Stabilizing selection on microsatellite allele length at arginine vasopressin 1a receptor and oxytocin receptor loci
Watts, P., Kallio, E., Koskela, E., Lonn, E., Mappes, T., & Mökkönen, M. (2017). Stabilizing selection on microsatellite allele length at arginine vasopressin 1a receptor and oxytocin receptor loci. Proceedings of the Royal Society B : Biological Sciences, 284(1869), Article 20171896. https://doi.org/10.1098/rspb.2017.1896
Julkaistu sarjassa
Proceedings of the Royal Society B : Biological SciencesPäivämäärä
2017Tekijänoikeudet
© 2017 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution
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The loci arginine vasopressin receptor 1a (avpr1a) and oxytocin receptor (oxtr) have evolutionarily conserved roles in vertebrate social and sexual behaviour. Allelic variation at a microsatellite locus in the 5′ regulatory region of these genes is associated with fitness in the bank vole Myodes glareolus. Given the low frequency of long and short alleles at these microsatellite loci in wild bank voles, we used breeding trials to determine whether selection acts against long and short alleles. Female bank voles with intermediate length avpr1a alleles had the highest probability of breeding, while male voles whose avpr1a alleles were very different in length had reduced probability of breeding. Moreover, there was a significant interaction between male and female oxtr genotypes, where potential breeding pairs with dissimilar length alleles had reduced probability of breeding. These data show how genetic variation at microsatellite loci associated with avpr1a and oxtr is associated with fitness, and highlight complex patterns of selection at these loci. More widely, these data show how stabilizing selection might act on allele length frequency distributions at gene-associated microsatellite loci.
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Royal Society PublishingISSN Hae Julkaisufoorumista
0962-8452Julkaisu tutkimustietojärjestelmässä
https://converis.jyu.fi/converis/portal/detail/Publication/27762406
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This research was supported by Biological Interactions Doctoral Programme (to E.L.), Academy of Finland (grant nos 257340, 119200, 115961, 140767 to E.K., 257729 to M.M. and 118603, 109165, 132190, 204284, 268670 to T.M.) and Center of Excellence in Evolutionary Research.Lisenssi
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