CONDITION-DEPENDENCE OF THE SEXUALLY DIMORPHIC TRANSCRIPTOME IN DROSOPHILA MELANOGASTER
Article first published online: 6 JAN 2010
DOI: 10.1111/j.1558-5646.2009.00938.x
© 2010 The Author(s). Journal compilation © 2010 The Society for the Study of Evolution
Additional Information
How to Cite
Wyman, M. J., Agrawal, A. F. and Rowe, L. (2010), CONDITION-DEPENDENCE OF THE SEXUALLY DIMORPHIC TRANSCRIPTOME IN DROSOPHILA MELANOGASTER. Evolution, 64: 1836–1848. doi: 10.1111/j.1558-5646.2009.00938.x
Publication History
- Issue published online: 2 JUN 2010
- Article first published online: 6 JAN 2010
- Received June 22, 2009Accepted November 24, 2009
Keywords:
- Condition-dependence;
- evolutionary genomics;
- life-history evolution;
- sexual selection
Sexually dimorphic traits are by definition exaggerated in one sex, which may arise from a history of sex-specific selection—in males, females, or both. If this exaggeration comes at a cost, exaggeration is expected to be greater in higher condition individuals (condition-dependent). Although studies using small numbers of morphological traits are generally supportive, this prediction has not been examined at a larger scale. We test this prediction across the transcriptome by determining the condition-dependence of sex-biased (dimorphic) gene expression. We find that high-condition populations are more sexually dimorphic in transcription than low-condition populations. High-condition populations have more male-biased genes and more female-biased genes, and a greater degree of sexually dimorphic expression in these genes. Also, condition-dependence in male-biased genes was greater than in a set of unbiased genes. Interestingly, male-biased genes expressed in the testes were not more condition-dependent than those in the soma. By contrast, increased female-biased expression under high condition may have occurred because of the greater contribution of the ovary-specific transcripts to the entire mRNA pool. We did not find any genomic signatures distinguishing the condition-dependent sex-biased genes. The degree of condition-dependent sexual dimorphism (CDSD) did not differ between the autosomes and the X chromosome. There was only weak evidence that rates of evolution correlated with CDSD. We suggest that the sensitivity of both female-biased genes and male-biased genes to condition may be akin to the overall heightened sensitivity to condition that life-history and sexually selected traits tend to exhibit. Our results demonstrate that through condition-dependence, early life experience has dramatic effects on sexual dimorphism in the adult transcriptome.

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