Abstract
The Japanese bigeye (Pristigenys niphonia) is a species in the genus Pristigenys and in the family Priacanthidae. To understand the phylogenetic relationship of Japanese bigeye in teleost, we firstly determined the complete mitochondrial genome of Japanese bigeye. The entire mitochondrial genome of Japanese bigeye is 16,519bp in length, including 13 protein-coding genes and 2 ribosomal RNA genes (rRNA), 22 transfer RNA genes (tRNAs), and 2 main non-coding regions. The overall base composition is 24.9% of T, 30.6% of C, 27.7% of A, and 16.8% of G. The gene arrangement, base composition, and tRNA structures of the complete mitochondrial genome of Japanese bigeye is consistent with those of other teleost. The complete mitochondrial genome of Japanese bigeye was used to construct phylogenetic tree, which shows that Japanese bigeye is clustered with the fishes of the order Perciformes. We expect that the availability of mitochondrial genome of Japanese bigeye will facilitate the further investigations of the taxonomic resolution, biogeography, and molecular systematic.
Keywords: Priacanthidae, Pristigenys niphonia, mitochondrial genome
The Priacanthidae, the bigeyes, are a family of 4 genus and 19 species of marine fishes. As one of the member of the family Priacanthidae, the Japanese bigeye (Pristigenys niphonia) is native to Western Pacific: Japan, East China Sea Shelf, Taiwan, South China Sea, Vietnam, Celebes, Australia and Indonesia (Iwatsuki et al. 2012). To research the taxonomic resolution and phylogenetic relationships of Japanese bigeye with other vertebrates, we sequenced the complete nucleotide sequence for the mitochondrial genome of Japanese bigeye. The samples were collected from the East China Sea (25.75°N, 123.47°E) .The specimen was preserved in 95% ethanol at herbarium which located Jilin Agricultural University (accession number:DK204).
Mitochondrial DNA was extracted and kept at −20 °C. The mitogenome of Japanese bigeye is a closed double-stranded circular molecule of 16,519 nucleotides (GenBank accession number: KX641477) and contains 13 protein-coding genes, 2 rRNA genes, 22 tRNA genes, the control region (CR), and the origin of the light-strand replication (OL). The base composition of Japanese bigeye is 24.9% of T, 30.6% of C, 27.7% of A, and 16.8% of G. The A + T (52.6%) content is higher than G + C (47.4%) content, which is similar to other fishes (Cheng et al. 2011a; Jin et al. 2012). Furthermore, the anti-G bias is ascertained in the third position of protein-coding genes, which brings Red bigeye in line with other vertebrate mitogenomes (Cheng et al. 2012a; Jin et al. 2013). The two ribosomal RNA genes 12S rRNA (954bp) and 16S rRNA (1703bp) are located on the heavy strand between tRNAPhe and tRNALeu (UUR), and being separated by tRNAVal gene. The 13 protein-coding genes are encoded on heavy-strand except for ND6, which is encoded on the light-strand. All the protein-coding genes start ATG, except for COI, which used GTG as the initiation codon. The stop codon of four protein-coding genes (ND1, COI, ATP8, and ND4L) is TAA, while ND6 end with TAG. The remaining protein-coding genes (ND2, COII, ATP6, COIII, ND3, ND4, ND5, and Cytb) have incomplete stop codon, either TA– or T––, which is common to vertebrate mitochondrial protein-coding genes (Xu et al. 2011; Cheng et al. 2012b; Liu et al. 2013). And, these incomplete termination codons are presumably complete as TAA via posttranscriptional polyadenylation (Ojala et al. 1981). The 22 tRNA genes, which contains two forms of tRNASer (UCN and AGY) and tRNALeu (UUR and CUN), scatter throughout the genome and range from 67 to 75 bp in size and the gene arrangement is typically as in most vertebrates. Among the 22 tRNA genes, 14 are located on the heavy-strand and 8 on the light-strand. Three tRNA clusters (IQM, WANCY, and HSL) are well conserved in Japanese bigeye as in other vertebrate mitochondrial genomes (Wei et al. 2013). Some overlaps occur in protein-coding genes and tRNAs ranging from 1 to 10 bp, which is similar to most vertebrates. The control region, which is determined to be 837bp, located between tRNAPro and tRNAPhe and this characterization is consistent with those of other teleost (Cheng et al. 2011b). Remarkably, the conserved motif 5′-GCCGG-3′, which is involved in the transition from RNA to DNA synthesis (Thomson et al. 1986), was identified in the mitogenome of Japanese bigeye.
Phylogenetic analysis result based on the complete mitochondrial genome sequences demonstrated that Red bigeye is clustered with the fishes of the order Perciformes (Figure 1). We expect that this mitogenome sequence data would play a crucial role in phylogenetic analysis of Red bigeye.
Figure 1.
Phylogenetic tree was constructed using the neighbour-joining method by MEGA 5 based on the complete mitochondrial genome sequences. The mitochondrial genome sequences used in phylogenetic analyses were derived from GenBank, accession no.: Cheilodactylus zonatus AP006013.1, Coreoperca whiteheadi KJ149811.1, Doederleinia berycoides AP009181.1, Gymnosarda unicolor AP012510.1, Histiopterus typus AP006807.1, Howella brodiei AP014536.1, Lutjanus argentimaculatus JN182927.1, L. bengalensis FJ171339.1, L. erythropterus KP939271.1, L. kasmira FJ416614.1, L. rivulatus AP006000.1, Micropterus salmoides DQ536425.1, Monodactylus argenteus AP009169.1, Pentaceros japonicus AB739063.1, Plectorhinchus lineatus KM099284.1, P. orientalis KP966562.1, Pristipomoides multidens KF430626.1, Pseudopentaceros wheeleri AB741956.1, Pterocaesio tile AP004447.1, Scombrops boops LC006297.2, Siganus canaliculatus KJ872545.1, Siniperca scherzeri KF746199.1.
Disclosure statement
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the article.
Funding
This study was supported by Key science and technology program of Jilin Province [20150204065NY], Special Fund for Agro-scientific Research in the Public Interest of China [201303091] and Construction Program of Modern Agricultural Industry Technology System of China [CARS-38].
References
- Cheng YZ, Xu TJ, Jin XX, Wang RX.. 2011a. Complete mitochondrial genome of the yellow drum Nibea albiflora (Perciformes, Sciaenidae). Mitochondrial DNA. 22:80–82. [DOI] [PubMed] [Google Scholar]
- Cheng YZ, Jin XX, Shi G, Wang RX, Xu TJ.. 2011b. Genetic diversity and population structure of miiuy croaker populations in East China Sea revealed by the mitochondrial DNA control region sequence. Biochem Syst Ecol. 39:718–724. [Google Scholar]
- Cheng YZ, Wang RX, Sun YN, Xu TJ.. 2012a. The complete mitochondrial genome of the small yellow croaker and partitioned Bayesian analysis of Sciaenidae fish phylogeny. Genet Mol Biol. 35:191–199. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheng YZ, Xu TJ, Jin XX, Tang D, Wei T, Sun YY, Meng FQ, Shi G, Wang RX.. 2012b. Universal primers for amplification of the complete mitochondrial control region in marine fish species. Mol Biol. 6:727–730. [PubMed] [Google Scholar]
- Jin XX, Wang RX, Zhao SL, Xu TJ, Shi G.. 2012. Complete mitochondrial genome of the striped sandgoby Acentrogobius pflaumii (Perciformes, Gobioidei). Mitochondrial DNA. 23:420–422. [DOI] [PubMed] [Google Scholar]
- Jin XX, Gao YH, Xu TJ, Shi G, Zhao SL, Sun YN.. 2013. Complete mitochondrial genome of the Asian freshwater goby Synechogobius ommaturus (Perciformes, Gobioidei). Mitochondrial DNA. 24:83–85. [DOI] [PubMed] [Google Scholar]
- Iwatsuki Y, Matsuda T, Starnes WC, Nakabo T, Yoshino T.. 2012. A valid priacanthid species, Pristigenys refulgens (Valenciennes 1862), and a redescription of P. niphonia (Cuvier in Cuvier & Valenciennes 1829) in the Indo-West Pacific (Perciformes: Priacanthidae). Zootaxa. 3206:41–57. [Google Scholar]
- Liu TX, Jin XX, Wang RX, Xu TJ.. 2013. Complete sequence of the mitochondrial genome of Odontamblyopus rubicundus (Perciformes: Gobiidae): genome characterization and phylogenetic analysis. Mitochondrial DNA. 3:423–432. [DOI] [PubMed] [Google Scholar]
- Ojala D, Montoya J, Attardi G.. 1981. tRNA punctuation model of RNA processing in human mitochondria. Nature. 290:470–474. [DOI] [PubMed] [Google Scholar]
- Thomson SM, Burnett DC, Bergmann JD, Hixson CJ.. 1986. Comparative inhalation hazards of aluminum and brass powders using bronchopulmonary lavage as an indicator of lung damage. J Appl Toxicol. 6:197–209. [DOI] [PubMed] [Google Scholar]
- Wei T, Jin XX, Xu TJ.. 2013. The first complete mitochondrial genome from Bostrychus genus (Bostrychus sinensis) and partitioned Bayesian analysis of Eleotridae fish phylogeny. J Genet. 92:247–257. [DOI] [PubMed] [Google Scholar]
- Xu TJ, Chen YZ, Liu XZ, Shi G, Wang RX.. 2011. The complete mitochondrial genome of the marbled rockfish Sebastiscus marmoratus (Scorpaeniformes, Scorpaenidae): genome characterization and phylogenetic considerations. Mol Biol. 45:392–403. [PubMed] [Google Scholar]

