Author
Listed:
- Michelle A. E. Anderson
(The Pirbright Institute
University of York)
- Estela Gonzalez
(The Pirbright Institute
University of York)
- Joshua X. D. Ang
(The Pirbright Institute
University of York)
- Lewis Shackleford
(The Pirbright Institute
University of York)
- Katherine Nevard
(The Pirbright Institute
University of York)
- Sebald A. N. Verkuijl
(The Pirbright Institute
University of Oxford)
- Matthew P. Edgington
(The Pirbright Institute
University of York)
- Tim Harvey-Samuel
(The Pirbright Institute)
- Luke Alphey
(The Pirbright Institute
University of York)
Abstract
CRISPR/Cas9-based homing gene drives have emerged as a potential new approach to mosquito control. While attempts have been made to develop such systems in Aedes aegypti, none have been able to match the high drive efficiency observed in Anopheles species. Here we generate Ae. aegypti transgenic lines expressing Cas9 using germline-specific regulatory elements and assess their ability to bias inheritance of an sgRNA-expressing element (kmosgRNAs). Four shu-Cas9 and one sds3-Cas9 isolines can significantly bias the inheritance of kmosgRNAs, with sds3G1-Cas9 causing the highest average inheritance of ~86% and ~94% from males and females carrying both elements outcrossed to wild-type, respectively. Our mathematical model demonstrates that sds3G1-Cas9 could enable the spread of the kmosgRNAs element to either reach a higher (by ~15 percentage point) maximum carrier frequency or to achieve similar maximum carrier frequency faster (by 12 generations) when compared to two other established split drive systems.
Suggested Citation
Michelle A. E. Anderson & Estela Gonzalez & Joshua X. D. Ang & Lewis Shackleford & Katherine Nevard & Sebald A. N. Verkuijl & Matthew P. Edgington & Tim Harvey-Samuel & Luke Alphey, 2023.
"Closing the gap to effective gene drive in Aedes aegypti by exploiting germline regulatory elements,"
Nature Communications, Nature, vol. 14(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36029-7
DOI: 10.1038/s41467-023-36029-7
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