Nature Ecology & Evolution· 2026Q1
Maternal inheritance accelerates sex chromosome degeneration and mitonuclear coevolution in a brood parasitic bird
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- 2026year
Short summary
Brood parasitic cuckoo finches with maternally inherited egg coloration show accelerated degeneration of their W sex chromosome and faster evolution of oxidative phosphorylation (OXPHOS) genes compared to related species.
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Key points
- Cuckoo finches with maternally inherited egg coloration exhibit accelerated W chromosome pseudogenization and gene loss.
- Rates of amino acid substitution are higher in both mitochondrial and nuclear-encoded OXPHOS genes.
- Acceleration in nuclear-encoded OXPHOS genes is proportional to their proximity to mtDNA-encoded residues.
- This links ecological selection on maternally inherited traits to sex chromosome degeneration and mitonuclear coevolution.
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract The coevolution of interacting mitochondrial and nuclear genes involved in the oxidative phosphorylation (OXPHOS) pathway has received growing attention as a critical component of organismal fitness1 and potential source of genetic incompatibilities2–4 that promote speciation5–7. However, in species with “ZW” sex chromosomes, the mitochondrial genome and female-specific W chromosome are effectively linked by their shared matrilineal history, such that selection on either should subject both to the accumulation of deleterious mutations via genetic hitchhiking8,9. Thus, enhanced ecological selection on maternally inherited traits should accelerate both W chromosome degeneration and mitonuclear coevolution, though this prediction has not been tested empirically. Here we show that brood parasitic cuckoo finches Anomalospiza imberbis, in which mimetic egg coloration is maternally inherited, have experienced accelerated W chromosome pseudogenization and gene loss in addition to higher rates of amino acid substitution in both their mitochondrial and nuclear-encoded OXPHOS genes. Using a structural model of respiratory complex I, we also show that the degree of acceleration in nuclear-encoded residues is a function of their proximity to mtDNA-encoded residues, providing strong evidence of compensatory mitonuclear coevolution. Our results link ecological coevolution at the species level to both sex chromosome degeneration and mitonuclear coevolution, highlighting genomic consequences of selection on non-recombining genome components.
The authors' abstract, as published at the source. Nature Ecology & Evolution, 2026 · DOI ↗
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Field: Genetics (Biochemistry, Genetics and Molecular Biology)
GeneticsBiochemistry, Genetics and Molecular Biology