Abstract
The CRISPR/Cas9 system is the most straightforward genome-editing technology to date, enabling genetic engineering in many insects, including the black soldier fly, Hermetia illucens. The white gene plays a significant role in the multifarious life activities of insects, especially the pigmentation of the eyes. In this study, the white gene of H. illucens (Hiwhite) was cloned, identified, and bioinformatically analysed for the first time. Using quantitative real-time polymerase chain reaction (qPCR), we found that the white gene was expressed in the whole body of the adult flies, particularly in Malpighian tubules and compound eyes. Furthermore, we utilised CRISPR/Cas9-mediated genome-editing technology to successfully generate heritable Hiwhite mutants using two single guide RNAs. During Hiwhite genome editing, we determined the timing, method, and needle-pulling parameters for embryo microinjection by observing early embryonic developmental features. We used the CasOT program to obtain highly specific guide RNAs (gRNAs) at the genome-wide level. According to the phenotypes of Hiwhite knockout strains, the pigmentation of larval stemmata, imaginal compound eyes, and ocelli differed from those of the wild type. These phenotypes were similar to those observed in other insects harbouring white gene mutations. In conclusion, our results described a detailed white genome editing process in black soldier flies, which lays a solid foundation for intensive research on the pigmentation pathway of the eyes and provides a methodological basis for further genome engineering applications in black soldier flies.
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Acknowledgements
We are grateful to Lingling Zhang of the Nankai University Public Experimentation Platform for helping us pull the microinjection needle.
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This work was supported by the National Natural Science Foundation of China (grant numbers 31830084, 31970440).
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Sui, Z., Wu, Q., Geng, J. et al. CRISPR/Cas9-mediated efficient white genome editing in the black soldier fly Hermetia illucens. Mol Genet Genomics 299, 5 (2024). https://doi.org/10.1007/s00438-023-02088-0
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DOI: https://doi.org/10.1007/s00438-023-02088-0