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MitoGenome Announcement

The mitochondrial genome of the ambush bug Carcinochelis bannaensis (Hemiptera: Reduviidae)

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Pages 990-991 | Received 13 Jul 2018, Accepted 29 Jul 2018, Published online: 29 Oct 2018

Abstract

The complete mitochondrial genome (mitogenome) of the ambush bug, Carcinochelis bannaensis, was determined in this study. The sequenced mitogenome is a typical circular DNA molecule of 15,335 bp, containing 13 protein-coding genes, two rRNA genes, 22 tRNA genes and a putative control region. All protein-coding genes initiate with ATN codons and terminate with TAA codons except for COII,COIII and ND5 use a single T residue as the stop codon. All tRNAs have the clover-leaf structure except for the tRNASer(AGN) and the length of them range from 61 to 71 bp. The control region is 797 bp long with an A + T content of 66.3%. The phylogenetic analysis result supports the monophyly of Phymatinae.

The ambush bug Phymatinae (Hemiptera: Reduviidae) is a diverse clade of predators and distinguished by the cryptic hunting behavior and morphologically diverse raptorial forelegs (Masonick et al. Citation2017). The genus Carcinochelis includes seven species distributed in the Oriental region of China. We sequenced the complete mitogenome of Carcinochelis bannaensis, the only one species which reaches the south of China in this genus (Cui et al. Citation2006). Voucher specimen (No. VCim-00115) was deposited at the Entomological Museum of China Agriculture University and the sequence was deposited in GenBank under the accession number KY069957.

The mitochondrial genome is a typical circular DNA molecule of 15,335 bp in size that encode 37 genes (13 protein-coding genes, 22 tRNA genes, and two rRNA genes) and a control region. Gene order is identical to the putative ancestral gene arrangement (Cameron Citation2014; Song et al. 2016; Li et al. Citation2017). Except for the control region, this mitogenome has seven inter-genic regions, which range from 1 to 55 bp in size. There are totally 60 bp overlapped nucleotides between neighboring genes in 15 locations, ranging from 1 to 17 bp in size.

The nucleotide composition of the whole mitogenome shows significantly AT bias. The A + T content is 70.7% with positive AT-skew (0.14) and negative GC-skew (–0.16). All protein-coding genes initiate with ATN as the start codon (four with ATT, five with ATG and four with ATA). The stop codon TAA is assigned to 10 protein-coding genes. Whereas COII,COIII and ND5 use a single T residue as incomplete stop codon which is commonly reported in true bug mitogenomes (Li et al. Citation2012). Among 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 (Jiang et al. Citation2016).

The length of the 22 sequenced tRNA genes range from 61 to 71 bp with the classic cloverleaf secondary structure. The lrRNA is 1242 bp long with an A + T content of 73.2%, and the srRNA is 761 bp long with an A + T content of 72.7%. The control region, which is located between srRNA and tRNAIle, is 797 bp long and is biased toward A + T (66.3%). Except the control region, another 55 bp noncoding region located between tRNAIle and tRNAGln, which has also been found in other ambush bugs.

Phylogenetic tree based on the maximum likelihood method shows Phymatinae is monophyletic, which is also recovered in previous molecular and morphological analyses (Weirauch and Munro Citation2009; Weirauch et al. Citation2014) (). The genus Carcinochelis is more closed to the genus Carcinocoris. The present data are largely congruent with recently published hypotheses in supporting paraphyly of Reduviinae (Hwang and Weirauch Citation2012; Liu et al. Citation2018).

Figure 1. Phylogenetic relationship of Carcinochelis bannaensis and other 17 species among Reduviidae. Phylogenetic tree was inferred from ML analysis of the 13 protein-coding genes and two rRNAs genes (12,697bp) and generated by IQ-TREE 1.6.5 (Trifinopoulos et al. Citation2016). The numbers beside the nodes are percentages of 1000 bootstrap values. Alphanumeric terms indicate the GenBank accession numbers.

Figure 1. Phylogenetic relationship of Carcinochelis bannaensis and other 17 species among Reduviidae. Phylogenetic tree was inferred from ML analysis of the 13 protein-coding genes and two rRNAs genes (12,697bp) and generated by IQ-TREE 1.6.5 (Trifinopoulos et al. Citation2016). The numbers beside the nodes are percentages of 1000 bootstrap values. Alphanumeric terms indicate the GenBank accession numbers.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

Funding for this study was supported by grant from the National Natural Science Foundation of China (No. 31760086).

References

  • Cameron SL. 2014. Insect mitochondrial genomics: implications for evolution and phylogeny. Annu Rev Entomol. 59:95–117.
  • Cui JX, Cai WZ, Rabitsch W. 2006. The Ambush Bugs of China: Taxonomic Knowledge and Distribution Patterns (Heteroptera: Reduviidae: Phymatinae). Zugleich Kataloge Der OÖ. 50:795–812.
  • 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
  • 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.
  • Li H, Leavengood JM, Jr, Chapman EG, Burkhardt D, Song F, Jiang P, Liu J, Zhou X, Cai WZ. 2017. Mitochondrial phylogenomics of hemiptera reveals adaptive innovations driving the diversification of true bugs. Proc R Soc B. 284:20171223.
  • Li H, Liu HY, Song F, Shi AM, Zhou XG, Cai W. 2012. Comparative mitogenomic analysis of damsel bugs representing three tribes in the family Nabidae (Insecta: Hemiptera). PLoS ONE. 7:e45925.
  • 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.
  • Masonick P, Michael A, Frankenberg S, Rabitsch W, Weirauch C. 2017. Molecular phylogenetics and biogeography of the ambush bugs (Hemiptera: Reduviidae: Phymatinae). Mol Phylogenet Evol. 114:225–233.
  • 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.
  • 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.
  • Weirauch C, Munro JB. 2009. Molecular phylogeny of the assassin bugs (Hemiptera: Reduviidae), based on mitochondrial and nuclear ribosomal genes. Mol Phylogenet Evol. 53:287–299.
  • Weirauch C, Berenger JM, Berniker L, Forero D, Forthman M, Frangenberg S, Michael A, Paiero SM, Udah O, Waston C, et al. 2014. An illustrated identification key to assassin bug subfamilies and tribes (Hemiptera: Reduviidae). Can J Arthrod Ident. 26:1–115.