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Mitogenome Announcement

The complete mitochondrial genome of frigate tuna (Auxis thazard) from South China Sea

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Pages 1971-1972 | Received 18 Apr 2019, Accepted 03 May 2019, Published online: 23 May 2019

Abstract

Auxis thazard is one of genus Auxis and widely distributed in tropical and subtropical waters. In this study, we described the complete mitochondrial genome of Auxis thazard. The genome is 16,506 bp in length, encoding the standard set of 13 protein-coding genes, 22 transfer RNA genes, 2 ribosomal RNA genes, and a non-coding D-loop, with a circular organization. The overall base composition of the whole mitochondrial genome was A (27.86%), T (24.88%), G (17.16%), and C (30.10%) with an AT bias of 52.94%. The longest protein-coding genes of these species was ND5, whereas the shortest ATP8.

The genus Auxis are cosmopolitan species and the smallest members of the tribe Thunnini, the true tunas (Infante et al. Citation2004). The existence of two distinct species, the narrow-corseleted Auxis thazard and the wide-corseleted Auxis rochei (Collette and Aadland Citation1996) is currently recognized. Morphologically, they are differentiated primarily by the width of the corselet under the origin of the second dorsal fin and by the anterior extent of the dorsal scaleless area above the pectoral fin. Both frigate and bullet tuna support very important commercial fisheries throughout the world. In fact, the total world catches of A. thazard and A. rochei was higher than 172,000 ton according to FAO Fishery Statistics (Collette et al. Citation2001; Catanese et al. Citation2008).

Here, we sequenced and annotate mitogenome of A. thazard form South China Sea to provide molecular information for genetically understanding of frigate tuna. The specimens of A. thazard were collected from the South China Sea (21°30′N, 118°30′E) on 19th September, 2017. Whole genomic DNA was extracted from muscle tissue of one specimen of A. thazard using TIANamp Marine Animals DNA Kit (TIANGEN, China). The concentration for use as a PCR template was adjusted to an A260 of about 0.05 to 0.2. The collected specimen and extracted DNA were stored in Guangdong Provincial Key Laboratory of Fishery Ecology and Environment. The complete mitochondrial genomes of A. thazard was sequenced using PCR primers designed from highly conserved regions of transfer RNA (tRNA) sequences of related species (Catanese et al. Citation2008) with additional specific primers designed as required from sequences already obtained. Long-PCR amplifications were performed by thermo-cycling using five pairs of primers and PCR amplicons were subjected to build up a genomic library and pair-end sequencing by MiSeq. The COI sequence of A. thazard was used as reference seeds for iterative assembly by MITObim v.1.8 (Hahn et al. Citation2013). SeqMan v.7.1.0 was used for the mitogenome assembly and annotation (Swindell and Plasterer Citation1997). Transfer RNA genes were predicted using online software tRNAScan-SE 1.21 (Lowe and Eddy Citation1997). All Protein coding gene (PCGs) are aligned independently, then concatenated to be applied for phylogenetic reconstruction with other Scombriformes in MrBayes v 3.12 (Ronquist and Huelsenbeck Citation2003) using a relaxed clock model.

The A. rochei mitochondrial genome forms a 16,506 bp closed loop (GenBank accession number: MK801690). The overall base composition of the whole mitochondrial genome was A (27.86%), T (24.88%), G (17.16%), and C (30.10%) with an AT bias of 52.74%. This mitochondrial genome represents a typical Auxis mitochondrial genome and matches with the A. rochei genome (Catanese et al. Citation2008), in which it comprises 13 protein-coding genes, 22 transfer RNA genes, and 2 ribosomal RNA genes (12S rRNA and 16S rRNA) and one A + T-rich region which could also be termed as control region. The ATG initiation codon is used in all protein-coding genes except COX1 (GTG), and the stop codons of all the 13 protein-coding genes were complete. Meanwhile, the longest protein-coding gene of these species was ND5 (1839 bp), whereas the shortest was ATP8 (168 bp). lrRNA and srRNA genes are 1652 and 950 bp in length respectively, and the length of D-loop is 557 bp. All the 22 typical tRNAs possess a complete cloverleaf secondary structure, ranging from 67 to 74 bp. The Bayesian inference phylogenetic tree showed that A. thazard firstly grouped with species of A. rochei (). We have the confidence to construct phylogenetic trees, based on the complete mitochondrial genomes, but the evolution history of cutlassfish still needs future research to be clearly resolved.

Figure 1. The Bayesian inference phylogenetic tree for Scombriformes based on mitochondrial PCGs and rRNAs concatenated dataset. The gene’s accession numbers for tree construction are listed as follows: Auxis rochei (AB103468), Katsuwonus pelamis (AB101290), Euthynnus alletteratus (AB099716), Euthynnus affinis (KM651783), Thunnus alalunga (KP259549), Thunnus thynnus (AB097669), Sarda orientalis (AP012949), Acanthocybium solandri (AP012945), Gymnosarda unicolor (AP012510), Gasterochisma melampus (JN086156), Cubiceps pauciradiatus (AP006038), Icosteus aenigmaticus (AP006026), Ruvettus pretiosus (AP012506), Peprilus triacanthus (AP012518).

Figure 1. The Bayesian inference phylogenetic tree for Scombriformes based on mitochondrial PCGs and rRNAs concatenated dataset. The gene’s accession numbers for tree construction are listed as follows: Auxis rochei (AB103468), Katsuwonus pelamis (AB101290), Euthynnus alletteratus (AB099716), Euthynnus affinis (KM651783), Thunnus alalunga (KP259549), Thunnus thynnus (AB097669), Sarda orientalis (AP012949), Acanthocybium solandri (AP012945), Gymnosarda unicolor (AP012510), Gasterochisma melampus (JN086156), Cubiceps pauciradiatus (AP006038), Icosteus aenigmaticus (AP006026), Ruvettus pretiosus (AP012506), Peprilus triacanthus (AP012518).

Disclosure statement

None of the co-authors has any conflict of interest to declare. The authors alone are responsible for the content and writing of the paper.

Additional information

Funding

Support was obtained from Central Public-Interest Scientific Institution Basal Research Fund, CAFS [NO. 2019HY-JC0203].

References

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