Mitonuclear interactions impact aerobic metabolism in hybrids and may explain mitonuclear discordance in young, naturally hybridizing bird lineages

Author:

McDiarmid Callum S.1ORCID,Hooper Daniel M.2ORCID,Stier Antoine34ORCID,Griffith Simon C.1ORCID

Affiliation:

1. School of Natural Sciences Macquarie University Sydney New South Wales Australia

2. Institute for Comparative Genomics and Richard Gilder Graduate School American Museum of Natural History New York New York USA

3. Department of Biology University of Turku Turku Finland

4. Institut Pluridisciplinaire Hubert Curien, UMR7178 Université de Strasbourg, CNRS Strasbourg France

Abstract

AbstractUnderstanding 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.

Funder

H2020 Marie Skłodowska-Curie Actions

Australian Research Council

Gerstner Family Foundation

Holsworth Wildlife Research Endowment

Publisher

Wiley

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