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Mitogenome Announcement

The complete mitochondrial genome of Monochamus dubius Gahan (Coleoptera: Cerambycidae)

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Pages 699-700 | Received 17 Nov 2020, Accepted 23 Jan 2021, Published online: 01 Mar 2021

Abstract

In this study, we sequenced the complete mitochondrial genome of Monochamus dubius Gahan 1894. The results showed that the length of complete mitochondrial genome was 16,029 bp with 22.22% GC content, containing 39.4% A, 38.4% T, 13.4% C, 8.8% G. There were 13 protein-coding genes (PCGs), 22 transfer RNA genes (tRNA), two ribosomal RNA genes (rRNA) and one AT-rich region. Phylogenetic analysis showed that M. dubius was clustered with Monochamus urussovii and Monochamus alternatus alternatus, and confirmed the sister relationship among the genus Monochamus, Anoplophora, and Aristobia from Cerambycidae. The complete mitogenome of M. dubius would help understand the classification and phylogeny of Chrysomeloidea.

Chrysomeloidea cover the two largest families, Cerambycidae (longhorn beetles) and Chrysomelidae (leaf beetles), each with more than 30,000 species and about a dozen subfamilies (Nie et al. Citation2020). Relationships among subfamilies of Chrysomelidae have been clarified over the past two decades (Reid Citation2000; Ge et al. Citation2011). However, up to date, phylogenetic relationships within Cerambycidae still remain understudied (Haddad et al. Citation2018). In recent decades, insect mitochondrial genome has been widely used in phylogenetic and population genetic studies at different levels due to its unique features (Salvato et al. Citation2008). Therefore, this study newly determined the complete mitochondrial genome of M. dubius from Cerambycidae. In addition, we built the phylogenetic tree based on the maximum likelihood method to understand the evolution relationship. The results provide important information for studying the evolution of mitochondrial genomes in this group.

The M. dubius adults were collected from Lianjiang, Fujian Province, China (East longitude 119.8002, North latitude 26.3284) by using sex pheromone traps. The specimens were deposited at −80 °C in the Key Laboratory of Integrated Pest Management in Ecological Forests, Fujian Agriculture and Forestry University (Jiankai Wu, [email protected]) under the voucher number TN-202009. The total DNA was extracted from the legs using Insect DNA Kit (Omega Bio-Tek, GA, USA) and purified using QIAquick Gel Extraction Kit (Qiagen GmbH, Germany). The mitochondrial genome was sequenced by the Illumina Hiseq 2500 (Illumina, CA, USA) at the Novogene (Beijing, China). A total of 66,458,876 clean reads were obtained by quality control and filtration from the 68,684,628 raw reads. After the de novo assembly of MitoZ and metaSpades software (Nurk et al. Citation2017), we obtained a 16,029 bp length complete mitochondrial genome of M. dubius with 22.22% GC content.

The characteristics of PCGs, tRNAs, rRNAs, and AT-rich region were obtained from the annotated result of mitoMaker (Bernt et al. Citation2013). The complete mitogenome sequence has been submitted to NCBI Genbank with accession number MW067124. In this study, 37 genes were annotated, including 13 PCGs, 22 tRNAs, 2 rRNAs. Thirteen PCGs are 10,911 bp in total, encoding 3,637 amino acids. Nine PCGs (ATP6, ATP8, COX1, COX2, COX3, CYTB, ND2, ND3, ND6) are clockwise coding, while four PCGs (ND1, ND4, ND4L, ND5) are counterclockwise coding. All PCGs stop with usual codons such as TAA and TAG, except ND5 which is stopped with the incomplete condon T. The rrnS and rrnL genes are 810 bp and 1234 bp in length.

To investigate its taxonomic status of M. dubius, the sequence alignment was performed with the MAFFT, according to mitochondrial genome sequence of 17 species from Chrysomeloidea which had been selected from Genebank BLAST according to the percent identity (Katoh and Standley Citation2013). Take the whole mitogenome of Cnidocampa flavescens (GenBank: KY628213.1) as an out-group, a maximum likelihood analysis of 11 Cerambycidae species and 6 Chrysomelidae species was performed with the software MEGA 7.0, following by calculating the bootstrap values with 1000 replications (Kumar et al. Citation2016). The resultant ML trees distinctly showed that the M. dubius constituted a monophyletic group with other 10 Cerambycidae. The monophyletic Cerambycidae that contains Lamiinae, Aseminae, Spondylinae and Lepturinae was assigned to the sister group to the clade of Chrysomelidae that consists of Chrysomelinae and Galerucinae in this study. Additionally, M. dubius was clustered together with M. urussovii and M. alternatus alternatus (). The complete mitochondrial genome of M. dubius will provide useful genetic information for the genetic evolution of M. dubius, as well as in other insects of Chrysomeloidea.

Figure 1. Maximum likelihood tree of the Monochamus dubius, Cnidocampa flavescens, and other 16 species of Chrysomeloidea based on the genome sequence. Numbers labeled on the branch are bootstrap values.

Figure 1. Maximum likelihood tree of the Monochamus dubius, Cnidocampa flavescens, and other 16 species of Chrysomeloidea based on the genome sequence. Numbers labeled on the branch are bootstrap values.

Disclosure statement

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

Data availability statement

The genome sequence data that support the findings of this study are openly available in GenBank of NCBI at [https://www.ncbi.nlm.nih.gov] (https://www.ncbi.nlm.nih.gov/nuccore/MW067124.1/) under the accession no. MW067124. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA688627, SRP300485, and SAMN17183230 respectively.

Additional information

Funding

This work was supported by the [Forestry Science Research Project of Fujian Forestry Department] under Grant [number Minlinke [2017] 03]; [Forestry Programs of Science and Technology in Fujian Province] under Grant [number Minlinke [2020] 29]; [horizontal research projects] under Grant [number KH200083A]; and [Undergraduate Training Program for Innovation and Entrepreneurship of China] under Grant [number 202010389003].

References

  • Bernt M, Donath A, Jühling F, Externbrink F, Florentz C, Fritzsch G, Pütz J, Middendorf M, Stadler PF. 2013. MITOS: improved de novo metazoan mitochondrial genome annotation. Mol Phylogenet Evol. 69(2):313–319.
  • Ge DY, Chesters D, Gómez-Zurita J, Zhang LJ, Yang XK, Vogler AP. 2011. Anti-predator defence drives parallel morphological evolution in flea beetles. Proc Biol Sci. 278(1715):2133–2141.
  • Haddad S, Shin S, Lemmon AR, Lemmon EM, Svacha PETR, Farrell B, Ślipiński ADAM, Windsor D, Mckenna DD. 2018. Anchored hybrid enrichment provides new insights into the phylogeny and evolution of longhorned beetles (Cerambycidae). Syst Entomol. 43(1):68–89.
  • Katoh K, Standley DM. 2013. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 30(4):772–780.
  • Kumar S, Stecher G, Tamura K. 2016. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 33(7):msw054.
  • Nie R, Vogler AP, Yang XK, Lin M. 2020. Higher-level phylogeny of longhorn beetles (Coleoptera: Chrysomeloidea) inferred from mitochondrial genomes. Syst Entomol. 45(1):188–204.
  • Nurk S, Meleshko D, Korobeynikov A, Pevzner PA. 2017. metaSPAdes: a new versatile metagenomic assembler. Genome Res. 27(5):824–834.
  • Reid CAM. 2000. Spilopyrinae Chapuis: a new subfamily in the Chrysomelidae and its systematic placement (Coleoptera). Invert Systematics. 14(6):837–862.
  • Salvato P, Simonato M, Battisti A, Negrisolo E. 2008. The complete mitochondrial genome of the bag-shelter moth Ochrogaster lunifer (Lepidoptera, Notodontidae). BMC Genomics. 9:331.