Propagation of seminal toxins through binary expression gene drives could suppress populations
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Final Published Version
Affiliation
Department of Entomology, University of ArizonaBIO5 Institute, University of Arizona
Department of Ecology and Evolutionary Biology, University of Arizona
Issue Date
2022
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Nature ResearchCitation
Hurtado, J., Revale, S., & Matzkin, L. M. (2022). Propagation of seminal toxins through binary expression gene drives could suppress populations. Scientific Reports.Journal
Scientific ReportsRights
Copyright © The Author(s) 2022. This article is licensed under a Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Gene drives can be highly effective in controlling a target population by disrupting a female fertility gene. To spread across a population, these drives require that disrupted alleles be largely recessive so as not to impose too high of a fitness penalty. We argue that this restriction may be relaxed by using a double gene drive design to spread a split binary expression system. One drive carries a dominant lethal/toxic effector alone and the other a transactivator factor, without which the effector will not act. Only after the drives reach sufficiently high frequencies would individuals have the chance to inherit both system components and the effector be expressed. We explore through mathematical modeling the potential of this design to spread dominant lethal/toxic alleles and suppress populations. We show that this system could be implemented to spread engineered seminal proteins designed to kill females, making it highly effective against polyandrous populations. © 2022, The Author(s).Note
Open access journalISSN
2045-2322PubMed ID
35428855Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1038/s41598-022-10327-4
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Except where otherwise noted, this item's license is described as Copyright © The Author(s) 2022. This article is licensed under a Creative Commons Attribution 4.0 International License.
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