| Literature DB >> 30086302 |
Ching-Jung Lin1, Fuqu Hu2, Raphaelle Dubruille3, Jeffrey Vedanayagam2, Jiayu Wen2, Peter Smibert2, Benjamin Loppin3, Eric C Lai4.
Abstract
Intragenomic conflicts are fueled by rapidly evolving selfish genetic elements, which induce selective pressures to innovate opposing repressive mechanisms. This is patently manifest in sex-ratio (SR) meiotic drive systems, in which distorter and suppressor factors bias and restore equal transmission of X and Y sperm. Here, we reveal that multiple SR suppressors in Drosophila simulans (Nmy and Tmy) encode related hairpin RNAs (hpRNAs), which generate endo-siRNAs that repress the paralogous distorters Dox and MDox. All components in this drive network are recently evolved and largely testis restricted. To connect SR hpRNA function to the RNAi pathway, we generated D. simulans null mutants of Dcr-2 and AGO2. Strikingly, these core RNAi knockouts massively derepress Dox and MDox and are in fact completely male sterile and exhibit highly defective spermatogenesis. Altogether, our data reveal how the adaptive capacity of hpRNAs is critically deployed to restrict selfish gonadal genetic systems that can exterminate a species.Entities:
Keywords: Drosophila simulans; RNAi; hpRNA; intragenomic conflict; sex ratio; siRNA; spermatogenesis
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Year: 2018 PMID: 30086302 PMCID: PMC6114144 DOI: 10.1016/j.devcel.2018.07.004
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270