Literature DB >> 33365779

Sequencing and analysis of the complete mitogenome of Doriprismatica atromarginata (Cuvier, 1804).

Thinh Dinh Do1, Mustafa Zafer Karagozlu1, Van Quan Nguyen2, Chang-Bae Kim1.   

Abstract

Doriprismatica atromarginata is a common nudibranch in the tropical and sub-tropical Indo-Pacific region. In this study, the complete mitogenome of D. atromarginata from Vietnam was recorded for the first time. The circular mitogenome had a size of 14,421 bp and consisted of 37 genes (13 protein-coding genes, two ribosomal RNA genes, and 22 tRNA genes). Phylogenetic tree based on amino acid sequences of coding genes demonstrated that D. atromarginata has sister group relationship with the genus Chromodoris.
© 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Chromodorididae; Doriprismatica atromarginata; Mitogenome; phylogenetic relationships

Year:  2019        PMID: 33365779      PMCID: PMC7706534          DOI: 10.1080/23802359.2019.1660276

Source DB:  PubMed          Journal:  Mitochondrial DNA B Resour        ISSN: 2380-2359            Impact factor:   0.658


Chromodorididae is a large family of the order Nudibranchia with over 300 recorded species (Johnson and Gosliner 2012). Based on a combination of morphological and molecular analyses, several cryptic and pseudo-cryptic species in this family have been detected recently (Matsuda and Gosliner 2018). Mitogenome is well known as a common marker for the resolution of taxonomic controversies (Gissi et al. 2008; Duchêne et al. 2011). However, to date, there are only seven mitogenomes of two genera (Chromodoris and Hyselodoris) from the family Chromodorididae recorded. In this study, we sequenced and analysed the mitogenome from a Chromodorididae species, Doriprismatica atromarginata. D. atromarginata collection was conducted by Scuba diving in Hon Me island (19°22′3.50″N, 105°54′59.44″E), Vietnam in July 2018. Upon collection, the specimen was vouchered and stored in the Department of Biotechnology, Sangmyung University (Voucher no. SMU0034). The methods for DNA extraction and mitogenome generation were described previously (Do et al. 2019). For the investigation of phylogenetic relationships, a tree was constructed based on amino acid sequences of protein-coding genes (PCGs). The neighbour-joining method with 1000 bootstrap replicates in MEGAX software was used for tree construction (Kumar et al. 2018). The D. atromarginata mitogenome (GenBank accession number: MN171300) was 14,421 bp in size, containing 13 PCGs, two ribosomal RNA genes, and 22 tRNA genes. Overall nucleotide composition was 29.4% A, 39.9% T, 17.5% G, and 13.2% C. Similar to recorded mitogenomes of Chromodorididae, D. atromarginata mitogenome is composed of 24 genes encoded on H-strand and 13 genes encoded on L-strand. Of 13 PCGs, nd5 was the longest gene (1680 bp) while atp8 (156 bp) was the shortest gene. For ribosomal RNA, 12S rRNA gene was 751 bp in length, and 16S rRNA gene was 1175 bp in length. There were 13 overlapping regions which ranging from 3 to 33 bp. The longest overlapping region was located between tRNAVal and 16S rRNA. For start codon, only nd6 started with ATT and nd4l started with ATA, the remaining genes started with ATG. For stop codon, two genes (nd5 and cytb) were terminated with TAG while remaining genes were terminated with TAA. The phylogenetic tree showed relationships between nudibranchs in the family Chromodorididae (Figure 1). It indicated that D. atromarginata have a close relationship with Chromodoris species (C. orientalis, C. annae, C. magnifica, and C. quadricolor).Itpositioned as sister to the genus Chromodoris and they formed a clade with the genus Hypselodoris. Our result is in agreement with the pattern in previous report by Johnson and Gosliner (2012) based on mitochondrial markers (16S rRNA and cox1). This is the first mitogenome record for the species and the third genus for the family Chromodorididae. For a better understanding of the phylogeny of the family, more mitogenomes from different genera should be sequenced and analysed.
Figure 1.

The phylogenetic tree of D. atromarginata in the Chromodorididae family based on amino acid sequences of mitochondrial protein-coding genes. GenBank’s sequences with accession numbers were obtained for the analysis. Triangular symbol represents D. atromarginata mitogenome. Phyllidia ocellate and Phyllidiella pustulosa (Phyllidiidae) were used for the outgroup.

The phylogenetic tree of D. atromarginata in the Chromodorididae family based on amino acid sequences of mitochondrial protein-coding genes. GenBank’s sequences with accession numbers were obtained for the analysis. Triangular symbol represents D. atromarginata mitogenome. Phyllidia ocellate and Phyllidiella pustulosa (Phyllidiidae) were used for the outgroup.
  5 in total

Review 1.  Evolution of the mitochondrial genome of Metazoa as exemplified by comparison of congeneric species.

Authors:  C Gissi; F Iannelli; G Pesole
Journal:  Heredity (Edinb)       Date:  2008-07-09       Impact factor: 3.821

2.  MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms.

Authors:  Sudhir Kumar; Glen Stecher; Michael Li; Christina Knyaz; Koichiro Tamura
Journal:  Mol Biol Evol       Date:  2018-06-01       Impact factor: 16.240

3.  Glossing over cryptic species: Descriptions of four new species of Glossodoris and three new species of Doriprismatica (Nudibranchia: Chromodorididae).

Authors:  Shayle B Matsuda; Terrence M Gosliner
Journal:  Zootaxa       Date:  2018-07-12       Impact factor: 1.091

4.  Traditional taxonomic groupings mask evolutionary history: a molecular phylogeny and new classification of the chromodorid nudibranchs.

Authors:  Rebecca Fay Johnson; Terrence M Gosliner
Journal:  PLoS One       Date:  2012-04-10       Impact factor: 3.240

5.  Mitogenome phylogenetics: the impact of using single regions and partitioning schemes on topology, substitution rate and divergence time estimation.

Authors:  Sebastián Duchêne; Frederick I Archer; Julia Vilstrup; Susana Caballero; Phillip A Morin
Journal:  PLoS One       Date:  2011-11-02       Impact factor: 3.240

  5 in total

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