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Complete mitochondrial genome of the headwater livebearer, Poeciliopsis monacha: the mother of clones

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Download by: [Ewha Womans University] Date: 26 July 2017, At: 22:12

Mitochondrial DNA Part B

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ISSN: (Print) 2380-2359 (Online) Journal homepage: http://www.tandfonline.com/loi/tmdn20

Complete mitochondrial genome of the headwater

livebearer, Poeciliopsis monacha: the mother of

clones

Yeon Seon Jeon, Shannon B. Johnson, Yong-Jin Won & Robert C. Vrijenhoek

To cite this article: Yeon Seon Jeon, Shannon B. Johnson, Yong-Jin Won & Robert C. Vrijenhoek (2016) Complete mitochondrial genome of the headwater livebearer, Poeciliopsis monacha: the mother of clones, Mitochondrial DNA Part B, 1:1, 793-794, DOI: 10.1080/23802359.2016.1197066

To link to this article: http://dx.doi.org/10.1080/23802359.2016.1197066

© 2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Published online: 29 Oct 2016.

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MITOGENOME ANNOUNCEMENT

Complete mitochondrial genome of the headwater livebearer,

Poeciliopsis

monacha: the mother of clones

Yeon Seon Jeona, Shannon B. Johnsonb, Yong-Jin Wona,cand Robert C. Vrijenhoekb

a

Division of EcoScience, Ewha Womans University, Seoul, South Korea;bMonterey Bay Aquarium Research Institute, Moss Landing, CA, USA; c

Department of Life Science, Ewha Womans University, Seoul, Korea

ABSTRACT

The sexually reproducing fish, Poeciliopsis monacha (Actinopterygii, Cyprinodontiformes, Poeciliidae), is the maternal ancestor of six hybrid biotypes that reproduce clonally. The gene content and order of its 16,818 bp mitochondrial genome is virtually identical with that of other sexually reproducing poeciliid fishes, providing no evidence for a mitochondrial involvement in the origins of all-female reproduction.

ARTICLE HISTORY Received 16 May 2016 Accepted 31 May 2016 KEYWORDS Mitochondrial genome; headwater livebearer (Poeciliopsis monacha); Poeciliidae

The headwater livebearer, Poeciliopsis monacha (Actinopterygii, Cyprinodontiformes, Poeciliidae), is native to the springs and arroyos of northwestern Mexico. It served as the maternal ancestor for six all-female biotypes: the gynoge-netic allotriploids P. 2monacha-lucida, P. monacha-2lucida, and P. monacha-viriosa-lucida; and the hybridogenetic allodi-ploids P. monacha-lucida, P. monacha-occidentalis, and P. monacha-latidens (Vrijenhoek 1998). Clonal reproduction arises spontaneously in interspecific hybrids with P. monacha mothers (Wetherington et al. 1987). Does its mitochondrial genome contain unusual characteristics that played a role in these origins?

Herein, we report the complete mitochondrial genome of P. monacha and compare it with a reference genome from other eight poeciliids (Figure 1). The specimen we examined was sampled from a headwater tributary of the Rıo Fuerte in Sonora, Mexico (26.908449N, 108.671743W; altitude 344 m), a locality from which P. monacha females were used to con-duct laboratory syntheses of hybridogenetic biotypes (Wetherington et al.1987). Genomic DNA was sequenced by 454 GS-Flex Titanium pyrosequencing (Roche Diagnostics Corporation, Bedford, CT) long-read version on a half-plate scale by Macrogen, Inc. (Seoul, Korea).

We used the web-based MitoAnnotator (Kashiwa, Chiba, Japan) (Iwasaki et al. 2013) to annotate the P. monacha genome. Using the PhyML (Guindon & Gascuel 2003) plugin on the Geneious v.9.04 (http://www.geneious.com/), a maximum-likelihood (ML) tree was constructed under the

GTR model based on the complete mitogenomic sequences of nine poeciliids and an outgroup species, Xenotoca eiseni, with 1000 bootstraps (Figure 1).

The P. monacha mitogenome examined in this study was 16,818 bp long (GenBank accession number: KX229692, a par-atype specimen’s museum number at the Natural History Museum of Ewha Womans University: EWNHMFI44) with an AT-rich (55.5%) base-composition: C (29.5%)> A (28.7%) > T (26.8%)> G (15%). It contained a non-coding control region (D-loop) and 37 genes typical of vertebrates: 2 rRNA genes; 22 tRNA genes; and 13 protein-coding genes. Individual tRNA genes showed the typical cloverleaf secondary structures. The protein-coding genes showed incomplete stop codons (T–– or TA–) that presumably were completed to a TAA stop codon by post-transcriptional polyadenylation (Ojala et al.

1981). The ML tree showed that P. monacha has a sister rela-tionship with the congeneric species, P. occidentalis.

The present analysis revealed nothing unusual in the P. monacha mitogenome that might contribute to the origins of the all-female alloploid biotypes. Length and AT-bias of the P. monacha mitogenome were similar to that of other eight poeciliids (16,533–16,771 bp, 52.2–59.1%). Gene compo-sitions and order were identical in all nine ingroup species. Nonetheless, this result does not exclude possible interactions between specific mitochondrial gene sequences and the nuclear genome. A search for factors that promote meiotic dysgenesis in hybrids involving P. monacha females resumes.

CONTACTYong-Jin Won [email protected] Division of EcoScience, Ewha Womans University, 52, Ewhayeodae-gil, Seodaemun-gu, Seoul, South Korea

ß 2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, dis-tribution, and reproduction in any medium, provided the original work is properly cited.

MITOCHONDRIAL DNA PART B: RESOURCES, 2016 VOL. 1, NO. 1, 793–794

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Disclosure statement

The authors report no conflicts of interest. The authors alone are respon-sible for the content and writing of the paper.

Fish were collected under permit #412.2.1.3.0 folio 4815 issued by the Departmento de Pesca, the Secretaria de Desarrollo Urbano y Ecologia, and the Departamento de Exteriores, Mexico, D.F.

Funding

Research was supported by grants from the U.S. National Science Foundation, 10.13039/501100003621 (BSR88-05361) and the David and Lucile Packard Foundation via the Monterey Bay Aquarium Research Institute to R. C. V. This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and future Planning (2015R1A2A2A01007117) to Y.-J. W.

References

Guindon S, Gascuel O. 2003. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol. 52:696–704.

Iwasaki W, Fukunaga T, Isagozawa R, Yamada K, Maeda Y, Satoh TP, Sado T, Mabuchi K, Takeshima H, Miya M. 2013. MitoFish and MitoAnnotator: a mitochondrial genome database of fish with an accurate and automatic annotation pipeline. Mol Biol Evol. 30:2531–2540.

Ojala D, Montoya J, Attardi G. 1981. tRNA punctuation model of RNA processing in human mitochondria. Nature. 290:470–474.

Vrijenhoek RC. 1998. Animal clones and diversity. Bioscience. 48:617–628.

Wetherington JD, Kotora KE, Vrijenhoek RC. 1987. A test of the spontan-eous heterosis hypothesis for unisexual vertebrates. Evolution. 41:721–731.

Figure 1. A maximum-likelihood tree of poeciliids constructed under the GTR model using the complete sequences of mitogenomes withXenotoca eiseni (GenBank accession number AP006777) as an outgroup. The asterisk indicated the species in this study. Bootstrap support was shown at nodes.

수치

Figure 1. A maximum-likelihood tree of poeciliids constructed under the GTR model using the complete sequences of mitogenomes with Xenotoca eiseni (GenBank accession number AP006777) as an outgroup

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