Abstract
The complete mitochondrial genome was determined for the flying gurnard Dactylopterus volitans belonging to the family Dactylopteridae. The total length of the D. volitans mitochondrial genome is 16,632 bp, which consists of 13 protein-coding genes, 22 tRNA genes, two rRNA genes, and a control region. It has the typical vertebrate mitochondrial gene arrangement. Phylogenetic analysis using mitochondrial genomes of 20 species showed that D. volitans formed a well-supported monophyletic group with other Dactylopteridae species.
Keywords: Mitochondrial genome, Syngnathiformes, Dactylopteridae, Dactylopterus volitans
The flying gurnard Dactylopterus volitans (Syngnathiformes, Dactylopteridae) notable for their tremendously enlarged and colorful pectoral fins is a bottom-dwelling fish of tropical waters in the Atlantic Ocean (Nelson et al. 2016). It is listed as least concern in the IUCN Red List of Threatened Species (Carpenter et al. 2015). Their phylogenetic position of this group, the family Dactylopteridae was changed from Scorpaeniformes to Syngnathiformes by Nelson (2016) based on the molecular evidence (Betancur et al. 2013; Near et al. 2013; Song et al. 2014); however, their taxonomic position remains controversial. In the current study, we first determined the complete mitochondrial DNA sequence of D. volitans and to analyze the phylogenetic relationship of this species with members of Syngnathiformes.
The D. volitans specimen used in this study was collected from high seas of the Western Central Atlantic (8.30 N, 14.00 W). Total genomic DNA was extracted from tissue of the specimen, which has been deposited in the National Marine Biodiversity Institute of Korea (Voucher No. MABIK 0001979). The mitogenome was sequenced and assembled using Illumina Hiseq 4000 sequencing platform (Illumina, San Diego, CA) and SOAP denovo assembler at Macrogen Inc. (Korea), respectively. The complete mitochondrial genome was annotated using MacClade ver. 4.08 (Maddison and Maddison 2005) and tRNAscan-SE 2.0 (Lowe and Chan 2016).
The complete mitochondrial genome of D. volitans (GenBank accession no. LC512458) is 16,632 bp long, and includes 13 protein-coding genes, 22 tRNA genes, 2 rRNA genes, and a control region. The ND6 gene and eight tRNA genes are encoded on the light strand. The overall base composition of the heavy strand is 27.92% A, 30.20% C, 16.29% G, and 25.59% T. Similar to the mitogenomes of other vertebrates, the AT content is higher than the GC content (Saccone et al. 1999). All tRNA genes can fold into a typical cloverleaf structure, with lengths ranging from 66 to 74 bp. The 12S rRNA (956 bp) and 16S rRNA genes (1,692 bp) are located between tRNAPhe and tRNAVal and between tRNAVal and tRNALeu(UUR), respectively. Of the 13 protein-coding genes, 12 begin with an ATG start codon; the exception being the COI gene, which start with GTG. The stop codon of the protein-coding genes is TAA in ND1, COI, ATP8, ND4L, ND5 and ND6; TA in ND2, ATP6 and COIII and T in the remaining four genes. The control region (870 bp) is located between tRNAPro and tRNAPhe.
Phylogenetic trees were constructed by the maximum-likelihood method using MEGA 7.0 software (Kumar et al. 2016) for the newly sequenced genome and a further 19 complete mitochondrial genome sequences downloaded from the National Center for Biotechnology Information. We confirmed that Dactylopteridae including D. volitans formed a monophyletic group together with other members of Syngnathiformes (Fistulariidae and Centriscidae) and this group formed a sister-group relationship with the family Pegasidae species with high statistical support (Figure 1).
Figure 1.
Phylogenetic position of Dactylopterus volitans based on a comparison with the complete mitochondrial genome sequences of 19 species. The analysis was performed using MEGA 7.0 software. The accession number for each species is indicated after the scientific name.
Funding Statement
This work was supported by grant from the National Marine Biodiversity Institute Research Program [2019M00600] and the Marine Biotechnology Program [20170488] funded by the Ministry of Oceans and Fisheries, Korea.
Disclosure statement
No potential conflict of interest was reported by the authors.
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