Sexually Antagonistic Selection

Current understanding

Sexually antagonistic (SA) selection arises when alleles that increase fitness in one sex impose a cost on the other. One of its most consequential effects in evolutionary genetics is its potential to reshape the architecture of sex chromosomes. When SA loci reside on autosomes, natural selection can favor chromosomal fusions that bring those loci into physical linkage with the sex-determining region, because such linkage ensures that each allele is reliably transmitted to the sex it benefits. This logic extends to unusual sex-chromosome systems: in organisms with univalent sex chromosomes (YO or WO systems, where one sex carries only a single sex chromosome with no pairing partner), SA-driven fusions between autosomes and the univalent Y or W would be positively selected whenever a beneficial-to-males (or beneficial-to-females) allele exists nearby. Over time, such fusions would convert a YO or WO system into a canonical XY or ZW system, providing a mechanistic explanation for why univalent systems appear evolutionarily transitory rather than stable endpoints. This theoretical argument draws on foundational work by Charlesworth & Charlesworth (1980) and van Doorn & Kirkpatrick (2007), and is articulated in the context of broader questions about why certain sex-chromosome configurations are rarely observed across taxa (Why not Y naught 2022, Finding 1).

The implication is that SA selection functions not merely as a force maintaining sex-limited alleles within existing sex chromosomes, but also as an active driver of sex chromosome turnover — continuously remodeling the genomic regions that differentiate the sexes by pulling new autosomal segments into the sex-determining linkage group.

Supporting evidence

Contradictions / open disagreements

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