It is found that using more than one gRNA reduced the efficiency of inheritance, especially in females, and this results show that gene drive performance depends strongly on biological context and design choices, and that strategies must be carefully optimized in the target species.
Abstract
Drosophila suzukii (Matsumura, 1931, Diptera: Drosophilidae) is a globally invasive pest of soft-skinned fruits that is currently controlled largely through the use of broad-spectrum insecticides. Increasing resistance to insecticides and regulatory pressures have motivated the development of genetic control strategies. We previously developed a CRISPR/Cas9-based homing gene drive targeting the coding sequence of the female-specific exon of the sex-determination gene doublesex, achieving highly efficient inheritance (94–99%) in both male and female germlines. A major limitation of homing gene drives is the formation of resistant alleles that evade cleavage yet retain gene function. Multiplexing guide RNAs (gRNAs) could reduce the formation of such functional resistance alleles. Here, we generated and tested homing constructs expressing one, two, or three gRNAs targeting different regions of the female-specific exon of doublesex, including the intron-exon splice junction. A single gRNA targeting the splice junction supported high inheritance in males but showed reduced efficiency in females. Combining this gRNA with a coding sequence-targeting guide further reduced drive efficiency, particularly in the female germline. Constructs expressing two gRNAs performed similarly whether guides were linked by transfer RNA (tRNA) sequences or expressed from independent promoters. Constructs expressing three gRNAs using tRNA processing showed consistently low drive inheritance in both sexes and low frequencies of target-site modification among non-drive progeny, consistent with reduced cleavage activity. Inheritance was significantly higher in male than female germlines for several constructs, indicating that germline context strongly influences drive performance. Our findings show that the strategy used for multi-gRNA expression, target site choice and sex-specific germline environments can influence gene drive efficiency, emphasizing the need to optimize construct design in the target species. Author Summary Spotted wing drosophila (Drosophila suzukii) is an invasive pest that damages soft skinned fruits such as berries and cherries. Control currently relies heavily on insecticides, but resistance and regulatory concerns are increasing the need for alternative approaches. We are developing genetic strategies for suppression of pest populations. We previously developed a gene editing system targeting a female-essential gene that showed very high biased inheritance (gene drive). However, a key challenge is that the system can sometimes create resistant individuals that are unaffected. One possible solution is to use using multiple gRNAs—molecules that direct gene editing to specific DNA sequences—to reduce the formation of these resistant individuals. In this study we found that using more than one gRNA reduced the efficiency of inheritance, especially in females. However, activity could be influenced by exactly where the DNA is targeted and how the guide RNAs are expressed. These results show that gene drive performance depends strongly on biological context and design choices, and that strategies must be carefully optimized in the target species.
It is indicated that higher drive conversion is associated with elevated expression of the promoter-associated gene in reproductive cells, but embryo resistance allele formation correlates with excessive female germline expression, and optimal drive performance requires restricting Cas9 expression to a tight quantitative and spatiotemporal window.
Ying Wu, Yunchen Xia, Ziyin Yao et al.· Nature Communications· 0 citations
This work develops a plasmid-based reporter system in budding yeast for the rapid identification of high-performing gRNAs in budding yeast and introduces BITREx 2.0, a dual-nicking strategy that targets both sides of the gene array.
Simple Summary The CRISPR-Cas9 and CRISPR-Cas12 systems recognize target DNA through base pairing with their guide RNAs, revolutionarily simplifying the design of DNA endonucleases with novel target-sequence specificity for genome editing and gene therapy, compared with endonucleases that rely on protein-based target recognition. The OMEGA (Obligate Mobile Element-Guided Activity) system, considered a precursor to Cas12, and likely to Cas9, in the CRISPR-Cas system, is widely present in the three domains of life as an auxiliary component of transposons. Recent studies have shown that the OMEGA system cleaves the site from which a transposon was excised, thereby inducing transposon restoration via gene conversion. It is now evident that the OMEGA system acts selfishly as a homing endonuclease. This article will focus on the selfish behavior of classical homing endonucleases and the OMEGA system, and discuss how it has evolved, been maintained, and adapted to new genomic environments.
This chapter outlines a comprehensive methodology for the design, assembly, and functional assessment of CRISPR/dCas9 systems optimized for tomato to investigate pathogen-associated responses.
Ananya Mukherjee, Shrabani Basak, Raghuvir Singh et al.· Methods in molecular biology· 0 citations
Insecticide resistance in mosquito vectors and antimalarial drug resistance in parasites threaten progress towards malaria elimination, prompting the development of alternative control strategies such as CRISPR-Cas9 gene drives. The sex determination gene femaleless (fle, AGAP013051), which is required for female development in Anopheles gambiae, is a promising target for population-suppression approaches aimed at disrupting female-specific genes that affect fertility or viability. However, its functions beyond sex determination remain unknown. Here, we engineered homing gene drives targeting fle and employed germline promoters with distinct temporal expression profiles, early-acting zero population growth (zpg, AGAP006241) and late-acting sporulation defective 11 (spo11, AGAP010898), to modulate Cas9 activity. The zpg-driven system achieved up to 98% transmission through males but caused complete sterility in hemizygous females due to early biallelic disruption of fle during germline development. Delaying cas9 expression with the spo11 promoter partially restored female fertility, although female transmission remained close to Mendelian levels (59%). These results reveal an essential role for fle in female gametogenesis in addition to its established function in sex determination. Population modelling predicts that releasing zpg-drive males at 16.9% of the wild-type male population could reduce female abundance by 95% within 36 generations. Collectively, our findings reveal a previously unrecognised reproductive function of fle that limits gene-drive spread and provide important insights for the design of vector-control strategies targeting genes with essential germline functions.
B. Fasulo, W. Garrood, J. Philpott et al.· bioRxiv· 0 citations
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