High resolution genomes of multiple Xiphophorus species provide new insights into microevolution, hybrid incompatibility, and epistasis

  1. Wesley C. Warren2
  1. 1The Xiphophorus Genetic Stock Center, Texas State University, San Marcos, Texas 78666, USA;
  2. 2Department of Animal Sciences, Department of Surgery, Institute for Data Science and Informatics, University of Missouri, Bond Life Sciences Center, Columbia, Missouri 65201, USA;
  3. 3Biochemistry and Cell Biology, Biozentrum, University of Würzburg, 97074 Würzburg, Germany;
  4. 4Institut de Génomique Fonctionnelle de Lyon, Ecole Normale Supérieure de Lyon, CNRS UMR 5242, Université Claude Bernard Lyon 1, F-69364 Lyon, France;
  5. 5Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;
  6. 6McDonnell Genome Institute, Washington University, St. Louis, Missouri 63108, USA;
  7. 7Department of Life Sciences, Texas A&M University, Corpus Christi, Texas 78412, USA;
  8. 8Developmental Biochemistry, Biozentrum, University of Würzburg, 97074 Würzburg, Germany
  1. 9 These authors contributed equally to this work.

  • Corresponding authors: y_l54{at}txstate.edu, phch1{at}biozentrum.uni-wuerzburg.de, warrenwc{at}missouri.edu
  • Abstract

    Because of diverged adaptative phenotypes, fish species of the genus Xiphophorus have contributed to a wide range of research for a century. Existing Xiphophorus genome assemblies are not at the chromosomal level and are prone to sequence gaps, thus hindering advancement of the intra- and inter-species differences for evolutionary, comparative, and translational biomedical studies. Herein, we assembled high-quality chromosome-level genome assemblies for three distantly related Xiphophorus species, namely, X. maculatus, X. couchianus, and X. hellerii. Our overall goal is to precisely assess microevolutionary processes in the clade to ascertain molecular events that led to the divergence of the Xiphophorus species and to progress understanding of genetic incompatibility to disease. In particular, we measured intra- and inter-species divergence and assessed gene expression dysregulation in reciprocal interspecies hybrids among the three species. We found expanded gene families and positively selected genes associated with live bearing, a special mode of reproduction. We also found positively selected gene families are significantly enriched in nonpolymorphic transposable elements, suggesting the dispersal of these nonpolymorphic transposable elements has accompanied the evolution of the genes, possibly by incorporating new regulatory elements in support of the Britten–Davidson hypothesis. We characterized inter-specific polymorphisms, structural variants, and polymorphic transposable element insertions and assessed their association to interspecies hybridization-induced gene expression dysregulation related to specific disease states in humans.

    Footnotes

    • Received October 25, 2022.
    • Accepted March 29, 2023.

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