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      The genome of the live-bearing fish Heterandria formosa implicates a role of conserved vertebrate genes in the evolution of placental fish

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          Abstract

          Background

          The evolution of complex organs is thought to occur via a stepwise process, each subsequent step increasing the organ’s complexity by a tiny amount. This evolutionary process can be studied by comparing closely related species that vary in the presence or absence of their organs. This is the case for the placenta in the live-bearing fish family Poeciliidae, as members of this family vary markedly in their ability to supply nutrients to their offspring via a placenta. Here, we investigate the genomic basis underlying this phenotypic variation in Heterandria formosa, a poeciliid fish with a highly complex placenta. We compare this genome to three published reference genomes of non-placental poeciliid fish to gain insight in which genes may have played a role in the evolution of the placenta in the Poeciliidae.

          Results

          We sequenced the genome of H. formosa, providing the first whole genome sequence for a placental poeciliid. We looked for signatures of adaptive evolution by comparing its gene sequences to those of three non-placental live-bearing relatives. Using comparative evolutionary analyses, we found 17 genes that were positively selected exclusively in H. formosa, as well as five gene duplications exclusive to H. formosa. Eight of the genes evolving under positive selection in H. formosa have a placental function in mammals, most notably endometrial tissue remodelling or endometrial cell proliferation.

          Conclusions

          Our results show that a substantial portion of positively selected genes have a function that correlates well with the morphological changes that form the placenta of H. formosa, compared to the corresponding tissue in non-placental poeciliids. These functions are mainly endometrial tissue remodelling and endometrial cell proliferation. Therefore, we hypothesize that natural selection acting on genes involved in these functions plays a key role in the evolution of the placenta in H. formosa.

          Electronic supplementary material

          The online version of this article (10.1186/s12862-019-1484-2) contains supplementary material, which is available to authorized users.

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          Most cited references47

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Innate immunity in plants: an arms race between pattern recognition receptors in plants and effectors in microbial pathogens.

            For many years, research on a suite of plant defense responses that begin when plants are exposed to general microbial elicitors was underappreciated, for a good reason: There has been no critical experimental demonstration of their importance in mediating plant resistance during pathogen infection. Today, these microbial elicitors are named pathogen- or microbe-associated molecular patterns (PAMPs or MAMPs) and the plant responses are known as PAMP-triggered immunity (PTI). Recent studies provide an elegant explanation for the difficulty of demonstrating the role of PTI in plant disease resistance. It turns out that the important contribution of PTI to disease resistance is masked by pathogen virulence effectors that have evolved to suppress it.
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              Redundans: an assembly pipeline for highly heterozygous genomes

              Many genomes display high levels of heterozygosity (i.e. presence of different alleles at the same loci in homologous chromosomes), being those of hybrid organisms an extreme such case. The assembly of highly heterozygous genomes from short sequencing reads is a challenging task because it is difficult to accurately recover the different haplotypes. When confronted with highly heterozygous genomes, the standard assembly process tends to collapse homozygous regions and reports heterozygous regions in alternative contigs. The boundaries between homozygous and heterozygous regions result in multiple assembly paths that are hard to resolve, which leads to highly fragmented assemblies with a total size larger than expected. This, in turn, causes numerous problems in downstream analyses such as fragmented gene models, wrong gene copy number, or broken synteny. To circumvent these caveats we have developed a pipeline that specifically deals with the assembly of heterozygous genomes by introducing a step to recognise and selectively remove alternative heterozygous contigs. We tested our pipeline on simulated and naturally-occurring heterozygous genomes and compared its accuracy to other existing tools. Our method is freely available at https://github.com/Gabaldonlab/redundans.
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                Author and article information

                Contributors
                henri.vankruistum@wur.nl
                joost.vandenheuvel@wur.nl
                travis@bio.fsu.edu
                ken@kenkraaijeveld.nl
                bas.zwaan@wur.nl
                martien.groenen@wur.nl
                hendrik-jan.megens@wur.nl
                bart.pollux@wur.nl
                Journal
                BMC Evol Biol
                BMC Evol. Biol
                BMC Evolutionary Biology
                BioMed Central (London )
                1471-2148
                26 July 2019
                26 July 2019
                2019
                : 19
                : 156
                Affiliations
                [1 ]ISNI 0000 0001 0791 5666, GRID grid.4818.5, Animal Breeding and Genomics Group, , Wageningen University, ; Wageningen, The Netherlands
                [2 ]ISNI 0000 0001 0791 5666, GRID grid.4818.5, Experimental Zoology Group, , Wageningen University, ; Wageningen, The Netherlands
                [3 ]ISNI 0000 0001 0791 5666, GRID grid.4818.5, Plant Sciences Group, Laboratory of Genetics, , Wageningen University, ; Wageningen, The Netherlands
                [4 ]ISNI 0000 0004 0472 0419, GRID grid.255986.5, Department of Biological Science, , Florida State University, ; Tallahassee, USA
                [5 ]ISNI 0000000084992262, GRID grid.7177.6, Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, ; Amsterdam, The Netherlands
                [6 ]ISNI 0000000089452978, GRID grid.10419.3d, Leiden Genome Technology Center Department of Human Genetics, , Leiden University Medical Center, ; Leiden, The Netherlands
                Author information
                http://orcid.org/0000-0002-5672-9760
                Article
                1484
                10.1186/s12862-019-1484-2
                6660938
                31349784
                8c57954f-7a96-4b57-9521-c9209bca420c
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 31 October 2018
                : 19 July 2019
                Funding
                Funded by: WIAS, WUR
                Funded by: European Union grants Network of Excellence LifeSpan FP6
                Award ID: 036894
                Funded by: IDEAL FP7
                Award ID: 259679
                Award Recipient :
                Funded by: PE & RC research grant
                Funded by: VIDI grant
                Award ID: 864.14.008
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Evolutionary Biology
                heterandria formosa,poeciliidae,placenta,matrotrophy,positive selection,gene duplication,molecular evolution,whole genome sequencing

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