Literature DB >> 36188670

The complete mitochondrial genome of Labidocera rotunda Mori, 1929 (Copepoda: Calanoida) from Jeju Island, Korea.

Jimoon Jun1, Hyeon Gyeong Jeong2, Hyeongwoo Choi1, Hyunmin Woo1, Donggu Jeon1, Young-Jin Seo1, Seong-Il Eyun1.   

Abstract

We sequenced the complete mitochondrial genome of the copepod Labidocera rotunda (family Pontellidae) collected from Ihotaewoo Beach in Jeju, Korea. The mitochondrial genome was 16,564 bp in length and contained 13 protein-coding genes (PCGs), 22 transfer RNAs, and two ribosomal RNAs. The concatenated phylogenetic tree of L. rotunda was reconstructed using the maximum-likelihood method based on the eight PCGs obtained from eight species of copepods including L. rotunda. The results of the phylogeny analysis showed that L. rotunda was closely related to the family Temoridae among the three families. The complete mitochondrial genome of L. rotunda analyzed for the first time in this study provides insight into the phylogenetic and evolutionary relationship of Labidocera.
© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Labidocera rotunda; Pontellidae; calanoid; copepod; mitochondrial genome

Year:  2022        PMID: 36188670      PMCID: PMC9518254          DOI: 10.1080/23802359.2022.2122748

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


The genus Labidocera Lubbock, 1853 occurs mostly in the surface waters (0–30 cm surface layer) of the warm temperate to tropical regions along the Indian Ocean and the Pacific Ocean (Fleminger 1967; Razouls et al. 2005–2022). To date, a total of 63 species are included in the genus Labidocera (Walter and Boxshall 2021) and new species continue to be added (Eyun 2017; Mulyadi 2021). With species-specific sexually modified anatomical features and relatively large size among the copepod, Labidocera has been a notable subject for examination of the ecological, distributional, and morphological relationships between closely related species (Fleminger 1967; Jeong et al. 2014). Despite its advantages in research, the mitochondrial genomes (mitogenomes) of Labidocera are yet to be made available. Therefore, we conducted the complete mitochondrial sequencing of L. rotunda. We collected L. rotunda from Ihotaewoo Beach in Jeju Island, South Korea (33°31′51.3″N, 126°25′15.4″E and 33°31′54.5″N, 126°25′33.6″E) using a conical net (mesh size 200 µm; mouth diameter 60 cm). Note that this site is not a protected area by the government and no permit was required. The voucher specimens were reexamined and cataloged at the National Marine Biodiversity Institute of Korea (https://www.mabik.re.kr/html/kr/, Hyeon Gyeong Jeong, hgjeong@mabik.re.kr) under the voucher number (MABIK CR00123334). Long and accurate PCR was performed to amplify the complete mitochondrial genome sequence using a set of universal primers (Wan et al. 2012) and designed primers. Sequencing was conducted using the primer walking method on an ABI 3730XL DNA Analyzer (Applied Biosystems, Inc., CA). Then, mitogenome annotation was initially conducted using the webservers, MITOS (Bernt et al. 2013) and MITOS2 (Donath et al. 2019), and manually modified based on the related species. The complete mitogenome of L. rotunda (NCBI accession number ON332184) is 16,564 bp in length, which is similar to the reported calanoid species (Eyun et al. 2007, 2017; Zhang et al. 2020). The mitogenome contains 37 genes comprising a conserved set of 13 protein-coding genes (PCGs), two ribosomal RNA genes (12S and 16S), and 22 transfer RNA genes. The overall base composition of the mitogenome is estimated to be 31.6% for A, 36.6% for T, 14.8% for C, and 16.9% for G, with a [A + T] content of 68.3%, which is similar to that of Phyllodiaptomus praedictus praedictus (family Diaptomidae) (69.4%) (Zhang et al. 2020). The concatenated phylogenetic tree of L. rotunda was reconstructed using the maximum-likelihood method with the substitution model of mtZOA + F+G4. Bootstrap analysis was performed based on the eight PCGs with 1,000 replicates to evaluate the confidence level of each clade (Figure 1). Tigriopus californicus (order Harpacticoida) was used as the outgroup in the phylogenetic tree. The well-supported bootstrap value of 100% indicates the close relationship between L. rotunda (family Pontellidae) and Eurytemora affinis (family Temoridae).
Figure 1.

Maximum-likelihood (ML) phylogeny of eight copepod species (seven from Calanoida including Labidocera rotunda and one species of Harpacticoida) based on the eight concatenated protein-coding genes of amino acid sequence. T. californicus (order Harpacticoida) was used as the outgroup. The numbers on the branches indicate ML bootstrap percentages (1,000 replicates). The GenBank and NCBI accession numbers for the published sequences are incorporated. The gray box indicates the L. rotunda analyzed in this study.

Maximum-likelihood (ML) phylogeny of eight copepod species (seven from Calanoida including Labidocera rotunda and one species of Harpacticoida) based on the eight concatenated protein-coding genes of amino acid sequence. T. californicus (order Harpacticoida) was used as the outgroup. The numbers on the branches indicate ML bootstrap percentages (1,000 replicates). The GenBank and NCBI accession numbers for the published sequences are incorporated. The gray box indicates the L. rotunda analyzed in this study. This study is the first to present the complete mitochondrial genome of L. rotunda. The results obtained here provide insights into the phylogenetic and evolutionary relationship of Labidocera.
  8 in total

1.  Genetic identification and molecular phylogeny of Pseudodiaptomus species (Calanoida, Pseudodiaptomidae) in Korean waters.

Authors:  Seong-Il Eyun; Youn-Ho Lee; Hae-Lip Suh; Sung Kim; Ho Young Soh
Journal:  Zoolog Sci       Date:  2007-03       Impact factor: 0.931

2.  MITOS: improved de novo metazoan mitochondrial genome annotation.

Authors:  Matthias Bernt; Alexander Donath; Frank Jühling; Fabian Externbrink; Catherine Florentz; Guido Fritzsch; Joern Pütz; Martin Middendorf; Peter F Stadler
Journal:  Mol Phylogenet Evol       Date:  2012-09-07       Impact factor: 4.286

3.  Morphological and genetic differentiation of heteromorphy in Labidocera rotunda (Copepoda, Calanoida, Pontellidae).

Authors:  Hyeon Gyeong Jeong; Ho Young Soh; Hae-Lip Suh
Journal:  Zootaxa       Date:  2014-02-10       Impact factor: 1.091

4.  Improved annotation of protein-coding genes boundaries in metazoan mitochondrial genomes.

Authors:  Alexander Donath; Frank Jühling; Marwa Al-Arab; Stephan H Bernhart; Franziska Reinhardt; Peter F Stadler; Martin Middendorf; Matthias Bernt
Journal:  Nucleic Acids Res       Date:  2019-11-18       Impact factor: 16.971

5.  Complete mitochondrial genome of the free-living earwig, Challia fletcheri (Dermaptera: Pygidicranidae) and phylogeny of Polyneoptera.

Authors:  Xinlong Wan; Man Il Kim; Min Jee Kim; Iksoo Kim
Journal:  PLoS One       Date:  2012-08-06       Impact factor: 3.240

6.  Phylogenomic analysis of Copepoda (Arthropoda, Crustacea) reveals unexpected similarities with earlier proposed morphological phylogenies.

Authors:  Seong-Il Eyun
Journal:  BMC Evol Biol       Date:  2017-01-19       Impact factor: 3.260

7.  Evolutionary History of Chemosensory-Related Gene Families across the Arthropoda.

Authors:  Seong-Il Eyun; Ho Young Soh; Marijan Posavi; James B Munro; Daniel S T Hughes; Shwetha C Murali; Jiaxin Qu; Shannon Dugan; Sandra L Lee; Hsu Chao; Huyen Dinh; Yi Han; HarshaVardhan Doddapaneni; Kim C Worley; Donna M Muzny; Eun-Ok Park; Joana C Silva; Richard A Gibbs; Stephen Richards; Carol Eunmi Lee
Journal:  Mol Biol Evol       Date:  2017-08-01       Impact factor: 16.240

8.  The mitochondrial genome of Phyllodiaptomus tunguidus Shen & Tai, 1964 (Copepoda, Calanoida) and its phylogeny.

Authors:  Xiaoli Zhang; Shaolin Xu; Ping Liu; Qi Huang; Huiming Li; Henri J Dumont; Bo-Ping Han
Journal:  Mitochondrial DNA B Resour       Date:  2020-06-22       Impact factor: 0.658

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.