Data

Data from: A sex-linked supergene controls sperm morphology and swimming speed in a songbird

Macquarie University
Clair Bennison (Aggregated by) Jon Slate (Aggregated by) Kang - Wook Kim (Aggregated by) Laura L. Hurley (Aggregated by) Lola Brookes (Aggregated by)
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.5061/dryad.p4238&rft.title=Data from: A sex-linked supergene controls sperm morphology and swimming speed in a songbird&rft.identifier=10.5061/dryad.p4238&rft.publisher=Macquarie University&rft.description=Sperm are perhaps the most diverse cells in the animal kingdom, with enormous morphological variation between taxa, between species, between males and within an ejaculate. Considerable interest in sperm diversity has arisen following the realisation that sperm competition (post-copulatory sexual selection) is a powerful selective force in many organisms, and that sperm morphology has co-evolved with female reproductive tract morphology. However, the relationship between sperm morphology, sperm motility and fertilisation success is only partially understood. The extent to which between-male variation is heritable is largely unknown, and remarkably few studies have investigated the genetic architecture of sperm traits, especially sperm morphology. Here we use high-density genotyping and gene expression profiling to explore the considerable sperm trait variation that exists in the zebra finch Taeniopygia guttata. We show that nearly all of the genetic variation in sperm morphology is caused by an inversion polymorphism on the Z chromosome acting as a ‘supergene’. These results provide a striking example of two evolutionary genetic predictions. First, that in species where females are the heterogametic sex, genetic variation affecting sexually dimorphic traits will accumulate on the Z chromosome. Second, recombination suppression at the inversion allows beneficial dominant alleles to become fixed on whichever haplotype they first arise, without being exchanged onto other haplotypes. Finally, we show that the inversion polymorphism will be stably maintained by heterozygote advantage, because heterozygous males have the fastest and most successful sperm with no apparent fitness cost.Usage NotesData from Kim et al 2017. Nat. Eco. Evol.&rft.creator=Clair Bennison&rft.creator=Jon Slate&rft.creator=Kang - Wook Kim&rft.creator=Laura L. Hurley&rft.creator=Lola Brookes&rft.creator=Nicola Hemmings&rft.creator=Simon C. Griffith&rft.creator=Terry Burke&rft.creator=Tim R. Birkhead&rft.date=2022&rft_rights= https://creativecommons.org/publicdomain/zero/1.0/&rft_subject=Other education not elsewhere classified&rft_subject=sperm velocity&rft_subject=sperm&rft_subject=inversion&rft_subject=Taeniopygia guttata&rft_subject=sperm morphology&rft_subject=supergene&rft_subject=Balancing selection&rft_subject=fertility&rft.type=dataset&rft.language=English Access the data

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Sperm are perhaps the most diverse cells in the animal kingdom, with enormous morphological variation between taxa, between species, between males and within an ejaculate. Considerable interest in sperm diversity has arisen following the realisation that sperm competition (post-copulatory sexual selection) is a powerful selective force in many organisms, and that sperm morphology has co-evolved with female reproductive tract morphology. However, the relationship between sperm morphology, sperm motility and fertilisation success is only partially understood. The extent to which between-male variation is heritable is largely unknown, and remarkably few studies have investigated the genetic architecture of sperm traits, especially sperm morphology. Here we use high-density genotyping and gene expression profiling to explore the considerable sperm trait variation that exists in the zebra finch Taeniopygia guttata. We show that nearly all of the genetic variation in sperm morphology is caused by an inversion polymorphism on the Z chromosome acting as a ‘supergene’. These results provide a striking example of two evolutionary genetic predictions. First, that in species where females are the heterogametic sex, genetic variation affecting sexually dimorphic traits will accumulate on the Z chromosome. Second, recombination suppression at the inversion allows beneficial dominant alleles to become fixed on whichever haplotype they first arise, without being exchanged onto other haplotypes. Finally, we show that the inversion polymorphism will be stably maintained by heterozygote advantage, because heterozygous males have the fastest and most successful sperm with no apparent fitness cost.

Usage Notes


Data from Kim et al 2017. Nat. Eco. Evol.

Issued: 11 06 2022

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