Analysis of complete chloroplast genome sequences and insight into the phylogenetic relationships of Ferula L.
Chloroplast genome
Comparative analysis
Ferula
Phylogenetic relationships
Journal
BMC genomics
ISSN: 1471-2164
Titre abrégé: BMC Genomics
Pays: England
ID NLM: 100965258
Informations de publication
Date de publication:
08 Sep 2022
08 Sep 2022
Historique:
received:
30
05
2022
accepted:
30
08
2022
entrez:
8
9
2022
pubmed:
9
9
2022
medline:
14
9
2022
Statut:
epublish
Résumé
Ferula L. is one of the largest and most taxonomically complicated genera as well as being an important medicinal plant resource in the family Apiaceae. To investigate the plastome features and phylogenetic relationships of Ferula and its neighboring genera Soranthus Ledeb., Schumannia Kuntze., and Talassia Korovin, we sequenced 14 complete plastomes of 12 species. RESULTS: The size of the 14 complete chloroplast genomes ranged from 165,607 to 167,013 base pairs (bp) encoding 132 distinct genes (87 protein-coding, 37 tRNA, and 8 rRNA genes), and showed a typical quadripartite structure with a pair of inverted repeats (IR) regions. Based on comparative analysis, we found that the 14 plastomes were similar in codon usage, repeat sequence, simple sequence repeats (SSRs), and IR borders, and had significant collinearity. Based on our phylogenetic analyses, Soranthus, Schumannia, and Talassia should be considered synonymous with Ferula. Six highly divergent regions (rps16/trnQ-UUG, trnS-UGA/psbZ, psbH/petB, ycf1/ndhF, rpl32, and ycf1) were also detected, which may represent potential molecular markers, and combined with selective pressure analysis, the weak positive selection gene ccsA may be a discriminating DNA barcode for Ferula species. Plastids contain abundant informative sites for resolving phylogenetic relationships. Combined with previous studies, we suggest that there is still much room for improvement in the classification of Ferula. Overall, our study provides new insights into the plastome evolution, phylogeny, and taxonomy of this genus.
Sections du résumé
BACKGROUND
BACKGROUND
Ferula L. is one of the largest and most taxonomically complicated genera as well as being an important medicinal plant resource in the family Apiaceae. To investigate the plastome features and phylogenetic relationships of Ferula and its neighboring genera Soranthus Ledeb., Schumannia Kuntze., and Talassia Korovin, we sequenced 14 complete plastomes of 12 species. RESULTS: The size of the 14 complete chloroplast genomes ranged from 165,607 to 167,013 base pairs (bp) encoding 132 distinct genes (87 protein-coding, 37 tRNA, and 8 rRNA genes), and showed a typical quadripartite structure with a pair of inverted repeats (IR) regions. Based on comparative analysis, we found that the 14 plastomes were similar in codon usage, repeat sequence, simple sequence repeats (SSRs), and IR borders, and had significant collinearity. Based on our phylogenetic analyses, Soranthus, Schumannia, and Talassia should be considered synonymous with Ferula. Six highly divergent regions (rps16/trnQ-UUG, trnS-UGA/psbZ, psbH/petB, ycf1/ndhF, rpl32, and ycf1) were also detected, which may represent potential molecular markers, and combined with selective pressure analysis, the weak positive selection gene ccsA may be a discriminating DNA barcode for Ferula species.
CONCLUSION
CONCLUSIONS
Plastids contain abundant informative sites for resolving phylogenetic relationships. Combined with previous studies, we suggest that there is still much room for improvement in the classification of Ferula. Overall, our study provides new insights into the plastome evolution, phylogeny, and taxonomy of this genus.
Identifiants
pubmed: 36076164
doi: 10.1186/s12864-022-08868-z
pii: 10.1186/s12864-022-08868-z
pmc: PMC9461113
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
643Subventions
Organisme : Taxonomic revision of polymorphic plant families of the flora of Uzbekistan
ID : FZ-20200929321
Organisme : The work was supported by the Third Xinjiang Scientific Expedition Program
ID : Grant No.2021xjkk0600
Organisme : the National Science and Technology Basic Program of China
ID : 2019FY100204
Organisme : the Shanghai cooperation organization partnership and international technology cooperation plan of science and technology projects
ID : 2021E01020
Organisme : Youth Innovation Promotion Association Foundation of the Chinese Academy of Sciences, China
ID : No. 2019429
Informations de copyright
© 2022. The Author(s).
Références
Pimenov MG, Leonov MV. The genera of the Umbelliferae: a nomenclator. Kew: Royal Botanic Gardens; 1993.
Sina AA. Kanon vrachebnoy nauki (Canon). In: Zaxidov TZ, editor. Book. 1. Tashkent: Academy of Sciences of the UzSSR; 1954. p. 549.
Shen GM. Chinese herbal medicine series: Ferula. Urumqi: Xinjiang people’s publishing house; 1986.
Nazari ZE, Iranshahi M. Biologically active sesquiterpene coumarins from Ferula species. Phytother Res. 2011;25(3):315–23.
pubmed: 21031633
doi: 10.1002/ptr.3311
Mahendra P, Bisht S. Ferula asafoetida: Traditional uses and pharmacological activity. Pharmacogn Rev. 2012;6(12):141–6.
pubmed: 23055640
pmcid: 3459456
doi: 10.4103/0973-7847.99948
Ajani Y, Ajani A, Cordes JM, Watson MF, Downie SR. Phylogenetic analysis of nrDNA ITS sequences reveals relationships within five groups of Iranian Apiaceae subfamily Apioideae. Taxon. 2008;57(2):383–401.
Kurzyna-Młynik R, Oskolski AA, Downie SR, Kopacz R, Wojewódzka A, Spalik K. Phylogenetic position of the genus Ferula (Apiaceae) and its placement in tribe Scandiceae as inferred from nrDNA ITS sequence variation. Plant Syst Evol. 2008;274(1–2):47–66.
doi: 10.1007/s00606-008-0022-2
Safina LK, Ostroumova TA, Pimenov MG. Carpology of the species of Ferula subgen. Merwia(Umbelliferae-Apioideae) and some taxonomic implications. Nord J Bot. 2015;33(2):140–50.
doi: 10.1111/j.1756-1051.2013.00315.x
Boissier PE. Flora orientalis sive, enumeratio plantarum in Oriente a Graecia et Aegypto ad Indiae fines hucusque observatae 2. Genève, Basel & Lyon: H.Georg; 1872. p. 1159.
Drude CGO. Umbelliferae. In: Engler A, Prantl K, editors. Die natürlichen Pflanzenfamilien, vol. 3. Leipzig: Verlag von Wilhelm Engelman (Druck von Breitkopf & Härtel in Leipzig); 1898. p. 63–250.
Korovin EP. Generis Ferula (Tourn.) L. monographia illustrata. Tashkent: Academiae Scientiarum UzRSS; 1947. p. 91.
Chamberlain DF, Rechinger KH. Ferula L. In: Hedge IC, Lamond JM, Rechinger KH, editors. Umbelliferae, Flora Iranica, vol. 162. Graz: Akademische Druck- und Verlagsanstalt; 1987. p. 387–426.
Safina LK, Pimenov MG. The carpoanatomical features of the species of the genus Ferula of the subgenus Peucedanoides (Apiaceae) in connection with the systematics of the genus. Bot Zhurn (Leningrad). 1983;68:730–9.
Safina LK, Pimenov MG. Feruly Kazakhstana. Alma-ata: Nauka Kazakhskoĭ SSR; 1984. p. 110.
Safina LK, Pimenov MG. Carpology of the species of type subgenus of the genus Ferula and some problems of their systematics. Feddes Repertorium. 2008;101(3–4):135–51.
Panahi M, Banasiak L, Piwczyński M, Puchałka R, Kanani MR, Oskolski AA, Modnicki D, Miłobędzka A, Spalik K. Taxonomy of the traditional medicinal plant genus Ferula (Apiaceae) is confounded by incongruence between nuclear rDNA and plastid DNA. Bot J Linn Soc. 2018;188(2):173–89.
doi: 10.1093/botlinnean/boy055
Ledebour CF, Bunge A, Meyer CA. Flora Altaica. Berolini: G. Reimeri; 1829. p. 197–206.
von Bunge A. Beitrag zur kenntniss der flor Russlands und der steppen Central-Asiens. St. Petersburg: Kaiserliche Akademie der Wissenschaften; 1851. p. 359.
Korovin EP. Ferula L. In: Schischkin BK, editor. Flora of the USSR. Moscow and Leningrad: Akad. nauk SSSR; 1951. p. 62–214.
She ML, Pu FD, Pan ZH, Watson MF, Cannon JFM, Holmes-Smith I, et al. Apiaceae (Umbelliferae). In: Wu ZY, Raven RH, editors. Flora of China. Beijing and St. Louis: Science Press and Missouri Botanical garden Press; 2005. p. 1–205.
Shen GM. Apiaceae (Umbelliferae). In: Shen GM, editor. Flora Xinjiangensis. Urumqi: Xinjiang Science & Technology Publishing House; 2011. p. 464–621.
Kuntze O. Plantae orientali-rossicae. Trudy Imp: S.-Peterburgsk. Bot. Sada. 1887;10:35–262.
Tojibaev KSh, Sennikov AN, Lazkov GA, Jang GG, Choi HJ, Chang KS, et al. Checklist of vascular plants of the Tian-Shan Mountain System. Pocheon: Korea National Arboretum; 2021. p. 607.
Korovin EP. The new genera and species of Umbelliferae from Kazakhstan flora. Trudy Instituta Botaniki: Akademiya Nauk Kazakhskoi SSR. 1962;13:242–62.
Pimenov MG, Kirillina NA. The carpology of Soranthus, Ladyginia, Eriosynaphe and Schumannia in connection with the problem of the taxonomic limits of the genus Ferula (Apiaceae). Botanicheskii Zhurnal. 1980;65:1756–66.
Govaerts R, Nic Lughadha E, Black N, Turner R, Paton A. The World Checklist of Vascular Plants, a continuously updated resource for exploring global plant diversity. Sci Data. 2021;8(1):215.
pubmed: 34389730
pmcid: 8363670
doi: 10.1038/s41597-021-00997-6
Qin XM, Shen KM. Taxonomic studies on the Genus Ferula and its close genera in Xinjiang. Arid Zone Res. 1990;7(4):23–33.
Hui H, Liu QX, Liu MH. Study on serum classification and genetic relationship of Ferula of Peucedaneae subtribe Ferulinae of Apiaceae in China. J Syst Evol. 2003;41(4):369–80.
Panahi M, Banasiak Ł, Piwczyński M, Puchałka R, Oskolski AA, Spalik K. Phylogenetic relationships among Dorema, Ferula and Leutea (Apiaceae: Scandiceae: Ferulinae) inferred from nrDNA ITS and cpDNA noncoding sequences. Taxon. 2015;64(4):770–83.
doi: 10.12705/644.8
Corriveau JL, Coleman AW. Rapid Screening Method to Detect Potential Biparental Inheritance of Plastid DNA and Results for over 200 Angiosperm Species. Am J Bot. 1988;75(10):1443–58.
doi: 10.1002/j.1537-2197.1988.tb11219.x
Jansen RK, Raubeson LA, Boore JL, dePamphilis CW, Chumley TW, Haberle RC, Wyman SK, Alverson AJ, Peery R, Herman SJ, et al. Methods for obtaining and analyzing whole chloroplast genome sequences. Methods Enzymol. 2005;395:348–84.
pubmed: 15865976
doi: 10.1016/S0076-6879(05)95020-9
Ravi V, Khurana JP, Tyagi AK, Khurana P. An update on chloroplast genomes. Plant Syst Evol. 2007;271(1–2):101–22.
Wicke S, Schneeweiss GM, dePamphilis CW, Muller KF, Quandt D. The evolution of the plastid chromosome in land plants: gene content, gene order, gene function. Plant Mol Biol. 2011;76(3–5):273–97.
pubmed: 21424877
pmcid: 3104136
doi: 10.1007/s11103-011-9762-4
Yang JB, Tang M, Li HT, Zhang ZR, Li DZ. Complete chloroplast genome of the genus Cymbidium: lights into the species identification, phylogenetic implications and population genetic analyses. BMC Evol Biol. 2013;13:84.
pubmed: 23597078
pmcid: 3644226
doi: 10.1186/1471-2148-13-84
Dong W, Liu H, Xu C, Zuo Y, Chen Z, Zhou S. A chloroplast genomic strategy for designing taxon specific DNA mini-barcodes: a case study on ginsengs. BMC Genet. 2014;15:138.
pubmed: 25526752
pmcid: 4293818
doi: 10.1186/s12863-014-0138-z
Ma PF, Zhang YX, Zeng CX, Guo ZH, Li DZ. Chloroplast phylogenomic analyses resolve deep-level relationships of an intractable bamboo tribe Arundinarieae (poaceae). Syst Biol. 2014;63(6):933–50.
pubmed: 25092479
doi: 10.1093/sysbio/syu054
Coissac E, Hollingsworth PM, Lavergne S, Taberlet P. From barcodes to genomes: extending the concept of DNA barcoding. Mol Ecol. 2016;25(7):1423–8.
pubmed: 26821259
doi: 10.1111/mec.13549
Hollingsworth PM, Li DZ, van der Bank M, Twyford AD. Telling plant species apart with DNA: from barcodes to genomes. Philos Trans R Soc Lond B Biol Sci. 2016;371(1702):20150338.
pubmed: 27481790
pmcid: 4971190
doi: 10.1098/rstb.2015.0338
Huang Y, Li X, Yang Z, Yang C, Yang J, Ji Y. Analysis of Complete Chloroplast Genome Sequences Improves Phylogenetic Resolution in Paris (Melanthiaceae). Front Plant Sci. 2016;7:1797.
pubmed: 27965698
pmcid: 5126724
Xie DF, Yu Y, Deng YQ, Li J, Liu HY, Zhou SD, He XJ. Comparative Analysis of the Chloroplast Genomes of the Chinese Endemic Genus Urophysa and Their Contribution to Chloroplast Phylogeny and Adaptive Evolution. Int J Mol Sci. 2018;19(7):1847.
pmcid: 6073864
doi: 10.3390/ijms19071847
Liang D, Wang H, Zhang J, Zhao Y, Wu F. Complete Chloroplast Genome Sequence of Fagus longipetiolata Seemen (Fagaceae): Genome Structure, Adaptive Evolution, and Phylogenetic Relationships. Life (Basel). 2022;12(1):92.
pmcid: 8778281
Wang N, Chen S, Xie L, Wang L, Feng Y, Lv T, Fang Y, Ding H. The complete chloroplast genomes of three Hamamelidaceae species: Comparative and phylogenetic analyses. Ecol Evol. 2022;12(2):e8637.
pubmed: 35222983
pmcid: 8848467
Fu CN, Mo ZQ, Yang JB, Cai J, Ye LJ, Zou JY, Qin HT, Zheng W, Hollingsworth PM, Li DZ, et al. Testing genome skimming for species discrimination in the large and taxonomically difficult genus Rhododendro. Mol Ecol Resour. 2022;22(1):404–14.
pubmed: 34310851
doi: 10.1111/1755-0998.13479
Goulding SE, Olmstead RG, Morden CW, Wolfe KH. Ebb and flow of the chloroplast inverted repeat. Mol Gen Genet. 1996;252(1–2):195–206.
pubmed: 8804393
doi: 10.1007/BF02173220
Huang J-L, Sun G-L, Zhang D-M. Molecular evolution and phylogeny of the angiosperm ycf2 gene. J Syst Evol. 2010;48(4):240–8.
doi: 10.1111/j.1759-6831.2010.00080.x
Zhu A, Guo W, Gupta S, Fan W, Mower JP. Evolutionary dynamics of the plastid inverted repeat: the effects of expansion, contraction, and loss on substitution rates. New Phytol. 2016;209(4):1747–56.
pubmed: 26574731
doi: 10.1111/nph.13743
Wen J, Xie DF, Price M, Ren T, Deng YQ, Gui LJ, Guo XL, He XJ. Backbone phylogeny and evolution of Apioideae (Apiaceae): New insights from phylogenomic analyses of plastome data. Mol Phylogenet Evol. 2021;161:107183.
pubmed: 33892097
doi: 10.1016/j.ympev.2021.107183
Gu C, Ma L, Wu Z, Chen K, Wang Y. Comparative analyses of chloroplast genomes from 22 Lythraceae species: inferences for phylogenetic relationships and genome evolution within Myrtales. BMC Plant Biol. 2019;19(1):281.
pubmed: 31242865
pmcid: 6595698
doi: 10.1186/s12870-019-1870-3
Liu X, Chang E-M, Liu J-F, Huang Y-N, Wang Y, Yao N, Jiang Z-P. Complete Chloroplast Genome Sequence and Phylogenetic Analysis of Quercus bawanglingensis Huang, Li et Xing, a Vulnerable Oak Tree in China. Forests. 2019;10(7):587.
doi: 10.3390/f10070587
Kim S-C, Lee J-W, Choi B-K. Seven Complete Chloroplast Genomes from Symplocos: Genome Organization and Comparative Analysis. Forests. 2021;12(5):608.
doi: 10.3390/f12050608
Rono PC, Dong X, Yang JX, Mutie FM, Oulo MA, Malombe I, Kirika PM, Hu GW, Wang QF. Initial Complete Chloroplast Genomes of Alchemilla (Rosaceae): Comparative Analysis and Phylogenetic Relationships. Front Genet. 2020;11:560368.
pubmed: 33362846
pmcid: 7756076
doi: 10.3389/fgene.2020.560368
Wanga VO, Dong X, Oulo MA, Mkala EM, Yang JX, Onjalalaina GE, Gichua MK, Kirika PM, Gituru RW, Hu GW, et al. Complete Chloroplast Genomes of Acanthochlamys bracteata (China) and Xerophyta (Africa) (Velloziaceae): Comparative Genomics and Phylogenomic Placement. Front Plant Sci. 2021;12:691833.
pubmed: 34194461
pmcid: 8238049
doi: 10.3389/fpls.2021.691833
Morton BR. Selection on the codon bias of chloroplast and cyanelle genes in different plant and algal lineages. J Mol Evol. 1998;46(4):449–59.
pubmed: 9541540
doi: 10.1007/PL00006325
Guisinger MM, Kuehl JV, Boore JL, Jansen RK. Extreme reconfiguration of plastid genomes in the angiosperm family Geraniaceae: rearrangements, repeats, and codon usage. Mol Biol Evol. 2011;28(1):583–600.
pubmed: 20805190
doi: 10.1093/molbev/msq229
Ren T, Li ZX, Xie DF, Gui LJ, Peng C, Wen J, He XJ. Plastomes of eight Ligusticum species: characterization, genome evolution, and phylogenetic relationships. BMC Plant Biol. 2020;20(1):519.
pubmed: 33187470
pmcid: 7663912
doi: 10.1186/s12870-020-02696-7
Lu H, Zhao WM, Zheng Y, Wang H, Qi M, Yu XP. Analysis of synonymous codon usage bias in Chlamydia. Acta Biochim Biophys Sin (Shanghai). 2005;37(1):1–10.
doi: 10.1093/abbs/37.1.1
Hassan S, Mahalingam V, Kumar V. Synonymous codon usage analysis of thirty two mycobacteriophage genomes. Adv Bioinformatics. 2009;2009:316936.
doi: 10.1155/2009/316936
Li WJ, Su ZH, Yang L, Cao QM, Fengi Y. Genetic diversity of the critically endangered Ferula sinkiangensis KM Shen (Apiaceae) and the implications for conservation. Turk J Bot. 2020;44(2):145–52.
Yang L, Hisoriev H, Kurbonova P, Boboev M, Bobokalonov K, Feng Y, Li W. High genetic diversity and low differentiation of endangered Ferula tadshikorum Pimenov in Tajikistan. GECCO. 2021;28:e01627.
Ren T, Yang Y, Zhou T, Liu ZL. Comparative Plastid Genomes of Primula Species: Sequence Divergence and Phylogenetic Relationships. Int J Mol Sci. 2018;19(4):1050.
pmcid: 5979308
doi: 10.3390/ijms19041050
Li B, Zheng Y. Dynamic evolution and phylogenomic analysis of the chloroplast genome in Schisandraceae. Sci Rep. 2018;8(1):9285.
pubmed: 29915292
pmcid: 6006245
doi: 10.1038/s41598-018-27453-7
Chen Y, Hu N, Wu H. Analyzing and Characterizing the Chloroplast Genome of Salix wilsonii. Biomed Res Int. 2019;2019:5190425.
pubmed: 31380427
pmcid: 6662467
Khan A, Asaf S, Khan AL, Al-Harrasi A, Al-Sudairy O, AbdulKareem NM, Khan A, Shehzad T, Alsaady N, Al-Lawati A, et al. First complete chloroplast genomics and comparative phylogenetic analysis of Commiphora gileadensis and C foliacea: Myrrh producing trees. PLoS One. 2019;14(1):e0208511.
pubmed: 30629590
pmcid: 6328178
doi: 10.1371/journal.pone.0208511
Wang L, Wuyun T-n, Du H, Wang D, Cao D. Complete chloroplast genome sequences of Eucommia ulmoides: genome structure and evolution. Tree Genet Genomes. 2016;12(1):15.
doi: 10.1007/s11295-016-0970-6
Shen X, Wu M, Liao B, Liu Z, Bai R, Xiao S, Li X, Zhang B, Xu J, Chen S. Complete Chloroplast Genome Sequence and Phylogenetic Analysis of the Medicinal Plant Artemisia annua. Molecules. 2017;22(8):1330.
pmcid: 6152406
doi: 10.3390/molecules22081330
Shen J, Li X, Chen X, Huang X, Jin S. The Complete Chloroplast Genome of Carya cathayensis and Phylogenetic Analysis. Genes (Basel). 2022;13(2):369.
doi: 10.3390/genes13020369
Li W, Zhang C, Guo X, Liu Q, Wang K. Complete chloroplast genome of Camellia japonica genome structures, comparative and phylogenetic analysis. PLoS ONE. 2019;14(5):e0216645.
pubmed: 31071159
pmcid: 6508735
doi: 10.1371/journal.pone.0216645
Tyagi S, Jung JA, Kim JS, Won SY. A comparative analysis of the complete chloroplast genomes of three Chrysanthemum boreale strains. PeerJ. 2020;8:e9448.
pubmed: 32685287
pmcid: 7337036
doi: 10.7717/peerj.9448
Hurst LD. The Ka/Ks ratio: diagnosing the form of sequence evolution. Trends Genet. 2002;18(9):486–7.
pubmed: 12175810
doi: 10.1016/S0168-9525(02)02722-1
Yang J, Kang GH, Pak JH, Kim SC. Characterization and Comparison of Two Complete Plastomes of Rosaceae Species (Potentilla dickinsii var. glabrata and Spiraea insularis) Endemic to Ulleung Island, Korea. Int J Mol Sci. 2020;21(14):4933.
pmcid: 7404287
doi: 10.3390/ijms21144933
Dong X, Mkala EM, Mutinda ES, Yang JX, Wanga VO, Oulo MA, Onjolo VO, Hu GW, Wang QF. Taxonomy, comparative genomics of Mullein (Verbascum, Scrophulariaceae), with implications for the evolution of Verbascum and Lamiales. BMC Genomics. 2022;23(1):566.
pubmed: 35941527
pmcid: 9358837
doi: 10.1186/s12864-022-08799-9
Lee-Yaw JA, Grassa CJ, Joly S, Andrew RL, Rieseberg LH. An evaluation of alternative explanations for widespread cytonuclear discordance in annual sunflowers (Helianthus). New Phytol. 2019;221(1):515–26.
pubmed: 30136727
doi: 10.1111/nph.15386
Zhang X, Deng T, Moore MJ, Ji Y, Lin N, Zhang H, Meng A, Wang H, Sun Y, Sun H. Plastome phylogenomics of Saussurea (Asteraceae: Cardueae). BMC Plant Biol. 2019;19(1):290.
pubmed: 31266465
pmcid: 6604455
doi: 10.1186/s12870-019-1896-6
Timme RE, Kuehl JV, Boore JL, Jansen RK. A comparison of the first two sequenced chloroplast genomes in Asteraceae: lettuce and sunflower. United States: Lawrence Berkeley National Laboratory; 2006. p. 1–33.
Pimenov MG. Glaucoselinum section (Schischk.) M. Pimen of genus Ferula L. (Umbelliferae). Moscow, Biologicheskie nauki: Nauchnye doklady vysshei shkoly. 1983;12:74–9.
Shan RH, She ML. Flora Reipublcae Popularis Sinicae, vol. 55. Beijing: Science Press; 1979.
Chen XY, Liu QX. Luteolin glycosides as taxonomic markers in Ferula and related genera. Biochem Syst Ecol. 1989;17(4):309–10.
doi: 10.1016/0305-1978(89)90008-2
Liu QX, Wu MY, Rao GX, Ye JS, Hui H. H-NMR detection of coumarin and its application in the chemical classification of Ferula. J Plant Resour Environ. 1999;8(1):46–51.
Du Q, Jiang M, Sun S, Wang L, Liu S, Jiang C, Gao H, Chen H, Li Y, Wang B, et al. The complete chloroplast genome sequence of Clerodendranthus spicatus, a medicinal plant for preventing and treating kidney diseases from Lamiaceae family. Mol Biol Rep. 2022;49(4):3073–83.
pubmed: 35059973
doi: 10.1007/s11033-022-07135-4
Meyer M, Kircher M. Illumina sequencing library preparation for highly multiplexed target capture and sequencing. Cold Spring Harb Protoc. 2010;2010(6):pdb prot5448.
pubmed: 20516186
doi: 10.1101/pdb.prot5448
Jin JJ, Yu WB, Yang JB, Song Y, dePamphilis CW, Yi TS, Li DZ. GetOrganelle: a fast and versatile toolkit for accurate de novo assembly of organelle genomes. Genome Biol. 2020;21(1):241.
pubmed: 32912315
pmcid: 7488116
doi: 10.1186/s13059-020-02154-5
Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, et al. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol. 2012;19(5):455–77.
pubmed: 22506599
pmcid: 3342519
doi: 10.1089/cmb.2012.0021
Wick RR, Schultz MB, Zobel J, Holt KE. Bandage: interactive visualization of de novo genome assemblies. Bioinformatics. 2015;31(20):3350–2.
pubmed: 26099265
pmcid: 4595904
doi: 10.1093/bioinformatics/btv383
Liu C, Shi L, Zhu Y, Chen H, Zhang J, Lin X, Guan X. CpGAVAS, an integrated web server for the annotation, visualization, analysis, and GenBank submission of completely sequenced chloroplast genome sequences. BMC Genomics. 2012;13:715.
pubmed: 23256920
pmcid: 3543216
doi: 10.1186/1471-2164-13-715
Kearse M, Moir R, Wilson A, Stones-Havas S, Cheung M, Sturrock S, Buxton S, Cooper A, Markowitz S, Duran C, et al. Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics. 2012;28(12):1647–9.
pubmed: 22543367
pmcid: 3371832
doi: 10.1093/bioinformatics/bts199
Lohse M, Drechsel O, Kahlau S, Bock R. OrganellarGenomeDRAW–a suite of tools for generating physical maps of plastid and mitochondrial genomes and visualizing expression data sets. Nucleic Acids Res. 2013;41(Web server issue):W575-581.
pubmed: 23609545
pmcid: 3692101
doi: 10.1093/nar/gkt289
Metsalu T, Vilo J. ClustVis: a web tool for visualizing clustering of multivariate data using Principal Component Analysis and heatmap. Nucleic Acids Res. 2015;43(W1):W566-570.
pubmed: 25969447
pmcid: 4489295
doi: 10.1093/nar/gkv468
Kurtz S, Choudhuri JV, Ohlebusch E, Schleiermacher C, Stoye J, Giegerich R. REPuter: the manifold applications of repeat analysis on a genomic scale. Nucleic Acids Res. 2001;29(22):4633–42.
pubmed: 11713313
pmcid: 92531
doi: 10.1093/nar/29.22.4633
Katoh K, Rozewicki J, Yamada KD. MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization. Brief Bioinform. 2019;20(4):1160–6.
pubmed: 28968734
doi: 10.1093/bib/bbx108
Darling AC, Mau B, Blattner FR, Perna NT. Mauve: multiple alignment of conserved genomic sequence with rearrangements. Genome Res. 2004;14(7):1394–403.
pubmed: 15231754
pmcid: 442156
doi: 10.1101/gr.2289704
Rozas J, Ferrer-Mata A, Sanchez-DelBarrio JC, Guirao-Rico S, Librado P, Ramos-Onsins SE, Sanchez-Gracia A. DnaSP 6: DNA Sequence Polymorphism Analysis of Large Data Sets. Mol Biol Evol. 2017;34(12):3299–302.
pubmed: 29029172
doi: 10.1093/molbev/msx248
Capella-Gutierrez S, Silla-Martinez JM, Gabaldon T. trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics. 2009;25(15):1972–3.
pubmed: 19505945
pmcid: 2712344
doi: 10.1093/bioinformatics/btp348
Zhang D, Gao F, Jakovlic I, Zou H, Zhang J, Li WX, Wang GT. PhyloSuite: An integrated and scalable desktop platform for streamlined molecular sequence data management and evolutionary phylogenetics studies. Mol Ecol Resour. 2020;20(1):348–55.
pubmed: 31599058
doi: 10.1111/1755-0998.13096
Stamatakis A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. 2014;30(9):1312–3.
pubmed: 24451623
pmcid: 3998144
doi: 10.1093/bioinformatics/btu033
Darriba D, Taboada GL, Doallo R, Posada D. jModelTest 2: more models, new heuristics and parallel computing. Nat Methods. 2012;9(8):772.
pubmed: 22847109
pmcid: 4594756
doi: 10.1038/nmeth.2109
Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Hohna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP. MrBayes 32: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol. 2012;61(3):539–42.
pubmed: 22357727
pmcid: 3329765
doi: 10.1093/sysbio/sys029
Letunic I, Bork P. Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation. Nucleic Acids Res. 2021;49(W1):W293–6.
pubmed: 33885785
pmcid: 8265157
doi: 10.1093/nar/gkab301
Rambaut A. FigTree 1.4.2 software, a graphical viewer of phylogenetic trees. Edinburgh: Institute of Evolutionary Biology University of Edinburgh; 2014.