Multiomics comparison among populations of three plant sources of Amomi Fructus

Amomi Fructus (Sharen, AF) is a traditional Chinese medicine (TCM) from three source species (or subspecies) including Wurfbainia villosa var. villosa (WVV), W. villosa var. xanthioides (WVX) or W. longiligularis (WL). Among them, WVV has been transplanted from its top-geoherb region Guangdong to its current main production area Yunnan for more than 50 years in China. However, the genetic and transcriptomic differentiation among multiple AF source (sub)species and between the origin and transplanted populations of WVV is unknown. In our study, the observed overall higher expression of terpenoid biosynthesis genes in WVV than that of WVX supplied possible evidence for the better pharmacological effect of WVV. We also screened ten candidate borneol dehydrogenase (BDH) genes that potentially catalyzed borneol into camphor in WVV. The BDH genes may experience independent evolution after acquiring the ancestral copies and the followed tandem duplications might account for the abundant camphor content in WVV. Furthermore, four populations of WVV, WVX and WL are genetically differentiated and the gene flow from WVX to WVV in Yunnan contributed to the increased genetic diversity in the introduced population (WVV-JH) compared to its top-geoherb region (WVV-YC), which showed the lowest genetic diversity and might undergo genetic degradation. In addition, TPS and BDH genes were selected among populations of multiple AF source (sub)species and between the top-geoherb and non-top-geoherb regions, which might explain the metabolite difference of these populations. Our findings provide important guidance for the conservation, genetic improvement, industrial development of the three source (sub)species, and identifying top-geoherbalism with molecular markers and proper clinical application of AF.

[1]  P. Yang,et al.  Chromosome-level genome assembly and functional characterization of terpene synthases provide new insights into the volatile terpenoid biosynthesis of Wurfbainia villosa. , 2022, The Plant journal : for cell and molecular biology.

[2]  Yan Liu,et al.  The sage genome provides insight into the evolutionary dynamics of diterpene biosynthesis gene cluster in plants. , 2022, Cell reports.

[3]  Xiaopu Yin,et al.  Transcriptome analysis reveals regulation mechanism of methyl jasmonate-induced terpenes biosynthesis in Curcuma wenyujin , 2022, PloS one.

[4]  Qing Dong,et al.  The Chromosome-Scale Assembly of the Curcuma alismatifolia Genome Provides Insight Into Anthocyanin and Terpenoid Biosynthesis , 2022, Frontiers in Plant Science.

[5]  D. Zhang,et al.  Allele-aware chromosome-level genome assembly of Artemisia annua reveals the correlation between ADS expansion and artemisinin yield. , 2022, Molecular plant.

[6]  David E. Hufnagel,et al.  A Chromosome-Level Genome of the Camphor Tree and the Underlying Genetic and Climatic Factors for Its Top-Geoherbalism , 2022, Frontiers in Plant Science.

[7]  P. Yang,et al.  Genome-Wide Identification of BAHD Superfamily and Functional Characterization of Bornyl Acetyltransferases Involved in the Bornyl Acetate Biosynthesis in Wurfbainia villosa , 2022, Frontiers in Plant Science.

[8]  D. Sankoff,et al.  Two divergent haplotypes from a highly heterozygous lychee genome suggest independent domestication events for early and late-maturing cultivars , 2022, Nature Genetics.

[9]  P. Pati,et al.  Plant Secondary Metabolite Transporters: Diversity, Functionality, and Their Modulation , 2021, Frontiers in Plant Science.

[10]  M. Newman,et al.  A Draft Genome of the Ginger Species Alpinia nigra and New Insights into the Genetic Basis of Flexistyly , 2021, Genes.

[11]  Q. Xia,et al.  Haplotype-resolved genome of diploid ginger (Zingiber officinale) and its unique gingerol biosynthetic pathway , 2021, Horticulture Research.

[12]  T. Marquès-Bonet,et al.  Ancient and modern genomes unravel the evolutionary history of the rhinoceros family , 2021, Cell.

[13]  Zhimin Zhao,et al.  Geographical origin discrimination of Amomi fructus using an ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry-based metabolomics approach combined with antioxidant activity analysis , 2021 .

[14]  D. Ro,et al.  The Taxus genome provides insights into paclitaxel biosynthesis , 2021, Nature Plants.

[15]  Lei Shi,et al.  The chromosome-based lavender genome provides new insights into Lamiaceae evolution and terpenoid biosynthesis , 2021, Horticulture research.

[16]  Heng Li,et al.  Haplotype-resolved de novo assembly using phased assembly graphs with hifiasm , 2021, Nature Methods.

[17]  Xin Hu,et al.  Constructing a Core Collection of the Medicinal Plant Angelica biserrata Using Genetic and Metabolic Data , 2020, Frontiers in Plant Science.

[18]  P. Su,et al.  Molecular cloning and functional identification of a high-efficiency (+)-borneol dehydrogenase from Cinnamomum camphora (L.) Presl. , 2020, Plant physiology and biochemistry : PPB.

[19]  Vineet K. Sharma,et al.  Genome sequencing of turmeric provides evolutionary insights into its medicinal properties , 2020, Communications Biology.

[20]  Menghua Wu,et al.  The scientific elucidation of daodi medicinal materials , 2020, Chinese Medicine.

[21]  B. M. Lange,et al.  Crop Wild Relatives as Germplasm Resource for Cultivar Improvement in Mint (Mentha L.) , 2020, Frontiers in Plant Science.

[22]  J. Flores,et al.  A Review of the Ephedra genus: Distribution, Ecology, Ethnobotany, Phytochemistry and Pharmacological Properties , 2020, Molecules.

[23]  Chase M Mason,et al.  Impact of genome duplication on secondary metabolite composition in non-cultivated species: A systematic meta-analysis. , 2020, Annals of botany.

[24]  C. Buell,et al.  Genome sequencing of four culinary herbs reveals terpenoid genes underlying chemodiversity in the Nepetoideae , 2020, DNA research : an international journal for rapid publication of reports on genes and genomes.

[25]  D. Qiu,et al.  Melatonin-mediate acid rain stress tolerance mechanism through alteration of transcriptional factors and secondary metabolites gene expression in tomato. , 2020, Ecotoxicology and environmental safety.

[26]  M. Raza,et al.  Transcriptional Factors Regulate Plant Stress Responses Through Mediating Secondary Metabolism , 2020, Genes.

[27]  Yuan Yuan,et al.  Molecular Pharmacognosy in Daodi herbs , 2020 .

[28]  Xiaofeng Liu,et al.  The MYB transcription factor CiMYB42 regulates limonoids biosynthesis in citrus , 2020, BMC Plant Biology.

[29]  Ling Li,et al.  Genome-wide investigation of WRKY transcription factors in sweet osmanthus and their potential regulation role in aroma synthesis. , 2019, Tree physiology.

[30]  Jinpu Jin,et al.  PlantRegMap: charting functional regulatory maps in plants , 2019, Nucleic Acids Res..

[31]  Steven L Salzberg,et al.  Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype , 2019, Nature Biotechnology.

[32]  Thomas Peterson,et al.  Benchmarking transposable element annotation methods for creation of a streamlined, comprehensive pipeline , 2019, Genome Biology.

[33]  Hui Ao,et al.  Comparison of Volatile Oil between the Fruits of Amomum villosum Lour. and Amomum villosum Lour. var. xanthioides T. L. Wu et Senjen Based on GC-MS and Chemometric Techniques , 2019, Molecules.

[34]  P. Bork,et al.  Interactive Tree Of Life (iTOL) v4: recent updates and new developments , 2019, Nucleic Acids Res..

[35]  Hui Wang,et al.  Comparison of the Active Compositions between Raw and Processed Epimedium from Different Species , 2018, Molecules.

[36]  M. Li,et al.  An Integrative Volatile Terpenoid Profiling and Transcriptomics Analysis for Gene Mining and Functional Characterization of AvBPPS and AvPS Involved in the Monoterpenoid Biosynthesis in Amomum villosum , 2018, Front. Plant Sci..

[37]  J. Richardson,et al.  Convergent morphology in alpinieae (Zingiberaceae): Recircumscribing amomum as a monophyletic genus , 2018 .

[38]  Huan Wang,et al.  RNA sequencing on Amomum villosum Lour. induced by MeJA identifies the genes of WRKY and terpene synthases involved in terpene biosynthesis. , 2018, Genome.

[39]  Yan Zhang,et al.  Comparison of Chemical Profiles, Anti-Inflammatory Activity, and UPLC-Q-TOF/MS-Based Metabolomics in Endotoxic Fever Rats between Synthetic Borneol and Natural Borneol , 2017, Molecules.

[40]  B. Fu,et al.  Borneol, a novel agent that improves central nervous system drug delivery by enhancing blood–brain barrier permeability , 2017, Drug delivery.

[41]  Guang-Huey Lin,et al.  Borneol Dehydrogenase from Pseudomonas sp. Strain TCU-HL1 Catalyzes the Oxidation of (+)-Borneol and Its Isomers to Camphor , 2016, Applied and Environmental Microbiology.

[42]  M. Gautier,et al.  rehh 2.0: a reimplementation of the R package rehh to detect positive selection from haplotype structure , 2016, bioRxiv.

[43]  Daisy E. Pagete An end-to-end assembly of the Aedes aegypti genome , 2016, 1605.04619.

[44]  Q. Wang,et al.  Metabolic engineering of terpene biosynthesis in plants using a trichome‐specific transcription factor MsYABBY5 from spearmint (Mentha spicata) , 2016, Plant biotechnology journal.

[45]  Zhonghua Liu,et al.  Molecular cloning and functional identification of a novel borneol dehydrogenase from Artemisia annua L. , 2015 .

[46]  Jing-zheng Song,et al.  Distinguishing Radix Angelica sinensis from different regions by HS-SFME/GC-MS. , 2015, Food chemistry.

[47]  Björn Usadel,et al.  Trimmomatic: a flexible trimmer for Illumina sequence data , 2014, Bioinform..

[48]  Yi-Bo Luo,et al.  Comparison of hypoglycemic and antioxidative effects of polysaccharides from four different Dendrobium species. , 2014, International journal of biological macromolecules.

[49]  Wei Shi,et al.  featureCounts: an efficient general purpose program for assigning sequence reads to genomic features , 2013, Bioinform..

[50]  Heng Li Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM , 2013, 1303.3997.

[51]  Zerihun A. Demissie,et al.  Molecular cloning and functional characterization of borneol dehydrogenase from the glandular trichomes of Lavandula x intermedia. , 2012, Archives of biochemistry and biophysics.

[52]  J. Dekker,et al.  Hi-C: a comprehensive technique to capture the conformation of genomes. , 2012, Methods.

[53]  Ruoting Zhan,et al.  Characterization and functional analysis of the genes encoding 1-deoxy-d-xylulose-5-phosphate reductoisomerase and 1-deoxy-d-xylulose-5-phosphate synthase, the two enzymes in the MEP pathway, from Amomum villosum Lour , 2012, Molecular Biology Reports.

[54]  Ruoting Zhan,et al.  Characterization and functional analysis of the genes encoding 1-deoxy-d-xylulose-5-phosphate reductoisomerase and 1-deoxy-d-xylulose-5-phosphate synthase, the two enzymes in the MEP pathway, from Amomum villosum Lour , 2012, Molecular Biology Reports.

[55]  H. Hong,et al.  Research of Chinese Drug Mahuang on its Resources and Quality Evaluation , 2012 .

[56]  A. Murphy,et al.  Tobacco nicotine uptake permease (NUP1) affects alkaloid metabolism , 2011, Proceedings of the National Academy of Sciences.

[57]  Gonçalo R. Abecasis,et al.  The variant call format and VCFtools , 2011, Bioinform..

[58]  Hu-Biao Chen,et al.  Comparison of contents of five ephedrine alkaloids in three official origins of Ephedra Herb in China by high-performance liquid chromatography , 2011, Journal of Natural Medicines.

[59]  M. DePristo,et al.  The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. , 2010, Genome research.

[60]  S. Ben-Shabat,et al.  Composition and stereochemistry of ephedrine alkaloids accumulation in Ephedra sinica Stapf. , 2010, Phytochemistry.

[61]  Gonçalo R. Abecasis,et al.  The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..

[62]  Janet M Thornton,et al.  The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative. , 2009, Chemico-biological interactions.

[63]  Yang Lu,et al.  [Study on natural borneol and synthetic borneol affecting mucosal permeability of gardenia extract]. , 2009, Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.

[64]  S. Horvath,et al.  WGCNA: an R package for weighted correlation network analysis , 2008, BMC Bioinformatics.

[65]  B. Persson,et al.  Medium- and short-chain dehydrogenase/reductase gene and protein families , 2008, Cellular and Molecular Life Sciences.

[66]  Sofia M. C. Robb,et al.  MAKER: an easy-to-use annotation pipeline designed for emerging model organism genomes. , 2007, Genome research.

[67]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.

[68]  P. Shannon,et al.  Cytoscape: a software environment for integrated models of biomolecular interaction networks. , 2003, Genome research.

[69]  P. Donnelly,et al.  Inference of population structure using multilocus genotype data. , 2000, Genetics.

[70]  OUP accepted manuscript , 2021, Journal of Pharmacy and Pharmacology.

[71]  Mosè Manni,et al.  BUSCO: Assessing Genome Assembly and Annotation Completeness. , 2019, Methods in molecular biology.

[72]  Jie Song,et al.  Pharmacology and Clinical Application of Plants in Epimedium L. , 2016 .

[73]  J. Brinckmann Geographical Indications for Medicinal Plants:Globalization, Climate Change, Quality and MarketImplications for Geo-Authentic Botanicals , 2015 .

[74]  Zhang Ya-qi Study on Volatile Constitutions and Quality Evaluation of Different Varieties of Fructus Amomis , 2010 .

[75]  F. Qin,et al.  Comparative studies on bioactivities of Yunnan introduced Amomum villosum and Amomum villosum , 2004 .

[76]  He Chuns Investigation Report on the Production and Market of Amomum villosum Lour. , 2003 .