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Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2019 Jul 19;4(2):2643–2644. doi: 10.1080/23802359.2019.1643800

The complete mitogenome of the granular torrent frog, Amolops granulosus (Anura: Ranidae)

An Huang a,b,*, Hongdi Luo a,b,*, Sangdawa Luo c, Haijun Li a,b, Qingyong Ni a,b, Yongfang Yao d, Huailiang Xu d, Bo Zeng a,b, Ying Li a,b, Zhimin Wei e, Mingwang Zhang a,b,
PMCID: PMC7706465  PMID: 33365663

Abstract

We obtained the complete mitochondrial genome of Amolops granulosus, which was 17,785 bp in length and it contained the 37 typical mitochondrial genes: 2 ribosomal RNAs, 22 transfer RNAs (tRNAs), 13 protein-coding genes (PCGs), and 1 control region (CR). The hotspot of gene arrangement was ranged as ‘W-gap-OL-gap-A-N-gap-C-Y’ which consisted with most published Amolops mitogenomes. Our phylogenetic results suggested the gene arrangement of ‘WANCY’ region can facilitate to distinguish the Amolops species as an efficient genetic marker.

Keywords: Mitochondrial genome, gene arrangement, Amolops granulosus


The genus Amolops is distributed across Nepal, northern India, western and southern China to Malaya and contains 58 species (Frost 2019). Recently, some mitochondrial genomes of genus Amolops have been reported that the tRNA gene cluster, ‘WANCY’, as a hotspot of mtDNA rearrangement, and it has provided evidence of rearrangements between species within the genus (Huang et al. 2014; Shan et al. 2016; Xue et al. 2016; Zhang et al. 2016). But the phylogenetic relationship of these species still remains controversial. In order to evaluate its phylogenetic position in the genus Amolops, we sequenced the complete mitochondrial genome of Amolops granulosus, a torrent frog which is an endemic species to China.

The sample was collected from Wawushan Mountain (29°38′38.98″ N, 102°55′48.06″ E, Sichuan, China) and placed in the College of Animal Sciences and Technology, Sichuan Agricultural University, China (voucher 20130258). Total genomic DNA was extracted from the muscle tissue using Ezup type animal genomic DNA extraction kit (Sangon, Shanghai) according to the manufacturer’s protocols. The DNA samples were sent to Personal Biotechnology Company (Shanghai, China) for library preparation and Illumina sequencing using a 2 × 251 paired-end strategy. The assembled sequence was annotated using MITOS web server (Bernt et al. 2013) and manually identified by comparing with related databases from GenBank.

In this study, the complete mitogenome of A. granulosus was 17,785 bp in length (GenBank Number: MH922934) and it contained the 37 typical genes: 2 ribosomal RNAs, 22 transfer RNAs (tRNAs), 13 protein-coding genes (PCGs), and a control region (CR). The length of 12S rRNA was 933 bp and of 16S rRNA was 1587 bp, while 22 tRNAs ranged from 65 to 72 bp, which were similar to other Amolops species. Among the 13 PCGs, most genes used ATG as an initiate codon, except for ND2 and COI, which started with ATT and ATA, respectively. For the stop codon, COI and ND5 ended with AGG, ND6 ended with AGA, ND2 and ATP8 ended with TAG, ND4L and Cytb stopped with TAA, while the remaining PCGs shared the incomplete terminal codon (TA or T). The hotspot of gene arrangement was ranged as ‘W-gap-OL-gap-A-N-gap-C-Y’ in the mitochondrial genome of A. granulosus, which consisted most published Amolops mitogenomes, with the exception of Amolops ricketti and Amolops wuyiensis.

Based on 13 PCGs from 26 Anura species, we depicted the molecular phylogeny in Figure 1. The best-fit nucleotide substitution models were determined using Partitionfinder (Lanfear et al. 2017). Bayesian analyses were conducted using MrBayes 3.2.1 with the Marko chain Monte Carlo (MCMC) for 10,000,000 generations and 1000 sampled generations (Ronquist et al. 2012). The phylogenetic tree showed that the seven Amolops species were divided into two clades, monophyly of (Amolops loloensis + Amolops tuberodepressus + Amolops mantzorum + Amolops chunganensis + A. granulosus) and (Amolops ricketti + Amolops wuyiensis) was strongly supported. Our phylogenetic results were not only congruent with previous studies, but also suggested the gene arrangement of ‘WANCY’ region can facilitate to distinguish the Amolops species as an efficient genetic marker (Xue et al. 2016; Yuan et al. 2016).

Figure 1.

Figure 1.

A phylogenetic tree based on the concatenated nucleotide sequences of 13 PCGs from 26 Anura species constructed with Bayesian inference (BI). Xenopus laevis and X. tropicalis were used as outgroups. Bayesian posterior probabilities are shown near the nodes.

Disclosure statement

No potential conflict of interest was reported by the authors.

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