Germline Cas9 promoters with improved performance for homing gene drive

Du, J., Chen, W., Jia, X. et al.,  Nature Communications,  15:4560. 2024.

Gene drive systems could be a viable strategy to prevent pathogen transmission or suppress vector populations by propagating drive alleles with super-Mendelian inheritance. CRISPR-based homing gene drives convert wild type alleles into drive alleles in heterozygotes with Cas9 and gRNA. It is thus desirable to identify Cas9 promoters that yield high drive conversion rates, minimize the formation rate of resistance alleles in both the germline and the early embryo, and limit somatic Cas9 expression. In Drosophila, the nanos promoter avoids leaky somatic expression, but at the cost of high embryo resistance from maternally deposited Cas9. To improve drive efficiency, we test eleven Drosophila melanogaster germline promoters. Some achieve higher drive conversion efficiency with minimal embryo resistance, but none completely avoid somatic expression. However, such somatic expression often does not carry detectable fitness costs for a rescue homing drive targeting a haplolethal gene, suggesting somatic drive conversion. Supporting a 4-gRNA suppression drive, one promoter leads to a low drive equilibrium frequency due to fitness costs from somatic expression, but the other outperforms nanos, resulting in successful suppression of the cage population. Overall, these Cas9 promoters hold advantages for homing drives in Drosophila species and may possess valuable homologs in other organisms.

More related to this:

Use of Insect Promoters in Genetic Engineering to Control Mosquito-Borne Diseases

Efficient somatic and germline genome engineering of Bactrocera dorsalis by the CRISPR/Cas9 system

CopyCatchers are versatile active genetic elements that detect and quantify inter-homolog somatic gene conversion

Toward a CRISPR-Cas9-Based Gene Drive in the Diamondback Moth Plutella xylostella

Meiotic Cas9 expression mediates gene conversion in the male and female mouse germline