A male-biased sex-distorter gene drive for the human malaria vector Anopheles gambiae.
Alekos SimoniAndrew M HammondAndrea K BeaghtonRoberto GaliziChrysanthi TaxiarchiKyros KyrouDario MeacciMatthew GribbleGiulia MorselliAustin BurtTony NolanAndrea CrisantiPublished in: Nature biotechnology (2020)
Only female insects transmit diseases such as malaria, dengue and Zika; therefore, control methods that bias the sex ratio of insect offspring have long been sought. Genetic elements such as sex-chromosome drives can distort sex ratios to produce unisex populations that eventually collapse, but the underlying molecular mechanisms are unknown. We report a male-biased sex-distorter gene drive (SDGD) in the human malaria vector Anopheles gambiae. We induced super-Mendelian inheritance of the X-chromosome-shredding I-PpoI nuclease by coupling this to a CRISPR-based gene drive inserted into a conserved sequence of the doublesex (dsx) gene. In modeling of invasion dynamics, SDGD was predicted to have a quicker impact on female mosquito populations than previously developed gene drives targeting female fertility. The SDGD at the dsx locus led to a male-only population from a 2.5% starting allelic frequency in 10-14 generations, with population collapse and no selection for resistance. Our results support the use of SDGD for malaria vector control.
Keyphrases
- copy number
- genome wide
- aedes aegypti
- mitochondrial dna
- plasmodium falciparum
- endothelial cells
- zika virus
- genome wide identification
- dengue virus
- transcription factor
- type diabetes
- drug delivery
- metabolic syndrome
- cancer therapy
- adipose tissue
- crispr cas
- skeletal muscle
- young adults
- dna binding
- insulin resistance
- pluripotent stem cells