De novo assembly and Transcriptome characterization of an endemic species of Vietnam, Panax vietnamensis Ha et Grushv., including the development of EST-SSR markers for population genetics
0301 basic medicine
Population genetics
Evolutionary biology
Plant Science
Gene
Genetic diversity
Agricultural and Biological Sciences
Conservation, EST-SSRs
Sociology
Expressed Sequence Tags
Elicitor Signal Transduction for Metabolite Production
Allele
0303 health sciences
Ecology
Loss of heterozygosity
High-Throughput Nucleotide Sequencing
Molecular Mechanisms and Medical Applications of Ginseng
Life Sciences
FOS: Sociology
Habitat
Vietnam
Pharmacological Effects of Licorice Roots
Conservation genetics
Research Article
Gene Flow
Genetic Markers
Pharmacology, Toxicology and Pharmaceutics
Population
Panax
Endangered species
Molecular Mechanisms of Plant Development and Regulation
Meta-analysis in Ecology and Agriculture Research
03 medical and health sciences
Panax vietnamensis
Biochemistry, Genetics and Molecular Biology
Genetics
Molecular Biology
Biology
Ecology, Evolution, Behavior and Systematics
Genome-wide Analysis
Demography
Pharmacology
Gene Expression Profiling
Endangered Species
Botany
Genetic Variation
Microsatellite
Molecular Sequence Annotation
15. Life on land
Genetics, Population
QK1-989
FOS: Biological sciences
Transcriptome
Microsatellite Repeats
Panax Ginseng
DOI:
10.1186/s12870-020-02571-5
Publication Date:
2020-07-29T17:02:53Z
AUTHORS (6)
ABSTRACT
AbstractBackgroundUnderstanding the genetic diversity in endangered species that occur inforest remnants is necessary to establish efficient strategies for the species conservation, restoration and management.Panax vietnamensisHa et Grushv. is medicinally important, endemic and endangered species of Vietnam. However, genetic diversity and structure of population are unknown due to lack of efficient molecular markers.ResultsIn this study, we employed Illumina HiSeq™ 4000 sequencing to analyze the transcriptomes ofP. vietnamensis(roots, leaves and stems). Raw reads total of 23,741,783 was obtained and then assembled, from which the generated unigenes were 89,271 (average length = 598.3191 nt). The 31,686 unigenes were annotated in different databases i.e. Gene Ontology, Kyoto Encyclopedia of Genes and Genomes, Nucleotide Collection (NR/NT) and Swiss-Prot for functional annotation. Further, 11,343 EST-SSRs were detected. From 7774 primer pairs, 101 were selected for polymorphism validation, in which; 20 primer pairs were successfully amplified to DNA fragments and significant amounts of polymorphism was observed within population. The nine polymorphic microsatellite loci were used for population structure and diversity analyses. The obtained results revealed high levels of genetic diversity in populations, the average observed and expected heterozygosity were HO = 0.422 and HE = 0.479, respectively. During the Bottleneck analysis using TPM and SMM models (p < 0.01) shows that targeted population is significantly heterozygote deficient. This suggests sign of the bottleneck in all populations. Genetic differentiation between populations was moderate (FST = 0.133) and indicating slightly high level of gene flow (Nm = 1.63). Analysis of molecular variance (AMOVA) showed 63.17% of variation within individuals and 12.45% among populations. Our results shows two genetic clusters related to geographical distances.ConclusionOur study will assist conservators in future conservation management, breeding, production and habitats restoration of the species.
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