Literature DB >> 30511017

Complete mitochondrial DNA genomes for two northeast Pacific mesopelagic fishes, the Mexican lampfish (Triphoturus mexicanus) and black-belly dragonfish (Stomias atriventer).

Benson R Truong1, Frank Gutierrez1, Andres Aguilar1.   

Abstract

Mesopelagic fishes are an important component of marine ecosystems, providing an important link between lower and higher trophic levels. This group of fishes are also highly abundant and make up a large portion of the marine vertebrate biomass. Here we report on the full mitochondrial sequences for two common mesopelagic fishes from the southern California bight: the Mexican lampfish Triphoturus mexicanus (Actinopterygii: Myctophidae) and the black-belly dragonfish Stomias atriventer (Actinopterygii: Stomiidae). T. mexicanus showed previously reported gene rearrangements for the Myctophidae. Phylogenetic analysis grouped S. atriventer with other Stomiiformes and T. mexicanus within the Myctophiformes.

Entities:  

Keywords:  Myctophidae; Stomiidae; gene rearrangements; mesopelagic; mitogenome

Year:  2017        PMID: 30511017      PMCID: PMC6269098          DOI: 10.1080/23802359.2017.1413293

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


Mesopelagic fishes make up the largest portion of the global vertebrate biomass (Gjøsaeter and Kawaguchi 1980; Kaartvedt et al. 2012; Davison et al. 2015). These fishes also make up an important component of marine food webs, as they are a link between plankton and higher-level predators (Gjøsaeter and Kawaguchi 1980; Cherel et al. 2008; Choy et al. 2012). Concordantly there is concern how this abundant and important fish community will respond to the impacts of climate change (Koslow et al. 2011; Asch 2015). Despite these features, there has been little genetic/genomic study on the mesopelagic fishes of the northeast Pacific. We assembled the complete mitochondrial genomes for two common mesopelagic fishes from the southern California bight: the Mexican lampfish (Triphoturus mexicanus) and the black-belly dragonfish (Stomias atriventer). Samples were obtained from an Isaacs-Kidd midwater trawl in the San Pedro Channel (33.55830 N, −118.42550 W) and specimens, tissue and DNA are vouchered at CSULA (#16-001 and #16-033). Total genomic DNA was extracted and each individual was sequenced on an Illumina HiSeqX (Illumina, San Diego, CA). A portion of the reads from each species were assembled using NOVOPlasty (Dierckxsens et al. 2017) with a portion of the mitochondrial cytochrome oxidase I gene used as the initial seed. Resulting assemblies were annotated with on the MitoFish website (Iwasaki et al. 2013) and protein coding genes were used in a partitioned Bayesian phylogenetic analysis. PartitionFinder2 (Lanfear et al. 2016) was used to identify partitioning schemes and best-fit models of molecular evolution for the protein sequences. The complete mitochondrial genome of T. mexicanus (Genbank accession no. MG321595) is 18,012 bp with two ribosomal genes (12S and 16S), 22 tRNAs and 13 protein-coding genes. It contained similar gene counts and organization as other Myctophidae and Lampanyctini (Poulsen et al. 2013). This includes the WANYC gene order, shifted tRNA-Cys and Tyr positions and a longer OL region (90 bp in T. mexicanus). Specific characteristics of the Lampanyctini found in T. mexicanus include the relocation of the tRNA-Glu and intergenic non-coding regions resulting in the CytB/T/E/P gene order. The assembled S. atriventer mitogenome (Genbank accession no. MG321596) is 17,596 bp with two ribosomal genes (12S and 16S), 22 tRNAs and 13 protein-coding genes. Stomias atriventer contains the typical vertebrate gene order that is also observed in another Stomiiformes (Diplophos sp. – Miya and Nishida 2000). Partitioned Bayesian phylogenetic analysis placed T. mexicanus sister to T. nigrescens with high posterior probability (Figure 1). S. atriventer placed in the Stomiioformes clade, sister to C. sloani + S. gracilis (Figure 1). This result is interesting given S. gracilis and Diplophos sp. are thought to be in the same family (Gonostomatidae), however a paraphyletic Gonostomatidae was found in a previous mitogenomic analysis (Miya et al. 2001) and the monophyly of the Stomiidae has been challenged with a mitochondrial and nuclear analysis of the family (Kenaley et al. 2014).
Figure 1.

Partitioned Bayesian phylogenetic tree of 3623 amino acid positions for 16 teleost species, T. mexicanus and S. atriventer are in boxes. Bayesian analysis was run over two chains for 5 × 107 generations, sampling each chain every 103 generations with MrBayes (Ronquist and Huelsenbeck 2003). The first 25% of sampled trees were discarded as burning and only posterior probabilities below 1.0 are shown. Genes and models of evolution for each partition are also reported. The MTMAM model of protein evolution (Cao et al. 1998; Yang et al. 1998) with gamma or gamma plus invariant sites was the best model for each respective partition based on BIC in PartitionFinder2. GenBank accession numbers are shown for additional species included in this analysis.

Partitioned Bayesian phylogenetic tree of 3623 amino acid positions for 16 teleost species, T. mexicanus and S. atriventer are in boxes. Bayesian analysis was run over two chains for 5 × 107 generations, sampling each chain every 103 generations with MrBayes (Ronquist and Huelsenbeck 2003). The first 25% of sampled trees were discarded as burning and only posterior probabilities below 1.0 are shown. Genes and models of evolution for each partition are also reported. The MTMAM model of protein evolution (Cao et al. 1998; Yang et al. 1998) with gamma or gamma plus invariant sites was the best model for each respective partition based on BIC in PartitionFinder2. GenBank accession numbers are shown for additional species included in this analysis.
  11 in total

1.  Use of mitogenomic information in teleostean molecular phylogenetics: a tree-based exploration under the maximum-parsimony optimality criterion.

Authors:  M Miya; M Nishida
Journal:  Mol Phylogenet Evol       Date:  2000-12       Impact factor: 4.286

2.  Mitogenomic exploration of higher teleostean phylogenies: a case study for moderate-scale evolutionary genomics with 38 newly determined complete mitochondrial DNA sequences.

Authors:  M Miya; A Kawaguchi; M Nishida
Journal:  Mol Biol Evol       Date:  2001-11       Impact factor: 16.240

3.  MrBayes 3: Bayesian phylogenetic inference under mixed models.

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

4.  Climate change and decadal shifts in the phenology of larval fishes in the California Current ecosystem.

Authors:  Rebecca G Asch
Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-09       Impact factor: 11.205

5.  The complex evolutionary history of seeing red: molecular phylogeny and the evolution of an adaptive visual system in deep-sea dragonfishes (Stomiiformes: Stomiidae).

Authors:  Christopher P Kenaley; Shannon C Devaney; Taylor T Fjeran
Journal:  Evolution       Date:  2014-01-30       Impact factor: 3.694

6.  Conflict among individual mitochondrial proteins in resolving the phylogeny of eutherian orders.

Authors:  Y Cao; A Janke; P J Waddell; M Westerman; O Takenaka; S Murata; N Okada; S Pääbo; M Hasegawa
Journal:  J Mol Evol       Date:  1998-09       Impact factor: 2.395

7.  Models of amino acid substitution and applications to mitochondrial protein evolution.

Authors:  Z Yang; R Nielsen; M Hasegawa
Journal:  Mol Biol Evol       Date:  1998-12       Impact factor: 16.240

8.  PartitionFinder 2: New Methods for Selecting Partitioned Models of Evolution for Molecular and Morphological Phylogenetic Analyses.

Authors:  Robert Lanfear; Paul B Frandsen; April M Wright; Tereza Senfeld; Brett Calcott
Journal:  Mol Biol Evol       Date:  2017-03-01       Impact factor: 16.240

9.  NOVOPlasty: de novo assembly of organelle genomes from whole genome data.

Authors:  Nicolas Dierckxsens; Patrick Mardulyn; Guillaume Smits
Journal:  Nucleic Acids Res       Date:  2017-02-28       Impact factor: 16.971

10.  Global trophic position comparison of two dominant mesopelagic fish families (Myctophidae, Stomiidae) using amino acid nitrogen isotopic analyses.

Authors:  C Anela Choy; Peter C Davison; Jeffrey C Drazen; Adrian Flynn; Elizabeth J Gier; Joel C Hoffman; Jennifer P McClain-Counts; Todd W Miller; Brian N Popp; Steve W Ross; Tracey T Sutton
Journal:  PLoS One       Date:  2012-11-28       Impact factor: 3.240

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1.  The complete mitochondrial genome of the longfin dragonfish Tactostoma macropus (Stomiiformes: Stomiidae).

Authors:  Minoru Ijichi; Tsuyoshi Takano; Masumi Hasegawa; Haruka Yashiki; Kazuhiro Kogure; Shigeaki Kojima; Susumu Yoshizawa
Journal:  Mitochondrial DNA B Resour       Date:  2018-04-23       Impact factor: 0.658

2.  A new gene order in the mitochondrial genome of the deep-sea diaphanous hatchet fish Sternoptyx diaphana Hermann, 1781 (Stomiiformes: Sternoptychidae).

Authors:  Nair Vilas Arrondo; André Gomes-Dos-Santos; Esther Román Marcote; Montse Pérez; Elsa Froufe; L Filipe C Castro
Journal:  Mitochondrial DNA B Resour       Date:  2020-07-15       Impact factor: 0.658

  2 in total

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