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Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2021 Jun 17;6(7):2024–2025. doi: 10.1080/23802359.2021.1937358

The complete mitochondrial genome of Diagramma pictum (Perciformes: Haemulidae)

Ming Chen a,b,c, Guowei Liao a, Zibo Li a, Houhua Chen a, Kai Zhang a,b,c, Rishen Liang a,b,c,
PMCID: PMC8344735  PMID: 34377787

Abstract

The painted sweetlips Diagramma pictum (Thunberg 1792) is an important fish for commercial fisheries which is widely distributed in the Indo-West Pacific Ocean. It can change its external coloration and pattern during their lives. The complete mitochondrial genome of D. pictum was determined in this study. The genome was 16,531 bp in length and consisted of 13 protein coding genes, 22 transfer RNA (tRNA), 2 ribosomal RNA (rRNA), and one noncoding control region. The overall base composition was estimated to be A: 27.5%; T: 24.7%; C: 30.9% and G: 16.9% with AT bias of 52.2%. The molecular phylogenetic result revealed that D. pictum did not form an independent branch but was tightly clustered inside the Plectorhinchus groups, closely related to the species Plectorhinchus chaetodonoides, indicating the close relationships between genera Diagramma and Plectorhinchus. These results may provide important genomic information for species evolution and mitogenome based phylogenetic analyses of D. pictum in the family Haemulidae.

Keywords: Mitochondrial genome, Haemulidae, Diagramma pictum, phylogenetic analysis


The painted sweetlips Diagramma pictum (Thunberg 1792) is an important fish for commercial fisheries. It belongs to the family Haemulidae of order Perciformes. It is widely found throughout the coastal inshore waters around the Indo-Western Pacific Ocean. Morphologically, D. pictum displayed diverse appearance and can change its external coloration and pattern during its life. Juvenile D. pictum has longitudinal dark bands along its body, as it grow to adult, the bands increased and break into numerous small round spots, making the juvenile quite distinct from its adult form (McKay 1984, 2001). In this study, we determined the complete mitochondrial sequence of D. pictum and analyzed the genome structure and organization as well as its phylogenetic status within the family Haemulidae.

The painted sweetlips D. pictum was collected from Nanao city, Guangdong Province, China (22°53'38″N, 114°48'88″E) in July 2019 by setting nets. The sample was deposited in the laboratory of College of Animal Science and Technology, Zhongkai University of Agriculture and Engineering, Guangzhou, China (23°37'93″N, 113°45'15″E, voucher number: ZK-201907DP01, collector Information: Rishen Liang, cheetahliang@126.com). Total genomic DNA was extracted from tissues using the Animal Genomic DNA isolation kit (TIANGEN, China). Sequencing of the mitogenome was performed on Illumina Novaseq 6000 platform and assembled using the de novo assembler SPAdes 3.11.0 (Dmitry et al. 2016). The annotations were performed with MITOS web server (http://mitos.bioinf.uni-leipzig.de/index.py) and the circular genome map was drawn using OGDRAW v1.2 (Lohse et al. 2007).

The complete mitogenome of D. pictum was circular and of 16,531 bp in length (GenBank accession number: MW411454), typically containing 13 protein coding genes, 22 transfer RNA (tRNA), 2 ribosomal RNA (rRNA), and 1 non-coding region. The overall base compositions of the genome were 27.5% for A, 16.9% for G, 24.7% for T, 30.9% for C, respectively. The AT content (52.2%) was higher than the GC content (47.8%). The genome structure, organization and base compositions were identical to those of other vertebrates (Zhang et al. 2019; Kim et al. 2020; Tabassum et al. 2020). 13 protein-coding genes found in D. pictum mitogenome use ATG as a start codon except for COI, which started with GTG. The use of stop codons varied among different genes, five genes ended with TAA: ND1, ND2, ATPase8, ND4L and ND5, one ended with TAG: ND6, one ended with AGG: COI, the remaining genes had incomplete stop codons, TA (ATPase6, COIII) or T: COII, ND3, ND4 and Cyt b.

We compared our D. pictum mitogenome sequence with Diagramma picta obtained from GenBank (AP009167), D. picta is a synonymy of D. pictum and D. pictum is a valid name (McKay 1984; McKay 2001; Froese and Pauly 2020). The result showed that there were 70 bp variable sites between the two samples and the sequence divergence value was 0.004%, indicating that some sequence variation and molecular differentiation exist at the intraspecific level. To investigated the molecular phylogenetic status of D. pictum in the family Haemulidae, mitogenome sequences of 7 Haemulidae and 2 Lutjanidae species available online in GenBank were downloaded and analyzed. Lutjanidae species were closely related to Haemulidae species and were used as outgroups (Mckay 1984; Miller and Cribb 2007). The molecular phylogenetic tree was constructed based on the nucleotide sequences of 12 proteins coding genes (except for ND6) by RAxML 8.0 using maximum-likelihood method with GTR + G + I model (Figure 1). The result revealed that D. pictum in our study was tightly clustered with D. picta. Species in Diagramma did not form an independent branch but were located inside the Plectorhinchus groups, closely related to Plectorhinchus chaetodonoides, and they were sister to cluster Plectorhinchus orientalis + Plectorhinchus vittatus + Plectorhinchus lineatus, revealing the close relationships within Diagramma and Plectorhinchus. This result was consistent with the previous phylogenetic studies of the Haemulidae fish (Sanciangco et al. 2011; Tavera et al. 2018). This mitochondrial genome provides important genomic information for species evolution and phylogenetic analyses of D. pictum in the family Haemulidae.

Figure 1.

Figure 1.

Molecular phylogenetic tree of Diagramma pictum with other Haemulidae species based on nucleotide sequences of 12 protein coding gene sequences constructed by maximum likelihood method. The accession number and species sites for these species are as follows: Diagramma picta(AP009167); Diagramma pictum(MW411454); Plectorhinchus chaetodonoides(MW411455); Plectorhinchus lineatus(KM099284); Plectorhinchus orientalis(KP966562); Plectorhinchus vittatus(KP976103); Plectorhinchus cinctus(KJ690267); Parapristipoma trilineatum(AP009168); Lutjanus erythropterus(KP939271); Lutjanus russellii(EF514208).

Funding Statement

The study was supported by the National Natural Science Foundation of China [No. 31802300] and the Natural Science Foundation of Guangdong Province, China [No. 2018A0303130104].

Disclosure statement

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

Data availability statement

The data that support the findings of this study are openly available in “NCBI” at https://www.ncbi.nlm.nih.gov/, reference number MW411454.

References

  1. Dmitry A, Anton K, Jeffrey SM, Pavel AP.. 2016. HYBRIDSPADES: an algorithm for hybrid assembly of short and long reads. Bioinformatics. 32(7):1009–1015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Froese R, Pauly D. FishBase. version (12/2020); 2020. www.fishbase.org.
  3. Kim P, Han JH, An SL.. 2020. Complete mitochondrial genome of Korean catfish, Liobagrus somjinensis (Actinopterygii, Siluriformes, Amblycipitidae), from South Korea. Mitochondrial DNA Part B. 5(1):866–868. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Lohse M, Drechsel O, Bock R.. 2007. Organellar Genome DRAW (OGDRAW): a tool for the easy generation of high-quality custom graphical maps of plastid and mitochondrial genomes. Curr Genet. 52:267–274. [DOI] [PubMed] [Google Scholar]
  5. McKay RJ. 1984. Haemulidae. In: Fischer W and Bianchi G, editors. FAO species identification sheets for fishery purposes. Western Indian Ocean (Fishing Area 51). Volume. 2. Rome: FAO; p. 1–11. [Google Scholar]
  6. McKay RJ. 2001. Haemulidae = Pomadasyidae. Grunts (also sweetlips, rubberlips, hotlips, and velvetchins). In: Carpenter KE, Niem VH, editors. The living marine resources of the Western Central Pacific, Volume 5. Rome: FAO; p. 2961–2989. [Google Scholar]
  7. Miller TL, Cribb TH.. 2007. Phylogenetic relationships of some common Indo-Pacific snappers (Perciformes: Lutjanidae) based on mitochondrial DNA sequences, with comments on the taxonomic position of the Caesioninae. Mol Phylogenet Evol. 44(1):450–460. [DOI] [PubMed] [Google Scholar]
  8. Sanciangco MD, Rocha LA, Carpenter KE.. 2011. A molecular phylogeny of the Grunts (Perciformes: Haemulidae) inferred using mitochondrial and nuclear genes. Zootaxa. 2966(1):37–50. [Google Scholar]
  9. Tabassum N, Kaure T, Park KD, Lee DS, Kim HW.. 2020. The complete mitochondrial genome of the doubled-lined mackerel Grammatorcynus bilineatus Rüppell, 1836 (Perciformes: Scombridae) from Beqa lagoon in Fiji. Mitochondrial DNA Part B. 5(3):3688–3689. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Tavera J, Acero PA, Wainwright PC.. 2018. Multilocus phylogeny, divergence times, and a major role for the benthic-topelagic axis in the diversification of grunts (Haemulidae). Mol Phylogenet Evol. 121:212–223. [DOI] [PubMed] [Google Scholar]
  11. Zhang Z, Cheng Q, Ge Y.. 2019. The complete mitochondrial genome of Rhynchocypris oxycephalus (Teleostei: Cyprinidae) and its phylogenetic implications. Ecol Evol. 9:7819–7837. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data that support the findings of this study are openly available in “NCBI” at https://www.ncbi.nlm.nih.gov/, reference number MW411454.


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