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Mitogenome Announcement

Mitochondrial genome sequence of black paradise flycatcher (Aves: Monarchidae) and its phylogenetic position

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Pages 454-455 | Received 20 Apr 2016, Accepted 20 Apr 2016, Published online: 08 Jul 2016

Abstract

We generated the complete mitochondrial genome of the black paradise flycatcher (Terpsiphone atrocaudata; Family: Monarchidae), an ecologically important insectivorous bird in Asian forest ecosystems. The mitogenome was 16,984 bp in length and consisted of 13 protein-coding genes, 22 tRNAs, two rRNAs and a control region. Gene composition and arrangement in the mitogenome were similar to those of related families Corvidae and Laniidae available in GenBank. However, tRNAAla was located between COXII and ATP8 genes in the mitogenome of T. atrocaudata while tRNALys, was in the same location in the mitogenomes of Corvidae and Laniidae. The phylogenetic tree based on the mitogenomes of T. atrocaudata and the related families supported that Monarchidae was the sister taxa to the clade of Laniidae and Corvidae. The mitogenome of T. atrocaudata will be a valuable genetic resource for phylogenetic analyses and implication of conservation and management of the species.

Black paradise flycatcher (Terpsiphone atrocaudata Eyton, 1839) also called Japanese paradise flycatcher is a passerine bird breeding mainly in the Korean Peninsula, Japan and Taiwan and migrating to China and Southeast Asia (Mizuta Citation1998; Del Hoyo et al. Citation2006; Kim et al. Citation2010, Citation2011). The species is an ecologically important insectivore in deciduous or mixed forest ecosystems of the breeding distribution but, unfortunately, the bird is suspected to be in rapid decline by habitat loss and, therefore, listed as Near Threatened of IUCN Red List (Del Hoyo et al. Citation2006; BirdLife International Citation2015).

Approximately one hundred species including T. atrocaudata belong to the monarch flycatcher family, Monarchidae (Gill & Donsker Citation2015). The systematic position of the family Monarchidae has been largely dependent on results of DNA–DNA hybridization (Sibley & Ahlquist Citation1990) and data from multilocus nuclear genes (Barker et al. Citation2002, Citation2004). However, comprehensive surveys of mitochondrial genome (mitogenome) for the phylogenetic placement of the family are lacking. Complete mitogenome plays a significant role in discussion of phylogenetic relationships (Eo and An. in press; Eo & DeWoody Citation2010) and implication of conservation and management (Eo et al. Citation2010) but, to our knowledge, no complete mitogenome has been reported from the family Monarchidae. Here, we sequenced the complete mitogenome of T. atrocaudata in order to provide further molecular resources for the biology, phylogenetic analysis and conservation of the species.

The specimen of T. atrocaudata was collected by CGRB (Conservation Genome Resource Bank for Korean Wildlife; CGRB3837), South Korea. We extracted genomic DNA from muscle tissue of the bird and prepared genomic libraries with an insert size of 300–700 bp. A HiSeq2500 sequencing platform (Illumina, San Diego, CA) generated about 5.8 million sequence reads corresponding to about 0.81 Gbp from genomic DNA of the black paradise flycatcher. We assembled the sequence reads into contigs using the default parameters in Newbler ver3.4 (Illumina, San Diego, CA).

The complete mitogenome sequence of a T. atrocaudata was 16,984 bp in length (GenBank accession no. KT901458) with 44.3% of the GC content. The mitogenome was composed of 13 protein-coding genes, 12S and 16S ribosomal RNAs, 22 transfer RNAs and a non-coding control region. The start codon was ATG in all protein-coding genes with an exception of the COXI (GTG). Gene composition, length and arrangement in the mitogenome were similar to those of related families Corvidae and Laniidae available in GenBank. However, tRNAAla was located between COXII and ATP8 genes in the mitogenome of T. atrocaudata while tRNALys, was in the same location in the available mitogenomes of the Corvidae and Laniidae.

A neighbor-joining (NJ) tree was reconstructed using 13 protein-coding genes of the T. atrocaudata mitogenome and all available complete mitogenomes of crows and allies in GenBank, with those of a Vireo olivaceus mitogenome as an outgroup (). Our NJ tree revealed that the family Monarchidae (Terpsiphone) was the sister taxa to the clade of the Laniidae (Lanius) and the Corvidae (Corvus, Nucifraga, Garrulus, Pica, Podoces, Urocissa, Cyanopica and Pyrrhocorax). The result is similar to those of the phylogenetic trees based on multilocus nuclear genes (Barker et al. Citation2002, Citation2004). The complete mitogenome of T. atrocaudata will be a valuable genetic resource for phylogenetic relationships and implication of conservation and management of the species.

Figure 1. Neighbor-joining tree based on 13 protein-coding genes from 20 crows and allies, Terpsiphone atrocaudata (KT901458) we sequenced and Vireo olivaceus as an outgroup. Numbers on branches represent bootstrap supports (1000 replicates).

Figure 1. Neighbor-joining tree based on 13 protein-coding genes from 20 crows and allies, Terpsiphone atrocaudata (KT901458) we sequenced and Vireo olivaceus as an outgroup. Numbers on branches represent bootstrap supports (1000 replicates).

Acknowledgements

The authors thank Conservation Genome Resource Bank for Korean Wildlife (CGRB) for donating samples of Terpsiphone atrocaudata. This work was supported by a grant from the National Institute of Biological Resources (NIBR), funded by the Ministry of Environment (MOE) of the Republic of Korea (NIBR 201503103).

Disclosure statement

The authors declare no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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