A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Mitonuclear interactions impact aerobic metabolism in hybrids and may explain mitonuclear discordance in young, naturally hybridizing bird lineages
Tekijät: McDiarmid, Callum S.; Hooper, Daniel M.; Stier, Antoine; Griffith, Simon C.
Kustantaja: Wiley-Blackwell
Julkaisuvuosi: 2024
Journal: Molecular Ecology
Tietokannassa oleva lehden nimi: Molecular ecology
Lehden akronyymi: Mol Ecol
Artikkelin numero: e17374
Vuosikerta: 33
Numero: 12
ISSN: 0962-1083
eISSN: 1365-294X
DOI: https://doi.org/10.1111/mec.17374
Verkko-osoite: https://onlinelibrary.wiley.com/doi/10.1111/mec.17374
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/393540554
Understanding genetic incompatibilities and genetic introgression between incipient species are major goals in evolutionary biology. Mitochondrial genes evolve rapidly and exist in dense gene networks with coevolved nuclear genes, suggesting that mitochondrial respiration may be particularly susceptible to disruption in hybrid organisms. Mitonuclear interactions have been demonstrated to contribute to hybrid dysfunction between deeply divergent taxa crossed in the laboratory, but there are few empirical examples of mitonuclear interactions between younger lineages that naturally hybridize. Here, we use controlled hybrid crosses and high-resolution respirometry to provide the first experimental evidence in a bird that inter-lineage mitonuclear interactions impact mitochondrial aerobic metabolism. Specifically, respiration capacity of the two mitodiscordant backcrosses (with mismatched mitonuclear combinations) differs from one another, although they do not differ significantly from the parental groups or mitoconcordant backcrosses as we would expect of mitonuclear disruptions. In the wild hybrid zone between these subspecies, the mitochondrial cline centre is shifted west of the nuclear cline centre, which is consistent with the direction of our experimental results. Our results therefore demonstrate asymmetric mitonuclear interactions that impact the capacity of cellular mitochondrial respiration and may help to explain the geographic discordance between mitochondrial and nuclear genomes observed in the wild.
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This work was supported by an Australian Research Council (ARC) Discovery Project to SCG and DMH (DP180101783), and a Holsworth Wildlife Research Endowment from Equity Trustees Charitable Foundation and the Ecological Society of Australia and a Macquarie University Research Excellence Scholarship to CSM. AS was supported by a ‘Turku Collegium for Science and Medicine’ Fellowship and a Marie Sklodowska-Curie Postdoctoral Fellowship (#894963). Gerstner Scholars Fellowship and the Gerstner Family Foundation, and the Richard Gilder Graduate School at the American Museum of Natural History provided support to DMH.
