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doi: 10.5061/dryad.2m6s2
In many species with internal fertilization, molecules transferred in the male ejaculate trigger and interact with physiological changes in females. It is controversial to what extent these interactions between the sexes act synergistically to mediate the female switch to a reproductive state or instead reflect sexual antagonism evolved as a byproduct of sexual selection on males. To address this question, we eliminated sexual selection by enforcing monogamy in populations of Drosophila melanogaster for 65 generations and then measured the expression of male seminal fluid protein genes and genes involved in the female response to mating. In the absence of sperm competition, male and female reproductive interests are perfectly aligned and any antagonism should be reduced by natural selection. Consistent with this idea, males from monogamous populations showed reduced expression of seminal fluid protein genes, 16% less on average than in polygamous males. Further, we identified 428 genes that responded to mating in females. After mating, females with an evolutionary history of monogamy exhibited lower relative expression of genes that were upregulated in response to mating and higher expression of genes that were downregulated—in other words, their post-mating transcriptome appeared more virgin-like. Surprisingly, these genes showed a similar pattern even before mating, suggesting that monogamous females evolved to be less poised for mating and the accompanying receipt of male seminal fluid proteins. This reduced investment by both monogamous males and females in molecules involved in postcopulatory interactions points to a pervasive role of sexual conflict in shaping these interactions.
Gene expression for 6 evolved populations x 2 sexes x 2 mating statusesThis text file contains the expression levels of 13995 genes from NimbleGen 12x135k arrays run for 6 experimentally-evolved populations. Males (virgin) and females (virgin and females) from each of the 6 populations were profiled, for 18 total transcriptional profiles.evolved_expression.txt
female post-mating response
female post-mating response
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