High resolution genomes of multiple Xiphophorus species provide new insights into microevolution, hybrid incompatibility, and epistasis
Because of diverged adaptative phenotypes, fish species of the genus have contributed to a wide range of research for a century. Existing 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 evol...
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Veröffentlicht in: | Genome research 2023-04, Vol.33 (4), p.557-571 |
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Zusammenfassung: | Because of diverged adaptative phenotypes, fish species of the genus
have contributed to a wide range of research for a century. Existing
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
species, namely,
,
, and
Our overall goal is to precisely assess microevolutionary processes in the clade to ascertain molecular events that led to the divergence of the
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. |
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ISSN: | 1088-9051 1549-5469 |
DOI: | 10.1101/gr.277434.122 |