Literature DB >> 33458044

The complete mitochondrial DNA sequence of Heterochaerus australis (Acoela, Convolutidae).

Bin Li1,2, Meijie Liao1,2, Miao Kong1,2, Yingeng Wang1,2, Xiaojun Rong1,2, Zheng Zhang1,2, Yongxiang Yu1,2.   

Abstract

One complete mitochondrial genomes (mitogenomes) was determined for Heterochaerus australis (Acoela, Convolutidae). Its mitochondrial genome size was 13,885 bp. The sequence contains 2 ribosomal RNA genes (rrnL and rrnS), 20 tRNA genes, and 12 protein-coding genes (PCGs). The A + T content of the complete mitochondrial genome sequence was 70.8%. The base composition showed a tendency of high AT. The resulted maximum likelihood (ML) tree supported that Acoela had a distant relationship with other orders of Turbellaria and the Xenacoelomorpha.
© 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Acoela; Heterochaerus australis; Xenacoelomorpha; mitogenome

Year:  2020        PMID: 33458044      PMCID: PMC7782523          DOI: 10.1080/23802359.2020.1797561

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


The taxonomic status of Acoela of Turbellaria is controversial. Some researchers believe that the Acoela belongs to Deuterostomia and should be removed from the Platyhelminthes and combined with the Xenoturbella japonica to form the Phylum Xenacoelomorpha (Philippe et al. 2011; Cinar 2014). Jondelius et al. (2011) interpreted the initial grouping of the Acoela and tunicates as a classical example of long-branch attraction (LBA). This is of particular relevance for Acoela species, which already demonstrate a very rapid rate of nucleotide substitution compared to other metazoans, leaving them vulnerable to LBA (Robertson et al. 2017). Here, we sequenced the mitochondrial genomes (mitogenomes) of Heterochaerus australis from Apostichopus japonicus breeding pond, and it has been indicated to be a new enemy species. In order to provide theoretical basis and scientific guidance for the taxonomic status of Acoela, mitochondrial gene composition, biological evolution, and molecular identification were studied. Heterochaerus australis was collected from Dalian, Liaoning Province of China (39.22N, 122.18E) in 2019 from sea cucumber culture ponds. The specimen was deposited into Fishery Barcode Data Base of China (YSF-ZW-4634). Total DNA was extracted using Omega Mollusk DNA Kit. The genome was sequenced by BGISEQ-500 method. The type of sequencing was PE100 and the length of the inserted fragment was 250 bp. The remaining reads were assembled using NOVOplasty. ORF Finder (http://www.ncbi.nlm.nih.gov/gorf/gorf. html) and BLASTx were used to determine the protein-coding genes (PCGs) using the invertebrate mitochondrial genetic code. The positions of transfer RNA (tRNA) genes were localized by ARWEN (Laslett andCanbäck 2008) and DOGMA (Wyman et al. 2004) using the invertebrate mitochondrial genetic code and the default search mode. The complete mitogenome sequences was 13,885 bp in length and has been deposited in the GenBank (Accession No. MT370508). The complete mitogenome contained 2 ribosomal RNA genes (rrnL and rrnS), 20 tRNA genes, and 12 protein-coding genes (PCGs). The A + T content of the complete mitochondrial genome sequence was 70.8%. The base composition showed a tendency of high AT. This phenomenon also appears in other species of Acoela (Mwinyi et al. 2010; Robertson et al. 2017). Phylogenetic trees based on the concatenated nucleic acid of 12 protein-coding genes. The branch lengths are determined with ML analysis. Heterochaerus australis is shown in bold. Numbers above or below branches denote bootstrap percentages (1000 replicates). Genbank accession numbers are shown for published sequences. A maximum likelihood phylogenetic tree of 7 species of Turbellaria and 1 species of Xenacoelomorpha was constructed based on the concatenated nucleic acid of 12 PCGs (Figure 1). In Acoela, only one species (P. rubra) clustered with other orders of Turbellaria, while the other four species (A. ylvae, I. pulchra, H. australis, S. roscoffensis) clustered into a single cluster, showing a distant relationship with other turbellarian. But X. japonica of Xenacoelomorpha is a separate branch.
Figure 1.

Phylogenetic trees based on the concatenated nucleic acid of 12 protein-coding genes. The branch lengths are determined with ML analysis. Heterochaerus australis is shown in bold. Numbers above or below branches denote bootstrap percentages (1000 replicates). Genbank accession numbers are shown for published sequences.

  6 in total

1.  Automatic annotation of organellar genomes with DOGMA.

Authors:  Stacia K Wyman; Robert K Jansen; Jeffrey L Boore
Journal:  Bioinformatics       Date:  2004-06-04       Impact factor: 6.937

2.  ARWEN: a program to detect tRNA genes in metazoan mitochondrial nucleotide sequences.

Authors:  Dean Laslett; Björn Canbäck
Journal:  Bioinformatics       Date:  2007-11-22       Impact factor: 6.937

3.  How the worm got its pharynx: phylogeny, classification and Bayesian assessment of character evolution in Acoela.

Authors:  Ulf Jondelius; Andreas Wallberg; Matthew Hooge; Olga I Raikova
Journal:  Syst Biol       Date:  2011-08-09       Impact factor: 15.683

4.  Acoelomorph flatworms are deuterostomes related to Xenoturbella.

Authors:  Hervé Philippe; Henner Brinkmann; Richard R Copley; Leonid L Moroz; Hiroaki Nakano; Albert J Poustka; Andreas Wallberg; Kevin J Peterson; Maximilian J Telford
Journal:  Nature       Date:  2011-02-10       Impact factor: 49.962

5.  The phylogenetic position of Acoela as revealed by the complete mitochondrial genome of Symsagittifera roscoffensis.

Authors:  Adina Mwinyi; Xavier Bailly; Sarah J Bourlat; Ulf Jondelius; D Timothy J Littlewood; Lars Podsiadlowski
Journal:  BMC Evol Biol       Date:  2010-10-13       Impact factor: 3.260

6.  The mitochondrial genomes of the acoelomorph worms Paratomella rubra, Isodiametra pulchra and Archaphanostoma ylvae.

Authors:  Helen E Robertson; François Lapraz; Bernhard Egger; Maximilian J Telford; Philipp H Schiffer
Journal:  Sci Rep       Date:  2017-05-12       Impact factor: 4.379

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.