Literature DB >> 36147362

The first complete mitogenome of Onychostoma ovale (Pellegrin & Chevey, 1936) with phylogenetic analyses.

Congqiang Luo1,2, Zemin Ma1,2, Ping Chen3, Pinhong Yang1,2.   

Abstract

Onychostoma ovale (Pellegrin & Chevey, 1936) is an endemic cyprinid fish that is widely inhabited in southern China, Vietnam, and Laos. In the present study, we first reported the complete mitochondrial genome of O. ovale. The mitogenome contained 16,600 bp with AT content of 56.2% and comprised of 13 protein-coding genes, 22 transfer RNA genes, two ribosomal RNA genes, and one control region (D-loop). Phylogenetic analyses suggested that Onychostoma species formed two major clades and the subspecies of O. ovale had close relationship with O. rarum. The mitochondrial genome of O. ovale provided a key aid for population genetics and phylogenetic inferences of Onychostoma in future research.
© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Onychostoma ovale; mitogenome; phylogenetic status

Year:  2022        PMID: 36147362      PMCID: PMC9487942          DOI: 10.1080/23802359.2022.2119819

Source DB:  PubMed          Journal:  Mitochondrial DNA B Resour        ISSN: 2380-2359            Impact factor:   0.610


Onychostoma is an important fish group in Cyprinidae that contains 23 valid species (www.fishbase.org). Onychostoma ovale (Pellegrin & Chevey, 1936) is a representative member in Onychostoma that is widely distributed in the Southern China, Vietnam, and Laos (Yue 2000; www.fishbase.org). Though this species has a wide distribution range, the species was not seen in recent field sampling in Southern China due to rare resources (Li et al. 2012; Zhang et al. 2020; Zhu et al. 2022), suggesting that more attention should be paid for this subspecies. To date, nevertheless, the information of this species is pretty poor as sparse researches have been conducted researches for this species, especially genetic studies. In this study, we first sequenced the whole mitochondrial genome of O. ovale and tried to resolve its phylogenetic status. Onychostoma ovale specimen was captured from local fishermen in a small local market of Du’an County, Guangxi Province, China (23.952N, 108.089E) on 27 July 2021. We diagnosed this sample according to the fish fauna by Yue (2000). Total genomic DNA was extracted from muscle tissue using a Genomic DNA Isolation Kit (QiaGene, Hilden, Germany). The sample and the total DNA were preserved in the fish collection of Hunan University of Arts and Science (www.huas.edu.cn, Zemin Ma and Flysu210610@163.com) under the voucher numbers LXBJ20210701. The complete mitogenome of O. ovale was obtained via sequencing the DNA using the Illumina MiSeq platform (Illumina Inc., San Diego, CA) and assembled by SPAdes 3.9.0 (Bankevich et al. 2012). The assembled mitochondrial genomes were annotated using the online tool MitoAnnotator (http://mitofish.aori.u-tokyo.ac.jp/annotation; Iwasaki et al. 2013). The annotated mitogenome was deposited in GenBank with the accession number ON120245. The complete mitogenome of O. ovale reached 16,600 bp in length with the A + T content (55.6%) was much higher than its G + C content (44.4%). It comprised of 13 protein-coding genes, two rRNA genes (12S rRNA and 16S rRNA), 22 tRNA genes, and a control region (D-loop), as observed in other fish species (Mascolo et al. 2018; Zhai et al. 2020). The initiation codon for all 13 PCGs was ATG except COI where it was GTG. With regard to the stop codon, six protein-coding genes (ND1, COI, ATP8, ND4L, ND5, and ND6) performed the routine termination codon (TAA or TAG), whereas five other protein-coding genes (ND2, COII, ND3, ND4, and Cytb) stopped with an incomplete stop codon T and two protein-coding genes (COIII and ATP6) stopped with an incomplete stop codon TA. In order to understand the phylogenetic status of O. ovale, we downloaded 11 published Onychostoma mitogenomes and constructed Bayesian inference (BI) and maximum-likelihood (ML) trees using the concatenated supergene that contained 13 protein-coding genes. The ML and BI trees were built using RAXML-VI-HPC (Stamatakis 2006) and MrBayes 3.2 (Ronquist and Huelsenbeck 2003), respectively. Acrossocheilus beijiangensis (GenBank no. KY131976) was selected as an outgroup. The best nucleotide substitution model of GTR + I+G was chosen using MRMODELTEST version 2.3 on the basis of the Akaike information criterion (Nylander 2004). Both trees consistently resolved two major clades, which was in line with a previous study by Zhai et al. (2020). In addition, this study indicated that O. ovale was closely related to O. rarum with high supported values (Figure 1). In future studies, the mitochondrial genome of O. ovale is helpful for phylogenetic inferences of Onychostoma. Furthermore, appropriate mitochondrial genes can be selected from O. ovale mitogenome to conduct conservation genetic studies of O. ovale populations.
Figure 1.

Maximum-likelihood tree showing the phylogenetic relationships among Onychostoma species using 13 protein-coding genes. Values on branches represent bootstrap values from maximum-likelihood analysis and posterior probability from Bayesian inference.

Maximum-likelihood tree showing the phylogenetic relationships among Onychostoma species using 13 protein-coding genes. Values on branches represent bootstrap values from maximum-likelihood analysis and posterior probability from Bayesian inference.

Ethical approval

Experiments were performed in accordance with the recommendations of the Ethics Committee of Hunan University of Arts and Science. These policies were enacted according to the Chinese Association for the Laboratory Animal Sciences and the Institutional Animal Care and Use Committee (IACUC) protocols.

Author contributions

Congqiang Luo and Zemin Ma: conception, design, analysis, investigation, interpretation of the data, and writing and revising the draft. Ping Chen: investigation. Pinhong Yang: design, investigation, and revising the draft. All authors agree to be accountable for all aspects of the work.
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1.  MrBayes 3: Bayesian phylogenetic inference under mixed models.

Authors:  Fredrik Ronquist; John P Huelsenbeck
Journal:  Bioinformatics       Date:  2003-08-12       Impact factor: 6.937

2.  SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing.

Authors:  Anton Bankevich; Sergey Nurk; Dmitry Antipov; Alexey A Gurevich; Mikhail Dvorkin; Alexander S Kulikov; Valery M Lesin; Sergey I Nikolenko; Son Pham; Andrey D Prjibelski; Alexey V Pyshkin; Alexander V Sirotkin; Nikolay Vyahhi; Glenn Tesler; Max A Alekseyev; Pavel A Pevzner
Journal:  J Comput Biol       Date:  2012-04-16       Impact factor: 1.479

3.  RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models.

Authors:  Alexandros Stamatakis
Journal:  Bioinformatics       Date:  2006-08-23       Impact factor: 6.937

4.  MitoFish and MitoAnnotator: a mitochondrial genome database of fish with an accurate and automatic annotation pipeline.

Authors:  Wataru Iwasaki; Tsukasa Fukunaga; Ryota Isagozawa; Koichiro Yamada; Yasunobu Maeda; Takashi P Satoh; Tetsuya Sado; Kohji Mabuchi; Hirohiko Takeshima; Masaki Miya; Mutsumi Nishida
Journal:  Mol Biol Evol       Date:  2013-08-16       Impact factor: 16.240

5.  The complete mitochondrial genome of the axillary seabream, Pagellus acarne (Perciformes: Sparidae).

Authors:  Celestina Mascolo; Marina Ceruso; Giuseppe Palma; Aniello Anastasio; Paolo Sordino; Tiziana Pepe
Journal:  Mitochondrial DNA B Resour       Date:  2018-04-01       Impact factor: 0.658

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