Literature DB >> 33366102

The mitochondrial genome of the black-tailed dasyure (Murexia melanurus).

Ran Tian1, Yuepan Geng1, Patrick B Thomas2,3,4, Penny L Jeffery2,3, Thomas Y Mutton5, Lisa K Chopin2,3, Andrew M Baker5,6, Inge Seim1,2,3,7.   

Abstract

In this study, we report the mitochondrial genome of the black-tailed dasyure (Murexia melanurus) of New Guinea. The circular genome is 17,736 bp in length and has an AT content of 60.5%. Its gene content - 13 protein-coding genes (PCGs), 2 ribosomal (rRNA) genes, 21 transfer RNA (tRNA) genes, a tRNA pseudogene (tRNALys ), and a non-coding control region (CR) - and gene arrangement are consistent with previous marsupial mitogenome assemblies.
© 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Dasyuridae; Mitochondrial genome; Murexia; New Guinea; dasyure; marsupial

Year:  2019        PMID: 33366102      PMCID: PMC7707616          DOI: 10.1080/23802359.2019.1677526

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


The marsupial family Dasyuridae (or carnivorous marsupials) includes ∼75 species native to mainland Australia and Tasmania, New Guinea, and other adjacent islands (Baker and Dickman 2018). The dasyurid subfamily Phascogalinae comprises three genera: Antechinus and Phascogale of Australia, and Murexia of New Guinea. Although morphological similarities exist, the current evidence suggests these genera derived from a common ancestor some 12.5 million years ago (Mutton et al. 2019). Murexia spp. have not received as much attention in evolutionary studies as their Australian counterparts within Phascogalinae, and genetic information on the various constituent species within Murexia is poorly represented. Here, we describe the complete mitochondrial genome of the black-tailed dasyure (Murexia melanurus). Murexia melanurus genomic DNA was extracted from ear tissue (voucher specimen ABTC46020) collected from Tibi, Papua New Guinea. Paired-end short-insert (200 bp) DNA libraries were sequenced by BGI (Hong Kong, China), to generate ∼30× genome coverage. Raw data were filtered using Flexbar v3.4.0 (Roehr et al. 2017). To remove microbial contaminants, we used bowtie2 v2.3.4.1 (Langmead and Salzberg 2012) to map reads to all bacterial and fungal sequences in NCBI Genomes, retaining 99.68% of reads. Two to 95 million reads were assembled using NOVOPlasty v2.7.2 (Dierckxsens et al. 2017), with the ND1 coding sequence from a partial M. melanurus mitogenome (GenBank: KJ868127) (Mitchell et al. 2014) as a seed sequence and the parameters ‘Type = mito, K-mer = 39, Genome range = 16,000–22,000’. The subset with the lowest number of reads which yielded a circular genome was retained (here: 12 M reads; 0.26% were assembled into a 17,736 bp contig at 179× coverage). Geneious Prime v2019.1.3 (Biomatters Ltd., Auckland, New Zealand) was used to align 95 M reads against the assembled contig and generate a consensus genome sequence, with a 75% masking threshold. The genome was annotated using GenBank features of the northern quoll (Dasyurus hallucatus; accession no. NC_007630). Various genome features were compared to the Virginia opossum (Didelphis virginiana), a seminal species in the marsupial mitochondrial genetics literature [e.g. see Janke et al. (1994) and Nilsson (2009)]. The M. melanurus mitochondrial genome (GenBank: MK977600) is 17,736 bp and has a base composition of 32% A, 28.5% T, 14.1% G, and 25.4% C. As in other marsupials, the genome has 13 protein-coding genes (PSGs), 2 ribosomal (rRNA) genes, and 21 transfer RNA (tRNA) genes. The genome shares unique features with all marsupial mitogenomes reported to date. These include: an ‘ACWNY’ tRNA gene re-arrangement (Paabo et al. 1991); a tRNA pseudogene (Janke et al. 1994; Dorner et al. 2001); and lack of an anticodon for aspartic acid, which is likely rescued by RNA-editing (Janke and Paabo 1993). In agreement with a recent molecular appraisal (Mitchell et al. 2014; Westerman et al. 2016), phylogenetic analysis revealed that M. melanurus and Murexia habbema are sisters, to the exclusion of the closely-related genera Phascogale and Antechinus (Figure 1). Maximum-likelihood (ML; estimated using IQ-TREE (Nguyen et al. 2015)) and Bayesian Interference (BI; implemented in MrBayes v3.2.7 (Ronquist and Huelsenbeck 2003)) gave the same tree topology.
Figure 1.

Phylogenetic tree of black-tailed dasyure (Murexia melanurus; indicated in bold blue font), nine other species in the marsupial family Dasyuridae, and the outgroup species Thylacinus cynocephalus. Because there are no complete mitogenomes from the genera Antechinus and Murexia in GenBank, phylogenetic reconstruction was performed with coding sequences of 12 protein-coding genes (excluding ND6). The number at each node is ML/BI bootstrap support value.

Phylogenetic tree of black-tailed dasyure (Murexia melanurus; indicated in bold blue font), nine other species in the marsupial family Dasyuridae, and the outgroup species Thylacinus cynocephalus. Because there are no complete mitogenomes from the genera Antechinus and Murexia in GenBank, phylogenetic reconstruction was performed with coding sequences of 12 protein-coding genes (excluding ND6). The number at each node is ML/BI bootstrap support value.
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Authors:  Maria A Nilsson
Journal:  Mitochondrial DNA       Date:  2009-12

4.  Rearrangements of mitochondrial transfer RNA genes in marsupials.

Authors:  S Pääbo; W K Thomas; K M Whitfield; Y Kumazawa; A C Wilson
Journal:  J Mol Evol       Date:  1991-11       Impact factor: 2.395

5.  Fast gapped-read alignment with Bowtie 2.

Authors:  Ben Langmead; Steven L Salzberg
Journal:  Nat Methods       Date:  2012-03-04       Impact factor: 28.547

6.  The marsupial mitochondrial genome and the evolution of placental mammals.

Authors:  A Janke; G Feldmaier-Fuchs; W K Thomas; A von Haeseler; S Pääbo
Journal:  Genetics       Date:  1994-05       Impact factor: 4.562

7.  Molecular phylogeny, biogeography, and habitat preference evolution of marsupials.

Authors:  Kieren J Mitchell; Renae C Pratt; Laura N Watson; Gillian C Gibb; Bastien Llamas; Marta Kasper; Janette Edson; Blair Hopwood; Dean Male; Kyle N Armstrong; Matthias Meyer; Michael Hofreiter; Jeremy Austin; Stephen C Donnellan; Michael S Y Lee; Matthew J Phillips; Alan Cooper
Journal:  Mol Biol Evol       Date:  2014-05-30       Impact factor: 16.240

8.  Flexbar 3.0 - SIMD and multicore parallelization.

Authors:  Johannes T Roehr; Christoph Dieterich; Knut Reinert
Journal:  Bioinformatics       Date:  2017-09-15       Impact factor: 6.937

9.  IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies.

Authors:  Lam-Tung Nguyen; Heiko A Schmidt; Arndt von Haeseler; Bui Quang Minh
Journal:  Mol Biol Evol       Date:  2014-11-03       Impact factor: 16.240

10.  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

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  1 in total

1.  The mitochondrial genome of the black-tailed dusky antechinus (Antechinus arktos).

Authors:  Yuepan Geng; Chen Yang; Han Guo; Patrick B Thomas; Penny L Jeffery; Lisa K Chopin; Andrew M Baker; Ran Tian; Inge Seim
Journal:  Mitochondrial DNA B Resour       Date:  2020-12-24       Impact factor: 0.658

  1 in total

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