Disassortative mating is a powerful mechanism stabilizing polymorphisms at sex chromosomes and other supergenes. The Alpine silver ant, Formica selysi, has two forms of social organization-single-queen and multiple-queen colonies-determined by alternate haplotypes at a large supergene. Here, we explore whether mate preference contributes to the maintenance of the genetic polymorphism at the social supergene. With mate choice experiments, we found that females and males mated randomly with respect to social form. Moreover, queens were able to produce offspring irrespective of whether they had mated with a male from the same or the alternative social form. Yet, females originating from single-queen colonies were more fertile, suggesting that they may be more successful at independent colony founding.We conclude that the pattern of asymmetric assortative mating documented from mature F. selysi colonies in the field is not caused by mate preferences or major genetic incompatibilities between social forms. More generally, we found no evidence that disassortative mate preference contributes to the maintenance of polymorphism at this supergene controlling ant social organization. K E Y W O R D Sants, disassortative mating, Formica selysi, genetic incompatibilities, mate preference, social polymorphism, supergene How to cite this article: Avril A, Zahnd S, Djordjevic J, Chapuisat M. No mate preference associated with the supergene controlling social organization in Alpine silver ants.
Sexually dimorphic phenotypes are thought to arise primarily from sex-biased gene expression during development. Major changes in developmental strategies, such as the shift from hemimetabolous to holometabolous development, are therefore expected to have profound consequences for the dynamics of sex-biased gene expression. However, no studies have previously examined sex-biased gene expression during development in hemimetabolous insects, precluding comparisons between developmental strategies. Here we characterized sex-biased gene expression at three developmental stages in a hemimetabolous stick insect (Timema californicum): hatchlings, juveniles, and adults. As expected, the proportion of sex-biased genes gradually increased during development, mirroring the gradual increase of phenotypic sexual dimorphism. Sex-biased genes identified at early developmental stages were generally consistently male- or female-biased at later stages, suggesting their importance in sexual differentiation. Additionally, we compared the dynamics of sex-biased gene expression during development in T. californicum to those of the holometabolous fly Drosophila melanogaster by reanalyzing publicly available RNA-seq data from third instar larval, pupal and adult stages. In D. melanogaster, 84% of genes were sex-biased at the adult stage (compared to only 20% in T. californicum), and sex-biased gene expression increased abruptly at the adult stage when morphological sexual dimorphism is manifested. Our findings are consistent with the prediction that the dynamics of sex-biased gene expression during development differ extensively between holometabolous and hemimetabolous insect species.
Most animals use olfaction to obtain important information from the environment, including the presence of food or mates. Insects detect odorants through receptors that are expressed in the sensory neurons of the olfactory sensilla, which cover the surface of the antennae. The olfactory capacities of an insect thus depend largely on the repertoire of the odorant receptors. Here, we study the repertoire of olfactory proteins in the stick insect Timema cristinae. We first generate transcriptomes from the antennae of adult males and females and identify, via homology searches, putative olfactory proteins of three different families: odorant binding proteins, odorant receptors, and chemosensory proteins (CSPs). We then attempt to categorize olfactory proteins likely involved in sexual communication by comparing gene expression between adults and juveniles, as well as between males and females. Notably, the olfactory proteins involved in the perception of food or abiotic environmental components, should be expressed in both adults and juveniles. By contrast, the olfactory proteins involved in sexual communication, such as the detection of sex pheromones, should be expressed in adults and often comprise different repertoires in males and females. Finally, we also tested whether olfactory proteins in general and the subset, with putative roles in sexual communication in particular, are under relaxed selection in the asexual species T. monikensis, a close relative of T. cristinae. We found that olfactory proteins are typically differentially expressed between juveniles and adults, but there is little overlap of differential expression between developmental stages and the level of sex bias in adults. Furthermore, while we find evidence that olfactory proteins are indeed under relaxed selection in the asexual species, there is no evidence that this is necessarily the case for olfactory genes with a putative role in sexual communication. Nevertheless, the list of olfactory genes generated in our study provides a useful tool for future studies on olfaction in Timema and other stick insects.
Sexually dimorphic phenotypes are thought to arise primarily from sex-biased gene expression during development. Major changes in developmental strategies, such as the shift from hemimetabolous to holometabolous development, are therefore expected to have profound consequences for the dynamics of sex-biased gene expression. However, no studies have previously examined sex-biased gene expression over development in hemimetabolous insects, precluding comparisons between developmental strategies. Here we characterized sex-biased gene expression at three developmental stages in a hemimetabolous stick insect (Timema californicum): hatchlings, juveniles, and adults. As expected, the proportion of sex-biased genes gradually increased over development. Sex-biased genes identified at early developmental stages were generally consistently male- or female-biased at later stages, suggesting their importance in sexual differentiation. We then compared the dynamics of sex-biased gene expression over development in T. californicum to those of the holometabolous fly Drosophila melanogaster by reanalyzing publicly available RNA-seq data from third instar larval, pupal and adult stages. In D. melanogaster, sex-biased gene expression increases abruptly at the adult stage when morphological sexual dimorphism is manifested. This supports the prediction that sex-biased gene expression mirrors phenotypic sexual dimorphism. Our study details for the first time the dynamics of sex-biased gene expression over development in a hemimetabolous insect and suggests that these dynamics differ extensively between holometabolous and hemimetabolous species.
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