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Dynamics of sex-biased gene expression over development in the stick insect Timema californicumuse asterix (*) to get italics
Jelisaveta Djordjevic, Zoé Dumas, Marc Robinson-Rechavi, Tanja Schwander, Darren James ParkerPlease use the format "First name initials family name" as in "Marie S. Curie, Niels H. D. Bohr, Albert Einstein, John R. R. Tolkien, Donna T. Strickland"
2021
<p style="text-align: justify;">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 (<em>Timema californicum</em>): 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 femalebiased at later stages, suggesting their importance in sexual differentiation. Additionally, we compared the dynamics of sex-biased gene expression during development in <em>T. californicum</em> to those of the holometabolous fly <em>Drosophila melanogaster</em> 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 <em>T. californicum</em>), 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.</p>
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA678950/You should fill this box only if you chose 'All or part of the results presented in this preprint are based on data'. URL must start with http:// or https://
https://doi.org/10.5281/zenodo.5639300You should fill this box only if you chose 'Scripts were used to obtain or analyze the results'. URL must start with http:// or https://
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Timema, sex-biased gene expression, development, Drosophila
NonePlease indicate the methods that may require specialised expertise during the peer review process (use a comma to separate various required expertises).
Evo-Devo, Evolutionary Dynamics, Evolutionary Ecology, Expression Studies, Genotype-Phenotype, Molecular Evolution, Reproduction and Sex, Sexual Selection
e.g. John Doe john@doe.com
No need for them to be recommenders of PCIEvolBiol. Please do not suggest reviewers for whom there might be a conflict of interest. Reviewers are not allowed to review preprints written by close colleagues (with whom they have published in the last four years, with whom they have received joint funding in the last four years, or with whom they are currently writing a manuscript, or submitting a grant proposal), or by family members, friends, or anyone for whom bias might affect the nature of the review - see the code of conduct
e.g. John Doe john@doe.com
2021-04-22 17:36:32
Nadia Aubin-Horth