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Mitogenome Announcement

Complete mitochondrial genome of Bombus breviceps (Hymenoptera: Apidae)

, , , , & ORCID Icon
Pages 604-606 | Received 03 Aug 2017, Accepted 24 Aug 2017, Published online: 05 Sep 2017

Abstract

The complete mitochondrial genome of Bombus breviceps, which belongs to the subgenus of Alpigenobombus in Bombus genus, was sequenced. This circular mitogenome is 16,743 bp (83.5% AT) in length, with two rRNA genes, 22 tRNA genes, and 13 protein-coding genes. All protein-coding genes are initiated with the common invertebrate initiation codon except TTA for ND2, and terminated by the typical stop codon TAA or TAG. tRNA-Ser (TCT) lacks a dihydrouridine (DHU) arm while other tRNA genes form a cloverleaf structure. Phylogenetic analysis shows that genus Bombus has a closer relationship with genus Melipona than any other genera in Apidae family, and B. breviceps clusters closer to B. lapidarius than any other bumblebees with sequenced mitogenome.

Bumblebees (Hymenoptera: Apidae) are a genus of pollinating insects, which play an important role in agriculture production and ecosystem balance (Fontaine et al. Citation2006; Velthuis and van Doorn Citation2006). There are 15 subgenera of bumblebees all over the world (Williams et al. Citation2008), however, to date, the sequenced mitochondrial genomes are only from two subgenera of bumblebees, Bombus and Melanobombus (Cha et al. Citation2007; Tang et al. Citation2015; Du et al. Citation2016; Takahashi et al. Citation2016; Nishimoto et al. Citation2017). Mitochondrial DNA sequences are commonly used to identify species and investigate the evolutionary relationship among them (Sankoff et al. Citation1992; Cameron et al. Citation2007). Bombus breviceps belongs to the subgenus of Alpigenobombus in Bombus genus and no mitochondrial genome from this subgenus was sequenced yet. Therefore, to further the phylogenic and genetic diversity analysis of bumblebees, we sequenced the complete mitochondrial genome of B. breviceps.

Male bumblebees were collected from Yuping town in Yunnan province, China (N 23.0116; E 103.6404). Specimen is stored in the CAAS Institute of Apicultural Research, Beijing, China (IAR), accession number: IAR-BR00007. The genomic DNA of B. breviceps was extracted from one single haploid drone, which was sequenced by Illumina’s HiSeq2500 (Illumina), with a read length of 250 bp. The resultant shotgun reads were assembled by DISCOVAR de novo (https://software.broadinstitute.org/software/discovar/blog/). We obtained a circular mitochondrial genome of 16,743 base pairs (bp) in length (accession number: MF478986). We analysed the mitogenome by MITOS web server (Bernt et al. Citation2013), and phylogenetic analysis was performed by MEGA7 software (Kumar et al. Citation2016).

In B. breviceps, the 16,743 bp of circular mitochondrial DNA encode 37 genes, including 13 protein-coding genes, 22 tRNA genes, and two rRNA genes. The overall base composition of B. breviceps mitogenome is 41.4% A, 42.1% T, 11.6% C, and 4.9% G. Of all these 37 genes, nine protein-coding genes and 13 tRNA genes are located on the heavy strand, while other 15 genes are on the light strand. Similar to other sequenced bumblebee species, ATP8-ATP6 and ND6-CYTB were overlapped with 19 bp and 13 bp, respectively (Du et al. Citation2016; Takahashi et al. Citation2016; Nishimoto et al. Citation2017). Eight of the thirteen proteins are started with methionine translated from two kinds of initiation codons, ATG (ATP6, COX3, CYTB, ND4, ND6) and ATA (COX1, ND1, ND3). Isoleucine can be the first amino acid of proteins in bumblebees with the codon of ATT (ATP8, COX2, ND4L, ND5). ND2 is a special case with TTA as start codon by reason of RNA editing. The stop codon of all protein-coding genes is TAA, except CYTB with TAG. Twenty one tRNA genes fold into secondary cloverleaf shape, and the remaining tRNA-Ser (TCT) lacks a dihydrouridine (DHU) arm.

Phylogenetic relationship of mitochondrial genomes coming from 24 closely related taxa was estimated with maximum likelihood method based on the JTT matrix-base model (Jones et al. Citation1992), using concatenated amino acid sequences of the 13 protein-coding genes in those mitochondrial genomes (). Megachilidae (Megachile sculpturalis) and Colletidae (Colletes gigas and Hylaeus dilatatus) are the sister groups of Apidae family within superfamily Apoidea (Debevec et al. Citation2012), which were used as outgroup (Huang et al. Citation2016; Tan et al. Citation2016; Zhang et al. Citation2017). The obtained phylogeny tree () suggests that bumblebees (Bombus) have a closer relationship with stingless bees (Melipona) than honeybees (Apis) or cuckoo bees (Nomadini). B. breviceps and B. lapidaries are representative bumblebee species from subgenus Alpigenobombus and Melanobombus, respectively (Williams et al. Citation2008). In the phylogeny tree, B. breviceps clusters closer to B. lapidaries than any other bumblebees with sequenced mitochondrial genome (), and this relationship is consistent with the simplified bumblebee subgeneric phylogeny (Williams et al. Citation2008). Complete mitochondrial genome is powerful as a supplementary way to classify different species of bumblebees.

Figure 1. Phylogenetic analysis of the 24 related mitochondrial genomes. Black triangle indicates the focal mitochondrial genome of this study. Numbers beside each node are percentages of 1000 bootstrap values. Mitochondrial genome sequences from Megachilidae (Megachile sculpturalis) and Colletidae (Colletes gigas and Hylaeus dilatatus) were used as outgroup. GenBank accession numbers were followed after their corresponding species names.

Figure 1. Phylogenetic analysis of the 24 related mitochondrial genomes. Black triangle indicates the focal mitochondrial genome of this study. Numbers beside each node are percentages of 1000 bootstrap values. Mitochondrial genome sequences from Megachilidae (Megachile sculpturalis) and Colletidae (Colletes gigas and Hylaeus dilatatus) were used as outgroup. GenBank accession numbers were followed after their corresponding species names.

Disclosure statement

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

Additional information

Funding

This work was supported by the Agricultural Science and Technology Innovation Program under Grant CAAS-ASTIP-2017-IAR-002; Elite Youth Program of Chinese Academy of Agricultural Sciences under Grant [to CS]; Ministry of Human Resources and Social Security of the People’s Republic of China under Grant [to CS].

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