A lethal mitonuclear incompatibility in complex I of natural hybrids.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 38200310.
- Also identified by DOI 10.1038/s41586-023-06895-8 and PMC identifier 10830419.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The evolution of reproductive barriers is the first step in the formation of new species and can help us understand the diversification of life on Earth. These reproductive barriers often take the form of hybrid incompatibilities, in which alleles derived from two different species no longer interact properly in hybrids<sup>1-3</sup>. Theory predicts that hybrid incompatibilities may be more likely to arise at rapidly evolving genes<sup>4-6</sup> and that incompatibilities involving multiple genes should be common<sup>7,8</sup>, but there has been sparse empirical data to evaluate these predictions. Here we describe a mitonuclear incompatibility involving three genes whose protein products are in physical contact within respiratory complex I of naturally hybridizing swordtail fish species. Individuals homozygous for mismatched protein combinations do not complete embryonic development or die as juveniles, whereas those heterozygous for the incompatibility have reduced complex I function and unbalanced representation of parental alleles in the mitochondrial proteome. We find that the effects of different genetic interactions on survival are non-additive, highlighting subtle complexity in the genetic architecture of hybrid incompatibilities. Finally, we document the evolutionary history of the genes involved, showing signals of accelerated evolution and evidence that an incompatibility has been transferred between species via hybridization.
Medical subject headings
- Electron Transport Complex I
- Fishes
- Hybridization, Genetic
- Genes, Lethal
- Genetic Speciation
- Mitochondrial Proteins
- Cell Nucleus