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Exploring the consequences of postmating-prezygotic interactions between the sexes.

ABSTRACT: The role of male-female interactions in the divergence of postmating-prezygotic reproductive traits has recently focused on sexual conflict as the selective force. While an association between mating costs and benefits suggests that antagonistic interactions may be important, a mosaic of processes may actually mediate the evolutionary dynamics of postmating-prezygotic interactions. Our study examines the ecological relevance of mating effects on females. We test this critical but often overlooked assumption in desert Drosophila, where the species' ecology provides a framework for evaluating the evolutionary implications of such mating consequences. We show that mating has a profound impact on an ecologically critical character--desiccation resistance. To explore what selective factors might underlie the observed population differences in mating effects, we test whether trends in the data match predictions based on the species' ecology. While these preliminary data are consistent with the expectation that the mating benefits are positively correlated with environmental conditions, further examination reveals an additional unanticipated association with the reproductive environment. This unexpected association challenges existing assumptions regarding the forces driving divergence of traits involved in mating.

SUBMITTER: Knowles LL

PROVIDER: S-EPMC1810077 | biostudies-literature | 2004 Aug

REPOSITORIES: biostudies-literature

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Exploring the consequences of postmating-prezygotic interactions between the sexes.

Knowles L Lacey LL Hernandez B Brodie BB Markow Therese A TA

Proceedings. Biological sciences 20040801

The role of male-female interactions in the divergence of postmating-prezygotic reproductive traits has recently focused on sexual conflict as the selective force. While an association between mating costs and benefits suggests that antagonistic interactions may be important, a mosaic of processes may actually mediate the evolutionary dynamics of postmating-prezygotic interactions. Our study examines the ecological relevance of mating effects on females. We test this critical but often overlooke ...[more]

PMID: 15504017

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Project description:In the Allonemobius socius complex of crickets, reproductive isolation is primarily accomplished via postmating prezygotic barriers. We tested seven protein-coding genes expressed in the male ejaculate for patterns of evolution consistent with a putative role as postmating prezygotic isolation genes. Our recently diverged species generally lacked sequence variation. As a result, ω-based tests were only mildly successful. Some of our genes showed evidence of elevated ω values on the internal branches of gene trees. In a couple of genes, these internal branches coincided with both species branching events of the species tree, between A. fasciatus and the other two species, and between A. socius and A. sp. nov. Tex. In comparison, more successful approaches were those that took advantage of the varying degrees of lineage sorting and allele sharing among our young species. These approaches were particularly powerful within the contact zone. Among the genes we tested we found genes with genealogies that indicated relatively advanced degrees of lineage sorting across both allopatric and contact zone alleles. Within a contact zone between two members of the species complex, only a subset of genes maintained allelic segregation despite evidence of ongoing gene flow in other genes. The overlap in these analyses was arginine kinase (AK) and apolipoprotein A-1 binding protein (APBP). These genes represent two of the first examples of sperm maturation, capacitation, and motility proteins with fixed non-synonymous substitutions between species-specific alleles that may lead to postmating prezygotic isolation. Both genes express ejaculate proteins transferred to females during copulation and were previously identified through comparative proteomics. We discuss the potential function of these genes in the context of the specific postmating prezygotic isolation phenotype among our species, namely conspecific sperm precedence and the superior ability of conspecific males to induce oviposition in females.

Dataset Information

Exploring the consequences of postmating-prezygotic interactions between the sexes.

Publications

Exploring the consequences of postmating-prezygotic interactions between the sexes.

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