Search Results (437)

Globba spp. is a perennial herbaceous plant of the Zingiberaceae family, characterized by its unique floral architecture and diverse coloration with high ornamental and medicinal value. However, research on the genetic basis of Globba is still insufficient, and only a limited number of molecular markers have been developed so far, which has greatly hampered the progress of its molecular breeding. Herein, we performed the first deep identification of genome-wide SSR markers based on the whole-genome data of G. sherwoodiana. A total of 276,809 SSR loci were identified with an average density of 189.24–297.49 SSRs/Mb within each chromosome. Mononucleotide repeat loci were most abundant, accounting for 58.95% of all SSRs, with dinucleotide and trinucleotide repeats accounting for 19.83% and 19.27%, respectively. Using G. sherwoodiana ‘MJ16’ and G. winitii C.H. Wright as parental lines, we constructed a hybrid F₁ population containing 173 individual plants. The coefficient of variation (CV) of the 10 phenotypic traits ranged from 13.09% to 27.43%, exhibiting a normal distribution. Phenotypic traits including terminal leaf width, inflorescence length, inflorescence width, secondary-inflorescence pedicel length, number of ornamental bracts, and basal inflorescence-bract length showed abundant variation, with all CV values exceeding 20%. Moreover, 27 polymorphic genomic SSRs (gSSR) were screened from the synthesized 192 primer pairs, amplifying a total of 203 alleles. On average, each marker detected 7.52 polymorphic loci, with a mean effective allele number of 3.63 and a mean polymorphism information content of 0.64, reflecting a relatively rich genetic diversity within the population. Through phenotype–marker association analysis, six gSSR loci were found to be significantly associated with six phenotypic traits. The highest interpretation ratio (16.86%) was observed for basal inflorescence-bract width. Three loci (gSSR48, gSSR105 and gSSR184) were simultaneously associated with more than two phenotypic traits, indicating a pattern consistent with pleiotropy or linkage. The informative gSSR markers and the association analysis results in this study provide an effective theoretical basis for germplasm identification, genetic diversity evaluation, and marker-assisted breeding of Globba. Full article

In this study, whole-genome resequencing was performed on the cold-tolerant variety ND-6 and the cold-sensitive variety ‘Sorbonne’. After evaluation, the Lilium davidii var. unicolor reference genome was selected to analyze SSR distribution characteristics. Whole-genome InDel identification and comparative analysis were conducted for the two varieties, yielding 34,812,909 and 24,497,857 InDels, respectively. Short InDels were predominant, with deletions slightly outnumbering insertions, mostly located in intergenic regions. Twenty pairs of SSR primers were screened and synthesized. Among them, 10 pairs amplified clearly, with a polymorphism rate of 82.6%, effectively distinguishing the two cultivars examined in this study. This study provides systematic data and a reliable marker resource for the analysis of lily genomic variation, laying a foundation for the identification of cold-tolerant germplasm; validation across additional cultivars and individuals will be required to extend their utility to broader germplasm. Full article

The FMD is an endangered species under first-class national protection in China. Comparative genomic investigation of microsatellite (SSR) in CDS may provide insights into adaptive evolutionary mechanisms and may inform conservation management strategies for captive populations. Here, we analyzed the FMD genome alongside five closely related ruminants: cattle (Bos taurus), red deer (Cervus elaphus), white-tailed deer (Odocoileus virginianus), sheep (Ovis aries), and goat (Capra hircus). Through genome-wide bioinformatic identification, we systematically compared the abundance, density, structural categories, repeat motifs, chromosomal distribution, and pathway enrichment analysis of SSR-containing genes in CDS. Furthermore, we performed synteny analysis and evaluated population genetic diversity. A total of 2509 SSRs in CDS were identified in the FMD, with a relative density of 62.61 loci/Mb. Trinucleotide SSRs were overwhelmingly dominant (88.46%) in the FMD. Notably, the FMD exhibited the highest relative abundances of both tetranucleotide and pentanucleotide repeats among the six species (2.37 and 2.18 loci/Mb, respectively), with pentanucleotide abundance approximately 5.6- to 9.1-fold higher than that of the other species. Chromosomal mapping revealed the highest SSR density in CDS regions on chromosome 27, while SSR-containing genes exhibited a heterogeneous pattern characterized by localized clustering. Synteny analysis demonstrated relatively conserved syntenic relationships between the FMD and goat, sheep, and cattle, with moderate conservation also observed with red deer and white-tailed deer, suggesting that SSR-containing genes in ruminants may remain highly conserved during chromosomal rearrangements. GO and KEGG analyses indicated that SSR-containing genes across all species were predominantly enriched in transcriptional regulation, RNA processing, and signal transduction pathways. Specifically, the FMD showed enrichment patterns associated with hypoxia response, mRNA processing, and epigenetic regulation, which may reflect lineage-specific transcriptional patterns, though the functional involvement of these SSRs remains to be experimentally validated. In addition, the five primer pairs screened in this study exhibited high polymorphism, with a mean polymorphism information content (PIC) of 0.93. The observed heterozygosity (Ho) was significantly lower than the expected heterozygosity (He), and the mean inbreeding coefficient (FIS) was 0.57, indicating heterozygote deficiency and an elevated risk of inbreeding in this captive FMD population. Collectively, our findings provide preliminary insights into the conserved patterns of microsatellite evolution and lineage-specific divergence in ruminants, offering a reference framework for comparative genomics and adaptive evolution research, as well as practical molecular markers for genetic management of captive populations. Full article

Euonymus alatus is a species of medicinal and ornamental value, yet high-quality chloroplast genome resources for this taxon remain scarce. The complete chloroplast genome of E. alatus was assembled and compared with 15 congeneric species to investigate genomic structure and evolutionary dynamics. The genome is 157,416 bp with a GC content of 37.3%, containing 131 genes and 156 repeats (67 tandem repeats, 49 dispersed repeats, and 40 SSRs). Divergence was concentrated in non-coding regions, with 14 hypervariable regions identified as potential markers. IR expansion occurred independently in E. fortunei and E. japonicus, while no genome-wide inversions were detected. 11 protein-coding genes were identified under positive selection, among which clpP exhibited the strongest signal, suggesting a possible role in adaptive evolution. Codon usage bias analysis revealed that both mutation pressure and natural selection shape codon usage patterns, with the latter playing a relatively prominent role; 17 optimal codons were identified. Phylogenetic analysis strongly supported E. alatus as sister to E. phellomanus. This study provides a valuable genomic resource for species authentication, phylogenetic revision, and breeding in this genus. Full article

Background: Clematis tangutica (Maxim.) Korsh. is a Tibetan medicinal plant, but its chloroplast genome and plastid gene evolution remain unexplored. Here, we assembled the complete chloroplast genome of C. tangutica and investigated the adaptive evolution of the ycf2 gene. Methods: Chloroplast DNA was extracted from fresh leaves and sequenced on the Illumina HiSeq PE150 platform. We then performed comprehensive genomic analyses, including genome structure characterization, repeat and SSR identification, comparative genomics, and positive selection analysis of the ycf2 gene. Results: The genome is 159,584 bp with a typical quadripartite structure, containing 134 genes and 23 SSRs. Comparative analyses revealed that ycf2 is the most variable gene among the 13 divergent loci identified. Positive selection analysis detected 12 significant sites in ycf2, all clustered in the middle region of the protein. Conclusions: This study provides the first complete chloroplast genome resource for C. tangutica, offers new insights into the adaptive evolution of ycf2 in Ranunculaceae, and yields molecular markers applicable to population genetics, phylogenetic studies, and conservation planning for this species of medicinal importance. Full article

Wild almond relatives are valuable reservoirs of allelic variation for crop improvement and conservation, yet Kazakhstan’s wild-almond genetic resources remain poorly characterised. We conducted an exploratory SSR assessment of 80 putative individuals from four taxon-locality groups (20 per group), each representing one sampled population: Prunus ledebouriana, P. tenella, P. petunnikowii, and P. spinosissima. Of 22 nuclear simple sequence repeat loci screened for cross-taxon transferability, 15 generated reproducible profiles and were retained; their even genome-wide distribution was not verified. Across the full dataset, the mean number of alleles was 3.55, the effective number of alleles was 2.62, expected heterozygosity (He) was 0.544, and 95.0% of loci were polymorphic. Missing genotypes ranged from 0.0% to 34.7% among groups, and six loci had at least 20% missing data. AMOVA attributed 76.5% of variation to within-group differences and 23.5% to among-group differences (PhiPT = 0.235, p = 0.001). PCoA, unbiased Nei distances, UPGMA, and descriptive Bayesian clustering separated the four sampled groups. A nine-locus sensitivity analysis that excluded the six high-missing loci retained P. spinosissima as the group with the highest mean He (0.699), whereas P. petunnikowii increased from 0.471 to 0.609. Thus, the low full-panel estimate for P. petunnikowii was not robust to missing data. Because taxon identity was fully confounded with locality and the marker panel was limited, the results are interpreted as a regional marker-transferability and methodological baseline rather than as species-wide or genome-wide inference. Full article

This study provides a genome-wide assessment of genetic diversity, fixation status, and population structure in 77 elite Korean popcorn (Zea mays L.) inbred lines using 100 SSR markers. The mean number of alleles per locus was 2.99, with an expected heterozygosity (He) of 0.373 and a mean polymorphic information content (PIC) of 0.321, indicating moderate but structured diversity within a relatively narrow breeding base. The low observed heterozygosity (Ho = 0.053) and high fixation index (F = 0.875) confirmed the advanced homozygosity of these inbred lines, although residual heterozygosity ranged from 2.00% to 12.12% among lines. Population structure analyses using Bayesian STRUCTURE (K = 2), principal coordinate analysis (PCoA), and UPGMA clustering consistently revealed two major genetic groups with substantial admixture and hierarchical substructure. Chromosome 6 exhibited complete fixation (F = 1.000), coinciding with previously reported popping-related QTL hotspots, thereby suggesting the possible role of directional selection during elite line development. For hybrid seed purity verification, 16–35 informative codominant SSR markers were identified for each F₁ hybrid combination, with umc2309 consistently polymorphic between the parental lines of all five tested commercial hybrid combinations. In addition, breeding-oriented subset optimization using PowerCore, CoreHunter, and their intersection retained 100% allele coverage while increasing the mean genetic distance by up to 16.0% and mean diversity indices by approximately 11%. These results demonstrate that redundancy within elite popcorn germplasm can be reduced without losing allelic representation, thereby improving parental discrimination, hybrid purity control, and breeding efficiency. Collectively, this study establishes a practical molecular framework for germplasm management, parental line discrimination, hybrid purity testing, and future popcorn breeding programs in South Korea. Full article

Background/Objectives: Ficus gasparriniana var. laceratifolia (H. Lév. & Vaniot) Corner is treated as a variety of F. gasparriniana and placed in Ficus subg. Ficus on morphological grounds, but complete plastome evidence for its plastid phylogenetic placement has been lacking. We assembled and analyzed its chloroplast genome to evaluate this morphology-based placement using plastid genomic evidence and to expand genomic resources for the genus. Methods: The plastome was assembled from paired-end reads using GetOrganelle and subsequently annotated. We characterized its genome architecture, simple sequence repeats (SSRs), codon-usage bias, inverted repeat (IR) junctions, and nucleotide diversity after standardizing sequence start positions and small single-copy (SSC) region orientation. Plastid phylogenetic relationships were inferred from four single-IR datasets: whole-plastome, coding, non-coding, and partitioned. Results: The 160,476-bp plastome exhibited the typical quadripartite structure and contained 110 unique genes. Its repeat composition and preference for A/U-ending codons were consistent with an AT-rich plastome, and 61 SSRs and five candidate variable regions represented potential marker resources for future Ficus studies. In all four phylogenetic datasets, F. gasparriniana var. laceratifolia was consistently grouped with F. pumila with maximum ultrafast bootstrap support (UFBoot = 100), conflicting with its morphology-based classification. Approximately unbiased (AU) tests rejected the sampled morphology-based constraint in every dataset, indicating that this morphology–plastid discordance was robust to dataset choice. Conclusions: This plastome provides a valuable genomic resource and reveals robust discordance between morphology-based classification and plastid phylogenetic placement. These findings provide a foundation for future nuclear-genomic and population-level tests of the alternative evolutionary scenarios underlying this discordance. Full article

Traditional Mediterranean grapevine landraces represent irreplaceable reservoirs of adaptive diversity, yet many regional germplasm pools remain poorly characterized, limiting conservation strategies and climate-resilient breeding. This study presents the first comparative genetic assessment of 154 local Vitis accessions from three historically interconnected but genomically underrepresented Mediterranean regions: Greece, Morocco, and Slovenia. Using 12 highly polymorphic nuclear SSR markers, we detected substantial genetic diversity (168 alleles; mean heterozygosity He = 0.881) with distinct regional signatures. Moroccan accessions exhibited the highest allelic richness and 11 private alleles, reflecting diverse agroecological adaptation. Slovenian germplasm formed a cohesive, genetically stable cluster with high effective allele numbers. Greek accessions exhibited the highest observed heterozygosity and 14 private alleles, consistent with the Aegean’s role as a major diversification hotspot. Despite >90% of variance occurring within individuals, AMOVA and pairwise FST (0.050–0.061) revealed low to moderate but significant geographic differentiation. Multivariate analyses (PCA, UPGMA) and Bayesian clustering (sNMF, K = 3) consistently resolved three regional genetic groups with varying admixture levels, consistent with a mosaic domestication model, as previously proposed for the Mediterranean basin, shaped by recurrent introductions, wild introgression, and region-specific selection. Our results show that peripheral Mediterranean germplasm harbors meaningful, regionally distinctive, substantial, non-redundant diversity not fully represented in surveys focused on climate adaptation, disease resistance breeding, and long-term genetic resource conservation. These findings challenge simplistic diffusion models and emphasize the strategic importance of geographically comprehensive sampling in grapevine conservation programs. Full article

The genus Aegilops comprises important wild relatives of cultivated wheat and represents a valuable genetic resource for wheat improvement. In this study, the complete chloroplast genomes of five Aegilops species (Ae. crassa, Ae. cylindrica, Ae. juvenalis, Ae. tauschii, and Ae. triuncialis) collected from Kazakhstan and Uzbekistan were sequenced, assembled, and comparatively analyzed. The chloroplast genomes exhibited a conserved quadripartite structure consisting of a large single-copy (LSC), a small single-copy (SSC), and two inverted repeat (IR) regions. Genome sizes ranged from 135,612 to 136,840 bp, with an identical GC content of 38% across all species. Comparative analyses revealed high structural conservation among chloroplast genomes, particularly within IR regions, whereas greater sequence divergence was observed in the non-coding regions of the LSC and SSC. Sliding-window analysis identified several highly polymorphic regions, including rpl32-trnL(UAG), ndhF-rpl32, trnC(GCA)-rpoA, psbA, and ndhD, which may serve as potential DNA barcodes and informative markers for phylogenetic studies. A total of 850 chloroplast simple sequence repeats (SSRs) were detected, predominantly A/T-rich mononucleotide repeats. Codon usage analysis demonstrated a conserved preference for A/U-ending codons across all species. Ka/Ks analysis indicated that most chloroplast protein-coding genes are under strong purifying selection, although relatively elevated evolutionary rates were detected in rpoA and ycf4. Phylogenetic analyses based on complete chloroplast genomes strongly supported sectional relationships within Aegilops and confirmed close maternal relationships among several species. Overall, this study provides chloroplast genome resources for Aegilops and contributes to understanding chloroplast genome evolution, phylogeny, and molecular marker development. Full article

Tomato (Solanum lycopersicum L.) is a globally important vegetable crop and a major dietary source of bioactive compounds, including lycopene, ascorbic acid, phenolics, and minerals. Modern tomato breeding has substantially improved yield, uniformity, and postharvest performance; however, these gains have often been accompanied by reduced flavor quality, lower nutritional value, and narrowing of the genetic base. This review synthesizes available evidence on Lithuanian tomato germplasm and evaluates its relevance for future breeding strategies aimed at enhancing genetic gain under Northern European conditions. The review integrates published data on genetic diversity, molecular characterization, morphological traits, fruit quality parameters, and yield performance of Lithuanian cultivars and hybrids developed in Lithuania. SSR-based studies indicate moderate genetic diversity, with mean expected heterozygosity of approximately 0.51 and mean PIC values of 0.47 in cultivars and 0.45 in hybrids, while also confirming a relatively narrow breeding pool. Lithuanian cultivars display substantial variation in fruit morphology, dry matter, soluble solids, firmness, lycopene, ascorbic acid, and yield. Traditional cultivars such as ‘Svara’, ‘Milžinai’, ‘Slapukai’, and ‘Balčiai’ show valuable nutritional and technological traits, whereas hybrids such as ‘Auksiai H’, ‘Adas H’, and ‘Ainiai H’ demonstrate improved productivity and firmness. The available evidence suggests persistent yield–quality trade-offs, particularly between productivity, soluble solids content, antioxidant accumulation, and postharvest performance. Although Lithuanian germplasm does not represent exceptionally broad genetic diversity, it contains regionally adapted material with stabilized trait combinations useful for breeding resilience, nutritional quality, and adaptation to temperate environments. Future progress will require broadening the genetic base and integrating traditional breeding with marker-assisted selection, genomic selection, GWAS, genome editing, multi-omics, and pangenomic approaches. Overall, Lithuanian tomato germplasm represents a locally adapted regional resource for translating genetic diversity into genetic gain in modern tomato breeding. Full article

(1) Background: Centella asiatica (L.) is a long-lived medicinal plant traditionally recognized for its wound-healing and anti-inflammatory properties. Despite the growing demand for diverse C. asiatica species in Korea, studies on genetic diversity remain limited. (2) Methods: Genome assembly data of C. asiatica from the NCBI database were utilized to develop genomic SSR markers. Genetic diversity and population structure were examined in 30 Korean native C. asiatica accessions using 90 SSR markers. (3) Results: Whole-genome sequencing revealed 376,751 SSR loci, from which 127,528 primer pairs were designed. Among 160 randomly selected primers, 90 showed consistent amplification and displayed high levels of polymorphism. Genetic analyses revealed that the MAF ranged from 0.15 to 1.00 (mean 0.55), the NA ranged from 1 to 15 (mean 5.6), the Ho ranged from 0.00 to 1.00 (mean 0.17), and the PIC values ranged from 0.00 to 0.88 (mean 0.52). Clustering analysis with 90 SSR markers revealed three clusters, whereas population structure analysis indicated two populations among the C. asiatica accessions. Furthermore, two minimum marker sets with five marker combinations were identified and proved useful to differentiate all C. asiatica accessions. (4) Conclusions: The newly developed SSR markers for C. asiatica hold promise for facilitating research endeavors pertaining to variety identification, genetic mapping, and marker-assisted selection. Full article

As pressures from climate change and global trade increase, developing cost-effective tools for origin tracking becomes essential to ensure the traceability and adaptability of forest reproductive material (FRM). Our objectives were (a) to test the efficiency of a set of nuclear microsatellite loci (nSSR) for revealing the genetic structures identified by high-input sequencing studies and (b) to verify this set of nSSR loci for genetic assignment of commercial seed lots into reference regions. We used 12 nSSR markers to genotype 220 trees from 11 populations representing the eastern Baltic, Scandinavian and southern European ranges of Norway spruce. The results showed that the populations from the eastern Baltic range had relatively higher allelic diversity parameters. The Bayesian clustering revealed a geographically consistent genetic structuring of Norway spruce populations by distinguishing the eastern Baltic from southern European and Scandinavian populations. GENECLASS analysis correctly assigned Lithuanian commercial seed lots into the Lithuanian reference region with markedly higher probability than to any other reference regions. Our study demonstrates promising results for origin identification of Norway spruce, particularly in contexts where high-resolution genomic approaches remain financially or logistically inaccessible. Full article

Sophora tonkinensis Gagnep. is an important medicinal shrub native to the karst regions of southwestern China, where long-term overharvesting and habitat fragmentation have markedly reduced wild resources. Although recent phytochemical, transcriptomic, and chloroplast genomic studies have improved understanding of this species, its maternally inherited population structure has remained unclear. To address this gap, we developed nine novel chloroplast simple sequence repeat (cpSSR) markers and used them to genotype 274 individuals from eighteen wild populations. A total of 41 alleles were detected, with 2–10 alleles per locus, indicating moderate to high polymorphism at the species level. By combining the nine cpSSR loci, we further identified 25 chlorotypes, including 19 private chlorotypes. Within-population chloroplast diversity was generally low, and five populations were monomorphic, whereas HJSE and LYNG retained comparatively high chlorotype diversity. Genetic differentiation among populations was extremely strong (mean FST = 0.808), whereas historical gene flow was very limited (Nm = 0.112), and AMOVA showed that 85% of total chloroplast variation occurred among populations. Taken together, chlorotype network analysis, chlorotype geographic distribution, UPGMA, PCoA, and exploratory STRUCTURE analysis supported three geographically structured chloroplast groups, indicating long-term restriction of seed-mediated dispersal across the fragmented karst landscape. These newly developed cpSSR markers and the derived chlorotype framework provide a practical basis for tracing maternal lineages, prioritizing conservation units, guiding ex situ germplasm sampling, and informing future breeding of this nationally protected species. Overall, the present results describe chloroplast-based maternal structure rather than total genome-wide diversity in S. tonkinensis. Full article

Background: The phylogenetic placement and chloroplast-inferred maternal relationships of commercial pluot cultivars remain unclear, largely because plastome-level evidence is limited for assessing their affinities with Prunus salicina and Prunus ussuriensis. Although chloroplast genome structure has been well characterized in angiosperms and in several Prunus species, complete plastome resources and comparative genomic evidence for commercial pluot cultivars remain scarce. Methods: Here, we assembled the complete chloroplast genomes of six commercial pluot cultivars and performed comparative genomic, phylogenomic, and divergence time analyses using representative Prunus species. Results: All genomes exhibited the typical circular quadripartite structure and ranged from 157,865 to 158,138 bp in length. Genome organization, GC content, and gene content were highly conserved, whereas the IR regions showed an elevated GC content of approximately 42.6%, owing to rRNA gene enrichment. IR boundary comparison revealed contraction at the IRb/SSC boundary in P. ussuriensis, while pluot cultivars were structurally more similar to P. salicina. In total, 370 SSR loci and four hypervariable regions, namely rpoB–trnC-GCA, petN–psbM, trnV-UAC–trnM-CAU, and trnP-UGG–psaJ, were identified as candidate molecular markers for Prunus germplasm identification and genetic analysis. Phylogenomic analysis resolved four major clades within Prunus and showed that ‘Flavor King’, ‘Flavor Supreme’, and ‘Flavor Queen’ grouped with P. ussuriensis, whereas ‘Flavorosa’, ‘Dinosaur Egg’, and ‘Flavorich’ grouped with P. salicina. Conclusion: Overall, this study provides the first comparative plastome analysis of six commercial pluot cultivars and offers chloroplast-level evidence for their maternal affinities within Prunus, together with useful marker resources for cultivar identification and germplasm evaluation. Full article