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Mitogenome Announcement

The complete mitochondrial genome of an endangered mangrove plant: Scyphiphora hydrophyllacea

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Pages 2779-2780 | Received 17 Jun 2020, Accepted 20 Jun 2020, Published online: 11 Jul 2020

Abstract

The complete mitochondrial genome of an endangered mangrove plant: Scyphiphora hydrophyllacea was analyzed in this paper, which is the first for the genus within the family Rubiaceae. The mitogenome sequence is 354,155 bp in length containing 3 ribosomal RNA genes, 16 transfer RNA genes, and 37 protein-coding genes. Gene ccmFc, ccmFn, rps3, rps13, rps10, rpl12, nad3 and cox1 contain one intron, gene cox2 and atp9 contain three introns and gene nad1, nad4 and nad7 contain four introns. Furthermore, Gene nad2 and nad5 have five introns. Gene nad1, nad2, nad5, nad7and Cox2 are trans-splicing genes. Phylogenetic analysis using the maximum likelihood method positioned S. hydrophyllacea closely with Asclepias syriaca in Gentianales.

Scyphiphora hydrophyllacea is one of the shrub mangrove plants belonging to Scyphiphora genus in the family Rubiaceae, which is a monotypic genus with a range from south India and Ceylon, Indochina and Hainan in China, through the Malay Archipelago and Philippines to tropical Australia and New Caledonia, Northward to the Solomon Islands and Palau (Tomlinson Citation1986). According to the categories and criteria of the International Union for the Conservation of Nature (IUCN) Red List of Threatened Species, S. hydrophyllacea was classified into the Least Concern (LC) category with the 20% global loss (Polidoro et al. Citation2010). Mitochondrial genome-based phylogenetic analysis would improve our understanding of the evolutionary relationship of this plant under tidal habitat. In this study, we sequenced and analyzed the complete mitochondrial DNA sequence of S. hydrophyllacea. This is the first complete mitogenome within the family Rubiaceae or even in Gentianales.

Fresh leaves were collected from one individual of S. hydrophyllacea in Sanya (N18°13′21.09″, E109°36′59.73″), Hainan Province, China. The total genomic DNA was extracted from three mixed fresh leaves of S. hydrophyllacea by using the modified CTAB method (Doyle Citation1987) in the laboratory of Hainan Normal University. Further, the specimen was also stored in the herbarium of Hainan Normal University (BHM-001). Genome sequencing was performed on an Illumina Hiseq X Ten platform with paired-end reads of 150 bp. In total, 50.4 Gb short sequence data with Q20 was 96.21% was obtained. The remaining high-quality reads were used to assemble the mitogenome using NOVOPlasty (Dierckxsens et al. Citation2016), where Asclepias syriaca (GenBank accession NC_022796.1) used as the seed sequence. The genes annotation in the mitogenome was doing with SPAdes v.3.9.0 (Bankevich et al. Citation2012) and some genes were annotated manually. The accession number in Genbank is MT610041. Four mitogenome sequences in Rosales were aligned including S. hydrophyllacea, Aegiceras corniculatum, one mangrove plant in Myrsinaceae was used as the out-group species. Phylogenetic analysis using the maximum likelihood algorithm was conducted with Mega X (Kumar et al. Citation2018).

The mitogenome of S. hydrophyllacea is 354,155 bp in length with GC content of 44.44%, which contains 3 ribosomal RNA genes (rrn5, rrn18 and rrn26), 16 transfer RNA genes, and 37 protein-coding genes. Gene ccmFc, ccmFn, rps3, rps13, rps10, rpl12, nad3 and cox1 contain one intron, gene cox2 and atp9 contain three introns and gene nad1, nad4 and nad7 contain four introns. Gene nad2 and nad5 have five introns. Gene nad1, nad2, nad5, nad7 and Cox2 are trans-splicing genes. Phylogenetic analysis with other four plant mitogenomes showed that S. hydrophyllacea is closest with Asclepias syriaca in Gentianales (). The useful genomic resources for characterization of genetic diversity of S. hydrophyllacea by the mitogenome will help for the study of evolution mechanism.

Figure 1. Maximum likelihood tree based on the sequences of five complete mitogenomes. Numbers in the nodes were bootstrap values from 1000 replicates. Scale in substitutions per site.

Figure 1. Maximum likelihood tree based on the sequences of five complete mitogenomes. Numbers in the nodes were bootstrap values from 1000 replicates. Scale in substitutions per site.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

The data that support the finding of this study are openly available in GenBank of NCBI at https://www.ncbi.nlm.nih.gov, reference number MT610041.

Additional information

Funding

This study was supported by Guangdong Provincial Key Laboratory of Plant Resource [2019plantKF09]; Fujian Provincial Key Laboratory of Marine Ecological Conservation and Restoration [EPR2020010].

References

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