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Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2019 Dec 9;5(1):19–20. doi: 10.1080/23802359.2019.1693922

Complete plastome of Leucanthemum maximum, the first in genus Leucanthemum

Haimei Chen a,*, Mei Jiang a,*, Liqiang Wang a, Jinwen You b, Chang Liu a,
PMCID: PMC7721026  PMID: 33366402

Abstract

Leucanthemum maximum is a perennial herb widely used in landscaping. Here, we reported the complete plastome of L. maximum. The plastome was 151,865 bp long, containing a large single-copy region of 84,369 bp, a small single-copy region of 18,450 bp, and two inverted repeats of 24,523 bp each. It encoded 112 unique genes, including 79 protein-coding, 4 rRNA, and 29 tRNA genes. The protein sequence of infA was distinctly truncated compared with those from other Anthemideae species. Phylogenetic analysis showed that the species is closely related to the genus Ismelia. This study provided a high-quality reference for future studies.

Keywords: Leucanthemum maximum, plastome, phylogenetic analysis


Leucanthemum maximum is a flowering plant from family Asteraceae, tribe Anthemideae. It is native to France and Spain, but it can be found to grow in the wild in other parts of the world as an introduced species and sometimes cultivated as an ornamental plant (Wikipedia 2019). L. maximum has a ploidy level of 2n = 12x = 108. The obtainment of the plastome is the first step to understand the phylogeny and phylogeography of a polyploidy complex (Greiner et al. 2012). For this reason, we sequenced and analyzed the complete plastome from L. maximum in this study.

The fresh leaves of L. maximum, identified by Professor Jinwen You, were collected from the Central China Medicinal Botanical Garden, EnShi, Hubei, China (Geospatial coordinate: N30.177764, E109.743937). The voucher sample is stored in the herbarium of Institute of Medicinal Plant Development (201808226). The genomic DNA was extracted with plant genomic DNA kit (Tiangen Biotech, China) and sequenced using the HiSeq 2500 platform (Illumina, San Diego, CA) following the manufacturer’s recommendations. The plastome was assembled with NOVOPlasty (v.2.7.2) (Dierckxsens et al. 2017) and annotated with CPGAVAS2 (Shi et al. 2019). The annotated genomic sequence has been submitted to GenBank with the accession number: MN518843.

The plastome of L. maximum is a typical circular DNA molecule with a total length of 151,865 bp. It has the conservative quadrilateral structure, including a large single-copy (LSC) region, a small single-copy (SSC) region, and a pair of inverted repeat (IR) regions, the length was 84,369, 18,450, and 24,523 bp. The overall GC content is 37.33%. The GC content of three regions is ranked as 43.10%, 35.41%, and 30.74% for IRs, LSC, and SSC, respectively. The plastome of L. maximum encoded 79 unique protein coding, 29 unique tRNA genes, and 4 unique rRNA genes. Among them, nine protein-coding genes (rps16, rpoC1, atpF, petB, petD, rpl16, rpl2, ndhA, and ndhB) contained one intron, and two protein-coding genes (ycf3 and clpP) contained two introns. The rps12 gene is a trans-spliced gene with the 5′ end located in the LSC region and the duplicated 3′ ends located in the IR regions. Four tRNA genes (trnK-UUU, trnS-CGA, trnE-UUC, and trnA-UGC) contained one intron. The infA gene coded a protein of 41 residues, significantly shorter than those from other Anthemideae species.

For the phylogenetic analysis, 75 protein sequences present in 17 additional Anthemideae species, two outgroup species (Nymphoides coreana and Menyanthes trifoliata), and L. maximum were retrieved using the ‘DownloadCOG’ module in PLasDB (http://www.herbalgenomics.org/plasdb). These protein sequences were aligned using the CLUSTALW2 (v2.0.12) program. The maximum likelihood method implemented in RaxML (v8.2.4) (Stamatakis 2015) was used to infer the evolutionary history, using the model of PROTGAMMACPREV. Subsequently, the bootstrap analysis was performed with 1000 replicates. As shown in Figure 1, L. maximum is closely related to the genus of Ismelia, with bootstrap values of 96, consistent with the current taxonomic classification. In the future, more plastome sequences from other Leucanthemum species are needed to determine their phylogenetic relationships.

Figure 1.

Figure 1.

Molecular phylogenetic analyses of plastomes in the tribe Anthemideae. The tree was constructed with the sequences of 75 proteins present in all 20 species by using the maximum-likelihood method implemented in RAxML. Nymphoides coreana and Menyanthes trifoliata were set as outgroups. The number on the top of the branch indicates bootstrap value, and the number at the bottom of the branch indicates the evolutionary distance. The accession numbers for the species are as follows: Artemisia annua: NC_034683.1, Artemisia argyi: NC_030785.1, Artemisia capillaris: NC_031400.1, Artemisia frigida: NC_020607.1, Artemisia fukudo: NC_044156.1, Artemisia gmelinii: NC_031399.1, Artemisia montana: NC_025910.1, Artemisia selengensis: NC_039647.1, Chrysanthemum boreale: NC_037388.1, Chrysanthemum lucidum: NC_040920.1, Crossostephium chinense: NC_042725.1, Ismelia carinata: NC_040110.1, Leucanthemella linearis: NC_043835.1, Opisthopappus taihangensis: NC_042787.1, Soliva sessilis: NC_034851.1, Chrysanthemum indicum: NC_020320.1, Chrysanthemum morifolium: NC_020092.1, Nymphoides coreana: NC_041481.1, and Menyanthes trifoliata: NC_041436.1.

Funding Statement

This work was supported by Chinese Academy of Medical Sciences, Innovation Funds for Medical Sciences (CIFMS) [2017-I2M-1-013], National Science Foundation Funds [81872966], and National Science &Technology Fundamental Resources Investigation Program of China [2018FY100705]. The funders were not involved in the study design, data collection and analysis, decision to publish, or manuscript preparation.

Disclosure of statement

No potential conflict of interest was reported by the authors.

References

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