Skip to main content
Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2019 Sep 20;4(2):3137–3138. doi: 10.1080/23802359.2019.1666690

The complete mitochondrial genome of the assassin bug Reduvius gregoryi (Hemiptera: Reduviidae)

Qiaoqiao Liu 1, Fan Song 1, Wanzhi Cai 1, Hu Li 1,
PMCID: PMC7707017  PMID: 33365887

Abstract

The complete mitochondrial genome (mitogenome) of the assassin bug, Reduvius gregoryi, was determined. The sequenced mitogenome is a typical circular DNA molecule of 16,477 bp, containing 13 protein-coding genes, 2 rRNA genes, 22 tRNA genes and a putative control region. Protein-coding genes all initiate with ATN codons and terminate with TAA codons except for ATP6, COI, COIII, ND4, and ND5 use a single T residue as the termination codon. All tRNAs have the clover-leaf structure except for the tRNASer(AGN) and the length of them range from 61 to 70 bp. The control region is 1731 bp long with an A + T content of 72.3%. Our phylogenetic analysis supported the polyphyly of Reduviinae and the sister relationship between Reduvius gregoryi and Reduvius tenebrosus.

Keywords: Mitochondrial genome, Hemiptera, Reduviidae, Reduvius gregoryi


The genus Reduvius Fabricius is one of the most speciose genera of assassin bugs (Hemiptera: Reduviidae) worldwide. About 197 species have been recognized in this genus so far (Weirauch et al. 2015). Most species occur in arid- and semi-arid areas in the Afrotropical, Oriental, and Palearctic regions. To date, only one mitogenome have been sequenced from the genus Reduvius (Jiang et al. 2016). Here, we sequenced the complete mitogenome of Reduvius gregoryi, which is the second representation of Reduvius. The samples were collected in Medog country, Xizang Autonomous Region, China (29°39′17″N 95°29′26″E). Voucher specimen was deposited at the Entomological Museum of China Agricultural University (No. VCim-00112) and the sequence was deposited in GenBank under the accession number KY069969.

This sequenced mitogenome is 16,477 bp long, including 37 genes (13 protein-coding genes, 22 tRNA genes, and 2 rRNA genes) and a control region. Gene order is identical to the putative ancestral arrangement of insects and other assassin bugs (Cameron 2014; Song et al. 2016; Li et al. 2017; Song et al. 2019). Except control region, this mitochondrial genome has one 182 bp inter-genic regions, which is between ND1 and tRNASer(UCN). There are totally 56 bp overlapped nucleotides between neighboring genes in 14 locations, ranging from 1 to 18 bp in size.

The nucleotide composition of the whole mitogenome is significantly biased toward A + T (71.1%) with positive AT-skew (0.19) and negative GC-skew (−0.26). All protein-coding genes initiate with ATN as the start codon (2 with ATA, 5 with ATT, and 6 with ATG). The stop codon TAA/TAG was assigned to 8 protein-coding genes. ATP6, COI, COIII, ND4, and ND5 used a single T residue as incomplete stop codon which is commonly reported in insect mitogenomes (Wang et al. 2014).

The length of the 22 sequenced tRNA genes range from 61 to 70 bp. Among all tRNA genes, only tRNASer(AGN) cannot exhibit the classic cloverleaf secondary structure, due to the deficiency of the dihydrouridine (DHU) arm which is typical feature of insect mitogenomes (Li et al. 2012). The lrRNA is 1255 bp long with an A + T content of 72.5% and the srRNA is 786 bp long with an A + T content of 71.8%. The control region, which is located between srRNA and tRNAIle, is 1731 bp long and is also significantly biased toward A + T (72.3%).

We analyzed nucleotide sequences of 13 protein-coding genes and 2 rRNAs with maximum likelihood (ML) method to understand the phylogenetic relationships within Reduviidae (Figure 1). The two Reduvius species were clustered into a branch with 100 bootstrap values. The subfamily Reduviinae was polyphyletic which was also recovered in previous comprehensive taxa-sampling studies (Weirauch 2008; Hwang and Weirauch 2012; Liu et al. 2018).

Figure 1.

Figure 1.

Maximum-likelihood (ML) phylogenetic tree of 16 Reduviidae species inferred from analysis of the 13 protein-coding genes and 2 rRNAs genes (12,697 bp) and generated by IQ-TREE 1.6.5 (Trifinopoulos et al. 2016). Number above each node indicates the ML bootstrap support values. Alphanumeric terms indicate the GenBank accession numbers.

Disclosure statement

All authors have read and approved the final manuscript. The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

References

  1. Cameron SL. 2014. Insect mitochondrial genomics: implications for evolution and phylogeny. Annu Rev Entomol. 59:95–117. [DOI] [PubMed] [Google Scholar]
  2. Hwang WS, Weirauch C. 2012. Evolutionary history of assassin bugs (Insecta: Hemiptera: Reduviidae): insights from divergence dating and ancestral state reconstruction. PLoS One. 7:e45523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Jiang P, Li H, Song F, Cai Y, Wang JY, Liu J, Cai WZ. 2016. Duplication and remolding of tRNA genes in the mitochondrial genome of Reduvius tenebrosus (Hemiptera: Reduviidae). IJMS. 17:951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Li H, Leavengood JM Jr, Chapman EG, Burkhardt D, Song F, Jiang P, Liu J, Zhou X, Cai WZ. 2017. Mitochondrial phylogenomics of hemipteran reveals adaptive innovations driving the diversification of true bugs. Proc R Soc B. 284:20171223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Li H, Liu HY, Song F, Shi AM, Zhou X, Cai WZ. 2012. Comparative mitogenomic analysis of damsel bugs representing three tribes in the family Nabidae (Insecta: Hemiptera). PLoS one. 7:e45925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Liu YQ, Song F, Jiang P, Wilson JJ, Cai WZ, Li H. 2018. Compositional heterogeneity in true bug mitochondrial phylogenomics. Mol Phylogenet Evol. 118:135–144. [DOI] [PubMed] [Google Scholar]
  7. Song F, Li H, Jiang P, Zhou X, Liu JP, Sun CH, Vogler AP, Cai WZ. 2016. Capturing the phylogeny of Holometabola with mitochondrial genome data and Bayesian site–heterogeneous mixture models. Genome Biol Evol. 8:1411–1426. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Song F, Li H, Liu GH, Wang W, James PD, Colwell D, Tran A, Gong SY, Cai WZ, Shao RF. 2019. Mitochondrial genome fragmentation unites the parasitic lice of eutherian mammals. Syst Biol. 68:430–440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Trifinopoulos J, Nguyen LT, Haeseler AV, Minh BQ. 2016. W-IQ-TREE: a fast online phylogenetic tool for maximum likelihood analysis. Nucleic Acids Res. 44:W232–W235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Wang Y, Li H, Wang P, Song F, Cai WZ. 2014. Comparative mitogenomics of plant bugs (Hemiptera: Miridae): identifying the AGG codon reassignments between serine and lysine. PLoS One. 9:e101375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Weirauch C. 2008. Cladistic analysis of Reduviidae (Heteroptera: Cimicomorpha) based on morphological characters. Syst Entomol. 33:229–274. [Google Scholar]
  12. Weirauch C, Russell K, Hwang WS. 2015. Reduvius frommeri, a new species of Reduviidae from the Western United States (Hemiptera: Reduviidae), with a synopsis of the Nearctic species of Reduvius fabricius. Zootaxa. 972:267–279. [DOI] [PubMed] [Google Scholar]

Articles from Mitochondrial DNA. Part B, Resources are provided here courtesy of Taylor & Francis

RESOURCES