were dried in the shade. The dried leaves were ground into powder in a mortar with liquid N2 and then filtered with a 50-mesh sieve. Five milliliters of EtOH-H2O (70:30, v/v) was used for every 0.05 g of powder, and then the solution was filtered with a 0.22-micron membrane. The EC was analysed by HPLC using a previously described method . All analyses were repeated three times using the identical HPLC system.
The TFC was examined according to the colorimetric method . In a microtiter tube, six milliliters of pure water were added to one milliliter of sample solution or standard catechin solution. After adding 300 µl of 5% NaNO2, the mixture was incubated for five minutes. Afterwards, 450 µl of 10% AlCl3 was added, and the mixture was allowed to stand for five minutes before adding three milliliters of one mole of NaOH and reacting for 30 min at room temperature. A spectrophotometer (Bio Tek Instruments, Winooski, VT, USA) was then used to measure the absorbance at 510 nanometers. The TFC was determined in milligrams of catechin equivalent (CAE) per gram of dried Epimedium powder (mg CAE/g).
Phenotypic data analysis
From 2019 to 2021, the LL and LA of the 109 F1 hybrid seedlings and two parents were measured from fresh leaves during the annual flowering period (mid-April) using LA-S software (Hangzhou Wanshen Detection Technology Co., Ltd.). All measurements were performed five times to guarantee the reliability of the results.
DNA extraction, library construction and sequencing
Using a modified cetyltrimethylammonium bromide (CTAB) method , DNA was extracted, and the DNA produced was evaluated using agarose gel electrophoresis. Our GBS libraries of the 111 genomic DNA samples were constructed using the previously described protocol . MseI and SacI were used to digest 200 nanograms of DNA from each sample for an hour at 37 °C. After adapter ligation, the fragments were amplified with KOD-Plus-Neo (TOYOBO., LTD., Life Science Department OSAKA JAPAN) using the two sequencing primers. Thereafter, the fragments were separated using a 2% agarose cartridge to capture a narrow distribution range of 380–480 bp and sequenced using 150 bp paired-end reads on the Illumina HiSeqTM 2500 platform (Illumina, Inc. ; San Diego, CA, US).
Genotyping and SNP identification
For quality control, the sequencing data were analysed using FASTP (V. 0.20.1) tool . Poly-G and poly-X read tails and reads with lengths < 15 bp were discarded. Using the BWA software package (v.0.7.17) , the filtered clean reads were aligned to the E. sagittatum genome. Then, the screened SNPs were divided into six LGs by mapping the locations on the E. sagittatum genome. Finally, mapping was conducted using read pairs with a single unique location in the E. sagittatum genomes. Haplotype Caller in GATK (v.188.8.131.52)  was used to find SNPs and inserts, and the variants were filtered. The remaining SNPs were then coded based on the division patterns ef×eg, hk×hk and lm×ll.
HDGM construction and evaluation
JoinMap 5  was used for HDGM construction under cross-pollinator (CP) patterns. The HDGM was developed using the regression mapping technique (Rec = 0.40, LOD > 1.0, Jump = 5, and ripple = 1). The markers of each LG were sorted using Kosambi’s mapping function, and HDGM distances were calculated in centimorgans (cM). Collinearity analysis and a haplotype map were used to assess the quality of the HDGM [46, 47]. The haplotype map  and collinearity analysis methods  were evaluated according to a previously described protocol.
QTL analyses were conducted on three consecutive years for two leaf size (LL and LA) traits and two flavonoid content (EC and TFC) related traits using MapQTL®v6.0 software , which employed the interval mapping (IM) method to evaluate QTL loci among 6 LGs for the HDGM. The LOD score significance threshold for each trait was assessed using a permutation test, and the IM model was used to search for potential QTLs on each LG. A QTL detected in all three years was defined as a stable QTL .
The analysis of variance, Pearson correlation, and frequency distribution were conducted using SPSS v. 25 (SPSS Inc., Chicago, IL, United States). The significance level was established at p < 0.05 for a two-tailed correlation test. The delineation result graph was generated using GraphPad Prism 9.0.0 software (GraphPad Software, Inc.).
The datasets generated or analysed during this study are included in this article (and its Additional file) or are available from the corresponding author on reasonable request. All raw data were submitted to the NCBI Sequence Read Archive: BioProject ID PRJNA910928.
Analysis of variance
Coefficient of variation
Expressed sequence tags- simple sequence repeat
Genotyping by sequencing
High-density genetic map
High-performance liquid chromatography
Logarithm of odds
Quantitative trait loci
Single nucleotide polymorphism
Total flavonoid content
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We thank the staff members of the Medicinal Plant Resources Group, Wuhan Botanical Garden, Chinese Academy of Sciences for field and technical support. The authors are grateful for the funding support. We also thank the two anonymous reviewers for their useful comments on an early version of this manuscript.
This research was supported by the National Natural Science Foundation of China (31670346, 32071675, 32270403), Biological Resources Programme, Chinese Academy of Sciences (KFJ-BRP-007-016), Key Scientific Research Talents Project of Wuhan Botanical Garden, Chinese Academy of Sciences (Y855281A05), and Wuhan Science and Technology Plan Project (2019020701011435).
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Yu, D., Huang, R., Yu, S. et al. Construction of the first high-density genetic linkage map and QTL mapping of flavonoid and leaf-size related traits in Epimedium. BMC Plant Biol 23, 278 (2023). https://0-doi-org.brum.beds.ac.uk/10.1186/s12870-023-04257-0
- Genetic linkage map
- Leaf size
- Epimedin C